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  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_008.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_007.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_006.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Doctors removed as many as 115 iron nails from man's stomach at a state-run hospital in Bundi
    MEGA419313_006.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Doctors removed as many as 115 iron nails from man's stomach at a state-run hospital in Bundi
    MEGA419313_001.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Doctors removed as many as 115 iron nails from man's stomach at a state-run hospital in Bundi
    MEGA419313_007.jpg
  • November 2, 2018 - Ankara, Turkey - Turkish doctors take part in a protest against violence in healthcare in Ankara, Turkey on November 2, 2018. 'We started this watches as a part of protests in response to the Turkish government's new draft law that will leave thousands of medical workers unemployed, instead of protecting us against violence in hospitals', a doctor said to the photographer during the protest. (Credit Image: © Altan Gocher/NurPhoto via ZUMA Press)
    20181102_zaa_n230_113.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: An x-ray of Bhola Shankar's stomach shows nails accumulated inside his body at a state-run hos
    MEGA419313_002.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Family members pay a visit to Patient Bhola Shankar recovering at a state-run hospital in Bund
    MEGA419313_004.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Patient Bhola Shankar recovering after surgery in a state-run hospital in Bundi, Rajasthan, In
    MEGA419313_003.jpg
  • EXCLUSIVE: By Sudipto Maity in India An Indian man complaining of stomach ache had over 100 iron nails removed from his intestine by doctors. The operation took place on Monday in the country's north west Rajasthan state. Reports said 42-year-old Bhola Shankar had reached the government hospital in Bundi town , complaining of excruciating pain. However, it was after conducting the initial tests that doctors were left baffled. X-ray of the patient showed a cluster of a rather unusual item in the man's stomach. A CT scan confirmed the suspicion. Operating on the patient, a team of surgeons, led by Dr Anil Saini, recovered and removed at least 116 iron nails. The team also shot a video of the operation, which showed nails being extracted from the intestine of the patient. Saini said, "This is the first such case I have come across," The doctor added it may be the first time something like this took place in Rajasthan. In 2017, doctors had removed at least 150 stationary pins from a patient's stomach in the same town. "What surprised us was the length of the nails. They measured 6.5 centimetres. To have such big iron nails removed from a patient's body is unprecedented," the senior doctor added. He also called it a bizarre case. Meanwhile, doctors have deemed the patient mentally imbalanced. "The patient is not able to narrate how the nails ended up in his intestine," Saini said, adding, "He is lucky the sharp objects did not puncture his organs, else, it could have proved fatal." The patient's younger brother said the former has been taking medicine for mental illness for the last two and half decades. However, he too couldn't explain how the nails ended up there. Doctors believe the man was in the habit of swallowing sharp objects as apart from the nails, doctors also extracted metal wires. Despite the lengthy operation, the patient was recovering well. 13 May 2019 Pictured: Dr Anil Saini who operated on Bhola Shankar shows the times extracted from his patient's stoma
    MEGA419313_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_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_009.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_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_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_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_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_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_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_007.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_003.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_005.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_004.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_006.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_002.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_007.jpg
