Connect
The Chordoma Foundation and many chordoma survivors are here to support you throughout your entire journey with chordoma, from diagnosis through to survivorship.
Join us in Boston on July 14-15 for a memorable event packed with opportunities to learn from experts and connect with other chordoma patients and family members!
We're committed to helping patients and caregivers every step of the way with our personalized Patient Navigation Service, an uplifting online community, Peer Guides, international Ambassadors, and a range of educational and support events.
Our Patient Navigators have extensive knowledge about chordoma and its treatment and are available at every step of your chordoma journey to answer your questions, provide information about treatment guidelines, help you find qualified doctors, and connect you with others in the chordoma community.
Chordoma Connections is our private, online community where chordoma patients and their loved ones can come together to share experiences, ask questions, and support one another.
If you’re interested in talking to someone who has been through a similar chordoma journey, our Peer Connect program can help.
In our support groups, you can come together with other people affected by chordoma to support and learn from one another, make new connections, and exchange information.
Our international volunteer Ambassadors help chordoma patients and their families outside the U.S. connect with local resources — and each other.
Our Uncommon Story series offers the opportunity to read what others have learned during their journeys with chordoma so that you can know what you might expect throughout your own. And when you're ready, you can share your own experience with the community!