Webinar Recap: Financial Assistance Resources for the Myasthenia Gravis Community
Affording care for myasthenia gravis remains a challenge for many patients. Find practical guidance on navigating patient financial support programs.
Tag: advice
What gives you hope?
The MG Community shares what keeps them going, despite the hardships of the disease.
Navigating College When You Live with Myasthenia Gravis
How does MG change the college experience?
Laughing Despite (and, Sometimes, Because of!) Myasthenia Gravis: An Interview with Jane Marla Robbins
An actor and author living with MG shares how humor helps her cope
We somehow always find a way to get back up: My MG story
Rose was diagnosed with myasthenia gravis in the summer of 2022. Born in Senegal, she has lived in Canada for 20 years. She works as a project manager and a content creator in the personal beauty industry. She first noticed MG symptoms while applying her makeup one day. She started seeing double and noticed her […]
How to Create a Fundraiser for the Myasthenia Gravis Foundation of America
If you’re passionate about supporting the MGFA, organizing a local fundraiser is a great way to raise awareness and generate funds for research, patient support, and advocacy.
Real Talk About MG
How to explain the rare neuromuscular disease myasthenia gravis