PLEASE Join TEAM RUN FOR ROSES and help fund a CURE!
It takes hours of treatments and handfuls of meds each day for those with CF to 'just breathe'. We walk / run for them because WE CAN. WILLYOU JOIN US?
Dear Friends,
If you have a loved one or know of someone who lives with CF or if you are just learning about CF, we are so appreciative that you are visiting our page!
Our family has been very committed to fighting for a cure for CF for over 17 years! Our daughter has become involved with a number of projects with the CFF and mental health and has been a CF Peer Mentor. In recent years, Katie worked with a group of researchers, adults with CF and parents of individuals with CF to review community and medical provider surveys to assess CF mental health research priorities. Katie has also been invited to join a few upcoming research projects, pending funding, related to mental screenings and evaluations, as well as invited to be one of the founding members for a mental health research group, PRIME: Prioritizing Research in Mental Health, to help address some of the key research questions around mental health and CF.
We humbly ask for your help on this journey. WE NEED YOU to PLEASE join us and help make life a little easier for those with CF by spreading awareness and raising funds that will go towards development of better treatments, meds and fund a CURE FOR CF.
There are approximately 40,000 Americans living with CF and 10 million who are carriers of one CF gene. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe.
By joining Team RUN FOR ROSES TODAY and making a donation you are helping add more healthier tomorrows for so many.
Your gift is 100% tax deductible.
THANK YOU for joining Team Run for Roses and "walking" with us on our PATH TO A CURE!
PLEASE share our story with your friends and family.
With warmest gratitude,
The Caul Family
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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.