← Return to Anyone have the FGFR3 antibody gene?

Discussion

Anyone have the FGFR3 antibody gene?

Neuropathy | Last Active: Jul 31 10:32am | Replies (147)
Comment receiving replies
@adamek3638

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.

Jump to this post

Replies to "I haven't been diagnosed with inability to sweat. I was positive for Igg vs FGFR3 antibody...."
Lisa Lucier, Moderator | @lisalucier | Feb 20, 2020

Hi, @adamek3638 - have you gotten the opportunity to talk to your doctor about the bulging veins, no sweat and constantly dry hands? If so, are you receiving any treatment for these issues?

VIEW AND REPLY
Hank | @jesfactsmon | May 19, 2020

Hi @adamek3638 I am interested in your comment regarding 5G's affect on SFN. I had not heard this before. I searched a bit online but only found a couple of passing references to this, nothing with any real info. Can you offer a link to any webpage with some info about this? Sounds like something to be aware of. Thanks much, Hank

VIEW AND REPLY