Committed to Community: Meet the 2017 Impact Grants Program Awardees

As an adult with cystic fibrosis, I know just how powerful and creative the CF community can be. That's why I'm excited to announce the four 2017 Impact Grant awardees who are making a positive impact on the CF community.

Nov. 21, 2017 | 4 min read
Piper Beatty Welsh, J.D., M.P.A.

It's no secret that the cystic fibrosis community is full of great ideas and has an even greater passion for standing together to help each other live fuller, more productive lives. As an adult with CF, I've known for a long time (36 years and counting!) how powerful and creative our community members can be, especially when it comes to finding new ways to serve others. And it is this spirit and drive that the Cystic Fibrosis Foundation seeks to encourage through the Impact Grants program, which offers up to $10,000 to programs designed by and for the CF community.

In 2016, we announced our first round of grants, which were given out to seven inspiring and innovative groups working to meet the needs of people with CF and their families. These grantees set out to make a difference -- from providing private online voice coaching, to family education days, to physical fitness programs. The programs have been so successful that we are renewing all 2016 Impact Grants for an additional year.

Now, we're excited to announce four new and exceptional programs as 2017 Impact Grant awardees. The Foundation is honored to be able to support these organizations in their efforts to provide new opportunities to the CF community.


The Cody Dieruf Benefit Foundation: “We Walk Together” Retreat for Mothers of Children with CF


The Cody Dieruf Foundation's “We Walk Together” program is a three-day retreat for mothers of children with CF that live in Montana, Idaho, and across the country. Retreats offer a safe space for mothers who share a connection through CF to come together for support, education, and community. Focus topics included anxiety and depression, self-care, living through a lung transplant, and offering hope for the future.

“I am a mother who is not alone. This retreat has been a turning point in my life. I am coming to have a better grip and more control of me. I need to take care of me so that I can take care of my child.” - Lanor, mother of a child with CF


CF Society, Inc.: CFS Gazette Newsletter

The CF Society's CFS Gazette Newsletter is written for people with CF of all ages and their families. The Gazette offers news about the latest medical advances and clinical trials, CF-friendly recipes, special profiles featuring community members, columns written by experts in the field of CF, and personal stories. Additionally, the Gazette contains cartoons, jokes, and games as part of its mission to provide people with CF and their families with both information and entertainment, as it emphasizes the old adage that sometimes laughter is the best medicine.


Meghan's Light, Inc.: 65 Wellness Wishes


Meghan's Light 65 Wellness Wishes grants 65 health-focused awards for wellness memberships and activities in and outside the hospital. Recipients are children and adults with CF treated at Boston Children's Hospital, with a percentage reserved for Boston Children's patients living in Western Massachusetts. The target number 65 references "sixty-five roses," a term used since 1965 by young children with cystic fibrosis trying to pronounce the name of their disease. The project honors Meghan's lifelong passion for fitness and supports recipients in incorporating wellness and fitness into their own lives.

“Meghan was able to show others that CF wasn't going to get in the way of her dreams and I hope that I can do the same to a new group of people.” - Jason, adult with CF


Kid Logistics

Kid Logistics, Inc. is a nonprofit organization dedicated to helping kids with CF in Mississippi live healthier, happier lives through exercise and activity. As part of its Kids Busy Living program, the organization funds participation in extracurricular activities such as summer camps and sports programs. They also provide educational tools for program providers about the special needs of children with CF and provide products, such as hand sanitizer and tissues, to aid in infection control.

Congratulations again to all the grantees!

Note: Applications for the 2018 Impact Grants Program will be available in early spring. Please visit or email for more information.

This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited to people with CF and their families, belong solely to the blog post author and do not represent those of the Cystic Fibrosis Foundation, unless explicitly stated. In addition, the site is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.

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Get Involved | About the CF Foundation

Piper  was first diagnosed with CF at 6 weeks old in 1981, and has since been the survivor of two double-lung transplants. Piper attended Emory University, received her J.D. from Columbia University Law School and then went on to earn her master's in public administration from New York University's Wagner School of Public Service. She is the owner and author of the popular CF and transplant blog, A Matter of Life and Breath, and lives in Colo. with her husband and puppy.

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