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  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_004.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_005.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_006.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_002.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_008.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_003.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_007.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_009.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_011.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_012.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_010.jpg
  • EXCLUSIVE: By Dinesh Dubey in India Something that started as a small white dot in the eyeball of three-year boy six months ago, has now gone on to cover his entire left eye and put his life at risk. Keffrien Reang who hails from Dhalai district of north Indian state of Tripura, has been diagnosed with retinoblastoma, a cancer that starts in the retina, the very back part of the eye. His poor parents are unable to bear the expenses of his treatment. Sanjit Reang (35), a small-time farmer who makes around Rs 4000 every month, and finds it difficult to support a family of five - his wife and three children. The disease started with a small white dot in the eyeball some eight to nine months ago. His parents took him to local doctors and "My second son has been diagnosed with ratinoblastoma last year. I know his condition is getting worse by the day, but I am not able to do anything for him,” says Reang. Around a year ago, they spotted a small off-white spot on the eyeball. The family initially thought it is a minor problem and ignored it thinking that the spot would go away on its own. But when the problem started to get worse, they took him to the local hospital. The doctors prescribed some ointments and medicines and sent them back, assuring that the problem would be solved. As time passed by, the problem started to worsen. “It was then we decided to take him to Agartala medical hospital. The boy was then referred to the regional cancer hospital and from there the boy was referred to another facility but nobody could give a proper diagnosis," says Reang. After a month-long diagnosis, the Agartala facility referred them to Regional Cancer Hospital in the same town. From there, they referred him to Shankar Netralaya in Guwahati in the neighbouring state of Assam. In the end, doctors at Dr B Barroah Cancer Institute, Guwahati, diagnosed that the boy has a retinoblastoma in the left eye. But the family couldn’t go ahead with his treatment as they couldn’t afford
    MEGA146159_001.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_002.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_008.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_007.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_011.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_010.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_001.jpg
  • October 13, 2017 - Rome, Italy, Italy - Teachers, parents and students in front of the House of Representatives in Montecitorio to apply for the approval of the law on ius sole. Approved by the House at the end of 2015 and since then waiting to be examined in the Senate, the law extends the criteria for obtaining Italian citizenship especially to children born in Italy by foreign parents or arrived in Italy when they were small. The event was organized by the network #Italianisenzittadership and ''I'm also Italy' (Credit Image: © Patrizia Cortellessa/Pacific Press via ZUMA Wire)
    RTI20171013_zaa_p133_279.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_006.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_003.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_004.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_005.jpg
  • EXCLUSIVE: Boy with webbed fingers, toes treated like a pariah in the neighborhood and at school, poor parents pin hope on crowdfunding to get their child treated By Sanjay Pandey in India Twelve-year-old Mannu Kumar is treated like a pariah in his neighborhood and at school because of his appearance. Mannu, standard III student, cannot run around like a regular boy of his age. He can't use hands for eating or any other purpose, nor can he wear shoes or slippers. Mannu suffers from Syndactyly, a rare genetic condition, because of which his hands and feet are fused-like. The disease causes abnormal fusion of hands and feet. The rare condition only affects one in 10 lakh people. Mannu, who hails from the Koderma of the east Indian state of Jharkhand, is the eldest child of Anand Kumar, a small-time grocery shop owner, and Rani Devi, a housewife. Mannu also has one sister and the medical expenses of his condition are quite a burden on the family. His parents have spent a fortune on his treatment in the last two years. They have sold family property and jewelry to arrange funds for the boy's medication