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.