Abigail’s Advocates for the Cystic Fibrosis Foundation 2024

Abigail is turning 5!

This past year has been busy, crazy, exciting, and wonderful. Abigail started school!! We were very anxious with her starting school and being around so many other little kiddos, but she has been our Warrior Princess. 2023 was the FIRST year we didn't have ANY HOSPITAL VISITS!!!!

As we look forward to the future and MANY more healthy years, we have to remember what Abigail has overcome. We have experienced an unexpected Cystic Fibrosis diagnosis, a 28-day NICU stay, 8 hospital stays, and quarantine for almost three years. Abigail has done 100’s hours of treatments and taken countless pancreatic enzymes, vitamins, high-fat foods, acid reducers, appetite stimulants, antibiotics, extra salt intake, and more. Even though it isn't always easy, we have watched Abigail grow into an independent, sassy, strong-willed, fearless, funny, stylish little girl who loves to play with her friends, cartwheels, color, and be outside. These last few years have been hard trying to find our new normal, but it has also been nothing short of beautiful. We have learned we have the most supportive friends and family praying for us. Your support has allowed us to learn and grow in parenthood. This year for Abigail’s 5th birthday, we hope to raise over $2,000 for the Cystic Fibrosis Foundation. The month of May is special. It is Cystic Fibrosis Awareness Month and Abigail’s birth month. In honor of Abigail’s birthday, we ask you to wear your Abigail’s Advocates shirt on May 11, 2024. This is ONE day after her birthday and the day of the CFF Great Strides Walk!
The QR code will take you directly to Abigail's Great Strides page!