Hi. My name is sue. I've got quite few things wrony with my body . on top off all them I av FM. Only diagnosed bout 5.yrs go, but like most off us with FM. Have ad it lot longer. Be nice to go on here n c what other people av to say ect. Thank you. Sue.
Introduction.: Hi. My name is sue. I've... - Fibromyalgia Acti...
Introduction.
Welcome Sue I am sure you will feel supported. By this Site & As I Do. Wishing You All The Best.😀
Welcome to the forum Sue you will find it a lovely supportive community. Have a look at our mother site Fibromyalgia Action UK as although you have had fibro a long time you might find some information that is new to you. If you have any questions ask away as there is usually somebody our the who has already experienced similar who can help. Look forward reading your posts.x
Welcome my dear I hope you enjoy the site as much as I do! I am just a old Texas girl! I say howdy and thank you ma'am . So welcome aboard my new friend!!
Hello. From one Sue to another. You will find a very friendly and helpful bunch here. Welcome aboard.
Yorky
Hi sue many here have many other conditions along side fibro but find the fibro is the icing on the cake , it is as my dr says one of the worse condition to deal with and to have other complications on top ,you wonder how you keep going , I found this site a life saver , some of us have become a little unhinged on here but laughter can keep the pain at baye , hope you decide to stay the more the merrier, and if you haven't been on one can I suggest a pain and fatigue clinic , it will help with pacing and exceptence and how to cope with this horrible conditions, we do get silly here but you need a giggle .
Hugs Chris 😊
Hi Craftysue1956
Welcome to the forum and it is wonderful to make your acquaintance. I sincerely hope that you find the forum useful, informative and loads of fun! I have pasted you a link below to our parent site, Fibromyalgia Action UK which rosewine mentioned to you. It hosts loads of useful Fibro information: fmauk.org/
I am so genuinely sorry to read that you have Fibro, and I sincerely hope that you are receiving adequate pain relief / medication from your GP or Medical Specialist? I do not know your personal situation, but FMA UK have a dedicated Benefit Helpline should you need any advice in that department? And they also have loads of other features from 'Fibro Groups' to 'Patient Handbooks.'
I want to genuinely and sincerely wish you all the best of luck and I look forward to seeing you around the forum.
All my hopes and dreams for you
Ken
Hi Sue, I am new on here. Went to my GP today and just broke down. Totally had enough. He actually listened and kindly told me that I wasn't dying from some awful illness and that every symptom I told him about was still the FM, which I refused to accept for the past 3 years. I'm hoping that talking to others and being more accepting will provide a glimmer of hope ☺️
Rachel x
Hi. Rachel. The only thing with the FM it brings lots of other elements with it. But don't give up n if u not satisfied c another Dr get 2nd option. Sum drs r very gud n no bout FM n sum drs don't no that much. Everything was put down to my bk problem , but after yrs , then when my neck n wrists started to play up I knew it was not all just down to my other bk problem., but had to keep going bk n forth to drs, then after a while was told got FM aswell. Not there are lots of other thibg S that cum along with the FM. Where do u live? I go to group once wk for FM suffers. Really gud n helpful n learn more all time. So hope u feeling bit brighter. Sending u gentle hugs. Lovely to speak to u on here. Oh n one thing I no u will no. But remember to pace yourself n thing u do. We r all so guilty of when we got a day were u think oh feel not to bad today. Then we over do things. But boy oh boy don't we suffer for long time after it. Take care. Hopefully speak to u again. Lv sue xx