Group photo of Duchenne Families cropped

Families Supporting Families

You are not alone. Whether you are dealing with a new diagnosis of Duchenne Muscular Dystrophy (DMD), or are further along in the journey, the Duchenne Family Support Group is here for you. Our helpline: 0800 121 4518

The DFSG is a UK national charity, run by families for families affected by DMD. We have been bringing people together for mutual support, information sharing and social activities since 1987.

All of our board of trustees and our Development Officer have experience of living with a family member with Duchenne.

The Summer Edition of the Duchenne News is out soon! The newsletter is packed with articles, stories and information about Duchenne.

If you have a family member with Duchenne muscular dystrophy, or you are a care professional with an interest in the condition, and you would like to receive the newsletter regularly, please sign up here.

Membership of the Duchenne Family Support Group is free and without obligation.

Captain Tom 100

Captain Tom Fundraising Logo

2021 has been a challenge for DFSG and like other small charities we are trying to raise money in many ways. Linking into Just Giving and Captain Tom100 is a way in which anyone can get involved and raise money. Find out more here


The London Marathon

The London Marathon is our biggest fundraising event, and its cancellation last year saw quite a big reduction in our income. However, it’s all systems go for the actual, and the virtual, London Marathon this year with both events taking place on Sunday, 3 October. We still have places available. Find out more here

Fundraise for the Duchenne Family Support Group when you shop online

Fundraise for Duchenne Family Support Group when you shop online
DFSG Logo