Breathe for Olivia was founded in 2009, one year after Olivia was diagnosed with Cystic Fibrosis. Our organization is made up of family and friends of Olivia who raise money and awareness, to benefit those living with Cystic Fibrosis and their families, through the Cystic Fibrosis Foundation. We do this through multiple fundraising events throughout the year. As parents, we do our best to help keep our daughter healthy by making sure she does her treatments and takes her medications. We assist her to every appointment and participate in her care treatment plans by making sure every decision made is the best choice for Olivia. We openly communicate with her and provide her with unconditional love and support. But as parents, we want to do more. We want to find the CURE for cystic fibrosis and free our daughter of this life long complicated disease. With the support of family and friends Breathe for Olivia came to life at a local 2009 Great Strides event. Together our family and friends and even complete strangers, made the commitment to walk with us and help raise funds for CF. But that’s not all they did, they provided us with an army full of people who showered us with encouragement, support, friendship, resources, faith, and never ending love. Each year team Breathe for Olivia grows bigger and stronger. In 2014, Breathe for Olivia became a qualified 501(c)(3) organization. Our goal is to increase the awareness of Cystic Fibrosis and help to raise funds that will be used for research to find the CURE. Team Breathe for Olivia wants to thank everyone for visiting this site and hope you consider joining our army in the fight against Cystic Fibrosis. Make sure to follow us on social media though Twitter, Instagram, Facebook, and Google+ for all of our latest fundraising activities and events. Thank you for your continued support in bringing us one step closer to finding a CURE! |
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