IBD Warriors Support and Awareness

28/08/2026

What People With IBD and Chronic Illness Wish You Knew 💜
Sometimes it’s not that we don’t want to make plans, or that we’re unreliable.
It’s that our bodies can change minute by minute.
One minute we’re feeling okay and looking forward to something. The next, we could be dealing with excruciating pain, overwhelming fatigue, or symptoms that make leaving the house impossible.
We can’t always predict when a flare or bad day will happen — and that can make making and keeping plans incredibly difficult.
Please remember, we’re not cancelling because we don’t care. Sometimes our bodies simply don’t give us a choice. 💜
Thank you, LeAnna, for sharing this important reminder with us. 💜

28/08/2026

Sending love to all of our beautiful Warriors 💜

28/08/2026

💜 A Little Thank You From Me to You 💜
Facebook hasn’t been showing me my list of Top Contributors / which means I haven’t been able to personally thank and recognise the people who regularly support this page.
So I wanted to take a moment to say this instead…
I see you. I appreciate you. I am so incredibly grateful for you. 🥹💜
Whether you comment, share a post, react to something, send a message, tell someone about this page, or simply quietly follow along — you are all a part of IBD Warriors Support and Awareness
This page and our group has always been about one thing: making sure no one facing IBD feels alone. 🫶🏻
Every single person who chooses to be part of this community helps make that possible.
Thank you for trusting this page.
Thank you for sharing your stories.
Thank you for supporting one another.
Thank you for being here. 💜🩵
To everyone who follows my Instagram too — thank you from the bottom of my heart. 💜
If you haven’t followed us there yet, I’ll leave the link below. 👇🏻( in the comments)
You are not just a follower. You are part of our IBD Warriors family. 💜

28/08/2026

💜 What I Wish More People Knew About IBD part 3

Sometimes the things people with IBD wish others understood aren’t the things you expect.

It’s the appointments.
The uncertainty.
The things we lose.
The invisible battles.
And even the strange reality of having a good day and still having IBD.

For this series, real people living with IBD have shared their own words and experiences — the things they wish more people truly understood.

These aren’t just quotes. They’re real lives. Real experiences. Real voices. 💜

Take a moment to listen. You might understand IBD a little differently because of them.

27/08/2026

💜 What I Wish More People Knew About IBD ( part 2 )

Behind every diagnosis is a person with a story, experiences, losses, challenges and strength that others may never see.
For this series, real people living with IBD have shared something they wish more people understood.
These are their words.
Their experiences.
Their truths. 💜
Because sometimes, the best way to understand IBD is simply to listen to those living it.
Swipe through, take a moment, and hear what they wish the world knew. 💜


💜 What I Wish More People Knew About IBD ( part 2 )

Behind every diagnosis is a person with a story, experiences, losses, challenges and strength that others may never see.
For this series, real people living with IBD have shared something they wish more people understood.
These are their words.
Their experiences.
Their truths. 💜
Because sometimes, the best way to understand IBD is simply to listen to those living it.
Swipe through, take a moment, and hear what they wish the world knew. 💜

26/08/2026

Shared with love to all our beautiful Warriors from Crohn's and Colitis Awareness

Today, we want to remind people that Crohn's and Colitis do not look the same for everyone.

Two people can have the same diagnosis and live completely different experiences.

One person's struggles may be visible. Another person's may be hidden.

Neither experience is less real. Neither person is "more sick" because their journey looks different.

26/08/2026

What people with IBD wish others knew ibdwarriors_support&awareness edition 😉 apologies for the deleted post earlier. Your voice matters . This is part one in our series .

25/08/2026

💜 Your voice matters.
What’s something you wish the world understood about living with IBD?
👇 Tell us in the comments — you might help someone feel a little less alone .
👇 Your voice could help raise awareness.