Cystic Fibrosis Foundation - Indiana Chapter

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

About CF:
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive system of approximately 30,000 children and adults in the United States. More than 10 million Americans are unknowing, symptomless carriers of a defective CF gene.

Sept 19 | VIP 5-6PM | General Admission 6-9PM | Tom Woods Aviation HangerFor those looking to experience the night in fi...
06/23/2026

Sept 19 | VIP 5-6PM | General Admission 6-9PM | Tom Woods Aviation Hanger

For those looking to experience the night in first class, we invite you to step into the VIP experience at Hope Takes Flight—where every detail is designed to bring you closer to the flavor, the moment, and the mission.

As a VIP guest, you’ll enjoy a curated experience that goes beyond the main event—including exclusive guided tastings personally led by the owners and winemakers of three boutique Napa Valley wineries: Amizetta, Benevolent Neglect, and Hyde Vineyards.

Don’t miss out—reserve your VIP spot today! https://events.cff.org/HTF2026

We’re incredibly proud of Cora for representing the cystic fibrosis community at the Cystic Fibrosis Foundation ’s 18th ...
06/23/2026

We’re incredibly proud of Cora for representing the cystic fibrosis community at the Cystic Fibrosis Foundation ’s 18th annual Teen Advocacy Day.

Cora is sharing their story with , , , , to highlight the urgent need to increase funding for the National Institutes of Health to sustain a robust research pipeline, support innovation, and accelerate progress toward treatments for every person with CF — and ultimately, a cure.

Join us for a memorable day on the green at the 65 Roses Golf Classic, while raising funds towards a cure for CF! Your p...
06/22/2026

Join us for a memorable day on the green at the 65 Roses Golf Classic, while raising funds towards a cure for CF!

Your participation helps support those living with cystic fibrosis, making a real impact while you enjoy a fun-filled day. Don’t miss out – spots are filling up fast! Register your Standard Foursome today at 65 Roses Golf Classic!
https://events.cff.org/65Roses26

It is with heavy hearts that we share the passing of our dear friend, advocate, and CF Fighter, Jen Weber.Born in 1973 a...
06/17/2026

It is with heavy hearts that we share the passing of our dear friend, advocate, and CF Fighter, Jen Weber.

Born in 1973 and diagnosed with cystic fibrosis at just 2½ years old, Jen dedicated her life to making a difference. She began volunteering with the Cystic Fibrosis Foundation at age 10 as an "Ambassador of Courage", and over the next four decades became one of the most influential voices in Indiana's CF community and beyond.

Jen served on the Indiana Chapter Board for many years, co-chaired numerous virtual CFF conferences, participated in national working groups focused on improving CF care, and tirelessly advocated for people living with cystic fibrosis. Her impact on our community is immeasurable.

Beyond her CF advocacy, Jen was an accomplished attorney who served the Indiana Supreme Court and used her talents to improve the lives of others. She founded Comfort Finders, a nonprofit that supports adults with CF and other chronic illnesses during hospital stays, and was deeply involved with the Indiana Donor Network, the World Transplant Games, and the Transplant Games of America.

Throughout her life, Jen faced challenges most people could never imagine, including three double-lung transplants. Yet she never stopped fighting—not just for herself, but for every person living with CF, every transplant recipient, and every family navigating difficult circumstances.

Jen embraced life with her trademark motto, "YOLO" — You Only Live Once — and encouraged others to do the same. She also ended nearly every message with a word that perfectly captured who she was: "Onward."

To Jen, onward meant moving forward with courage, purpose, and hope, regardless of the obstacles ahead.

While we did not achieve a cure during Jen's lifetime, we honor her legacy by continuing the work she cared so deeply about. The CF community is stronger because of Jen Weber, and her influence will continue to be felt through the countless lives she touched.

Thank you, Jen, for your leadership, your friendship, your advocacy, and your unwavering spirit.

Onward. 💜

Elevate your 65 Roses Golf Classic experience with a Red Rose Foursome!Get the ultimate VIP treatment while supporting t...
06/16/2026

Elevate your 65 Roses Golf Classic experience with a Red Rose Foursome!

Get the ultimate VIP treatment while supporting those living with cystic fibrosis! Register your Red Rose Foursome today at 65 Roses Golf Classic!

https://events.cff.org/65Roses26

06/11/2026
Want the ultimate Purple Tie Ball experience? Treat yourself to a VIP Ticket and enjoy exclusive perks while supporting ...
06/10/2026

Want the ultimate Purple Tie Ball experience? Treat yourself to a VIP Ticket and enjoy exclusive perks while supporting the CF Foundation in style.

This is your all-access pass to a memorable night!
💜Pre-event VIP tasting experience featuring signature cocktails made from a variety of spirits and passed o hors d'oeuvres.
💜Chef-crafted meal
💜Full bar access throughout the evening

Purchase your VIP ticket today: https://events.cff.org/indianaptb26

Thank you, TWO MEN AND A TRUCK®  Indianapolis for being a Paddle Sponsor for the 2026 Purple Tie Ball!We are truly thank...
06/08/2026

Thank you, TWO MEN AND A TRUCK® Indianapolis for being a Paddle Sponsor for the 2026 Purple Tie Ball!

We are truly thankful for the businesses whose generous sponsorship made this event possible. Your commitment not only brings our community together, but also strengthens our shared mission to cure cystic fibrosis and offer hope to every person and family affected by it.

Last night was every bit as legendary as the Leaders and Legends who attended!Thank you to everyone who joined us for ou...
06/05/2026

Last night was every bit as legendary as the Leaders and Legends who attended!

Thank you to everyone who joined us for our second annual Leaders & Legends event. This special evening brought together longtime supporters and those newer to the mission to share stories, build connections, and celebrate the strength of our cystic fibrosis community.

Today, on 65 Roses Day (6/5), we're reminded that progress happens when people come together with a shared purpose. From CF fighters and their loved ones to dedicated volunteers, advocates, and corporate supporters, this community continues to inspire hope and drive change.

Together, we honor the past, carry this mission forward across generations, and move closer to the day when CF stands for Cure Found.

This 65 Roses Day (6/5), join the 65 Roses Club: a dedicated group of monthly donors committed to helping cure cystic fi...
06/05/2026

This 65 Roses Day (6/5), join the 65 Roses Club: a dedicated group of monthly donors committed to helping cure cystic fibrosis.

As a monthly donor, you can spread your support into smaller gifts that add up to real progress. This steady, reliable stream of revenue helps enable the Foundation to fund innovative research, drug development, and provide high-quality, specialized care so that we can get closer to a cure for cystic fibrosis.

Joining is easy — set up automatic monthly giving through the donation page and know your support is working for people with CF every month, without any extra steps.
https://give.cff.org/65rosesclub/donate?rbref=65RD26ch&donate=35&unitid=Indiana

Address

8445 Keystone Crossing #135
Indianapolis, IN
46240

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