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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.
I’m on the more severe side (bedridden, tubefed, unable to speak) but it’s nice to meet someone else with the disease too.
My condolences. Hope you find some relief.
Very informative. I know a couple of people who might be in this category and should read this.
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
