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Sharing the story of our family and our daughter who was diagnosed with Spinal Muscular Atrophy, type 1

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Month: March 2017

Diagnosis day
Blake · grief

Diagnosis day

March 9, 2017 BlakesMama4 Comments

A year ago today, Jeff, Blake and I sat in an exam room at Seattle Children’s Hospital. I was holding my sweet baby girl as she was falling asleep. We were alone, waiting for the doctors to come back in. They were going to tell me something I already knew. They were going to tell… Continue reading Diagnosis day

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