Can anyone share what life with Conn's Syndrome is like?
My endo is working up my labs to explore possible Conn's Syndrome. I'm trying to wrap my head around what life with Conn's would be like. I see a lot of videos on what it is but very little about what it's like to live with this condition. I have undetectable renin which of course throws my ARR off.
CT Scan with no contrast came back clear. My endo is leaning towards bilateral Conn's Syndrome.
Thanks in advance. I look forward to hearing from you!