ME/CFS An introduction and how the medical industry has failed sufferers.

What is Chronic Fatigue Syndrome?

Chronic Fatigue or ME/CFS is a complex multi-system illness, characterised by debilitating fatigue, body wide pain, and exercise intolerance where there are no bio-medical markers. It’s a spectrum disorder so some individuals are able to function with relative normality, attending work and social activities and at the other end of the spectrum, patients (need a better word – sufferers maybe?) may be completely housebound or bed bound and need additional care.

Why talk about it?

The #millionsmissing campaign – there are millions of people who are affected and because they cannot leave their house, they cannot integrate into society leaving them feeling forgotten and depressed with a complete lack of support. Language around ME/CFS consists of lazyitis, the yuppy flu and this language serves to further segregate those who are experiencing it. There is a huge need for more research and that starts with more awareness.

Who does it effect?

ME/CFS can affect children and adults alike but more commonly, it is seen in mid-teens, early twenties and mid-forties. It seems to affect more women than men – is this because it is less reported in men than it is with women?

Papers/sources for referencing:

Age of onset: https://meassociation.org.uk/about-what-is-mecfs/ and https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-014-0167-5

Age of onset and general ME/CFS description: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370741/

Chronic fatigue syndrome/myalgic encephalomyelitis (or encephalopathy): diagnosis and management:

https://www.nice.org.uk/guidance/cg53/chapter/1-Guidance#diagnosis

What is ME/CFS?:

https://www.cdc.gov/me-cfs/about/index.html

Book: Health Psychology.

Vitamin d deficiency: https://bmjopen.bmj.com/content/7/11/e015296

 

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