What we do

The Duchenne Family Support Group (DFSG) exists to provide support for families with children diagnosed as having Duchenne Muscular Dystrophy (DMD).

The DFSG is a national charity run by families for families affected by DMD. It provides a positive national support network of parents, their families and professionals.

The DFSG helps bring families together for mutual support, sharing of information and experience, and social activities. The DFSG produces a quarterly newsletter, has an informative website and also offers a family help line. Families can ring the office about any questions or problems they may have, and we can also try and put them in touch with a family in their area. Please see https://dfsg.org.uk/

Is there a charge to use this service?

No

Can anyone use this service?

Anyone can contact us directly

Service details for this family support services

Language: English only

• Can provide specialist support for families of children with disabilities / additional needs Yes Please contact to discuss your child(s) needs further.
• Relevant staff have a valid current DBS? No

 Address

 You can send post here:

78
York Street
W1H 1DP

 Website

https://www.dfsg.org.uk/index.php