When you donate your birthday to Dysautonomia International, your support helps fund critical dysautonomia research, clinician education, patient empowerment programs and much more. You can create an easy birthday or anytime fundraiser at: facebook.com/fund/Dysautono…

Congratulations to Kate Bourne, who just defended her PhD based on her outstanding research on #POTS ! Up next… medical school! 👏👏👏

Dysautonomia can cause various symptoms, and some can be new and catch us off guard. What do you do when experiencing a new symptom? #TuesdayTips

Sjogren's is estimated to impact 4M Americans, but 75% remain undiagnosed. If you have #dysautonomia with dry eyes, dry mouth, any form of neuropathy, or any family history of an autoimmune disease, we encourage you to get screened for Sjogren's. #SjogrensAwarenessMonth

#SillySaturday Most people living with #dysautonomia benefit from a high salt diet. But it's important to eat a HEALTHY high salt diet. Here are some tips on nutritious ways to get your salt, and how to calculate your sodium vs salt intake: dysautonomiainternational.org/salt

Join us for the 9th Annual Race to Beat POTS in West Chester, PA on June 2nd, in person or virtually! Details at racetobeatpots.org. Run, walk, wheelchair roll, or come out to show your support, meet other #POTS families and #MakeNoiseForTurquoise !

Duke University researchers are asking people diagnosed with POTS or nOH to complete this brief survey about your experiences with compression garments to help them understand the needs of our patient community.
redcap.duke.edu/redcap/surveys…

#TBT It's #SjogrensAwarenessMonth , a great time to watch these outstanding lectures from Dr. Brent Goodman on the relationship between dysautonomia and Sjogren's and how Sjogren's dysautonomia is treated.

youtu.be/N77sfyQB63A?fe…

youtu.be/qls_KKxsVrg?fe…