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ME / Cfs support thread for those in the parallel universe

(1 Post)
gotmychocolateimgood Mon 03-Jun-19 15:29:35

Back story: I was diagnosed with ME 3 months ago and am unable to work. Really missing work right now. Symptoms began 5 years ago after a nasty chicken pox hit followed by labyrinthitis. I can potter at home, slowly, care for myself but struggle with horrendous fatigue and sleep 15 hours out of 24. Spaced out and headachey. Sensitive to light and sound. Creeping, itching sensations but luckily not much pain.
Would be nice to chat to others! 🙂

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