I live with Crohn’s
Put yourself at the center without having to explain everything.
Start this role →TeamCrohns helps people living with Crohn’s and the people they choose to stand beside them turn support into clear, respectful action.
Choose your position
The person living with Crohn’s stays at the center. Everyone else learns how to offer support without taking control, demanding details, or pretending to be a medical expert.
Put yourself at the center without having to explain everything.
Start this role →Stay close without turning love into control or constant problem-solving.
Start this role →Believe what you are told, protect privacy, and make help specific.
Start this role →Keep showing up when plans change and the right words are hard to find.
Start this role →Create practical flexibility without demanding a diagnosis story.
Start this role →Use your voice, time, or platform without speaking over people with Crohn’s.
Start this role →Do one useful thing
Start with one practical action. Ask first. Complete what was agreed. Do not demand an update, explanation, or public acknowledgment.
Tell one trusted person whether you want listening, practical help, quiet company, or space. No medical explanation is required.
Use one question: “Do you want me to listen, help with something, give space, or help contact a professional?”
Respond to a changed plan or difficult day without cross-examination, comparison, or a demand to prove how bad it is.
Try: “Thinking of you. No update or reply needed. I’m here.” Then let the message stand.
Ask about access, scheduling, communication, or workload in a private setting—not in front of coworkers or classmates.
Direct someone to NIDDK or the Crohn’s & Colitis Foundation instead of reposting a treatment claim without context.
Current community action
Ask someone what would be useful. Complete one agreed action. Do not demand an update, explanation, or public thank-you.
Specific, private, and easy to decline.
No improvising with medical advice.
No proof, praise, update, or post required.
Story standard
TeamCrohns will publish support-in-action stories only after contributor review, image-rights confirmation, and written publication approval. The launch roster will not be faked to make the site look populated.
The Team Code
Support begins with permission. The person living with Crohn’s decides what is useful, what is private, and when the answer is no.
Nobody needs a diagnosis history, medication list, symptom log, or surgery details in order to be a respectful supporter.
Team members do not interpret symptoms, rank treatments, or tell someone to start, stop, or change medical care.
Food, medication, weight, appearance, disability, surgery, ostomies, work capacity, and canceled plans are not material for public judgment.
No product, diet, mindset, supplement, routine, or individual is presented as a cure or guaranteed path.
A story is not content inventory. Publication requires consent, contributor review, image rights, and a correction or withdrawal path.
One network. Different jobs.
Michael’s complete lived-experience story, Crohn’s education, and broader mission.
Daily-life operating layerWork, school, travel, relationships, setbacks, movement, confidence, and rebuilding.
Care-preparation deskAppointment, care-team message, medication-list, and after-visit organization.

From Michael
Michael built TeamCrohns from lived experience with Crohn’s—not medical authority. The goal is direct: help good people replace uncertainty with one respectful action.