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HDFN Voices

The latest insights and perspectives from people who have lived and struggled with HDFN

  • Taylor Jeans It takes a village: Why support was vital for my HDFN-affected family

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  • Taylor Jeans My infant affected by HDFN needed an emergency transfusion—here’s how it went

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  • Taylor Jeans Intrauterine blood transfusions as a treatment for HDFN: a first-person account

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  • Taylor Jeans A survivor’s tale: my experience with phototherapy as a treatment for HDFN

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Your news and information resource for living with hemolytic disease of the fetus and newborn
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Rare Disease Companion (RDC) is a network of news and information websites that supports people living with rare diseases. Through accurate, authentic, and compassionate news coverage, feature-length articles, and patient-friendly educational material, RDC provides insights into living with rare diseases at every point along the patient journey.

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