Works by the CF Community 2024

We’re highlighting three creators who are helping raise awareness for cystic fibrosis. They’re voicing the many ways people experience the disease by sharing a part of their life through written and spoken works.

Sept. 3, 2024 | 4 min read
A professional headshot of Sarah Dobson
Sarah Hyndshaw
An adult with CF writing in a journal at an outdoor table
A headshot of Barbara Todd

Barbara Todd

Host, Air of Optimism

Air of Optimism is a six-episode collection of interviews with my incredible friend Bernadette. Bern was born with cystic fibrosis in 1967, when very little was known about the disease. I have been friends with Bern for over 35 years and am constantly in awe of her incredible attitude and drive to survive. In each episode, we walk through a moment of her life including early childhood, becoming a nurse, having a child, and ultimately receiving a lung transplant. We explore her life after transplant and include an incredibly touching interview with Bernadette’s daughter, who is now 24. This podcast is for everyone, including someone with CF, a parent of a child with CF, a child of someone with CF, anyone who has had or may need a transplant, or anyone who loves a story of optimism!


A headshot of Barbara Washburn

Barbara Washburn

Author, My Queen Rox

My Queen Rox is a short but impactful story about my long-distance friendship with Roxy, a woman I met through a phone app who had CF. Through the hardships of her CF journey, we coped by escaping into roleplay texting, where we adventured to locations we could only dream of visiting together. This story is a fun but emotional ride through my experience with Roxy and CF. It shows just how meaningful you can be to someone else, even if you are only a text on a screen.

I had always dreamed of becoming a published author. Roxy, through enduring her own struggles, pushed me to fulfill my dream. She helped me believe in myself and encouraged me to write this book. Through her friendship, I learned how to love without boundaries, let go when I have no control, and always keep my promises. I wrote this book for her and to fulfill her dream of helping others, including me, to overcome their pain, hardships, and loss — specifically those who have CF. She wanted everyone to know just how special and amazing they are, no matter who they are, where they are from, or what they must endure.

My Queen Rox is not only a dedication to an amazing woman with CF, but also our dreams made whole. Per Roxy’s (loving) demand, portions of all proceeds will be donated to the CF Foundation and other amazing organizations.


Ashley Wilson

Ashley Wilson

Author, Beauty Grown From Thorns

Beauty Grown From Thorns is a collection of 65 original poems that brings readers into a new element and light to Ashley Wilson's art. Ashley Wilson is an author and producer residing in Los Angeles. Known for sharing her faith and experiences living with cystic fibrosis online, Ashley wrote this poetry book to bring awareness to cystic fibrosis, inspire, and share words of healing.

“This book has been seven years in the making. Actually, I never imagined these poems would be published. I always thought these words would stay locked away and the key would be thrown out. These pages are filled with excerpts from the heart and are very deep and personal. I wrote these poems during times when I did not know how to process my emotions. Over time, the words I once wrote in the midst of pain grew to become words of strength and healing.

I hope as you read these poems, you can grieve, be inspired, find healing, or even relate, as I have come to learn you are not alone in the raw experiences that life brings.”

Interested in sharing your story? The CF Community Blog wants to hear from you.

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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A professional headshot of Sarah Dobson

Sarah is a communications specialist on the Community Engagement team at the Cystic Fibrosis Foundation. In her role, Sarah supports the marketing and promotion efforts for community programs like community conferences, CF Peer Connect, Community Voice, Tomorrow's Leaders, and Compass. She also manages the Community Blog. In her spare time, Sarah enjoys gardening, reading, and wrangling her pitbull-boxer mix, Beau. She currently lives in Georgia with her husband, an adult with CF. 

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