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Author: Tracy McQuire

DAC @ Diabetes Canada Conference 2025

The Diabetes Canada Professional Conference is a key opportunity for our Network to connect, learn, and share progress. This agenda highlights Diabetes Action Canada’s activities throughout the week — from presentations and panels to special events that showcase our collaborative, patient-oriented research.

Wednesday November 26th, 2025

Time SessionSpeakers
13:15 – 16:15DCS1 – Eat Well, Move Smart, Live Strong: A Practical Workshop on Diabetes and Women’s HealthJane Yardley
Cydney Prusky
Nicole “Nikki” Fraser Heslin
Susie Jin
14:45 – 16:15 SPECIAL EVENT
(CanScreen T1D): Can We Prevent Type 1 Diabetes in Canada?
👉 Register here for the CanScreen T1D Symposium

Thursday November 27th, 2025

TimeSessionSpeakers
7:30 – 8:30SPECIAL EVENT FOR MEMBERS:
DAC Networking Breakfast
👉 Register here for the DAC Breakfast
10:30 – 11:45DCS4 – Lifetime Achievement & Early Researcher Awards LecturesDavid Campbell
Rémi Rabasa-Lhoret
14:30 – 15:45DCS8 – Clinical Practice GuidelinesZaina Albalawi
Virginie Blanchette
Barbara J. MacDonald
Arnav Agarwal
Iliana C. Lega
14:30 – 15:45DCS9 – Emerging Adjuvant Therapies in Type 1 Diabetes (& LADA)Melissa-Rosina Pasqua
Alanna Weisman
Nadine Taleb
Sonia Butalia
19:00SPECIAL EVENT
Premiere of Low Priority (Sequel to Low)
👉 Register here to attend the Low Priority premiere

Friday November 28th, 2025

TimeSessionSpeakers
10:30 – 11:45DCS10 – Compassion in Practice: Supporting Clients Through Diabetes Distress and Mental Health ChallengesJessica Kitchler
Ciara Stevens
Sarah Moore-Vasram
Sonja M. Reichert
11:55 – 12:15CC08 – Obesity Treatment in Motion: Navigating Decision Points TogetherSatya Dash
13:00 – 14:14AS04 – Practicalities of screening for kidney disease in diabetesSheldon W. Tobe
Rick Ward
Jo-Anne Wilson
Christopher Tran
Calvin Ke
14:30 – 15:45DCS14 – Complications of DiabetesPedro Geraldes
Vaibhav Patel
Joan Krepinsky
Jacqueline Beaudry
16:00 – 17:15DCS15 – Beyond Basics: Further Topics in Diabetes TechnologyAlanna Weisman
Michael C. Riddell
Rémi Rabasa-Lhoret
Bikrampal Sidhu

Saturday November 29th, 2025

TimeSessionSpeakers
9:15 – 10:30AS05 – Transforming Type 1 Diabetes: Strategies for early detection and delay onset therapeuticsPeter Lin
Peter Senior
Susie Jin
Elizabeth Rosowlowsky
10:45 – 12:00DCS19 – Type 2 Diabetes Remission – Evidence, Impact, and Future DirectionsMegan Racey
Diana Sherifali
Brian McKenna
Mark Ewer
Lindsay Sawatsky
Sonja M. Reichert
13:00 – 14:15ORAL ABSTRACT: DCO3 – Economic Analysis and Return on investment (ROI) for Diabetic Retinopathy (DR) Screening and Treatment through Diabetes Eye Screening Program (DESP) among uninsured patient populations living with diabetes and seeking careAleksandra Stanimirovic

Islet and Stem Cell Innovation in Focus at DAC’s September Network Action Session

On September 25, 2025, Diabetes Action Canada (DAC) hosted its third Network Action Session, bringing together researchers, Patient Partners, community leaders, and trainees from across the country. These sessions are designed to spark conversation, share knowledge, and identify ways to move patient-oriented research in diabetes forward.

