April 11, 2015, San Clemente,CA: please support Team Miles for Myles. Jay Alders signed art for charity auction along with a great music show by some real talented and caring musicians.
Myles was diagnosed with Cystic Fibrosis when he was three weeks old. The day that Myles was diagnosed our life changed and from that moment forward we made it our mission to help CURE Cystic Fibrosis. That is why we walk, hike, fundraise to ulimately find a CURE!
Myles has had a very busy year starting kindergarten, riding his bike, playing baseball and trying basketball for the first time. He has also been extremely busy working hard to stay healthy by balancing the many medications, treatments, clinical trial appointments, doctors appointments, and therapies that he must do on a regualr basis to stay healthy. Myles is such a trooper, he tackles Cystic Fibrosis with such strength and bravery! His strength astonishes us on a daily basis. We feel blessed and thankful for yet another healthy year for Myles.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. We walk for our son Myles and all of his friends that have Cystic Fibrosis as well as those that we do not personally know.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Our family would love for our friends and family to join team Miles For Myles and walk for a CURE! We are dedicated to walk for CF until CF stands for CURE FOUND!!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Live. Fight. Breathe.