This is the fifth aniversary of Team MAXpedition! Thank you over and over to everyone that continues to support the CF Foundation and Team MAXpedition each year.
For anyone not familiar with why this is so important to us: Our son Max (4yo) was diagnosed with Cystic Fibrosis 2 weeks after birth. He spends over an hour doing respiratory therapy treatments and takes an insane amount of medications each day (~20 pills, 2 nebulizers, 3 liquid meds, and Orkambi). CF is considered a rare genetic disorder so we rely heavily on research that is funded by the Cystic Fibrosis Foundation to search for effective treatments and one day a cure.
Max is one of approximately of 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. We walk for them. Will you join us? To become a member of our team, just click on the "Join our Team" button. From there you can make a donation and start your fundraising.
By becoming a member and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
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.