Thread by @AbyssPearl

My doctor dismissed me, my wordsw my symptoms, for 10 years (20 if you take the rest) then didn't see me for a few years.
Fast forward i'm very severe ME almost dying. He came because i've been almost dying for months. After YEARS.

He did ask me why he hadn't see me these past

https://twitter.com/PutrinoLab/status/1654956335891374081

few years.
Well I became housebound then completely bedridden, bedbound, because they didn't listen to me.

This was such an insult.

When I gave him (again) the list of symptoms I've been having and complaining about for 10 years, the reply was so insulting.

I was 100% bedridden. For weeks, months. At this point. In the dark. No energy. Difficulty breathing and speaking. Out of breath. Hurting like hell. Lost a lot of weight. Dehydrated.

He SIGHED. At my list of symptoms. Said that this was "a lot" like I was exagerating, inventing,

that it's not possible to have all of this. I said that these have been the same symptoms I had for 10 years. One adding to the list every month. The same symptoms they told me it was nothing. The same they dismissed for 10 years.

I was dying 🙂
Still dismissed me.

To the question : why haven't I seen you for a long time?

I said : because you never listened to me, and never took my pain and symptoms seriously.

The reply : me ? I would never do that.

Then procedeed to dismissed me again, the list, the sighs everything. Did nothing to

help me. (but obviously psychologising, and saying things (that could have helped) but never acted on it.)

They watch you die.

#pwme #meawarenessmonth #severeme #verysevereme #realityofMECFS #mecfs #MyalgicEncephalomyelitis #MyalgicE #dismissedpatients #millionsmissing #pots

I'm in France btw.
This really does happen everywhere in the world. We need to share more from various countries.