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  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_013
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399219

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_005
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399220

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_004
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399221

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_002
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399222

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_003
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399223

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_017
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399224

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_011
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399225

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_009
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399227

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_016
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399228

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_008
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399229

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_001
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399230

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_012
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399232

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_007
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399231

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_010
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399234

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_018
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399233

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_006
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399235

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_014
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399236

    (c) Dukas

     

  • FEATURE - Besuch beim Hausarzt - Symbolfotos
    DUK10150689_015
    FEATURE - Besuch beim Hausarzt - Symbolfotos
    ROTTERDAM - A general practitioner examines a patient during a visit to the doctor's office in Rotterdam. Everyone sometimes doubts whether a visit to the general practitioner or out-patient clinic is necessary. You often err on the side of caution and call or go anyway. Do you want to know whether a visit to the doctor is necessary? / 110722
    *** Local Caption *** 39399237

    (c) Dukas

     

  • FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    DUK10150411_003
    FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    EXCLUSIVE: **NO NEW YORK POST, NEWS CORP OR RTL USAGES**
    Doctors have successfully removed a metal figurine of the Hindu god Krishna from a man's throat – after he swallowed the metal object.
    Vinayak Kolkekar, 48, accidentally gobbled it while glugging holy water on Tuesday (21 June).
    The object became lodged in his throat, blocking his food pipe and choking him.
    Kolkekar was taken to hospital where an X-ray revealed the deity residing there, with the left leg of the figurine obstructing the food pipe.
    He underwent emergency surgery KLE hospital in Belgavi, Karnataka, India.
    The patient is doing well following the surgery and has been discharged from the health centre.
    Pictured: GV,General View
    Ref: SPL5321665 250622 EXCLUSIVE
    Picture by: Jam Press/TIM / SplashNews.com


    World Rights, No Australia Rights, No Netherlands Rights, No Russia Rights, No United Kingdom Rights, No United States of America Rights
    *** Local Caption *** 39277608

    (c) Dukas

     

  • FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    DUK10150411_002
    FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    EXCLUSIVE: **NO NEW YORK POST, NEWS CORP OR RTL USAGES**
    Doctors have successfully removed a metal figurine of the Hindu god Krishna from a man's throat – after he swallowed the metal object.
    Vinayak Kolkekar, 48, accidentally gobbled it while glugging holy water on Tuesday (21 June).
    The object became lodged in his throat, blocking his food pipe and choking him.
    Kolkekar was taken to hospital where an X-ray revealed the deity residing there, with the left leg of the figurine obstructing the food pipe.
    He underwent emergency surgery KLE hospital in Belgavi, Karnataka, India.
    The patient is doing well following the surgery and has been discharged from the health centre.
    Pictured: GV,General View
    Ref: SPL5321665 250622 EXCLUSIVE
    Picture by: Jam Press/TIM / SplashNews.com


    World Rights, No Australia Rights, No Netherlands Rights, No Russia Rights, No United Kingdom Rights, No United States of America Rights
    *** Local Caption *** 39277612

    (c) Dukas

     

  • FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    DUK10150411_001
    FEATURE - Beim Trinken von heiligem Wasser: Ärzte operieren erfolgreich verschluckte Metallfigur des Hindu-Gottes Krishna aus dem Rachen von Vinayak Kolkekar
    EXCLUSIVE: **NO NEW YORK POST, NEWS CORP OR RTL USAGES**
    Doctors have successfully removed a metal figurine of the Hindu god Krishna from a man's throat – after he swallowed the metal object.
    Vinayak Kolkekar, 48, accidentally gobbled it while glugging holy water on Tuesday (21 June).
    The object became lodged in his throat, blocking his food pipe and choking him.
    Kolkekar was taken to hospital where an X-ray revealed the deity residing there, with the left leg of the figurine obstructing the food pipe.
    He underwent emergency surgery KLE hospital in Belgavi, Karnataka, India.
    The patient is doing well following the surgery and has been discharged from the health centre.
    Pictured: GV,General View
    Ref: SPL5321665 250622 EXCLUSIVE
    Picture by: Jam Press/TIM / SplashNews.com




