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Author: Linxi Mytkolli

From Rain to Realizations: A Fellow’s Journey at the Diabetes Canada Conference


One of the most memorable things about this year’s Diabetes Canada Conference didn’t really have much to do with the conference itself—it was the weather. It rained every single day, but that didn’t stop the DAC Fellows from forging new friendships, presenting innovative ideas for the diabetes community, and having just a little sugar and fun!

This was my third time attending the Diabetes Canada Conference, and it never fails to be a fantastic networking and learning opportunity. This year was even more special because of our presentation showcasing materials created as part of the Diabetes Action Canada Fellowship.

Going into the presentation, I knew that my cohort of eight Fellows was the very first to take part in this groundbreaking fellowship. What I didn’t know, however, was how few presentations at the conference actually featured people with lived experience. Hearing the passion and dedication of my fellow Fellows as they answered questions about their projects was nothing short of spectacular. Their work will provide so much value to the diabetes community, and learning from them has been incredibly impactful.

Sometimes it was as simple as, “How did I not think of that?” Other times, it was more profound: “I’ve lived with diabetes for 31 years—how did I not know this?”

Throughout the conference, there were countless opportunities to attend impactful sessions. What stood out to me most was the high volume of Indigenous-focused sessions. These were incredibly informative, and I hope they will continue at future conferences. The Indigenous community is an important and often underrepresented part of the broader diabetes community, and these learnings are essential.

The long days, engaging sessions, and the hustle of navigating through vendor alley all reminded me of one unifying truth: we are a community. When you break down the thousands of conversations happening at the Halifax Convention Centre, we all want the same things. We want to reduce the stigma surrounding diabetes, explore technology and tools to better manage it, and understand how this chronic illness impacts all aspects of life.

A heartfelt thank you to Diabetes Action Canada and my fellow Fellows for an absolutely incredible presentation and conference experience. Thank you to the delegates who shared their time and conversations with me, and to Diabetes Canada and their presenters, who made the sessions come to life.


About the Author:
Ryan Hooey is a passionate advocate for accessibility and a person living with type 1 diabetes (T1D) for over 30 years. As part of the Keeseekoowenin First Nation, Ryan is dedicated to improving equitable access to medication, technology, and care for people with diabetes. He is the Manager, Major Gifts at CNIB, a Patient Partner with Diabetes Action Canada’s Diabetic Retinopathy Screening program, and a Catalyst for Change Award recipient. Ryan also hosts the AMI Book Review segment on Accessible Media Inc., where he highlights audiobooks and interviews authors.


About the Fellowship:
The Diabetes Action Canada (DAC) Research to Action Fellowship is a pioneering programme that equips individuals with lived or loved experience of diabetes to bridge the gap between research and real-world application. Fellows collaborate with researchers, patient partners, and community members to co-create culturally relevant tools and solutions that improve diabetes awareness and care. This initiative reflects DAC’s commitment to amplifying patient voices and fostering equity in diabetes research and practice.

From the Road to the Conference: Lessons in Connection and Care


A Different Kind of Journey

The last time I travelled to meet my fellowship cohort, I rode in on my motorcycle. That was back in May, and I was healthy then—able to walk on my own and barely acquainted with this group of dedicated individuals.

I was in awe of how much talent the other Fellows brought to the table. Their education, experience, and perspectives as patients, professionals, and cultural representatives were incredible. While I know my own background is valid, it sometimes feels mundane in comparison.

Flying into Halifax for the Diabetes Canada Conference this time was different. I wasn’t as healthy, and I needed help to make the trip. It was humbling but also heartening to see how this team supported each other. Meeting my DAC partner’s fiancée, someone I had only met over Zoom, added a personal and meaningful connection to the experience.

Building Connections and Sharing Ideas

The conference brought our cohort’s online bond into the real world. Many of us faced arduous travel delays, but eventually, we all made it to Halifax. Sitting down over meals, discussion tables, and coffee (always coffee) brought out our best conversations. My loquacious nature took over—it often does when I’m surrounded by great minds.

The Diabetes Canada Conference itself was vibrant, a testament to the talent, imagination, and dedication of this community. The health, advocacy, and diabetes communities are drenched with passion for improving lives. Talks like those on islet research reminded me how much work goes into pushing science forward.

