Hi Everyone, I would like to ask everyone a favor.... Please take a minute to visit the link for Raegan's Walkers below and read about our cause and why it is important to us.  My (future) step-daughter has Cystic Fibrosis and last year her aunt and I formed "RAEGAN'S WALKERS" and joined the Sooner-Chapter of the Cystic Fibrosis Foundation.  On our team page is information about CF, and Raegan.  There is a video at the beginning that you can watch that will help you understand a little about what Raegan and our family goes through daily with this illness.  Since the illness only affects about 300,000 young children and adults, it's not one of those HOT TOPICS that major corporations is jumping to support and fund research.  Therefore, it is up to friends and family of the patients to get the word out and support the foundation to help find new drug therapies and hopefully one day a cure.  So, If you have an extra min to stop by and learn a little please do so.  If you happen to have an extra $1.00 to deposit into our team fund at the Cystic Fibrosis Foundation we would greatly appreciate it.  If not and you can pass the information along to a few friends who might that would be great too.  Our walk is going to be held in Oklahoma City on May 10, 2009... YES! The Saturday before Mother's Day!  I can't think of any better way to spend it.  If you happen to live in the area and would like to join our team... let me know.  I could use a few new team members.     http://walkersforlife.blogspot.com/ Robin R Inge "Life is not measured by the number of breaths we take, but by the number of moments that take our breath away"