These past few years fund raising for our daughter Emma towards a cure for Cystic Fibrosis has been incredibly humbling. We have received so many donations from family, friends, colleagues, customers, and even total strangers. Along the way, I have answered questions about the disease, what it means to Emma, how it effects our family, and what we are expecting for the future. For those who are still curious, check out this YouTube link to a quick discription of what CF is. Even though it is for kids, it does a great job.
https://youtu.be/FMAOEOmLoUE
This a couple years ago, another breakthrough drug was released!! Emma has been taking this treatment and has been doing great, they have made amazing strides. This is all do to your donations.
With this all being said, lets get things started off right and hit our goal to find a cure for Emma!!!!
Thank you all for all your generosity!!
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!
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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.