Bullseye Rash
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Re:fibro or lyme?
by Robin123
In FMS Support Forums > General & Support
"Hi there. Well, a few years ago I recieved a dx of fibromyalgia and mixed connective tissue disorder (that one is autoimmune, like having lupus, RA, and scleroderma), but have no ANA factor.
I have never been happy with this dx. Have always felt there is something else going on. SO my husband and I are constantly looking things up on the net.
He came across an article where some lady wa"
In FMS Support Forums > General & Support
"Hi there. Well, a few years ago I recieved a dx of fibromyalgia and mixed connective tissue disorder (that one is autoimmune, like having lupus, RA, and scleroderma), but have no ANA factor.
I have never been happy with this dx. Have always felt there is something else going on. SO my husband and I are constantly looking things up on the net.
He came across an article where some lady wa"
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help finding a Dr
by myhusbandhaslyme
In Lyme Disease Support Forums > General & Support
"Hi, is there anyone out there that can give me a name and phone# of a specialist. My husband has battled this for 4 years and none of the drs he has seen seem to understand the disease and the severity that he is going thru. Please help with any suggestions.
"
In Lyme Disease Support Forums > General & Support
"Hi, is there anyone out there that can give me a name and phone# of a specialist. My husband has battled this for 4 years and none of the drs he has seen seem to understand the disease and the severity that he is going thru. Please help with any suggestions.
"
Related Discussions:
Severity of Lyme ... posted in Lyme Disease Support Group
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I think it's Lyme
by erleichda
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have some questions. Several years ago, I had a large red ring on my arm. It looked just like the ones you see from people who have Lyme disease. The doctor said it looked like Lyme but that I couldn't get it here. I didn't get sick so I didn't take it further. With time, it faded.
A few years later, I developed severe fibromyalgia symptoms with full-body pain, fatigue"
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have some questions. Several years ago, I had a large red ring on my arm. It looked just like the ones you see from people who have Lyme disease. The doctor said it looked like Lyme but that I couldn't get it here. I didn't get sick so I didn't take it further. With time, it faded.
A few years later, I developed severe fibromyalgia symptoms with full-body pain, fatigue"
Related Discussions:
Lyme Disease and ... posted in Lyme Disease Support Group
Lyme Disease - Ea... posted in Lyme Disease Support Group
Lyme Disease - Ea... posted in Lyme Disease Support Group