Also great gif 😆

Thank you 🤍

@whitneydafoe.bsky.social @mecfsnews.bsky.social @karenwestphysio.bsky.social @malnutritionme.bsky.social @thesicktimes.org @meactnet.bsky.social @aaronca11.bsky.social

t.co/EznZ9NoczS

Same. Sometimes we got to pick our battles. I had a jaw specialist ask me but he seemed like he didn’t truly want to understand, so I gave a short answer and went back to talking about TMJ pain.
🪫 too low on mental energy.

That’s interesting , any idea how it fixed your allergy?

If you have MECFS especially together with EDS carefully consider the risks of the vaccine. Many of us became much more severe with new health issues from it (not returned to baseline since 2021)

Imagine everything they could’ve done for me since childhood.I could’ve had a life , it’s been pure misery since age of 11. I could’ve had a life but nobody listened or cared.
My life is over now.I never got the chance to be me and experience everything that made life worth livingThey let me suffer

When something is so very wrong but ignored 😢

extreme memory loss, unable to concentrate and extreme difficulty processing information. Feel my head is inflamed and my brain is being squeezed all the time. Maybe I could’ve had a life if they helped in the past or now.
Nobody ever helped me and now life isn’t worth living anymore

[3/3] Every night I don’t remember most of what happened during the day, many gaps in my memory.
Does anyone else with ME or LC experience this? I’ve been living like this for many years, most of my twenties.

#MECFS #LongCOVID #PCVS #neurology

[2/3] I experience disorientation, confusion, and have difficulty thinking clearly. Mentally I black out.
When it gets really bad, I have intense vertigo, nausea, and visual disturbances (more severe than usual).

UK