Newly diagnosed?
If you or someone you care about has recently been diagnosed with chordoma, we are here to help with answers to your questions, important steps to consider, and ways to get support.
What you should know
Chordoma Foundation Updates
Record Number of Labs Apply For CF Seed Grants
Momentum Surges Following Chordoma Research Workshop and Community Conference
Chordoma Foundation Presents First Annual Uncommon Awards
New Radiation Therapy for Chordoma Patients Open at MGH
Watch the stories
Featured champion
The Laird Family
One thing Alison Laird delighted in most during her eight-year battle with chordoma was proving her doctors wrong. A woman of amazing strength and spirit, she wasn’t about to let cancer rob her of the things she enjoyed...
Featured researcher
Dr. Gary Gallia
There are many diseases that were fatal 50 years ago, that are now curable. I want that to happen for chordoma.” Armed with a grant from the Chordoma Foundation, Gallia is moving us closer to that outcome...
Chordoma Biobank
Contribute to Our BioBank
Patient tissue is critical for research needed to find a cure. Our Biobank enables patients to help advance research by donating excess tissue. Learn how to contribute »









