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​ The days after the holidays can feel strangely unmoored. Not quite rest. Not quite routine. Just that in-between space where your body is tired, your rhythm is off, and everything that used to feel automatic suddenly takes effort. If you’ve been feeling that lately, you’re not behind. You’re recalibrating. I wrote a new post this week about what it actually looks like to rebuild daily rhythm after the holidays when you live with chronic illness. Not the “get back on track” version. Not the color-coded schedule version. The gentler, more honest version that starts with where your energy really is right now. In it, I talk about why jumping straight back into routines often backfires, how rhythm can be more supportive than rigid structure, and what it means to build your days around stability instead of pressure. It’s less about doing more and more about creating anchors you can return to, even on low-energy days. If routines have felt fragile, or if you’ve been quietly wondering whether you’re doing something wrong because things still feel off, this post is for you. It’s meant to feel grounding, not demanding. Something you can read slowly, or skim, or come back to when you have the capacity. You can read the full post here: 👉 How to Gently Rebuild Your Daily Rhythm After the Holidays When You Have a Chronic Illness​ However you move through this season, I’m really glad you’re here. Warmly,
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đź’ŞI create resources to help people adapt to living with chronic illness so they can thrive.
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...
Hi Reader, When I was first diagnosed, I thought the hardest part would be the symptoms. I was wrong. The symptoms were real, yes. Disorienting. Limiting. Sometimes scary. But what caught me off guard was everything around them. The silence. The well-meaning comments. The identity shift. The subtle pressure to “handle it well.” I originally wrote a version of this post in 2024. I recently went back and fully updated it to reflect what I understand now — with more clarity, more depth, and more...
Hi Reader, There’s a belief I hear over and over again in the chronic illness community. “I’m just bad at boundaries.” It sounds self-aware. Responsible. Honest. But it’s usually carrying something heavier underneath. When you’re living with chronic illness, unpredictable energy, and fluctuating symptoms, boundaries that protect energy aren’t a personality trait. They aren’t about being confident enough or assertive enough. They’re about adapting to reality. In this week’s post, I’m breaking...