Spotlight on Islet and Stem Cell Therapy

A highlight of the session was a presentation by Dr. Peter Senior, who shared his expertise on the future of islet and stem cell therapy. While islet cell transplants offer the promise of eliminating the need for insulin in people with type 1 diabetes, challenges such as donor shortages and immune rejection remain. Dr. Senior underscored the importance of pairing scientific advances with the lived experiences of those directly impacted, reminding us that research must remain connected to patient priorities.

📺 Missed the session? Watch the full recording here


Featured Resources & Initiatives

  • DAC 2024 Collaborators Report
    Highlights include the Research to Action Fellowship, Diabetes Research Connect, research impact in Diabetic Retinopathy Screening (DRS) and Lower Limb Preservation (LLP), and the DAC Workshop.
    👉 Read the report
  • New Article in Diabetologia
    Linxi Mytkolli, DAC’s Director of Patient Engagement, is the lead author of “Diabetes in four dialects: a global call for equity across lived, loved, learned and laboured experiences,” introducing DAC’s 4Ls framework.
    👉 Read the article
  • Sustaining Momentum to Implement the Diabetes Framework
    Developed in partnership with Diabetes Canada and CIHR INMD, this report identifies future diabetes research priorities and emphasizes the need to embed equity, data/registries, community care, and knowledge mobilization tools into the work ahead.
    👉 Read the Grey Paper
  • New Publications from DAC Researchers
    • Type 2 Diabetes Remission: A Systematic Review and Meta-analysis of Nonsurgical Randomized Controlled Trials (Lead: Dr. Diana Sherifali) 👉 Read more
    • Automated Insulin Delivery Systems and Glucose Management in Children and Adolescents With Type 1 Diabetes (Lead: Dr. Jon McGavock) 👉 Read more
    • Feasibility of a Co-designed Technology-enabled Collaborative Care Program for Young Adults With Type 1 Diabetes and Diabetes Distress: A Protocol (Lead: Dr. Carly Whitmore) 👉 Read more

Welcoming a New Team Member

DAC is pleased to welcome Elise Kammerer as Project Lead for the Connect1d Canada platform. Based at the Alberta Diabetes Institute, Elise brings a strong background in implementation science, knowledge mobilization, and co-designing research with people with lived experience. Her work has focused on improving care for children with medical complexity and advancing equity in research and practice.


Upcoming Events

  • DAC Breakfast at the Diabetes Canada Conference (for those already going to the conference)
    🗓 November 27, 2025 | ⏰ 7:30 AM
    👉 Register here
  • Next DAC Network Action Session
    January 2026 (exact date and time TBD)

Stay Connected


✨ DAC thanks all members and partners who continue to make these sessions a space for learning, connection, and collective action. We look forward to building on this momentum in 2026.

Understanding Type 2 Diabetes Remission: New Research, New Resources

For people living with type 2 diabetes (T2D), conversations about management and remission can be complex and at times carry feelings of shame or stigma. Research studies often use very strict protocols and narrowly selected participants, making it hard to see how results translate into real life.

A new systematic review and meta-analysis, recently published in Diabetes Care, helps shed light on what T2D remission really means and how it can be achieved. This is the first study of its kind to evaluate both pharmacological (medication-based) and non-pharmacological (behaviour-based) approaches across 18 randomized controlled trials in 11 countries.

👉 Read paper here

What is T2D Remission?

Remission in T2D means that blood glucose levels return to the normal range without the need for diabetes medication. While this does not mean “cure,” it can significantly improve health outcomes and quality of life.

What Did the Research Find?

  • People were more likely to achieve T2D remission with multi-modal approaches, combining strategies such as medication, nutrition, physical activity, and health coaching.
  • Behavioural interventions, primarily focused on low calorie diets, showed the strongest results, with significantly higher T2D remission rates compared to standard care.
  • Additional benefits included improved A1C, weight loss, reduced hypoglycemia, and better quality of life.

