Team Pritchard is back and fundraising for a cure for CF. We are walking in person this year. So many of you have donated through the years to our team and we thank you for helping make the life of our children and others with CF better. Anderson Pritchard, just turned 13 this month. Our youngest, Katherine Pritchard, recently turned 9. The continued generosity of my friends and family over the past 12 years has always been humbling to me as we strive towards finding a cure for CF. We have seen amazing advances in those 12 plus years. Anderson and Katherine continue to do well and enjoy life to the fullest.
Anderson has had a great year. Nothing major to report this year! He continues to hunt, fish, and play the bagpipes!
Katherine had sinus surgery this year and was able to get her sinus back under control! The doctor said she was full of infection. She loves to play with dolls, spend time outside, and play the piano.
Let's lace up our tennis shoes and walk to support Anderson and Katherine. The support we have been shown over the years means the world to us and we look forward to this event each year. We are excited to be able to walk in person again this year!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts. Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Real progress has been for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Please consider making a donation to my Great Strides fundraising campaign today!
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting groundbreaking research and medical progress. Your gift is 100-percent tax deductible.
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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.