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Hid and Sick

Crohn's Disease and other invisible challenges
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Knots within my gut, can’t get far enough I decided that I need a place where I can write about my illness without directly bugging the people I know and love. They hear enough out of me, you know? The illness in question is Crohn’s Disease, and besides giving you […]

An introduction

Today I gave myself my once-a-month Stelara shot. And these days, I also think, "Is this the last one?" Every day I ask, "What can I do to help? How can I be most of use?"

Is this the last time?

Assorted IVs with text over top that says "Been alive for five years" and a cartoon of a woman holding her abdomen underneath

Five years ago, my life drastically changed. Five years ago, I almost died. I didn't die. I lived, but I was transformed.

Been Alive for Five Years

There’s been quite a few discoveries and advances in research on IBD lately, with some possibilities for new treatments as well. That’s exciting news! Some of the things that have happened in 2023 – 2024 include positive outcomes with stem cell therapy, an oral medication to treat Crohn’s Disease, and […]

But What Does It MEAN?

My scar has become a symbol of everything that's happened to me. I love it, because it's part of me and those surgeries saved my life. I hate it because it altered my body in ways that I'm struggling to love, and I don't recognize myself because of that. It's the representation of all the things I can't yet do or I've lost because of this illness.

This is me, look at my scars

1 comment

Crohn's Disease plays havoc with one's regular diet. Trying to figure out what to eat can trigger disordered eating patterns.

It’s a complicated relationship

6 comments

Chronic illness changes you, and it's okay to mourn who you were or be angry about what you've lost. One of my biggest struggles is a two pronged one: knowing what I can handle in this new form, and reinforcing to others that I'm not capable of everything that I used to be able to do.

Chronic Illness Changes You

2 comments
White text says "mental health is part of Crohn's Disease" over an image of a shadowed sad person in a tunnel

It's important to talk about mental health struggles, and medical trauma is often ignored in this context. This is my current journey to correct that.

Mental Health is Part of Crohn’s Disease

2 comments
Background pic of leaf close-up showing veins, colored in pink and blue. Text on top says "the opposite of juicy" in white cursive.

Last time I updated, I mentioned that I was due to get a CT scan [properly, a CT Enterography] and that I'd update after that happened with the results. Except things didn't go exactly as planned. They couldn't get an IV going. Keep reading to see how that went, and why.

The opposite of juicy

...I got my official diagnosis, Crohn's Disease. I cried with relief when that happened, because it was an answer, finally, to what had been going on. Not a great answer, but at least an actionable one.

My journey to a diagnosis, part two

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My gut trouble started in my early 20s. Actually, that's not accurate. Looking back with the information I have now, I realize that signs were there much earlier.

My journey to a diagnosis, part one

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About This Site

I’m Christiane Knight: writer, artist, ne’er-do-well, Crohnie.

Let me tell you what life with an invisible, incurable illness is like in words that will give you all the emotions and with poop jokes that will make you cringe. Humor is my antidote to horror, and unflinching honesty is 100% my jam.

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    • Is this the last time?
    • Been Alive for Five Years
    • But What Does It MEAN?
    • This is me, look at my scars
    • It’s a complicated relationship
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  • Medical Fun (2)
  • My Journey (6)
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