Progress
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is feeling OK
I got fibromyalgia and lymes disease in Dec. of 1999 and was living my life in bed I was in so much pain. Finally the lymes disease was taken care of, but nothing was done for the fibro which was causing extreme pain in my spine (especially the lower spine... it feels like someone is pulling it out.. and then I had all thses other symptoms like migranes, IBS, insomnia, depression, memory loss ... I can forget an entire conversation I had... Irritable Bladder Syndrome, and soreness in my neck and back that gets worse as the day goes on. At first many doctors just told me it was in my head. Then finally I found a doctor that diagnosed me with fibro, but the bad news was he said there was no cure. I refuse to believe that. In my heart I know some day I will be free of this. I just don't know when, where, or how.
Come & Take a look at Our New Support Group http://dailystrength.org/groups/su...
Sometimes with fibromyalgia I get things a little mixed up. I think the top portion should have gone down here. But I recently moved to LA to follow my life long dream to me an actress, and it's been very challenging physically. When I'm on set I have to take pain pills to get through an all day shoot, becaue I'm consantly up on my feet doing somethng or waiting. It's been hard because I left me support system (my family and friends) and I don't know anyone out here. if I'm feeling really bad, I don't have anyone to call to go to the drug store to pick up my meds. So needless to say it's been a challenge. But I'm pushing through. I'm trying to find a doctor here that treats fibromyalgia and pain managemaent, but I don't know where to start. I feel very isolaed. That's why I wanted to join this group.