A video about the reality of severe ME

The reality of Severe ME/CFS

Most people don’t really know what ME/CFS is. And that means a lot of their opinions and judgements on it are shaped by how it is portrayed in the media, which hasn’t always been friendly to us sufferers.

I just wanted to share this video posted last year by Palo Alto Online so those who don’t know what ME/CFS does to sufferers and those close to them, can see it for themselves.

If you’d like to help Ron Davis, there is a new fun challenge raising money for his research.

Laura Chamberlain

Laura is a writer blogging about living with chronic illness, namely Lyme Disease, Myalgic Encephalomyelitis (ME/CFS) and Fibromylagia.

She likes food, cats, bad jokes. Unfortunately, her boyfriend is allergic to the last two...

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