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How many ppl here are on this protocol & had all NEGATIVE tests?And how much progress have you had?Also in regards to neuropathy

Submitted by SS In Oregon on Wed, 2007-08-01 01:43

If you have large or small fiber neuropathy how much has CAPi helped you? I have to ask because the neurologists RN got me so down today over the phone saying that I must have permanent nerve damage but that hopefully the burning and prikly pain wont lead to numbness soon. I hated hearing this. I mean this symptom is so new and already I am trying to hard to think positive, that my moisture glands are not destroyed. Any info appreciated. Thank you!

‹ Just saying hello Adding large fiber autonomic neuropathy to my diseases.... ›

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