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HDFN Voices

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

  • Emily Hamby Making informed decisions for my alloimmunized baby

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  • Taylor Jeans What to expect from weekly check-ups if your infant has HDFN

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  • Taylor Jeans Protecting my child with HDFN: The invisible battle of a rare disease

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  • Taylor Jeans How HDFN affected my child’s physical and cognitive growth

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  • Emily Hamby My anti-Kell diagnosis: Trying to understand the threat of HDFN

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  • Taylor Jeans Adapting to life changes after bringing home my daughter with HDFN

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  • Taylor Jeans Coping with medical trauma from my HDFN-affected pregnancy

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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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