A Social Network for Men with Fibromyalgia, Chronic Fatigue or Pain
Hi,
I just been diagnosed with fibro( I believe shots in the dark) by two doctors (neurologist/rhumatologist). They did very little testing except for the "push/pull" stuff. I purshed pretty hard on the last doctor (he didn't like it). I had two spots that correlated with FMS. I viewed some of the information on the progressive nature of fobro. It feels like the pain is getting worse and is spreading to different parts of my body. It seems like every week, there is a new problem with how I feel. I used to do a lot of exercise; now I do none. I'm afraid of making things even worse.
I wonder if some of what I have is MPS. I've read about that too. I wish is was MPS. Can anyone share their experience with MPS or fibro in terms of what the impact of even light exercise is for them. I feel like I'm made of glass and afraid to do anything. I asked the rhumatologist for a bone scan test and she said that we do that after someong gets a fracture. What nonsense. Also does anyone is the New York City area know of a goo doctor or place to go for treatment. Thanks.
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Permalink Reply by Hans Miniar Jónsson on June 20, 2010 at 2:36pm
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