Amy Neyer

Mom. Physical therapist. Writer. Special needs advocate.

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MCAS and rare disease

The Terrifying Uncertainty of Having a Child with an Illness that Changes Every Day (Today’s Parent, Aug 2018) IMG_4720.JPG

How I Honor My Son on Rare Disease Day (The Mighty, Feb 2017)2016_11_Neyer Family-16

When I Accepted My ‘New Normal’ While Caring For My Son With a Rare Disease (The Mighty, Nov 2016) cropped-fullsizeoutput_b1b5-3.jpeg

The Reality of Becoming a ‘Rare Disease Parent’ (The Mighty, May 2016) 2016_11_Neyer Family-11

 

 

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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

Recent Posts

  • Expressing Motherhood
  • Flipping my guilt into gratitude
  • Feeding tube awareness week
  • Expressing Motherhood
  • Connecting with parents online helped me survive parenting a son with special needs

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Email
neyer.amy@gmail.com

 

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