Thank you for visiting my page. This is our the 23rd year participating in the Great Strides campaign aimed at finding the cure for cystic fibrosis.
Change is something we have learned to live with. In 2017, Danny received a port and began daily IV infusions, we had to re-arrange all schedules in order to incorporate his new medical regiment. In 2018, we began the vetting process for a lung transplant, visited different hospitals for extended stays and testing. In 2019, the big move to North Carolina where Danny was accepted for listing at UNC. In August of 2019, Danny was admitted into the hospital with pneumonia and on September 25th 2019, he passed away.
We plan to continue the fight we started together to find an END to this horrific disease. We will continue to do this the same way Danny lived his life, FULL THROTLE!!!
This years walk will be held at Zoo Miami on April 6th. You can donate directly on this page. You can create your team under Team Running with Danny and have others join you in this effort.
Please share this with friends, family and collogues and help us continue to raise funds so that others with cf do not need to go through what Danny did.
You can visit our website www.runningwithdanny.org to read more about Danny and his life as well as follow us on social media on the Running with Danny pages on Facebook, Instagram and Twitter.
Our family thanks you for the continued support and generosity you have shown us throughout the years. Not only are we continuing the fight to raise life saving funds for medical research but will be celebrating Danny’s fight and keeping his legacy alive.
Thank you and God Bless!!!
Mike, Mari, Joanna, Michael and Danny
Please email us with any questions @ mike.runningwithdanny@gmail.com
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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.