What the Cancer Experience Registry Means to Bladder Cancer Patients with Dr. Kimberly Papay Rogers

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In Episode 21 of Bladder Cancer Matters, host Rick Bangs talks with Kimberly Papay Rogers, PhD, the Director of Research at the Cancer Support Community. Rick and Dr. Rogers discuss her work on the Cancer Experience Registry, an online research survey that helps enhance cancer care, improve health care policies, and ensure support services better reflect the needs of people affected by cancer.

They also talk about:

  • What a cancer registry is
  • What has been learned from the Cancer Experience Registry so far
  • Why bladder cancer was added to the registry
  • Who can and should participate in the bladder cancer patient survey
  • The findings’ expected impact on bladder cancer treatment and experiences

Disclaimer: The views and opinions expressed in this podcast are those of the speakers and guests and do not necessarily reflect the views or positions of the Bladder Cancer Advocacy Network.

Dr. Kimberly Papay Rogers