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HDFN Voices

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

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

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  • Taylor Jeans How to easily explain HDFN to friends and family 

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  • Taylor Jeans What to expect during and after a C-section due to HDFN

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  • Taylor Jeans When life-saving HDFN medication is denied by your insurance

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  • Taylor Jeans My journey with HDFN: Year one in review

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  • Taylor Jeans Weekly MCA Doppler monitoring for my HDFN-affected infant

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  • Taylor Jeans What to pack for an outpatient blood transfusion

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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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