I wrote this post last week and forgot to post it, it is still relevant so thought I would post it now. I was thinking today about why it is so hard for doctors, family, friends and colleagues to believe or understand the impact FMS has on a person. Thinking back to when I was [...]

Fibro and Me

Are you in pain now? Does it really hurt all over? You can't always be in pain, can you? You can't be tired! Yes, yes and yes!!! These are the sort of questions I get asked all the time and I know it can be hard to understand or believe that someone can be tired [...]