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Continue reading →: What I Wish Healthy People Knew About Life with Crohn’s
If I could sit down with every healthy person in my life, here’s what I’d want them to know: 💜 I don’t “choose” to be flaky. I cancel plans because my body makes the decisions—not me. 💜 I don’t look sick, but I feel sick. Just because I’m not in…
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Continue reading →: The Anxiety of Leaving the House with Crohn’s
Every time I leave the house, I go through the checklist: ✔ Bathroom locations mapped out – Because I can’t afford surprises.✔ Emergency bag packed – Meds, wipes, extra clothes—just in case.✔ Exit strategy planned – Because Crohn’s doesn’t wait until I’m ready. And yet, even with all the planning,…
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Continue reading →: The Reality of Parenting with Crohn’s (And Why I’m Not a “Bad Mom”)
Some days, I have the energy to be the fun mom—the one who plays, bakes cookies, and builds forts in the living room. Other days, Crohn’s wins. 💔 I have to say “not today” when my kids ask me to play outside.💔 I rely on easy meals when I wish…
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Continue reading →: Why I Stopped Apologizing for My Crohn’s
For years, I felt like I had to apologize for my illness. 💭 “Sorry for canceling again.”💭 “Sorry I need to rest.”💭 “Sorry for asking if there’s a bathroom nearby.” But one day, I stopped. Because I realized—I didn’t choose this. ✔ I don’t owe anyone an apology for taking…
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Continue reading →: The Emotional Toll of Living with an “Invisible Illness”
If I had a dollar for every time someone said, “But you don’t look sick,” I’d be able to afford all my Crohn’s meds out of pocket. Living with an invisible illness is exhausting—not just physically, but emotionally. 💔 People assume I’m fine because I “look okay.” Just because I’m…
