Guest guest Posted December 12, 2003 Report Share Posted December 12, 2003 On or about Thursday, December 11, 2003 7:12 PM [GMT+1=CET], mt <mtien@...> sprinkled letters onto the page, saying: > Hi, Kezzi, > > I read your story. It is well done and I really appreciate your > sharing of your experiences. I understand your initial symptoms..... > > Just Bradford microscope which diagnosed Lyme for you? Did you try > EDS(electrodermal Screening) ever? I love to know more about how you > were diagnosed. > > mei Hi Mei, Thank you... I have never been 'formally' diagnosed with Lyme - just borreliosis. Stage III Lyme is suspected based on my long histstory and symptoms. I hadn't heard of EDS but the only yhing I can tell you for certainty about future tests is that I have been disabled for so long that I have been unable to work since 1988 and have no money for testing. My mother paid for my last consultancy and microscopy as she was determined to get to the bottom of my illness as no treatment has ever made any difference to me. I am certain now that my GBS(CIDP) diagnosis wasa wrong one... Regards, Kezzi. . . My story - http://tinyurl.co.uk/8ebv Quote Link to comment Share on other sites More sharing options...
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