Three moments from the conference stood out to me:

  1. An unintentional “brain date” with Michael, Ciara, and Grace taught me that while my patient perspective is unique, it’s not ubiquitous. We need to engage more people, especially those who don’t typically participate.
  2. Katherine Mackett’s presentation on the P2P peer support programme was inspiring. This structured mentorship model is transferable to many other chronic conditions. I would love to champion this idea further.
  3. A chance meeting with Kelly and Rebecca from the Métis Nation highlighted the importance of cultural connection in healthcare. Their passion for making positive change left a lasting impression, and I’m determined to help strengthen ties between them and DAC.

Reflections and Gratitude

Reflecting on the experience, I see how much effort everyone put into making this fellowship successful. From Linxi to Tracy, Julie, Ryan, Matt, Cindy, and so many others, it was a privilege to work alongside such talented individuals.

Flying home was bittersweet. While I was happy to return to my family, leaving this incredible group behind wasn’t easy. Even now, as I wrap up work and chat with Matt about final touches for our projects, I can’t help but feel proud of everything we’ve accomplished together.

À bientôt,
Al


About the Author:
Al Martin is a heavy-haul trucker, husband, and father of two teenagers who also happens to be a passionate patient advocate. As a Patient Partner with Diabetes Action Canada (DAC) and Obesity Canada, Al champions mental health inclusion in healthcare. Al and his wife both live with type 2 diabetes and obesity, bringing both lived and loved experiences to their advocacy work. When he’s not driving trucks or riding motorcycles, Al enjoys writing and studying physics.


About the Fellowship:
The Diabetes Action Canada (DAC) Research to Action Fellowship is a pioneering programme that equips individuals with lived or loved experience of diabetes to bridge the gap between research and real-world application. Fellows collaborate with researchers, patient partners, and community members to co-create culturally relevant tools and solutions that improve diabetes awareness and care. This initiative reflects DAC’s commitment to amplifying patient voices and fostering equity in diabetes research and practice.

Bridging Cultures and Care: A Journey from Research to Action


My journey to the Diabetes Canada Conference began in May 2024, when I was honoured to be selected as one of eight awardees for the Diabetes Action Canada (DAC) Research to Action Fellowship. This groundbreaking programme empowers individuals with lived or loved experiences of diabetes to bridge the gap between research and practical applications. For me, this fellowship held deeply personal significance.

My grandfather had diabetes, but health issues were rarely discussed openly in my community. Although diabetes was part of my family’s story, I had little understanding of what living with it truly entailed. While my academic background gave me a solid grasp of the biology behind diabetes, the fellowship helped me uncover the profound human and cultural dimensions that go far beyond the science.

During the fellowship, I collaborated with a teammate to develop a project focused on culturally relevant diabetes management and prevention for Black and South Asian communities. We aimed to address the health inequities disproportionately affecting these groups by creating resources tailored to their unique cultural and systemic challenges. Through focus groups, we engaged directly with community members, gathering insights and refining our project based on their feedback.

These discussions underscored the importance of empathy, inclusion, and culturally relevant strategies. For instance, we emphasized using familiar terms like “sugar” instead of “diabetes,” explored ways to enjoy cultural dishes while managing blood glucose, and highlighted techniques like refrigerating rice to stabilise glycaemic control.

The Diabetes Canada Conference marked the culmination of months of learning, collaboration, and hard work. Presenting on a panel with the largest number of patient partners ever included in a single session at the conference was both humbling and inspiring. It reinforced the importance of centring the voices of those directly impacted by research and translating scientific knowledge into tools and solutions for real-world challenges.

Insights Beyond the Science

Through this fellowship, I gained a deeper appreciation for what it means to live with diabetes. Listening to and learning from people with lived experiences brought a new level of understanding—something no textbook could teach.

I came to appreciate the financial burden of managing diabetes, from insulin and medical devices to supplies like test strips and glucose sensors. I even tested a glucose sensor myself, briefly stepping into the shoes of someone managing this condition daily.

