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  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_010.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_002.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_004.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_012.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_008.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_001.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_011.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_003.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_005.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_006.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_009.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_007.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_006.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_004.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_007.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_009.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_002.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_003.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_008.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_001.jpg
  • By Dinesh Dubey in India A newborn baby weighing just 400 grams has survived after her premature birth and gained normalcy after completing a six-month-long clinical course, with her parents and doctors having struggled hard to keep her alive and healthy. The girl was discharged from the hospital in Udaipur on Thursday. Neonatologist Sunil Janged, who led a team of doctors and nursing staff for ensuring the girl's incredible survival, claimed that she was the smallest newborn baby to survive in India and South Asia. The last reported such survival was a baby, Rajni, weighing 450 grams, at Mohali in 2012. The girl, named Manushi by the nursing staff of Vivanta Children's Hospital, was born to a couple married for 35 years. When her mother’s blood pressure became uncontrollable halfway through her pregnancy and the ultrasonography revealed absence of blood flow to the foetus, a caesarean section was conducted on her on June 15, 2017. Baby Seeta is the smallest baby ever to survive not in India but also in South Asia. Doctors calls her "our miracle baby", saying: "She’s just fought and fought and fought against all the odds. But she’s made it." Born to a couple married for 35 years, when her blood pressure was uncontrollable halfway through her pregnancy and the ultrasonography revealed fetoplacental insufficiency [ absent blood flow to fetus. So she was taken up for emergency caesarean section on June 15,2017. Baby Seeta weighed just 400 grams and measured just 8.6 inches when she was born, her minuscule feet only slightly bigger than a fingernail. She was not breathing when she was born. But the couple decided to fight to keep her alive. “When the baby was born, we were uncertain of what could happen,” Dr Sunil Janged, Chief Neonatologist said. The baby required artificial breathing support to regularize her breathing and then she was quickly transferred to Jivanta neonatal ICU. The baby was managed & looked after at Jivanta Neonatal ICU under precise care
    MEGA144195_005.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_003.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_011.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_002.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_008.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_007.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_010.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_005.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_006.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_004.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_001.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_009.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_024.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_031.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_002.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_004.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_006.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_017.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_026.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_028.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_034.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_036.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_038.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_001.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_003.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_007.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_005.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_008.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_009.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_010.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_011.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_013.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_012.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_014.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_019.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_021.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_022.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_023.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_033.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_035.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_040.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_015.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_018.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_016.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_020.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_027.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_030.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_029.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_037.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_039.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_025.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_032.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_041.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_002.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_007.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_004.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_009.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_008.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_010.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_003.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_001.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_005.jpg
