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DUK10151175_001
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Aria Kean is still always smiling (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - meaning *** Local Caption *** 3959
(c) Dukas -
DUK10151175_002
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Aria Kean in hospital (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - meaning he will dona *** Local Caption *** 3959
(c) Dukas -
DUK10151175_005
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Joe, Gemma and Aria together (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - meaning he wi *** Local Caption *** 3959
(c) Dukas -
DUK10151175_006
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Gemma and Aria out for dinner together (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - mea *** Local Caption *** 3959
(c) Dukas -
DUK10151175_008
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Joe Kean with his daughter Aria (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - meaning he *** Local Caption *** 3959
(c) Dukas -
DUK10151175_007
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Joe and Aria enjoying the sunshine together (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency *** Local Caption *** 3959
(c) Dukas -
DUK10151175_003
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Gemma says she can't wait to do more fun activities with Aria after the liver transplant (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's l *** Local Caption *** 3959
(c) Dukas -
DUK10151175_009
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Gemma with Aria enjoying the sunshine (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it becomes an emergency - mean *** Local Caption *** 3959
(c) Dukas -
DUK10151175_004
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Aria has just had open heart surgery to close a hole in her heart (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver donor if it *** Local Caption *** 3959
(c) Dukas -
DUK10151175_010
SCHICKSALE - Die kleine Aria Kean aus Suffolk braucht zwei Wochen nach einer OP am offenen Herzen wahrscheinlich eine Leberspende von ihrem Vater
Aria Kean was diagnosed with the rare liver disease called Biliary atresia (Collect/PA Real Life)
Newlyweds on tenterhooks as baby girl who had heart surgery 2 weeks ago awaits liver transplant with dad ready to be emergency living donor Devoted newlyweds whose adorable baby girl was whisked into hospital three days into their honeymoon and had open heart surgery two weeks ago are now on tenterhooks as the "smiley" tot awaits a liver transplant. When within days of little Aria Kean being born on 21 October 2021 she showed signs of baby jaundice, including yellow skin, her parents, financial advisor Joe Kean, 29, and service advisor Gemma Kean, 27, were not worried as they knew the condition was common. But when it failed to clear a series of hospital trips followed and, aged seven weeks, she was diagnosed with biliary atresia - a rare disease affecting the bile ducts, gallbladder and other structures involved in producing bile, which is made by the liver to aid digestion. Aged eight weeks, Aria had a Kasai procedure - surgery that can help re-establish bile flow from the liver to the intestine by joining the two directly - which worked for a few months, but doctors went on to tell her parents she needed both a liver transplant and surgery to close a hole in her heart. Now, one week after his daughter's open heart surgery lasting four hours, Joe, of Red Lodge, Suffolk, said: "The liver transplant will change everything for Aria. "She is so happy and smiley all the time, but she has never been well, she has only ever been poorly. "Because of her liver, it has affected her hitting her milestones. With the transplant, she will be like a different baby, with all this energy. "She only had heart surgery on Tuesday July 26 and she is already doing so amazingly. "We cannot wait for her to have the transplant now." Hoping for a liver transplant in the next few weeks, if no donor is found, Joe will become his daughter's living liver do *** Local Caption *** 3959
(c) Dukas -
DUK10145893_008
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593208
(c) Dukas -
DUK10145893_013
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593202
(c) Dukas -
DUK10145893_012
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593201
(c) Dukas -
DUK10145893_002
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593209
(c) Dukas -
DUK10145893_009
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593204
(c) Dukas -
DUK10145893_003
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Dominic Sadler-Smith and Jodie Weeder with their daughter Posie-Aurora Sadler-Smith in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593200
(c) Dukas -
DUK10145893_005
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Dominic Sadler-Smith and Jodie Weeder with their daughter Posie-Aurora Sadler-Smith in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593211
(c) Dukas -
DUK10145893_011
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Dominic Sadler-Smith and Jodie Weeder with their daughter Posie-Aurora Sadler-Smith in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593203
(c) Dukas -
DUK10145893_010
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Dominic Sadler-Smith and Jodie Weeder with their daughter Posie-Aurora Sadler-Smith in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593205
(c) Dukas -
DUK10145893_007
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593207
(c) Dukas -
DUK10145893_006
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593210
(c) Dukas -
DUK10145893_004
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593212
(c) Dukas -
DUK10145893_001
SCHICKSALE - Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen
Keine eigenen Beinknochen: Posie-Aurora Sadler-Smith aus Sudbury hat ihre ersten Prothesen angepasst bekommen -- Collect photos showing Posie-Aurora Sadler-Smith at her home in Sudbury, Suffolk. See story SWSYlegs - By Kate Pounds A little girl born without bones in her legs has taken her first steps on her new prosthetic limbs after bravely having an amputation. Posie-Aurora Sadler-Smith, one, was diagnosed with limb problems during her 20 week scan, but medics didn't know she had fibular hemimelia until she was born. The disability - where part or all of the fibula is missing - usually only impacts one leg, but Posie was missing nearly all the bones from both her lower limbs. The little fighter defied the odds to learn to crawl, using all her strength in her upper body to get around, and even haul herself on to the sofa for a cuddle with dog Seuss. / action press *** Local Caption *** 36593206
(c) Dukas -
