I am familiar with those support groups & some members but, again, they are not in the vicinity of the City-- are quite a distance away.
Geographically, the doctors outside the 128 belt (highway surrounding Boston) aren't really of help to those of us who can't get out to those suburban and rural areas.
I have my feelers out and posted on MassLyme yahoo groups--
of which all the State support group leaders are members--
and am still waiting to hear about a substitute who TAKES INSURANCE.
I'll contact the director of px care at my PCP's clinic tomorrow who might be able to help.
The only alternative my Md's office assistant gave us was a terrible Md in the same clinic who is completely lyme un-friendly and a great integrative PCP who isn't taking any more patients, unfortunately.
I need to find an INTEGRATIVE PCP who TAKES INSURANCE. This is HUGE for me and others b/c of the very few LLMDs in Mass who cannot (or refuse to b/c of time constraints) function as PCPs and/or who we can't visit often enough because of distance.
Posts: 571 | From Massachusetts | Registered: Oct 2008
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