NewsNotes Celebrating 2024 // Looking Ahead 2025

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CHILDREN’S DIABETES FOUNDATION  CELEBRATING 2024 / FIRST LOOK 2025

EXECUTIVE BOARD: Arlene Hirschfeld, Board Emeritus

Barbara Davis, Chairman

Cameron van Orman

Cindy Wells

Dana Davis, CDF Executive Director

Dan Feiten, M.D.

David Asarch

Deidre Hunter

Joe Smolen, Vice-Chairman

John H. Sampson, MD, PhD, MBA, MHsc

Lori Finch, Guild Representative

Ken Rickel

Lisa Corley

Nancy Davis Rickel

Marian Rewers, M.D. Ph.D.

Richard Abrams, MD

Sandip Garg

Shane Hendryson, Secretary

Shawn Hunter, Treasurer

Stacy Robinson

Stephen Daniels, M.D., PhD

Steve Lucas

SCIENTIFIC ADVISORY BOARD:

Richard S. Abrams, M.D.

Director, Colorado Preventive Medicine, Rose Medical Center; Clinical Professor of Medicine, University of Colorado Denver

Mark Atkinson, Ph.D.

Professor of Pathology & Pediatrics, Director, University of Florida

Diabetes Institute

Ezio Bonifacio, Ph.D.

Professor for Preclinical Approaches to Stem Cell Therapy, Center for Regenerative Therapies, Dresden, Germany

Robert Eckel, M.D.

Professor of Medicine, Physiology and Biophysics, University of Colorado School of Medicine

Matthias Hebrok, Ph.D.

Professor in Residence and Director, Diabetes Center, University of California, San Francisco

Steven Kahn, M.B., Ch.B.

Professor of Medicine, Director of the Diabetes Research Center, University of Washington

Rudolph Leibel, M.D.

Professor of Pediatrics and Medicine, Co-Director, Naomi Berrie Diabetes Center, Columbia University

Alvin Powers, M.D.

Professor of Medicine, Molecular Physiology/Biophysics, Division Director, Vanderbilt University

William Tamborlane, M.D.

Professor of Pediatrics, Yale University School of Medicine

AN EVENING OF INSPIRATION, ENTERTAINMENT,AND CELEBRATION

A heartfelt thank you to everyone who joined, supported, and celebrated the 38th Carousel of Hope Ball at The Beverly Hilton in Beverly Hills, California on October 5, 2024. Hosted by Barbara Davis and co-chaired by Dana Davis, this extraordinary event brought together leaders in entertainment, philanthropy, and business to raise critical funds for the Children’s Diabetes Foundation (CDF) and the Barbara Davis Center for Diabetes (BDC)

We extend our deepest gratitude to Barbara Davis, whose unwavering dedication and inspired vision continue to make this event a success. Barbara reminds us, “The incidence of diabetes has doubled over the last twenty years, with projections indicating it will increase by 54% by 2030. Marvin and I began this mission over 44 years ago when our daughter Dana was diagnosed with type 1 diabetes. Our dream was to build a clinic that would offer the most advanced treatments, prevent complications, and conduct groundbreaking research.”

Over the decades, the Carousel of Hope has amassed more than $115 million for diabetes research, care, and support. This

substantial sum has directly benefited the Children's Diabetes Foundation and the Barbara Davis Center for Diabetes, which focus on patient support, diabetes education, and research for a cure—reaching the “brass ring.” This year’s event raised an impressive $2.1 million through the ticket sales and sponsorships, live and silent auctions, and live appeal donations.

AN UNFORGETTABLE EVENING

This year’s Carousel of Hope was more than just a celebration— it was a mission in motion. Guests were treated to an extraordinary evening filled with inspiring stories, star-studded performances, and a shared commitment to finding a cure for type 1 diabetes.

The evening’s host David Foster, served as both the host and music director, set the tone for a night of entertainment and impact for this year's event. The production was managed by George Schlatter, with Clive Davis and Quincy Jones returning as Music Chairmen.

INSPIRING MOMENTS

Our evening’s invocation was led by CDF Advocate siblings Caleb and Zoe Alula who asked for, “one day, the world will see an end to type 1 diabetes, and that all who suffer from it will be restored to full health.” Zoe and Caleb both live with type one diabetes, Caleb for seven years and Zoe for six. Zoe has been living with type one since she was less than a year old.

Another memorable moment of the night was when Dancing With The Stars professional dancer Rylee Arnold told her story of being diagnosed three years ago at age 16. Rylee shared, that her type 1 diabetes would push her to become a better person and to become more motivated to accomplish her dreams. She made a promise to herself to advocate for other type ones to live their dream life.

Lastly, the presentation of the “Inspirational Lifetime Achievement Award” to legendary Diane Warren who was honored for her contributions to music and philanthropy was presented by David Foster. Followed by Jimmy Jam who received the “Brass Ring Award,” recognizing his impact in the music industry and his advocacy for diabetes awareness presented by Terry Lewis and Max Harris.

SHOW-STOPPING PERFORMANCES

The evening’s entertainment was a showcase of world-class talent:

• Upcoming talent MaKenzie Thomas opened the star-studded evening, followed by David Foster delivering a special performance of “Happy Birthday” for Barbara Davis in honor of her birthday

• Gladys Knight sang her crowd favorites like “You’re the Best Thing,”

• “Use my Imagination,” “Neither One of Us”, and GRAMMY winning “Midnight Train to Georgia,” followed by upcoming talent Luke K.

• Closing out the night, Jason Derulo captivated the audience with stunning renditions of… “Trumpets,” Whatcha Say,” and “Savage Love” drawing guests out of their seats up dancing and to the stage.

MEANINGFUL IMPACT

Thanks to the generosity of our guests, sponsors, and donors, funds raised from this year’s Ball will support vital diabetes research, clinical care, and education through the Barbara Davis Center for Diabetes and the Children’s Diabetes Foundation.

We extend our deepest gratitude to our generous sponsors:

• Presenting Sponsor: Dexcom

• Underwriting Sponsor: Sanofi

• Additional Sponsors: American Airlines, The Beverly Hilton, Variety, Deb & Bill MacMillan, and Fox Corporation.