and diagnosis. Since his parents are uneducated they couldn't pick on the early signs of the disease and his diagnosis was made only this year in July. Now it is in an advanced stage and doctors have told them that it would take at least Rs 10 lakh for reconstructing Mannu’s hands and feet. Doctors informed the parents that the estimated cost of treatment, including neuro and plastic surgery procedures, would come to approximately Rs 10 lakh. Moreover, the family would have to shell out Rs 5 lakh for the treatment process to begin. Since the family has already exhausted all their resources in the last two years, on the boy's medication, they have started a fundraiser to raise money for his further treatment. His mother Devi said: ‘It is the curse of the God that my son was born like this and I am worried about his future. ‘I’m afraid he might struggle to lead a no
    MEGA177869_009.jpg
  • March 30, 2019 - Riga, Latvia, Latvia - Latvia, Riga, 30.03.2019. The second Parents 'meeting organized in Riga by the Russian Union of Latvia and the parents' Community. The purpose of the Meeting is to put forward demands to the Ministry of education to rectify the situation in the school system. (Credit Image: © Russian Look via ZUMA Wire)
    20190330_zaf_l75_002.jpg
  • March 30, 2019 - Riga, Latvia, Latvia - Latvia, Riga, 30.03.2019. The second Parents 'meeting organized in Riga by the Russian Union of Latvia and the parents' Community. The purpose of the Meeting is to put forward demands to the Ministry of education to rectify the situation in the school system..In the photo: Miroslav Mitrofanov - member of the European Parliament (Credit Image: © Russian Look via ZUMA Wire)
    20190330_zaf_l75_001.jpg
  • May 10, 2017 - Rome, Italy, Italy - Sit-in to Rome in the place where three gypsy sisters last night died in the rooftop of their camper - stationed in a car park - where they lived with their parents and other 6 brothers who were saved. In a commercial camera video camera, a man faced with an outbreak, throws an incendiary bottle against the camper. Surveys for now have not excluded any track, whether it's vengeance or racial gesture. The garrison took place in the place.Sit-in to Rome in the place where three gypsy sisters last night died in the rooftop of their camper - stationed in a car park - where they lived with their parents and other 6 brothers who were saved. In a commercial camera video camera, a man faced with an outbreak, throws an incendiary bottle against the camper. Surveys for now have not excluded any track, whether it's vengeance or racial gesture. (Credit Image: © Patrizia Cortellessa/Pacific Press via ZUMA Wire)
    RTI20170510_zaa_p133_222.jpg
  • March 28, 2019 - Srinagar, Jammu and Kashmir, India - Members of Association of Parents of Disappeared Person (APDP) are seen holding Placards during a silent protest in Srinagar..A demonstration of Association of Parents of Disappeared Persons (APDP) held in summer capital Srinagar today seeking information about their beloved ones. The APDP is demanding the setting up of a commission to probe the disappearances of people in Kashmir. According to the APDP, some 8,000 to 10,000 people have gone missing since the beginning of the Kashmir conflict in 1989. (Credit Image: © Idrees Abbas/SOPA Images via ZUMA Wire)
    20190328_zaa_s197_059.jpg
  • Former first lady Barbara Bush, wife of former President George H.W. Bush and mother of former President George W. Bush, died Tuesday at her home in Houston. She was 92. Barbara Bush had been in failing health, suffering from congestive heart failure and chronic obstructive pulmonary disease. George and Barbara, who celebrated their 73rd wedding anniversary on Jan. 6, hold the record for the longest-married presidential pair. Mrs. Bush was known for her wit and emphasis on family. One of her primary causes was literacy. She founded the Barbara Bush Foundation for Family Literacy in 1989 to carry forth her legacy in the cause for literacy. PICTURED: Oct. 16, 1991 - Florissant, Missouri, U.S. - US First Lady BARBARA BUSH reads ''Brown Bear Brown Bear'' to the children with Missouri Governor JOHN ASHCROFT at a ''Parents as Teachers'' parent and child group at the Ferguson-Florissant School District October 16, 1991 in Florissant, Missouri. (Credit Image: © White House/Planet Pix via ZUMA Wire)
    19911016_zaa_p138_001.jpg
  • Former first lady Barbara Bush, wife of former President George H.W. Bush and mother of former President George W. Bush, died Tuesday at her home in Houston. She was 92. Barbara Bush had been in failing health, suffering from congestive heart failure and chronic obstructive pulmonary disease. George and Barbara, who celebrated their 73rd wedding anniversary on Jan. 6, hold the record for the longest-married presidential pair. Mrs. Bush was known for her wit and emphasis on family. One of her primary causes was literacy. She founded the Barbara Bush Foundation for Family Literacy in 1989 to carry forth her legacy in the cause for literacy. PICTURED: Oct. 16, 1991 - Florissant, Missouri, U.S. - US First Lady BARBARA BUSH reads ''Brown Bear Brown Bear'' to the children with Missouri Governor JOHN ASHCROFT at a ''Parents as Teachers'' parent and child group at the Ferguson-Florissant School District October 16, 1991 in Florissant, Missouri. (Credit Image: © White House/Planet Pix via ZUMA Wire)
