Melissa’s Rap: When one suffers from an autoimmune or other chronic condition (or several), a new doctor can bring hope as well as fear. Hope that THIS is the one; the doctor who will finally find what works so you can function in your life. Fear that they will 1) not understand, 2) put your current treatment at risk and 3) will implement treatments that do more damage than good.
Recently I started a new job and with it came a new insurance company. The new company doesn’t cover my old primary care physician (PCP), so I had to find another one. This is a scary prospect when you have as many health conditions as I do. I have been laughed out of the office by a PCP who didn’t believe I had Lyme disease, even though I had it in black and white: CDC-positive. I have had to fight to stay on medications that have made a tremendous difference in my symptoms, because that doctor didn’t support that brand/treatment/dosage, etc. Many PCP’s don’t know what to do with me because I have so many things going on, it is difficult to know what to treat and how those treatments interact with each other.