HDFN Voices
The latest insights and perspectives from people who have lived and struggled with HDFN
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What to expect from weekly check-ups if your infant has HDFN
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Protecting my child with HDFN: The invisible battle of a rare disease
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How HDFN affected my child’s physical and cognitive growth
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My anti-Kell diagnosis: Trying to understand the threat of HDFN
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Adapting to life changes after bringing home my daughter with HDFN
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Coping with medical trauma from my HDFN-affected pregnancy