    19911016_zaa_p138_001.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_018.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_014.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_012.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_006.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_003.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_001.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_013.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_011.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_008.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_009.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_007.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_002.jpg
  • ** NO USA TV AND NO USA WEB **Olivia Jade's a walking testament to what Sunday Funday looks like ... never mind her parents are engulfed in the biggest college admissions scam in American history. We got Lori Loughlin's youngest daughter out Sunday in L.A. where she was dressed like your regular ol' college student but without the responsibilities anymore. We got her arriving at Fred Segal and took another stab at getting her take on her parents allegedly paying $500k in bribes to get her and her sis into USC under false pretenses. 06 May 2019 Pictured: Olivia Jade. Photo credit: TMZ/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA412791_005.jpg
  • ** NO USA TV AND NO USA WEB **Olivia Jade's a walking testament to what Sunday Funday looks like ... never mind her parents are engulfed in the biggest college admissions scam in American history. We got Lori Loughlin's youngest daughter out Sunday in L.A. where she was dressed like your regular ol' college student but without the responsibilities anymore. We got her arriving at Fred Segal and took another stab at getting her take on her parents allegedly paying $500k in bribes to get her and her sis into USC under false pretenses. 06 May 2019 Pictured: Olivia Jade. Photo credit: TMZ/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA412791_002.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_017.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_016.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
    MEGA461133_005.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_015.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: CHA Fertility Center. Photo
    MEGA461133_010.jpg
  • EXCLUSIVE: A mother gave birth to someone else’s babies after an IVF mix-up, a new lawsuit claims. The woman and her husband, from Queens, New York, are suing CHA Fertility Centre, in Los Angeles, after giving birth to children who didn't share their ethnicity. The clinic is run by Dr. Joshua Berger and co-owner Simon Hong. The Asian couple, who are referred to as Y.Z. and A.P. in court documents, married in 2012 and tried relentlessly--both naturally and with medical assistance--to get pregnant. After countless disappointment, the couple visited CHA Fertility Center with the hopes of becoming parents. In January 2018, Dr. Berger and Mr Hong met with the couple and walked them through months-long medicine, vitamin tests, and several procedures to yield eight embryos. In total, the couple says they spent $100,000 on the entire process. In September, the pair were excited after learning female embryos were successfully planted and they were pregnant with twins. Their joy, however, was short-lived when the ultrasound revealed they were instead having twin boys. Dr. Berger dismissed the sonogram and tried to calm their concerns by revealing when his wife was pregnant they were originally having a boy but gave birth to a girl. Y.Z. and A.P's nerves were calmed for a moment, and on March 30, 2019, A.P. delivered the children via C-section and was met with an unspeakable mix-up. The babies were indeed boys but did not share their Asian ethnicity. Even worse, the boys weren't related to one another. Y.Z and A.P. unknowingly were surrogate parents and had to give the children up to their respective parents who were also clients of CHA Fertility Center. The couple was so embarrassed and heartbroken they haven't told their family or close friends. For Y.Z and A.P, the experience has left them with "permanent emotional injuries from which they will not recover," the suit says.The amount they are suing for is also undisclosed. 07 Jul 2019 Pictured: Dr. Joshua Berger. Photo cre
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  • Embargoed to 0001 Monday May 29 File photo dated 30/07/14 of a piggy bank. Piggy bank-raiding parents are plundering nearly £50 a year typically from their children's savings, a survey has found.
