Cystic Fibrosis Foundation · [email protected]

March 26, 2025 at 2:31 PM

Infection Research Spotlight

Read the latest news on detection, phage research March Update Research into infections continues to be a top priority for the Cystic Fibrosis Foundation. Chronic infections and drug-resistant bacteria remain key challenges — even for those who take modulators, such as Trikafta.   Research In…

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  Cystic Fibrosis Foundation · [email protected]

March 20, 2025 at 8:20 PM

Together: a Community Update

Get to know our new National Volunteer Advocacy Committee co-chairs March 20, 2025  Meet Our New National Volunteer Advocacy Committee Co-Chairs    Kirk Astroth, an adult with cystic fibrosis, and Brittney Householder, a godmother to a teen with CF, will lead our volunteer advocacy effort…

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  Cystic Fibrosis Foundation · [email protected]

March 18, 2025 at 10:55 AM

Register now for our genetic therapy research webinar

Just 2 days out! This Thursday, March 20     CF Foundation Supporter, genetic therapies, including RNA therapy and gene therapy, could potentially work for every person with cystic fibrosis — even those who can't benefit from CFTR modulators.   Join us this Thursday, March 20 at 7 p.m. ET…

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  Cystic Fibrosis Foundation · [email protected]

March 6, 2025 at 9:20 PM

Together: a Community Update

Register for our upcoming research webinar March 6, 2025  Ask Your Questions About Genetic Therapy Research Genetic therapies, including RNA therapy and gene therapy, could potentially work for any person with cystic fibrosis, including people with nonsense and rare mutations. If you have…

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  Cystic Fibrosis Foundation · [email protected]

February 27, 2025 at 4:40 PM

Bring your idea to life — join our Impact Grants webinar!

Learn how to secure up to $10,00 for your CF-focused program Have an idea that could empower people with cystic fibrosis or their families? Join us for an informational webinar March 13 at 3 p.m. EST to learn more about the Impact Grants application process. During this webinar, CF Foundat…

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  Cystic Fibrosis Foundation · [email protected]

February 20, 2025 at 9:11 PM

Together: a Community Update

Read our response to NIH funding cuts February 20, 2025  CF Foundation Responds to NIH Funding Cuts  We oppose the decision by the National Institutes of Health (NIH) to cut the reimbursement rate for indirect costs — funding that covers expenses such as equipment and lab space. The rapid…

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  Mary Dwight - CF Foundation · [email protected]

February 20, 2025 at 11:56 AM

Advocate, we need your voice now

Tell Congress to protect programs that support people with CF Advocate,   Today, volunteers from across the country are participating in the 18th annual March on the Hill to deliver a timely message: we need Congress to protect the National Institutes of Health (NIH), the U.S. Food and Drug…

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  Cystic Fibrosis Foundation · [email protected]

February 14, 2025 at 2:16 PM

Show your love every month – join the 65 Roses Club

💕 Your support makes our hearts full 💕 Friend, as a dedicated member of the cystic fibrosis community, we invite you to become part of something special.   The 65 Roses® Club is a group of individuals who are committed to making an impact for people with CF through monthly giving.   As a mon…

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  Cystic Fibrosis Foundation · [email protected]

February 12, 2025 at 9:11 PM

Research and care update: January/February edition

Our latest must-read developments January/February UpdateHighlights New modulator Alyftrek approved Study results on Trikafta and GI symptomsFunding for research into lung transplant complication CF Foundation Responds to NIH Funding Cuts The CF Foundation is opposed to the recent deci…

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  Cystic Fibrosis Foundation · [email protected]

February 6, 2025 at 9:18 PM

Together: a Community Update

Take our brief survey to share your insights February 6, 2025  Share Your Insights on Digestive System Issues and Aging With Cystic Fibrosis   As the CF Foundation continues work to support its next strategic plan, we have identified two areas of community concern to further explore: digest…

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  Cystic Fibrosis Foundation · [email protected]

