Today, August 1, marks the beginning of SMA (Spinal Muscular Atrophy) Awareness month. August is my least favorite month of the year. On the 10th, we will come around to the second anniversary of Blake’s death. The only thing that helps me through this month is trying to do good in her name and making… Continue reading SMA awareness month
This space of mine has been neglected lately. Between home life, my day job and The Sunshine Co., I feel like I’m going in a million directions. There are so many things that will stop me in my tracks because of my grief. So far, one of those things just happens to be dates. Today,… Continue reading Diagnosis day take 3
This time last year, we started fundraising for the annual Cure SMA Walk-n-Roll that happens in our area. CureSMA is an organization we were introduced to shortly after Blake’s diagnosis. They do a lot of important and helpful things for families like ours during their most difficult times, all while passionately trying to find a… Continue reading Team Blake
Still Finding Sunshine 