Join us.

No experience needed — just a voice.

For patient families

If you or your child lives with a rare disease and you'd like to connect with our community — in the US or Morocco — we'd love to hear from you.

For young advocates

Interested in joining an iCAN KIDS chapter, or curious what it's like to advocate on Capitol Hill? Reach out. No experience needed — just a voice.

For organizations

Project RARE welcomes partnership inquiries from patient organizations, hospitals, researchers, and advocacy groups.

Contact

Reach out anytime

📧 Email: info@projectrare.org

📷 Instagram: @project.rare

📍 Washington, DC

We typically respond within a few days. For partnership inquiries, please include your organization's name and a brief description of your work.