LymeNet Flash: LLMD in Northern California?

This is topic LLMD in Northern California? in forum Seeking a Doctor at LymeNet Flash.

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Posted by alextaylor14 (Member # 25124) on :

I have been having problems for the past two years and have seen countless doctors. I have just recently been to Stanford to be checked for MS and ALS. Can someone recommend an LLMD in Northern California? I live Modesto,CA and would be willing to travel almost anywhere including the bay area.

Thank You..

Posted by Robin123 (Member # 9197) on :

Hi Alex - am pm'ing you.

Posted by Siciliano (Member # 15920) on :

Hi, [hi]

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

I have sent you a private message (pm) also.

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!
[Smile]

Posted by jblral (Member # 8836) on :

Recommend you join the CaliforniaLyme on-line support group:

http://health.groups.yahoo.com/group/CaliforniaLyme/

There are members in your area who can tell you about doctors.

Also, the California Lyme Disease Association website maintains a list of support groups throughout the state. Check for one in your area:

http://lymedisease.org/california/california_support_groups.html