Kyra

myastheniagravis hashtag performance

#MyastheniaGravis: Awareness, strength, living, sharing, struggles, diagnosis, treatment, support, autoimmune, chronic, invisible illness, education, community, resilience, inspiring, advocacy, hope, understanding.
**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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**Update: I added my venmo to my bio if anyone wants to help. Everyone has been so kind. I am going
#myastheniagravis #medicalgaslighting #mg #anxiety
Replying to @LisaM #mg #myastheniagravis #vyvgarthytrulo #chronicillness #remission
#greenscreen Dr McSteamy from Greys has #als #lougehrigsdisease #neuromusculardisease #myastheniagra
Replying to @maplebugs #symptoms #ALS #lougherigsdisease #myastheniagravis #mg #lamberteatonmyasthen
#CapCut What it’s like living with #LEMS, an ultra rare #neuromusculardisease. I don’t talk abou
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#CapCut What it’s like living with #LEMS, an ultra rare #neuromusculardisease. I don’t talk abou
I could go on and on, but if you are chronically ill, please try and have a support system. Wether i
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I could go on and on, but if you are chronically ill, please try and have a support system. Wether i
Just not feeling it today #chronicillness #migraine #pituitartytumor #myastheniagravis #sunt #trigem
K infusion and birthday pastry’s #chronicillness #migraine #pituitartytumor #myastheniagravis #sun
I was severely gaslit and this disease left me bedridden for two years. I was then in a wheelchair a
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I was severely gaslit and this disease left me bedridden for two years. I was then in a wheelchair a
Big blood return celebration!! Since o got my double lumen placed, I’ve been having some difficult
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Big blood return celebration!! Since o got my double lumen placed, I’ve been having some difficult
Replying to @learningtosee a little about my journey. It has involved moving across the country, bei
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Replying to @learningtosee a little about my journey. It has involved moving across the country, bei
Having MG isn’t fun at all- BUT I see it as a superpower.   My body lets me know that I’m sick b
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Having MG isn’t fun at all- BUT I see it as a superpower. My body lets me know that I’m sick b
Jen is back at it again today at the MGFA 2025 Annual Conference in Phoenix, Arizona!  #myastheniagr
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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Replying to @Bee 🐝 It’s a lot of info at once but if you have ANY questions, I can answer from
PT was good but I'm exhausted now. Fatigue and possible flare-up is showing up.  Do any of you take
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PT was good but I'm exhausted now. Fatigue and possible flare-up is showing up. Do any of you take

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