As you may know from posts in prior years, my younger sister, Rachel, has Cystic Fibrosis. It is a terrible disease that currently has no cure. Every day she is faced with the tough challenges of having CF. Doctors appointments, treatments, and lots of medicine are just some of the things that she goes through to maintain lung function. Advancement in CF meds have made improvements for people with CF, but there’s still a ways to go.
Every year, my family (along with CF families nationwide) works hard fundraising and promoting awareness about Cystic Fibrosis. More research is crucial in creating and testing new medicines, and ultimately finding a cure. Research, however, is not possible without funding. Please consider donating to this cause, which is so close to my heart.
If you would like to make a donation to support the Cystic Fibrosis Foundation, I would be forever grateful. There is a link above.
Again thank you for reading this and thank you for your support!
"Until CF stands for Cure Found",
James VanLandingham
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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.