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Part of Sickle Cell Disease on Somebody To Talk To

OneSCDvoice archive

Explore reporting, meetings, people, education, community stories and resources from the original OneSCDvoice website.

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3,376 pages

  1. People

    Maria Grazia Roncarolo, MD

    Healthcare Providers · Healthcare/Research · Hematology · Pediatrics/Child Care

  2. People

    Mona Robbins, PhD

    Patient Support Professionals · Healthcare/Research · Psychiatry/Psychology

  3. Community stories

    ‘Every Time It’s A Battle’: In Excruciating Pain, Sickle Cell Patients Are Shunted Aside

    Patient Stories · QUALITY OF LIFE · Emergency Departments/Hospitalizations · Feelings and Experiences · HealthCare Issues/Services · Healthcare/Research · Living with SCD/Quality of Life · mistrust · Psychosocial · Racism · Stigma

  4. Community stories

    Kyriako Damavoletes Talks About the Stigma of Sickle Cell Disease

    Patient Stories · QUALITY OF LIFE · Discrimination · Feelings and Experiences · Living with SCD/Quality of Life · Stigma

  5. Community stories

    My Story: “Any Day Without Pain Is a Good Day!”

    Patient Stories · QUALITY OF LIFE · Feelings and Experiences · Living with SCD/Quality of Life · Pain

  6. News and meetings

    National Sickle Cell Disease Poll of African Americans Dispels Long-Held Views

    Clinical Trials and Research

  7. Community stories

    Pioneering a New Therapy for Sickle Cell Disease

    TREATMENTS · Community Interviews · Clinical Trials · Disease Management · Investigational Therapy/Future Therapy

  8. Videos and visuals

    Sickle Options Video Library

    video libraries · Definitions · Disease Basics · Sickle Cell Disease/Sickle Cell Anemia

  9. Community stories

    Sickle Strong Initiative – Dr. Marie Ojiambo

    Patient Stories · disease awareness/support · patient advocacy · Resources/Patient Support

OneSCDvoice archive — page 200 | oneSCDvoice