Hello! My name is Samantha and I am 22 years old and have cystic fibrosis. I had a rough start to life being sick all the time. I left high school from how sick I got. It wasn’t until my pediatric CF clinic at rush university figured it out and practically saved me. They diagnosed me with cystic fibrosis in my teens. Once I turned 18, I moved to the adult cystic fibrosis team. I am now seen at the university of Chicago and get the best care. I am now healthy, have a full time job and got my own car which is a Tesla! I still do treatments daily. Vest, nebulizers, inhalers and sinus rinses along with sinus sprays. I spend about an hour morning and night, sometimes more. My sinuses are very diseased with cystic fibrosis and required sinus surgery. We are walking for a cure. It would be amazing to completely get my life back and no more treatments. Even with a full time job and all my accomplishments, I am very tired. It’s very exhausting. I qualify for no big CF drugs like trikafta. I hope in the future my genes will qualify me.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.