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Anyone with neuropathy

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Hi, was diagnosed in October with lyme [misdiagnosed for several months prior to

that]. I believe I've had this since last spring, but not entirely sure. I'm

currently on abx treatment but have ordered Buhner's core protocol to begin as

well.

One of the symptoms lyme has brought into my life is neuropathy. Since

September, I have had a burning feeling on my skin. My doctor says it's

neuropathy and since antibiotic treatments have not touched this problem, he

says this may be a lingering symptom. I don't like this idea and trying to find

alternatives to help with this.

Has anyone had this symptom, or currently does? And what can be done? There

must be something.

Thanks,

Kate

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