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Let’s Go There: From Ostomy Surgery to the Rugby World Cup

October 1, 2025

Cass Bargell

Credit: Dante K Photography  My Ostomy Journey My name is Cass Bargell, and I have many different identities that I’m proud of. I’m an analyst on the Data Science & Analytics team at the Crohn’s & Colitis Foundation, a USA Rugby National Team player, and an IBD pati...

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Cass Bargell - ostomate and professional rugby player with ulcerative colitis

Five Tips to Navigate Life with a Chronic Illness like IBD

July 5, 2023

Rachel Peifer

Dewey Thom running during a Team Challenge Event    When Dewey Thom was a teenager in the 1970s, he started experiencing stomach pains, which led to a series of invasive tests over a period of many months. Finally, his gastroenterologist told him he had ulcerative colitis...

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Dewey Thom Great Highway

Volunteer to Make IBD Visible

December 6, 2022

One of the best ways to Make IBD Visible is to join the fight to find cures for Crohn’s disease and ulcerative colitis and improve the lives of people living with IBD. As a volunteer-fueled organization, the Crohn’s & Colitis Foundation relies on the passion and dedication of our vo...

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My Crohn's Journey

December 3, 2022

Jordan Leftwich

Hey! My name is Jordan Leftwich. I’m 17 years old and I’m a professional international model and actress. Although, one main thing that makes me different is that I have Crohn’s disease. I’ve probably been living with Crohn’s disease my entire life but I was only diagnosed around 2018, ...

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A voice of support for veterans with IBD

November 11, 2022

Trei McMullen

Army veteran and security subject matter expert Trei McMullen was finally diagnosed with ulcerative colitis when he was 26 years old, after struggling with symptoms since he was 18. Today, McMullen has joined the Crohn’s & Colitis Foundation’s Business Advisory Council and wants to ...

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What it's like to be LGBTQ+ with IBD

June 15, 2021

Joseph Cobucci

Every June during Pride, I'm reminded of how fortunate that I am. I can live in a country where I'm free to be myself and share my life openly with my husband of 20 years. I know that we can thrive because our life consists of lots of love and support. Support from the many facets of ou...

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What it’s like to live with IBD around the world

May 18, 2021

Michael Osso

More than 10 million people worldwide live with Crohn’s disease or ulcerative colitis. Living with these diseases is very individual and no patient experiences the same symptoms or manifestations of disease. But what bonds everyone — regardless of whether they live in the United States,...

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Giving thanks and appreciating the small things

November 18, 2020

Rachel Stackiewicz

During the chaotic times that we are living in, it is more important than ever to reflect on the things we are appreciative of. It can be easy to forget to be thankful for the things we find normal in our everyday lives, such as our families, our homes, our education, our jobs, and more...

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Learning to advocate for myself as an IBD patient

October 9, 2020

Making hard decisions and advocating for what is best for me is all part of being an IBD patient. Growing up, I was knocked down by this disease countless times and had to advocate for second opinions or treatment plans that would improve my quality of life and help me achieve remission...

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IBD: My reason to ride

July 31, 2020

Before I was diagnosed with IBD, my life was fueled by a simple reason: I woke up, got on my bicycle, and trained each day to win bike races. I worked hard and made sacrifices to become the best professional athlete I could be. It all seemed straight forward, really. But things suddenly...

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