Muscular Dystrophy Family Foundation Inc

The Muscular Dystrophy Family Foundation (MDFF) mission is to increase the quality of life and independence of Hoosiers with neuromuscular diseases – and empower their families – through advocacy, education, and financial assistance. 

Costs associated with necessary equipment can be unaffordable for many families living with muscular dystrophy.  Wheelchairs can cost from $15-80k depending on type.  Accessible vans can run $30-60k or more for reliable transportation, and home modifications for accessibility can often be well above $10k.

In the U.S. alone, there are about 250,000 people with some form of muscular dystrophy and thousands newly diagnosed each year. There is no cure for these progressive diseases and for many families, support beyond medical care is critical to their emotional needs and overall health outcomes.

MDFF provides year-round support to Hoosier families by offering:

--cost-free social family outings to create a sense of community and healthy recreational breaks from illness

--adaptive equipment (ramps, lifts, wheelchairs, etc) and home modifications vital to increased independence and accessibility

--one-of-a-kind accessible van giveaway each year, allowing reliable transportation, greater mobility, and a sense of freedom to enjoy life

--scholarships to pursue education goals and financial awards to encourage pursuit of a dream or goal

MDFF is here to help families get what they need to live safer, more independent lives.