You don't have to face neuromuscular diseases alone. Each year, hundreds of people with a neuromuscular disease, and their loved ones, turn to the MDFF for support. We offer comprehensive support programs to ensure clients' medical and emotional needs are taken care of. Our staff and medical directors from our clinics will help you through every stage of your family journey. From wheelchairs to van lifts to communication devices and beyond, we can help you get the equipment you need to live with No Boundaries®.
MDFF is funded by direct contributions of cash, stock, gifts in-kind, estates, wills and trusts, from individuals and businesses, corporate sponsors, and proceeds from special events. MDFF is one of the restricted funds that administered by St. Vincent Foundation located at Indianapolis, Indiana. MDFF is an Indiana local agency that offers financial assistance to Indiana residents only.
Kim Bryan Stoneking, CAE - Executive Director
MDFF Board of Directors
Tim Doyle - President
Emily Munson - Vice President
Tom Olinger - Secretary
Matt Haab - Treasurer
Derek Miller - Past President
The Muscular Dystrophy Family Fund provides services to children and adults regardless of races, ages and genders.