Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.
Did many of you have difficult time being diagnosed with FMS and obtaining a good overall treatment plan? Do you have doctors who do believe in you, who care, listen and empathize with your condition.
It took so long and so many doctors to FINALLY initally be diagnosed (and then the other varied diagnoses crossed wires to complicate life more). When I was given the initial diagnoss of Fibro I was sooooooo relieved and then researching and learning all of its symptoms and the contentions of doctors that come with a FMS diagnoses then caused me anxiety. Sigh.
I was diagnosed in summer of 2000 after nearly 3 yrs of misinformed doctors. My heart goes out to each of you fellow FMS sufferers and my hope is for doctors to become more informed re the care and treatment of FMS/CFS overall.
with thanks new friends,,,
It took so long and so many doctors to FINALLY initally be diagnosed (and then the other varied diagnoses crossed wires to complicate life more). When I was given the initial diagnoss of Fibro I was sooooooo relieved and then researching and learning all of its symptoms and the contentions of doctors that come with a FMS diagnoses then caused me anxiety. Sigh.
I was diagnosed in summer of 2000 after nearly 3 yrs of misinformed doctors. My heart goes out to each of you fellow FMS sufferers and my hope is for doctors to become more informed re the care and treatment of FMS/CFS overall.
with thanks new friends,,,
deleted_user
Oh, yeah. It took 5-6 years for me to get a FMS diagnosis. I started with Hypothroidism which we started to treat, but then 2-3 years into that treatment I still felt rotten and was sick all the time. I had to push my Internal Medicine doctor to keep looking and had to shed a few tears in front of her and hope that she would somehow sense my desperation and frustration. (Also, I think having a female doctor helped me). Her nurse finally mentioned Fibro to me for the first time and we started down that road. My Internist first prescibed my drugs and then after 6-12 months I went to a Rheumotologist that was just fantastic and he helped me get adjusted to a new lifestyle and deal with the pain/fatigue management. I also had a sleep study done that confirmed the fibro. I think I had a fairly easy diagnosis road when I listen to all of the stories on this site.
deleted_user
I was diagosis a long time ago. My new dr right now is great. I keep bring in articles for her to read and stay updated.That is my only advise I give to people. Its up to you to keep your dr informed. With so many illnesses out there, I think its hard for them to keep up with everything. After all they are only human
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I miss traveling with my husband. Has anyone found a specific site regarding cruising for widow/widowers or any sightseeing trips. Not interested in being with couples and kids,,,I realize a cruise ship will have a portion size of families and couples, but perhaps they also put together a part of the cruise ship for groups of widows/widowers????
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A friend sent this to me..As far as I can see, grief will never truly end.It may become softer overtime, more gentleand some days will feel sharp.But grief will last as long as Love does - ForeverIt's simply the way the absence of your loved onemanifests in your heart. A deep longing accompaniedby the deepest Love some days. The heavy fog mayreturn and the next day, it may recede.Once again, it's...
