LymeNet Flash: LOS ANGELES, CALIF. LLMD NEEDED

This is topic LOS ANGELES, CALIF. LLMD NEEDED in forum Seeking a Doctor at LymeNet Flash.

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Posted by fifi25 (Member # 16675) on :

i need help finding a llmd in los angeles ca

we don't have the test result yet.

but my daughter has been suffering from severe headache, stiff neck, numbness in her sides, funny heart beat , sleepless night, sweat & swollen in her legs.

Posted by bettyg (Member # 6147) on :

sent pm to fifi with LA NAMES....using meg's list!

Posted by Peedie (Member # 15355) on :

Meg has a good list. I will PM you about my LLMD which is pretty close to you.
TC
Peedie

Posted by fifi25 (Member # 16675) on :

thanks peedie,
i called the office and they don't take insurance.

if you please send me additional names, i will really appreciate it.

Meg didn't send me anything yet. i keep checking.

thanks everyone for your help.

Posted by bettyg (Member # 6147) on :

fifi,

I SENT YOU MEG'S LIST; you have received it by thru ME!

Posted by Peedie (Member # 15355) on :

FIFI - I sent you a list also. Go to top of Flash Discussion Directory and look for flashing "you have a private message" in red, and click in.

TC Peedie

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