Hi,
I'm new to this forum, so thank you kindly for any help in advance. I have a few of the issues associated with Dysautonomia, specifically looking for advice regarding POTS. Diagnosed a few years ago now, had some success with medications and exercise therapy, but had ups and downs as I'm sure we've all had. Until now I've always had exercise intolerance, pain, fatigue, and presyncope episodes when standing with dizziness, feeling hot, vision problems, etc. No actual fainting. But now I'm experiencing actual syncope (no warning, but quick recovery I think). I haven't seen my cardiologist yet, as my appointment is a while away, and she's hard to get into (didn't feel this was an 'emergency'). I'm not certain this is Pots related, since it has never been part of my presentation.
I guess I'm wondering if anyone else has experienced a change in their Pots over time, especially since people seem to either have syncope in their diagnosis or not, from the people I've heard, so perhaps mine is a non-cardiac issue and I should just go to the local doctor (I live in Australia).
Thank you.