January 23, 2025 at 9:12 PM

Together: a Community Update

BreatheCon is February 7-8! January 23, 2025  Register for BreatheCon 2025   Whether you were diagnosed with cystic fibrosis at birth or recently received a diagnosis, there’s a spot for you at BreatheCon! This two-day virtual experience offers opportunities to share stories and perspective…

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  Cystic Fibrosis Foundation · [email protected]

January 21, 2025 at 4:29 PM

Our National Annual Meeting is tomorrow night

Don't miss your chance to register!   You're invited to the Cystic Fibrosis Foundation’s National Annual Meeting Wednesday, January 22, 2025 8 p.m. ET / 5 p.m. PT  LEARN HOW WE'RE SHAPING THE FUTURE Time is running out to secure your spot for this vital conversation with Foundation lead…

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  David Elin - CF Foundation · [email protected]

January 10, 2025 at 2:02 PM

Stay informed: Join us for an advocacy community update

A look at what's ahead for CF advocacy in 2025 Hello Advocate,    You’re invited to join us Tuesday, January 14 at 2 p.m. EST for a CF advocacy community update. We are excited to share our 2025 advocacy priorities including how we plan to work with the 119th Congress and engage with CF adv…

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  Cystic Fibrosis Foundation · [email protected]

January 9, 2025 at 9:18 PM

Together: a Community Update

The FDA has approved a new triple-combination modulator January 9, 2025  FDA Approves New, Once-a-Day CFTR Modulator for People With Cystic Fibrosis  The FDA has approved a new triple-combination modulator, Alyftrek, for people with cystic fibrosis ages 6 years and older who have a mutation…

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  Cystic Fibrosis Foundation · [email protected]

January 7, 2025 at 4:36 PM

Don't miss Q&A with CF Foundation leaders!

Save your spot now for our National Annual Meeting You are invited to the Cystic Fibrosis Foundation’s National Annual Meeting Wednesday, January 22, 2025 8 p.m. ET / 5 p.m. PT  REGISTER NOW!   President and CEO Michael Boyle, MD, and Executive Vice President and Chief Operating and Finan…

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  Cystic Fibrosis Foundation · [email protected]

January 1, 2025 at 2:16 AM

This is your final chance to give in 2024

Don’t miss your opportunity to give. Let’s cure cystic fibrosis Time is nearly up. Can you help us make investments in the most promising CF science toward a cure for all people with cystic fibrosis? COUNT ME IN Every day without a cure is one day too many for people who live with this d…

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  Cystic Fibrosis Foundation · [email protected]

December 31, 2024 at 8:16 PM

Time is running out

Don’t wait — your support is critical in the fight against CF CF Foundation Supporter, every person with cystic fibrosis has a unique journey. While we’ve made significant advances with more therapies than ever before, people with CF need more breakthroughs and ultimately, a cure.   Don't mis…

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  Cystic Fibrosis Foundation · [email protected]

December 31, 2024 at 1:17 PM

Every day without a cure is one too many

Help drive critical research forward — make your gift today As the year ends, we reflect on the progress we’ve achieved together, while recognizing how much more we need to do. Your support is needed today to help cure cystic fibrosis.   Every day without a cure is one day too many for peop…

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  Cystic Fibrosis Foundation · [email protected]

December 30, 2024 at 4:25 PM

Working together for a future without CF

A special message from our Senior VP and Chief Development Officer Dear CF Foundation Supporter,   Reflecting on the past year, I am struck by how much we have achieved together for people living with cystic fibrosis in advancing our pursuit of a cure, excellent care, and community connection…

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  Cystic Fibrosis Foundation · [email protected]

December 27, 2024 at 4:10 PM

CF doesn’t wait. Neither can Emilee.

