Count Me In: Partnering With Patients to Accelerate the Pace of Cancer Research With Melissa Mirick

At the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago, Oncology Data Advisor sat down with Melissa Mirick, Partnership Manager of Advocacy Groups at Count Me In, a nonprofit research initiative that engages patients and enables them to accelerate cancer research by sharing their samples, their clinical information, and their voices. Ms. Mirick shares more about Count Me In and its mission, including:

  • How Count Me In uses collected data to advance cancer research
  • What the collection process involves
  • Where and when the data is made available
  • What clinicians should know about Count Me In and why it’s important for them to be involved
  • How clinicians can connect their patients with Count Me In
  • How anyone who is interested in becoming involved can get started
  • And more!

About Melissa Mirick 

Melissa Mirick is the Partnership Manager of Advocacy Groups at Count Me In. She works with patient advocacy groups across the United States and Canada and builds collaborative relationships to share information about Count Me In’s projects with patients and their caregivers.

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