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  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young man being rushed on a gurney, to get help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire
    RTI20170404_zaa_d118_010.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young boy being rushed on a gurney, to get help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_011.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - Men in masks and hazmat suits push a boy to the hospital on a gurney. The young victim, was a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. Death toll at 70 and rising, many childern. The airstrikes appear to have targeted clinics treating the wounded in Khan Sheikhoun, Idhib Province it is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_012.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young man on a gurney, getting help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_007.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A baby getting help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_003.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young man getting help in a ambulance, after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_002.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young boy being rushed on a gurney, to get help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    20170404_zaa_d118_011.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A young boy being rushed on a gurney, to get help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    20170404_zaa_d118_011.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A medic helps a victim of nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances came to the border in Hatay Province, Turkey for medical evacuation of victims after the Syrian toxic gas attack, then to be brought to Turkish medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_006.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - Ambulance rushes to help victims of a deadly nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances came to the border in Hatay Province, Turkey for medical evacuation of victims after the Syrian toxic gas attack, then to be brought to Turkish medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_009.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - ACIL Emergency facility and ambulances wait for  victims of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances came to the border in Hatay Province, Turkey for medical evacuation of victims after the Syrian toxic gas attack, then to be brought to Turkish medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_005.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - Ambulances gather to help victims of a nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances came to the border in Hatay Province, Turkey for medical evacuation of victims after the Syrian toxic gas attack, then to be brought to Turkish medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    RTI20170404_zaa_d118_004.jpg
  • April 4, 2017 - Hatay, Hatay Province, Turkey - A baby getting help after being a part of a supposed nerve gas attack (possibly the powerful and lethal sarin nerve gas) in north-western Syria. First reports place the death toll at 70 to 100, many childern. Several reported that airstrikes had targeted clinics treating the wounded. Khan Sheikhoun, Idhib Province is a rebel-held town of 165,000. Around 30 Turkish ambulances gathered at the border in Hatay Province for medical evacuation of victims after the Syrian toxic gas attack, to be brought to Turkey for immediate medical aid. (Credit Image: © Ferhat Dervisoglu/Depo Photos via ZUMA Wire)
    20170404_zaa_d118_003.jpg
  • April 4, 2017 - Khan Sheikhoun, Idhib Province, Syria - Syrian Civil Defense aka the White Helmets, helping young child victim, after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defense via ZUMA Wire)
    RTI20170404_jlr_z03_005.jpg
  • April 4, 2017 - AlHabeet, Idhib Province, Syria - Children victims from a result of shelling with chemical materials of the town of AlHabeet are wrapped in a blanket. Syrian Civil Defense aka the White Helmets, helped these young victims, after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defense via ZUMA Wire)
    RTI20170404_jlr_z03_002.jpg
  • April 4, 2017 - Khan Sheikhoun, Idhib Province, Syria - Syrian Civil Defense aka the White Helmets, helping a victim, after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defense via ZUMA Wire)
    RTI20170404_jlr_z03_003.jpg
  • April 4, 2017 - AlHabeet, Idhib Province, Syria - Children victims from a result of shelling with chemical materials of the town of AlHabeet are wrapped in a blanket. Syrian Civil Defense aka the White Helmets, helped these young victims, after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defense via ZUMA Wire)
    20170404_jlr_z03_002.jpg
  • April 4, 2017 - Khan Sheikhoun, Idhib Province, Syria - Syrian Civil Defense aka the White Helmets, helping victims after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defence via ZUMA Wire).
    20170404_jlr_z03_005.jpg
  • April 4, 2017 - Khan Sheikhoun, Idhib Province, Syria - Syrian Civil Defense aka the White Helmets, helping victims after morning attack of a suspected serious lethal gas (most likely sarin nerve gas), in rebel-held Idlib Province in northwestern Syria, near Turkey (population 165,000). A score wounded and over dozen already dead, others might die shortly as a after effect of exposure to deadly gases. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Syria Civil Defense via ZUMA Wire).