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  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_006.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_008.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_012.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_010.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_007.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_001.jpg
  • March 28, 2019 - Srinagar, J&K, India - A relative of a disappeared youth seen holding a placard during a silent protest in Srinagar..The Association of Parents of Disappeared Persons (APDP) staged a silent protest here in Srinagar against the human rights violation in Kashmir. They said that the custodial killing of Rizwan Pandit due to torture is yet another case among hundreds of cases of human rights violations in Kashmir. (Credit Image: © Saqib Majeed/SOPA Images via ZUMA Wire)
    20190328_zaa_s197_066.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_019.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_002.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_003.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_014.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_013.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_009.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_011.jpg
  • Jennifer Aniston's parents seen leaving her 50th Birthday party. 09 Feb 2019 Pictured: Jennifer Aniston. Photo credit: Rachpoot/P&P/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA355630_002.jpg
  • Jennifer Aniston's parents seen leaving her 50th Birthday party. 09 Feb 2019 Pictured: Jennifer Aniston. Photo credit: Rachpoot/P&P/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA355630_001.jpg
  • The teenager was held captive for 88 days before escaping. The Wisconsin house where Jayme Closs Opens a New Window. was held captive has been revealed. And RadarOnline.com has exclusive images of the now infamous property. As the 13-year-old recovers from her trauma with her family the true horror of her ordeal is coming to light. The cabin is situated in rural Eau Claire Acres in Gordon, Wisconsin. It is located ten miles outside of Gordon and 70 miles from where Jayme was abducted – according to neighbors the development has few year-round residents. The teenager was found alive after she was abducted in October, and her parents, James Closs and Denise Closs, were murdered in their own home in Barron, Wisconsin. Jake Thomas Patterson, 21, is in custody on two charges of first- degree intentional homicide in the deaths of Jayme’s parents and one count of kidnapping. Since she escaped Jayme has been pictured smiling in photos shared to Facebook alongside her aunt, who is now acting as her legal guardian. Police confirmed Patterson, from Gordon, Wisconsin, is currently being held in custody. 13 Jan 2019 Pictured: Wisconsin Home Where Jayme Closs Was Held Captive. Photo credit: AMI/MEGA TheMegaAgency.com +1 888 505 6342
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  • The teenager was held captive for 88 days before escaping. The Wisconsin house where Jayme Closs Opens a New Window. was held captive has been revealed. And RadarOnline.com has exclusive images of the now infamous property. As the 13-year-old recovers from her trauma with her family the true horror of her ordeal is coming to light. The cabin is situated in rural Eau Claire Acres in Gordon, Wisconsin. It is located ten miles outside of Gordon and 70 miles from where Jayme was abducted – according to neighbors the development has few year-round residents. The teenager was found alive after she was abducted in October, and her parents, James Closs and Denise Closs, were murdered in their own home in Barron, Wisconsin. Jake Thomas Patterson, 21, is in custody on two charges of first- degree intentional homicide in the deaths of Jayme’s parents and one count of kidnapping. Since she escaped Jayme has been pictured smiling in photos shared to Facebook alongside her aunt, who is now acting as her legal guardian. Police confirmed Patterson, from Gordon, Wisconsin, is currently being held in custody. 13 Jan 2019 Pictured: Wisconsin Home Where Jayme Closs Was Held Captive. Photo credit: AMI/MEGA TheMegaAgency.com +1 888 505 6342
    MEGA337201_030.jpg
  • October 31, 2018 - Manhattan, New York, United States - A child seen dressed up in Halloween outfit during the parade..Hundreds of parents and Children dressed in Halloween costume take part in the 27th Annual Kids Halloween Parade in Washington Square Park in New York City. The annual Children's Halloween Parade is organized by New York University and Manhattan Community Board. (Credit Image: © Ryan Rahman/SOPA Images via ZUMA Wire)
    20181031_zaa_s197_029.jpg
  • October 6, 2018 - Kolkata, West Bengal, India - Parents, children suffering from cerebral palsy and social worker participate in a cultural program to celebrate World Cerebral Palsy Day. World Cerebral Palsy Day observes annual on October 6 to celebrate and affirm the lives of the 17 million people living with cerebral palsy (CP) (Credit Image: © Saikat Paul/Pacific Press via ZUMA Wire)
