Thread by @AbyssPearl

What I mean is that they saw me before. They saw me sick. They saw me moderate, mild, severe. They heard and witness the dozens of symptoms accumulating for years. They saw it. I didn't know what was happening to me. I checked SO MANY OF the mecfs symptoms for YEARS.
#meawareness

https://twitter.com/AbyssPearl/status/1655157519088513026

doctors even diagnose me orthostatomic hypotension, orthostatic intolerance, then pots. the raynauds, like a lot of these conditions. But they did nothing about it. "It will disappear" Guess what ? It got worse. i even had a test for an illness that causes red blood cells to not

be able to transport the oxygen through the body. like they all saw that something was wrong but it was "nothing"

Of course they kept blaming the fact that I was sick and getting worse on me. "I wasn't doing enough" while I was overworking and probably in crashes all the time.

I didn't know what was mecfs didn't know about it for years and years. everybody kept blaming me and my laziness (mind you I also struggled with chronic migraines, big allergies, endometriosis, the low blood pressure since being a CHILD (Teen for endo) so no I wasn't fucking lazy

If you add the mistreatment, the gaslighting, the abuse. And the anxiety and depression all of this caused.
I was killing myself at school cause it was the thing to do and no one recognized my illnesses.

They were no awareness, mental health didn't exist, endo didn't exist.

And apparentely these days "mecfs do not exist" for a lot of people 🤡 and if it does, "there's not such thing as severe or very severe mecfs"
well yes actually it DOES exist. you don't know or don't want to see it or don't acknowledge it.

This is why we all need raising

awareness for #ME #MECFS #SEVEREMECFS #VerySevereME #pots #oi #oh #MyalgicEncephalomyelitis #MyalgicE #ChronicPain #chronicillness #millionsmissing #pwme #dontletmeDIE