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Hello neurotalk community!
Hi Everyone,
I'm new here and glad to have found this community. I was diagnosed with Lyme neuroborreliosis two years ago with a CDC positive western blot. I'm looking forward to sharing info with a wider group of folks who suffer from neuro-related illnesses because I believe we can learn so much from each other and the cross-over connections between diagnoses. I am having positive results with long-term combined antibiotics, though I still have quite a ways to go in getting back on the road to good health. Best regards, Anka |
Welcome! We look forward to getting to know you!
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Thanks, Gigi
Thanks, Gigi.
I'm curious, how did you figure out you had Lyme? It took years before I figured out something was going on (I kept thinking it was just my stressful life and circumstances). It was on a forum like this one that my husband saw my symptoms listed and then we learned how to get Lyme testing done. What a relief to have a target to go after! I've found some really helpful folks through support groups and forums. It's amazing the things people are dealing with and how much we can learn from each other, regardless of what we're suffering from. Good healing! Anka |
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