Max was diagnosed with Cystic Fibrosis when he was 10 days old. he went from a healthy 6lb baby to a very fragile 5lb baby very quickly. when the dr called and told me they needed to speak to me in person, I knew what was coming. I knew I was a carrier for CF I knew Brian was too. but we had 3 healthy kids already and I knew there was a 75% chance that a new baby would be born healthy as well. 75% are pretty great odds. Unfortunately Max wasn’t as lucky as my other 3 children. When he was 10 days old he started with medications.
This beautiful boy is the light of my life. I need your help to make his life a long and healthy one.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. 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.