We explored the mental health toll of diabetes, from burnout to anxiety over fluctuating glucose levels. Conversations about topics like dating, disclosing diabetes to a new partner, and the potential link between trauma and diabetes opened my eyes to the condition’s profound psychological, social, and cultural dimensions.

A Paradigm Shift

Research is often seen as an academic pursuit, but in health, it has the power to directly improve lives and address systemic inequities. To achieve this, we must shift from treating research as a purely scientific exercise to embracing it as a tool for change—rooted in empathy, equity, and the lived experiences of those it serves.

Patient partners are essential to this transformation. By bringing invaluable lived experiences into the research process, they ensure that studies are relevant, inclusive, and actionable. This fellowship reaffirmed my belief in a “for us, by us” approach, where solutions are co-created with the people they aim to serve.

The Diabetes Canada Conference was a step in the right direction, but there is still much work to be done. To my fellow researchers, healthcare professionals, and advocates: let’s commit to prioritising equity, making space for patient partners, and using research to create a better, healthier world for all.

A heartfelt thank you to Diabetes Action Canada and CIHR SPOR Network for championing this vision. Together, we can transform how research is conducted and how it serves those who need it most.


About the Author:
Cindy Lufuluabo is pursuing a Master’s in Public Health at the University of Montreal, with a focus on health equity and improving health outcomes for marginalised communities. As the daughter of Congolese immigrants, she is passionate about culturally competent care and bridging the gap between research and practice to reduce health disparities. Through the Diabetes Action Canada Research to Action Fellowship, Cindy developed tools to improve diabetes awareness and care for Black communities.


About the Fellowship:
The Diabetes Action Canada (DAC) Research to Action Fellowship is a pioneering programme that empowers individuals with lived or loved experiences of diabetes to bridge the gap between research and action. Fellows receive training in patient-oriented research and knowledge mobilisation, collaborating with community members and researchers to develop culturally relevant and impactful solutions. This initiative represents DAC’s commitment to amplifying patient voices and fostering equity in diabetes research and care.

Webinar – How to Develop a Knowledge Mobilization Plan for your Grants or Existing Research Projects: Introducing the KMap Tool

Join us on February 6, 2025, from 1-2 p.m. (EST) for a live webinar on How to Develop a Knowledge Mobilization Plan for your Grants or Existing Research Projects: Introducing the KMap Tool.

Planning for knowledge mobilization (KM) involves preparation, intention, and action. If done early, it can optimize both the mobilization and application of research results and outputs.

Hosted by: Dr. Monika Kastner, Scientific Lead, DAC KM-IS Program

What you’ll learn:

  • What the KMap Tool is and how it can help you plan for your grants or existing research projects
  • The importance of knowledge mobilization (KM)
  • How to use the KMap too,
  • Tips to write the KM section of your grants for clinical or preclinical research projects

Looking Ahead to 2025: Hopes and Reflections from the DAC Community

At Diabetes Action Canada (DAC), we know that research is about more than data—it’s about people, their lived experiences, and the hope for a better future. This guiding principle was at the heart of our first-ever DAC Patient Partners Holiday Gathering, where we watched The Human Trial and came together to discuss our hopes and dreams for the future of diabetes research and care.

A Community of Diverse Voices

Our gathering brought together an incredible range of perspectives:

  • Lived experience of T1D, T2D, gestational diabetes
  • Loved experience of MODY, T2D, T1D
  • Labored experience in research and allied health
  • Learned experience in biochemistry, pharmaceuticals, and more

This rich diversity underscored the strength of the DAC patient partner community. Together, we reflected on the progress being made and the work that lies ahead.

Gratitude and Hope

Throughout the discussion, one sentiment rang clear: gratitude. Gratitude for the researchers and clinicians working tirelessly to push the boundaries of what’s possible. Gratitude for the power of storytelling in The Human Trial, which gave a face to the struggles and triumphs of those seeking better treatments. And gratitude for the sacrifices and contributions of everyone who participates in the journey of research—whether as clinical trial participants or as patient partners helping to shape the future of care and innovation.

Patient participation and partnership are both profound acts of generosity, each with its own kind of sacrifice. As a community, we deeply value the efforts of everyone who contributes, whether by sharing their story, collaborating on research protocols, or providing insights that make studies more patient-centered.

