Has anyone found anything to help the sweating? I didn't know until recently that sweating is part of fibro. I also found out that taking cymbalta is a culprit too and makes it very bad for me. I can't take the sweating. I am 52 and know the difference between the hot flashes and the awful sweating.
And does anyone get the awful back pain that would run across the back just under the shoulder blades? It's awful. I can take the lower back pain, but the upper I just can't. My muscles on my shoulders and across the bones in the front under the neck. (having a brain fog for the name) and back there are hurting pretty much right now. I had a whole body massae the other night thinking it would help, but it didn't. Does moist heat help at all? I have tried it other places. I am using voltaren, but that helps only a little.
Why do doctors feel this isnt' a real disease? the pain is certainly real. I have noticed my skin is on the gray side of color right now. I was scared of cancer because I see people with cancer having gray looking skin. My liver or kidey on the right side is painful too.
Just venting. I try not to tell my husband everything. He has seen me laying and covered up since last week and sleeping during the day. That's not me. I could never sleep during the day at all. And if he sees me covered up, he knows something is wrong. I think worrying about me has given him aches and pains too.
thanks for listening.
I have one good friend, but she has not been sick much at all in her life. a cold here and there. She tries to understand, and my children, adult ones, don't bother either. Why is this such a lonely disease.
Deb