http://www.voltairenet.org/article166027.html
I have suffered since 2008. Found out about morgellons in 2011 and then the corellation to lyme in 2013. Heartbreaking the way it decimates lives. I heard in a rense radio show, it as a weapon, is meant not to kill but to incapacitate, creating a burden upon the immediate family, community and eventually the society. I was an activist for awareness for some years but tend to keep it to myself.
It is more common in Missouri than they want to admit. I know there are people struggling with diagnosis, doctors, and failed treatment to symptoms. I have great animosity towards dr. Anadkat of wash u. Who i found out after nearly a year of bullshit treatments had diagnosed me with trictolomania, an impulse control disorder. His diagnosis procedure was terribly flawed and no biopsy or bloodwork was used. It was not the delusional parasotitus diagnosis that lyme/morg patients usually recieve but it was just as devestating. By 2013 i was divorced, deemed unfit for work, and would later lose my house and estate. My wife, family and friends thought my condition psychological and indeed i was going to pieces but first and foremost it was a physiological problem.
https://steemit.com/blog/@wakeupsheeps/forgotten-history-3-plum-island-and-lyme-disease