Supporting The CF Gala

Join us in our mission to raise funds and awareness for Cystic Fibrosis Canada through the FaceOff with CF Gala. Together, we can make a difference.

Inspiring

Making a Difference in the Fight Against Cystic Fibrosis

The FaceOff with CF Gala has a rich history of supporting Cystic Fibrosis Canada and making a positive impact on the lives of those affected by this disease. Through our gala sponsors, silent auction, and ticket sales, we have raised significant funds to support research, advocacy, and patient care programs.

Itinerary

Face Off with CF Gala

Schedule:

Time PM (MST)	Events
4:30	Sponsor Reception – sponsors only
5:00	Mix and Mingle reception – All attendees
6:30	Ballroom Doors Open
6:40	Welcome
6:50	Dinner is served
8:15	Introductions and Awards
8:45	Break
9:00	Silent Auction closes
9:10	On Site Live Auction
9:30	CF Guest Speaker
9:45	Key to the Cure
10:00	Break
10:10	Hot Stove hosted by Bob Stauffer
10:50	Closing remarks”

Inspiring

Meet Our Team

Meet the team behind the gala.

Stacy Hipkin

I have proudly been involved with this event for 15 years, serving as the chairperson for the last five. I became involved with Cystic Fibrosis Canada 17 years ago when my son was diagnosed at the age of three. We quickly learnt that there was no cure for cystic fibrosis and at that moment my husband and I vowed we would fundraise and advocate for him and everyone battling this disease until a cure was found. Thanks to donated dollars, we are getting closer. Medical advancements are leading to longer lives and better quality of life, but we are not there yet. Please join us on Sept 12, 2026 at the JW Marriott, together lets make a difference to the over 4300 Canadians with Cystic Fibrosis. Hope to see you all there.

Deanna Hipkin

For the past 5 years, I have been involved with the gala in support of my nephew, Carter, who was diagnosed with cystic fibrosis (CF) at a young age. As there is currently no cure for CF, it has become my mission to help raise awareness and funds to support Carter and all those affected by this disease.

We are thrilled to invite you to join us on Sept 12, 2026 at the JW Marriott, for an unforgettable night dedicated to making a difference in the lives of those living with CF. Together, we can help fund the research needed to one day make CF stand for CURE FOUND! Your support can truly help change lives.

We look forward to seeing you there!

Erin Clemmer

I became involved with Cystic Fibrosis Canada at the end of 2022, when my daughter was diagnosed with CF at just 6 weeks old. As much as it shook our world, finding the support within this community has changed our lives for the better. I have worked behind the scenes with the gala since 2023, with 2026’s event being my first in a co-chair position. Finding a cure for Cystic Fibrosis has become my passion and to be part of The Face of with CF Gala is such an honour.

Esther Cantafio

When I started fundraising for cystic fibrosis in 2005, I couldn’t have imagined how deeply this cause would become woven into the fabric of my life. Through car washes, golf tournaments, and countless events, I’ve watched in awe as research advances have transformed CF from a condition with a life expectancy of just 23 years to one where patients are living well into their fifties. But my connection with the Hipkin family, especially Carter and Stacy, truly drives my commitment. They’ve shown me why every dollar raised matters, why every event counts, and why we can’t stop until we find a cure. Now, as a member of the Face Off with CF Gala Executive Committee, I’m more motivated than ever to be part of this remarkable journey. I invite you to join us on Sept 12, 2026 , at the JW Marriott, as we continue our vital work in making CF stand for ‘Cure Found’.

Winter Dzaman

Winter Dzaman is proud to serve as a committee member for Face Off with CF, a charity event dedicated to supporting research for the treatment and cure of Cystic Fibrosis (CF). Winter’s journey with the organization began through a deep, personal connection with Stacy Hipkin, the committee chair, and her son Carter, who has cystic fibrosis around 9 years ago. Winter first met Stacy and Carter when Carter was a young boy, advocating for a cure not only for himself but for countless other children battling CF.

