About The Muscular Help Foundation (MHF)
MHF exists to deliver unforgettable experiences in the UK (which the charity calls Muscle DreamsTM) designed to help children and young people whose lives are afflicted by the muscle wasting disease, muscular dystrophy, the single biggest genetic killer of children in our world today.
About Muscular Dystrophy (MD)
Muscular dystrophy is a relentless, cruel and unforgiving disease. In the UK alone, there are some 60,000 sufferers being robbed of their mobility, independence and finally for those children with the most severe type (mainly boys) their lives. Despite ongoing global research efforts, there is still no cure or treatment to delay or reverse the disease.
About MHF’s Founder
Michael McGrath was diagnosed with muscular dystrophy in 1984 when he was in his late teens. Over the past 25 years, the deteriorative nature of the disease has meant that Michael, who was once extremely competitive and loved his sports, has today lost his ability to walk and now uses a powerchair (known affectionately as his ‘chariot’) to get around. Michael brings a deep understanding of the disease as well as the challenges and frustrations that sufferers and their families must face – at the heart of this understanding lies the reason and the motivation that MHF came to be, with the simple aim to deliver amazing experiences for those whose lives are, like Michael’s, being slowly destroyed by this remorseless disease.
Through the charities Muscle DreamsTM programme, selected beneficiaries are given the opportunity to live a dream, or perhaps fulfil a cherished ambition.
With its entrepreneurial spirit, corporate mindset, dynamic approach and determined focus, the charity’s Trustees and Friends have established a vibrant resource network, rooted in the notion that delivering real experiences for those with muscular dystrophy is far beyond the scope of any one individual or organisation.