LOOKING AHEAD

As we reflect on the incredible success of this year’s Carousel of Hope, we look forward to continuing the fight against type 1 diabetes. Thank you for being part of this unforgettable evening. Together, we are moving closer to our ultimate goal: a cure for diabetes

For more information about the Children’s Diabetes Foundation and ways to get involved, please visit ChildrensDiabetesFoundation.org.

Mark your calendars and save the date for The Carousel Ball on October 11, 2025

EVENT HIGHLIGHTS

The evening featured opportunities for guests to contribute while enjoying exclusive activities:

• Sanofi hosted an engagement space with a photo booth and two artists who sketched attendees. Attendees also interacted with the Sanofi team to learn more about their Screen For Type 1 initiative.

• Live Auction: Led by auctioneer Halie Behr, guests bid on luxury experiences including stay and play at Rancho Valencia Resort & Spa, a tropical island stay at the Four Seasons Resort Maui, and a Galapagos getaway expedition for two by Lindblad Expeditions. The live auction also featured a rhinestone-encrusted guitar signed by Dolly Parton, dazzling 18-karat yellow gold and diamond hoop earrings by Roberto Coin donated by XIV Karats LTD, and one-of-a-kind sculpture named “Yume” by Daniel Mazzone

• Special Guests: The event welcomed a host of notable attendees, including Annie Bosko, Ashley Benson, Berry Gordy, Carter Kench, Ed Begley Jr., Janice Dickinson, Josh Flagg, Kathy & Rick Hilton, Kelsey Bascom, Linda Thompson, Nicole Avant, Nigel Lythgoe, Stephen Nedoroscik, Suzanne de Passe, Ted Sarandos, and more!

THE LEGACY OF THE CAROUSEL OF HOPE HORSE DESIGN

A CONVERSATION WITH NANCY LOCKSPIESER

The artwork for the Carousel of Hope has become iconic. How did you get started as an artist?

My love for art started as a child. I’d sit on my father’s lap while he was on his amateur radio in our sunroom, and I’d draw. It was a formative experience that stayed with me. Later, I pursued graphic design and printmaking, starting with layouts on artboards and progressing through hands-on experimentation and learning. I’ve always enjoyed blending creativity with physical processes, like using a printing press.

How did you become involved with the Children’s Diabetes Foundation?

In 1976, when we moved to Denver, I had two friends whose children were diagnosed with juvenile diabetes. One became my best friend, and the other introduced me to the Foundation through her work on a golf fundraiser. My husband also had a colleague, Dr. Stephen Gabby, on the board. Through them, I learned about the need to raise awareness and funds, and I became deeply inspired to help.

The Carousel of Hope covers are stunning and quite memorable. How did the design process begin?

Barbara gave me clear direction for the covers: they needed to feel soft and Renoir-like, with pastel tones. I used textured sandpaper and pastels for many of the original pieces, starting with the horses and then adding children’s portraits. Each design represents the energy and optimism of the event. The carousel itself became a metaphor for uplifting motion, community, and hope.

How has the artwork evolved over the years?

I created the first covers for the Carousel of Hope when it began in Denver in 1978, and then again when the event moved to California in 1990. While I stepped back for several years, other talented artists like John Mancicchi continued the tradition. I returned in 2008 to pick up where I left off, building on the legacy we had started.

What message do you hope to convey through your artwork?

I want to celebrate energy, community, and the hope for a better future. The carousel is a joyful symbol that brings people together—families, friends, and supporters—all working toward a cure for diabetes.

What advice do you have for aspiring artists? Be playful and embrace the process. Art isn’t about perfection—it’s about expression, motion, and connection. For me, the carousel represents all those things, and it’s a perfect vehicle for sharing that message.

Nancy's original Carousel of Hope logo design.

BARBARA DAVIS CENTER: MEET THE DOCTOR

TODD ALONSO, MD,

PEDIATRIC ENDOCRINOLOGY

A Passion for Diabetes Care at the BDC

We are proud to highlight the incredible individuals at the Barbara Davis Center for Diabetes (BDC) who dedicate themselves to improving the lives of those living with diabetes. We sat down with Dr. Todd Alonso whose journey into diabetes care is as inspiring as his daily work.

HOW DID YOU GET INTO DIABETES CARE?

My journey into diabetes care began quite unexpectedly during my second year of medical school in Houston. Like many students, I was enticed by the promise of a free lunch during a faculty talk. Little did I know that lunch would change the course of my career.

The speaker was a pediatric endocrinologist, and as he described his work, I found myself captivated. He talked about the long-term relationships he developed with his patients, the blend of clinic and hospital care, and the meaningful impact he could make in their lives. In just 15 minutes, I knew: This is what I want my job to look like. This is what I want to do for a living.

Later that semester, I requested a rotation in his clinic. Spending a few afternoons in November with him and his patients solidified my interest. I loved the continuity of care, the close bonds he had with patients and families, and the opportunity to make a lasting difference.

As I continued my training in pediatric endocrinology, I kept coming back to this field, and every experience confirmed it was the right path for me. I hadn’t initially considered focusing solely on diabetes—most endocrinologists work more broadly across conditions—but everything changed when I interviewed at the Barbara Davis Center in 2013.

What struck me about the BDC was its singular focus. The entire building, the entire team, is dedicated to one condition: diabetes. The expertise, collaboration, and passion of the staff were unparalleled. I knew immediately that this was where I wanted to be.

More than a decade later, I feel privileged to be part of such a unique and innovative community. The BDC is a place where we not only deliver world-class care but also build lasting relationships with patients and their families, making a real difference every day.

HOW LONG HAVE YOU BEEN WITH THE BDC AND HOW DID THEY FIND YOU?

The job market for pediatric endocrinologists is unique—most positions are tied to large children’s hospitals in major cities. While training in Dallas, I was initially looking at opportunities within Texas, in places like Dallas, Fort Worth, and Austin. Leaving Texas, where I was born and raised, hadn’t even crossed my mind.

