GREAT STRIDES, a Walk supporting the CF Foundation, will take place at Brier Creek Park, Morrisville, Saturday, May 18th 2024 . We, along with Allison, other families, care providers, friends and spirited supporters will be "making strides" on May 18th, we ask that you support our effort, and the 2024 GREAT STRIDES Walk.
Allison is in her final semester at University of South Carolina and will be graduating May 3 with a BSN in Nursing. This past year, she has successfully managed clinicals 2-3 days a week as well as her health and CF regimen of daily vest treatments, breathing treatments and oral medications throughout the day. In July, Allison will begin her nursing career at Duke University Medical Center working in the Pediatric unit.
Since starting Trikafta( (elexacaftor/ivacaftor/tezacaftor), a triple combination therapy available to treat patients who have at least one F508del mutation, which is estimated to represent 90% of the CF population)in September 2019, Allison has been very healthy. No hospitalizations since July 2019 and a few viruses requiring oral antibiotics. Trikafta really has been a game changer for Allison and so many others fighting Cystic Fibrosis.
It has been a challenging and incredible journey since diagnosis March 1, 2001, learning and seeing very encouraging advances over the last 23 years. With continued support, we are confident research will progress at a similar pace and the rarest CF gene mutations will be addressed, including Allison's.
2024 Goals-help us build on the successes of previous years, raise awareness, continuing our efforts to fund the research for therapies providing a higher quality of life and treat the root cause of CF; let's advance research to address rare and specific mutations. We need your support in helping those with CF reach the milestones that many take for granted, and increase the median age of those with CF. Let's help CF kids and adults breathe easy.
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 life-saving research and medical progress. Your gift is 100-percent tax deductible.
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.