Anyone else have fibermyolgia?

I was diagnosed with fibermyolgia over 14 years ago and suffer pain that will never go away. I've have migrates that I went to the hospital with and got shots for only to have the shot have to affect on me what so ever. I feel for anyone who has or will be diagnosed with fibermyolgia.

I don't have fibermyolgia, but have an online friend that does. We talk about it a lot, but that's because I ask questions about it (nothing personal though) so that way I can understand what she is going through. Her's is to the point where she it's hard to get out of bed somedays and other days it would be like she had no problems at all. She goes to a pain clinic for it, but she always tells me that she don't think it's helping all that much.