Your support is vital for our success Emilee Pehrson, a 44-year-old with cystic fibrosis, was first hospitalized when she was 15.   “At the time, it felt like the beginning of the end,” she said. “It meant no matter if I did everything perfectly, CF was still going to affect my life.” MAKE…

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  Mike Boyle, Cystic Fibrosis Foundation · [email protected]

December 26, 2024 at 8:59 PM

Hallmarks of excellence in 2024

A message from our President and Chief Executive Officer Dear Friend,   This year, we continued to transform all areas of our work to help people with cystic fibrosis. Here are some exciting highlights that community members like you made possible. I could not be more grateful, and I hope you…

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  Cystic Fibrosis Foundation · [email protected]

December 19, 2024 at 4:15 PM

Join us for our National Annual Meeting!

Don’t miss this opportunity to ask CF Foundation leadership your questions You are invited to the Cystic Fibrosis Foundation’s 2025 National Annual Meeting  Wednesday, January 22 at 8 p.m. ET/5 p.m. PT  RESERVE YOUR SPOT TODAY Join us for an inspiring conversation with Michael Boyle, MD, P…

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  Cystic Fibrosis Foundation · [email protected]

December 18, 2024 at 6:06 PM

Research and care update: December edition

Our latest must-read developments December UpdateFeatured This Month: New funding for potential gene editing therapy  Anti-infective enters Phase 2 trial New daily care check-in tool  Foundation Funds Development of Gene Editing Therapy  We have agreed to invest up to $15 million in ReCod…

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  Cystic Fibrosis Foundation · [email protected]

December 12, 2024 at 9:23 PM

Together: a Community Update

Our latest CF research update December 12, 2024  CF Research Update The Cystic Fibrosis Foundation has agreed to invest up to $15 million in ReCode Therapeutics to fund the development of a gene editing therapy for people with CF.     Read the announcement »   COST-CF Survey Results…

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  Cystic Fibrosis Foundation · [email protected]

December 11, 2024 at 7:05 PM

Thank you for sharing your experience with health care costs

Read the results from the 2024 cost burden survey Earlier this year, the Cystic Fibrosis Foundation and Dartmouth College, asked you to share your experiences with health care costs and how they may impact you and your family. You generously shared your experiences, and the results are now avai…

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  Cystic Fibrosis Foundation · [email protected]

December 10, 2024 at 8:27 PM

You're the key to a cure

Make a difference this holiday season Joseph Rosano, a pharmacist from Connecticut, has no personal connection to cystic fibrosis.   However, after being nominated for Connecticut’s Finest, an event hosted by the CF Foundation that recognizes outstanding professionals, he felt compelled to d…

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  Cystic Fibrosis Foundation · [email protected]

December 4, 2024 at 5:24 PM

GivingTuesday has ended, but our work has not

Make an impact by donating now The strength and support of the cystic fibrosis community continues to amaze us.   We reached our GivingTuesday goal, and thanks to our supporters and the generosity of the Stremick family, we raised critical funds needed to advance CF research and improve the …

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  Cystic Fibrosis Foundation · [email protected]

December 4, 2024 at 12:18 AM

GivingTuesday is almost over ...

Lock in your donation before midnight CF Foundation Supporter, GivingTuesday is almost over — but it’s not too late to show your support for the cystic fibrosis community. MAKE YOUR GIVINGTUESDAY GIFT People with CF, like Amanda, continue to face significant challenges.   “At 27, I mad…

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  Cystic Fibrosis Foundation · [email protected]

December 3, 2024 at 7:16 PM

We need your support this GivingTuesday

Help us unlock the match! This GivingTuesday, your donation will have double the impact, thanks to a $250,000 matching gift from the Stremick family. Your matched donation lays the foundation for tomorrow’s breakthroughs and helps ensure we can continue to support high-quality, specialized c…

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  Cystic Fibrosis Foundation · [email protected]

December 3, 2024 at 12:24 PM

2X the impact for GivingTuesday

Children like Bradley are counting on YOU Today is GivingTuesday and we are counting on YOU to double the impact for people with cystic fibrosis. Thanks to the Stremick family, your donation will be matched, dollar-for-dollar up to $250,000. DOUBLE YOUR GIFT While innovative treatments h…

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  Cystic Fibrosis Foundation · [email protected]

December 2, 2024 at 4:30 PM

Our GivingTuesday match starts TODAY!

