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Patient Support Resources

The C.W. Bill Young Cell Transplantation Program (Program) includes an Office of Patient Advocacy to support patients and families throughout the transplant process. As the contractor for the Program's Office of Patient Advocacy, the National Marrow Donor Program® (NMDP) provides many resources and services for patients and their families, including:

  • One-on-one case managers to help patients and their families understand the disease and treatment options and learn about insurance and financial matters. This assistance is free through the Office of Patient Advocacy (not a U.S. Government Web site).
  • Educational presentations as well as printed and audiovisual materials. This information is free of charge and some materials are translated.
    • Patient Teleconferences (not a U.S. Government Web site)
    • Request Patient Materials (not a U.S. Government Web site)
    • Translated materials include:
      • (Spanish) Español (not a U.S. Government Web site)
      • (Tagalog) Tagalog (not a U.S. Government Web site)
      • (Vietnamese) Tieng Viet (not a U.S. Government Web site)
      • (Chinese) Chinese (not a U.S. Government Web site)
      • (Korean) Korean (not a U.S. Government Web site)


Last Updated: June 20, 2007

Survivorship Symposium
The 2nd annual Celebrating a Second Chance at Life survivorship symposium, held in Dallas, Texas September 20-21, 2008 was an inspiring and educational event. Survivors came to learn from the experts, and from each other, how to live well after transplant.

Organizations Across the Country
Select your information needs and view a listing of organizations and their contact numbers.

Answers to Your Questions
Find answers to questions asked by other patients.
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