A Demonstration of Dysautonomia (POTS)

Thank you for making such an informative video. So many people think that POTS is "all in your head"...a made up disorder, a disorder caused by anxiety. Thank you for providing such a clear explanation is such a professional manner. Credibility is priceless! I will share this with my family and friends.

Wow, thats crazy. I am so sorry to hear you have pots. This is a great video. Informative and interesting. Thanks

My heart rate also jumps around, and my blood pressure goes so low when I stand up, that people can see it. My face turns green and white, and we have to 'abort' taking my blood pressure. Or else, I will faint on the floor. I coined the term, "Brittle Dysautonomia" because my dysautonomia is unpredictable, has wide swings in vital signs, and my response to medications has been variable.

Thank you for posting this video.

great demonstration. i have inappropriate sinus tachycardia.... and i am 24 years old..... my heart rate goes up to 160 sometimes for no reason......

God bless you for such an awesome demonstration ! I've been struggling with this life destroying condition for most of my life, but has become devastating in the last 6 years of my life - and only in the last 2 years have we discovered what my illness actually is. Again, very well done and I hope there will be more attention and for this illness to be taken more serious in the medical field. - -- -Blessings !

Superb video, well done in making this and educating the public.

On my TILT test my pulse was 170bpm in 2 mins and they stopped the test, so it's good you mentioned a TILT test as it's a vital diagnostic tool.

I have no symptoms of EDS, though I do know a lot of POTS people seem to have both. I have other autoimmune disorders though, in addition to Dysautonomia.