I imagine more of the learned Lyme folk here have read this book, but I am just beginning the Pamela Weintraub book, "Cure Unknown"---And boy, oh boy, if I was questioning before my symptoms & lyme indicators, this book not only does the parallel, but just incenses me even more that the medical community has divided & blatantly ignored sufferers.
I know lyme groups, local & otherwise exist--& recent political bill passing to do further research, but is anything at all happening with activism to make treatments the here & now?!
