Magdalena Grace Roberts

One of the coolest parts of writing is that I get to meet so many wonderful people. Although I really enjoy all the stories I write, occasionally I'll meet someone who makes a huge impact.

This week I was working on a story about the March of Dimes and I had the pleasure of meeting (over the phone) Julie and Noah Roberts. The Roberts' daughter Magdalena Grace was born with Trisomy 18, a chromosomal defect where most babies don't make it to full term, and if they do, less than ten percent live to see their first birthday. In January, at 167 days old, Magdalena passed away, leaving her parents of course heartbroken, but determined to keep her memory alive. After hearing this story, I can tell you this little girl was so special and has touched my heart beyond belief. And I didn't even get to meet her!

As mother to two sweet baby girls, I cannot imagine what Noah and Julie are going through. Despite the heartbreak, these two have the most amazing, joyful spirit. Where most would be asking why she had to leave them so soon, they are thanking God for the time they had with their daughter and praising Him for this blessing. Oh, to be more like them. They truly see God in everything around them, even the loss of their precious little girl. Please join me in praying for this family. I'm sure it doesn't get any easier as time passes. Pray that God continues to give them peace and pray that Magdalena's story continues to point people toward Jesus as it already has for so many.

The Roberts have also organized a team, Magdalena's Feet, for the March of Dimes' March for Babies walk, which will take place in May. Check out the Roberts' blog to find out more and to read Magdalena's story. I promise you will be blessed by this sweet family.