POTS In the News
These are wonderful awareness pieces about people just like you. We can learn from each other as we advocate for ourselves and raise awareness about postural orthostatic tachycardia syndrome.
Blogs about Living with POTS
Many people blog as a way to deal with their own lives that have been altered by chronic illness and to raise awareness. Standing Up to POTS does not endorse, nor is it affiliated with any of the blogs listed. We are not responsible for content of individual blogs.
Webinars about Issues Related to POTS, EDS, and Mast Cell Activation Syndrome
Webinars are seminars given to patients or other health practioners at professional conferences that are later posted on the Internet. This is a great way to hear the latest from experts in the field about topics relevant to you and your family.