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By Disabled People for Disabled People

Thursday, 20 February, 2020

People with Chronic Fatigue Syndrome/ME share what it’s really like – Insider

“The best way to describe what I experience is a brain fog that sometimes simply won’t lift.” iStock / Getty Images Plus

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After months of struggling both mentally and physically to do simple tasks, dealing with constant, extreme exhaustion that wouldn’t go away no matter how much I slept, in 2015, a doctor told me I had Chronic Fatigue Syndrome (CFS).

Having never heard of it, my response was skeptical, and somewhat annoyed — similar to when you’re told “it’s only a virus” after having a miserable cold for weeks on end.

Click here to read full article https://www.insider.com/what-its-like-to-have-chronic-fatigue-syndrome-myalgic-encephalomyelitis-2019-11

Categories :
  • Chronic Fatigue Syndrome me/cfs
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  • Myalgic Encephalomyelitis ME/CFS
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