Looking for a LLMD near macon ga

Hi. Im looking for a LLMD near macon GA that uses treatments other than antibiotics. Any information would be appreciated.

Thank you GA Hunter. Can you email me his name and address?

I didn't know there were any LLMDs in Georgia. I lived north of Atlanta. I saw a naturopath in Roswell who has Lyme, but it seemed to be more about money than help.

The LLMD I have seen before is near Nashville.

....... AP in Suwanee, or Alpharetta, GA (mixed reviews)

........RB in Roswell


........AP in Roswell (Naturopath)

........KB in Marietta

,,,.....and a clinic in Newnan.


There are some good reviews from prior patients, but not current forum members.

If you recognize those above...and they aren't considered lyme literate....please let me know, and I'll remove them (or add comments) from my list.

I have no faith in supposed GA LLMD's. The few I called were infectious disease MD's and we all know how that is going to go.

Georgia Hunter said...
I have no faith in supposed GA LLMD's. The few I called were infectious disease MD's and we all know how that is going to go.

Being an ID Doc doesn’t necessarily negate lyme literacy

Dr J is an ID doc.

WalkingbyFaith, SA in Savannah is the one I was talking about that may be OK. I've had a patient or two from there and their treatment program wasn't bad. I could probably help her but most physicians don't need help from someone like me.

If I were sick again, I'd see Dr Simon Yu (I should be able to say his name because he isn't a LLMD) in St Louis.

I should add that I am not a good patient. I question everything and trust no one. Even if I had the best doctor, if I wasn’t all in and didn’t or couldn’t trust them and the process, I would likely sabotage my chances for recovery. I am a very stubborn person who needs to understand a lot in order to trust. My issues probably stem partially from having dealt with minor disabilities and health issues lifelong and being hurt by doctors or having doctors who gave my minor issues no concern, basically leaving me to figure out how to function and cope on my own.

My PCP had another patient with Lyme who was using a walker or wheelchair. SA got him recovered or mostly recovered with her treatment plan.

From the beginning, she has rarely talked to me about Lyme/co at all and instead talks to me mostly about mold and parasites. Those are the things she thinks are my biggest problems. She is likely correct on that. I have had the biggest responses/herxes trying to treat those issues.

Post Edited (WalkingbyFaith) : 5/7/2020 6:44:43 AM (GMT-6)

Georgia Hunter said...
I could probably help her but most physicians don't need help from someone like me.

I’d say most physicians DO need help from someone like you. When I ask most physicians hard questions, they have no answers and the responses I get make it clear that their level of scientific knowledge and understanding is far more superficial than I ever imagined. YOU, on the other hard, have a deeper level of scientific knowledge and contemplation than anyone I know of and are way beyond my comprehension. I would guess you are beyond most average doctor’s’ comprehension.

My impression of the two alternative doctors I have seen is that they go to conferences and pick up information from other experts but don’t have mastery of the information. They probably do know more and are more competent than they seem to me. Like I said, I am not a good patient - too much critical thinking for my own good (and everyone else’s, too).

Yu has a really good knowledge of protozoans but also treats according to what he finds. Anyone who goes to see him has no recommended treatment until he assesses you. He is unconventional using an acupuncture meridian assessment that is not used my most. He's a big dental cavitation guy too.

And yes, the last neurologist I talked with had absolutely no clue about the question I asked him. He didn't even know anything about the question much less the answer.