    World Rights, No Australia Rights, No Netherlands Rights, No Russia Rights, No United Kingdom Rights, No United States of America Rights
    *** Local Caption *** 39277611

    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_015
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805520
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_014
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805525
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_013
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Hinweisschild zur Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805501
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_012
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805533
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_011
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805515
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_010
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    A300 Zero G beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805505
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_009
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805512
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_008
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    A300 Zero G beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805541
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_007
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Fläschchen mit Dosierungen von Comirnaty beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805531
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_006
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805521
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_005
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Hinweisschild zur Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805546
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_004
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805534
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_003
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805492
    (c) Dukas

     

  • NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    DUK10147151_001
    NEWS - Coronavirus: Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport
    Impfaktion beim Pressetermin zur außergewöhnlichen Impfaktion im historischen Airbus A300 Zero G am Köln Bonn Airport. Das Flugzeug wurde bis 2014 zur Simulation von Schwerelosigkeit bei sog. Parabelflügen eingesetzt. Köln, 21.12.2021 *** Local Caption *** 36805523
    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_013
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Matthew proposed to Amy in December 2020 (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Am ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_004
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy after recent knee operation (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has lau ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_012
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy and Matthew after Amy's most recent jaw operation (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and afte ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_003
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy after a jaw operation (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has launched ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_007
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy with her dad Paul (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has launched a Go ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_002
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy with her mum Christine (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has launched ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_005
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy as a child with dad Paul (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has launch ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_011
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy as a child with mum Christine (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has l ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_008
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy with older siblings Gary and Claire (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_010
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Baby Amy with her older siblings Gary and Claire (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_006
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy and Matthew are due to get married in 2023 (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_001
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy and Matthew met through their work (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy ***

    (c) Dukas

     

  • SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    DUK10146829_009
    SCHICKSALE - Sucht nach einer OP-Finanzierung: Amy Stewart leidet an der sehr seltenen und angeborenen Kleidokranialen Dysplasie
    Amy and Matthew on the beach (PA Real Life) *** Bride-to-be with agonising "one in a million" condition meaning she was born
    with no collarbone needs private surgery to walk down the aisle pain free
    By Jack Clover, PA Real Life
    A bride-to-be with a "one in a million" condition that saw her born with no collarbone and
    whose spine is agonisingly twisted like the letter C - making it impossible to carry a child - is
    desperate for private surgery so she can walk down the aisle pain free and start a family.
    Born with cleidocranial dysostosis (CCD) - a birth defect affecting teeth and bones present in
    one in every million people, according to medical experts, Amy Stewart, 27, has been in
    agony since falling down some stairs and fracturing her spine in August 2020.
    Diagnosed with CCD after being born with a wide forehead, an open skull at the top, no
    collarbone and three rows of teeth, she flourished despite countless operations and being
    bullied at school - landing a job with the emergency services and falling in love.
    But Amy, of Milton Keynes, Buckinghamshire, now fears that unless she can raise £38,000
    towards private treatment, she will still be in agony when she marries her fiancé, Matthew
    Woollard, 38, a fellow emergency services worker, on 1 June, 2023, and that they will never
    be able to have children.
    Also suffering with kyphoscoliosis - a spine that curves to the side and forwards or
    backwards at the same time - she said: "My spine is much weaker than most people, so when
    I fell down a flight of stairs not only did I fracture it, but my kyphoscoliosis has deteriorated
    rapidly, reducing my quality of life significantly."
    Seeking private help when her NHS doctors did not see surgery on her spine as an option,
    according to Amy, she was offered a lifeline by a private specialist who can perform a spinal
    fusion as soon as January 2022 - making the prohibitive factor the cost of around £40,000 for
    surgery and aftercare.
    Now Amy has launch ***

    (c) Dukas

     

