Snarf said...
My LLMD takes BCBS, Aetna, and Medicare. He writes the lyme/bartonella diagnosis on the paperwork, etc. I pay my copay for the visit and a small fee for the prescriptions. Things like glutathione IVs are not covered, but at least the visits, meds, and labwork (with exception of Igenex) is all covered.
There are two LLMD's in my area that take insurance. I know that the receptionists at my current doctor make it very clear when they answer calls that he is NOT a "Lyme Doctor"...he is an integrative GP. Maybe that's the difference?
\That must be it.
I wasn't aware of the insurance situation until late summer last year. I've had Medicaid for 12 years now and it's wonderful! I guess my Internist wasn't aware of the LLMD situation either when he called the one in Missouri for me, as he was as unhappy as I was when I told him they said they were cash up front only, and how much the first consult was. He knew I'd not be able to afford it. My disability is only $733. a month to live on.
I know that there are others here in the same financial boat as I, and it's a shame, but I've had this getting progressively worse for so many years I've no hope in reversing anything anyway.