That changed when Dr. Rob Slover from the Barbara Davis Center sent an email to pediatric endocrinology programs seeking to hire Spanishspeaking physicians. The BDC had recently lost two Spanish-speaking providers and was eager to fill this gap for their large population of Spanishspeaking patients.

I had minored in Spanish and enjoyed using the language in patient care, so I reached out. After a Skype interview (my first- and only-time using Skype!), I was invited to visit the BDC. From the moment I arrived, I was impressed by the team, the center’s focus, and the opportunity to make a meaningful impact.

The idea of living in Denver and raising a family here was also incredibly appealing. The process moved quickly, and I’ve never looked back. Joining the BDC has been an incredible experience, both professionally and personally.

DO YOU HAVE PERSONAL A TYPE 1 CONNECTION?

Growing up, I had friends here and there who lived with type 1 diabetes, but I didn’t have any close family members or personal relationships with someone managing the condition. However, over time, that has changed. Today, I feel deeply connected to type 1 through the many friends, colleagues, and patients I work with daily. These relationships have given me a profound appreciation for the challenges and resilience of those living with type 1 diabetes.

WHAT MAKES YOUR DEPARTMENT AND TEAM AT THE BDC SO UNIQUE?

In 2015, the Barbara Davis Center supported me in taking a year-long course in quality improvement, marking the start of an exciting new chapter in our commitment to improving patient care. At the time, the center didn’t have anyone dedicated to leading these efforts, and I was thrilled to take on the challenge of building a team to drive this work forward.

Quality improvement is all about tackling operational challenges in a way that leads to meaningful and lasting change. Quick fixes only provide temporary relief, but by analyzing data and understanding how our systems truly function, we can identify opportunities for real improvement. Together, our team has worked to address critical processes—like reducing the time it takes for patients to start on insulin pumps or ensuring non-English-speaking families have the same seamless experience as Englishspeaking families.

These efforts require a multidisciplinary approach. Our team brings together providers, educators, and administrative staff to deeply understand how every step of a process works. By sharing this understanding, we can identify inefficiencies, eliminate redundancies, and ultimately create better workflows that save time and improve outcomes for our patients. For example, we’ve retooled the insulin pump start process to make it faster and more consistent, and we’re continuing to refine it based on patient and team feedback.

A core focus of our work is ensuring that the latest advancements in diabetes care reach patients as quickly and effectively as possible. This means addressing not only the science behind new therapies but also the operational challenges of implementation.

For example, when technologies like continuous glucose monitors (CGMs) or therapies like teplizumab (T-zeild) become available, our team works closely with industry partners to prepare. At the BDC we also have the unique advantage of robust research teams who have worked with these technologies for years before they are available for clinical use, and we’re able to leverage their expertise. We map workflows, set expectations, and ensure our team is ready to meet the needs of our patients from day one.

Leading this quality improvement team has been incredibly rewarding. It’s not just about analyzing data or redesigning workflows—it’s about fostering collaboration across the center and building a culture of innovation and excellence. Every improvement we make benefits the health and experience of our patients and seeing our team’s efforts translate into better care is the greatest reward.

WHAT HAS CHANGED WITH DIABETES CARE IN THE TIME YOU HAVE BEEN PRACTICING?

The most significant change we experience daily in diabetes care is the incredible advancement in technology, particularly in insulin pumps and continuous glucose monitors. These tools have become not only more sophisticated but also seamlessly integrated. Today, nearly all of our patients using an insulin pump have it paired with a CGM for automated insulin delivery—a transformative shift.

This integration has been a game changer. It's directly responsible for the improvements we’ve seen in our patients' average blood sugar levels and A1Cs. For a long time, we experienced a plateau in A1C outcomes, even as scientific advancements were being made. But about five or six years ago, that started to change.

Since then, we’ve seen a steady improvement in our patients' A1Cs, a trend mirrored across pediatric diabetes clinics in the U.S. After analyzing the data and publishing several studies, it’s clear that these improvements are driven by the widespread adoption of CGM technology and automated insulin delivery systems. This progress is a testament to how innovative tools can significantly enhance the quality of life for patients with diabetes.

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TELL ME ABOUT A PATIENT EXPERIENCE THAT HAS REALLY IMPACTED YOU AS A PROVIDER?

I’ve encountered so many moments with patients and families that have challenged what I thought I knew, reshaped my understanding, or made me question my perspective. These moments are invaluable—they remind me to stay open-minded and to allow my patients and their families to teach me things I may not have considered.

One moment that stands out was with a father of a type one child. After I had worked with his family for some time, he shared something that profoundly changed how I approach new diagnoses. He said, “You know, Dr. Alonso, when our son was diagnosed, we got so much information and support from the center. But no one told us it was going to be OK. And we really needed to hear that.”

That insight has stayed with me. Now, whenever I meet families, whose child has just been diagnosed, I make sure to convey that message of hope. I frame it in a way that is both truthful and realistic. I’ll say something like, “If we work together, if we follow this plan, and if we provide the right support, I expect your child to do well. I expect them to stay healthy and thrive.”

At the same time, I acknowledge the challenges ahead. Diabetes can be incredibly difficult, and there will be struggles. For some families, it will be harder, and some kids may face setbacks. But even in those cases, I want families to know that we’ll be there to support them every step of the way.

kids, playing Ultimate Frisbee, and woodworking. I recently completed a reclaimed wood wall at home.

WHAT IS YOUR FAVORITE COLOR?

Red. As a kid, my parents planned to move me to another bedroom for my baby sister. When asked about my room's color, I said red. They painted it blue.

WHAT’S YOUR FAVORITE FOOD OR DISH TO MAKE?

I'm passionate about cooking, especially experimenting with tacos. I love pairing them with ingredients like smoked pork or seafood, which adds variety to the dish.

DO YOU HAVE PETS?

My boys have fish, lizards, a snake, and we have a very calm and lazy dog.

