Dear Family & Friends,
It’s Great Strides time of year again!
The Cystic Fibrosis Foundation’s largest national fundraising event is Great Strides, with walks being held throughout the United States! Great Strides Seattle is on Sunday, May 21st, 12 noon at Seattle Center.
We would love to have you join Team Super G for this easy 3 mile walk. Last year Team Super G raised over $10,000! And with your help we can do it again!
Click on the link to sign up for the walk. If you are unable to attend the walk and would like to support the CF Foundation please consider a donation. Any amount will make a difference!
The Cystic Fibrosis Foundation’s mission is to cure cystic fibrosis and raise awareness about this rare, genetic, life-shortening disease that makes it difficult to breathe. The Foundation leads the way in innovative research and drug development. Nearly every Cystic Fibrosis drug on the market today has been researched and developed by the Foundation.
As many of you know, our grandson, Greyson, has Cystic Fibrosis. He was diagnosed with CF at two weeks old and luckily he was started on therapeutic treatments right away. Today Greyson is an energetic 6 ½ year old boy who loves going to first grade, making new friends, playing on the playground at the park with his little sister Olivia, and he’s also looking forward to the start of T Ball season! We feel very fortunate that Greyson’s health has been very good this last year and his doctors from the CF Clinic at Seattle Children’s Hospital are pleased with his growth and continued good health.
There are now approximately 40,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day just to breathe. Many of these people struggle on a daily basis to maintain their health, however major advancements have been made in specialized CF care that have added years and improved quality of life for those living with Cystic Fibrosis. Although there is still so much work to do, the lives of many people with CF are still cut far too short.
Please join Team Super G and the CF Foundation in finding a cure to help all people with Cystic Fibrosis live longer, healthier lives and to pursue their dreams. We’re looking forward to the day when CF stands for Cure Found!
Thank you,
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: