My niece, Kailyn has Cystic Fibrosis. She is 11 years old. Breathing treatment, meds, doctor appointments, blood draws, throat cultures and other medical test are all still part of her life. She continues to grow and is becoming a caring, loving and beautiful young lady that likes having fun, fishing and all things family.
What is Cystic Fibrosis? CF is a genetic, life shortening lung disease that makes it difficult to breathe.
Because of your support, progress is being made with new treatments, therapies and drugs. Her hope and mine is a cure will be found. Every year we get closer!
Would you join me again and help us fight to find a cure? I am asking for your support to keep our hope alive. Thank you!
If this your first time, PLEASE help us get one breathe closer to a cure.
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift is 100-percent tax deductible.
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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.