The Power of Storytelling

The evening also highlighted the importance of creative forms of knowledge mobilization. It’s one thing to read a paper about cell therapy or a clinical trial; it’s another to watch a film that captures not only the science but the human experiences, hopes, and challenges behind it.

Creative storytelling, like The Human Trial, has a unique ability to convey what numbers alone never could. It allows us to connect on a deeper level and appreciate the far-reaching potential impacts of research, reminding us of the humanity at the heart of the work we do.

The Role of DAC

As we listened to these reflections, it became clear how DAC can continue to support this vision. The DAC community plays a critical role in:

  • Helping researchers understand what to study by elevating patient priorities.
  • Supporting grant applications with patient-informed insights.
  • Co-designing protocols that reflect real-world needs and barriers.
  • Advising on the composition and function of advisory committees.

DAC is uniquely positioned to connect researchers with patient partners at every stage, ensuring that the lived realities of people impacted by diabetes are at the center of research design, execution, and translation.

A Call to Action: The 4Ls

As we look toward 2025, we invite everyone in our community to join us in shaping a brighter future for diabetes care and research:

  • Lived experience: Share your story and help researchers understand what truly matters in the lives of people living with diabetes. Your voice can shape the priorities and direction of research.
  • Loved experience: Use your perspective as a family member, friend, or caregiver to help inform what matters most for those you care about and support. Your input is vital to ensuring that research reflects the broader diabetes community.
  • Laboured experience: If you work in healthcare, research, or a related field, partner with us to connect your work with patient partners. Our tools, data, and patient insights can help shape, refine, and elevate your projects.
  • Learned experience: Collaborate with us to integrate patient partners into your work. Whether it’s co-designing studies, spreading the word, or sharing results, we’ll help you make your work more impactful and patient-centered.

Looking Forward

2025 promises to be a year of growth and opportunity for DAC and the broader diabetes community. Together, we can strengthen the connection between research and the people it’s meant to serve. We’ll continue to build bridges, amplify voices, and foster hope—one story, one study, one connection at a time.

Stay tuned for more updates, events, and opportunities to get involved. Together, we’re shaping a future filled with gratitude, collaboration, and progress.

Linxi Mytkolli
Director of Patient Engagement

Knowledge Mobilization Team Launches KMap Tool

In the summer of 2024, the DAC 2.0 Knowledge Mobilization-Implementation Science (KM-IS) Program team undertook a review of the overall program and its tools and resources. This mid-point review inspired several updates, including a revision of the KM planning tool to optimize its user-friendliness.

Now called the KMap Tool (Knowledge Mobilization Action Planning), the new name reflects the tool’s role as a “map” that guides the user as they move through various steps in the journey to create a KM plan for a particular project. Each of the five steps includes a description and examples, with additional guidance tips offered for some of the steps. A worked project example is also provided to illustrate considerations for each step and what a completed KM plan table looks like.

“The ‘map’ analogy was intentional as the tool serves to provide a structured roadmap to systematically think through important questions about your research and KM goals when planning for knowledge mobilization,” says Julie Makarski, co-lead DAC 2.0 KM-IS Program.

This new version of the tool now includes an introductory page with pertinent information about the tool and how to use it. The KMap Tool is available as a fillable document, to facilitate its completion and editing by multiple team members. It can be completed as a team or initiated by one team member and then circulated to the team for continued refinement. The KM plan that is generated can then be used as a blueprint to execute the KM activities outlined in the plan and is appropriate for a grant application or existing research project.

“Planning for knowledge mobilization involves preparation, intention, and action, and if done early during the design stage of research projects, can optimize both the dissemination and application of research results and outputs,” says Monika Kastner, Scientific Co-Lead for the DAC 2.0 KM-IS Program. “The KMap tool guides users to create a comprehensive KM plan, which can then be used to execute their KM activities.”

The KMap tool debuted at the November 2024 Diabetes Canada Pre-Conference workshop, where it was very well received. Workshop attendees were provided the opportunity to apply the tool using an example project and rated the tool highly for clarity and ease of use. All attendees indicated that they would use the tool for their work and would recommend it to others. 

