Breathe With Me

Breathe With Me is a social media community group trying to raise funds for cystic fibrosis research by focusing on outreach to the non-CF community. The group leads its campaigns by asking the general public to “try breathing like a person with cystic fibrosis.”

Condition Awareness & Advocacy

Here is a list of conditions this partner raises awareness and advocacy for:

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Patient Worthy Posts on Cystic Fibrosis

Woman Gets a Flu Shot to Pay Tribute to Her Friend with Cystic Fibrosis

Sometimes in moments of tragedy, there is a bright silver lining that helps us learn, and that’s exactly what Amber Briggle was aiming to do.

Is the FDA Approving Drugs too Quickly?

At times there seems to be no happy medium in life. A recent article in Bloomberg claims that the speed at which the FDA is

DISORDER: The Rare Disease Film Festival — When Art Becomes Heart

The holiday season and end of the year/decade is upon us! As schedules slow down and we begin to reflect, I too began to take

These Two Canadian Brothers Have Cystic Fibrosis, But Only One Has Access to Effective Treatment

According to a story from globalnews.ca, Andre and Joshua Laroque are nine and seven years old respectively. The brothers, being close in age, spend a

Artist Finds Inspiration in his Cystic Fibrosis

Many artists draw inspiration from events in their lives. Dylan Mortimer is no exception, as his art is inspired by his cystic fibrosis. He

A Recent Discovery Could Help Cystic Fibrosis Patients Avoid Lung Transplants

According to a story from thejournal.ie, a recent study has discovered a new method for bringing down inflammation in cystic fibrosis. The study authors have