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<blockquote data-quote="JMichal" data-source="post: 373280" data-attributes="member: 5744"><p>I know what you are dealing with as I have been with Lyme for over 5 yrs. I believe a great many more of us have Lyme but attribute it to aging. I did until I really got sick & was diagnosed. I thought I was losing my mind at 46, and thought I had throat cancer. Never smoked. Also had more than 20 other terrible symptoms. I went to a support group on line for Lyme and found a Doc in Springfield MO. We hit it very aggressively. 4 different antibiotics for 6 weeks each, large doses. I haven't felt this good as I have for the past 6 months in 5 yrs. I just hope it's gone and not in remission.</p><p></p><p>This is very serious stuff that the AMA is just not aware of at the local level. My freind in OK was Diagnosed last summer. Both of our Docs claimed " We don't have that here". BS!!!</p><p>Neither was going to file the case with the CDC until I called and told them I will call the CDC. They then reported as required by feds.</p><p></p><p>My springfield Doc says Lyme may be the cause of Lou Gherigs and Multiple Sclerosis, as all his patients with these have tested positive for Lyme (He calls it Boreallia Borgdorfei) spelling may not be 100%. </p><p></p><p>I felt I needed to post this to make others aware. But cow crazy 101 if you wish to talk with someone about this for info or support please PM me. We all need help in times like this.</p><p></p><p>JMichal</p></blockquote><p></p>
[QUOTE="JMichal, post: 373280, member: 5744"] I know what you are dealing with as I have been with Lyme for over 5 yrs. I believe a great many more of us have Lyme but attribute it to aging. I did until I really got sick & was diagnosed. I thought I was losing my mind at 46, and thought I had throat cancer. Never smoked. Also had more than 20 other terrible symptoms. I went to a support group on line for Lyme and found a Doc in Springfield MO. We hit it very aggressively. 4 different antibiotics for 6 weeks each, large doses. I haven't felt this good as I have for the past 6 months in 5 yrs. I just hope it's gone and not in remission. This is very serious stuff that the AMA is just not aware of at the local level. My freind in OK was Diagnosed last summer. Both of our Docs claimed " We don't have that here". BS!!! Neither was going to file the case with the CDC until I called and told them I will call the CDC. They then reported as required by feds. My springfield Doc says Lyme may be the cause of Lou Gherigs and Multiple Sclerosis, as all his patients with these have tested positive for Lyme (He calls it Boreallia Borgdorfei) spelling may not be 100%. I felt I needed to post this to make others aware. But cow crazy 101 if you wish to talk with someone about this for info or support please PM me. We all need help in times like this. JMichal [/QUOTE]
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