Jenn Scheetz
Every person living with Cystic Fibrosis has a story as unique as they are; Owen is no exception. But unique as they are, they all have one thing in common - a life shortening disease that currently has no cure. While advancements in Owen's young 17 years have been outstanding people are still dying way too young.
Owen is doing extremely well thanks to the advances made in treatments and therapies developed/funded by the Cystic Fibrosis Foundation. Hard to believe but he will be finishing his junior year of high school in June and turn 18 in August! He stays busy with soccer, lacrosse, and video games. :)
As we have for the past 15 years, our family is committed to walking at Great Strides Lancaster to raise funds and awareness for CF. We hope you can join us! Please use the link to join our team or make a donation to support a truly life changing organization!
Owen is doing extremely well thanks to the advances made in treatments and therapies developed/funded by the Cystic Fibrosis Foundation. Hard to believe but he will be finishing his junior year of high school in June and turn 18 in August! He stays busy with soccer, lacrosse, and video games. :)
As we have for the past 15 years, our family is committed to walking at Great Strides Lancaster to raise funds and awareness for CF. We hope you can join us! Please use the link to join our team or make a donation to support a truly life changing organization!
Comments