Still standing after 20 years of chronic Lyme disease AKA post sepsis.
Once we understand what the disease is, the next question, invariably, is, “what’s the treatment?” Thank you, MontanaNAR, for raising the question. These reports were compiled by Kathleen, of ActionLyme. She says: Read these 4 reports, all new, and… Read More ›
I had the most wonderful conversation last night with one of my best Lyme friends. It spanned four hours, at least four different phones, two dropped calls (one due to a dead battery) and the gamut of topics, from shoes… Read More ›
After 19 years of having Lyme disease, it’s imperative to have a bad attitude. Seems unhealthy, one might think. Well, so is having a disease of immune suppression–similar to AIDS–with no known cure, no effective treatment, and very little acknowledgement. … Read More ›
When I began my transformation from victim to activist, I had to understand the disease process. My world had just been turned upside-down by my daughter’s diagnosis. After a period of anguished grieving, my logical side took over. I knew… Read More ›