Lyme Disease Protocols: Where To Start

By the time I had been diagnosed with Lyme Disease I had spent years seeing specialists who’d greet me with shrugged shoulders and send me away with more questions than answers. When I was finally diagnosed with Lyme Disease, I was relieved to have a label to my symptoms, terrified about ending up in a wheelchair and overwhelmed by the unknown all at once. First, there was the issue of not knowing much about my own disease. I knew much of my time was about to be spent researching something I’d prefer to know nothing about (even though years later I actually quite love researching infectious diseases). And when I did start looking into my disease, it got confusing really fast. Between the doctors disregarding the existence of Lyme, the dispute between protocols and the conspiracy theories, I was pretty pissed off that of all things, this was my ultimate sentence. Read more “Lyme Disease Protocols: Where To Start”