Just wanted to say hello. I'm new and I neaver been treated for Lyme Disease -- I have had all tests come back neg. ELISE & Western Blot was the only ones they did. Now --I have to find Lyme literate doctor to treat me as no one gives the proper tests and by this time it has spread to my brain/nervous system /joints stomach. I have had an MRI that shows 2 white spots in my brain in the white matter and two in back of lobe in white matter. Now I am so sound sensitive I can't bear even a spark of sound to a book being turning a page . Anyone else going through this ?-- and how many here have not been treated due to being misdiagnosed. Is been seven long hard years for me . Just wondering all. :-)