Living with a neuromuscular disease means facing new challenges every day.
Enroll with MDFF today to participate in all the exciting programs and activities offered!
How We Help Indiana
The Muscular Dystrophy Family Foundation uses its collective resources to help those with a neuromuscular disease live safer, more independent lives. Some examples of past types of support we’ve provided include:
- Adaptive Equipment
(e.g., ramps, lifts, wheelchairs, and wheelchair components) - Home Modifications
(e.g., bathroom modifications and bathroom equipment) - Transportation
(e.g., van conversion assistance, transfer seats, and vehicle lifts)
Accessible Van Giveaway Program
The Muscular Dystrophy Family Foundation regularly awards wheelchair-accessible vans to families needing reliable transportation.
Learn About the Van Giveaway Program
Events
The Muscular Dystrophy Family Foundation hosts free, fun-filled social events throughout the year to strengthen our community and help families make connections.
We also host fundraising events which enable us to continue our everyday impact on local families coping with MD.
Timothy J. Doyle Golf Outing
The Timothy J. Doyle Golf Outing will be held Monday, May 12, 2025. We’ll be at Hillcrest Country Club again for our annual golf outing in honor of MDFF’s former president, Tim Doyle. Early Bird Tickets are available until March 11. Register here
Mobility Gala: Shake Rattle and Roll
MDFF is upping the ante with a fresh new take on our annual fundraiser!
Friday, September 19, 2025; Biltwell Event Center
Join us for a marvelous evening of dinner, cocktails, auction, and gaming entertainment with a 50’s style theme!
“My long, portable ramp from MDFF donors has opened doors (almost literally) for me. It’s unlikely that I would have ever been able to visit my daughter in Florida without it. Thank you so much.”
James, Limb-Girdle Muscular Dystrophy Patient
MDFF Portable Ramp Recipient
Mission
The Muscular Dystrophy Family Foundation uses the power of giving to increase the quality of life and independence of people with muscular dystrophy—and empower their families—through advocacy, education, and financial assistance.