You, Me and Richard Marx All #TakeaBreathforCF

Why did so many people “take a breath for CF” last week? Uniting action and purpose catapults #TakeaBreathforCF, with some help from your favorite celebrities.

June 3, 2016 | 3 min read
Emily Dulcan

You may have noticed a flurry of online activity last weekend in the cystic fibrosis community around the hashtag #TakeaBreathforCF. Singer-songwriter and musician Richard Marx (of pop fame in the '80s and '90s, so there's definitely some fandom happening in my corner) wanted to raise awareness about CF during May's CF Awareness Month with a social media campaign. He knew a simple concept and hashtag would be key for spreading the message on social, and #TakeaBreathforCF was born.

Oh boy, did it take off! After Richard posted the video of himself taking a breath, a wave of other celebrities joined in. Some of my favorites came from Arsenio Hall, Bob Saget, Olivia Newton-John and Blues Traveler. And everyone on the digital team at the Foundation was pumped to see Shania Twain, CeeLo Green and Jane Lynch posting videos as well. 

But, the best part for me was watching the CF community get involved. You posted your own breath videos, and you asked your favorite celebrities and heroes to join in. You thanked the celebrities who had already posted and, without a doubt, brought the cause of curing CF even closer to their hearts.

I've been pondering why this campaign did so well. First, we had lots of great celebrities get on board and, of course, that helps a lot! Second, it was easy to participate: Take a breath and donate.

Finally, and most importantly, I think the concept of a single breath really resonated with everyone. For those of us with healthy lungs, a single deep breath just happens, followed by breath after automatic breath. But for people living with CF, a single breath can be a struggle, painful or nearly impossible -- a monumental effort. Asking people with healthy lungs and people with CF to all take a breath for CF unifies us in action, thought and purpose.

I am grateful for everyone -- famous or not -- who has taken a breath for CF. Let's keep this momentum going, because every breath brings more awareness to the fight against CF. 

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.

Share this article
Get Involved

Emily is the online community events lead at the CF Foundation. She comes to the Foundation after serving for three years as digital director at the Peace Corps. Emily has worked as a digital strategist for nonprofits, agencies and political campaigns, including three years with Organizing for America. In 2006, Emily earned a master's degree in cross-cultural journalism from the Missouri School of Journalism. She loves traveling, reading, exercising, cooking and eating well.

Recent Community Posts
An Unexpected CF Diagnosis
Blog | 5 min read
Reclaiming My Identity After Starting Trikafta
Blog | 8 min read
The Impact of Advocacy Beyond the Hill
Blog | 6 min read