New or suspected diagnosis
Including questions about the doctor’s experience with chordoma, diagnosis, surgery, and radiation
Chordoma is a complex disease to treat. Patients often wonder what types of questions they should ask their doctors to help them make the most informed decisions about their care.
We developed these lists of questions to ask about treatment with input from chordoma patients, caregivers, and the members of our Community Advisory Board on what they found important to ask their doctors. You may not need to ask all the questions on these lists and there may be questions you want to ask that are not listed, but we hope these will be a helpful starting point.
Some helpful tips to consider:
Including questions about the doctor’s experience with chordoma, diagnosis, surgery, and radiation
Including questions about the doctor’s experience with recurrent chordoma, surgery, re-irradiation, and other options
Including questions about systemic therapy and clinical trials
Including questions about how palliative care specialists can help with pain management, physical therapy, rehabilitation, and mental health counseling
Including questions about causes of pain and pain management options
Including questions about complementary and alternative medicine
Including questions about treatment costs and disability benefits in the United States
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.