Looking ahead, the KM-IS Program will be offering a live webinar about the tool on February 6, 2025 from 1:00-2:00pm(EST). The webinar will provide information about KM planning for both pre-clinical and clinical research projects, a walk-through of the KMap tool, and tips for writing the KM section of grants. Save the date! Webinar registration will open in January 2025.

Visit the KM Practice Tools page to try the KMap Tool!

DAC-Supported Projects Receive Grants

The entire team at Diabetes Action Canada (DAC) is thrilled to celebrate that eight out of the ten research projects funded through the CIHR Operating Grant: Knowledge Mobilization in Diabetes Prevention and Treatment received our support!

Of these projects:

“We are thrilled to see CIHR funding projects that recognize the vital role of Patient Partners in Knowledge Mobilization”, says Tracy McQuire, Diabetes Action Canada’s Executive Director. “We look forward to working alongside these teams to help move this important research to action and impact.”

The funded projects are:

Congratulations to all of the funded teams!

Learn more about DAC’s Knowledge Mobilization Consultation Service and Practice Tools.

Celebrating the Life of Patient Partner David Wells

Everyone at Diabetes Action Canada was saddened to learn about the passing of our longtime Patient Partner, David Wells on November 22, 2024.

David lived in Fredericton, New Brunswick and had been a Patient Partner with DAC since 2018 and the Maritime SPOR Support Unit (MSSU) since 2013. His work as a patient advocate and research partner had an enormous impact and is a lasting testament to his commitment to improved healthcare for all.

From 2005-2011 David chaired the New Brunswick Surgical Care Network Advisory Committee, which designed and implemented new procedures that reduced surgical wait times in New Brunswick by 50-70%. During 2012-2015 he was the patient representative on the New Brunswick Primary Health Care Steering Committee, which changed the delivery of primary health care in New Brunswick by producing an extensive guidelines document adopted for Family Medicine New Brunswick in 2017. Dave served on five DAC committees, and as a patient partner on multiple CIHR grants. He also co-facilitated several course on patient-oriented research.

“David was one of the first Patient Partners I had the privilege to work with after joining DAC. As a former professor, he had a remarkable way of organizing and sharing his thoughts, often using a flip chart and marker to guide us through his feedback. When the flip chart wasn’t in use, one of his late wife’s beautiful quilts would often grace the room—a touching tribute to her memory. David was a passionate advocate for SPOR, and his contributions were instrumental in shaping our programs, refining our implementation plans, and fostering a culture of patient-oriented diabetes research,” says Tracy McQuire, Diabetes Action Canada’s Executive Director. “On a personal level, I will deeply miss David as my friend. Over the years, I had the joy of getting to know him better, often calling to check in and share a conversation. He was truly a pleasure to know, and his absence will be profoundly felt by all who had the honor of working with him.”

Marina Hamilton, Maritime SPOR SUPPORT Unit Executive Director, also shared her condolences on David’s passing. “David was a founding member of the Maritime SPOR SUPPORT Unit Patient/Public Partner Council and New Brunswick Provincial Steering Committee. We remember him as a passionate leader of our patient-oriented research training, bringing a wealth of knowledge and lived experience to every session. His stories deeply resonated with MSSU staff and the research community, leaving a lasting impact.”

The Diabetes Action Canada Collective Patient Circle were saddened to learn of David’s passing and shared many remembrances of their work with him.

“Thank you for letting us know about David’s passing. I remember working with him on the Do’s and Don’ts project. He was such a champion of patient engagement and a wealth of knowledge and experience. It was always lovely to chat with him in person at the DAC workshops and I’m glad I got to see him this past year in Toronto.” 


“I wanted to share how engaged Dave was during our session this past May; he really engaged with the art and was one of the big reasons we changed the session style. I will always remember his engagement and enthusiasm.”

“I will also remember how much he loved hot and sour soup, his beautiful quilts behind him in his Zooms, and his naps during meetings.”  

Learn more about David Wells on this tribute page.

