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Anyone have the FGFR3 antibody gene?

Neuropathy | Last Active: Apr 7 6:29pm | Replies (146)
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@johnbishop

Hi @adamek3638, I would like to add my welcome to Connect along with @lisalucier and other members. Have you been diagnosed for the inability to sweat symptom or found anything that helps? Mayo Clinic has some information on the condition here:

Anhidrosis - Symptoms & Causes:
-- https://www.mayoclinic.org/diseases-conditions/anhidrosis/symptoms-causes/syc-20369400?page=0&citems=10

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Replies to "Hi @adamek3638, I would like to add my welcome to Connect along with @lisalucier and other..."
Kathy84 | @adamek3638 | Feb 19, 2020

I haven't been diagnosed with inability to sweat. I was positive for Igg vs FGFR3 antibody. I noticed constantly dry hands, no sweat at all. And I noticed buldging veins - especially in my apartment, where they were testing 5g. This technology is a killer for people with small fibers neuropathy.

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