National Cystic Fibrosis Awareness Month
On National Cystic Fibrosis Awareness Month, we listen louder, learn more, and make sure no one feels invisible.
Why it matters
WELCOME TO MAY
May is National Cystic Fibrosis Awareness Month, a time to support those affected by CF.
THE STORY
Cystic fibrosis (CF) is a progressive genetic disorder that affects the lungs and digestive system, making it difficult for the body to breathe and absorb nutrients. It is caused by mutations in the CFTR gene, which regulates salt and water movement in and out of cells. In the United States, approximately 30,000 individuals are currently living with this chronic illness. As a result, National Cystic Fibrosis Awareness Month, observed every May, plays a pivotal role in raising awareness about the disease and promoting research efforts.
During this month, various organizations, including the Cystic Fibrosis Foundation, work tirelessly to educate the public about CF and its impact on patients and families. Events such as fundraising walks, educational seminars, and community outreach are organized to engage individuals in understanding the challenges faced by those living with cystic fibrosis. Through these initiatives, people become more informed about the importance of early diagnosis and advancements in treatment options.
Moreover, advancements in treatment have significantly improved the quality of life for those with CF. Therapies such as CFTR modulators have transformed the management of the disease, allowing many to lead healthier, more active lives. While these advancements are promising, continuous research and funding are crucial to finding a cure. National Cystic Fibrosis Awareness Month serves as a reminder of the ongoing need for support and advocacy in the fight against this debilitating disease.
Community involvement is essential during this observance, not only to support those affected by CF but also to foster a sense of unity and hope. By participating in local events or sharing information on social media, individuals can contribute to a larger movement dedicated to improving the lives of those living with cystic fibrosis. This May, let us come together to raise awareness, support families, and advocate for a future free from cystic fibrosis.
Awareness is the first step toward change.
WORTH KNOWING
Support CF Research
Donate to organizations dedicated to cystic fibrosis research.
Join a Fundraiser
Participate in walks or runs to raise awareness.
Educate Yourself
Read up on cystic fibrosis and its implications.
Wear Purple
Show your support by wearing purple this May.
AROUND THE WORLD
DID YOU KNOW?!
CF's Genetic Basis
Cystic fibrosis is caused by mutations in the CFTR gene.
Salt and CF
People with CF often have salty sweat due to chloride imbalance.
Lifespan Improvements
Advancements in treatments have increased life expectancy for CF patients.
CF in Newborns
Newborn screening for CF is now standard in many states.
CF Research Funding
The Cystic Fibrosis Foundation invests heavily in research.
Global CF Awareness
Many countries participate in raising awareness for CF.
CF Impact on Families
CF affects not only patients but their families as well.
READ MORE
Breath of Life
A Journey with Cystic Fibrosis
This memoir chronicles the author’s life with CF, highlighting challenges and triumphs.
The Cystic Fibrosis Kit
A Guide for Kids
This book helps children understand cystic fibrosis in a friendly, accessible way.
Living with Cystic Fibrosis
A Comprehensive Guide
An informative resource for families navigating life with CF.
Cystic Fibrosis: New Perspectives
Scientific Insights
A collection of studies on the latest research and treatments for CF.
PAIR IT WITH
Support the CF community.
Work together for awareness.
Cystic fibrosis knows no borders.
Show compassion for those with CF.
Spread the Word
Help raise awareness for cystic fibrosis this May. Share information and support those affected by this disease.
How to celebrate
Small, doable ways to celebrate National Cystic Fibrosis Awareness Month.
- Share one reputable resource with your network.
- Donate to a patient-led organization working on cystic fibrosis awareness.
- Check in on someone you know who's living with it.
- Book the screening or appointment you've been putting off.
- Listen more than you speak.
Celebration ideas by audience
For families
Have the real conversation at the table — stigma-free, no lecture.
For kids
Answer questions honestly and age-appropriately.
For couples
Check in with each other's appointments, screenings, and follow-ups.
At the office
Share vetted resources and encourage people to use their benefits.
At school
Bring in an expert, survivor, or advocate to speak for a class period.
In your community
Run a donation drive, a walk, or a listening session for those affected.
On your own
Reach out to someone you know is living with it. Ask how they're doing for real.
