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      <title>Henrietta Lacks - Chapter 36, 37, 38 by Nora Joyce</title>
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      <pubDate>2025-09-09 00:40:58 UTC</pubDate>
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         <title>How can researchers balance the need for scientific progress with respecting patient and family autonomy today?</title>
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         <pubDate>2025-09-09 00:42:33 UTC</pubDate>
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         <title>How does the Lacks family’s experience highlight the connection between poverty, lack of education, and powerlessness in medical decision-making?</title>
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         <pubDate>2025-09-09 00:43:14 UTC</pubDate>
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         <title>Do the benefits to global health from HeLa cells outweigh the ethical violations against Henrietta and her family? How do we decide when benefits “outweigh” harms?</title>
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         <title>Should families always be consulted when genetic data from a deceased person could reveal information about descendants? Why or why not?</title>
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         <title>What kinds of harm can occur when communities feel excluded or exploited by medical research, even beyond physical health risks?</title>
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         <title>What does “justice” look like for the Lacks family today — financial compensation, public recognition, healthcare access, or something else?</title>
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