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LLMD in Southern California

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Lyme Disease
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Elleon
Regular Member
Joined : Feb 2014
Posts : 364
Posted 8/26/2020 3:18 PM (GMT -7)
Hello All,

I posted a couple weeks ago about some new symptoms I've been having. I've been to a neurologist, a gastroenterologist, my PCP, no one can find anything wrong.

Which points to my Lyme relapsing. Does anyone know any LLMDs in Southern California? I can travel to San Diego, LA, Santa Barbara, anywhere within a few hours of Orange County, CA.

My email is listed in my profile to message me.

Thank you!
Elleon
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Missymoe
New Member
Joined : Jan 2021
Posts : 6
Posted 1/15/2021 8:45 AM (GMT -7)
Hello elleon,
I am also in so cal and recently have been exposed. I am working with Dr Lehman in LA. Her consult was 175, and she immediately wrote me a script of antibiotics. Three different ones along with nystatin for Candida. If you habe ins you can try to fill you script . I have Kaiser so I had to pay cash which was 500. Also they are hard to get s hold of I suggest emailing them. Its tough but you need those antibiotics to cut the load down. Or at least I did. Also you should definitely start on some herbs. Buhner is who I started with. Along with the antibiotics. Except with flagyl.
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Elleon
Regular Member
Joined : Feb 2014
Posts : 364
Posted 1/15/2021 9:34 AM (GMT -7)
Thanks for the reply.

Is she a lyme literate doctor? Did she test you and you were positive?

Just wondering because i've had it for 7 years now, not sure how I'll test, probably not positive since it's been so long. But the symptoms are lingering.
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Missymoe
New Member
Joined : Jan 2021
Posts : 6
Posted 1/16/2021 4:47 PM (GMT -7)

Elleon said...
Thanks for the reply.

Is she a lyme literate doctor? Did she test you and you were positive?

Just wondering because i've had it for 7 years now, not sure how I'll test, probably not positive since it's been so long. But the symptoms are lingering.

No I tested positive with infections disease doctor they my insurance (lucky I guess). Yes she is, but she did not test me, because I showed markers already. Then they treat as of you also ha e co infections. Igenex is where you can get testing. Again, costly and your md has to sign off on it. You order the kit And they fill out the form and sign. I also spoke to another dr in Irvine, that is from the east coast and has had Lyme. He sends blood to a lab in New Jersey that is compared to Igenex he says and it’s less money. Idk it’s all so expensive and frustrating and scary. I go next Thursday, I can let you know how it goes. His name is Darin Ingels.
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