this post was submitted on 10 Jul 2024
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[–] [email protected] 5 points 4 months ago (1 children)

I have ME/CFS. I have it relatively mildly and it's still the worst thing that's ever happened to me. I used to get migraines once or more per week so bad that I would vomit and could do nothing but go to bed and try to sleep. I would rather go back to that.

[–] [email protected] 7 points 4 months ago (1 children)

I’m on the more severe side (bedridden, tubefed, unable to speak) but it’s nice to meet someone else with the disease too.

[–] [email protected] 3 points 4 months ago

My condolences. Hope you find some relief.

[–] [email protected] 2 points 4 months ago* (last edited 4 months ago) (1 children)

Very informative. I know a couple of people who might be in this category and should read this.

[–] [email protected] 3 points 4 months ago

This website helped one of my friends a lot when they were first wondering if they had the condition :) https://me-cfs.github.io/useful-resources.html