Dysautonomia/POTS FAQ

Here are the helpful links for dysautonomia:

http://heartdisease.about.com/cs/womensissues/a/dysautonomia.htm
http://www.dinet.org (forum)
http://www.dynakids.org/Documents/DebbieDysautonomiaArticle.pdf
http://www.wrongdiagnosis.com/d/dysautonomia/symptoms.htm
http://www.mvprolapse.com/dysautonomia.html

Ways to contact me:
twitter.com/RachelDianeFTW
myspace.com/tha_handwarmer
Message me if you would like my email, and if you could provide some proof that youre not a spammer/stalker that would be great.

Comment this video as well if you have any questions whatsoever!!

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• POTS
• dysautonomics
• help
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[ninoninochile]

You do a beautiful and important labor spreading this information. Hope you feel good today and everyday... Thank you!!.

[1210donna]

you've done a fab job :-) 

[rx2mozart]

thanks this was really helpful.

[Elevate4Him]

auw you're so cute! i love you!

[Jazzyteach65]

you have my support ;}

[biebersshawtys13]

@homeintheclouds tHANKSS(:

[LouLou3078]

Hi, sorry you have this disease. Thank you for posting this video. I have MS (Multiple Sclerosis). I have most of these symptoms plus a few other different ones.

Have you looked into being tested for CCSVI . An ultrasound to the neck vein to see if you have any narrow of the veins, CCSVI (Chronic Cerebro-Spinal Venous Insuffiency). A lot of people with Autoimmune Diseases are testing Positive for CCSVI. Clinical Trials are being conducted around the World. Type in CCSVI on U Tube,.

[homeintheclouds]

@biebersshawtys13 :/ i'm really sorry to hear that. i hope you can jump back into school soon! it sucks getting back on track :/

[homeintheclouds]

@surferbuddhist wow, that sucks :/ i'm really sorry to hear that! i hope you feel better soon <3

[homeintheclouds]

@ChrisVitchev wow, way outside the norm are ya? :) lol. i do still have dysautonomia. i'm still kind of getting over a flare up.