I’ve lived with CFS/ME for 6/7 years now, it has been tough coping with this illness as not many doctors fully understand the condition and there isn’t much help when it comes to reducing the symptoms, but there is a lot of network support out there from people who either live with the condition themselves or know someone who does, I find this a great source of help as it means I’m not alone and I can talk about how I’m feeling and what I’m going through to someone who truly gets it. Not everyone has the same symptoms, but none of us ever think we have it worse as we all know we’re going through it and we’re doing it together with the help and support from one another.
Information on International CFS/ME Awareness Day, a Worldwide day event which is on the 12th May 2018.
— Read on www.whathealth.com/awareness/event/internationalcfsmeawarenessday.html
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