  • EXCLUSIVE: Michael Jackson’s doctor Conrad Murray is set to cause new anguish for the family of the late singer after giving a shocking new interview about the star’s father Joe Jackson. The disgraced 65-year-old medic - who was found guilty and jailed for the King of Pop’s manslaughter – has made astonishing claims about the family patriarch just over a week after his death. Jackson, who was the brains behind the Jackson 5 group, died in LA on June 27 aged 89 with his wife Katherine by his side. But just days after Joe’s death, Murray unleashed a brutal verbal attack and branded him one of the “worst father’s in history” in a video obtained by US website ‘The Blast’. In other shocking claims he also addressed allegations that pop singer Michael – who died at the age of 50 on June 25, 2009 – was chemically castrated as a child via hormone injections to delay puberty and maintain his high-pitched voice. The former doctor said in the video: “Joe Jackson was one of the worst fathers to his children in history. “The cruelty expressed by Michael that he experienced at the hands of his father, particularly the bad treatment and moreover, the fact that he was chemically castrated to maintain his high pitched voice is beyond words. “I knew and cared for Michael very well and he told me of the many sufferings at the hands of his father that he encountered. “It was dreadful and beyond imagination and words. “I would not shed a single tear for the passing of this cruel and evil man, Joe Jackson. “It is said that only the good die young. I hope Joe Jackson finds redemption in hell.” Michael Jackson was under the care of Murray at the time of his passing in 2009. The doctor was subsequently convicted of involuntary manslaughter and served two years in prison for administering the lethal dose of the powerful anesthetic, propofol, that killed the pop star. In 2010 Joe Jackson filed a wrongful death lawsuit against Murray but later dropped the
    MEGA248972_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_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_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_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_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_006.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_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_001.jpg
  • April 20, 2020, Paris, Ile-de-France (region, France: Mobile clinic of the NGO Doctors without borders (DWB). A patient takes his weight in the NGO truck during a consultation by an MSF doctor. The clinic is installed next to the Aurore association which provides packed lunches to the poor (Credit Image: © Michael Bunel/Le Pictorium Agency via ZUMA Press)
    20200420_zaa_p164_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_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_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_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_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_022.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_005.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_006.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_004.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_002.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_003.jpg
  • A urology doctor delivered a baby boy during an eight-hour Air France flight from Paris to New York. Dr Sij Hemal, 27, was moments away from enjoying a glass of champagne in first class when he had to jump into action after 41-year-old passenger Toyin Ogundipe went into labor. Dr Hemal, a second-year urology resident at Cleveland Clinic’s Glickman Urological and Kidney Institute, safely delivered the baby — who was named Jake — before tying the umbilical cord with a makeshift surgical clamp… a shoe string. By chance, Dr Hemal had been seated next to a French pediatrician Dr. Susan Shepherd, who was able to help and gave the baby boy a clean bill of health upon delivery. Dr Hemal had been on a day-long journey from New Delhi, India, when the drama unfolded, and was making his way back to the U.S. after attending his best friend’s wedding the day before. “I was pretty tired from jet lag,” Dr Hemal said. “I thought I’d just have a drink and fall asleep. As it turned out, I’m glad I didn’t drink anything.” Ms Ogundipe, a banker who resides between the UK and Nigeria, was traveling with her four-year-old daughter Amy when she suddenly went into labor about midway into the December 17 flight, just as the jet skirted the southern coast of Greenland, 35,000 feet below. An emergency landing would have required a two-hour diversion to a U.S. military base in the Azores Islands, so Dr. Hemal recommended to the pilot they continue to JFK International Airport, which was still four hours away. “Her contractions were about 10 minutes apart, so the pediatrician and I began to monitor her vital signs and keep her comfortable,” Dr Hemal explained. The doctors used instruments and supplies in the flight’s scanty medical kit to routinely check Ms Ogundipe’s vital signs, including blood pressure, oxygen rate and pulse. But within the course of an hour, Toyin’s contractions accelerated; they occurred seven, then five and finally two minutes apart. “T
    MEGA147966_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_016.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_004.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_003.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_005.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_002.jpg
