65 LaRosas - Walk with us and/or support us

65 LaRosas

Fundraising for Cincinnati Great Strides

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65 LaRosas

We are now well over 30 years participating in Great Strides For CF. It is our premier fundraiser each year and we hope this year will be the same. Our family appreciates each and every person who prays for us and supports us. Tre will be 31 by this year's event and got engaged in February 2025 to a wonderful person who we cherish and are blessed with. Her name is Jessica Maria Burns. We wholeheartedly believe Alyssa brought them together as one of her best Lysswinks so far and is our guardian angel as we move through life. We can't wait to celebrate their marriage next year. In the meantime, we invite you to take part in Great Strides by joining our team, walking and/or supporting us. We promise, you belong here! This event is always a rewarding, fun-filled day where you can help advance the care and research needed to cure cystic fibrosis. By walking with us, you'll enjoy not only the natural camaraderie (yes, lots of laughter!), but the important impact we are making together.



While the CF Foundation has made incredible progress, we still need a cure because there is still much unknown about the future of our loved ones. The fear and anxiety continues. Plus, we still have lots of individuals who don't benefit from the current treatments and we need more. This will require time, funding, and persistence \u2013 but with you on our team \u2013 we are ready to go the distance.



Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?



Love, Frank, Sue, Alyssa, Tre, Jessica, and our pups

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$100
raised of $5,000 goal
 

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4 Participants

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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.