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Robin1237 - October 20

There's a good post at http://flash.lymenet.org, in Medical Questions, called "To those who were 1st diagnosed w/fibro, but turned out to be Lyme". 28 posts there so far. It's an eye-opener. I'm included in it. Me: 25 years of fibro, that's actually Lyme disease from a tick bite on my foot in 1981. But I had no symptoms at the time, so when my symptoms started, I didn't know they were related to the tick bite. I developed sore shoulder muscles, a stiff neck, head-to-toe muscle pain, unstable joints that need constant chiropractic care, insomnia, depression, light sensitiviy, sound sensitivity, chemical sensitivity, loss of smell, TMJ, lost my period due to abnormally elevated prolactin, developed low thyroid, got constipated, later got swollen ankle and knee joints, and by the way, that's only some of the Lyme symptoms. The bacteria can go anywhere and inflame any part of us. Good news is as soon as you understand what you're dealing with, you can start to treat it more effectively, with antibiotics, oxygen treatment, herbs, supplements, electromagnetic machines -- it's something we have to learn about. So I would like to see you guys go over to the site I'm recommending and then come back here and discuss what you think of what people are posting over there!

 

coop - October 21

I just spent about an hour at http://flash.lymenet.org. What I found is a site wrought with confusion,misinformation and paranoia. I found no sound medical advise what so ever. (There are however people espousing govt sprayed "chemtrails" as the cause of their "lyme".) Everyone who is confused by Robin's constant repetitive posts rambling on about lyme should go there and check it out for themselves.

 

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