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Bone Marrow/Stem Cell Transplant Frequently Asked Questions
This booklet is intended for patients, caregivers, and families as they prepare for and enter the world of bone marrow/stem cell transplant. It was written as a helpful resource to give patients and families tools, information, encouragement, and support during their transplant journey.
The nbmtLINK values your opinions and would like to hear what you think about Frequently Asked Questions. When you are finished reading this publication, please take our five-minute online survey at: http://www.zoomerang.com/Survey/WEB22FR8MBW4RS
Your feedback will be used to help evaluate Frequently Asked Questions and aid us in the creation of future programs and resources for bone marrow/stem cell transplant survivors.
Use the right-hand menu to view an online version of this guide.
Click here to purchase a copy of this guide (Bilingual: English/Spanish)
Click here to download a PDF version of this guide (4852K/74pg)
Founded in 1992, the nbmtLINK is an independent, nonprofit organization funded entirely through the generosity of individuals, corporations, and foundations. Tax deductible contributions are welcomed and enable us to create and sustain programs and services.
The mission of the National Bone Marrow Transplant Link is to help patients, caregivers, and families cope with the social and emotional challenges of bone marrow/stem cell transplant from diagnosis through survivorship by providing vital information and personalized support services.
The information in this booklet should not be a substitute for medical advice, and the listed resources are not intended to be endorsements. Please consult with your physician regarding your medical decisions and treatment.
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