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LLMD's in St. Louis Area

Hi everyone!

I have been treated by an LLMD here in Texas for the past 8 months for Babesia and Anaplasma.  I am doing much better and am no longer on Mepron, and I am down to only 200mg/day of Doxy.  

I am moving to St. Louis on Friday and wondered if anyone has any recommendations for doctors in the area. I have tried contacting the Lyme support group, but the phone number has been disconnected and their website domain is inactive.  

I would love any information anyone could give me, thanks!!
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Avatar universal
Ditto mojogal --

You could email to

                -- contact  [at]  ILADS   [dot]   org  ---

that's their referral function.  Best wishes!
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1763947 tn?1334055319
Email ILADS they can give you a list of names there. Hope you have a smooth move!
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