Understanding POTS
What's POTS?
POTS stands for Postural Orthostatic Tachycardia Syndrome, and if you've never heard of it, you're not alone. It's a dysfunction of the autonomic nervous system, which is the part of your body that regulates things you never have to think about, like your heart rate and blood pressure. For people with POTS, something as simple as standing up causes the heart rate to spike abnormally, and that triggers a whole chain reaction. Dizziness, extreme fatigue, brain fog, and feeling like your body is working against you every single day.
Getting diagnosed requires a tilt table test where your heart rate and blood pressure are monitored as you move from lying down to standing upright. It sounds straightforward but for most of us the road to that test was anything but.
What makes POTS especially tricky is that it often develops after a major event, a pregnancy, surgery, trauma, or a viral illness. An estimated one to three million people in the US are living with it, and yet so many go years without answers, feeling dismissed, confused, and honestly just exhausted from trying to explain something that most people have never even heard of.

Navigating Life with POTS
While there isn't a cure for POTS, a combination of medications and lifestyle adjustments can significantly help in managing its symptoms and enhancing the overall quality of life. Sharing my personal experiences with POTS is a way to connect with others who might be facing similar challenges. I hope that by understanding the realities of this condition and the strategies I've employed, you can find inspiration and practical advice to keep moving forward, even when things feel overwhelmingly difficult.
Useful Information and Advice
When I was first navigating POTS I felt completely alone. Nobody really talks about it, and finding information that actually made sense was exhausting. I spent so much time digging through random corners of the internet just trying to understand what was happening in my own body. It was a lot.
What I want you to know is that reliable information exists, you just have to know where to look. And that's honestly part of why I'm here. POTS research is still evolving and new studies are coming out all the time, so staying on top of it matters. I'm not a doctor, not even close, but I am someone who has been living this for a long time and has done a whole lot of homework along the way.
Below are some of the resources I actually trust and go back to. Bookmark them, share them, send them to the person in your life who still doesn't quite get what you're going through.
Some Helpful Resources:
https://www.ninds.nih.gov/health-information/disorders/postural-tachycardia-syndrome-pots
https://www.dysautonomiainternational.org/page.php?ID=30
*Always seek your primary doctor/specialist*