Hi Brujah, I know that feeling, you just have to try to get on with living as best you can do not let the symtopms of fibro rule your life I know that is hard to do sometimes but we all have to give it a try. We all cope in our different ways I do not know how to private message on here so I can email you, I added a website in my last post but it ...

Hi there Brujah, My name is Jaki and I was diagnosed last year and have had this for 22 years, it does help talking to other sufferes and I to go to a group meeting held every 3rd Wed of the month at ArrowPark Hospital, I am 34 but there are loads of people on here of all ages and severaty of this condition. Anything I can do to help please ask.

Hi Jayne and Jayne I was refered to Dr Williams by my ortho surgen, he was so great, listened to my every word and looked at my whole medical file and history, he then made the FMS diagnosis, I too didnt know wheather to hug him or cry, I sat there stunned to finally have a name for what I was going through after 22 years of thinking noone ...

Hi Jayne  I see Dr Williams at the pain clinic at Caltterbridge, Go to your gp and ask for a referal, hes Pete Williams and hes great, I am taking Tramado (sr) 150 mgs and Celebrex as thats kinder to your stomach, and with having IBS its good, I Take amytryptiline aswell and thinking of upping my dose as I am not sleeping ...

Hi Jayne  I have to live close to you as I go to clatterbridge aswel, I have FMS and was diagnosed last year after 22 years tryin to get someone to listed to me and find out what was wrong, I have found talking to others who suffer the same is very helpful especial as you do not feel alone and can find ways of telling friends and family how ...

Hi Andy, I had trouble getting my DLA back again after they decided that I was better, so when I tried again 1st I wrote to my gp telling her how my disability affected me so she knew excatly how bad I was and told her that she would be asked to fil in a DLA form for me.  Next I filled out the form and where it asks, how far can you ...

Hi I have been emailing my local MPs and MEPs to get them to go the the Awareness day, we need as many as possible to attend, for more details of this go to fmauk.org. I was diagnosed with fibro last year after suffering for 22 years yes I said 22 years this is why we need the awareness say so more people with this condition do not have to wait ...