That balance—offering honest expectations while instilling hope—has become a cornerstone of how I care for my patients and connect with their families. It’s a small but powerful reminder that, even in the face of something as daunting as a new diagnosis, what people often need most is the reassurance that they’re not alone and that things can turn out OK.

WHAT DO YOU DO FOR FUN WHEN YOU ARE NOT AT THE BDC? HOBBIES?

I have four sons, so I'm heavily involved in youth baseball, supporting and watching their games. Beyond that, I enjoy fishing and camping with my

WHAT MOTIVATIONAL OR INSPIRATIONAL ADVICE DO YOU HAVE FOR TYPE 1S?

Embrace the journey of self-improvement with patience and small, consistent steps. Remember, it's not about being perfect but about making progress. Each day, choose one small thing you can commit to, like a healthy habit or a moment of mindfulness. This approach leverages the power of incremental change, allowing you to build a life of wellness and fulfillment. Your path is yours alone, and every small step forward is a victory towards a better you.

BARBARA DAVIS CENTER

A VISION OF HOPE THE FUTURE OF DIABETES

The theme of 2024’s Empowering Patients for Individualized Care (EPIC) Diabetes Conference, “The Future of Diabetes,” was forward-looking and practical. The event was packed with workshops and panels covering vital topics like:

• Prevention and Delay of Type 1 Diabetes

• Innovative Insulins: Exploring faster insulins, inhaled insulin, and weekly basal insulin options

• Adjunctive Therapies and Obesity Medications for managing diabetes and overall health

• Emerging Diabetes Technologies and their role in simplifying and enhancing care

The expert speakers and workshops offered actionable insights and gave participants hope, showing how cutting-edge research and advancements in diabetes care are improving outcomes and quality of life.

WORKSHOPS THAT MADE A DIFFERENCE

This year’s workshops were tailored to meet the unique needs of both adult and pediatric participants, with specialized tracks designed for their respective challenges. Each session featured a focused presentation followed by a dynamic Q&A session, where attendees had the rare chance to ask questions directly to leading experts in the field.

From breaking down complex concepts to tackling the personal nuances of diabetes care, the workshops exemplified the conference's mission of empowering education. Attendees walked away with tools, strategies, and connections they could apply immediately in their own lives.

BUILDING CONNECTIONS

One of the most memorable moments of the day was the diabetes-themed Bingo game, which provided a fun and interactive way for participants to connect with one another. This activity fostered a sense of community that reminded everyone that they are not alone on their diabetes journey. Sharing stories, learning together, and building friendships were just as impactful as the expertled workshops.

A COMMUNITY EFFORT

The 7th Annual EPIC Diabetes Conference was a true community-driven effort, made possible by the generous support of King Soopers, which provided $10 gift cards for attendees.

We also extend our heartfelt thanks to our exhibitors, who shared their expertise and showcased groundbreaking advancements in diabetes care: Abbott, ADA, Beta Bionics, Diabetes Resource Nurses of Colorado, Diabetes Sangha, Dexcom, Genteel, Jewels for Hope, Lilly Diabetes, Medtronic, Novo Nordisk, Omnipod, Sanofi, Tandem, and Xeris Pharmaceuticals. Their contributions played a key role in creating an engaging and informative experience for everyone.

Additionally, a huge thank-you to the EPIC Committee—Dr. Halis Akturk, Dr. Erin Cobry, Dana Davis, Sydney Lundgren, and Regina Reece—for their tireless dedication to planning and executing such a meaningful event.

VOICES OF THE COMMUNITY

Here’s what attendees had to say about the conference:

• "The opportunity to interact with renowned clinicians and industry leaders was invaluable. The workshops allowed me to leave feeling informed and inspired."

• "Hearing about the latest research and FDA approvals gave me hope I hadn’t felt before. The dedication of the speakers was amazing."

• "The sessions were so relevant, especially the updates on new insulin and devices. I left with a renewed sense of control over my care."

• "I loved the community feel and the shared experiences—so powerful to know we’re not alone in this journey."

• "The device demonstrations were incredibly helpful. It was great to see all the options and how far technology has come."

LOOKING AHEAD

As the day concluded, one thing was clear: the EPIC Diabetes Conference is not just about education—it’s about connection, empowerment, and progress. We’re already looking forward to this year’s event, taking place on May 3, 2025 with the theme of Mind, Body, and Soul.

To all who attended, participated, or supported the 2024 conference: thank you for making it a truly impactful day. Together, we’re paving the way for a brighter, healthier future for the diabetes community. See you next year!

BARBARA DAVIS CENTER

2024 ATDC CONFERENCE

The 33rd Annual Practical Ways to Achieve Targets in Diabetes Care (ATDC) Conference, held from July 10–13, 2024, once again proved to be a cornerstone event for advancing education and innovation in diabetes care. Over the past three decades, the ATDC Conference has solidified its reputation as an essential resource for healthcare professionals focused on diabetes management and cutting-edge technology.

This year’s conference brought together over 450 attendees from across the United States and around the globe, representing a wide range of disciplines, including endocrinologists, internists, pediatricians, family physicians, physician assistants, nurse practitioners, dietitians, social workers, medical residents, fellows, and Certified Diabetes Care and Education Specialists (CDCES). With 43% of attendees identifying as healthcare providers, the conference continued to foster robust engagement and interaction.

PROGRAM HIGHLIGHTS

The 2024 program provided invaluable insights into the latest trends, tools, and therapeutic approaches in diabetes care. Key sessions included:

• Obesity and Diabetes Treatment Innovations: A deep dive into the comparison of GLP-1 receptor agonists versus bariatric surgery for managing obesity, with discussions on long-term outcomes and patient selection.

• The Evolving Role of CGMs in T2D: Sessions addressed the expanding use of continuous glucose monitors (CGMs) in Type 2 diabetes (T2D) management, particularly in inpatient settings, and strategies to reduce hospitalizations.

• Advancing Technology: Updates on hybrid closed-loop systems (HCL) and artificial intelligence (AI)-powered algorithms for diabetes management, along with practical insights into implementing clinical decision support systems.

