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Order the 2022-2023 Portraits of Cystic Fibrosis calendar today!

When I published the first Portraits of Cystic Fibrosis calendar (PCFC) 18 years ago, it was to let the world know we existed. I wanted people to see the beautiful faces of the people with Cystic Fibrosis. It was also to inspire others with the disease, their families, and friends. The PCFC is a constant reminder of who the CF community is through the years; we’re babies, adults, college students, scientists, families, athletes, and the CF support community. This year, as we continue to make it through the pandemic together, I was reminded how strong we are as individuals and as a community.

The Portraits of Cystic Fibrosis 2022-23 calendar showcases many of the smaller foundations throughout the United States and Canada & the wonderful CF warriors who run them. The purpose is to show our reasons why. I have two daughters (Molly, 26 years old, and Emily, 24 years old) with Cystic Fibrosis (CF). I started the Bonnell Foundation to help others. I knew the need and wanted to help fill it. I hope that you enjoy each person’s story from the perspective of the person with CF. We all support the CF community in different ways, but we advocate together.

I am grateful to my friends (who are my family) in this calendar who do so much to make the world a better place for people with CF.

The Portraits of Cystic Fibrosis calendar is dedicated to everyone with CF, their caregivers, and anyone in the CF community.

We’re grateful to all the pharmaceutical companies working on drugs to correct the underlying condition of this terrible disease. There is much to be thankful for and much work to do.

$25.00

This is a gorgeous black and white, 15 month calendar that showcases many of the smaller foundations throughout the United States and Canada & the wonderful CF warriors who run them. The purpose is to show our reasons why. I have two daughters (Molly, 26 years old, and Emily, 24 years old) with Cystic Fibrosis (CF). I started the Bonnell Foundation to help others. I knew the need and wanted to help fill it. I hope that you enjoy each person’s story from the perspective of the person with CF. We all support the CF community in different ways, but we advocate together.