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DUK10118755_003
FEATURE - Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3000 Pfund im Internet bestellt
Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3.000 Pfund im Internet bestellt -- Kelly Snipes age 37 who suffers with a rare sleeping disorder at her home in Basildon Essex. A mum-of-three who suffers from a rare sleeping disorder has told how she has spent £3k in bizarre internet shopping sprees - while fast asleep.Kelly Snipes, 37, regularly woke up in the mornings to find email receipts for items she unconsciously bought on-line during the night.One day a delivery lorry turned up outside her home containing a full-sized plastic basketball court she didn't realise she had bought. / action press *** Local Caption *** 29798416
(c) Dukas -
DUK10118755_002
FEATURE - Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3000 Pfund im Internet bestellt
Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3.000 Pfund im Internet bestellt -- Kelly Snipes age 37 who suffers with a rare sleeping disorder at her home in Basildon Essex. A mum-of-three who suffers from a rare sleeping disorder has told how she has spent £3k in bizarre internet shopping sprees - while fast asleep.Kelly Snipes, 37, regularly woke up in the mornings to find email receipts for items she unconsciously bought on-line during the night.One day a delivery lorry turned up outside her home containing a full-sized plastic basketball court she didn't realise she had bought. / action press *** Local Caption *** 29798414
(c) Dukas -
DUK10118755_001
FEATURE - Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3000 Pfund im Internet bestellt
Im Schlaf gekauft: Kelly Snipes hat unbewusst Waren im Wert von über 3.000 Pfund im Internet bestellt -- Kelly Snipes age 37 who suffers with a rare sleeping disorder at her home in Basildon Essex. A mum-of-three who suffers from a rare sleeping disorder has told how she has spent £3k in bizarre internet shopping sprees - while fast asleep.Kelly Snipes, 37, regularly woke up in the mornings to find email receipts for items she unconsciously bought on-line during the night.One day a delivery lorry turned up outside her home containing a full-sized plastic basketball court she didn't realise she had bought. / action press *** Local Caption *** 29798411
(c) Dukas -
DUK10143063_001
SCHICKSALE - Allen Widrigkeiten zum Trotz: Bethany Meloche will vor ihrem 30. Geburtstag trotz ihrer genetischen Nervenerkrankung 30 Länder der Welt bereisen
Bethany at the Leaning Tower of Pisa, in Italy. PA REAL LIFE/COLLECT *** Author makes bucket list to visit 30 countries before she is
30 despite severe mobility problems caused by genetic
nerve disease
By Susan Clark and Jessica Frank-Keyes, PA Real Life
A remarkable woman with a genetic nerve disease which greatly restricts her mobility has
vowed to complete her bucket list and visit 30 countries before she is 30 in November - with
just three left to go.
Diagnosed with Charcot-Marie-Tooth disease (CMT), when she was 12, author Bethany
Meloche, 29, has always refused to let her disease define her - despite having a severe form
that saw her using a wheelchair at 15 and unable to stand by 18.
Instead of giving in, she met her husband, Josh, 31, a software engineer, through online
dating, had surgery enabling her to walk with sticks and even moved continents from
Michigan, USA to Bayswater, west London, saying: "It is easy to look at someone with a
progressive disease like me and say, 'Well, theres not much we can do.'
"But I decided a long time ago I didnt want CMT to define me.
Also the author of a book about living with her condition - How Should A Body Be? - Bethany,
cites childhood memories of seeing her grandmother wearing leg braces, which she now
knows was because she, too, had CMT.
I remember when I was l very young watching my Grandma May put on these giant, clunky
leg braces," she said.
"At that age, I just thought, thats what grandmas did - they wore big Grandma shoes."
And no one mentioned CMT to Bethany, despite her always having an imbalanced gait when
she walked, which indicated she had the condition - as they wanted to protect her.
She said: I was very close to Grandma May, who passed away in 2010, following a stroke,
and I think she was very close to me because she saw from my gait Id inherited the
condition.
