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The latest #MyastheniaGravis treatments are making a difference for many: hubs.la/Q03rT0wy0 #MGawareness

Read more about Valerie's #myastheniagravis journey ow.ly/jIs750W8K2y

Join us on June 30 for "The Changing MG Conversation," a special MG Awareness Month webinar with Dr. Jeffrey Rosenfeld of Loma Linda University. Dr. Rosenfeld will argue why this is an unprecedented time to be part of the MG Community. Register: ow.ly/ZCUI50We96z

“MG is a huge barrier – it takes so much from us – but you’ve got to take it back. Don’t let it take away your joy. I started getting back to music one little bit at a time. Slowly but surely, you build up those muscles and you build up the courage.” - Dania

What is myasthenia gravis? Learn more in this informative YouTube video. Share with friends and family who need to know. youtu.be/1nsRqTqn2r8?si…

Seronegative #myastheniagravis, meaning your blood does not contain antibodies known to cause MG, is an especially difficult form on the disease.

For all the #MGWarriors out there: we see you. #MGAwarenessMonth #MyastheniaGravis

As #MGAwarenessMonth draws to a close, we're excited to share details on our new Virtual Adaptive Yoga program designed specifically for those with neuromuscular disorders, including #myastheniagravis. Created in partnership with patient advocate Deborah Vick and NMD Pharma's

, Every year, we join forces to help the world know about myasthenia gravis. Thank you for an incredibly productive month, turning awareness into action!

Tips for managing MG and summer heat on #IndependenceDay: * Know your limits. Don't be afraid to turn down invitations or leave early. * Cold + Refreshing + Hydrating = Your snack mantra! * Use MGFA's Partners in MG Care list for care while traveling. ow.ly/K2PM50WiHUU

From MG to MD, read one man's MG story of hope and persistence ow.ly/brq050WleKt

"Living with chronic illness and navigating work is basically a job in itself." Find strategies in this MGFA webinar, sponsored by Immunovant. ow.ly/gVWl50WleKJ

Join us to learn more and ask your questions about participating in a clinical trial. This webinar is sponsored by argenx. Register: myasthenia.org/mgfa-events-we…

Read the rest of Greg Olson's inspiring blog post: mglifebygreg.com/find-joy

You don't need to walk your #MyastheniaGravis journey alone. Register for the MG Walk. mgwalk.org

Programs are available to help you cover the cost of medical care when you live with myasthenia gravis. Learn more about grants from partner organizations: myasthenia.org/living-with-mg… *Note - these funds are available to United States residents.

If you have MuSK MG, learn more about this important study - musk1000.smhs.gwu.edu

What you do after getting the diagnosis can help shape the path that your #myastheniagravis will take. Here is what volunteer Rebecca wishes she knew when she was diagnosed. myasthenia.org/blog/2021/10/1…

"Say ahhh!" is not straightforward when you live with muscle weakness and fatigue. Check out these tips for a successful dentist visit from dentist and MG patient Dr. Gene Casagrande. ow.ly/nNaM50WrcWu

If you are sweating under a heat dome right now, read these tips for staying cool. Hot weather can exacerbate myasthenia gravis symptoms. Take care! myasthenia.org/blog/2024/06/2…