I'm curious how living in extreme heat climate affects your hEDS? I was recently diagnosed with hEDS and POTS and while I think I can trace back my symptoms for quite some time, I have no real idea how long I've been having issues because I've really adapted my life for quite some time. However, I have lived in a very hot climate for nearly 2 decades and as of late it has started to really affect me negatively, and I'd love to know how anyone adjusts, accommodates, etc.
Thank you!