Hey Ryan's Hope Team!!!
Hoping and Praying you are all feeling healthy and happy!!
It has been a crazy year and seems like it flew by!! It was just yesterday we were walking virtually and joining together to raise money for Cystic Fibrosis.
Well, thanks to COVID.... the Great Strides Walk to cure Cystic Fibrosis is virtual again. We miss all of you and were really hoping to be able to see everyone this year! Although VERY disappointing....We are still fighting to find a cure and could use your help!!
Ryan has been doing so well on the new drug TRIKAFTA and we are sooooo THANKFUL for that!!!! Although new medications and treatments are improving the quality of life for many CFers...there is still no cure!! Every year when Great Strides comes around, I hear so many stories from the CF community.....some happy and some sad. I am reminded that this fight is NOT over!! Real progress has been made in the search for a cure, but the lives of people with CF are still cut FAR TOO SHORT!
Let's find a CURE for this devastating disease!!
In 27 years, we have raised thousands and thousands of dollars and I truly believe all of the advances they have made to find a cure for CF is because of friends like you!!! Our team has always been filled with so much love and support that there will NEVER be any words to express our gratitude!!!
Help us reach our team fundraising goal of $5,000 by donating to our team!! Your support will help add "tomorrows" to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. All donations are 100% tax deductible!
Thank YOU for all of your love, support and prayers!
We couldn't do it without you!
Lets make CF stand for CURE FOUND!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.