Still, challenges remain: studies varied widely in design, used strict eligibility criteria, and often applied inconsistent definitions of T2D remission. This makes it difficult to know how well these findings apply across diverse populations.

Beyond the Numbers: Knowledge Products Co-Designed with Patients

At Diabetes Action Canada, we believe research should not stop at publication—it must be translated into resources that people can understand and use. This work was led by Dr. Diana Sherifali and her team, who brought together an integrated Knowledge Translation (iKT) group to ensure the research was informed by diverse perspectives. Diabetes Action Canada was invited to join this team, contributing alongside patient partners, researchers, healthcare professionals, and decision-makers to help shape resources grounded in lived and living experience.

Together with our partners at Knowing Diabetes—a hub for trusted information, research opportunities, and expert insights—we’ve developed three key knowledge products:

  1. Graphic Novel
    A powerful story following one woman’s journey with newly diagnosed T2D, capturing the emotions, challenges, and successes of striving for T2D remission.
    👉 Read the graphic novel
  2. Two-Part Video Series: “Evidence-Based Takes”
    Short, accessible videos narrated by Dr. Megan Racey, breaking down what the research means and sharing helpful messages for people considering T2D remission.
    👉 Watch Part 1
    👉 Watch Part 2
  3. Blog Post
    A plain-language reflection on what T2D remission research tells us—and why it matters for people living with diabetes.
    👉 Read the blog

Why This Matters

These tools are designed to increase awareness, promote dialogue, and support informed decision-making around T2D remission. By making the evidence more accessible, we hope to encourage future research that not only tests T2D remission programs, but also considers their long-term sustainability and alignment with patient priorities.


Explore more at Knowing Diabetes and share these resources with your community. Together, we can reduce stigma, spark conversation, and support people living with type 2 diabetes in exploring their options for T2D remission.

New Grey Paper Calls for Stronger Links Between Research and Policy to Improve Diabetes Care

Diabetes Action Canada is proud to have partnered with Diabetes Canada and the Canadian Institutes of Health Research Institute of Nutrition, Metabolism and Diabetes (CIHR INMD) in planning the 2025 Diabetes Research Workshop, which brought together leading researchers, policymakers, and patient partners from across the country. The findings are captured in a new report, Sustaining Momentum to Implement the Diabetes Framework: Diabetes Research Workshop. (Grey Paper 2025).

Turning Research into Action

The Grey Paper makes one point clear: world-class diabetes research must be mobilized into policy and practice if it is to improve health outcomes for the more than four million Canadians living with diabetes. Despite decades of discovery, major gaps remain in access, equity, and integration of proven approaches into health systems.

At the workshop, participants identified priority areas where knowledge mobilization and patient partnership are essential:

  • Equity in care – Targeting interventions at the intersection of diabetes, social determinants, obesity, and cardiometabolic disease yields the highest return on investment.
  • Surveillance and data – Canada needs better diabetes registries and integrated social data to guide policy decisions. Models such as CanScreen T1D, BETTER, CAPACITY, and Connect1d Canada already demonstrate how registries can improve care.
  • Health services and policy research – Evaluating new care models in primary and community settings is critical to reaching structurally underserved populations.
  • Knowledge mobilization tools – Researchers need support to communicate evidence effectively to policymakers. The Grey Paper highlights that CIHR INMD has adopted DAC’s KM consultation service and tools as a national model.

Why It Matters

The report underscores that without coordinated action, Canada risks worsening inequities and rising costs. For example:

  • Diabetes costs the health system $18 billion annually.
  • Only ~40% of underserved Ontarians receive retinopathy screening, despite it being a proven intervention to prevent blindness.
  • Lower-limb amputations have risen in Ontario’s diabetes population over the past decade, even as stroke and heart attack rates have fallen.
  • Out-of-pocket costs can reach $18,300 per year for type 1 diabetes, forcing many to skip or delay treatment.

