08/30/2021
This beach~going~beauty turned 20 years old this month!
Olivia is thriving, in good health, and enjoying the best life has to offer!
The Breathe for Olivia foundation has been going strong for many years, raising hundreds of thousands of dollars for the Cystic Fibrosis Foundation, and giving to individuals and families personally affected by this disease.
Although we will never stop being advocates for Cystic Fibrosis, the time has come that we shut our doors and spend some time slowing down and enjoy life, instead of focusing our time on fundraising all year long.
This does NOT mean that we want you to stop supporting and donating to this amazing foundation, but instead please donate and support those living with Cystic Fibrosis through here:
https://www.cff.org/CentralPA/
We can not THANK our supporters enough for all your kindness, gratitude, donations, friendships, opportunities, and LOVE you have shown Olivia, our family, and our foundation!
I hope you realize what a difference you made in our lives and in EVERYONES lives that live with Cystic Fibrosis.
Blessings to you all đź’śđź’śđź’ś
THANK YOU!