Research Participants

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Sickle Cell Disease Association of America Empowers Research and Better Health Care

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The Sickle Cell Patient Experience

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Parents and Physician Collaborate to Build Patient Advocacy Group From The Ground Up

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Family Concerns and Stress About Going Back Into Public During the Pandemic

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Patient Advocacy Leadership at Its Finest. The Global Liver Institute Rallies Stakeholders to Face Down Liver Disease for Many.

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The Sickle Cell Disease Association of America Empowers Research and Better Health Care

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Using Data to Bring Change for Minority Health: An Interview with Dr. Gary Puckrein, President & CEO of the National Minority Quality Forum

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What Are Clinical Trials and How Do They Benefit Participants?

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Providing Mental Health Services in Underserved Asian Communities

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Mental Illness: Patient Advocate Wenora Johnson speaks of her family and coping with mental illness in minority communities.