I have been ill for sometime but diagnosed only a couple of months ago.....I suppose i now know im not going mad but the fatigue is sooo hard to come to terms with...very depressed with it at the mo.......
newly diagnosed: I have been ill for... - Fibromyalgia Acti...
newly diagnosed
hi, you'll never be alone with it now, there are many people on this site with personal experience to share. I'm sorry you are very depressed, it's a lot to deal with. Ask away.
regards, sandra
Hello
we have all been there and we understand how you feel. get as much information on fibro as possible google is great and go and see your dr and get on an anti-depressant its harder to deal with the pain when our minds are in a bad place.
here is you want advice on anything you can private message me if you prefer x
keep smiling it does get better x
Hi,
Welcome!
Just ask what you need comment reasonably on anything.
Personally blogging is fine but actual support group is better in long term.I belong to a group & count them as friends I can talk to & get feedback. enjoy
Hi yup you need an anti depressant maybe with a muscle relaxant that gets you on a even keel and it helps me sleep too a problem many other people on here have terrible trouble with. Before I got my meds I didn't sleep and it was so hard ... Now although I have good and bad days the fact I now get sleep is such a help it's amazing how much better you feel after sleeping properly. Don't be afraid to ask your gp for meds ... Mine practically forced mine on me I thought being given anti depressants was awful. I am so glad he did the difference they have made is incredible I have gone from a sleep deprived zombie to a functioning person again.
Take care xx
welcome to the world of wonderful fibro freinds, you will never feel alone on here we will always be here to help with advice and you will be able to share your experiences and help others to know doubt , chin up you are not alone xx teresa xx
hello and welcome to the sight where people do understand ..
yes fatege is the killer to get used to but do not be hard on yourself you are not alone keep going back to doctor and get the balance right fot you ...
it is about finding a balance there is no shame in having a nap i do often .. life is good if you can balance out the FMS with meds and friends
Gentle dyslexic hugs
Thanks everyone for your support..much needed apnd appreciated
Welcome to our Fibro family, At least now you have a diagnosis you know what you are up against, I have learned so much since I joined this site. xx