On the 4th of November 2017 our world changed forever – a chance meeting in the park would finally give us the answers we were seeking for 4 years, unfortunately the answer was Duchenne Muscular Dystrophy. Our cheeky boy Charlie takes this diagnosis in his stride every day, he fights the battle of constant pain, falls and the knowledge this condition is currently fatal. But what we do have is HOPE! Hope that a cure will be found to stop this deadly disease, hope that our boy will become the man he deserves to be, hope that babies born today will be able to run as fast as they can and feel the wind in their face.
This is why we walk, this is why we fight each and every day to raise awareness and much needed funds for research to eradicate this disease forever.
Family, friends and supporters please join us on the 16th of February to join our team to walk and if you can’t walk please donate, every single dollar helps.