  • By Sanjay Pandey in India for MailOnline This 40-year-old gritty man not only survived 12 hours with a 5ft long and tree branch lodged in his neck and head, but also managed to travel 60km with the (wood) staff to a private hospital in Bangalore, India. Farm labourer Nanjesha HN, who hails from Amruthur in Tumkur district of south Indian state of Karnataka, had met with a road accident and got himself impaled on the branch (3cm in diameter) on December 22. The staff pierced through his neck - entering from the left of the neck and exiting on the right side behind the ear. A team of doctors from Sparsh Hospital, Yeshwantpur, successfully removed the branch and saved his life. Four months on, the patient has recovered well and is able to narrate his own story. “On December 22, I was riding a two-wheeler from my house and was heading toward Kunigal to attend the funeral of a relative. I veered to my left to avoid an oncoming truck. But I lost my balance and impaled myself on a dried up branch lying on the ground,” said Nanjesha, still struggling to speak clearly. “It pierced through my neck and emerged on the other side from behind my ear. I was bleeding profusely and had to keep my mouth wide open, gasping for breath. At that time, I didn’t know whether I would live to see the next morning. But I never gave up and kept fighting for survival,” he added. Luckily for Nanjesha, a passersby spotted him and called an ambulance. Though the vehicle reached in 20 minutes and he was taken to the nearby Kunigal government hospital, the doctors refused to take his case. “The doctor didn’t even touch me. I was still on the ambulance, so they decided to take me to another nearby hospital in Belluru Cross,” Nanjesha recalled. From there, he was taken to a private medical college where doctors administered first aid. Since the patient’s airways were obstructed, the doctors had to do a tracheostomy near his throat to provide an air passage to help him breathe. “I w
    MEGA419759_006.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_018.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_016.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_015.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_014.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_017.jpg
  • EXCLUSIVE: **WARNING CONTAINS NUDITY**Just when Egyptian woman Eman Ahmed’s drastic weight loss — from a whopping 500kg to 176kg merely in three months — and controversies around the story was making international headlines, there was another woman, pegged as of India’s heaviest, who quietly underwent a second round of barbaric surgery to lose further weight at a private hospital in Mumbai. Amita Rajani, the 44-year-old resident of Vasai, weighed around 300kg and was bed-ridden for around nine years. She lost 165kg in two years. After second operation, she has lost 10kg in one month. Doctors say she will be 70 by next April. "Bariatric surgery has given me a new lease of life," said Amita after her second surgery at Laparo Obeso Centre in Mumbai on April 02. More than a month after the second operation, she now weighs 125kg. "My life has changed drastically. Until 2015, I was confined to my bedroom for almost eight years as I could barely walk a few steps. Now, I can walk a few kilometers at a stretch, drive my car to work, go out shopping. I have literally got my life back. Now, I walk for at least 2km daily, earlier I needed help to turn from one side to another in the bed. The obesity had ruined my personal, professional and social life. Whenever I want I take out my car, go for a long drive or go meet my relatives and friends and wedding and birthday parties,” said Amita, who works as a share trader, adding that her friends have organized a reunion to celebrate her transformation. Amita’s weight gain, however, did not happen suddenly. It happened over the years. Amita was 116kg when she was in class 10. "In 2007, we consulted doctors in UK but since I was born with a single kidney, they said it would be a high-risk surgery," said the lady who once ran a small soft toy factory in the city. Until 2015, Amita needed four to five people to help her stand. "Today, I step out of home every day and my mother teases me about it.'' Amita kept gaining weight t
    MEGA173444_001.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_010.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_016.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_011.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_001.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_008.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_003.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_006.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_009.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_012.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_015.jpg
  • EXCLUSIVE: Erramatti Mangayamma, 73, was so desperate and determined to have a baby that she ‘underaged herself’ to avoid the chances of being ruled out for the IVF treatment. "She lied about her age to avail the treatment. But after fact-checking with her husband and kin, who in turn submitted her school records, we discovered that she was born on September 1, 1946. And we got to know about this after she conceived,” said Dr. S Umashankar, who headed the team of doctors at Ahalya Nursing Home in the southern Indian Andhra Pradesh state's Guntur town. The doctors told the family that they have to live in the hospital during the entire course of pregnancy. “I told her husband that I cannot let you go home as they would jeopardise our treatment plan,” said Dr Uma Shankar. 
Erramatti and her husband were fine with that arrangement. “But we didn’t know how to organise funds for such a pro-longed treatment and stay at the hospital.
It was then the hospital administration told us that we don’t need to worry about the expenses as the entire cost of treatment would be borne by the hospital trust,” said the new mother. The hospital authorities knew that they were staring at an even bigger challenge after they discovered that woman was carrying twins. It was a double whammy for the team. First the woman was 73 and not 65 as claimed by her and secondly, she had conceived twins. “We formed three teams for her. One to look at her nutrition status, second one looked at her cardiac and other health parameters and the third one looked into her pregnancy status,” said Dr Uma Shankar. So finally six-decade-long wait came to end. Mangayamma gave birth to two healthy baby girls on Sept. 5 morning. “Now, no one call me sterile. I thank god and the doctors who have this possible,” said an emotional Erramatti struggling to hold back her tears. Hailing from Nelapartipadu village in East Godavari district, Mangayamma was childless after 54 years of marriage. Sh
    MEGA497373_014.jpg
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