Have had lyme for 5 years, treated be Lyme Dr., antibiotic 6 mos. Thought I was getting better and it morphed into another nightmare condition, am allergic to almost everything and again am neurologically impaired. New Lyme Dr. said Mast Cell Activation Syndrome and only knows of one neurologist who deals with it. She is not accepting any new patients. Have been very patient these 5 years with losing job, losing friends, and being sick, scared and isolated, and now a whole new thing. Another mystery disease. Trying to hold on. If I have to, willing to go out of state.
Posts: 5 | From colorado | Registered: Apr 2017
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