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Still Finding Sunshine

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

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How we do it
Family

How we do it

July 17, 2016July 17, 2016 BlakesMama4 Comments

“I don’t know how you do it. I would just die.” Someone said this to us, not long ago. At first I was taken aback for a moment, mostly because I feel ill every time I hear the word “die”. Those three letters, put together, cut me way too deep. I hate them. This lady… Continue reading How we do it

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