The DFSG is a national charity run by families for families affected by Duchenne muscular dystrophy. It provides a positive national support network of parents, their families and professionals. It helps bring families together for mutual support, sharing of information and experience, and social activities.
The charity offers:
- family outings and events each year
- workshops and an annual conference
- telephone support
- a subsidised annual group holiday
- DFSG fundraising events.
To learn more about the charity, visit their website at: dfsg.org.uk