Myasthenia Gravis Foundation of America Inc

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#MyastheniaGravis Foundation of America (MGFA) is the largest nonprofit patient advocacy organization dedicated solely to improving the lives of people with MG. For a world without MG

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800633798

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Address: 355 Lexington Ave Fl 15, New York CityWeb: Sign in to see organisation websiteFacebook: MyastheniaGravisFoundationX (Twitter): myastheniaorgICO: 800633798

Home | Myasthenia Gravis Foundation of America Search Newly Diagnosed Guidance if yourenewly diagnosed with MG Read More Connect With Others Find the support you need Read More MG Research Latest clinical researchand discoveries Read More Volunteer Today. Get involvedwith MGFA Read More Welcome MGFA is the largest leading patient advocacy organization solely focused on myasthenia gravis. We support those living with MG and create connections for the MG community. Learn more about our mission What is myasthenia gravis.

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Ann

So grateful for the support and resources MGFA provides! It's uplifting to see a community come together for a common cause. πŸ’œ #HopeForMG

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Myasthenia Gravis Foundation of America Inc

"I was diagnosed with MG in 2023. It took them a year to diagnose me, but I have MuSK MG, which is very hard to treat. It's a hard disease to deal with but I do it.

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Kate

1. What are some ways the Myasthenia Gravis Foundation of America (MGFA) can enhance community engagement and support networks for those newly diagnosed with MG?

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Lucille

2. How can advancements in clinical research for Myasthenia Gravis be better communicated to patients and their families to ensure they are informed about the latest treatment options and resources available?

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Monica

Just learned about the importance of early diagnosis and support for MG! Let's spread the word and help those affected find the resources they need. Together we can make a difference! 🌟 #MyastheniaGravis #MGFA

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