Guest guest Posted January 24, 2010 Report Share Posted January 24, 2010 Bridget, I understand your anger and frustration.When I first became chronically ill my primary MD said it was psychosomatic! That was 5 years ago in NY state. I have since moved to western Mass. where I was finally diagnosed last June. My new primary MD, who is young and a good listener, at first questioned the test results after calling an infectious disease specialist. But when I reported to her my severe, incapacitating reaction (herx) to one month of Doxycyline (ordered by different MD who finally diagnosed my illness) she agreed I had Lyme. The next hurdle came when I went for my yearly physical in Dec. I brought my DVD of Under Our Skin and a 20 page paper (from online) about treating chronic Lyme & Co-infections by a well-known NYC neuro-psychiatrist. She gave me a look of disapproval when I told her how many antibiotics I " d been taking under the care of my LLMD. She said, " All the spirochetes have been killed by now. " Well, she promised to look at the paper and the DVD. I also gave her info & website of my LLMD, who is prominent in the field. If our family doctor is not Lyme Literate, we have to find some skillful means to educate them--without bruising their sense of authority. My initial reaction to my primary MDs ignorance (not her fault) of chronic lyme, was a bit defensive. I think our relationship is improving. She's a caring person. She called me about a possible abnormality in some red blood cells from my routine blood work and faxed the results of all lab to my LLMD. She ordered a repeat CBC, in case it might indicate babesia. She read the paper and is planning to watch the DVD when she has time. My advice: don't lose your cool during appointments and see if you can find good solid evidence--research from online or the book Cure Unknown by Pamela Weintraub or the ILADS guidelines for treatment to prove that the CDC/IDSA guidelines are being disputed by treating physicians & some researchers. S/he might not be aware that the Attorney General of Connecticut is investigating conflicts of interest not disclosed by the IDSA panelists who updated the guidelines in '06. In fact, a new panel was formed--excluding any physicians who had made more than $10,000 treating patients for chronic Lyme because they may have been motivated to over-treat for financial gain! This is touched on briefly in the film. You don't want an adversarial relationship with your family doctor. But if your doc isn't open-minded, it might be time to find one who is. That's my two cents, Kim [ ] test results So I was fuming last night, just thinking about my family doctor a couple weeks ago saying I supposedly was diagnosed with lyme, but got a negative result from the CDC, well I thought of a good one for people to say if their doc gives them crap, I know people that have had negative pregnancy tests time after time when they were indeed pregnant, so maybe tests aren't always accurate!!!!! Just thought I'd throw that out there, kinda makes you think, just because it doesn't show a positive test, doesn't mean there isn't something there. Bridget Quote Link to comment Share on other sites More sharing options...
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