Most people would never know by looking at him, that Logan Moore has Cystic Fibrosis (CF). He is smart, funny, active, and social. He makes friends where ever he goes. He is confident, brave, and well spoken- a natural born leader. Most people can see these things in Logan.
What they don't know, is that Logan is a fighter. He works hard every day to stay as healthy as possible. Logan has been admitted to a hospital over a dozen times. He spends 3 total hours a day sitting, hooked up to a special machine that helps clear his lungs so he can breathe. Logan takes 18-25 pills each day.... and that's when he's healthy. He also takes 11 inhaled medicines a day. He even has to go to school with his PICC line in and do IV infusions in the nurses office when he gets sick. Through it all he wears a smile. He doesn't complain- he just keeps fighting each step of the way.
Along his journey Logan has aquired quite a crew of people to support him in his fight. He has, and will continue, to touch the lives of the people around him. There is no cure for CF, but they are close. Additional money is needed to help further the research efforts.
We are hoping you will join in Logan's Crew! There are so many ways to help: Join us in our walk on May 21, 2011 in Olympia. Click on the donate now button on the right so we can help improve the lives of all people with CF. At the very least, take a moment to stop by the Logan's Crew Blog and pass it along to your friends. Awareness is important! Go to loganscrew.blogspot.com (this blog- lol)to learn more about Logan and CF. Check back often as I will update frequently.
Thanks for your support,
The Moore Family &
Logan's Crew!
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