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The Slone Epidemiology Center at Boston University is enrolling patients who have been recently diagnosed with multiple myeloma in a voluntary research project called the Patient Registries at Slone: Myeloma. The registry gathers important information about the impact of myeloma and its treatments on patients’ physical, emotional, social, and economic well-being.

Since myeloma is not a very common disease, it is essential for the registry to enroll as many patients as possible. It is also important that the registry includes patients from all regions of the U.S. and from all walks of life. Together, you and others facing the challenges of myeloma can provide valuable information that will help doctors better understand the disease and in turn, help myeloma patients now and in the future.


Due to a lack of funding, the registry is now closed. We appreciate your interest and apologize for any inconvenience. For more information, email us at mminfo@slone.bu.edu.

To view our presentations:

To view the poster presented at the 2007 annual meeting of the American Society of Hematology (ASH), click here.

To view the poster presented at the 2008 annual meeting of the American Society of Hematology (ASH), click here.

Last Updated: January 11, 2011

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