  • SCHICKSALE - Gesicht ihrer Töchter zum ersten Mal deutlich sehen: Kayley Storey kann mit Hilfe einer Spezialbrille ihre Makuladegeneration ausgleichen
    DUK10145505_016
    SCHICKSALE - Gesicht ihrer Töchter zum ersten Mal deutlich sehen: Kayley Storey kann mit Hilfe einer Spezialbrille ihre Makuladegeneration ausgleichen
    Kayley and Ryan tied the knot in September 2020 during lockdown (Collect/PA Real Life). *** Former X Factor contestant gets gift of sight
    for her birthday thanks to miracle glasses allowing
    her to see her daughters face clearly for first time
    By Harriet Bullough, PA Real Life
    A former X Factor contestant was given the gift of sight for her birthday when miracle
    glasses allowed her to see her daughters face clearly for the first time.
    Professional artist Kayley Storey, 33, was just 15 when she was diagnosed with rare
    Stargardt disease, an inherited eye condition affecting an area of the retina known as the
    macula and reducing central or detailed vision.
    While she refused to let it hold her back auditioning for the 2009 X Factor alongside Olly
    Murs and getting to the final 12 girls she relied on her HGV mechanic husband, Ryan,
    35, to describe even her favourite TV shows to her. And when their daughter, Ivy, was
    born last December, she could not see her face clearly.
    But on August 22, Kayley, of Gillingham, Kent, says she had the best birthday ever,
    thanks to a pair of special glasses which enabled her to at last see Ivy properly.
    She said: It was magical. I was lent the glasses to try, but if I can get a pair, itll change
    everything. I can watch Ivy in her Christmas plays and do her homework with her.
    Kayley first realised something was seriously wrong with her eyes when she was 15
    going to the doctor when she could no longer see the board clearly in lessons.
    She said: First I couldnt see the board, then I noticed my teachers faces disappearing,
    so I went to the optician.
    My first two tests were inconclusive, then I was diagnosed with Stargardt disease.
    It was a real shock for my whole family, as we have no history of it.
    Left unable to focus on objects or people, Kayley found the condition very difficult to deal
    with.
    She said: Its like someone has poured a big tub of glitter in the middle of my eye.
    Its really isolating. If Im in a roo *

    (c) Dukas

     

  • SCHICKSALE - Gesicht ihrer Töchter zum ersten Mal deutlich sehen: Kayley Storey kann mit Hilfe einer Spezialbrille ihre Makuladegeneration ausgleichen
    DUK10145505_007
    SCHICKSALE - Gesicht ihrer Töchter zum ersten Mal deutlich sehen: Kayley Storey kann mit Hilfe einer Spezialbrille ihre Makuladegeneration ausgleichen
    Kayley, pictured here with Ivy, was diagnosed with Stargardt Disease when she was 15 years old (Collect/PA Real Life). *** Former X Factor contestant gets gift of sight
    for her birthday thanks to miracle glasses allowing
    her to see her daughters face clearly for first time
    By Harriet Bullough, PA Real Life
    A former X Factor contestant was given the gift of sight for her birthday when miracle
    glasses allowed her to see her daughters face clearly for the first time.
    Professional artist Kayley Storey, 33, was just 15 when she was diagnosed with rare
    Stargardt disease, an inherited eye condition affecting an area of the retina known as the
    macula and reducing central or detailed vision.
    While she refused to let it hold her back auditioning for the 2009 X Factor alongside Olly
    Murs and getting to the final 12 girls she relied on her HGV mechanic husband, Ryan,
    35, to describe even her favourite TV shows to her. And when their daughter, Ivy, was
    born last December, she could not see her face clearly.
    But on August 22, Kayley, of Gillingham, Kent, says she had the best birthday ever,
    thanks to a pair of special glasses which enabled her to at last see Ivy properly.
    She said: It was magical. I was lent the glasses to try, but if I can get a pair, itll change
    everything. I can watch Ivy in her Christmas plays and do her homework with her.
    Kayley first realised something was seriously wrong with her eyes when she was 15
    going to the doctor when she could no longer see the board clearly in lessons.
    She said: First I couldnt see the board, then I noticed my teachers faces disappearing,
    so I went to the optician.
    My first two tests were inconclusive, then I was diagnosed with Stargardt disease.
    It was a real shock for my whole family, as we have no history of it.
    Left unable to focus on objects or people, Kayley found the condition very difficult to deal
    with.
    She said: Its like someone has poured a big tub of glitter in the middle of my eye.
    Its r *

    (c) Dukas

     

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