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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Looking for LLMD in CT

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Author Topic: Looking for LLMD in CT
pjpape
Junior Member
Member # 36659

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I have been tested (blood) for 14 spirochetes, all of which have come back negative as have traditional Lymes tests.

I saw a Naturopath who has been using energy testing for 20 years. He found me highly toxic for Borrelia, Babesia and Ehrlichia to start. I will see him again next week as I had had a colonoscopy the day prior to our appointment.

I was diagnosed with MS more than 10 years ago. Although I have been 90% compliant with treatment, having MS has never resonated with me and what I've read about Lymes has.

The Naturopath gave me 2 homeopathic formulas which have made a tremendous difference since day1. I have hope again!

If I need to do the antibiotics in addition to the energy medicine/homeopathy, he can't prescribe for me. Any suggestions?

Posts: 1 | From clinton, ct | Registered: Mar 2012  |  IP: Logged | Report this post to a Moderator
t9im
Frequent Contributor (1K+ posts)
Member # 25489

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PM of MD's sent.

If your Lyme test was / is the elisa then I suggest the Western Blot done by Stonybrook, Igenex or one of the other ones who don't use the NIH standard WB kit.

It's amazing there is a controversy to this insidious disease and I've found it easiest to show a couple of u tube video's on the controversy.

http://www.youtube.com/watch?v=PVPRWiukp_M

http://www.youtube.com/watch?v=8yk0C-uX9cU

If you watch this video you can see some of the miss diagnosis.

http://www.youtube.com/watch?v=3nIuIF6q8FA&feature=related

http://www.youtube.com/watch?v=V-lHDA863TM&feature=related

Dr. B's Advanced Topics in Lyme disease.

http://researchednutritionals.com/FactSheets/Burrascano's%20Advanced%20Topics%20in%20Lyme%20Disease%20_12_17_08.pdf

--------------------
Tim

Posts: 1111 | From Glastonbury, CT | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
dmc
Frequent Contributor (1K+ posts)
Member # 5102

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print out the green booklet from http://lymepa.org

Check out & order Dr. P's video presentation from the University of New Haven website.

It's #5

http://www.newhaven.edu/unh/lyme/

Check out Dr. Terry Wahls Foundation on Facebook...she says how Tick Diseases can trigger MS and for pete's sake, you live at the CT shore.

I've been DX MS since 1988 guess what!!! IT IS LYME! Have been treated Lyme, Bartonella, & Babesios since 2003.

never did MS drugs...No new lesions, non enhanced since 2003 when I finally went to a LLMD & treated for the TBIs. That's 9 years...unheard of for so-called "MS" people.

Sending you blessings to get proper answers.

Posts: 2675 | From ct, usa | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
   

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