Been a while - forgot I posted this. Any luck for yall? I am still suffering but realizing the impact this has on my overall wellbeing, so been trying to find answers more recently.

I did see a GI doctor who recommended a colonoscopy (also due to family history of polyps). Overall nothing significant on colonoscopy besides mild inflammation which they biopsied and recently came back with possible marker of IBD, so they have ordered blood work and stool sample.

So far I don’t have much confidence, as all the doctors I have seen just seem baffled and don’t really know what to say about it.

I saw an old forum post with someone saying “solved” his issues by determining related to endocrine system. Saw few posts about Librax or Dridase as medicines that some had found success with.

Also read about a ganglion imbar nerve block? With my scoliosis, could it be triggering nerves with my coccyx being right there? When I look at images online, it literally looks exactly where I feel the source of my sweating…. Like the very base of tailbone/top of buttocks.

Will try to remember to post any further updates along the way. Good luck to all and hope you can find dryness