  • A 75-year-old man suffering from a rare disease has grown a Hellboy-like horn on his head. Shyamal Lal Yadav, hailing from Sagar district of Madhya Pradesh in central India, suffered an injury on his head five years ago. Yadav claims that a horn-like structure started developing in the middle of his head after that. Yadav saw several doctors, but ‘all of them looked clueless’. He finally got the horn sliced with the help of a barber. “I thought to myself finally I had got good riddance from the devil’s horn. But my happiness was short-lived,” said Yadav. As feared, the horn started to grow back on his head and he was completely clueless about his next course of action Fortunately, the growth did not cause any physical discomfort or snowball into a medical issue. But, it had certainly made him a laughing stock. He was embarrassed to roam around in public with the unnatural growth on his head. “I kept doing the rounds of hospitals, but nothing happened. Then I asked my barber to cut the horn with the shaving blade. He did manage to cut it off, but the horn grew back in some time at the same spot,” said the ‘real-life Hellboy’. According to Yadav, he travelled to Bhopal (around 170km from Sagar) and Nagpur (around 388km from his home) to consult senior experts, however, had to come back as he could not afford the cost of the operation. The medical fraternity was in a tizzy as they hadn’t witnessed anything like that. His quest finally ended at a private clinic run by Dr. Vishal Gajbhiye in his home town Sagar. Dr. Gajbhiye said,” “The four-inch horn was solid and had sizable thickness.” The physician carried out a CT scan to ensure that the horn wasn’t deep enough to require the intervention of a neurosurgeon. The physician went ahead with the head surgery to remove the horn. After the horn was removed, the surgeons used the skin of Yadav’s forehead to fill up the gap through plastic surgery. Dr. Gajbhiye calls it a rare case and claimed t
    MEGA503504_001.jpg
  • Jun. 23, 2007 - Close-up of female doctor thinking at her desk.. Model and Property Released (MR&PR) (Credit Image: © Cultura/ZUMAPRESS.com)
    20070623_baf_cu5_084.jpg
  • July 13, 2017 - Thessaloniki, Thessaloniki, Greece - Anti-Juncker demonstrations. .Jean-Claude Juncker,  European Commission President, named Honorary Doctor of the Law School of the Aristotle University of Thessaloniki (AUTH) (Credit Image: © Achilleas Pagourtzis/Pacific Press via ZUMA Wire)
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  • September 6, 2017 - Biloxi, MS, USA - An ABC film crew follows Singing River Hospital's Dr. Tyler Sexton, a real life inspiration for shows like ABC's ''The Good Doctor'' to debut locally on Sept. 25. Sexton makes his rounds at the hospital's newborn nursery, while being filmed for a feature to promote the show. (Credit Image: © Karen Nelson/TNS via ZUMA Wire)
    RTI20170906_zaf_m67_059.jpg
  • April 20, 2020, Paris, Ile-de-France (region, France: Mobile clinic of the NGO Doctors without borders (DWB). The clinic is installed next to the Aurore association which provides packed lunches to the poor (Credit Image: © Michael Bunel/Le Pictorium Agency via ZUMA Press)
    20200420_zaa_p164_019.jpg
  • April 20, 2020, Paris, Ile-de-France (region, France: Mobile clinic of the NGO Doctors without borders (DWB). Under a tent set up by the NGO, a nurse finished filling out papers. The clinic is installed next to the Aurore association which provides packed lunches to the poor (Credit Image: © Michael Bunel/Le Pictorium Agency via ZUMA Press)
    20200420_zaa_p164_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_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_041.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_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_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_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_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_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_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_040.jpg
  • February 2, 2020, Zouping, Binzhou Township, Shandong Province, China: Overwhelmed with emotion, nurses hug. Hands and hugs as nurses comfort each other. They are part of a eight nurse and doctors team, taking care of patients who have new coronavirus COVID-19 pneumonia, in the isolation ward in Zouping People's Republic Hostipal with a empty bed behind them. (Credit Image: © Dong Naide/TPG via ZUMA Press)
    20200202_zaa_t49_005.jpg
  • ALL HANDS ON DECK: February 2, 2020, Zouping, Binzhou Township, Shandong Province, China: Overwhelmed with emotion, nurses hug. Hands and hugs as nurses comfort each other. They are part of a eight nurse and doctors team, taking care of patients who have new coronavirus COVID-19 pneumonia, in the isolation ward in Zouping People's Republic Hostipal. (Credit Image: © Dong Naide/TPG via ZUMA Press)
    20200202_zcc_t49_005.jpg
  • February 2, 2020, Zouping, Binzhou Township, Shandong Province, China: Overwhelmed with emotion, nurses hug. Hands and hugs as nurses comfort each other. They are part of a eight nurse and doctors team, taking care of patients who have new coronavirus COVID-19 pneumonia, in the isolation ward in Zouping People's Republic Hostipal with a empty bed behind them. (Credit Image: © Dong Naide/TPG via ZUMA Press)
    20200202_zan_z03_005.jpg
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