Diabetes Action Canada at the Diabetes Canada/CSEM Professional Conference: A Recap

In November, the DAC team was in Halifax to attend the Diabetes Canada/Canadian Society of Endocrinology and Metabolism Professional Conference. The event, which takes place over four days, was full of highlights.

On Wednesday, November 20, our Knowledge Mobilization Team, led by Dr. Monika Kastner and supported by Research Assistant, Isabella Herrington, hosted a workshop aimed at helping participants build capacity and capability in knowledge mobilization and implementation science.

DAC team members, including Director of Patient Engagement Linxi Mytkolli, participated in the MyRoad training day on Wednesday. All of our Research to Action Fellows were invited to attend this full day training and education session and Linxi was a guest speaker. In addition, a number of DAC trainees took part in the day.

Thursday morning kicked off bright and early with our first ever DAC breakfast at the conference. Our members and partners joined us for an hour of networking, program updates and a meal. Scientific co-lead Gary Lewis offered welcome remarks, Executive Director, Tracy McQuire introduced new DAC resources, and Linxi updated attendees on the Fellowship and our KM program.

Here’s a quick recap of the updates we shared:

  • Patient Engagement: A new streamlined recruitment form lets you request patient partners in minutes, with tailored one-on-one support for your projects.
  • Knowledge Mobilization: Improved five-minute request form for one-on-one consultations to amplify your research impact.
  • Digital HealthDiabetes Research Connect, launched with CPCSSN, connects patients and providers through innovative solutions.
  • Community Hub: The DAC Hub, a global first, is a comprehensive database of diabetes organizations, support groups, and online communities offering peer support and connection.
  • DAC Member Presentations: Explore the full list of DAC-affiliated sessions at the conference.

 Click here to access all updates and resources!

See photos from our time at the conference on Instagram!

Throughout Thursday, DAC members were speakers at the sessions. Two of many highlights? Peter Senior participated in a plenary talk on islet transplants and Diane Wherrett provided an update on the CANScreen program, which aims to screen children across Canada for type 1 diabetes antibodies.

On Friday, DAC members Sonia Butalia and Baju Shah were featured speakers on a session highlighting updates to the Diabetes Canada Clinical Practice Guidelines. As part of the updates, the T1D leads also referenced a DKA awareness project led by Bruce Perkins and Patient Partner Wajeeha Cheema.

A major highlight of Friday was the session, Implementation and Knowledge Translation in Diabetes: From Research to Community to Lived Experience, where our eight Research to Action Fellows presented their projects for the first time. The panel, which was attended by hundreds of conference participants, was noted as a highlight for many – and there were more than a few tears shed by those moved by the lived experience perspectives.

Women with diabetes was a major focus of Friday’s sessions, with DAC’s Lorraine Lipscombe discussing gestational diabetes – including a DAC-supported program aimed at reducing type 2 diabetes risk in women with the condition – and Iliana Lega presenting on diabetes and menopause. Kaberi Dasgupta also presented an oral abstract on gestational diabetes as part of the scientific oral presentation.

On Friday evening, the conference hosted a poster session and several DAC members and trainees presented, many of them discussing DAC-supported projects. Presenters included Linxi, Jamie Boisvenue, Saania Tariq, Jim Bowen and Valeria Rac.

Saturday, Calvin Ke and Jacqueline Beaudry were the featured speakers at the Innovators and Emerging Leaders in Canadian Research session. Both researchers are DAC members, including patient partnership at the heart of their work. In a concurrent session, Bruce Perkins presented the latest on T1D and exercise, including tips for how healthcare teams can better support people living with the condition.

Saturday was also a big day for our Indigenous partners and colleagues with Celeste Theriault, Executive Director of the National Indigenous Diabetes Association presenting Forging Ahead: A distinctions-based pathways approach for Indigenous Diabetes Management. Rosylnn Baird and Autumn Watson also presented Examining the Model of Care and Impact of the Indigenous Diabetes Health Circle on Indigenous Communities: A Case Study Using Ethnographic Approach as part of the Indigenous Science & Content Oral Abstract Presentations. We hope that moving forward these conferences continue to host a wealth of Indigenous voices.

It was a wonderful week of engaging with colleagues and partners from across Canada and beyond. Our team could not be prouder of how much patient-oriented research has become a part of this meeting and the diabetes research and care community overall.

