Caregiving for a Blood or Marrow Transplant Patient

The National Marrow Donor Program's Office of Patient Advocacy and BMTInfoNet are conducting a caregiver survey to learn more about the experiences of people caring for blood or marrow transplant patients. Completing this survey is voluntary and anonymous; no personal identifying information is collected. At the end of this project, survey results may be submitted for publication. The results of this survey will be used to develop materials and services to support transplant patient caregivers.

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