Living with a neuromuscular disease means facing new challenges every day.
Watch our video from Jacob Buehler on Tim Doyle’s passing and the future of MDFF.
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.
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.
MDFF Feud: Honoring Tim's Legacy
Register here for the 2024 Feud event on Thursday, September 12. Enjoy a silent auction, live auction, great food, drinks, and a DJ and dancing!
Holiday Party
MDFF Families, don’t skip this year’s Holiday Party on December 8, 2024. We will be hosting the event at The Marriott Indianapolis North starting at 1:00 pm.
Register Here: https://www.mdff.org/2024-holiday-party-registration
“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.