All things about living with POTS
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…
Not too long ago, I shared a post about the POTS and vagus nerve connection. I’ve been fascinated with this connection and what I learned from the two books I read on the topic. I’ve been especially intrigued by how to stimulate the vagus nerve. But if you haven’t read…
If you feel fatigue after exercise, you’re not alone. In the POTS world, patients can often feel worse after exercise, especially in the early months of an exercise program. Extreme fatigue after exercise is also very common in Chronic Fatigue Syndrome (ME/CFS). Until I reached a certain fitness level, I…
Did you know that there’s a nerve in the human body that’s connected to POTS? It’s called the vagus nerve. Maybe you’ve heard of it before. The vagus nerve actually regulates many important functions in the body—so many, that it’ll probably surprise you just how much this not-so-little nerve is…
Hi, friends! Guess what? You don’t need to sacrifice traveling with a chronic illness like POTS. While traveling may trigger symptoms, I have POTS travel tips that you can try for reducing symptoms and traveling safely and comfortably. For example, you should pack a bag of essentials with everything you…
It’s hot, hot, HOT in NYC! Is it just me, or does this summer seem to be one heatwave after the next? All these ninety-degree days have been putting my methods of controlling my POTS symptoms to the test. If you’re wondering how to survive the heat with POTS, then…
In the last few months, I’ve received a lot of messages and comments from people who developed POTS after having COVID-19. With that being said, I wanted to drop a special post dedicated to these people. Disclaimer: I am not a doctor or medical professional. Everything I share on this…
Ever stand up too fast and feel like a blackout or fainting episode is imminent? As someone with POTS, I get this all the time. Although, I consider myself lucky that I don’t faint (usually!). But for others with POTS, vasovagal syncope, or other forms of orthostatic intolerance, fainting happens…