LymeNet Flash: LLMD needed in MN

This is topic LLMD needed in MN in forum Seeking a Doctor at LymeNet Flash.

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Posted by cjbrklich (Member # 24607) on :

I was diagnosed in Sept. of 09 after showing symptoms since July of 09. My regular dr. gave my anti-biotics for 3 weeks. I felt better for awhile but now my joint pain is back. I contacted my dr. and she only gave me a new Rx for the same pain pills but I could take more during the day. They really are'nt helping as much as they were before. I need a LLMD. I'm very new to all of this. I just found this group today and found a couple groups on FB last week. I'm learning alot which is good and scary at the same time.

Posted by Siciliano (Member # 15920) on :

Hi, [hi]

cjbrklich and WELCOME to our lyme site. We're glad you came to us for help.

I have sent you a private message (pm), click on the flashing envelope.

Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!
[group hug]

Posted by LymeXtu (Member # 24590) on :

Hi cjbrklich I am also new here, my 12 yr old son has Lyme and we are in Minnesota, we are seeing a LLMD in St Louis Park that we have been very happy with so far. I got his name from Minnesota Lyme Action, he is new to Lyme but seems to be very well trained. I am planning on asking him if this group can start giving out his name and contact info. If you PM me I guess I can give you his name and number.(sorry this is all new to me too).