CHANGES: Pt. 1, Living with Postural Orthostatic Tachycardia Syndrome (POTS) part 1

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Uploaded by on Dec 15, 2010

The Dysautonomia Information network presents a film that provides ANSWERS, medical interviews, personal testimonies, facts and statistics about Postural Orthostatic Tachycardia Syndrome (POTS). For more information, please visit www.dinet.org

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Education

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Uploader Comments (justadbeer)

  • True, but this video is geared towards POTS patients. With POTS patients EDS may or may not be present. Both my wife and son have POTS (my son to a lesser degree) and both show symptoms of joint hyper-mobility.

  • there are six parts total...please watch them all,

  • Please, could you put spanish subtitles?

  • @ramona7990

    I'm not sure how to do that, but i will look into it and see if it is possible.

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  • actually its under my comments !

  • Hello all. I'm spreading awareness for POTS and other illnesses through my own personal story on my blog. Please click my name and see my profile description!

  • They don't mention that with EDS, POTS is a permanent condition...

  • It's really important to watch part two also.

  • Thank you so much for this video series. I live with POTS and NCS, and I really appreciate you addressing the impact it has on our lives, in particular, how it affects relationships and how others perceive us as fakers because we "look fine." I'd love to connect with others who have POTS - please contact me through my page gatewaytobeing. Thanks again.

  • @justadbeer Ok. Thanks and sorry if you don't have time for it :)

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