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My Great Strides Story

Debra Lenihan

Fundraising for Avon Great Strides

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Debra Lenihan

Team AJ was formed in 1997 in honor of my daughter, Amy, and my son, Jason, both were born with Cystic Fibrosis. 

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.  

Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$1,525
raised of $15,000 goal
 

Achievements

Leader

Team AJ

$1,525

Recent Donations

Christine Tormey$20
Jane Stapleton$65
This donation is in lieu of flowers for Kathleen Kenny,s family. Kathleen s granddaughter Debra lenihan has cystic fibrosis
Mariellen Lenihan$250
In memory of Kathleen Kenny
Daniel OConnell$65
In memory of Kathleen Kenny
Janice Crisci$100
Anonymous
Tin and Deb Lenihan$500
Donation made in memory of Kathleen Kenny RIP
John Lenihan$50
In memory of a great woman, aunt, and CF supporter
Rose Conway$100
Mary Kate Garrett$50
John Ruane
In memory of Kathleen Kenny
Karen Wieman$100
We are so sorry for your loss, Kevan. Sending you love and prayers. Love, The Wieman Family

Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.