• Managing Diabetes in Unique Populations: Plenaries explored managing diabetes during pregnancy (GDM), across the menstrual cycle, and in special populations such as toddlers and the elderly.

• Type 1 Diabetes (T1D):

• Updates on early-stage T1D detection using antibody screening and the use of teplizumab to delay disease onset.

• The growing prevalence of T1D during the COVID-19 pandemic and its immunological underpinnings.

• Exploring adjunctive therapies such as SGLT-2 inhibitors and GLP-1 receptor agonists to enhance T1D management.

• Regulatory and Clinical Updates: FDA representatives discussed regulatory pathways for diabetes devices and the latest clinical guidelines for managing T1D and diabetic kidney disease.

HANDS-ON WORKSHOPS AND TECHNOLOGY SESSIONS

One of the most celebrated aspects of this year’s event was the Hands-On Technology Session, which provided attendees with the opportunity to interact with cutting-edge devices, including CGMs, insulin pumps, alternate insulin delivery (AID) systems, and hybrid closed-loop technology. This interactive format allowed participants to gain practical skills and insights they could immediately apply in their practice. Additionally, a new session focused on meal planning and AID systems, offering practical considerations for integrating technology into everyday diabetes management.

KEY CLINICAL TRIALS AND EMERGING THERAPIES

The program also featured updates on pivotal clinical trials, including the SUMMIT and SURPASS CVOT studies, and their implications for clinical practice. Discussions also centered on newer therapeutic approaches, such as the use of fenofibrates, mineralocorticoid receptor antagonists (MRAs), and GLP-1 analogs in diabetic kidney disease and retinopathy.

FORMAT CHANGE A SUCCESS

The 2024 conference introduced a new schedule, beginning with a half-day session on Wednesday and concluding with a full-day session on Saturday. This change allowed for a more streamlined experience while still delivering an expansive curriculum across the four-day event.

LOOKING AHEAD

As we look ahead to the 34th Annual ATDC Conference, scheduled for July 23–26, 2025, attendees can expect even more engaging sessions, hands-on workshops, and networking opportunities. The 2025 program will delve deeper into topics such as integrating CGM and pump data into EMR systems, managing diabetes with advanced AI algorithms, and exploring newer therapeutic avenues for T1D and T2D. Our format will change slightly from 2024 with a full-day session on Wednesday and a half-day session (ending with lunch) on Saturday in 2025.

Registration for the 2025 conference opened in November 2024, and more information will be available at www.atdcconference.com/program

We thank all attendees, speakers, and sponsors for making the 2024 ATDC Conference a success and look forward to welcoming you again next year!

PaY it forwarD! pink panther books

Children’s Diabetes Foundation is proud to publish

AFirstBookforUnderstandingDiabetes,the go-to guide for diabetics all around the world!

Support a newly diagnosed family by purchasing a book today!

The Go-To Diabetes Books for over 50 Years! the pink panther books

The Children’s Diabetes Foundation publishes several different books to help educate patients and their families. The Pink Panther books are essential references for those involved with the management of type 1 diabetes.

For more information, or to order your book today, scan the QR Code below or call 303-863-1200.

DIABETES NEWS

ROADBLOCKS AND REVELATIONS

NAVIGATING LIFE AFTER MY SON’S T1D DIAGNOSIS

Cassie Bailey, mom to a child with T1D and paid Sanofi spokesperson

Before my son Josiah’s type 1 diabetes (T1D) diagnosis, he was the most fun, energetic, and inquisitive boy you’d ever meet. He was filled with joy; a child who embraced life with open arms.

In an instant, everything changed. Seemingly overnight, my little boy became a shadow of himself. He was lethargic, losing weight, and thirsty all of the time. I tried my best not to worry, rationalizing every symptom I saw: “He’s probably just playing too much” or “He might have an infection that his five-year old body is struggling to keep up with.” But deep down, my gut as a mom told me something was wrong.

I’ll never forget the day he collapsed at the bottom of the stairs. Immediately, my whole world faded – and my sole purpose became doing everything in my power to make sure my once healthy and happy child was safe. My husband and I sprang into action and took him straight to the hospital emergency room, where the doctor diagnosed him with T1D. I’ll never forget what she said when she told us.

“You guys are so lucky you brought him in, because he might not have woken up the next morning.”

As a parent, hearing those words was simply unfathomable. All you want to do is to protect your child – to shield them from pain or illness or, of course, disease. That said, neither my husband nor I knew anything about T1D or its symptoms. How could I have prevented this from happening when I didn’t have the information necessary to act?

Josiah, like far too many others, experienced diabetic ketoacidosis (DKA) when he was first diagnosed –which is a serious complication of T1D that can be life-threatening. Looking back, he had all the signs and symptoms of DKA, but we didn’t know what to look out for. It’s hard not to blame yourself as a parent. But I couldn’t shake the feeling that we could’ve done something if we were more knowledgeable about T1D, its associated risk factors, and warning signs.

Thankfully, Josiah recovered from DKA and has since gone on to live a very typical childhood. Our story, however, is not an isolated one, and should serve as a cautionary tale for the cost of not knowing about a T1D diagnosis – and the importance of early screening for T1D in being able to take charge of your health.

In the days following my son’s diagnosis, my husband and I got to work, undergoing a very necessary (and very lonely) crash course in T1D. We had to drop everything to learn how to navigate the complexities of this disease. It felt like climbing the side of a mountain.

I believe strongly that had we just known sooner, we would have been better prepared. We would have felt better equipped to find the right care team and outline a more thoughtful plan of action for my son’s health. And, most importantly, we would have known the signs, and we may have been able to reduce the likelihood of Josiah having to go through DKA.

Through this experience, my husband and I decided that we didn’t want to take another moment with our family for granted. That’s why we hit the road, embracing life in an RV so we could spend more time with our children and feel more present at every step. In a way, it gave us the space to breathe and feel more prepared for the challenges ahead – something we wished we could have had from the very beginning.

