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    Experiences of family building counseling and perceptions of reproductive technology among adults with sickle cell disease.

    August 24, 2026 · PloS one

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    Key takeaway

    This study found that Black adults with sickle cell disease want more support and clear information from their doctors about how SCD affects having children. This matters because it shows our community needs earlier, regular conversations about family planning options and help affording treatments like IVF.

    Why this matters for our communities

    Research in hematology helps close long-standing gaps in how Black and African American families are studied, diagnosed, and cared for. Use findings like this one to start informed conversations with your care team — not as a substitute for personal medical advice.

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