DUK10139773_013
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534064
(c) Dukas -
DUK10139773_012
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534070
(c) Dukas -
DUK10139773_011
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534069
(c) Dukas -
DUK10139773_010
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534073
(c) Dukas -
DUK10139773_009
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto monsignor Corrado Lorefine, l'arcivescovo del capoluogo siciliano
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic monsignor Corrado Lorefine
*** Local Caption *** 31534074
(c) Dukas -
DUK10139773_008
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534081
(c) Dukas -
DUK10139773_007
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto monsignor Corrado Lorefine, l'arcivescovo del capoluogo siciliano
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic monsignor Corrado Lorefine
*** Local Caption *** 31534075
(c) Dukas -
DUK10139773_006
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto monsignor Corrado Lorefine, l'arcivescovo del capoluogo siciliano
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic monsignor Corrado Lorefine
*** Local Caption *** 31534078
(c) Dukas -
DUK10139773_005
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534083
(c) Dukas -
DUK10139773_004
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca con il padre maglia rosa
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin with her father *** Local Caption *** 31534071
(c) Dukas -
DUK10139773_003
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534082
(c) Dukas -
DUK10139773_002
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin
*** Local Caption *** 31534066
(c) Dukas -
DUK10139773_001
NEWS - Verstorben bei der TikTok Blackout Challenge: Beerdigung der zehnjährigen Antonella Sicomoro in Palermo
Foto Alberto Lobianco - LaPresse
cronaca
26-01-2021 Palermo
La tragedia su TikTok, oggi l'ultimo saluto ad Antonella Sicomoro
Nella Foto il feretro della piccola su una bara bianca con il padre maglia rosa
Photo Alberto Lobianco - LaPresse
news
26-january -2021 Palermo - Italy
TikTok - funeral of Antonella Sicomoro
In the pic coffin with her father *** Local Caption *** 31534072
(c) Dukas -
DUK10126161_012
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507779
(c) Dukas -
DUK10126161_011
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas's spine. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507768
(c) Dukas -
DUK10126161_010
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas's spine. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507769
(c) Dukas -
DUK10126161_009
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas in a brace. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507770
(c) Dukas -
DUK10126161_008
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507771
(c) Dukas -
DUK10126161_007
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507772
(c) Dukas -
DUK10126161_006
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507773
(c) Dukas -
DUK10126161_005
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas's spine. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507774
(c) Dukas -
DUK10126161_004
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas in a brace. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507775
(c) Dukas -
DUK10126161_003
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507776
(c) Dukas -
DUK10126161_002
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas kickboxing. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507778
(c) Dukas -
DUK10126161_001
FEATURE - Der Skoliose zum Trotz: 11-jährige Kickboxerin sammelt Geld für ihre Wirbelsäulenoperation
Izzy Harwood-Lucas and sister Thalia. An 11-year-old kickboxer is racing against time to raise money for surgery to fix a triple curve in her spine - so she can carry on kicking. See NATIONAL story NNspine. Martial arts fanatic Izzy Harwood-Lucas was diagnosed with a severe scoliosis curve this summer and has not one, but three, bends in her spine. Normally kids with the condition only have one curve so her case was quite unusual. But if the family go for treatment on the NHS, her spine will be fused, meaning she cannot carry on with her kickboxing. So they are trying to raise the £60,000 pounds for a more advanced treatment that will allow her to continue with the sport that she has been doing since she was three. But they only have until March to raise the cash before a growth spurt could make the new treatment unfeasible. The family were out walking their dog when they noticed Izzy's back was hunched over. / action press *** Local Caption *** 30507777
(c) Dukas -
DUK10119720_003
FEATURE - Neuer Banksy in Bristol?
This new stencil artwork down an alleyway in Bristol is set to send the street art world into a frenzy - for a while at least - about whether Banksy has painted in his home town again or not. The work appeared overnight a couple of days ago down an alleyway off a main road into Bristol city centre, and it is either a real genuine - but as yet unconfirmed - Banksy, or it is someone having something of a dig at him. Works of street art that ARE painted by Banksy are almost always eventually confirmed by either his Instagram account, or by ‘the Pest Control’ people who operate a service which authenticates Banksy’s work for anyone who asks. The work features a girl with a backpack standing in front of a crayon house, with the words ‘Intellectual Property’ and ‘Keep Out’ written on them. This is a direct copy and mix-up of a 2011 work by Banksy, called Crayon House Foreclosure, which was painted on the wall of a neighbourhood in Los Angeles. *** Local Caption *** 29970422
(c) Dukas -
DUK10119720_002
FEATURE - Neuer Banksy in Bristol?
This new stencil artwork down an alleyway in Bristol is set to send the street art world into a frenzy - for a while at least - about whether Banksy has painted in his home town again or not. The work appeared overnight a couple of days ago down an alleyway off a main road into Bristol city centre, and it is either a real genuine - but as yet unconfirmed - Banksy, or it is someone having something of a dig at him. Works of street art that ARE painted by Banksy are almost always eventually confirmed by either his Instagram account, or by ‘the Pest Control’ people who operate a service which authenticates Banksy’s work for anyone who asks. The work features a girl with a backpack standing in front of a crayon house, with the words ‘Intellectual Property’ and ‘Keep Out’ written on them. This is a direct copy and mix-up of a 2011 work by Banksy, called Crayon House Foreclosure, which was painted on the wall of a neighbourhood in Los Angeles. *** Local Caption *** 29970421
(c) Dukas -