Witnessing Carter’s bravery and determination, and hearing his story, made Winter reflect deeply on the privileges of having a healthy family. The thought of a child standing in front of strangers, discussing the complexities of medical procedures and navigating a life defined by illness, weighed heavily on Winter’s heart. It sparked a strong resolve to support the fight for a cure in any way possible.

Through sponsorship and volunteering, Winter has worked alongside the Face Off with CF committee to fundraise and raise awareness for Cystic Fibrosis. With a strong belief in the power of community and the importance of bringing about positive change, Winter remains committed to making a difference in the lives of families living with CF.

Beyond this cause, Winter is an active member of the community, working in the promotional industry and dedicating time to charitable initiatives. Passionate about wine, gardening, and philanthropy, Winter holds a garden in the local community garden program and volunteers regularly with several local charities by donating her time any chance she gets.

Having worked with great Philanthropists in the city, Winter has supported many charities, Winter continues to stand with the CF community, driven by a shared goal of finding a cure and offering hope to families everywhere that are affected by this disease.

Shae-Lynn Hipkin

My dedication to finding a cure for Cystic Fibrosis started at a young age, after my brother’s diagnosis. There were many hurdles and challenges we overcame as a family, which in the end caused us to become stronger together. As a family we have made the commitment to do everything in our power to raise awareness. We want to bring forward new avenues from donated funds that will benefit the lives of those with Cystic Fibrosis and hopefully one day no longer have to think about this life limiting disease. I look forward to seeing you all there and having a great night together!

Sharjeel Khan

My perspective on cystic fibrosis changed forever when I was 14 and learned about my classmate’s daily challenges with CF. It opened my eyes to the reality that so many families face, and I knew I wanted to be part of the solution. Joining the Face Off CF Gala committee gives me the opportunity to transform that early inspiration into meaningful action for the CF community.

Bradley Velsink

When I first partnered with Face Off CF Gala through my agency in 2023, I saw an opportunity to make a real difference. Digital marketing isn’t just about reaching audiences – it’s about connecting people to causes that matter. I’m honored to join the committee and continue using my expertise to raise awareness and funds for cystic fibrosis research.

Volunteers?

Are you looking to volunteer at the FaceOff With CF Gala?

Experience an unforgettable evening at the FaceOff with CF Gala

Support Cystic Fibrosis Canada and make a difference in the lives of those affected by this disease. Join us for a night of celebration and fundraising.

Cystic fibrosis (CF) is the most common fatal genetic disease affecting Canadian children and young adults. At present, there is no cure. That is why the 65 Roses Sports dinner has been active in Edmonton for over 30 years. We are making progress, but we still need your help to find a cure. That is why this event takes place. Each year the CF team puts on an amazing dinner and charity auction where sponsors and guests have the opportunity to mix and mingle with our CF Ambassador Ryan Nugent Hopkins. This event is a must attend for those that want to make a difference in the lives of CF patients. Having Ryan as our ambassador and advocate has elevated the profile of our event and ensured we can draw on supporters to attend and more importantly support the cause. As an individual that has been active in CF fundraisers for the past 30 years, I can attest that this is an event you don't want to miss. Ryan and his wife Bre along with some other Oilers make this a night to remember.

John Windwick

ATB

Inspiring

Impacting Lives, Raising Funds, and Celebrating Success: FaceOff with CF Gala

Every year, the FaceOff with CF Gala brings together passionate individuals and generous sponsors to make a difference in the lives of those affected by Cystic Fibrosis. With a silent auction, inspiring stories, and a night of celebration, we raise vital funds to support Cystic Fibrosis Canada’s mission.

Honorary Chair

Ryan Nugent-Hopkins

We are thrilled to welcome Ryan and Breanne Nugent-Hopkins as the honorary chairs of this year’s FaceOff with CF Gala.

Their commitment to supporting the cystic fibrosis community and dedication to making a difference in the lives of those affected by this condition is truly inspiring. With their passion and leadership, we are confident that this year’s event will be a tremendous success, bringing hope and raising crucial awareness and funds for CF research. Together, we look forward to creating meaningful and lasting impact.

Thank you, Ryan and Breanne, for joining us in this important cause.