The largest patient advocacy organization dedicated solely to MG. Support groups, a patient registry, the myMG symptom tracking app, webinars, and a curated books and media list.

https://myasthenia.org/

Focused on wellness and quality of life alongside medical treatment, not instead of it.

https://mgholisticsociety.org/

MGteam is a free online community for people living with myasthenia gravis and the people who care about them. Here, you can connect with others who truly understand, share your story, and find practical, medically reviewed information about symptoms, treatments, and research.

https://www.mgteam.com/abouthttps://www.mgteam.com/about

Patient support hub with an advocacy group directory and a mental health webinar series, since rare disease and mental health go hand in hand more than people talk about.

https://morethanmg.com/

Several states have their own MG foundations (California, Michigan, Illinois, and others), often with local support groups and sometimes financial or clinic assistance. Worth a search for your specific state, MGFA’s site links out to several of these.