Sweet Nash
My Story
May is Cystic Fibrosis Awareness Month and on the 18th we walk for our sweet boy and all those who are fighting this disease.
This year has been a year of learning and growing in our understanding of CF and how to navigate the effects of this disease on Nash.
All in all, he has thrived and done amazingly well due to the fabulous care his mommy and daddy have given him! You wouldn’t even know he had CF if you saw him in person. He is such a happy, sweet, silly, into all things toddler!
In order for him to stay healthy, there is a lot of prep that goes into taking care of his medical needs each and every day. That is why bringing awareness to this disease and raising money for Nash and all those who suffer from CF is so important to our family!
Please consider joining me by walking either in person or virtually and let’s make medical history! Team “Nash Strong” all the way!
Most of all, we would appreciate your continued prayers for Nash, Jessica and TJ as they continue this walk each and every day!
Thank you so much!
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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.