Guest guest Posted April 23, 2004 Report Share Posted April 23, 2004 OK so here's my question then. If we are too believe that was he says about the below is how it goes then what happens to those of us who fall into this " Post Lyme Syndrome " category? What do we do about it? Stay this way? Sit and wait to die? I wish someone could answer this. Robyn In a message dated 4/22/2004 2:57:00 PM Eastern Daylight Time, Robynn@... writes: Post-Lyme disease syndrome. A small percentage of patients with well-documented Lyme disease may develop disabling musculoskeletal pain, neurocognitive symptoms, or fatigue along with or soon after symptoms of the infection (S59-S62). This post-Lyme disease syndrome, or chronic Lyme disease (the terms are used interchangeably), which is similar to chronic fatigue syndrome or fibromyalgia, persists for months or years after standard antibiotic treatment of the infection. In a study of such patients who then received intravenous ceftriaxone for 30 days followed by oral doxycycline for 60 days, or intravenous or oral placebo preparations for the same duration, no significant differences were found between the groups in the percentage of patients who said that their symptoms had improved, gotten worse, or stayed the same (81). Therefore, it is hypothesized that B. burgdorferi may trigger immunologic or neurohormonal processes in the brain that cause persistent pain, neurocognitive, or fatigue symptoms, despite spirochetal killing with antibiotic therapy (82). Among B. burgdorferi-infected patients, a prior history of depression or anxiety seems to be a risk factor for the development of chronic Lyme disease (83). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2004 Report Share Posted April 23, 2004 I think those people who have gotten better need to write STeere. I don't know if it would really help, but it is a thought. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2004 Report Share Posted April 23, 2004 So he is saying that those of us with Chronic Lyme or Post Lyme syndrome usually " have had past history of Depression or Anxiety " , reading between the lines this sounds oddly like the 'You just want to be ill " syndrome I was mis-dxed with years ago. How about the fact that Lyme messes with our brain chemistry and causes those symptoms in some? Maybe 'if' they came up pre-Lyme dx its because those people went awhile before the dx? People can go months or years after courses of abx and still have latent Lyme. Hasnt he heard of Cyst form Lyme? God forgive me but I hate that man. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 24, 2004 Report Share Posted April 24, 2004 , You are absolutely right, and he is so " guarded " by the same peer reviewers that his articles always get published when others that disagree with him don't get their articles in any of the journals. I have been following this since 1993......he is totally wrong. connie, MI Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 24, 2004 Report Share Posted April 24, 2004 I do think you reach a point you should stop abx treatment, that you are causing more harm than good to your body.....especially if you are not feeling better on the abx treatment. At some point, the body needs to be repaired..........and yes that repair will take months, and perhaps years.........the lyme and all the drugs have caused damage and imbalance that needs healing and correcting.......extensive testing needs to be done to determine how to help begin the repair........I'm living proof. The tricky part is knowing when enough treatment is enough.......only you and your Dr. can determine that. ConnieKnwnj When our bodies & minds are out of balance....... ........we suffer! Quote Link to comment Share on other sites More sharing options...
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