I tried calling them in SLC and no answer. They
are still waiting for the equipment to get there before they will let them go
home. Here are some pics from the past two days. |
playing with Mom. |
Aweee we love our Blake |
Blake Evan Smith has a Neuromuscular Disease. We decided to create this website full of pictures and stories for our family, friends, and other families confronted with a Neuromuscular Disease. It is our hope that we can help or inspire others by sharing Blake's Journey.
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