I’ve lived with Ulcerative Colitis for 25+ years.
Not quietly. Not gracefully. But honestly.
This space is for the real ones, those fighting UC and invisible illness with grit, fear, humor, and hope.
Let’s build something real.
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#UlcerativeColitis#IBD
I was diagnosed with #UlcerativeColitis when I was 15. After 25 years, I've decided to tell my story, and try my best to help people along the way. Our latest newsletter issue has posted. Sign up today. It's Free.
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Anemia is one of the most common (and overlooked) complications in IBD!
Low Hgb? It’s not “just anemia” — it’s a clue to investigate & intervene.
Submit 🗳️ below & 👀 for anemia in IBD #back2basics 🧵this Monday
Some days you feel like a walking flare. Other days you almost forget you have IBD. Both are real. Both are valid. You do not owe anyone consistency. #IBD#Crohns#UlcerativeColitis#FlareAndFortitude
Crohn’s advice people trust isn’t from experts. It’s from patients. Real stories. No filters. Just truth. Read why that matters https://t.co/4zosCAkFD4 #Crohns#PatientVoices#HealthTrust
@CrohnsDiseaseUK The most trusted voices in Crohn’s care are the ones living it every day. Lived experience builds trust faster than titles ever could. Keep elevating patient truth. #Crohns#PatientVoices#FlareAndFortitude
If you’re already missing #DDW2025, then get a head start on planning for #DDW2026! Mark your calendars now for May 2-5, 2026, in Chicago, IL!
We can’t wait to see our #AGAGastroSquad there in-person or online – start planning by visiting https://t.co/CzUitdxI12.
@NTforIBD This is so real. Chronic illness can shrink your world fast. But with the right support, boundaries, and honesty, connection is still possible. We’ve lived it. #IBD#ChronicIllnessLife#FlareAndFortitude
Flare and Fortitude is not about perfection. It is about showing up anyway. Raw, real, and relentless. We are just getting started. #UlcerativeColitis#IBD