I’m hoping to.

 

I’m merely trying to understand what happens in real-life to people with moderate degrees of aldosterone impairment when they drink a lot of water and don’t do anything to compensate for it.  There _is_ something called a "thirst mechanism", so I don’t mean it to come off as cold and detached.  I know this is more of a social support group than a CAH "tech support" forum, but that’s why this is the place to find people with every-day experience who may have run into this stuff.  People in my family don’t talk about their medical issues, much less seek treatment.