But I wasnt diagnosed until I was 12. Id been tripping over, then I experienced what felt
like a bolt of lightning
(c) Dukas -
DUK10111773_013
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, and her left ear after the failed surgery .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_012
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, with children Bethany,6, and baby Bobbie,2.Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_011
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48..Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_010
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, with children Bethany,6, and baby Bobbie,2.Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_009
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, and partner Martyn Smith,41, with children Bethany,6, and baby Bobbie,2.Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_008
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, and her left ear after the failed surgery .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_007
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, and her left ear after the failed surgery .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_006
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_005
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48..Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_004
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, with her partner Martyn Smith, 41.Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_003
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_002
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, .Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10111773_001
FEATURE - Loch im Ohr: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom
SONDERKONDITIONEN: Satzpreis!
Loch im Ohr wird zur Qual: Junge Mutter leidet am seltenen Kanal-Dehiszenz-Syndrom / 140119 ***
Collect of Pam Roberts,48, with her partner Martyn Smith, 41...Pam suffers from Superior Semicircular Canal Dehiscence (SSCD), which means she is constantly haunted by the sound of her own body.See National News story.NNbrain. A 'fun-loving' mum has become a shell of her former self because she is tortured by the sound of her eyeballs moving and the insides of her body.Pam Roberts, 49, suffers from Superior Semicircular Canal Dehiscence (SSCD) which means she can constantly hear her heart beating, her bowels moving and her body digesting food.The rare condition has caused a hole between her brain and her inner ear which means she is forced to listen to the sounds of her body 24 hours per day.Pam, from Maidstone in Kent, said: "The most difficult thing for me is having my voice all the time like a broken kazoo - I can't ever escape it. *** Local Caption ***
(c) Dukas -
DUK10131308_006
SCHICKSALE - Genesung: Epileptikerin malt Kühe und ist seitdem anfallsfrei
Lauren Terry (Collect/ PA Real Life) *** Actress whose life was ruled by epilepsy swaps her
fast-paced routine for running her own cow portrait
business and has been seizure-free for two years
By Laura Withers, PA Real Life
A trained actress whose life was blighted by terrifying epileptic seizures believes that
leaving the stage to paint portraits of cows has "cured" her of the stress triggers that led
to her elliptic episodes.
Seizure-free for two years, Lauren Terry 31, of York, stumbled on her unusual "treatment"
back in 2011 when, a self-taught artist, she copied a picture of a cow from a greetings
card and gave it to her dad, Justin, 64, a retired tailor.
So impressed by her efforts that he had it framed, when the shop owner suggested it was
good enough to exhibit, Lauren rose to the challenge - holding her first exhibition in
Wykeham, North Yorkshire, in 2012.
I had 18 cow portraits and at my first exhibition I sold six, which I was chuffed with, she
said. They were sold for up to £450 each, which was a decent amount of money.
Then, using £5,000 from her savings and with £1,000 invested by her mum, Jude, 63, now
her business partner, she launched her new artistic venture.
A side project until 2016, when she and her husband, James, 31, an area sales manager with whom she is expecting her first child in May - moved from London to Yorkshire, and
she ditched acting to paint cows full-time, Lauren soon began to reap extraordinary health
benefits.
For her life had been blighted by epilepsy - a condition affecting the brain and causing
seizures - since she was 10 years old.
First experiencing absence seizures, causing lapses in awareness, she would briefly lose
consciousness.
It felt like Id gone into a deep daydream or into some sort of trance, she
explained. Sometimes Id completely zone out and my teacher would assume I wasnt
paying attention.
