LymeNet Flash: LLMD in Buffalo, Western NY

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in Buffalo, Western NY - Support Groups In WNY

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Topic: LLMD in Buffalo, Western NY - Support Groups In WNY

McStorch
Junior Member
Member # 20987

posted

Hi! I am really new to this. Diagnosed and treated (not very well) in July 2009 and I am very sure, based on western blot and symptoms that it is back. MD says not enough criteria met to warrant treatment. Nice.

I have an appointment with Dr. P who is on the LLMD list for NY. In Buffalo, NY. Wondering if anyone has any experience with this DR. Charges $280 for initial consult and will not accept insurance. Is this the norm?

Also, does anyone know of a support group in WNY? I am trying to sponge up as much info on LD as I can before I start this journey.

Thanks All!!

Posts: 6 | From PA | Registered: Jun 2009 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Very much the norm... back in a minute...

Read this:

http://flash.lymenet.org/ubb/ultimatebb.php/topic/2/13239

scroll all the way down to info on insurance

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

TS96
LymeNet Contributor
Member # 14048

posted

There are support groups, one in the Syracuse area and one in Farmington, NY, near Rochester.
PM me for more info on the Rochester one if you need it.

Anyone, please chime in if you know of one in the Buffalo area.

--------------------
Bart Henslea 1976
Fibro/CFS/arthritis 2004
Lyme diagnosed 2007
3 1/2 years treatment with oral combos, Cowden, IV roc. BW herbs. Off all abx in 12/10. Feeling good.

Posts: 647 | From NY | Registered: Dec 2007 | IP: Logged |

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