Patients
Resources just for you
Information for patients and their families ranges from data about transplant outcomes for those considering transplant to best practices in follow-up care for patients post-transplant.
Click the links below to learn more about CIBMTR resources available for patients.
Additional Resources
Additional information and resources for patients can be found through the following websites:
- NMDP website
- C.W. Bill Young Cell Transplantation Program website
- Related websites (including Patient Advocacy Groups)
Patients: Contact your healthcare provider immediately for reports of problems with your treatment or problems with products received for your treatment. CIBMTR uses de-identified data and is unable to associate reported treatment problems, adverse events, or corrections of information with a center, clinical trial, or healthcare provider.