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DUK10163096_002
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_013
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_011
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_003
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_001
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_010
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_008
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_007
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_006
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_009
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_004
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_012
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10163096_005
Emma hat 'nen Blindenhund: Emma Norman aus Biggleswade hat die ZSD Augenerkrankung und ist auf ihren Assistenzhund Archie angewiesen
SONDERKONDITIONEN: Satzpreis!
WORDS BYLINE: Deborah Cicurel
She was just a normal kid, running around with her friends and having fun dancing - until a devastating diagnosis.
When Emma Norman was six her parents noticed her squinting at the TV but they didn’t think too much of it.
However, Emma, now 33, would soon find out that she had Cone Rod Dystrophy and would eventually go blind.
Emma, a Pilates and meditation breathwork instructor from London, living in Biggleswade, Bedfordshire, believes the stereotypes around blindness made accepting her diagnosis even harder — and she wants to challenge outdated ideas around sight loss.
“Life before my diagnosis felt pretty normal,” she remembers.
“I was just like any other kid—running around with friends, dancing around to my favourite TV shows and records. I even skipped crawling and went straight to walking, and I was reading and talking from a very young age, so nobody noticed anything unusual.
“To me, everything seemed fine because that was just my normal. It wasn’t until my parents started picking up on little things—like me squinting at the TV or struggling to see animals at the zoo when they pointed them out—that they became curious.
“At first, they thought I was just being cheeky, pretending not to see things, but when I kept squinting at the TV, they decided to take me to the optician. They assumed I was probably just short-sighted and needed glasses.
“In my early years at school, I only needed to sit closer to the board, but beyond that, I didn’t notice anything different. I guess what I saw—how I saw—was just my normal.
“When I first started squinting, my parents thought I probably just needed glasses for short-sightedness, like the other kids in my class.
“The optician gave me my first pair of multi-coloured glasses in the meantime while they arranged for the doctors to refer me to Moorfields Eye Hospital, as they could tell something more was going on.
“After getting the gl *** Local Caption ***
(c) Dukas -
DUK10146696_020
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245482
(c) Dukas -
DUK10146696_006
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245485
(c) Dukas -
DUK10146696_001
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245469
(c) Dukas -
DUK10146696_022
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245471
(c) Dukas -
DUK10146696_011
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245475
(c) Dukas -
DUK10146696_008
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245452
(c) Dukas -
DUK10146696_021
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245455
(c) Dukas -
DUK10146696_017
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245453
(c) Dukas -
DUK10146696_012
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245464
(c) Dukas -
DUK10146696_018
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245450
(c) Dukas -
DUK10146696_004
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245467
(c) Dukas -
DUK10146696_007
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245461
(c) Dukas -
DUK10146696_013
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245433
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245436
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245441
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245432
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DUK10146696_010
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245415
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DUK10146696_003
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245430
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DUK10146696_009
ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245431
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245428
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245425
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245437
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ROYALS - Sophie von Wessex besucht die Disability Initiative in Camberley
Gräfin Sophie von Wessex (GB), beim Besuch der Disability Initiative anlässlich des Internationalen Tages der Menschen mit Behinderungen in Camberley, Grossbritannien, 1. Dezember 2021. *** Local Caption *** 02245411
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DUK10146016_005
NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612261
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DUK10146016_007
NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612264
(c) Dukas -
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612263
(c) Dukas -
DUK10146016_012
NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612260
(c) Dukas -
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612266
(c) Dukas -
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612262
(c) Dukas -
DUK10146016_011
NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Irschenberg, Bayern, Deutschland, BRD, /
Irschenberg, Bavaria, Germany, Europe, *** Local Caption *** 36612259
(c) Dukas -
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Inntaldreieck, Bayern, Deutschland, BRD, /
Inn Valley Triangle, Bavaria, Germany, Europe, *** Local Caption *** 36612257
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Inntaldreieck, Bayern, Deutschland, BRD, /
Inn Valley Triangle, Bavaria, Germany, Europe, *** Local Caption *** 36612258
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Inntaldreieck, Bayern, Deutschland, BRD, /
Inn Valley Triangle, Bavaria, Germany, Europe, *** Local Caption *** 36612268
(c) Dukas -
DUK10146016_009
NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Inntaldreieck, Bayern, Deutschland, BRD, /
Inn Valley Triangle, Bavaria, Germany, Europe, *** Local Caption *** 36612269
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NEWS - Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung
Gigantischer LKW-Stau von der Grenze bis München wegen österreichischer LKW-Blockabfertigung / Gigantic truck traffic jam from the border to Munich due to Austrian truck block clearance / Inntaldreieck, Bayern, Deutschland, BRD, /
Inn Valley Triangle, Bavaria, Germany, Europe, *** Local Caption *** 36612265
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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
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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
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