The rare disease OS

You are not alone.

Rareix is the home for rare disease patients, caregivers, and communities. Find your people, find the right trial, find a specialist who gets it, free, forever.

A connected community

300M

people live with a rare disease

7,000+

distinct rare diseases

5-7 yrs

average time to diagnosis

Start here

Everything a rare disease patient needs, in one place.

Communities

Built for rare, one community at a time.

We go deep before we go wide. Each community gets a focused, modern home, starting with two where the need is sharpest.

Featured community

Featured community

Ehlers-Danlos Syndrome

The Ehlers-Danlos community is large, digitally native, and deeply underserved. Patients spend years being told their symptoms are anxiety, growing pains, or in their head, long before anyone connects the dots.

~1 in 500

live with hEDS / HSD

10-22 yrs

average time to diagnosis

10+

wrong diagnoses, on average

The platform

More than a website, a rare disease operating system.

Live now

Disease communities

A modern, focused home for each condition, not a forgotten subreddit or a decade-old forum.

Live now

Clinical trial matching

Every study on ClinicalTrials.gov, matched to your condition and explained in plain English.

Live now

Specialist directory

Find rare-disease-aware doctors and centres, so you stop starting from scratch.

In build with the community

Symptom & treatment journalAI navigation assistantInsurance denial toolkitPeer matching
Help shape what's next

Our belief

Rare as identity, not illness.

300 million people, each condition rare, together the size of a nation, and no modern home built for them. We're building it, patient-first, and we're never selling that trust.

Founding members

Be one of the first 500.

Founding members get early access, a founding badge, and a genuine say in what we build next. We build Rareix with the community, not at it.

We will never sell your data. Read our plain-English data charter.