Through the life services of Advocacy, Education and Consultation, Muscular Dystrophy Family Fund will enhance and strengthen the lives of individuals with neuromuscular diseases and to provide, or direct their families to valuable resources in helping our clients become successful contributors to the community.
MDFF exists to provide resources, services, and adaptive equipment to enable patients with neuromuscular diseases and their family members to live independent and productive lives.  The resources include the areas of:
  • Advocacy
  • Education
  • Emotional Support
  • Individual Education Programs (IEPs)
  • Sponsorship of Clinics
  • Mobility
  • Neuromuscular Community
Thanks to the generosity of our donors, the MDFF continues to succeed in its mission to provide adaptive equipment and emotional support to individuals and families affected by one of over 40 neuromuscular diseases.
To return to the Muscular Dystrophy Family Fund, click here.









 

 
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