mecfs hashtag performance
#MECFS: Awareness. Chronic illness. Devastating. Energy limitations. Pain. Brain fog. Post-exertional malaise (PEM). Advocate. Invisible disease. Support. Community. Hope. Research needed. Diagnosis struggle. Understanding.
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Replying to @The_quad_father Yes, I can walk. No, that doesn’t mean I don’t need my wheelchair.
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Not every wheelchair user is paralyzed. Not every disability is visible. And not everything you see
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YouTuber and science communicator Dianna Cowern shares her experience with Long COVID and ME/CFS. Af
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Physics Girl has been bedridden for 2 years suffering from Long Covid and ME/CFS For years Dianna ha
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BEFORE the Vs existed #chronicillness #epilepsy #potssyndrome #dysautonomia #mecfs #myalgicencephalo
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ME is serious, complicated, & debilitating (and fatigue is not “being tired) #mecfs #chronicillnes
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What people think chronic fatigue looks like: “just a little tired.” What it actually feels like
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should i post the messages? also now extremely stressed bc the lab work is insanely important and wi
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feel free to leave more below! these are just my favorites 🌷 for hopefully all energy levels! �
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At the top of my page! #chronicillness #epilepsy #potssyndrome #mecfs #myalgicencephalomyelitis #dys
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