04/22/2023
🫁💜Be BRAVE, Be STRONG, BE A WARRIOR💜🫁
To be one of the toughest around living with such a rare diagnoses means you are each one of those three things and so so much more. Cystic Fibrosis effects roughly 70,000 worldwide, that number seems rare, until you are lucky enough to personally know TWO of those badass WARRIORS. Simon and Abel have been fighters from the beginning and this fight hasn’t been one they have or will ever have to fight alone. The love and support coming from their parents, Krista and Jake and their sweet baby sister, Hallie is enough to MOVE MOUNTAINS. By the grace of God they have remained asymptomatic and we pray they always stay that way.
Seeing these two boys be the toughest they can be is such an inspiration. In support of all our warriors and their families that fight each day and Cystic Fibrosis month coming up in May, we are launching a fundraiser and need your help! We will be selling locally handmade earrings with varying purples as the primary color to continue showing CF support! If earrings are not for you, or someone you know but you’d still like to donate, contact the CF momma, Krista Chenoweth, directly or do your own research and pick your favorite CF Charity.
Stay tuned and be on the lookout for our post coming soon with information regarding ordering and designs that will be available!
Stay Salty Friends! 💜
