Join our team and help add tomorrows!
See us on Facebook too!
www.facebook.com/TheJTeamCure/
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. We walk for them.
Josalyn was diagnosed 6 days after birth with Cystic Fibrosis. As parents, our number one concern was to keep her healthy, learn everything we could about CF, and do what we could to help make a difference. That is when "The J Team" was started. If is our way to help create awareness, and help to raise necessary money for research and development to find a cure, and to stop CF from taking those that we love away from us.
The walk in Grand Haven, MI is beautiful, we follow the boardwalk along Lake Michigan and the State Park. There will be water and food available for participants, and every year we have participated the weather has been perfect! In 2023 we raised over $29,000 and this year we are hoping to raise over $30,000! With your help we can get there.
We encourage you to bring your kids, strollers, cameras, and make the day memorable. Great Strides is a fun, family-friendly event whose goal is to raise money, awareness, and support for people with CF and their families.
For those that are going to be joining us for the walk this year, we will once again be selling our "The J Team" T-Shirts to everyone that walks, and the proceeds from those shirts will be donated to the CF Foundation as well. We will be selling them for $15/each, and we will reach out to you directly once you sign up to get sizes. We will also be doing corporate sponoship for the shirts this year as well, so if your company is interested in sponosring, please let us know!
We encourage you to sign up and come walk with us, or if you cannot make it, please consider donating by choosing a team member to donate through, and helping to make a difference and to find a cure for CF.
Thank you very much for your support!
Tony, Laura, Josalyn, Kate and Alex
Connect With Us
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.