Amy Neyer

Mom. Physical therapist. Writer. Storyteller.

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When I Accepted Our ‘New Normal’ While Caring for My Son With a Rare Disease

January 16, 2019January 16, 2019 / AN

The Mighty, Nov 2016

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MCAS, Rare disease, Special needs parenting

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← When My Child Is Developing at a Different Pace, I Remember This

How I Honor My Son on Rare Disease Day →

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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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