Donate now for DOUBLE the impact Tomorrow is GivingTuesday, and we are counting on YOU to bring us closer to a cure for cystic fibrosis. Thanks to the Stremick family, donations starting today will be matched, dollar-for-dollar, up to $250,000. You can make twice the impact for all people wi…

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  Mary Dwight, CF Foundation · [email protected]

November 21, 2024 at 12:37 AM

The work ahead: What this election means for CF policy

Our priorities from today on As Washington and state governments prepare for leadership changes in January, the Cystic Fibrosis Foundation remains guided by one principle: ensuring that people with CF have the opportunity to live long, fulfilling lives. We continue to engage and educate polic…

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  Lou & Nancy Stremick, CF Foundation · [email protected]

November 19, 2024 at 4:21 PM

Stand with us this GivingTuesday

Your support is critical as we work to cure CF Dear Friend,   We are Lou and Nancy Stremick, grandparents to Ella, a 19-year-old (adult!) who has cystic fibrosis. Like all grandparents, Ella and all our grandchildren mean the world to us, and we would do absolutely anything for them. With Gi…

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  Cystic Fibrosis Foundation · [email protected]

November 14, 2024 at 9:14 PM

Together: a Community Update

GivingTuesday is just two weeks away! November 14, 2024  Save the Date for GivingTuesday  GivingTuesday is just two weeks away, and we have exciting news! Starting Monday, December 2, your donation will be matched, dollar-for-dollar, up to $250,000 thanks to Lou and Nancy Stremick, whose 19…

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  Cystic Fibrosis Foundation · [email protected]

November 11, 2024 at 4:02 PM

You're invited to our NACFC Q+A

Join us tomorrow! Join our NACFC Live Event! Every year, the North American Cystic Fibrosis Conference brings together thousands of scientists, clinicians, and caregivers from around the world to discuss the latest advances in cystic fibrosis research, drug development, and care. Tomorrow, dur…

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  David Elin - CF Foundation · [email protected]

November 4, 2024 at 2:19 PM

Tomorrow is Election Day

Are you ready to vote? CF Foundation Supporter,    Election Day is tomorrow, November 5! As you prepare to make your voice heard, please take a minute to confirm your plan to vote based on your state’s requirements and processes. CONFIRM YOUR VOTER REGISTRATION Voting is an important way…

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  Cystic Fibrosis Foundation · [email protected]

October 31, 2024 at 8:13 PM

Together: a Community Update

Register for our live NACFC highlights webinar November 12 October 31, 2024  Join our Live NACFC Highlights Event with Q&A Interested in learning about the latest cystic fibrosis research and care highlights from the North American Cystic Fibrosis Conference? Join us live, November 12 a…

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  Cystic Fibrosis Foundation · [email protected]

October 25, 2024 at 1:14 PM

Now live! NACFC 2024 recordings now available

Watch on YouTube NACFC Recordings Now on YouTube Recordings from this year’s North American Cystic Fibrosis Conference are now available on YouTube. Hear CF professionals from across the globe share the latest in cystic fibrosis research, drug development, and care during plenaries, symposia, …

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  Cystic Fibrosis Foundation · [email protected]

October 23, 2024 at 7:16 PM

Research and care update: October edition

Our latest must-read developments October UpdateFeatured This Month: Efforts to improve newborn screening “Bionic Pancreas” study enrollingNew mental health study for children Join Our Live NACFC Highlights Webinar Interested in learning about the latest cystic fibrosis research and care …

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  Cystic Fibrosis Foundation · [email protected]

October 17, 2024 at 8:13 PM

Together: a Community Update

ROSE UP is just 1 week away - Register now! October 17, 2024  ROSE UP to Help Cure CF ROSE UP is celebrating its fifth anniversary, and the big day is one week away! It’s not too late to register, choose an activity, and raise funds to show your support for everyone living with cystic fibro…

