Latest Post
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
LATEST FROM THE MGFA INSIDER BLOG
My MG Story: Danielle’s Journey with Seronegative Myasthenia Gravis
Danielle wants to share her treatment journey to help others understand the challenges of finding the right approach.
Running for a World Without MG: Kristy’s Story
Kristy shares her MG story and why helping others living with the disease is important to her.
MGFA Advocacy Update
Learn more about Rare Disease Week on Capitol Hill and hear the latest on our advocacy efforts.
MGFA and Bionews Partner to Deliver Myasthenia Gravis News to Wider MG Community
Myasthenia Gravis News, delivered by Bionews, is an online news source intended to provide the myasthenia gravis (MG) community with the most recent news and information about MG, as well as first-hand community perspectives from patient and caregiver columnists.
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 […]
A Mother’s Commitment
"The driving force behind my commitment to the MGFA is to help people know about MG."
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
Physical Therapy and Myasthenia Gravis – Webinar Recap
Is it safe to do physical therapy or exercise when you have myasthenia gravis?