Having two children born with Cystic Fibrosis is a cruelty I would wish on no mother.
My son Mark died young. Fortunately, my daughter Michelle has benefited from medical advancements, but her struggle remains intense and ongoing. My “story” is certainly one of anguish and despair. But, surprisingly, the decades of battle with this insidious disease have also embellished my life with faith, promise, and an endless appreciation of so many who’ve stood by in support. To them I owe a debt which I’ll never be able to repay but for which I’m eternally grateful.
From the beginning, the Cystic Fibrosis Foundation has fought the good fight alongside me. I can’t emphasize enough their selfless potential for bringing our fight to a liberating conclusion. Please join me in their effort.
Marty—Michelle’s Mom
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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.