My Great Strides Story
I'm walking for our dear friends the O'Leary's...here's their story.... We are once again walking in Great Strides to raise money to find a cure for Cystic Fibrosis for our son Casey and all others who courageously battle this disease.
Those of you who follow CF news know that many CF patients are currently benefiting from life changing oral medications that minimize CF symptoms to the point that they no longer need to follow the exhausting routine of drugs and therapies to keep them healthy. They are expecting to live many decades longer than they ever expected.
Casey is not eligible to take these miracle drugs. His CF is caused by what are termed rare or nonsense CF mutations. The Cystic Fibrosis Foundation is dedicated to finding a cure for all CF patients and is now focusing in on rare and nonsense mutations. Their motto is "until it's done". Research and clinical trials are currently underway not only to develop medications to treat CF symptoms for these patients but also for a true cure, an end to CF, for all patients. Both of these goals are within reach.
This science costs money and that is where we need your help. Please consider making a donation to the Cystic Fibrosis Foundation to help Casey and all the others afflicted with this horrible disease. With your help we can make CF stand for CURE FOUND!
You can support me!
By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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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.