Team Scottie 2024
Scott is living the full life we always dreamed of. He got married in May of 2023 and is celebrating his 28th miraculous year of life - good things happen in May. This year I’m taking a passenger seat to my son who’s taking the baton of fundraising on himself. I will never stand completely on the sidelines when it comes to CF - feel free to donate to our page if you are moved to do so !! We are off celebrating the life God has so generously and graciously given us in Scott Jr and Sarah too.
His life will never be easy - but it will always be GOOD because he's a fighter and lives it the best he can EVERY day!!
He continues to look ahead to the promising future God has set before him. I remind him almost daily - he's an overcomer !! He still wants to be the first person "never hospitalized" w/ CF complications. Help me make all his dreams come true! Please help me raise the much-needed research money to assist the foundation in making CF stand for Cure Found. UPDATE - still living the dream ....never been !!
Many years ago, I asked him what it's like to have CF - his candid reply, "like riding a roller coaster, blindfolded". Help me stop the "ride" and let him live a normal life one day - free of Cystic Fibrosis ) I assure you it's been more like Mr. Toad's wild ride for me too - but God is faithful, and we are thankful!
We are VIRTUALLY participating in the actual event this year. So if you are willing sign up to "virtually walk" like me, or donate, or go and walk in our honor if you are local ....we appreciate any and all support - always !!
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.
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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.