myastheniagravis hashtag performance
#Myastheniagravis on TikTok: Sharing struggles, triumphs, and daily life with MG. Raising awareness, connecting patients, advocating for research, and fostering community through relatable content.
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**Update: I added my venmo to my bio if anyone wants to help. Everyone has been so kind. I am going
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Just an update for my friends over here. If you have MG, Check medication contraindications bc you c
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Tag anyone from this list please also, drop anyone extra you can think of I can reach out to please!
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This happened because of a contraindicated medication with my disease, Myasthenia Gravis. I had a to
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I want to thank soooooooioo many of you for all of your love support and encouragement over the last
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#greenscreen Dr McSteamy from Greys has #als #lougehrigsdisease #neuromusculardisease #myastheniagra
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I have addressed this before when he did the SAME thing and this one is worse. #myastheniagravis #do
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Replying to @maplebugs #symptoms #ALS #lougherigsdisease #myastheniagravis #mg #lamberteatonmyasthen
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Replying to @judyrodriguez812 I couldn't even swallow and ice chip without aspirating. I have a whol
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JUST BECAUSE ITS RARE DOESNT MEAN IT DOESNT EXIST! I can’t believe it’s been almost three years
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JUST BECAUSE ITS RARE DOESNT MEAN IT DOESNT EXIST!!! It gets worse. I have more guys don’t your wo
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Today is a much needed #restday which is a mandatory reality when you live with #chronicillness Th
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Replying to @learningtosee a little about my journey. It has involved moving across the country, bei
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Replying to @john Drakeford thank you! I’ll be looking into this! Hoping for less flares in my fu
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I was severely gaslit and this disease left me bedridden for two years. I was then in a wheelchair a
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Big blood return celebration!! Since o got my double lumen placed, I’ve been having some difficult
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Replying to @Bee 🐝 It’s a lot of info at once but if you have ANY questions, I can answer from
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