Amy Neyer

Mom. Physical therapist. Writer. Special needs advocate.

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How I Honor My Son on Rare Disease Day

January 16, 2019January 16, 2019 / AN

The Mighty, Feb 2017

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MCAS, Rare disease

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

Turning My Pain Into Gratitude as I Parent My Son With Complex Needs →

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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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