We’re already looking forward to next year.

DAC @ DC Conference

From November 20 – 23rd, Diabetes Action Canada will be taking part in the Diabetes Canada Professional Conference in Halifax. Our researchers, fellows and patient partners will be involved as speakers and attendees. This is an important opportunity to share our latest research updates and to network and engage with the diabetes community in Canada.

We are excited to share the following updates with our members:

  1. Patient Engagement – Streamlined form and process to connect researchers with Patient Partners.
  2. Knowledge Mobilization – Renewed 1:1 KM consultation process and DAC specific tools.
  3. New Digital Health Research Connect – DAC/CPCSSN initiative linking 1,500 primary care providers and 2 million patients.
  4. Community Hub – First-of-its-kind global database of diabetes support groups, organizations, charities and more.
  5. DAC Members at DC Conference – A guide to our members in action below!

Throughout the conference, we’ll be sharing highlights from DAC-affiliated presentations and events, as well as updates from our first DAC breakfast on Thursday morning. Follow along on our LinkedIn and/or Instagram where we’ll be sharing posts regularly.

If you are attending, be sure not to miss out on content related to patient-oriented research. Check out the schedule for DAC speakers below.

Wednesday, November 20, 2024

TimeSessionSpeakers
1:30 – 4:30 p.m.DC 2411 – Knowledge Mobilization with DACMonika Kastner
Julie Makarski
1 p.m. – 7 p.m.Trainee Event with MyRoadLinxi Mytkolli

Thursday, November 21, 2024

TimeSessionSpeakers
9 a.m. – 10 a.m. DC/CSEM01 – Dr. Harold Copp Lecture: Advances in Islet & Stem Cell Transplant: Celebrating 25 Years of the Edmonton ProtocolTimothy Keiffer
Peter Senior
Breay Paty
11:15 – 12:30 p.m.DC2412 – Exploring Cardiovascular, Renal, and Metabolic management in Diabetes CareJulie Loveshin
Kristin Clemens
Abhinav Sharma
Sonia Butalia
12:45 – 13:45 p.m.AS2402 – Enhancing Uptake and Use of Glucose Sensing TechnologyJames Kim
Elizabeth Rosolowsky
Michelle Stewart
Jean-Francois Yale
14 – 15:15 p.m.Clinical Care and Educational Oral Abstract Presentations
DC2439 – A1c versus Oral Glucose Tolerance Test for Chronic Glycemic Surveillance in Women with Previous Gestational Diabetes
Ravi Retnakaran
14 – 15:15 p.m.DC2413 – Sustaining Beta Cell function in Diabetes: New developments in screening and treatment approachesDiane Wherrett,
Ravi Retnakaran,
Alanna Weisman

Friday, November 22, 2024

TimeSessionSpeakers
8:30 – 9:30 a.m.CPG UpdatesJames Kim
Baiju Shah
Jeremy Gilbert
Sonia Butalia
Zaina Albalawi
Sheldon Tobe
Harpreet Singh Bajaj
Phil McFarlane
Brandy Wicklow
Ilana Halperin
10 – 11:15 a.m.DC2430 – Forging The Path: An Interdisciplinary Approach to Diabetes Foot CareAhmed Kayassi
Jolene Heil
Virginie Blanchette
Zaina Albalawi
10 – 11:15 a.m.CSEM2406 – Menopause: Lessons to Learn from the Canadian Longitudinal Study on AgingIliana Lega
Gillian Einstein
Laurie Mereu
10 – 11:15 a.m.Scientific Oral Presentations (Basic)
 