Unfortunately, I, like many other caregivers, was completely caught off-guard by my son’s T1D diagnosis. But it doesn’t have to be this way. Thanks to T1D autoantibody screening, families and loved ones can better understand their risk of developing the disease earlier –offering much-needed, potentially life-saving information that may help to prepare for the future.

No one should ever have to endure what we experienced with Josiah. As a mother, I won’t sugar coat it: It was terrifying. Through T1D autoantibody screening, however, we could’ve learned sooner about Josiah’s risk of developing T1D and planned accordingly to ensure he didn’t suffer the consequences that came along with his unexpected diagnosis.

For this reason and more, I’m proud to bring awareness to the importance of early screening for T1D. Please don’t wait, talk to your doctor about T1D screening, which is available around the country. Visit ScreenForType1.com for additional resources on T1D autoantibody screening and learn about screening options.

Watch The Bailey Family's T1D Diagnosis Story here.

PATRICIA ANN MCALISTER (WARD)

TYPE 1 HERO

Pat McAlister was a light in the world of type one diabetes (T1D). Pat was diagnosed as a young girl and always wanted to meet an older person living with T1D. When Pat was diagnosed no such person existed. She decided she had to become that person. Pat lived for over 76 years with T1D and was an inspiration to all who met her. Pat enjoyed attending Guild meetings and digital support groups where she would share her life story along with a positive outlook on life. Even after all that Pat had been through, she still looked and talked about T1D in a optimistic manner. Pat wanted the younger generations to see her and to know that they could still live a healthy and happy life with T1D. They could still have the career of their dreams, have children, travel, and more.

Pat told one story about how she traveled across the country with her school. Once she arrived at the destination, she hopped off the train and found reporters waiting for her. They were so shocked that someone with T1D was able to travel so far, even back then Pat was an inspiration. When Pat was diagnosed, she was told that she would never be able to have children, and she decided to prove those doctors wrong. Pat had always wanted to have a daughter named Beth. So she did just that. She had her daughter Beth along with a son named Mike. Pat lived with her family in Denver, Colorado where she received her master’s degree and started teaching computers at Metro State University.

We thank Pat for everything she did for the type one community. She touched many hearts and inspired so many. Her impact is everlasting.

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Each month

CDF receives your gift...

...nearly 130 more children in America have been diagnosed with type 1 diabetes

...a type 1 patient has used at least 3 CGM sensors

THANK YOU for your crucial monthly support!

...the Barbara Davis Center treats another 625 patients

...a type 1 patient has used at least 10 pods for their tubeless insulin pump

Continuous Giving Member

Are you able to make support for type 1 diabetes a monthly priority and become a CGM - a Continuous Giving Member with CDF today?

We would love for you to become a CGM - a Continuous Giving Member and part of CDF’s monthly giving program! It’s a wonderful way to automate your giving conveniently and consistently while helping to sustain CDF’s mission each and every month. When you join this group of special supporters, you can choose where you want your monthly gift to go or select ‘area of greatest need’. You can also adjust or cancel your monthly contribution anytime.

This special group of supporters receive additional member perks detailed in the benefits chart on the page to the right.

2024 EMPOWER TIED TO A CURE DENVER GOLF TOURNAMENT

A DAY OF COMMUNITY, FUN, AND IMPACT

A heartfelt thank you to everyone who joined, supported, and celebrated this year’s Empower Tied to a Cure Denver Golf Tournament presented by RE/ MAX in honor of Ian McDonald! This extraordinary event brought together golf enthusiasts, advocates, and donors for an unforgettable day at the stunning Sanctuary Golf Club, nestled in the foothills of the Rockies.

With its breathtaking views, lush landscapes, and tranquil atmosphere, Sanctuary Golf Club offered the perfect setting for a scenic yet challenging game, all while supporting a powerful cause.

A DAY TO REMEMBER

This year’s tournament wasn’t just a game of golf—it was a mission in action. Thanks to your generosity and participation, we raised $350,000 to benefit the Children’s Diabetes Foundation (CDF) and the Barbara Davis Center for Diabetes!

We are deeply grateful to our dedicated event chairmen: Joe Smolen, Michael McDonald, Dan Fuller, and Todd Schieck, whose leadership and passion made this event a success.

INSPIRING MOMENTS

One of the most moving highlights of the day was hearing from our CDF advocate, 11-year-old Sophia Reynolds, who shared her story of living with type 1 diabetes for the past six years. Sophia’s heartfelt words at the "Pay It Forward" hole reminded us all why we came together: to make life better for families like hers.

EVENT HIGHLIGHTS

The tournament was packed with exciting opportunities and activities:

• Celebrity Long Drive Hole: Featuring Andrew Eigner, the 2023 World Long Drive Champion Amateur Division holder with 451 yards for the longest competitive drive, and raised over $4M for charities.

• Exclusive Prizes: Players competed for a chance to win a trip to Pebble Beach, as well as two luxury cars complements of McDonald Automotive hole-in-one challenges.

• Silent Auction: Golfers and guests had the opportunity to bid on an incredible array of unique and sought-after items.

MEANINGFUL IMPACT

Thanks to the generosity of our attendees, sponsors, and donors, the funds raised will support diabetes research, patient services, and education efforts aimed at improving the lives of those living with T1D.

We extend our deepest gratitude to:

• Title Sponsor: Empower

• Presenting Sponsor: RE/MAX

• Eagle Sponsor: McDonald Automotive

• Birdie Sponsors: Capital Group-American Funds, Columbia Threadneedle, Morningstar Retirement, and Sierra Pacific Windows

Your support and contributions have helped us move one step closer to the ultimate goal—a cure for type 1 diabetes.

LOOKING AHEAD

Save the date: Tuesday, August 19, 2025. We’re already gearing up for this year’s tournament, and we’d love to see you there! Mark your calendars and join us as we continue to drive impact and support the T1D community.

For more information or to secure your spot, please contact Lindsay Klatt at Lindsay@ ChildrensDiabetesFoundation.org. Thank you for being part of this incredible tournament. Together, we are making strides toward a brighter future for those living with type 1 diabetes.

