All things about living with POTS
In my four years of having a POTS diagnosis, I’ve learned (sometimes the hard way!) what can make my POTS worse. Knowing these POTS triggers, like the summer heat, dehydration, and my menstrual cycle, has helped me adapt to a lifestyle where I’m prepared for these triggers or avoid them…
Hi, friends! I have POTS diet tips woven throughout different blog posts, but I don’t have one post dedicated to compiling all these diet tips in one neat and tidy place. Plus, I’m really interested in nutrition and how what you eat can fuel and nourish your body. So I…
Hey there! You’ve probably landed on this page because you know someone with POTS and you need awesome gift ideas. Or, maybe you have POTS and you want to put some new items on your wish list for friends and family. Whatever the case may be, you’ve come to the…
Hello, friends! I’m very excited to share today’s post. For the past month, I’ve been training for running a 5k with POTS! This is huge for me because I haven’t run a 5k race—or any races at all—since before I got my POTS diagnosis. It took so much work and…
Many people with Postural Orthostatic Tachycardia Syndrome, or POTS, need to eat a high-salt diet. The good news is that there are a lot of foods out there packed with sodium to help us get the salt we need. But not all the options are the healthiest, and if you…
When I was in grad school a few years ago, my POTS brain fog was at its worst. Before I had POTS, I never dealt with brain fog, but once I started experiencing it, it was really distressing. Whereas I usually felt like a mentally sharp, well-spoken person, I suddenly…
This week, I returned to New York City after a weeklong trip with my sister to Acadia National Park in Maine. And I can’t say enough how much of an amazing trip this was! My sister and I had always talked about going on a cross-country trip together, and while…
April is a memorable month for me. And not just because I love spring and fresh flower blossoms and a world thawing from winter. The month also marks an important anniversary for me. Can you guess it from this post’s title? It’s when I received my POTS diagnosis and put…
It’s been almost three years since I was diagnosed with POTS. Sometimes, I need to do things differently than the way I used to before my life with POTS. And you know what? That’s OK. The biggest thing I’ve learned since my diagnosis is that I needed to become a…
If you put the words “running” and “POTS” together, it looks and sounds a bit contradictory. They are two words that don’t seem to go together, given what POTS is and the taxing nature of running. But running with POTS, at least in my experience, doesn’t have to be impossible…