Cystic Fibrosis Foundation - Connecticut Chapter

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Cystic Fibrosis Foundation - Connecticut Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis.

The Connecticut Chapter is helping to advance the Cystic Fibrosis Foundation’s mission to find a cure for every person with cystic fibrosis, and provide all people with CF the opportunity to lead long, fulfilling lives.

Today, at 32, Stephen Picard, adult living with cystic fibrosis, continues to show what it means to keep moving forward....
10/22/2026

Today, at 32, Stephen Picard, adult living with cystic fibrosis, continues to show what it means to keep moving forward.

From playing Division II hockey to completing four World Marathon Majors, Stephen has never let cystic fibrosis define what’s possible. Since starting Trikafta in 2020, his lung function has increased from 88% to 100%, helping him pursue new goals, build a career he loves and give back to the CF community.

Stephen’s journey is a powerful reminder of how far we’ve come and why we can’t stop now. Together, we’ll keep going until every person with CF can live a long, healthy life.

But every experience with CF is different. People still struggle with this disease, and lives are lost every year. You can help rewrite this future.

When you donate today to the Connecticut 2026 Annual Fund, your gift will be doubled, dollar-for-dollar, up to $10,000. That means your donation can help fuel twice the progress! Double your donation to support our mission now: https://give.cff.org/connecticut/Donate?rbref=26CTMsocial01&donate=250.

We are proud to announce Greg and Debbie Sullivan as the recipients of the 2026 Paul Drury Legacy Award.Their longstandi...
10/20/2026

We are proud to announce Greg and Debbie Sullivan as the recipients of the 2026 Paul Drury Legacy Award.

Their longstanding support of the Foundation and unwavering dedication to our mission have helped bring hope, progress, and opportunity to those impacted by cystic fibrosis. Through their generosity and commitment, Greg and Debbie embody the spirit of the Paul Drury Legacy Award and inspire us all in the pursuit to find a cure for cystic fibrosis.

Join us on Nov. 21 at the Hartford Marriott Downtown to celebrate Greg and Debbie: https://events.cff.org/roseball.

There is no cure for cystic fibrosis, but your support can help change that reality. Now through Oct. 30, your donation ...
10/19/2026

There is no cure for cystic fibrosis, but your support can help change that reality.

Now through Oct. 30, your donation can go even further. Thanks to the Gelfenbien Family and the Laura Norton Fund, gifts to the 2026 Annual Fund will be matched, dollar-for-dollar, up to $10,000.

That means your gift can fuel twice the progress: from advancing today’s therapies to investing in genetic research with the potential to benefit everyone with CF.

Together, we can rewrite the future of cystic fibrosis. Make your gift now: https://give.cff.org/connecticut/Donate?rbref=26CTMsocial01&donate=250.

We are proud to announce that Prisco Panza, President of Winsupply of Shelton, and Gina Panza, Head of School at St. Tho...
10/16/2026

We are proud to announce that Prisco Panza, President of Winsupply of Shelton, and Gina Panza, Head of School at St. Thomas's Day School, will be honored as the 2026 Titans at the Connecticut Rose Ball. Their shared commitment to leadership, generosity, and service reflects the very spirit of this honor and continues to make a meaningful impact in advancing the Cystic Fibrosis Foundation's mission to cure cystic fibrosis.

Join us Nov. 21 at the Hartford Marriott Downtown for an unforgettable evening of Hollywood glamour, inspiration and celebration as we recognize Prisco and Gina and advance the mission of the Cystic Fibrosis Foundation. Rose Ball features exquisite cuisine, open bar, elevated silent auction, and live music.

Secure your tickets or table, learn more about sponsorship: https://events.cff.org/roseball.

Join us in congratulating Yale University School of Medicine CF Center (Pediatric Program) on receiving a 2026 Outstandi...
10/16/2026

Join us in congratulating Yale University School of Medicine CF Center (Pediatric Program) on receiving a 2026 Outstanding Care Center Partnership Award at the North American Cystic Fibrosis Conference (NACFC)!

This recognition celebrates care centers that go above and beyond in partnering with the Cystic Fibrosis Foundation to support people with CF and their families through community engagement, education, advocacy, and connection.

We are grateful for the dedication of the team at Yale University School of Medicine CF Center (Pediatric Program) and their commitment to helping strengthen and support the CF community. Thank you for being such an incredible partner in our mission.

Yale Pediatrics, Yale New Haven Hospital

Did you know that you can join a research study outside of your usual CF care center? Many studies offer compensation an...
10/14/2026

Did you know that you can join a research study outside of your usual CF care center? Many studies offer compensation and reimbursement for travel costs, making participation possible even if a study is far from home. Use the Clinical Trial Finder and filter by location to see study opportunities in your area and beyond: cff.org/finder.

Did you know you can support the Cystic Fibrosis Foundation through a donor-advised fund (DAF)? A DAF is a charitable gi...
10/08/2026

Did you know you can support the Cystic Fibrosis Foundation through a donor-advised fund (DAF)? A DAF is a charitable giving account that allows you to contribute cash, stocks, or other assets, receive an immediate tax deduction, and recommend grants to the causes you care about most. It's a flexible and easy way to support the CF Foundation with a one-time or recurring gift, or in the future as a beneficiary.

Learn more about giving through a DAF: https://www.cff.org/get-involved/other-ways-give

Please consult your DAF sponsor and financial or legal advisor regarding DAF giving. The Cystic Fibrosis Foundation cannot provide tax or legal advice.

Choosing a health insurance plan isn't always straightforward, and there isn't a perfect option. If you're feeling overw...
10/08/2026

Choosing a health insurance plan isn't always straightforward, and there isn't a perfect option. If you're feeling overwhelmed, are unsure where to start, or want a second opinion, Compass can help you compare plans, understand trade-offs, and choose the option that best supports you or your child’s healthcare needs.

Learn more and prepare now: https://www.cff.org/support/choosing-insurance-coverage-cystic-fibrosis.

Address

101 Centerpoint Drive, Suite 107
Middletown, CT
06457

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Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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+18606327300

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