Hope for Gabriel - Cure Duchenne

Six years ago our lives changed forever! Our beautiful little boy Gabriel was diagnosed with Duchenne Muscular Dystrophy, a progressive- life limiting-  muscle wasting disease. 

We sat in a hospital room and listened to the doctors explain that our son's muscles were slowly wasting away, he was going to lose the ability to walk and as he grew older, wheelchairs, breathing machines and disability equipment were going to become part of his life. 
The doctors told us that Duchenne was incurable with a limited life expectancy of late teens - early twenties... 
With tears in our eyes we watched our son  innocently playing , whilst the world crumbled under our feet. We were scared for his future and heartbroken - we still are - but we know we have to be strong to help our son fight this disease. 

Our Gabriel is kind, loving and a very brave little boy. He gets on with all the hospitals visits, clinical tests and many different specialists without a complain.  

With the kind support of  family and friends, we fundraise to aid clinical research and hope to give our little boy a happy fulfilling life! 

Please support our cause!

You can follow our journey by visiting our facebook page www.facebook.com/hopeforgabriel

Thank you for your support,

Ana & Steve ( Gabriel's mummy and daddy)


  • Anonymous 
    • £200 (Offline)
    • 2 mos
  • Alex Levin 
    • £30 
    • 7 mos
  • Lara Stavrinou  
    • £40 
    • 7 mos
  • Seda Durham 
    • £30 
    • 7 mos
  • Eleni Polycarpou 
    • £25 
    • 7 mos


Ana Chadwick 
London, Greater London, United Kingdom
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