How about in nearby states ? What are Texas patients doing to improve?
Posted by tclimb (Member # 29508) on :
I contacted the support group coordinator in OK a few months ago for a friend, she gave a few names which I passed on, don't now have.
try locating support group for state. This web site has links to those contacts. start in TX if that doesn't work CAll coordinator in OK, she picked the phone right up.
Posted by kday (Member # 22234) on :
I wish I could tell you. Helpful doctors exist in TX, but the ones I found don't want any patients referred to them because of the pitbulls that run the Texas medical board.
There's a couple good NDs, and I could share that info since they aren't attacked.
Posted by Lymetoo (Member # 743) on :
To find your STATE Lyme Disease Association-
Web search: [your state], ``Lyme Disease Association'' and be sure that group is ILADS-minded
moving to Seeking a Doctor
Posted by jkmom (Member # 14004) on :
I am in TX. I have been to LA, MO, CT, VT, DC, and CA for LLMD's.
I've also been to one in TX, but he has been driven out.
I have seen some TX doctors that will treat but not per ILADS, so if you can't travel, you might be able to find someone to help.
I just stumbled on to the TX doctors when I was looking for alternative health care. I wasn't going to them for Lyme but they knew about it and did treat it, just not the way I wanted to treat it.
Most of the out of state doctors I have been to require in office visits periodically but do a lot of phone consults, so traveling expenses are reduced.
Posted by annxyzz (Member # 20404) on :
I am thankful for replies and hope I will receive a helpful lead. I have no idea where to start after three years of self treating .
Posted by Peacek (Member # 30633) on :
I am new here, but I live in North Texas as well. Is there a LLD in LA? Or OK? thanks