LLMD recommendations??

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Regular Member

Date Joined Oct 2009
Total Posts : 289
   Posted 10/8/2009 2:25 PM (GMT -7)   
Hi everyone- i really need to get started with some testing to see exactly what i'm dealing with- if anyone has a great LLMD please respond and email me specifics- walkingflame7@yahoo.com.  I live in texas- so someone in texas or at least in surrounding states would be great. Thanks for the help!

Veteran Member

Date Joined Oct 2009
Total Posts : 699
   Posted 10/8/2009 10:47 PM (GMT -7)   

I live in California so can't help with a recommendation. I found my LLMD by contacting ILADS. They don't have a formal referral system, but I told them I was having a difficult time finding a doctor in my area and they helped me. I had to call them to get the information.


Regular Member

Date Joined Oct 2008
Total Posts : 222
   Posted 10/8/2009 11:53 PM (GMT -7)   
Also if you go on Lymenet they have a doctor r fine section on their forum and there are at least two poeple who have been keeping an ongoing list of doctors seen by lyme paitents and they try to keep patient comments and everything. very helpful.

The Lyme Disease Association also has a referral dataase online you have to sign up and login to get it.

And if you contact your state or local lyme disease support group they always can help.

Good Luck to you.

Or ask around in places like here or other sites... and gather up names that way.

Just DO NOT ASK the American Lyme Disease Foundation or the IDSA (my opinion).
The will not give you any doctors who believe in chronic lyme disease if you do ask them for a
referral list..(from my experience).

Veteran Member

Date Joined Mar 2009
Total Posts : 4717
   Posted 10/9/2009 9:16 AM (GMT -7)   
Hi finding,

Did I give you Tickers email addy yet? She is a long time member of these forums and helps new members find a good doctor around their area. She also knows which ones NOT to go to.

Here is her info:


You can also try stephanie@turnthecorner.org
**You never know how STRONG you are....until being STRONG is the ONLY choice you have**

Co-Moderator Lyme Disease Forum

Regular Member

Date Joined Oct 2009
Total Posts : 289
   Posted 10/13/2009 1:57 AM (GMT -7)   
thank you Cajungrl, i finally found someone but i think i will email ticker anyway just in case i need a back up. Maybe i will ask her what she knows about the doc i am going to see too- D. F in Lousiana (well his assitant actually)
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