It’s been nine months since I published the epilogue for my story about Hadley Ferguson, my intrepid friend with multiple system atrophy. I thought you might appreciate this update in her own words, written for the 2017 MSA Coalition’s fundraising effort on this Giving Tuesday.
Dear friends and family,
I am 40 years old, a mother to a beautiful daughter, a wife to the most amazing husband, a daughter to wonderful loving parents, friend to many supportive dear people, and I have Multiple System Atrophy (MSA). I was originally diagnosed in 2010 with Young Onset Parkinson’s disease. At…