Our Great Strides Story
Dear Friends & Family,
As some of you may or may not know, our son Mason was diagnosed with Cystic Fibrosis in 2014. Since the day he came into our lives we knew that he was something special. He has opened our eyes to how precious life can be and how to not take anything for granted, even something as simple as breathing. He's currently an energetic four year old that loves going to school and playing with his friends, but unlike normal four year olds he has to take 24 pills a day and sit through breathing treatments twice a day to keep his lungs clear. He takes them like a champ although I'm pretty sure he'd rather be at the park riding his scooter.
There are approximately 30,000 other Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers. This year and every year, I will walk for them, my son, and hope you will support us in our efforts.
Real progress has been made in the search for a cure. Although there still is no cure for this genetic disease, the CF Foundation is making great strides and there are very promising drugs in trials. If would like to learn more about CF, the best source for the most current information is at http://www.cff.org. By walking on May 13th, we are helping add tomorrows to the lives of people living with cystic fibrosis. Will you join us? Please support us by making a donation to our Great Strides fundraising campaign today.
|Mason's Minions - Join Team||Raised|
|Suzanna & Mike O'Donnell||$7,100.00|
|Denotes a Team Leader|