Coleman needs your prayers....

I know it's been quiet a while since I've posted. It's just been busy, busy, busy around here. Which is a good thing. I just wanted to ask a favor of everyone on behalf of my little guy, Coleman......

PRAY! PLEASE! We all have one BIG contact in Heaven...call on Him. Pray for a miracle! If you do NOTHING else...just pray! Coleman Larson is 4, he will be 5 on December 10. His twin Caden has been a trooper for the last 2 1/2 years that Coleman has been fighting a beast known as Medulloblastoma...BRAIN CANCER! Together they are TEAM LARSON! Coleman has endurred brain surgery, chemo, radiation, CT scans by the dozen, MRIs that he no longer has to be sedated for...he is a pro, multiple lines, port-a-caths, a stem cell harvest and transplant and two relapses. His fight is getting harder and there are less and less options for him.

If you would like to, I know they would be very greatful to receive a birthday card. They love to get mail and they are very appreciative of every peice of mail they receive. Again, their birthday is December 10, 2008. Here is their address:

Coleman & Caden Larson

c/o Team Larson

Box 251

Callender, Iowa 50523

How can a doctor look into these eyes and say, "We are out of options."? Coleman and his family are in IOWA. But they are "regulars" at the Ronald McDonald house in NYC. Team Larson needs YOU, those of you who kept reading even though tears are streaming down your face, to PRAY, and PRAY like you've never prayed before! Because if TEAM LARSON has taught me ANYTHING it's to NE-VA DIV UP!

They got back home Saturday afternoon and are going to be able to spend Thanksgiving with their family for the first time in 2 years. However, when they got home, due to side effects of this new treatment, Coleman can no longer walk without falling. So, he is having to be carried everywhere. Can you imagine how frustrating and frightening this is for him and his family? He is still a happy little boy, just very scared and confused. HE NEEDS YOUR PRAYERS.

Coleman and Caden will tell you exactly what they think of Cancer if you ask. Peggy, their mom asked them and this is what they said:

Coleman explains, “It’s hard to be hooked up to a pole all day when it’s a sun-shiny day, ann be in your hos-pita woom all day when yoa don’t wanna be there ann wish ya tould be outside in-said, but NO, ya tan’t. I wish that no more tids would det tancer, tuz it's tewwible to haffa do all-a the suff what ya dotta do. If no more tids dot it, then we tould all yust be no-mal wif no more pokes."

Coleman’s twin Caden chimed in and gave his two cents, “Cancer is the worse day of my wife (life) because you don’t getta pway wif your brudder when ya weally want to. Sometimes the hospital is fun …if ya aren’t froe-in up wike Coleman does sometimes. I wish that no tids ever det tancer, so they tan haff fun all-a their days until they be daddies."

Thanks for hangin' in there and loving Coleman already! How can anyone not love this kid and pray for him continously??

For more info on Coleman Larson and his family, go to http://www.carepages.com/ and register (it's FREE and takes seconds). Click on Visit and type in ColemanScott (all one word). Be prepared to fall in love. This is ONE AMAZING FAMILY!!!!!