So after reading several threads here tonight, I came to the conclusion that many of us have done the same thing I have done too, and that is we've all gone to doctor after doctor after doctor with no answers. So I think "going to doctor after doctor with no answers" (or something like that) should be added to the list of Lyme symptoms!
What do you all think?
Chronic Lyme Disease, Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, Pancytopenia, chronic malabsorption/malnutrition, etc.; G-Tube; Currently TPN-dependent.
Meds: Zofran, Pulmicort, Heparin (to flush PICC line), Claritin, Colloidal Silver (used topically), IV Milk Thistle, probiotics.