Diabetes Action Canada’s Role

For Diabetes Action Canada, the Grey Paper is a strong validation of our mission: ensuring that diabetes research is not only excellent but also translated into policy and practice. Through our Knowledge Mobilization program, national registries and data initiatives, and patient-partnered research, we are building the bridge between discovery and real-world impact.

This report is both a roadmap and a call to action: to work together across sectors so that every person in Canada has access to prevention, treatment, and support that is timely, equitable, and evidence-based.

👉 Read the full Grey Paper here

Diabetes in Four Dialects: A Global Call for Equity

We are proud to share that Linxi Mytkolli, Director of Patient Engagement at Diabetes Action Canada, is the lead author of a new article published in Diabetologia: “Diabetes in four dialects: a global call for equity across lived, loved, learned and laboured experiences.”

The 4Ls framework—Lived, Loved, Learned, and Laboured—has been the foundation of Diabetes Action Canada’s approach to patient engagement. It recognizes that expertise in diabetes is not limited to clinical or academic settings. Instead, it is shaped by:

  • Lived: the daily experiences of people living with diabetes
  • Loved: the support of family, friends, and caregivers
  • Learned: the knowledge of researchers and academics
  • Laboured: the work of healthcare providers, policymakers, and advocates

By bringing these four perspectives together, the framework ensures that diabetes research and care reflect the realities of all those affected.

Why this matters

Patient advocates rarely appear in leading scientific journals, let alone collectively across 15 countries as in this article. Publishing in Diabetologia shows what is possible when science makes space for diverse voices and creates opportunities to mobilize this expertise nationally and internationally.

📖 Read the full article here

Supporting the Whole Health of Young Adults with Type 1 Diabetes: A New Approach to Diabetes Distress

Young adults with type 1 diabetes (T1D) face daily self-management challenges that go far beyond blood sugar levels. Mental health struggles (including diabetes distress (DD)) are common, yet care systems often fail to address the emotional and psychological realities of living with diabetes. A new pilot study is changing that.

The TECC-T1D3 trial, supported by Diabetes Action Canada and co-designed by young adults with lived experience, is testing a virtual, technology-enabled collaborative care model tailored to the needs of young adults navigating life with T1D and DD.

Here are three key elements of this innovative project:

1. Mental health is diabetes care—especially for young adults

The protocol aims to address a critical gap in care: traditional diabetes services often prioritize glycemic outcomes over emotional well-being. Yet nearly 40% of people with T1D experience diabetes distress, which can impact self-management, mental health, and long-term outcomes. TECC-T1D3 has been co-designed to offer a more holistic model, centering emotional support as part of everyday diabetes care.

2. Co-designed, patient-led solutions are needed

TECC-T1D3 was co-developed with young adults living with T1D, whose insights shaped everything from intervention design, the content, to the recruitment strategy. As a result, the intervention is delivered virtually through a health coach, supported by a virtual care team, and uses everyday technologies like phone calls and text messaging to reduce cognitive burden. Most importantly, TECC-T1D3 has been designed to prioritize trust, flexibility, and connection—values identified by patient partners as essential to success.

3. Scalable and compassionate care is possible

Unlike many mental health interventions that rely on specialized personnel or proprietary technology, TECC-T1D3 has been intentionally designed for scalability. Health coaches are selected based on relational skills rather than clinical credentials, making it possible to scale the model across diverse communities while maintaining personalized, culturally responsive support.

As the trial progresses, findings will inform the next stage of implementation—laying the foundation for broader, patient-informed mental health support in diabetes care across Canada.

Learn More
Read the full TECC-T1D3 protocol, published in Digital Health: https://journals.sagepub.com/doi/10.1177/20552076251365134

Diabetes Action Canada is proud to support this important work and the patient partners whose leadership is transforming how care is delivered.

