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Lyme Disease Board Index
Pages: 1 2 3 4 5 6 7 8 9 10 11 ... 18Showing 1 - 20 of 353 for i have lyme disease and no one will help me. (0.157 seconds)


... Thank you, I will keep you posted. Im seeing my new endo april 17th then the GI doctor on the 19th. I feel its either........ adrenal fatigue, my thyroid still, candida, celiac, or lyme disease. Its definitely one of them. No doubt in my mind. ... (10 replies)
... Hi everyone, I am new here so I will introduce myself. ... (4 replies)
... Hello! I'm so happy to have found this. Ticker or anyone else who may have answers, please help me. ... (3 replies)

... Yes I know. Im sure this is nothing new for those of you who have been educating yourselvs on the subject of Lyme Disease. But for me its very new. I dont know what to do. I am in denial one minute and thinking Im just crazy or a hypochondriac. ... (4 replies)
... I really feel for you, honest. I thought it was an acceptance problem as that is so normal, yes it is! ... (20 replies)
... Hello, I've just registered here and need some feedback from people who've had Lyme disease. I'll try to make this as short as I can.... ... (5 replies)
... Let me share a story with you...I went to see a infectious disease specialist over the summer. He gave me his opinion and told me after three months of treatment, there is no way the infection could have survived. ... (39 replies)
RM10?
Dec 18, 2006
... Hi, Kat. I found the Primal Defense on Garden of Life, but not the RM10. ... (2 replies)
... I have no idea even if every person in the states came down with Lyme I think they would find a way to shove under the carpets! ... (18 replies)
... Hey everyone...I've been reading through the posts and I noticed some things here, maybe some of you will agree, maybe some of you won't. ... (39 replies)
... or a while now and have been waiting to post until I'd learned a bit more about Lyme Disease, but there is so much conflicting information all over the internet, and the doctors around here know so little about it, that I realize now is as good a time as any. ... (5 replies)
... change my family doctor gave me some valtrex thinking maybe I just had some virus. After 3 pills I couldn't see out of my left eye. I felt that I haa reaction to the valtrex but the opthamologist, neurosurgeon, and MS specialist all blew that off because they said valtrex will not do that. ... (42 replies)
... OK so here's how it all started. In August 2006 I came down with symptoms of headache, fast heart rate, and increased thirst sensations. This was about a week and a half after I had gone camping, and ironically the day before I took the MCAT, which is the acceptance test used by medical schools. ... (4 replies)
... law. Sorry, my oversight! Still though, I think my point is valid. Seeing her go through what you would call a "classic" case of Lyme Disease is not by any means uncommon. ... (36 replies)
... I'd really appreciate your help in editting this document I am putting together to discuss my dx journey with a couple of docs I can talk to. One is a young intern in neurology. I would love to be able to influence her. ... (3 replies)
... I am sorry you have been sick for so long. ... (10 replies)
... of a principal that is requiring a doctor's note for any and all further absences he has. ... (19 replies)
... how hard it was to get DX, how many people we know with the disease, the connection btw Lyme and so many autoimmune diseases as well as others, how much we pay for dr. visits, treatment, etc.? ... (17 replies)
... months. I am just going to post a timeline here. I am going for my first visit to a rheumatologist on Wednesday so I need this for them anyway. ... (11 replies)
... I am new to this board and if I stray into forbidden territory, please, let me know. ... (5 replies)


Associated Tags: dermatomyositis, lyme, western blot

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