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It's Dysautonomia Awareness Month! Share our "What is POTS?" video below on your social media channels with the hashtag #31DaysofDys to raise awareness! bit.ly/whatispots

Dysautonomia impacts over 70M people worldwide. People living with dysautonomia often look healthy, despite many experiencing debilitating symptoms. Help us make dysautonomia more visible by donating at dysautonomiainternational.org/donate and share this post for #DysautonomiaAwarenessMonth!

The reason you never feel “good enough” is because you’re looking for validation from people who don’t understand YOU or what YOU want and they probably don’t even understand themselves. The only place you should look for validation is in the mirror.

Day early- but happy 5TH birthday to my nephew cam! Aunt Maddie loves you so much! Whether you want to be a power ranger, ninja kid, or NFL player when you grow up I will support you every step! ❤️

So much heartbreak in my life lately- so glad I get to escape for a week and clear my mind. ❤️💔

Not ready to leave California 😢 red eye flight- please allow me sleep ❤️

(In)patiently waiting for my doctors to allow me to return back to work and see the outside world. Also, I’m hoping when I recover, my POTS flare goes back with it. I didn’t get 3 years into this illness for Covid to take me back to square one 😭

Chronic illness probs 🤣

When you see the nurses rolling in the EKG machine you know they’re prepping your room 🤣🤣🤦🏼‍♀️

Honored to have been recognized by my company today for what I do everyday! So glad I found this company. ❤️ I’ve had so many opportunities in the 1 1/2 yrs I’ve been here and can’t wait to see what’s in store for my future.

Climbing up my career ladder 🪜 🙏🏻 grateful to be given these opportunities. I have gained so much knowledge this past year and a half and am ready to shine in my new role. ❤️

Had my bi-annual echocardiogram today after seeing my cardiologist. I had someone ask me if the testing will ever end- the short answer is no. Having heart disease and chronic illness never means no breaks! Plus being a Covid long hauler 🤦🏼‍♀️

#Dysconf2022 Dr. Blitshteyn S Blitshteyn MD, FAAN, FANA, Dysautonomia Clinic's message on #POTS, shared during #DysConf2022 today. Stop psychologizing these patients and learn to properly diagnose and treat POTS, an autonomic nervous system disorder. #MedTwitter

.Sen. Kirsten Gillibrand Please include $10M for #POTS research in NIH's FY2023 funding. Millions of Americans like me are suffering from this devastating illness with no FDA approved treatments. Connect with @dysautonomia for details.

POTS is a complicated and potentially debilitating chronic illness. Help us to raise awareness by liking and sharing! standinguptopots.org #POTS #dysautonomia #spoonie