Crohn’s Fighters shares lived experience and trusted resources. It does not diagnose, prescribe, or replace your care team. Read the boundary · Urgent emergency help ↗

Lived experience + trusted Crohn’s resources

THE DISEASE IS REAL.
SO IS THE FIGHT IN YOU.

Crohn’s Fighters is a lived-experience and resource platform for people navigating Crohn’s disease, IBD, treatment, surgery, pain, fatigue, uncertainty, and life beyond the diagnosis.

Personal experience. Trusted sources. No miracle claims.

Michael “Mike J.” Jannicelli, founder of Crohn’s Fighters.
FOUNDED FROM LIVED EXPERIENCE.Not a white coat. Not a miracle pitch. A real person building the resource he wished existed.
Source-ledAuthoritative organizations linked directly
Honest boundariesNo diagnosis, dosing, or individualized treatment
Human firstThe person is always larger than the disease

Start where you are

YOU DO NOT NEED THE WHOLE ROADMAP TODAY.

You need the next right place to start. Pick the path that best matches what you are dealing with now.

01

NEWLY DIAGNOSED

Get the basics, organize questions, and find trusted sources.

Start here
02

IN A FLARE OR STRUGGLING

Use an organization checklist for your next care-team conversation.

Get organized
03

EVALUATING TREATMENT

Build better questions without asking a website to choose care.

Prepare questions
04

FACING SURGERY

Gather questions and trusted external resources.

Find resources
05

LIVING WITH CROHN’S

Work, fatigue, travel, relationships, identity, and everyday life.

Live beyond diagnosis
06

SUPPORTING SOMEONE

Help without controlling. Listen, learn, and protect your capacity.

Support someone
Mike Jannicelli outdoors.

From Mike J.

I KNOW WHAT IT FEELS LIKE WHEN THE DISEASE STARTS TAKING OVER THE STORY.

“I cannot tell you which treatment is right for you.”

I can tell you that you deserve clear information, a healthcare team that listens, people who understand, and a life that is not reduced to your worst day.

Read Mike’s full story →

Understand Crohn’s

CLEAR INFORMATION WITHOUT PRETENDING THE DISEASE IS SIMPLE.

Start with source-based context, then go directly to government and major nonprofit resources. Higher-risk clinical pages stay blocked until real review is documented.

SOURCE-BASED

WHAT CROHN’S IS

A chronic inflammatory bowel disease that can affect different parts of the digestive tract.

Read the overview
SOURCE-BASED

CROHN’S VS. COLITIS

Two forms of IBD with important differences in location and inflammation pattern.

Read the overview
SOURCE-BASED

HOW DIAGNOSIS WORKS

History, examination, laboratory tests, endoscopy, and imaging may all play a role.

Read the overview
SOURCE-BASED

TREATMENT OVERVIEW

There is no single treatment path for every person. Care decisions belong with your team.

Read the overview

EDITORIAL STATUS

Source-based patient education. Not medically reviewed. Sources checked July 31, 2026. See how evidence and experience stay separate.

Between appointments

THE MEDICAL FACTS MATTER. SO DO THE THINGS BETWEEN APPOINTMENTS.

Lived-experience guidance — not medical advice
01

Write questions down.

02

Bring one medication list.

03

Ask what happens if the plan fails.

04

Keep copies of labs and imaging.

05

Describe symptoms without shame.

06

Surgery is not personal failure.

07

Fatigue is not laziness.

08

You may ask for another opinion.

Resource center

TRUSTED PLACES TO GO WHEN YOU NEED MORE THAN A SEARCH RESULT.

No affiliate tracking. Direct links to government, regulators, major disease organizations, and official registries.

02

CROHN’S & COLITIS FOUNDATION

Patient education, support groups, and navigation.

Explore resources
03

FDA + CLINICALTRIALS.GOV

Official medication and clinical-study information.

Explore resources

Living with Crohn’s

THE DISEASE AFFECTS MORE THAN THE GUT.

Work. Fatigue. Pain. Food uncertainty. Travel. Bathrooms. Relationships. Insurance. Body image. Purpose.

Explore everyday life →

Fighter stories

NO TWO STORIES ARE THE SAME. NONE SHOULD BE USED AS A PRESCRIPTION.

No invented patients, no instant publishing, no borrowed faces. Every future story requires consent, privacy choices, and moderation.

STORY PUBLISHING IS NOT OPEN YET.

The workflow is built. Real consent comes first.

See the story standard

The Fighter Code

FIGHTING DOES NOT MEAN PRETENDING YOU ARE NEVER TIRED.

Crohn’s Fighters heritage badge
01

Tell the truth about what is happening.

02

Ask better questions.

03

Keep your records.

04

Protect your mental health.

05

Let people help.

06

Do not confuse internet confidence with medical evidence.

07

Respect that another path may be different.

08

Build a life larger than the diagnosis.

09

Keep going when you can.

10

Rest when you need to.

Join the Fighters List

USEFUL UPDATES. NO PANIC. NO MIRACLE CLAIMS. NO FILLER.

The form is ready but will collect nothing until a real secure endpoint and privacy workflow are connected and tested.

Not yet connected — no information is being collected

Your diagnosis is not your identity

YOU ARE NOT YOUR DIAGNOSIS. YOU ARE STILL HERE.