In Living COGI 2025

Many of you know that I have been living with Ulcerative Colitis, a form of Inflammatory Bowel Disease, for over 20 years. You also know that I’m a strong advocate for better treatments and — most importantly — a cure.

As an Ambassador for COGI (The Color of GI Illnesses), I’m committed to helping eliminate the disparities that Black and Brown people face when navigating this disease.

Here’s why this work matters:

• Black IBD patients are diagnosed on average 2 years later than other patients — often after the disease has already progressed.

• Many Black and Brown patients report not being believed about their symptoms or pain.

• Studies show that some medical students and clinicians still hold the false belief that Black people have a higher pain tolerance — a myth that directly impacts the quality of care.

• Delayed diagnosis means delayed treatment, which can lead to more severe disease, more complications, and fewer treatment options.

This isn’t just a healthcare issue — it’s a social justice issue. And it’s exactly why COGI exists.

COGI is working every day to bring awareness, education, advocacy, and community to people of color living with Crohn’s, Ulcerative Colitis, and other GI conditions. We’re fighting for earlier diagnosis, better care, and equity across the board.

COGI support programs were created to provide patients with the tools they need to navigate their diagnosis, amplify their voices, and remind them that they are truly seen and valued. These programs have reached over 500 patients and counting, offering critical support that fosters community, understanding, and empowerment. 

Your donations will enable us to expand these essential services, including mental health resources and support groups, which play a vital role in the overall well-being of patients.