I am twenty years old, and in June of 2014 I was diagnosed with Chronic Late Stage Lyme Disease along with five other co-infections. Like many others struggling with this disease, it took me many years (six to be exact) to find out what was ailing me. Although many of my symptoms limited me in middle and high school, it wasn't until I started treatment that I reached my roughest patch yet.
It seemed as if my life had changed nearly over night; I spent most of my days in bed with crippling fatigue, migraines, GI troubles, and wide spread joint pain. Because of my worsening condition, I had to make the crushing decision (more like the decision was made for me by doctors) to remain at home to receive treatment instead of returning to school out east.Read More