TUESDAY, AUGUST 19, 2025

RECOGNITION & BRANDING OPPORTUNITIES

Putting Green Sponsor: $5,000

Player Gift Sponsor: $4,200

Lunch Sponsor: $3,000

Driving Range Sponsor: $3,000

Brunch Sponsor: $3,000

Bar Sponsor: $3,000

Post Golf Reception Sponsor: $3,000

Golf Cart Sponsor: $3,000

Hole Sponsor: $1,500

Snack Bag Sponsor: $1,000

TOURNAMENT CONTACT

For more information on sponsor benefits please contact Lindsay Klatt at Lindsay@ChildrensDiabetesFoundation.org or 303-628-5109.

Payments and donations can be made throught the QR code.

2024 MCDONALD AUTOMOTIVE TIED TO A CURE GOLF FLYAWAY

A VEGAS ADVENTURE FOR A TYPE 1 CURE

Last year’s McDonald Automotive Tied to a Cure Las Vegas Golf Flyaway Tournament was nothing short of spectacular! On Thursday, October 24, 2024, 108 passionate golfers gathered in Las Vegas to experience an unforgettable day at the prestigious Shadow Creek Golf Course, followed by a luxurious stay at the Bellagio Hotel

With breathtaking views, world-class amenities, and a shared purpose of supporting type 1 diabetes (T1D) research and care, the event raised over $260,000 for the Children’s Diabetes Foundation—an outstanding accomplishment that will help drive impactful change for individuals and families affected by T1D.

A DAY OF UNFORGETTABLE EXPERIENCES

The day began early with a slate of engaging activities designed to energize and inspire:

• Poker games and an open bar set the stage for camaraderie and fun.

• A high-end liquor pull, offered unique items and experiences for guests to enjoy.

• A delicious breakfast provided by Epicurean Catering fueled participants for the day ahead.

Before the golf began, Michael McDonald, President of McDonald Automotive and Event Co-Chair, delivered remarks about his personal connection to the cause, sharing the story of losing his nephew to T1D. Attendees also heard heartfelt remarks from other co-chairs and were deeply inspired by Jacob and Asher Reich. Jacob is 11 years old and has had type 1 for eight years. Asher is eight years old and does not yet have T1D, but he has all five T1D antibodies. Asher was diagnosed with type one antibodies 2 years ago. Since then, he is seen every three months at the Barbara Davis Center for monitoring, he also wears a CGM to monitor his blood sugar. The live auction held onboard the plane added a touch of excitement, a made for an exhilarating start to the day.

MEANINGFUL IMPACT

Thanks to the generosity of our attendees, sponsors, and donors, the funds raised will support diabetes research, patient services, and education efforts aimed at improving the lives of those living with T1D.

We extend our deepest gratitude to:

• Title Sponsor: McDonald Automotive

• Eagle Sponsor: Lockton Companies

• Birdie Sponsors: Haley Custom Homes, Joe Sakic, Patrick Williams, and Roger Parker

• Live and Silent Auction Donors: Jay Leno's Garage, Kroenke Sports Charities, KTLA, Shadow Creek Golf Course, Spago, and Joe Sakic

Special thanks to Jacob and Asher Reich and their parents, Jenny Hoffman and Josiah Reich, for sharing their stories, and to Dan “Smackintosh” McIntosh, the Professional Long Driver, whose skills wowed attendees.

CELEBRATING LEADERSHIP AND DEDICATION

This event’s success would not have been possible without the unwavering commitment of our cochairs: Michael McDonald, Dan Fuller, Joe Smolen, and Todd Schieck. Their leadership, dedication, and passion continue to make the Tied to a Cure Golf Flyaway a standout event year after year.

LOOKING AHEAD

As we reflect on this extraordinary day, we are reminded of the power of community and the difference we can make together. To all who attended, donated, and supported this event, thank you for helping us drive progress toward a cure for type 1 diabetes.

We can’t wait to see you again at this year’s Tied to a Cure Golf Flyaway!

FOUNDATION NEWS

RUN FOR THE RING 5K & KIDS FUN RUN CELEBRATES 10 YEARS!

A massive thank you to everyone who contributed to the success of our 10th Annual Run for the Ring 5K Walk/Run & Kids Fun Run, raising nearly $31,700 for The Guild of the Children’s Diabetes Foundation.

A LANDMARK DAY

The event took place on Saturday, August 3, 2024 at the University of Colorado Anschutz Medical Campus. The day started with a welcoming speech by Keefer from 97.3 KBCO and an inspiring National Anthem by Gaven Qendall, followed by a runner warmup and diabetes exercises led by Michelle Shaw from Zyia Shawesome Active Wear and Medtronic

We had a remarkable turnout with 32 teams and 450 participants, all united in the pursuit of reaching the brass ring, a symbol of our collective aim to find a cure for type 1 diabetes.

KIDS FUN RUN

The kids' event was enlivened by the Pink Panther Mascot, who encouraged the little ones as they ran. The fun continued with Creamies popsicles, foam parties, hamster balls, and an obstacle course, ensuring a day full of joy for families.

AWARDS AND RECOGNITIONS

A special thanks to the Denver Broncos Cheerleaders for joining us this year! Congratulations to our 5K top male finisher Luke Urban, top female finisher Courtney Alberts, and our largest team, BDC Research Division, who had 35 members this year! Congratulations to our Top Fundraiser, Owen Young, for raising a whopping $2,900!

SPECIAL THANKS

A tremendous thank you to our sponsors who we could not have done it without:

Platinum: Sanofi

Gold: Vectra Bank

Silver: Abbott Diabetes Care, The Benson Hotel, Dexcom

Award Ceremony: Runners Roost

Water Station: Eldorado Natural Spring Water

COMMUNITY SPIRIT

Thank you to this year’s event chairs, Katie Grassby and Angie Anderson. A big shout out to KBCO’s Keefer for being the Run for the Ring emcee! Our heartfelt thanks to the volunteers and committee members who made it all possible: Lori Finch, Christy Alberts, Kimber Jones, Lyn Schaffer, Sue Finger, Sophie Johnson, Sherie Shaffer, and Christy Vasey. Their hard work fostered a sense of community and purpose. The overwhelming success of the 10th Annual Run for the Ring underscores the strength of our collective effort and spirit. Thank you to all who participated and supported this noble cause!

