Crohn’s is more than just a stomach disease. It’s a mental battle, too.

For years, I thought I was just stressed. But then I realized—living with a chronic illness comes with a constant undercurrent of anxiety and depression.

💭 Anxiety:
✔ Worrying about when the next flare will hit.
✔ Scanning for bathrooms everywhere I go.
✔ Wondering if people think I’m lazy for needing to rest.

💭 Depression:
✔ Mourning the life I had before Crohn’s.
✔ Feeling isolated because no one truly gets it.
✔ The exhaustion of fighting a never-ending battle.

Some days, my mental health struggles more than my stomach. But here’s what helps:

Therapy – Talking to someone who understands chronic illness grief is life-changing.
Self-compassion – I remind myself I’m doing the best I can with what I have.
Support system – Whether it’s online friends or family who truly care, I lean on them.

Crohn’s isn’t just physical. It takes a toll on your mind, too. And that’s why it’s okay to ask for help.

Stay Strong.

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I’m Kelly

Welcome to My Crohnstipated Life, a space where I share the raw, real, and often humorous journey of living with Crohn’s disease. From unpredictable flares to parenting while managing a chronic illness, this blog is a mix of personal stories, practical tips, and a whole lot of laughter—because sometimes, humor is the best medicine. Whether you’re living with Crohn’s, love someone who is, or just want a peek into the rollercoaster of chronic illness, I’m glad you’re here. 💜 Stay Strong.

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