Raremark

What we’re doing

We’re crowdsourcing and organizing the wisdom of experts: patients, parents, and caregivers who deeply understand what it’s like to live with a rare disease every day.

We believe free access to information is key to helping everyone better understand, manage, and talk about the rare condition that’s part of their life.

And that’s what our vision is all about: shaping a future where all rare conditions are understood and treated.