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POTS SYNDROME

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Uploaded by on Jun 1, 2010

Pots Awareness! (for best results watch in HD) This is a video about what Postural Orthostatic Tachycardia Syndrome is and for my friends and other people to understand what happens to people who have this condition. Please Subscribe & comment!

the song is: Thats how it is by Paul Freeman

(I don't own all of the pictures)

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People & Blogs

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Standard YouTube License

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Uploader Comments (Potsgirl22)

  • @Lev8mysoul and @ncantu2011 Thank you so much! I am so glad this video was so helpful! Hopefully it helped your friends and family understand more about this not very well known illness.

    Keep spreading awareness!

    - Caroline :)

  • @cobaltgnome23 I'm glad my video helped you! I hope that you find answers and a diagnoses soon!

    -Caroline

  • Fantastic video! Thank you from a fellow POTSIE

  • @thehaynes4 Thank you! 

  • @NeverShoutAlex19 No problem! Thanks for spreading awareness :) Thanks for telling me part of your story! (I only said part because I know most of our stories are o so long!)

    - Caroline

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All Comments (27)

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  • I am 18, and had all of those symptoms since I was 14. I was 14 when I first fell to the ground (blacked out). I have blacked out many times...Recently I was diagnosed by a cardiologist that I have POTS. I was on a heart monitor/event monitor for a month before they made the diagnosis. Have POTS made me get severe anxiety, and since I am on anxiety medicine, my doctor won't prescribe me anything to help POTS. One of the side effects of the anxiety medicine I am taking now, helps with POTS.

  • I am 46 and was recently diagnosed with POTS. I shared this video with my friends to help them understand what I am going through. I received emails thanking me for sharing this. Everytime I watch your video, I cry and thank you at the same time for this helpful video.

  • You did an excellent job with this. My daughter, age 17 also has pots. To help the rest of the family to understand more about this I'm passing it on. TY very much.

  • @justind1997 Thank you and I wish all the best to you too!

  • I had mono for about a year and was confined to bed for about six months. After i got over the mono i still felt horrible, so we went to so many doctors until one said i had fibromyaltia. Ive been taking meds for that but they havnt worked. Im hoping now if i tell my docs about POTS (which encompasses all my symtoms) they will finally be able to do something about my dizzyness which has put me in a wheelchair at school and so many other places.

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