Hi! I'm Jo Ann Avery's grandmother. Avery was diagnosed with cystic fibrosis at just 9 days new. It was a diagnosis that none of us were expecting. Avery is currently a healthy, thriving 5 year old. She takes a mulitvitamin, artificial pancreatic enzymes and a CFTR modulator drug daily. She also does compressive vest therapy. It's been a great stride thus far, and we have a lifetime to go! It is because of your generous support that we will, one day, find a cure for this terrible lifelong disease. Every donation goes towards finding ne medications and expanding research to hopefully one day find a cure and make CF a thing of the past. Thank you for your donation!
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!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?
Achievements:
Jo Ann Parham
Event: New Orleans
| Team: Avery's Army
Jo Ann's Fundraising Goal: $2,500.00
| Amount Raised: $751.07
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.