Neuropathy Message Board
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| I have had PN since 2004 and in 2008 was also diagnosed with Autonomic Neuropathy. Over the years, I have had B12 checked on a regular basis, and it was always within normal ranges. Then, in 2009 I was referred to a Neuromuscular Clinic. The doctor there did a full B panel. And found my B6 too low. Normal ranges are 5.0 to 30.0. Mine was 2.6.
I was started on 100 mg daily of B6. I did some internet research on B6 (Pyridoxine) deficiency. I realize I can’t state the sources, but here are quotes from some of the articles I found:
[QUOTE]Pyridoxine deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Pyridoxine deficiency, or a subtype of Pyridoxine deficiency, affects less than 200,000 people in the US population.[/QUOTE]
[QUOTE]Pyridoxine deficiency causes blood, skin, and nerve changes. [B][COLOR="Blue"]This vitamin is unique in that either deficiency or excess can cause peripheral neuropathy[/COLOR][/B].[/QUOTE]
[QUOTE]Pyridoxine absorption is reduced in elderly persons and in patients with intestinal disease or who have undergone surgery.[/QUOTE]
[QUOTE]Acquired deficiency is associated with inflammatory disorders and with concurrent use of several medications.[/QUOTE]
Several medications were listed that could contribute to a Pyridoxine deficiency, but two jumped out for me: anticonvulsants and antidepressants. I am on both. And, since I have also had abdominal surgery 13 times, I probably have a double whammy.
Within a month of taking the B6 supplements, I started to come alive again. That lasted about 3 months, when I started to feel the slide. The next time I saw the doctor, my B6 level had fallen even lower to 1.9.
I was told to increase the B6 until I was feeling good again. I am now at 200 mg a day, and feeling like joining the human race. If your doctor has suggested B6 supplements, he may be right.
Probably the only question I would have for you is this: Is he just having you ‘try’ it, or is his recommendation supported by lab tests? Aussie,
How much nerve damage symptoms do you feel the b12 treatment actually reversed for you? How much time did it take? The more I read about this deficiency the more the symptoms seem related. But I do have motor dyfunction in my hands that I hope heals.I also have a slight tremor in my hands. Could this be a part of the nerve damage, and if so can it heal? |
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