Patient Partners Lead National Co-Design Sessions to Build New Diabetes Resources

Diabetes Action Canada is supporting a series of national virtual co-design sessions this month, led by Patient Partners through the Research-to-Action Fellowship. These sessions bring together people with lived, loved, laboured, or learned experience of diabetes to shape tools that respond to real community needs.

This initiative is grounded in the principles of patient-oriented research and collaborative innovation. Rather than traditional focus groups, these sessions are designed as working sessions where participants co-create alongside Fellowship teams.

Participants are offered an honorarium in recognition of their time and contributions. Each session will last 1.5 hours and includes light preparation and follow-up.

Session Topics Include:

  • What People with Diabetes Wish Nurses Knew — Addressing stigma and bias in care
  • Cell Therapy 101 — Demystifying stem cell treatment in type 1 diabetes
  • Hormones & Diabetes — Navigating puberty, pregnancy, and menopause
  • AID 101 — Exploring automated insulin delivery tools and lived experience
  • Right Diagnosis Toolkit — Responding to misdiagnosis in Black, Indigenous, and racialized communities

Open to people in Canada aged 16+, these sessions are part of a broader effort to ensure that new resources reflect the priorities and realities of the communities they are meant to serve.

For more information, visit: https://lnkd.in/edZhZ5pE

When Research Saves Sight and Dollars: The ROI of Patient Partnership in Health Policy

At this year’s CAHSPR conference in Ottawa, Diabetes Action Canada member Aleksandra Stanimirovic, also part of the UHN Program for Health System and Technology Evaluation (PHSTE), presented on behalf of her team members Troy Francis, Jim Bowen, and Valeria Rac; collaborators from South Riverdale Community Health Centre (Rebecca Merritt and Ann Phillips); and Judy Hung from Toronto Western Hospital. Together, they made a strong case for how patient-partnered research can demonstrate that population-based diabetic retinopathy screening, with treatment access for underserved populations, delivers exceptional return on investment for individuals, communities, and the health system.

Co-developed with Patient Partners Debbie and Malcolm Sissmore and Ryan Hooey, the study evaluated the cost-effectiveness of Ontario’s tele-retina screening program for diabetic retinopathy, focusing on structurally underserved populations. Three care models were compared, and population-based screening emerged as the most cost-effective.

The numbers tell a powerful story:

  • $27 saved for every $1 invested when regular screening is paired with low-cost therapy
  • $7.66 saved for every $1 invested when paired with high-cost therapy
  • Improved early detection and prevention of avoidable vision loss
  • Reduced long-term healthcare costs tied to advanced eye disease and disability

But the real ROI goes beyond economics.

Because the study was shaped by individuals with lived experience, the research addressed real-world barriers to access and delivery. Patient Partner insights directly informed the modeling assumptions—ensuring relevance, legitimacy, and impact.

Now, these findings are informing active conversations with health system leaders about scaling diabetic retinopathy screening province-wide. This is patient-oriented research influencing real policy—and driving smarter, more equitable investment.

And this work doesn’t stop at the abstract. Stay tuned for the upcoming peer-reviewed publication, and continued leadership from Diabetes Action Canada in advancing research that saves sight, limbs —and public dollars.

From Ideas to Action: DAC’s Network Session Showcases Community-Driven Solutions

On May 27, 2025, Diabetes Action Canada hosted another Network Action Session, bringing together a diverse community of researchers, Patient Partners, trainees, and community leaders committed to advancing diabetes care and patient-driven research.

The event featured a research talk from Dr. Holly Witteman, who introduced CommuniT1D / CommunauDT1, an innovative, community-led peer-support platform specifically designed for people living with type 1 diabetes. This initiative responds directly to a long-standing request from DAC’s Patient Partners for accessible, community-focused support.

For those who missed it, the full session recording is now available online here.

