As I reflect on the last few weeks, those are the words that came to mind.

Yep, it’s true.  I, Sarah Kasner, am the one who gave Caleb & Duncan Duchenne Muscular Dystrophy.  I am the carrier, and I had no flipping idea.

Celebrating birthdays for a child with Duchenne is bittersweet.  Caleb can’t wait to turn 5 tomorrow, he has been talking about it for months and he has this idea that you always get the same number of presents as the age you are.