Looking for LLMD in Los Angles, California

Hello,
I have been treated for lyme since September in New York, but I just moved to Los Angeles. I have being seeing Zhang since October, but I am interested in knowing as much as I can and all the options. I'm not sure if I should be taking more abx or not. Since there is no timeline to this - it's hard for me to know if I am doing "well" or if I should be doing more.

I also need a PCP, and I would love to find someone who has some lyme literacy - though I know that isn't easy to find - and it's not the same as an ILADS MD. So any ILADS MD or PCP with Lyme Literacy recs in Los Angeles would be very helpful.
Thank you!

Post Edited (PandaFox) : 1/11/2020 11:21:45 PM (GMT-7)

Hi PandaFox!

Good to see you here. Others should be along soon but Girlie holds the database and can provide great recommendations so don't be shy about emailing her. She's a GEM.

I didn't have a PCP while I treated Lyme--my LLMD provided that pretty well. And I had fairly good insurance at the time...until I didn't. Can share that story.

I was also lucky to see a nurse who used to work under my LLMD and I can recommend her to you as well. I've been out of the scene for a couple yrs so I'm betting there are LL practitioners in LA who will be great for you.

-p