The content on this blog is for informational & educational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare professional with any medical questions regarding diagnosis, new health regimen, or treatment.
When Joe Burrow said football wasn’t fun
anymore, NFL media looked for drama. I heard something different: the quiet grief that comes when your body no longer does what it once could. This post is about chronic illness, grief, resilience, & learning to keep going when your body lets you down.
A quirky, heartfelt look at the little things, big moments, and hilarious chaos that add up to… well, ME.
It all started with an uncoordinated girl, a TV without cable, and a blond quarterback who stole my heart before I even knew what a down was.”
If you’re new to the world of POTS — or if you’ve been living with it and still feel like you’re trying to solve a medical escape room — this post breaks down the basics in plain English. Think of it as your starter guide to a condition that’s anything but simple, written by someone who lives it every single day.
Life with chronic illness is a fourth-quarter comeback every single day — but I’m learning how to move the chains one play at a time.