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  Cystic Fibrosis Foundation · [email protected]

October 3, 2024 at 8:21 PM

Together: a Community Update

Submit your original artwork for our BreatheCon art contest October 3, 2024  Enter our BreatheCon Art Contest    Adults with cystic fibrosis: Do you want an opportunity to see your artwork featured on our 2025 BreatheCon promotional and event materials? Submit your original artwork for our …

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  Elizabeth Holden, CF Foundation · [email protected]

October 1, 2024 at 5:02 PM

Advocacy in Action: We're on a roll

The impact of your voice   Preparing for the 2024 General Elections The Cystic Fibrosis Foundation believes in empowering our community to advocate for the needs of people with cystic fibrosis. This includes providing nonpartisan tools to help enable the CF community to exercise their right…

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  Cystic Fibrosis Foundation · [email protected]

September 30, 2024 at 7:21 PM

Your NACFC recap is here

Catch up on the highlights At this year’s North American Cystic Fibrosis Conference (NACFC), scientists, clinicians, and caregivers from around the world came together to discuss the latest advances in cystic fibrosis research, drug development, and care. In case you missed them, you can cat…

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  Cystic Fibrosis Foundation · [email protected]

September 25, 2024 at 2:01 PM

NACFC starts tomorrow!

Don't miss out - register today The North American Cystic Fibrosis Conference (NACFC) starts tomorrow! There's still time to join us virtually to hear the latest advances in cystic fibrosis research, drug development, and care.   Register now to join the virtual NACFC platform to watch the …

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  Cystic Fibrosis Foundation · [email protected]

September 19, 2024 at 8:17 PM

Together: a Community Update

Help guide the Foundation's work in the years ahead September 19, 2024  Help Inform the Foundation’s Priorities  To continue accelerating toward our mission to cure cystic fibrosis and provide all people with CF the opportunity to live long, fulfilling lives, the Foundation is developing ou…

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  Mary Dwight - CF Foundation · [email protected]

September 17, 2024 at 11:17 AM

It’s National Voter Registration Day

Resources to help you cast your ballot Dear CF Foundation Supporter,    Today is National Voter Registration Day, the nation's largest nonpartisan civic holiday dedicated to celebrating our democracy, and the CF Foundation is celebrating by encouraging the cystic fibrosis community to registe…

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  Cystic Fibrosis Foundation · [email protected]

September 12, 2024 at 1:06 PM

NACFC is just two weeks away!

Join us online September 26-28 Don't miss out! Just two weeks until the North American Cystic Fibrosis Conference (NACFC) kicks off — save your virtual seat now to join us online September 26-28! RESERVE YOUR SPOT This annual meeting brings together scientists, clinicians, and caregivers…

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  Cystic Fibrosis Foundation · [email protected]

September 5, 2024 at 8:15 PM

Together: a Community Update

ROSE UP is October 24 September 5, 2024  How Will You ROSE UP? ROSE UP, a fundraising event that brings the entire cystic fibrosis community together to get creative and advance the mission of the Foundation, is October 24! You can choose any activity to ROSE UP — whether it’s sports, bakin…

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  Cystic Fibrosis Foundation · [email protected]

August 22, 2024 at 8:17 PM

Together: a Community Update

Register for the North American Cystic Fibrosis Conference (NACFC) August 22, 2024  Virtual Registration Now Open for the North American Cystic Fibrosis Conference (NACFC) Join us online September 26-28 to hear the latest advancements in cystic fibrosis research, drug development, and care …

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  Cystic Fibrosis Foundation · [email protected]

August 15, 2024 at 8:01 PM

NACFC live event registration now open!

Join us online September 26-28 The North American Cystic Fibrosis Conference (NACFC) is back September 26-28!   Save your virtual seat now to hear the latest advances in cystic fibrosis research, drug development, and care during three plenaries, as well as six sessions prioritized and chos…

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