I just got diagnosed with POTS. It is completely disabling. I'm living in a fog most of the time and so incredibly dizzy and lightheaded. I have fainted this past week just from sitting upright.
I know very little about POTS. I even forget what it stands for without googling it. I already knew about orthostatic hypotension as this is what I was diagnosed with about ten or more years ago. But I've been told in the ER that POTS is different.
I read online that a good percentage of POTS patients are comorbid with autism and hypermobile Ehlers Danlos. I have both of those.
Could anyone who has POTS tell me more about it, their symptoms, the treatment etc? I can't get in to see a cardiologist until June. I would like some info in the mean time.
I know very little about POTS. I even forget what it stands for without googling it. I already knew about orthostatic hypotension as this is what I was diagnosed with about ten or more years ago. But I've been told in the ER that POTS is different.
I read online that a good percentage of POTS patients are comorbid with autism and hypermobile Ehlers Danlos. I have both of those.
Could anyone who has POTS tell me more about it, their symptoms, the treatment etc? I can't get in to see a cardiologist until June. I would like some info in the mean time.