The North Pole was reached in April 2002 and the South Pole in January 2004 – in so doing, Michael made history by becoming the first disabled person in the world to have successfully led expeditions to both Poles. What makes this achievement all the more remarkable is that in 1984, aged just 18yrs, Michael was himself diagnosed with MD.
The charity was first known as ‘pole2pole’ before being later renamed ‘The Muscular Help Foundation’ and then finally ‘The Muscle Help Foundation’. Learn more about the charity’s impact, the team and its current Trustee Board.
Rooted in the idea that well executed, shared experiences can be powerfully transformative in nature, MHF delivers what it calls Muscle Dreams for children, young people and young adults (8-28yrs) in the UK with the muscle wasting disease, Muscular Dystrophy (MD) and allied neuromuscular conditions – these highly-personalised, restorative experiences are uplifting, joyful and often cathartic in nature. See testimonials from some of our beneficiaries, families, volunteers and also special messages of support from Sir Kenneth Branagh (an MHF Patron) and Sir Richard ‘Dickie’ Attenborough to name a few.
MHF is a small (currently one full-time paid member of staff), multi-award winning charity (entrenched in family values) with national reach. It has a singular focus to deliver 657 Muscle Dreams, one life-changing experience for every muscle in the human body.
Anchored at the heart of the charity is a unique initiative designed to allow anyone to quickly grasp, support and champion our work – learn more about the #powerof657 and how you can get involved by either fundraising for us, joining our Muscle Warrior tribe as a volunteer or becoming a strategic corporate partner.
As of October 2020, MHF will have delivered 312 Muscle Dream experiences – it’s impact is being felt across the UK by beneficiaries, families, their friends and the wider community including schools.
MHF has over many years established friendships and partnerships with other muscular dystrophy charities across the UK such as Spinal Muscular Atrophy UK, the Eileen McCallum Trust, DMD Pathfinders, Duchenne Family Support Group (DFSG) and Muscular Dystrophy UK as well as relationships with many UK hospices including: Acorn’s Children’s Hospice, Hope House Hospice, Chestnut Tree House Hospice, The J’s Hospice, Keech Hospice, Naomi House & Jack’s Place Hospice, Shooting Star Chase Hospice and Ty Hafan Hospice to name but a few.
MHF is a member of Together for Short Lives, a leading UK charity for children with life-threatening & life-limiting conditions. The charity is also a member of the Fundraising Regulator, Stewardship (helping the Christian community in the UK to give and to receive), the Disabled Children’s Partnership (DCP), the UK Genetic Disorders Partnership Network via Genetic Disorders UK (national charity working to improve the lives of individuals and families living with a genetic disorder) and Genetic Alliance UK (consisting of over 200 patients organisations working to improve the lives of patients and families affected by all types of genetic conditions).