WE ARE HERE TO HELP
If you or someone you care about is dealing with chordoma, our Patient Navigation Service can answer your questions, explain treatment options, help you find qualified doctors, and more.
Leading the search for a cure
We proactively and strategically initiate, manage, and fund research across the globe to accelerate the development of effective treatments and ultimately a cure for chordoma.
What you should know
Chordoma Foundation Updates
Uncommon Awards presented for remarkable contributions
Chordoma Foundation Biobank Collaborates with Children’s Hospital of Philadelphia
Chordoma Connections takes off, fueled by Lee-Straus Family Fund for Patient Empowerment
Debra Jarvis to keynote International Chordoma Community Conference
Learn from Experts
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What are the most important things a chordoma patient should know?
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What should chordoma patients look for in a treatment team?
Featured champion
Smith Anderson team
Behind everything the Foundation has accomplished in the past decade is nearly half a million dollars of pro-bono services from our dedicated legal team at Smith Anderson, LLP.
Featured research
Chordoma Genome Project
Results of the Chordoma Genome Project provide the most comprehensive insights to date about how chordoma forms, and important clues about how it could be treated.
Chordoma Biobank
Contribute to Our Biobank
Patient tumor tissue is critical for research needed to find a cure. Our Biobank enables patients to help advance research by donating excess tumor tissue.