Helena Bonham Carter: New Patron of Action Duchenne

Duchenne Muscular Dystrophy has no cure. It is caused by mutations in the dystrophin gene which prevent correct readings of the genetic code. This results in no dystrophin, an essential muscle protein, to be produced in the body. No dystrophin allows a progressive wasting of the muscle, limiting mobility in teenage patients (boys and men). Premature deaths happen from respiratory or cardiac problems since the heart muscle is affected by the genetic defect.

Duchenne affects 2,500 people in the UK and about 40,000 people worldwide.

Nick Catlin, CEO of Action Duchenne said; “Helena Bonham Carter and our other supporters provide an incredible boost to all Duchenne sufferers and their families. It is uplifting that people whose lives are untouched by this disease are still able to demonstrate compassion and support for families that are affected by this devastating, life-limiting condition. We are very grateful to all our patrons and the support that they give – our fundraising efforts will continue to be a focus to find a cure for this disease.”

Click here ( http://www.actionduchenne.org/ ) for more information about the charity and the disease.