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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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#1 | ||
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Guest
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Hi Ada,
I really hope your PCP can help by recommending someone else. Ada I am very ill myself. My pain level is way down, I am very sick still. I am doing everything I can. You need to find a Lyme Literate MD. Hugs, Roz Here is a article. http://www.confrontinglyme.com/foreward.html Last edited by buckwheat; 07-25-2007 at 11:33 PM. |
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Administrator
Community Support Team
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Hello Ada
we do have a Lyme Disease forum here that isnt all that active re discussion, but does have a lot of very helpful info re Lyme Also, one of our members BlackRoze has Lyme and has a wealth of info and experience related to it that may be helpful to you Lyme can be very serious and it is oh so important to have knowledgable qualified professional care if you do in fact have this disease hope that helps a bit with info for you here is the link to the NT Lyme disease forum http://neurotalk.psychcentral.com/forumdisplay.php?f=91 Cheri
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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Magnate
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I will go over and read on that forum and PM Blacckroze.
I have been so sick here lately. I called my Dr. and I see him as the last patient tomorrow so we can decide on turning my VNS off until I feel better. I really don't want to do it. We had planned on turning it up Monday and he didn't get the call from the company on how to do it a different way to keep it from messing with my breathing. Now we may decide to turn it off. I am going to try and find a Dr. to check me for it. Roz gave me a good article that explains the problems with getting help for it, but I am going to check and see if I can find someone who might know something about it. Thanks again, Ada |
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Magnate
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Thank you for you concern and help on the lyme disease.
I just wanted to let you know I saw my PCP today and he ordered bloodwork to see if I have it or not. He explained it to me but I'm no good at explaining it. He called those places Erytherna Migrans. I don't know if I'm spelling this right. The man writes pretty good. A lot better then me but some letters I am not sure of. He said it will take awhile to get the bloodwork report back due to it going to Denver. He's hoping they don't cancell it as they did the 3 test the Immunologist ordered. I'm glad he's doing it. I didn't want to have to go looking for another Oncologist. Ada |
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Junior Member
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