Harper’s Hope for Cystic Fibrosis 2024-Relaunch

Eleven years ago, our world turned upside down when we found out our newborn, Harper, had something called Cystic Fibrosis. At the time, we knew very little about this disease that would, in many ways, dictate the kind of parents we would learn to become. We have had many ups and downs through the years, but many of our highest moments in this medical journey have been the direct result of the work done by the Cystic Fibrosis Foundation.
While Harper is not able to sit across the table from another CF fighter to share experiences and encouragement, we as a family have grown and been strengthened by the people God has placed in our lives in spite of this disease through the CF Foundation.
We would like to invite you to share in this fight with us.
Your shirt purchase donated funds to the research that creates medicines like Trikafta for people like Harper. Trikafta has changed Harper’s life for the better. She is stronger and healthier than she has ever been. However, we must keep fighting, because there are still too many people who need tot he fighting chance that Trikafta has given Harper.
Will you help us?