Find all needed information about Pots Support. Below you can see links where you can find everything you want to know about Pots Support.
Providing information and support about postural orthostatic tachycardia syndrome (PoTS) for sufferers, medical professionals, family, and friends - aiming to raise awareness.
https://themighty.com/2016/11/pots-and-dysautonomia-support-groups-and-feeling-alone/
Laney Rogers, a woman with postural orthostatic tachycardia syndrome (POTS), explains how a support group for those with dysautonomia has helped her to feel less alone living with a chronic illness.
http://www.standinguptopots.org/
STANDING UP to POTS is committed to increasing awareness for postural orthostatic tachycardia syndome (POTS) within the medical community and raising money to support POTS research. POTS is a form of dysautonomia, and is caused by malfunctioning of the autonomic ("automatic") nervous system.
https://www.drugs.com/answers/support-group/postural-orthostatic-tachycardia-syndrome/
Nov 09, 2016 · Ask questions and get answers about Postural Orthostatic Tachycardia Syndrome. Our support group helps people share their own experience. 16 questions, 75 members.
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https://withasideofsaltpotssupport.blogspot.com/
I created "With a Side of Salt" to educate and empower patients along their journey. Educate. Empower. I'm not quite sure what happened to either of those goals over the years. I remember when I first started my blog, I was brainstorming names for my blog and texting the names back and forth with my friend.
https://www.nhs.uk/conditions/postural-tachycardia-syndrome/
Postural tachycardia syndrome (PoTS) is an abnormal increase in heart rate that occurs after sitting up or standing. Some typical symptoms include dizziness and fainting. It's sometimes known as postural orthostatic tachycardia syndrome. PoTS affects a range of people but is most common in girls and women aged 15 to 50.
http://www.dysautonomiainternational.org/page.php?ID=24
We know how valuable it can be for patients and caregivers to connect with others in their own community who are facing similar challenges. That is why we have compiled the following list of volunteer-led local dysautonomia support groups. Please note that Dysautonomia International cannot verify the accuracy of information posted on the groups.
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