This is SMA Video

The Strong family, who started the Gwendolyn Strong Foundation (named for their daughter), put together an awareness video about Spinal Muscular Atrophy to show at their annual golf fundraiser. It's absolutely beautiful and I hope you will all take a few minutes to watch it. Nicholas and I feel so honored that his birthday picture made the final cut...look for us at 0:40.

Click here to watch the video.

We also wanted to thank our friends and family members who left such kind comments about my previous blog post. Nicholas is doing wonderfully now and thankfully we have not had any more scares. We feel so blessed to be loved by each and every one of you.