    RTI20170404_jlr_z03_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_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_013.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_012.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_022.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_023.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_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_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_040.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_003.jpg
  • April 4, 2017 - Khan Sheikhoun, Syria - A young boy lying on the ground, hurt by what rescue workers described as a suspected gas attack (most likely sarin never gas), in rebel-held Idlib, Syria. Idlib is a city in northwestern Syria, capital of the Idlib Governorate, near Turkey and 59 kilometers south west of Aleppo. It has an elevation of nearly 500 meters above sea level, population around 165,000. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Edlib Media Center via ZUMA Wire)
    RTI20170404_zba_r01_644.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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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_027.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_030.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_029.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_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_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_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_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_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: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_002.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_011.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_004.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_007.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_012.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_005.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_008.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_006.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_010.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_009.jpg
  • EXCLUSIVE: By Sherbien Dacalanio in Philippines A Filipino family is desperately trying to raise funds required for separation of their conjoined twins attached at the forehead despite the risk of them dying in the operation. Chiara and Charina, 7, from Roxas in Palawan, were born with craniopagus. The conjoined wins’ struggle starts with waking up and till the time they go to sleep. In between of everything, whatever daily chores everyone does is excruciating painful and difficult for them. From bathing, to eating, while going to school, they need to manage their heads that is stuck to each other sharing an artery. Sonia Nortega, 37, the mother of twins, says: “We conducted a series of medical procedure on the twins, such as MRI and CT Scan. Much to our dislike, the reports suggest that it will be a risky affair to separate Chiara and Charina. In the arterial studies there is clear arterial crossover and sharing between the twins. In addition the venous studies show a very robust outflow circulation in the larger venous vessels. There is also very poor central deep drainage in the veins.’ “But we have decided to go ahead with the process anyway. I am well aware that during the process we might end up losing one of the twins. If one of them gets cured and starts leading a normal life, I would know the other sister’s sacrifice was worth. I am positive and believe in the miracles of science. I wishes to send my daughters to better surgeons, who can handle the risk of this case and cure her daughters. My heart says that they both would survive the operation and would be able to lead a normal life,” the said 37-year-old mother of five. The Nortegas have three other children that were born normal without any complication and lead normal life. After the doctors told the family that the separation of the twins possible is but involves a risky operation, a local charity withdraw its earlier financial support. Now, the Nortegas are finding it difficult to raise f
    MEGA191446_001.jpg
  • April 4, 2017 - Khan Sheikhoun, Syria - A victim lying on the ground, wounded and some dead, hurt and killed by what rescue workers described as a suspected gas attack (most likely sarin never gas), in rebel-held Idlib, Syria. Idlib is a city in northwestern Syria, capital of the Idlib Governorate, near Turkey and 59 kilometers south west of Aleppo. It has an elevation of nearly 500 meters above sea level, population around 165,000. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Edlib Media Center via ZUMA Wire)
    RTI20170404_zba_r01_654.jpg
  • April 4, 2017 - Khan Sheikhoun, Syria - Medics spray down a victim lying on the ground, hurt  by what rescue workers described as a suspected gas attack (most likely sarin never gas), in rebel-held Idlib, Syria. Idlib is a city in northwestern Syria, capital of the Idlib Governorate, near Turkey and 59 kilometers south west of Aleppo. It has an elevation of nearly 500 meters above sea level, population around 165,000. The inhabitants are overwhelmingly Sunni Muslims, although there is a significant Christian minority. (Credit Image: © Edlib Media Center via ZUMA Wire)
    RTI20170404_zba_r01_646.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_014.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_019.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_025.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_032.jpg
  • July 5, 2018 - London, England, United Kingdom - 10 Downing Street is pictured as the Government called for an emergency Cabinet, after Amesbury Poisoning, London on July 5, 2018. Britain is holding an emergency cabinet meeting on July 5, over a couple who were left critically ill after being exposed to the same nerve agent used on a former Russian spy earlier this year. Home Secretary Sajid Javid will be chairing the talks in London, as counter-terrorism police lead an investigation into the incident in Amesbury, a village in southwest England. (Credit Image: © Alberto Pezzali/NurPhoto via ZUMA Press)
    20180705_zaa_n230_152.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_003.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_002.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_016.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_005.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_007.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_014.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_009.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_011.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_015.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_004.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_006.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_013.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_008.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_012.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_010.jpg
  • EXCLUSIVE: **NO WEB UNTIL 6pm GMT 20th August** The world’s first transgender ref made her debut at QPR’s training ground in London. Taxi driver Lucy Clark, 46, took charge of hundreds of non-league games as Nick but revealed at the weekend how she felt trapped in a man’s body. Lucy, who has three kids, reffed QPR’s female youth team v Parkwood Ladies at the Championship side’s West London training ground. QPR’s Jess Painter said after her side’s 4-2 win: “The ref was great — one of the best we’ve ever had.” With a pink whistle and a ponytail, the arm-tattooed official formerly known as Nick booked one woman for a scything tackle in the second half during the home side's 4-2 win. Lucy was watched by supportive wife Avril from the sidelines and Kellie Moloney, the former boxing promoter called Frank who became a woman. Dressed all in black, Lucy showed no nerves officiating during the London and South East Women's Football's Premier League opening day clash. 18 Aug 2018 Pictured: Lucy Clark. Photo credit: W8Media / MEGA TheMegaAgency.com +1 888 505 6342
    MEGA264376_001.jpg
  • Jun. 07, 2010 - Young woman in modern waiting room. Model and Property Released (MR&PR) (Credit Image: © Cultura/ZUMAPRESS.com)
    20100607_baf_cu5_076.jpg
  • August 23, 2019, Madison, Illinois, USA: GRAHAM RAHAL (15) of the United States  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_102.jpg
  • August 23, 2019, Madison, Illinois, USA: ZACH VEACH (26) of the United States  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_095.jpg
  • August 23, 2019, Madison, Illinois, USA: Crewmembers of MATHEUS LEIST (4) of Novo, Hamburgo Brazil  prepare their car to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_094.jpg
  • August 23, 2019, Madison, Illinois, USA: ED CARPENTER (20) of the United States  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_097.jpg
  • August 23, 2019, Madison, Illinois, USA: SANTINO FERRUCCI (19) (R) of the United States  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_100.jpg
  • August 23, 2019, Madison, Illinois, USA: TAKUMA SATO (30) of Tokyo, Japan  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_101.jpg
  • August 23, 2019, Madison, Illinois, USA: WILL POWER (12) of Toowoomba, Australia  prepares to qualify for the Bommarito Automotive Group 500 at World Wide Technology Raceway in Madison, Illinois. (Credit Image: © Walter G Arce Sr Grindstone Medi/ASP)
    20190823_zaa_a161_103.jpg
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