Amy Neyer

Mom. Physical therapist. Writer. Special needs advocate.

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When My Son’s Phlebotomist Made Me Cry

January 16, 2019January 16, 2019 / AN

The Mighty, May 2018

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MCAS, Rare disease, Special needs parenting

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The terrifying uncertainty of having a child with an illness that changes every day →

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#ExMoShow Expressing Motherhood Food allergies gratitude MCAS MCAS and rare disease parenting Rare Rare disease special needs Special needs parenting Tube feeding

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neyer.amy@gmail.com

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