Aaawwww, thanks bruce. Being an Alien isn't easy, LOL.
I was diagnosed in 2010. Many docs were afraid to deal with Lyme because there was conflict with the insurance companies and many mainstream disease specialists on how to treat the disease and for how long. They were finding that it was taking more than the standard 10 day antibiotic treatment and many docs were threatened with losing their licenses if they broke protocol. As a result, many doctors stopped treating suspected Lyme patients. A few hung on, though but the last time I read anything about it they were still being chewed on by the insurance companies and medical boards.
My doctor wanted me to see a Communicable Disease Specialist but my insurance was only for Catastrophic coverage. So I handed him a copy of Buroscano's essay on treatment of Lyme and told him congratulations, he was about to become a Lyme specialist. Bless him, he did read the study and later told me he had several patients beside me who were being treated for Lyme.
The interesting thing is that the studies are now venturing into the question of how many people being treated for MS actually have untreated Lyme Disease? Mainly because the brain lesions that show up on an MRI due to MS exactly mimic those that Lyme Disease produce. The material out there relating to Lyme is pretty overwhelming and the sad thing is there is not one good thing that a tick does for the environment or society in general.