r/NHSandME↗
ME/CFS + Fibro patients sharing news + NHS treatment
Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Fibromyalgia and possibly long COVID, are eerily similar sad diseases. These diseases utterly destroy the quality of life for countless thousands of people. Probably over 99% of patients using our wonderful NHS are treated well. However, regrettably, some are not. It's our belief those with ME/CFS/FM are disproportionately dissatisfied with the treatment they've received from the NHS. This sub provides testimonies from NHS patients.
562 subscriberssince 2021
r/NHSandME has 562 members.
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