Coleman Family: Marshmallows for dinner...yes please!!!

Sunday, October 16, 2011

Marshmallows for dinner...yes please!!!

She's so good at sharing!

3 comments:

Anonymous said...: Oh it's such a highlight of my day checking in to see how Maggie is doing! She has captured my heart and ive never even met your family! What a wonderfully devoted mother you are.... And what a curious and sweet big girl she is :). Have a wonderul joy-filled week!; October 16, 2011 at 11:16 PM
Rachel said...: Made me smile! Thanks!
xxoo; October 17, 2011 at 8:34 AM
steph said...: That is MY kind of dinner! Can I come over? Love you !!!! xoxo; October 18, 2011 at 5:52 PM

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Whit and I have been married for 9 years now. How time flies when you are having fun. We have the most precious baby boy named Jonas. He is in Heaven right now, waiting for us to return to him. We miss him every minute. We also have a little girl named Maggie, who has the same disease that her brother had. Time with her is limited as well, so we continue to do what we did with her brother...enjoy every minute! We are so blessed to have the most beautiful children and even though our time with them will be short, we know we will be with them again!

Jonas Mathie

Jonas was born on December 2, 2007. At six weeks old Jonas was diagnosed with a genetic disorder called SMA (spinal muscular atrophy). SMA Type I is a terminal genetic disease that results in loss of nerves in the spinal cord and weakness of the muscles connected with those nerves. Jonas beat the odds and lived with us for almost three years! He returned to heaven November 18, 2010. Every day we had with him here on earth was our heaven. We are better people because of Jonas and miss him everyday.