These educational resources are a wealth of information that can help you learn even more about chordoma.
The basics on chordoma, including who gets it, where it's located in the body, what types there are, and if it's genetic.
Chordoma Foundation Patient Navigators provide personalized information and support to anyone affected by chordoma, anywhere in the world, at any stage of their journey. Your Patient Navigator will use their extensive knowledge of chordoma to help answer your questions, provide information about treatment guidelines, help you find qualified doctors, talk with you about side effects, and connect you with others in the chordoma community who have been through a similar journey.
