Hi! I'm Yogagirl--a bit new to the site, but not new to lyme. My husband has been under treatment for lyme for months. I myself never got tested because my joints felt fine. However, I did have some neuro symptoms sneeking up on me. I thought I was having anger management problems because I'd have these sort of "rages". I had a lot of stress from a job I didn't like (and that I used to explain my 3 month -long headache problem). Then I started to black out entire 2-3 hour blocks of time while working as a nurse in a critical care unit (want me taking care of your mom?). So, I has to stop working for a while. I hope I get my brain back soon because money is starting to get tight. Got the Western Blot...IGeneX and CDC Positive. Guess if I would have listened to hubby and believed, I'd be halfway to feeling better right now.
What I want to know, has anyone else out there been so skeptical? Is anyone outthere a healthcare worker suffering the cognitive deficits that can go along with the neurological damaged possible with lyme disease?
Thanks, Yogagirl