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#mecfs

11 clips from 6 authors · 2.4M total views. Every clip opens with its own counters and comments.

i’ve been slowly working on a faq post for like a month and a half now — @angelfairer

1.4M@angelfairer

This is a total game changer! Introducing the all-in-one Rollator and — @kaya.mieko

488.7K2:54@kaya.mieko

educational repost on PEM source: batemanhornecenter #mecfs #myalgicen — @angelfairer

371.7K@angelfairer

Replying to @Qv_411 what do i do for my husband? #mecfs #chronicillnes — @angelfairer

46.2K1:54@angelfairer

This is probably the most vulnerable thing I’ve shared on the internet — @faythegay

24.4K9:59@faythegay

Having different ways of describing, even quantifying pain, disability — @littlemissdiagnosed

15.9K1:30@littlemissdiagnosed

Patients with severe Long COVID & Myalgic Encephalomyelitis can’t acce — @erinrackham

8.3K2:27@erinrackham

I’m grateful and lucky to be in the “post”-trauma from my most severe — @erinrackham

3.9K2:56@erinrackham

Things are really hard right now, but that’s real life. If you have to — @faythegay

2.4K9:55@faythegay

Long covid and an immune system that sucks led to pots, mecfs, mcas, a — @askdrmom

1.5K1:35@askdrmom

What should I name my butterfly? #mecfs #myalgicencephalomyelitis — @faythegay

1.4K3:49@faythegay

Top authors

@angelfairer3 clips @kaya.mieko — TikTok avatar

@kaya.mieko1 clip @faythegay — TikTok avatar

@faythegay3 clips @littlemissdiagnosed — TikTok avatar

@littlemissdiagnosed1 clip @erinrackham — TikTok avatar

@erinrackham2 clips @askdrmom — TikTok avatar

@askdrmom1 clip

Related tags

#myalgicencephalomyelitis #pots #chronicillness #longcovid #heds #chronicpain #ifs #dysautonomia