Or, Id just stop in the middle of crossing a road and my parents would be yelling,
Lauren, wh
(c) Dukas -
DUK10105604_031
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_030
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson,5, with her sister Kinzley, 10 and brother Parker, 13 and mother Kendra Larsen, 36, and father Eric Larsen, 38...Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21 *** Local Caption *** / action press
(c) Dukas -
DUK10105604_029
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_028
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_027
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5 in hospital with her mother Kendra Larsen, 36, during one of her many hospital visits since 2012.. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_026
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_025
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5 in hospital with her mother Kendra Larsen, 36, during one of her many hospital visits since 2012.. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_024
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_023
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_022
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_021
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson,5, with her sister Kinzley, 10 and brother Parker, 13..Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_020
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_019
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_018
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_017
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_016
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larsen, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_015
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_014
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson,5,mother Kendra Larsen, 36, on the Ririe Reservoir. Idaho...Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_013
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_012
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_011
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_010
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson,5, with her sister Kinzley, 10.Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_009
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_008
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5 in hospital with her mother Kendra Larsen, 36, during one of her many hospital visits since 2012.. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_007
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5, surfing with her father Eric Larsen, 38, on Ririe Resevoir, Idaho. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. July 21 2018. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_006
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5 in hospital during one of her many hospital visits since 2012.. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_005
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_004
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE.. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_003
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_002
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10105604_001
SCHICKSALE - Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit
SONDERKONDITIONEN: Satzpreis!
Als 5-jährige schon 90 Knochenbrüche: Die kleine Hadley leidet an der Glasknochenkrankheit/ 2018 *** Collect of Hadley Larson, 5 in hospital with her mother Kendra Larsen, 36, during one of her many hospital visits since 2012.. Hadley suffers from osteogenesis imperfecta, also known as Brittle Bone Syndrome, making her incredibly FRAGILE. . See story SWNYsurf.A ‘china doll’ five-year-old who has suffered 90 broken bones in her short lifetime overcame her disease to go surfing with her dad. Hadley Larson, five, has osteogenesis imperfecta, also known as Brittle Bone Disease, and has been in and out of hospital since she was born in 2012.A lack of the protein collagen means Hadley's bones are so brittle they can shatter in an instant, and a light fall can leave her with serious injuries. So mom Kendra Larsen, 36, says she was stunned when Hadley asked her if she could try to surf with dad Eric Larsen, 38, on a daytrip to Ririe Reservoir, Idaho, on July 21. *** Local Caption *** / action press
(c) Dukas -
DUK10131308_004
SCHICKSALE - Genesung: Epileptikerin malt Kühe und ist seitdem anfallsfrei
Lauren Terry (Collect/ PA Real Life) *** Actress whose life was ruled by epilepsy swaps her
fast-paced routine for running her own cow portrait
business and has been seizure-free for two years
By Laura Withers, PA Real Life
A trained actress whose life was blighted by terrifying epileptic seizures believes that
leaving the stage to paint portraits of cows has "cured" her of the stress triggers that led
to her elliptic episodes.
Seizure-free for two years, Lauren Terry 31, of York, stumbled on her unusual "treatment"
back in 2011 when, a self-taught artist, she copied a picture of a cow from a greetings
card and gave it to her dad, Justin, 64, a retired tailor.
So impressed by her efforts that he had it framed, when the shop owner suggested it was
good enough to exhibit, Lauren rose to the challenge - holding her first exhibition in
Wykeham, North Yorkshire, in 2012.
I had 18 cow portraits and at my first exhibition I sold six, which I was chuffed with, she
said. They were sold for up to £450 each, which was a decent amount of money.
Then, using £5,000 from her savings and with £1,000 invested by her mum, Jude, 63, now
her business partner, she launched her new artistic venture.
A side project until 2016, when she and her husband, James, 31, an area sales manager with whom she is expecting her first child in May - moved from London to Yorkshire, and
she ditched acting to paint cows full-time, Lauren soon began to reap extraordinary health
benefits.
For her life had been blighted by epilepsy - a condition affecting the brain and causing
seizures - since she was 10 years old.
First experiencing absence seizures, causing lapses in awareness, she would briefly lose
consciousness.
It felt like Id gone into a deep daydream or into some sort of trance, she
explained. Sometimes Id completely zone out and my teacher would assume I wasnt
paying attention.
Or, Id just stop in the middle of crossing a road and my parents would be yelling,
Lauren, wh
(c) Dukas -