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  • August 27, 2017 - Kolkata, West Bengal, India - A heart breaking astonishing situation - little child with parents and other family members,Father  holding a huge oxygen cylinder and Mother holding the baby with the pipe inside nostrils of the little child rushing from one to the other department of the hospital for treatment without any support at the heritage hospital, Medical College,Kolkata on 27.8.2017  (Credit Image: © Sandip Saha/Pacific Press via ZUMA Wire)
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  • EXCLUSIVE: Wayne and Coleen Rooney are spotted boarding a skiff with two of their boys and Coleen's parents. 30 May 2017 Pictured: Wayne Rooney, Coleen Rooney. Photo credit: Queensofthenorth/MEGA TheMegaAgency.com +1 888 505 6342
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  • EXCLUSIVE: Coleen Rooney is spotted at the beach in Barbados with her parents and 3 kids. 24 May 2017 Pictured: Coleen Rooney. Photo credit: Queensofthenorth/MEGA TheMegaAgency.com +1 888 505 6342
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  • May 10, 2017 - Srinagar, Jammu and Kashmir, India - Relatives of missing Kashmiri youths participate in a sit-in protest organized by the Association of Parents of Disappeared Persons (APDP) in Srinagar, Indian controlled Kashmir, Wednesday, May 10, 2017. According to APDP about 8,000-10,000 people have gone missing since the beginning of the Kashmir conflict in 1989, mostly arrested by Indian security agencies. (Credit Image: © Zahid Bhat/Pacific Press via ZUMA Wire)
    RTI20170510_zaa_p133_070.jpg
  • December 10, 2016 - Washington, DC, USA - Parents and kids hold signs.  Children's Rally for Kindness takes place at Trump International Hotel in Washington DC on December 10, 2016 organized by the Takoma Parents Action Coalition.  According to their FaceBook page, it was a call to President-elect Donald Trump: ''to remember these lessons as he prepares to take office and implement policies that will affect the lives of children and families across our diverse nation.''.''All over the world, across cultures and countries, children learn the same basic lessons: .Ã’be kind,Ó .Ã’tell the truth,Ó .Ã’be fair,Ó .Ã’respect everyone,Ó .Ã’treat others the way you want to be treated,Ó .Ã’donÕt touch others if they donÕt want to be touched. (Credit Image: © Carol Guzy via ZUMA Wire)
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  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_016.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_018.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_005.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_017.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_015.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_020.jpg
  • Indian doctors were at their wit’s end after excising as many as 500 teeth from a seven-year-old’s palate in Chennai, India. The young patient was only three when his lower right jaw started to swell up but was left undiagnosed for four years as his parents lacked the right knowledge. The doctors diagnosed it to be a rare case of "compound composite ondontome", the boy was brought to the hospital with a swelling in his lower right jaw. "Later as swelling increased, the parents brought the boy to our hospital," said P.Senthilnathan, Professor -Department of Oral and Maxillofacial Surgery at at the Saveetha Dental College and Hospital on Wednesday. According to the doctors, the patient's family was worried that the swelling was carcinogenic. An X-ray and CT-scan of the boy's lower right jaw showed a lot of rudimentary teeth following which the doctors decided on the surgery. A team of doctors operated on the boy for five-long hours and successfully removed 526 teeth-like structures from his mouth. "We opened up the jaw after administering general anaesthesia and saw a bag/sack inside it. The sack, weighing about 200 grams, was carefully removed and was later found to contain 526 teeth -- small, medium and big sized,” said Dr Senthilnathan. Dr. Pratibha Ramani, Professor and Head of Department of oral and maxillofacial pathology, said, “Social consciousness on emerging environmental hazards is imperative. Every tissue information is patient’s right, surgical decision making is the key and final diagnostic expert is the pathologist.” According to the doctors, this is the first ever case documented in the world in which in an individual has been found to have so many minute teeth. Though some were very tiny particles, the doctors said, they had the properties of teeth. It took five long hours for the doctors to remove all the minute teeth from the sack. "It was reminiscent of pearls in an oyster," the doctors said. "The boy was normal three days after the sur
    MEGA476488_004.jpg
  • The teenager was held captive for 88 days before escaping. The Wisconsin house where Jayme Closs Opens a New Window. was held captive has been revealed. And RadarOnline.com has exclusive images of the now infamous property. As the 13-year-old recovers from her trauma with her family the true horror of her ordeal is coming to light. The cabin is situated in rural Eau Claire Acres in Gordon, Wisconsin. It is located ten miles outside of Gordon and 70 miles from where Jayme was abducted – according to neighbors the development has few year-round residents. The teenager was found alive after she was abducted in October, and her parents, James Closs and Denise Closs, were murdered in their own home in Barron, Wisconsin. Jake Thomas Patterson, 21, is in custody on two charges of first- degree intentional homicide in the deaths of Jayme’s parents and one count of kidnapping. Since she escaped Jayme has been pictured smiling in photos shared to Facebook alongside her aunt, who is now acting as her legal guardian. Police confirmed Patterson, from Gordon, Wisconsin, is currently being held in custody. 13 Jan 2019 Pictured: Wisconsin Home Where Jayme Closs Was Held Captive. Photo credit: AMI/MEGA TheMegaAgency.com +1 888 505 6342