LOOKING AHEAD

We’re already gearing up for next year’s run, and we’d love to see you there! Mark your calendars for August 2, 2025 and join us as we continue to drive impact and support the T1D community.

For more information regarding sponsorships, please contact Mackenzie Atencio at Mackenzie@ChildrensDiabetesFoundation. org. Thank you for being part of this incredible event. Together, we are making strides toward a brighter future for those living with type 1 diabetes.

2024 CHARLOTTE TUCKER SCHOLARSHIP THE GUILD

The Guild of the Children’s Diabetes Foundation was delighted to award $4,000 scholarships to 20 outstanding students from the Barbara Davis Center for Diabetes, all of whom are embarking on higher education to chase their dreams. These scholars are entering diverse fields, driven by ambition and resilience. We celebrate these remarkable students as they step into a promising future.

CHARLOTTE TUCKER SCHOLARSHIP RECEPTION

A special reception for the Charlotte Tucker Scholarship recipients was held on June 6, 2024 at the Joy Burns Center on the University of Denver’s campus. Guild President and Charlotte Tucker Scholarship chair Lori Finch opened the event, welcoming recipients, their families, and guests. Lindsay Klatt, the guest speaker, encouraged students with the inspiring message that they, in learning to manage their type 1 diabetes, already had the tools in their toolbox to excel in college. Lori Finch and Stephen Edmonds, a Selection Committee member, introduced each awardee, sharing personal anecdotes about them and presenting them with certificates of recognition. The scholars then each expressed gratitude to The Guild and the Children's Diabetes Foundation, sharing stories that were both inspiring and humorous, reflecting their resilience through challenging times.

We extend heartfelt thanks to Lori Finch, our Charlotte Tucker Scholarship Chair, for her dedication. We also acknowledge the diligent work of the Scholarship Committee, including Paul Buchholz, Elizabeth Hamer, Stephen Edmonds, Cheryl Lebsock, Brenda Neyman, Diane Bishop, and Sharon Sager. These members reviewed 27 applications for the 2024-2025 school year, a task made difficult by the caliber of all applicants.

Gabrielle Bhatti Colorado State University
Melina Collier The George Washington University
Ava Dow-Peterson University of Colorado Colorado Springs
Luke Jakobsen University of Colorado Boulder
Xiomara Hernandez University of Northern Colorado
Cienna Daniels University of Colorado Colorado Springs
Gabrielle de Leeuw Embry-Riddle Prescott
Alexander Hess Colorado School of Mines

SCHOLARSHIP OPPORTUNITIES

FOR 2026-2027

The Guild continues its tradition of supporting education, offering scholarships to high school seniors and college students who are patients of the Barbara Davis Center.

Applications for the upcoming 2026-2027 academic year can be found at ChildrensDiabetesFoundation.org/Charlotte-Tucker-Scholarship. Applications open in the fall of 2026. For more information, or have any questions, please reach out to Mackenzie Atencio at 303-628-5116 or via email at Mackenzie@ChildrensDiabetesFoundation.org.

THE GUILD

Olivia Stoolman Arizona State University
Bennett Stewart University of Colorado Boulder
Ryan McClendon Colorado State University
Austin Kalivas Colorado School of Mines
Aubrey Ledall University of Colorado Boulder
Dennis Joseph (DJ) Smith University of the Cumberlands Williamsburg, Kentucky
Na’Kia Napue University of Colorado Denver
Finnegan LaVelle Benedictine College
Aidan Sobolevsky Purdue University
Avery Waters University of Colorado Colorado Springs
Adam Stevenson University of Northern Colorado
Mauricio Jaquez University of Colorado Denver

Children’s Diabetes Advisory Board Members and Guild Presidents

THE GUILD PRESIDENTS:

Founding President, Amy Davis, 1978

Kay Stewart 1981

Carol Roger 1982

Joy Burns 1983

Charlotte Tucker 1984

Karen Aylsworth 1985

Carol Roger 1986

Norma D’Amico 1987

Melissa Tucker 1988

Janet Knisely 1989

Loretta Tucker 1990

Donna Douglas 1991

Jane Weingarten 1992

Jamie Angelich 1993

Nancy Cowee 1994

Georgia Imhoff 1995

Helenn Franzgrote 1996

Linda Broughton 1997

Marty Jensen 1998

Suzy Love 1999

Gretchen Pope 2000

Sally Frerichs 2001

Helen Hanks 2002

Diane Sweat 2003

Bonita Carson 2004

Margy Epke 2005

Chris Foster 2006

Debbie Gradishar 2007

Sally Newcomb 2008

Gail Johnson 2009

Sharon Kamen 2010

Judy McNeil 2011

Gina Abou-Jaoude 2012-13

Dalyla Creaghe 2014

Shelley Lucas 2015

Tangy Buchanan 2016

Christy Alberts 2017

Barb Oberfeld 2018

Cheryl Lebsock 2019

Lisa Corley 2020-21

Lori Finch 2022

Katie Grassby 2023

ADVISORY BOARD:

Sir Michael Caine

Mrs. Lisa Corley

Mr. and Mrs. Robert A. Daly

The Honorable Diana DeGette, U.S. House of Representatives, Colorado

Mr. Neil Diamond

Mr. Placido Domingo

Mr. John Elway

Mr. David Foster

Mr. Kenny G

Mr. David Geffen

Mr. Magic Johnson

Mr. Quincy Jones

Ms. Sherry Lansing

Mr. Jay Leno

Mr. Lionel Richie

Mrs. Adrienne Ruston Fitzgibbons

Mr. George Schlatter

Ms. Maria Shriver

Ms. Brenda Richie

Ms. Barbera Thornhill

Miss Joan van Ark

Mrs. Cindy Wells

Mr. Gary L. Wilson

Mr. Stevie Wonder

See complete list at ChildrensDiabetesFoundation.org

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