Welcome
Our efforts to accelerate cures and help patients get the best care and outcomes possible are in service of the worldwide chordoma community. The support and resources you'll find throughout our entire site are available to individuals in any country. And no matter where you're located, you can contribute to our shared mission.
In addition, because the chordoma diagnosis and treatment journey can vary by country, we offer additional local resources in some countries, including Brazil, Canada, France, Germany, Israel, Italy, Spain, the Netherlands, and the UK. We're grateful to our international Ambassadors, who have helped develop our local resources based on their own experiences as patients and caregivers.
Visualize the worldwide chordoma community
There’s strength in numbers. By making ourselves more visible, those of us affected by chordoma can bring much-needed attention to our situation and the urgency of our shared mission to find cures.
Hover over the map to see how many patients in your country are in our network.
Number of chordoma patients in our network
Use the form below to be accounted for on our map.
Three reasons to join our network and be seen:
- Help others feel less alone
- Draw attention to the needs of chordoma patients in your region
- Encourage companies and researchers to open clinical trials in your area
Be counted!
Our map partners
We're thankful to the following organizations who support our chordoma community map, and who are our partners in serving the worldwide chordoma community.
Our Ambassadors
Our volunteer Ambassadors help chordoma patients and families outside the U.S. connect with local resources — and each other. They also help distribute educational materials to medical centers and identify chordoma-experienced doctors in their countries, ensuring that patients have good local treatment options. We are grateful to be working with such an amazing, committed group of Ambassadors, and we encourage you to connect with an Ambassador in your country.
Ways to help
We know chordoma is a solvable problem. How fast it gets solved depends on the contributions of every one of us affected: whether by donating, hosting a fundraiser, or participating in research. There are lots of opportunities for each of us affected by chordoma to fuel research advances that will dramatically improve treatments and outcomes.