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  • EXCLUSIVE: Wayne and Coleen Rooney are spotted boarding a skiff with two of their boys and Coleen's parents. 30 May 2017 Pictured: Wayne Rooney, Coleen Rooney. Photo credit: Queensofthenorth/MEGA TheMegaAgency.com +1 888 505 6342
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  • SOUTH AFRICA - Durban - 08 June 2020 - South Africa - Durban -  08 June 2020 - After almost three months, most grade 7 pupils of Ekuthuleni primary school in Kwamashu and other schools are finally back at school.<br />
But despite a desperate last-minute scramble by the basic education department, some schools will remain closed, most of them because they lack water and proper sanitation. Schools are scheduled to open today. Teacher unions and parents are questioning decisions that led to the safety of schools given the massive spike in COVID-19 infection rates in SA.<br />
Picture: Motshwari Mofokeng/African News Agency (ANA)
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  • SOUTH AFRICA - Cape Town - 6 July  2020  - Parents picketing outside Merrydale Primary in Mitchell's Plain.They are against the returning of grade R and Grade 11 pupils to school during the Covid-19 lockdown because of safety. Picture: Phando Jikelo/African News Agency(ANA)
    MerrydalePrimary267.jpg
  • December 10, 2016 - Washington, District of Columbia, U.S. - Children's Rally for Kindness takes place at Trump International Hotel, organized by the Takoma Parents Action Coalition.  According to their FaceBook page, it was a call to President-elect Trump: 'to remember these lessons as he prepares to take office and implement policies that will affect the lives of children and families across our diverse nation.'. (Credit Image: © Carol Guzy via ZUMA Wire)
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  • South Africa - Durban -  08 June 2020 -   Schools are scheduled to open todaybut the decision has not been unopposed. Teacher unions and parents as well as the South African Human Rights Commission have slammed Angie Motshekga's decision questioning the safety of schools given the massive spike in COVID-19 infection rates in SA. Tobi Primary School in Umbumbulu has open its doors. Picture Leon Lestrade/African News Agency(ANA).
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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_002.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_003.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_007.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_008.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_009.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_011.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_013.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_012.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_014.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_018.jpg
  • EXCLUSIVE: Battling a rare health condition that has left half of her face disfigured, a 24-year-old Indian woman says she tries to live positively despite jeers by people. Sasikala K, from Chennai, the capital of India’s southern Tamil Nadu state, suffers from plexiform neurofibromatosis, which has taken a toll on her face, affecting the right side. However, she admits her confidence has taken a hit of late. Sasikala, who prefers to live boldly and does not cover her face, likes dressing up and wearing make-up, much like girls her age, though she finds it difficult to execute them owing to her complications. She was only six-months-old when her parents noticed a part of her face swelling. However, they waited for another one and a half years to get medical help. “I have always been very bold, however, with age, the condition progressed and no one has come for help,” she says, adding, “I am slowly losing my confidence.” According to medical experts, her condition affects the face and craniofacial region of the body. It can also affect the neck and other parts of the body, depending upon the host. The family had not considered the deformity to be a big issue until Sasikala turned six and the face started to swell at an unusual rate. Now, almost 18 years later, she finds it difficult to execute daily chores like eating and brushing. The 24-year old is an employee at an embroidery unit run by a trust. Sasikala took it up as a means to support her family after completing her diploma in nursing and unable to land a job in the hospitality sector. Kumar, 54, Sasikala’s father, says his daughter has been under the knife four times, but it has only gotten worse. “She was six when doctors operated upon her for the first time,” Kumar says. “The result was satisfying and she looked normal,” he added. However, the joy was short-lived, as the tumours grew back again. Kumar says upon approaching the doctors again, he was told that it could be controlled but wou
    MEGA506733_019.jpg
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