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looking for llmd in orlando fl

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Posted 12/11/2015 3:58 PM (GMT -5)
llmd in orlando fl??
Posted 12/11/2015 5:42 PM (GMT -5)
Welcome to our community. reminder!

Since you are new to the forum, I'd like to point out the thread at the top of the page titled: "New To Lyme?...Start Here!" It's full of good information - symptom lists, info on probiotics, detoxing ideas, and much more!

I hope you keep coming back here to read, ask questions. Also, feel free to share your 'story'

Also, you should enable your email option - we don't post the names of the LLMD's here for privacy reasons. Members can email you the names once your email is enabled.
Posted 12/11/2015 5:56 PM (GMT -5)
If anyone knows of a doctor anywhere in Florida please email me! Desperately looking for a doctor! Any help is greatly appreciated.
Posted 12/11/2015 7:52 PM (GMT -5)
Hi Theycallmegumby - welcome to our community!

I see you have posted in several threads for a Dr. in Florida...so I won't answer all of them.

I see you have enabled your email option - that is great. We don't post the names on here - for privacy reasons..so members can email you with names.

You can also contact the ILADS Physician Referral - here is the link:

ilads.org/ilads_media/physician-referral/

Since you are new to the forum, I'd like to point out the thread at the top of the page titled:"New to Lyme?...Start Here!" It's full of great information- symptom lists,info on probiotics, detoxing suggestions, and much more.
Posted 12/11/2015 8:04 PM (GMT -5)
Thank you girlie, I read that first. I actually have been diagnosed with lymes, and bartonella, treated for babesia(sp?) and have 2 different strains of blood clotting disorders. I know one is the MTFHR and I honestly can't remember the other, because I just got told today by my doctors office they won't see me anymore because they don't think they can help anymore. I have the list of all the medications I can take, what I've taken, what's the best combination (so sad factiv isn't available anymore). I don't eat gluten anymore, minimal dairy, no processed foods, no meats that have any hormones or steroids, a variety of colors of fruits and vegetables, and I buy as many of them from farmers markets as I can to ensure they're local and not being sprayed with anything when they're coming into the country
Posted 12/11/2015 8:13 PM (GMT -5)
So the Dr. who was treating you wasn't a LLMD? Was it your PCP that was treating you?

How long were you in treatment?
Posted 12/11/2015 8:42 PM (GMT -5)
No unfortunately it was a LLMD, but the nurse practitioner in the office was not up to par. And they had the requirements that you had to see the doctor one month, and the nurse practitioner the next. And the np would just ask me what I wanted to take and do, and would then the doctor even started saying the same thing. They were alright and more up to date with lymes, but I needed them to acknowledge that I have bartonella worse than lymes, and that the cowden protocol wasn't working for me(it was causing serious skin discoloration) and when I said I wanted to try Chinese herbs they said I was on my own with that, and to just let them know...:(
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