Each year we come together to walk in the Annapolis Great Strides walk to raise awareness and money for the Cystic Fibrosis Foundation. We walk to support my niece Aurora, my sister Vanessa and my brother in law Jeff. Through these gatherings of family, friends and neighbors, I’m so happy to announce that the Scientists & Doctors at the CFF have found a treatment called Trikefta- a treatment that is not a cure, but that is extremely beneficial for 90% of all people with Cystic Fibrosis, including Aurora! Aurora started taking Trikefta in 2021 and she has been doing very well! But there are still approximately 10% of people with CF who can't take Trikefta, so we STRIDE ON- we will continue raising money until we have a treatment for all those born with CF!!
PLEASE JOIN ME IN WALKING WITH US THIS YEAR or help us by making a donation. EVERY DOLLAR COUNTS AND IS SO VERY APPRECIATED!! THANK YOU!!
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.
Raised the amount of money defined for this milestone
Personal Progress:
of Goal
$1,550
Raised
$3,000.00
Fundraising Honor Roll
Rolander Family Foundation
Kathleen Mackey
$50
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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.
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.