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#1 |
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I know there has to be other Fibro sufferers here. Its such an insidious and painful disease. Would be nice to have a place where we can share stories, support one another, discuss new medications and therapies that might help us.
Jewel |
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#2 |
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Bump...I cant be the only one here with Fibro.
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#3 |
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I have it too.. Though in the last year or so it hasn't bothered me as much as it use to. I firmly belive that my aches and pains are not nearly as bad because my head is in a better place than it use to be. Actually a lot of my health problems are a lot better.
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#4 |
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Yes, your emotional state DOES have a big effect on Fibro.
Genlte hugs, Jewel |
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#5 |
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*raising hand*
I am in what is probably my worst fibro flare in over 10 years. Not a happy camper, C |
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#6 |
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#7 |
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Awww honey, Im so sorry. Sleep is the single most important thing for us fibro sufferers. And please be kind to yourself my friend. I know its not easy. Has anyone tried Cymbalta? Ive been on it since it came out. It doesnt help the pain, but it helps the fibro fog and some other symptoms that I have.
I need to unburden my soul about something that I am very very scared about. I had some labwork done a few weeks ago and got the results today. I tested postive for an autoimmune disease that require further labwork and tests. It could be lupus. Who knows. Im scared to death. Those of you who know me, know I have already been put thru the ringer these past 7 years healthwise. I know that I will get thru this just like I have everything else. But Im scared. And tired. Ive had my fill. I try and have a positive attitude and not complain. So Im sorry if it comes off like that. Im glad we started this thread and can support each other. Gentle hugs, Jewel |
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