Guest guest Posted September 25, 2000 Report Share Posted September 25, 2000 In a message dated 9/25/2000 2:00:28 AM Eastern Daylight Time, rod@... writes: Steere study: << CONCLUSIONS: Lyme disease may trigger fibromyalgia, but antibiotics do not seem to be effective in the treatment of the fibromyalgia. >> Boy Pepi you were right to say take this with a grain of salt! My fibromyalgia like pain is much better with antibiotic therapy.....after 5 years of being misdiagnosed with FMS, unable to find anything including pain meds to relieve the symptoms, my tender points are MUCH better.....I no longer cringe when my kids hug me!!! (And I do not take any pain meds) I certainly would not advocate taking antibiotics if no " infection " source......but I know how hard it is to get a proper dx. Happy (Maine) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2000 Report Share Posted September 25, 2000 Happy, if you find more of his articles, his or Sigals they contradict themselves and each other constantly. Pepi Steere study: > << CONCLUSIONS: Lyme disease may trigger fibromyalgia, but antibiotics do not > seem to be effective in the treatment of the fibromyalgia. > >> > Boy Pepi you were right to say take this with a grain of salt! > My fibromyalgia like pain is much better with antibiotic therapy.....after 5 > years of being misdiagnosed with FMS, unable to find anything including pain > meds to relieve the symptoms, my tender points are MUCH better.....I no > longer cringe when my kids hug me!!! (And I do not take any pain meds) I > certainly would not advocate taking antibiotics if no " infection " > source......but I know how hard it is to get a proper dx. > Happy (Maine) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2000 Report Share Posted September 26, 2000 In a message dated 9/25/00 2:00:40 AM, rod@... writes: << -------------------- This is written by Steere, so read it but take all its meaning with a grain of salt, after all he doesnt believe in Chronic Lyme. So that is all in our heads! >> Actually, mine is (today) in my fingers, neck, head, feet, ribs, knees. . . .. .LOL I have to share with you all a great Lyme Fog moment: Today I went into the bathroom just off our kitchen (sort of a half-bath guest bathroom) and just stood there for a minute, forgetting why I was in there. Then I remembered. I was looking for the peanut butter! (I wouldn't be surprised if one one of my foggier days I put the peanut butter away in the medicine cabinet! ) --charlotte Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2000 Report Share Posted September 26, 2000 Who is Steere? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2000 Report Share Posted September 26, 2000 Who is Steere? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2000 Report Share Posted September 26, 2000 Thanks Pepi. Good health and good luck!! Jo-Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 26, 2000 Report Share Posted September 26, 2000 > Who is Steere? > Dr Steere is one of the original Drs that put a name to Lyme Disease back in the 70's. He is , virtually sinle handedly, responsible for many Lymies to not be able to get treatment. He has The Ear of the medical establishment at large and has them convinced ( without good scientific backup ) that we are suffering from " Post Lyme Syndrome " whatever that means. He is pretty much the Anti-Christ of Lymies, ( No offense meant there ) He Sigal and another that i cannot remember the name of now, UGH, are the on insurance companies payroll ,they testify as an 'expert' . answer ya? hope so!!! LOL Pepi Quote Link to comment Share on other sites More sharing options...
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