Research to Action Fellowship: Empowering Patient-Led Innovation

The session also highlighted DAC’s Research to Action Fellowship, which empowers Patient Partners to lead transformative projects that bridge research and community action. The Fellowship’s resource library, featuring impactful projects from its inaugural cohort, has already seen over 10,000 downloads across more than 30 countries.

The current cohort of fellows is actively addressing critical issues such as:

  • Cell Therapy 101: Making stem cell treatments understandable and accessible.
  • Women’s Health & Diabetes: Addressing gender-based disparities in diabetes care.
  • Automated Insulin Delivery 101: Simplifying complex insulin delivery systems.
  • Uncovering Misdiagnosis: Tackling diagnostic biases impacting Black and Brown communities.
  • Diabetes Stigma: Working to reduce stigma in clinical and community environments.

Explore these valuable resources in full here.

Save the Date

Stay tuned for our next DAC Network Action Session coming in September 2025—exact date and time to be announced soon.

To stay connected, follow Diabetes Action Canada on LinkedIn or visit our website at www.diabetesaction.ca.

Have ideas for future sessions? We welcome your input and encourage you to reach out anytime.

Creating Change Through Conversation: Reflections from Our Indigenous-Led Anti-Racism Training

By Sasha Delorme, Chair of the Indigenous Patient Circle, Diabetes Action Canada

What am I doing to create change in this world—for my children, and for future generations? I’m working to make space for honest, open conversations about racism. And not just conversations—transformative ones.

Earlier this spring, the Indigenous Patient Circle (IPC) hosted its second anti-racism training workshop in Magog, Quebec. What made it particularly powerful was that the entire day was planned and facilitated by patient partners.

A small group of eight of us boarded a shuttle at 7:30 a.m., making the 90-minute drive to a quiet ski resort in Magog. By 9:00, we were setting up for a full day of learning and dialogue with research trainees and health system professionals.

Before the day officially began, I had the honour of meeting Elder Gregoire Canapé, who welcomed me with warmth and kindness—taking my hand and gently pressing his cheek to mine, first on the left, then on the right. In keeping with protocol, I offered him tobacco in gratitude for the teachings and prayers he would share with us that day. (As a reminder: it’s customary to offer tobacco when requesting prayers, teachings, or guidance from an Indigenous Elder.)

We opened the workshop, as always, in circle. The circle symbolizes unity and equality, and it creates a safe space for everyone to share their experiences, thoughts, and questions freely.

Elder Gregoire began by smudging the room and sharing stories, teachings, and a prayer and song in his language. His presence filled the space with calm and joy—his teachings were met with smiles and quiet reflection. And since he spoke French fluently, one of our team members stepped in with some spontaneous translation—bringing both clarity and a few moments of laughter.

Later, we welcomed Elder Barb Nepinak to the circle. She shared teachings on the importance of water, the significance of tobacco, and demonstrated how to make a tobacco tie—reminding us of the ceremonial elements that ground our work in community, respect, and tradition.

We also heard from guest speakers: an anti-Indigenous racism facilitator from the First Nations Health and Social Services of Manitoba (FNHSSM), and the Indigenous Initiatives Manager from the CKD Network. They spoke about Indigenous cultural safety and the resources their organizations are creating to better support care and research in Indigenous contexts.

Our facilitators—each of them Indigenous patient partners—shared their lived experiences of racism in healthcare. These stories were powerful and at times difficult to hear. In hindsight, we realized that some content could have benefited from a trigger warning, and we’ll be more mindful of that in future sessions.

At the end of the workshop, we asked the participants—many of whom were research trainees—what they had learned. Their reflections were raw and honest. Several admitted they had never been taught the true history of colonization or how it continues to shape the health of Indigenous Peoples today.

That moment reminded me why these workshops matter. They don’t just teach cultural practices—they invite a reckoning with history. They build bridges between lived experience and structural change. They are, in every way, a step toward reconciliation.

If you ever have the opportunity to attend one of our anti-racism workshops, I encourage you to come with an open heart. The journey toward change begins with listening—and continues with action.

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