In the comments below Our Team's roster, please watch (link) "Willem's Journey - Breathe" video. Or copy this URL to your browser:
https://drive.google.com/file/d/1aSEfgmKt7_ruACJ6dZGMjSV3D__wsI8Q/view?usp=sharing
Join our team and help fight CF and add tomorrows!
It's been another difficult year with Covid and even harder for those with Cystic Fibrosis. While we are blessed and full of gratitude for my upcoming 4th “Lungaversary” of my double lung transplant, a lung transplant is not a cure for Cystic Fibrosis. So we support the CF Foundation in its research. Fundraising for research has been successful in developing many treatment modulators that help this group of people try to live a life. The most recent being Trikafta, that has tremendously helped many maintain a level or improve lung function. Yet there are still more that don’t have this option and hope for something more. The Cystic Fibrosis Foundation is making great strides towards a cure. We hope to see one in our lifetime, but they need our help. Would you please consider a donation and join us on this fight for a cure?
Thank you for your support. Until CF Stands for Cure Found,
Willem and Kathy Wery
Wery Warriors Team
Connect With Us
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.