There is a form of PN that is inherited. It is called Charcot Marie Tooth, and has no cure. This is diagnosed by a special DNA test, which is done by Athena labs and maybe some others.
There are several variants of this genetic problem, and the test is different from the others now offered on TV and otc. It is also much much more expensive for this specific DNA test.
Here is a site with more information:
What is CMT? | Charcot-Marie-Tooth Association
We don't have many posters here, because once diagnosed, self help isn't often effective. These patients may have nutrient deficiencies but fixing those only help with the problems that
co-exist with the CMT. Our forum can help with daily life like choosing shoes, and other comfort solutions, though.
Having PN for only 2 months or a brief time, the possibility of CMT is not often brought up. Short time frames can suggest other causes, which may wane, or flare in the future. CMT is usually progressive with no wane.
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei
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Weezie looking at petunias 8.25.2017
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