Amy Neyer

Mom. Physical therapist. Writer. Storyteller.

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

January 16, 2019January 16, 2019 / AN

Today’s Parent, Aug 2018

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Food allergies, MCAS, Rare disease, Special needs parenting, Tube feeding

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← When My Son’s Phlebotomist Made Me Cry

Connecting with parents online helped me survive parenting a son with special needs →

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#ExMoShow Expressing Motherhood Food allergies gratitude growth mindset MCAS MCAS and rare disease parenting Rare Rare disease Speaking special needs Special needs parenting Storytelling Tube feeding update

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neyer.amy@gmail.com

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