My Great Strides Story
In September we welcomed to the family the most perfect little peach - Georgia . Her parents, Steven & Emily, are not just family, but also close friends. Entering into parenthood is already jarring and filled with a lot of questions and unknowns, add in learning and adapting to a diagnosis like CF - these two have been the definition of strength. Georgia is lucky to have many people who love her, but the most lucky that she has Steve & Em as her parents, who will go to the ends of the earth to ensure they are doing everything in their power so that she has the best life.
Your donation, whether it be joining us for the walk (in-person or virtual!), monetary, prayer, or just a note that you’re rooting for Georgia - would be a cherished example of how many people the Wehr family has on their team.
A little more on CF itself, and the impact you’d be making:
Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person, and as people with CF live longer than ever before, their disease can become more complicated, leading to serious health issues.
The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.
Your support makes a difference.
By donating to my fundraising goal, you will help advance our mission for a cure for all. Please consider joining us and helping make CF stand for Cure Found.
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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.