I walk for our son Logan and for our CF community! We found out about Logan's diagnosis through prenatal screening almost 7 years ago. Since then we have grown stronger as a family and parents. We have learned more about how to live with CF and pushed our capacity for hope more than we ever dreamt possible. Our passion is bigger than ever as we push for a CF Cure! We are so grateful for the support of each and every one of you! In the past 5 years you have shared our story, walked beside us and donated last year alone nearly $10k!
Will you join Logan and support our mission to make medical history again this year?
All we need of you is to click on the "Join our Team" button. By becoming a member of our team, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Cystic fibrosis is a life-threatening, genetic disease that causes persistent lung infections and progressively limits the ability to breathe.
A little more about Logan and Cf...
Under it all Logan bravely fights Cystic Fibrosis…every day, 365 days a year. There is no holiday for the average 3 breathing treatments, 2 sinus rinses, 25 enzymes/pills every day. We are always “on guard” for the simple cough, sneeze or runny nose! Each cold, virus, infection calls for immediate action and increased treatments as each “simple” illness creates permanent scarring on his lungs.
We are amazed as we watch who Logan is growing to be! He is a fighter and a lover of all things space! This year Logan bravely started Kindergarten, proudly shows off that he swallows 5 large enzymes capsules at once and is taking the lead at doing his own breathing treatments. He shows us he can and WILL do it all! We have been very fortunate that overall Logan has been healthy and we count each day of good health as a victory! To learn more about our daily routine, watch Logan's video from last year: https://youtu.be/eDKRqCqHy58