Alexena is my niece and she has Cystic Fibrosis. We found out in 2011. We walk and raise funds and awareness every year for her and others with CF. She doesn't look on the outside most of the time like most that have Cystic Fibrosis do not. Help me help her and others with CF get the treatments they need and deserve to live the best lives they can to the fullest just like the rest of us have the opportunity to.
Team Xena's Warriors is going to walk in Erie, Pennsylvania for the 2023 walk for a cure. Join our team, make a donation and spread the word to help educate yourself and others about what Cystic Fibrosis is and how your support could mean the future for my niece and others with CF.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
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. I will not stop striding until all those with cystic fibrosis have a cure. Will you join me? Please consider donating to my Great Strides fundraising campaign today!
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting groundbreaking research and medical progress towards a cure. Please help me reach my fundraising goal! I do all kind of different fundraisers with different little incentives as prizes if you make direct donations to the CFF. And i mail prizes to the winners so never be shy about donating and then sending me a message to be put down for a drawing. Help me and be one of my niece Alexena's many warrior against Cystic Fibrosis.
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.