Columnist Writes About Her Diagnosis Day 30 Years Ago
Morning! Wanted to share my latest column with you all. In it, I reflect on my diagnosis day (well, from what my parents have told me) and reflect on how my family must have felt receiving a diagnosis like SMA type I. Back then, very little was known about SMA and there wasn’t much hope in terms of treatments and life expectancy. I’m sure many of you can relate. What have you been told about your diagnosis story?
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