Haven’t heard anything from the endocrinologist yet.
The polyuria isn’t worse; but it’s not better either. To be honest, I don’t know what “better” would even look like. Part of me wonders is this Cowden’s Syndrome related, or Lhermitte-duclos Disease related? Or both. Neither? What the crap is causing it?
I have decreased my water, inadvertently or subconsciously, I don’t know. But what I do know is that I shouldn’t do that…I just can’t help it really. I just can’t help it.
So I am doing this instead. If I sweat a lot I don’t use the bano as much. And I’m kind of less frustrated. At least temporarily.