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Hi Reader, For a long time, I thought pacing meant cutting back. Doing less. Cancelling more. Shrinking my life until it fit inside my energy. And honestly? That framing made me resist it. What I eventually realized is that pacing with chronic illness isn’t about restriction. It’s about structure. It’s about protecting your baseline so you’re not constantly recovering from energy crashes. That shift changed everything for me. Because once pacing became foundational instead of reactive, my days stopped swinging so wildly between “I can do everything” and “I can barely function.” In this week’s post, I’m breaking down what pacing with chronic illness actually protects, why good days can be the trickiest to manage, and how to build routines that flex with fluctuating energy instead of fighting it. If you’re tired of the boom-and-bust cycle, I wrote this for you. You can read it here: Pacing With Chronic Illness – The Fundamentals That Make Everything Else Work​ |
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Hi Reader, Have you ever had a day where nothing on your list looked that hard — and you still couldn't get through it? That's what this week's post is about. Not the flare day, not the obvious crash. The day that just feels heavier than it should, and you can't quite point to why. I've been sitting with this one lately. There's something in my own life I'm not ready to name specifically, but it's been quietly occupying space in the background of every day. And what I keep noticing is how...
Hey there Reader, If you've ever hit a wall trying to decide something completely ordinary — what to eat, whether to rest, how to sequence your afternoon — and felt genuinely depleted by it, this week's post is for you. Decision fatigue is a real and researched phenomenon. But most of what's been written about it was designed for people whose decision-making day starts fresh. Ours doesn't. By the time we get to the "normal" decisions of the day, we've already run through a full round of...
Hey Reader, This week's post started with a question I've been sitting with for a while: why does managing a chronic illness feel like a full-time job even on days when nothing happens? The answer, it turns out, is that something is always happening. It's just invisible. Tracking symptoms. Researching. Translating what your body is doing into language that will be taken seriously in a twelve-minute appointment. Holding a hundred administrative details that no one else is holding. This is real...