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how to find LLMDs and Support Groups



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05/04/2008 18:01
fin24
Lime Green Ribbon
Posts: 95
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If youre having trouble locating info for your state/area/country try the following

1. www.lymediseaseassociation.org

(LDA , click physisican referral and support group links)the Dr referrals limit you to 3 requests a month (I think) and I know Ive used up my limit already for others, sorry

2.www.lymeneteurope.org

( has a lot of U.S. members too)

post for help--great site for valid info on all things Lymie!!

and www.lymediseaseaction.org.uk/

3.www.lymenet.org

click 'find a Dr' and post

( this may take a long while as theyve been VERY slow lately to get back to people and theyve recently begun a controversial policy of asking you for a LOT of personal info--so if you are at all wary--dont give it to them)

4.GOOGLE

"your state" Lyme support groups"

a few links should pop up, go to them and get the phone or email contacts for the groups then contact them and ask them for a list of reputable Lyme professionals as well as who to avoid!!

good luck

Fin

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