DC2420 – Unveiling Gaps in hESCβ-cell Function: Combining Single-cell Electrophysiology and scRNA-Seq
Jasmine Maghera
10 – 11:15 a.m.DC2414 – Implementation and Knowledge Translation in Diabetes: From Research to Community to Lived ExperienceMary Jung
Linxi Mytkolli
Holly Witteman
Matt Larsen
Senaya Karunarathne Jeremy Storing
Natalie Mangialardi
Al Martin
Cindy Lufuluabom
Rosan Wesley
Ryan Hooey
11:30 – 12:45 p.m.DC2415 – Advancing Diabetes Treatment: The Future of GPCR-Targeted TherapiesJonathan Campbell
Robert Screaton
Erin Mulvihill
11:30 – 12:45 p.m.DC2435 – Updates in Gestational DiabetesLorraine Lipscombe
Celeste Durnwald
Rachel Bon
2:15 – 3:30 p.m.DC2416 – From Parents to Children: The Legacy of Diabetes and ObesityBrandy Wicklow
Jennifer Thompson
Jennifer Bruin
Jonathan McGavock
2:15 – 3:30 p.m.DC2429 – Precision Diagnosis in DiabetesAlanna Wesiman
Diane Wherrett
Akshay Jain
Jeremy Gilbert
3:35 – 3:55 p.m.DCC13 – From Awareness to Action: Shining a Light on Presymptomatic Type 1 DiabetesBruce Perkins
4:00 – 5:15 p.m.Scientific Oral Presentations (Clinical)
 
DC2421 – Preliminary analyses from a step count and weight track and target Feasibility Trial in Gestational Diabetes
Kaberi Dasgupta

Research Hour

5:15 – 6:30 p.m.Co-Creating a Global Type 1 Diabetes Support Group Repository: A Knowledge Mobilization ProductLinxi Mytkolli
Assessing the Impact of a Community-Based Narrative Film about Diabetes and Homelessness on Audience Members’ Knowledge, Attitudes, and BeliefsSaania Tariq
Differences in Attendance of Referrals made to a Tertiary Diabetes Education Centre by Referral Location and Neighbourhood DeprivationSaania Tariq
Community-Based Tele-Retina Screening for Diabetic Retinopathy Supported by Provincial Healthcare Administrative Data Session: Community-Based Tele-Retina Screening for Diabetic Retinopathy Supported by Provincial Healthcare Administrative DataJim Bowen
Valeria Rac
Understanding patient-focused registries for diabetes: A Scoping Review of Published LiteraturePaige Alliston
Investigating the Impact of Medical Trauma by Age at Diagnosis in People Living with Type 1 Diabetes using Epistemic Network AnalysisJamie Boisvenue
Nature versus Nurture of glucose homeostasis trajectories in youth across different ancestries)Kaossarath Fagbemi
Imputation across HLA/MHC alleles using multiple machine learning-based simulation methods shows high concordance with HLA/MHC typing in autoimmune Type 1 DiabetesErica Kleinbrink

Saturday, November 24, 2024

TimeSessionSpeakers
7:15 – 8:15 a.m.Cardiorenal Connection: Interdisciplinary Management and the Cardiorenal ConnectionStravroula Christopoulos
Lisa DeMolitor
Christopher Tan
David Cherney
Aakash Modi
9:40 – 10:55 a.m.DC2431 – Exercise as MedicineChristopher Shields
Bruce Perkins
Gabrielle Schmid
9:40 – 10:55 a.m.DC2409 – Forging Ahead: A distinctions-based pathways approach for Indigenous Diabetes ManagementCeleste Theriault
9:40 – 10:55 a.m.Indigenous Science & Content Oral Abstract Presentations
 
DC2437 – Examining the Model of Care and Impact of the Indigenous Diabetes Health Circle on Indigenous Communities: A Case Study Using Ethnographic Approach
Roslynn Baird
Autumn Watson
9:40 – 10:55 a.m.DC2418 – Innovators and Emerging Leaders in Canadian ResearchCalvin Ke
Jacqueline Beaudry
Rebecca Hull-Meichle
11:10 – 12:25 p.m.DC2432 – Exploring Models of Care to Support Transitions in Diabetes CareLisa Brothers Yetman
Fred Melindy
Tamara Spaic
Rayzel Shulman
Lisa DeMolitor
11:10 – 12:25 p.m.DC2432 – Innovative Strategies in Glucose ManagementMourad Ferdaoussi
Kacey Prentice
Christine Doucette
12:35 – 13:35 p.m.CSEM2413 – CSEM Rising Stars SymposiumMelissa-Rosina Pasqua
Iliana Lega
Breay Paty