In the fall of 2009 I was finally diagnosed with chronic Lyme disease and co-infections after a long, frustrating two years visiting different doctors, trying to get a diagnosis for my declining health.
While I still have pain off and on, most days I don’t feel so much like a Lymie, especially since many of my friends have similar aches and pains. I’m not going to say we’re getting older but you know, it happens.
When I was first diagnosed I agreed to high doses of antibiotics. I acted out of fear and ignorance, I thought this was the only way I would regain my health.