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Peripheral Neuroapthy

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LDN is not a pain killer. It probably won't help your neuropathy.

I have chronic neurological lyme disease and have " cactus foot " most of the time

as a result of the scarring in my CNS that this illness has caused for me. You

know, that feeling that your foot is constantly asleep, so that numbness,

prickling, and tingling doesn't ever really go away. Its tolerable most of the

time, but there are times its unbearable.

Best thing to use for your neuropathy is a drug called MetaNX which is basically

B6, B12, and Folic Acid in their natural/active state (L-methylfolate, Pyridoxal

5'-phosphate, and Methylcobalamin). I take it twice a day and it helps. Ask

your Dr. about it.

Other things to do are to soak the affected extremity in hot water with a good

heaping of epsom salts. The heat increases the blood flow to the extremity

which can ease the neuropathy.

Also, Lidocane based products can help numb the extremity, reducing the

discomfort.

Other than that....not much else to do but just deal with it.

- KenC.

>

> I'm new here... hoping to talk to some of you about LDN and if it can really

help with the severe pain of Peripheral Neuraopthy?

>

> I've had it for 3+ years due to using the antibiotic LEVAQUIN in the QUINOLONE

family of antibiotics.

>

> Severe pain legs/feet/arms/hands. Stabbing, burning, etc. 24/7

>

> Has anyone experienced this condition and used LDN successfully?

>

> Thankyou for any help you can give.

>

> Rose Terry

>

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