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  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_011.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_006.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_003.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_007.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_001.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_008.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_010.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_005.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_002.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_004.jpg
  • EXCLUSIVE: By Sanjay Pandey and Supito Maity in Sao Paulo A 28-year-old Brazilian woman crippled by sheer weight and disproportionate size of tumours in her lower limbs is pleading for help from the netizens. Karina Rodini, who was fired from her job and is forced stay unmarried due to her medical condition, says the disease took a heavy toll on her personal and professional life. Karina has spent most of her adult life hiding it in public. But after last year’s botched up surgery in a state-run hospital, her ‘legs have become double the size and no clothes fit her’, making her a pariah in the locality. Karina suffers from type one neurofibromatosis, a genetic condition marked by changes in skin colour and the growth of non-cancerous cysts in different parts. The disease affects one in 4000 people globally. According to the US National Library of Medicine, patient with type one neufibromatosis are born with one mutated copy of the NF1 gene in each cell. It said, "In about half of cases, the altered gene is inherited from an affected parent. The remaining cases result from new mutations in the NF1 gene and occur in people with no history of the disorder in their family." Karina, from Sao Paulo, was just two when ‘coffee milk’ patches started to appear on her skin. She said due to the lack of formation of lumps, the doctors could barely make out what ailed her. “I was diagnosed with neurofibromatosis when I was only two years old, at first it was only ‘coffee milk’ patches so the doctor couldn’t do anything because there were no lumps or tumours,” she said. The cysts started to show up almost nine years later. One year later, when she was 12, Karina underwent a surgical procedure to remove a cyst, weighing around nine kilograms, from her uterus. According to her, the cavity gave her a semblance of a pregnant woman. Being the oldest child among three, Karina has always received love from her mother, Fatima M. Abou Ali, 58, a single woman, who raised
    MEGA348608_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_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_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_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_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_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_001.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_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_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_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_009.jpg
  • June 6, 2017 - inconnu - A breakthrough 3D printer has been unveiled which can work like a production line using a conveyor.Currently 3D printers use a stationary print bed.Printing long objects would take several print runs and some glue. The BlackBelt from Stephan Schürmann replaces the print bed of old with a conveyor belt, which allows for continuous printing.It easily surpassed a €50,000 Euros goal on crowd-funding site Kickstarter on the first day of its month-long campaign.The BlackBelt has been 3 years in development and is production ready.It has carbon fibre composite conveyor belt that allows for continuous printing of long objects, with the option of going even longer by adding a roller module. It can also create continuous batch production of smaller single build parts, like a factory production line.The build area is given as 340 mm wide, 340 mm high and an infinite length, and the interchangeable print heads can be set at four different angles.That means creators don't need to rely on support structures for overhangs in complex prints.Its Dutch-based maker says that the BlackBelt can be made available as either a desktop unit or a floor-standing machine, and can be customized to match buyer needs. The pre-production prototype has been tested with three types of print plastics though Schürmann does suggest that other materials may be supported.The expected retail price is €9,500 Euros for a desktop model, or €12,500 Euros for a freestanding version, but significant reductions are being offered to Kickstarter backers. Delivery is estimated to start in October. # IMPRIMANTE 3D INDUSTRIELLE (Credit Image: © Visual via ZUMA Press)
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  • July 6, 2018 - Wakefield, Yorkshire, UK - Wakefield UK. The scene where Elsie Frost's body was found in Wakefield in 1965. The family of murdered Elsie Frost are to lobby the Attorney General for a fresh inquest, which would allow police to put evidence implicating Peter Pickering into the public domain. The family have launched a crowdfunding campaign to meet the legal costs of the move, which they say would bring them an element of justice after the opportunity to see Pickering prosecuted was robbed from them by his death earlier this year. In 1965 the body of 14 year old Elsie Frost was found on the steps next to a railway bridge in the Lupset area of Wakefield. Elsie had been stabbed 5 times & died of shock & blood loss, despite a massive manhunt there has never been a conviction of anyone responsible. In 1966 a coroner presiding over the inquest into Elsie's death decided Ian Bernard Spencer was the man guilty, he was cleared by two courts. In March 2018 after the death of Peter Pickering who was convicted of the 1972 manslaughter of 14 year old Shirley Boldy near Barnsley, West Yorkshire police said they had ''strongly suspected'' he was responsible & ''it was our expectation'' the Crown Prosecution Service would have decided to charge him in due course. (Credit Image: © Andrew Mccaren/London News Pictures via ZUMA Wire)
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman, is strapped into the JB-10 Jetpack flying machine as he prepares for a flight around the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839717.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839710.JPG
  • David Mayman before he piloted the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman, alongside the JB-10 Jetpack flying machine at the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839594.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839551.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839715.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839555.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839546.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839713.JPG
  • David Mayman, alongside the JB-10 Jetpack flying machine at the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839694.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839691.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839596.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839557.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839546.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839540.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839188.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839170.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839156.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839130.JPG
  • David Mayman, is strapped into the JB-10 Jetpack flying machine as he prepares for a flight around the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839717.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839718.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839714.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839710.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839713.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839704.JPG
  • David Mayman before he piloted the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839701.JPG
  • David Mayman, alongside the JB-10 Jetpack flying machine at the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839694.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839691.JPG
  • David Mayman, alongside the JB-10 Jetpack flying machine at the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839680.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839597.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839596.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839594.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839540.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839534.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839516.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839188.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839177.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839174.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839153.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839150.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839712.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839704.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839688.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839555.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839550.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839534.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839516.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839721.JPG
  • David Mayman, is strapped into the JB-10 Jetpack flying machine as he prepares for a flight around the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839719.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839688.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839557.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839551.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839152.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
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  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839119.JPG
  • David Mayman, is strapped into the JB-10 Jetpack flying machine as he prepares for a flight around the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839719.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839720.JPG
  • David Mayman pilots the JB-10 Jetpack flying machine over the Royal Victoria Docks in east London on its maiden flight in the UK to mark the launch of an equity crowdfunding campaign on Seedrs.
    28839714.JPG
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