Top Tweets for #MGFA on Twitter.

Search results for #MGFA

Myasthenia Gravis Foundation of America @MyastheniaOrg

3 weeks ago

These are just a few of the ways that we at the MGFA aim to create a world without MG. We're so grateful for your support as we work to connect patients with resources, create community, raise awareness, and more. #MGFA #MGStrong

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Phlegm Wadd @SeeFred1

a month ago

Make gaslighting funny again #MGFA

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Myasthenia Gravis Foundation of America @MyastheniaOrg

a month ago

Scott Bejda's story is one of resilience and determination. Living with #myastheniagravis for more than 20 years, he has made his mark on hip-hop media, interviewing industry giants while managing his symptoms. Learn more at the #MGFA blog: ow.ly/xt1I50QZUnk

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Myasthenia Gravis Foundation of America @MyastheniaOrg

a month ago

Thanks to the @EveryLifeOrg for organizing Rare Disease Week on the Hill! Advocates — including those with MG like Siobahn — are making a difference. Read about her experience at the #MGFA blog: ow.ly/ahlg50QWZcJ #RareDiseaseWeekOnTheHill

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Myasthenia Gravis Foundation of America @MyastheniaOrg

a month ago

Want to feel more in control of your healthcare experience? Heather Finlay-Morreale, MD, shares her tips on how to make the most of your doctor appointments in #MGFA's most recent blog. ow.ly/lbFU50QStMG

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Be seen and heard! Become the story of hope newly diagnosed #myastheniagravis patients need to hear, and strengthen our campaign of turning awareness into action. Reach out today to share your unique MG journey. ow.ly/Vhko50QPbYn #MGStrong #MGFA #Autoimmune #RareDisease

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

How are you preparing for MG Awareness Month? Here are #MGFA's tips for getting a head start. Explore our full #MGAwarenessMonth Toolkit here: ow.ly/kGRv50QNSVt #MGstrong #MGFA

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Newly diagnosed with myasthenia gravis? Bridget Noujaim sheds light on her MG journey — from diagnosis to living life fully. Read her story: ow.ly/QvP150QL1tu via @GoodRx #MyastheniaGravis #MGStrong #MGFA

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East Side Eagles @EastSideEagleMB

2 months ago

The 2024 MGFA Online Registration is now open. Eligible Birthdates: Born between 01/01/2010 and 12/31/13 eastsideeaglesmb.ca/mgfa-registrat… In person dates available to assist please contact [email protected] 📸: Ang Deneka Photos Athletics #mgfa #fbmb #eastsideeagles

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East Side Eagles @EastSideEagleMB

2 months ago

Girls football registration opens March 4. More information on our website eastsideeaglesmb.ca #mgfa #winnipeg #204 #mbfootball #girlsinsports

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VICKtorious @vicktorious_npo

2 months ago

This year I could not be in DC but I still can share my story! @ForwardRolling #RareDisease #Advocacy #EhlersDanlosSyndrome #EdsSociety #MGFA #MyastheniaGravis myasthenia-gravis.com/living/rare-di…

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Join us at MGFA’s Community Health Fair in SF on Mar 2, 10AM-2PM, to navigate MG with experts. Free resources & community support await! Thanks to our sponsors Alexion and argenx! Register now: ow.ly/sEmr50QGOhE #MGFA #MGStrong

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

This #RareDiseaseMonth, you can make a difference in #MyastheniaGravis research. Join the MGFA Global Patient Registry at mgregistry.org. Your participation matters! #MGFA #MGstrong #PatientRegistry

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Celebrate #RareDiseaseMonth by registering for the 2024 National Patient Conference in Tampa, FL, Apr 28-30, FREE for MG patients & caregivers! This is a unique opportunity to connect & learn. Will we see you there? ow.ly/BQYx50QyTyZ #MGFA #MGStrong #RareDisease

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Spread love this February 💕 #RareDiseaseMonth meets #ValentinesDay, a perfect time to embrace the MG Community with open arms. Share your support and connect with MG patients just like you at #MGFA's Community hub: myasthenia.org/MG-Community

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Mark #rarediseaseMonth by equipping yourself with knowledge! The #MGFA Wellness Webinar "What’s Your Antibody?" by Dr. Srikanth Muppidi addresses the vital role of understanding antibody status in managing a #raredisease like myasthenia gravis. ow.ly/Jz8k50QyT6q #MGStrong

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Myasthenia Gravis Foundation of America @MyastheniaOrg

2 months ago

Maximize your doctor visits! Join our webinar with Dr. Heather Finlay-Morreale from UMass Medical School. Get expert tips on effective patient care, Feb 22 at 3PM ET. #WellnessWebinar #PatientCare #MGFA #MGStrong Register here: ow.ly/qQXt50QySYT

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Myasthenia Gravis Foundation of America @MyastheniaOrg

3 months ago

Join us this #RareDiseaseMonth in funding the path to a future without Myasthenia Gravis. Your donation to #MGFA supports crucial research and hope. Let’s make a difference together. Contribute today: ow.ly/YmKC50Qzky2 #MGStrong