Running a 5K With POTS

Running a 5k With POTS

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…

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My Favorite Salty Snacks for POTS

salty snacks for POTS patients

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…

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The October Slide and How to Cope With It

Girl looking out over lake with a rainbow

We’re sliding into October, which means I’m pulling out my favorite cardigans, dusting off my knee-high boots, and buying fall-scented (and flavored!) everything. But when you live with a chronic illness, it can also mean gearing up for a worsening of your symptoms. It’s a phenomenon in the chronic illness…

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8 Ways to Deal With POTS Brain Fog

ways to deal with POTS brain fog

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…

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My Journey With Endometriosis (So Far)

my journey with endometriosis

Today, I have something different that I’d like to talk about because it’s a part of my life with chronic illness and something I’ve been struggling with for years. I want to share my journey with endometriosis. I’ve put it off for a while because talking about this and sharing…

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Moving Out of NYC in a Heatwave

moving in a heatwave with POTS

I’ve said it before, but I’ll say it again: Heat is my number one enemy when it comes to Postural Orthostatic Tachycardia Syndrome. Even when I’m feeling good and not dealing with bad symptoms, all it takes is a little (or a lot, in the case of a few weeks…

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What’s in My Chronic Illness Day Bag?

Chronic illness day bag of essentials

Warmer weather and summer are here, bringing vacations, day trips, and other fun adventures with them. Mike and I are big fans of taking day trips on the weekends. It gives us a chance to explore somewhere new in New York City or within a reasonable traveling distance outside of…

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Traveling With POTS: Acadia National Park

Traveling with POTS to Acadia National Park

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…

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I Got Engaged and Then I Got COVID

Hi, friends! What exciting and terrible news I have to share in today’s blog! I don’t typically post much about my personal life, but when major life news and things that affect my health happen, I open up to share with you all. As this blog’s title alludes to, I’ve…

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How I’m Doing 3 Years After My POTS Diagnosis

pots diagnosis reflection

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…

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