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Find support, or help research

People near you who know what living with Myasthenia gravis is like, and ways you can help find better treatments.

Support groups in United States

  • Conquer Myasthenia GravisUS nonprofit helping myasthenia gravis patients and families with support, education and community.
    All of United States
  • Genetic and Rare Diseases Information CenterNIH information center (GARD) providing reliable information on genetic and rare diseases to patients and families via website and contact center.
    All of United States
  • Muscular Dystrophy AssociationUS nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS and related neuromuscular diseases.
    All of United States
  • Myasthenia Gravis Association (MGA)Kansas City-based association offering support groups, education, new patient packets and resources for people with myasthenia gravis and their families.
    Kansas City, MO
  • Myasthenia Gravis Foundation of AmericaThe largest US patient advocacy organization solely dedicated to myasthenia gravis: support, education and research funding.
    All of United States
  • Myasthenia Gravis Foundation of Michigan (MG-MI)Serves the Michigan myasthenia gravis community with patient support, support meetings, education, newsletters, a provider directory and advocacy.
    Grand Rapids, MI
  • The MG AllianceUS coalition of nonprofit myasthenia gravis organisations offering support groups, education, awareness, advocacy and events for patients and families.
    All of United States
  • The Myasthenia Gravis Association of Colorado (MGAC)Denver-based volunteer association serving people with myasthenia gravis and families through education, publications, support groups, chats and research funding.
    Colorado
  • The Myasthenia Gravis Association of Western PennsylvaniaWestern Pennsylvania association serving people with myasthenia gravis through support groups, a mental health toolkit, newsletters, education and events.
    Pittsburgh, PA
  • National Organization for Rare DisordersUS national rare disease alliance of patient organizations: education, patient assistance programs, rare disease database and policy advocacy.
    All of United States

Contact details come from each group's own page and are checked every 3 months.