
We rally for Tali.
Tali was born in November 2021 with cystic fibrosis – a rare, progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. When we first began learning about CF, we were comforted and encouraged by the impressive history, progress and ongoing research pipeline driven by the Cystic Fibrosis Foundation.
The Cystic Fibrosis Foundation is the world's leader in the search for a cure for CF and supports a broad range of research initiatives to tackle the disease from all angles. The foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Their work has and will continue to have a direct impact on Tali’s quality of life. This is why your support for this cause means so much to us.
Great Strides, the Cystic Fibrosis Foundation’s largest national fundraising event offers hope to those living with cystic fibrosis. Each year, approximately 125,000 people participate in nearly 300 walks across the country to support the Foundation’s mission. Team “Rally for Tali” will be taking part for the first time, walking 5km on May 22nd, 2022.
We walk for Tali and for all the CF warriors.
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. your support truly matters. Together, we can make “CF” stand for “Cure Found”.
Please consider joining our team and walking with us or donating to support this incredible cause.
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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: