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Author: Tracy McQuire

MEDIA RELEASE: Canada takes leadership role at Global Summit to End Diabetes Stigma

Next week, advocates, researchers, clinicians, and people living with diabetes from more than 30 countries will gather in Jaipur, India, for the inaugural Global Summit to End Diabetes Stigma.

This landmark event will bring together global voices, lived experience, and evidence to confront one of the most persistent and overlooked barriers in diabetes: stigma. The Summit will feature more than 150 contributions, including over 100 digital submissions, and will help shape a global roadmap for action.

Canada will play a visible leadership role in that work. Diabetes Action Canada (DAC), a Trailblazer Partner of the Summit, will be represented by more than 12 network members attending and presenting across panels, workshops, film screenings, and digital contributions.

DAC’s presence reflects a distinctly Canadian model of patient-partnered leadership. Funded through CIHR’s Strategy for Patient-Oriented Research and based at University Health Network, DAC works alongside more than 400 patient partners across Canada to co-design research, programs, and tools grounded in lived experience.

DAC members contributed more than 20 accepted abstracts to the Summit, spanning panels, spotlight sessions, workshops, and digital contributions. In advance of the Summit, DAC is also helping host pre-Summit film screenings, including Low and Low Priority, creating space for storytelling, reflection, and dialogue on the realities of diabetes stigma.

DAC’s Research-to-Action Fellowship will also be strongly represented throughout the program. Of the nine fellowship projects developed over the last two years, seven will be presented at the Summit. In addition, the fellowship itself is featured through a digital contribution highlighting it as a model for reducing diabetes stigma through community-led knowledge mobilization.

The Canadian presence at the Summit also extends to national leadership. Member of Parliament The Honourable Sonia Sidhu will be speaking on Day 2 of the Summit. She has played a key role in advancing Canada’s Diabetes Framework and brings an important policy perspective to the global conversation.

Linxi Mytkolli, Director of Patient Engagement at Diabetes Action Canada, serves on the Summit’s international Steering Committee and will emcee the event. Laurie Lepine, Francophone Engagement Coordinator at DAC, is also part of the team supporting the delivery of the Summit.

“As someone living with diabetes, I know stigma is not just a concept or a policy issue. It can shape how you are spoken to, how seriously you are taken, and how safe you feel asking for care or telling the truth about what you need,” said Mytkolli. “What makes this Summit so powerful is that it brings people together not just to name that harm, but to build something better together. That is the work we believe in at DAC, too.”

Tracy McQuire, Executive Director of Diabetes Action Canada, said the scale of DAC’s contributions reflects the strength of research shaped with communities, not just for them. “Through CIHR’s Strategy for Patient-Oriented Research, Canada has helped build a model where people with lived experience are true partners in shaping research and solutions. To see more than 20 DAC abstracts accepted, seven fellowship projects featured, and our members contributing across the program is incredibly meaningful. We are proud to bring that approach to a global effort to end diabetes stigma and improve care.”

Based at University Health Network, DAC is anchored in one of the world’s leading academic health systems. Earlier this year, Toronto General Hospital, part of UHN, was ranked #2 in the world, underscoring the global strength of the institution supporting this work.

The Global Summit builds on the international momentum to end diabetes stigma, including the Pledge to End Diabetes Stigma, which has engaged thousands of individuals and organizations across 119 countries, and aims to produce a global roadmap for action across healthcare, research, and policy.

Diabetes Action Canada will continue sharing reflections, stories, and contributions from its Canadian delegation throughout the Summit.

About Diabetes Action Canada

Diabetes Action Canada is a national research network funded through the Canadian Institutes of Health Research Strategy for Patient-Oriented Research and based at University Health Network. DAC brings together people living with diabetes, loved ones, researchers, clinicians, and decision-makers to co-design solutions that improve lives and health systems. Through a national network of 400+ patient partners and initiatives including the Research-to-Action Fellowship, DAC advances more equitable, person-centred diabetes research and care across Canada.

Media Contacts

Linxi Mytkolli
linxi.mytkolli@uhn.ca

Tracy McQuire
tracy.mcquire@uhn.ca

Understanding and Preventing DKA: New Research Highlights Real-World Barriers and Opportunities for Change

Diabetic ketoacidosis (DKA) remains one of the most serious emergencies faced by adults living with type 1 diabetes. Even today, DKA leads to thousands of hospital visits in Canada each year. While prevention is absolutely possible, the steps involved: checking ketones, interpreting results, adjusting insulin, and knowing when to seek urgent care, can feel confusing or overwhelming in real life.

A new Canadian study published in the Canadian Journal of Diabetes shines fresh light on why DKA remains so hard to prevent and what could help. For people living with type 1 diabetes, families, and clinicians, the findings reveal the everyday challenges that often go unseen. For the health‑care system, this work highlights the need for clearer education and better tools to support timely action.

👉 Read the full article here: https://www.sciencedirect.com/science/article/pii/S1499267125003995?via%3Dihub

What the Researchers Wanted to Learn

This research team, led by Diabetes Action Canada (DAC) member Dr. Bruce Perkins, and supported by patient partners, including DAC Research to Action Fellow, Wajeeha Cheema, set out to understand the behavioural and practical barriers that make DKA prevention difficult. Instead of focusing only on clinical factors, they explored the lived experiences of adults with type 1 diabetes and the clinicians who support them.

Their goals included:

  • Understanding why ketone testing is often delayed or avoided
  • Learning how people interpret ketone results and decide what to do
  • Exploring the emotional and system‑level factors that affect sick‑day management
  • Identifying what makes someone hesitate to seek emergency care—even when they know it’s needed

To gather these insights, the team conducted three focus groups with people living with type 1 diabetes, a caregiver, and health‑care professionals from across Canada. Recruitment through DAC’s national research registry, Connect1d (connect1d.ca), was valuable, ensuring the study included people with lived experience who could speak authentically about day‑to‑day challenges.

What the Study Revealed

Participants described a mix of emotional, logistical, and knowledge‑based barriers that can make DKA prevention harder than it appears on paper.

Key findings included:

  • Limited understanding of ketones and their risks. Many participants were unsure when to test for ketones, what the numbers meant, or how ketones differ from typical blood glucose changes.
  • Difficulty remembering sick‑day steps. With so many daily diabetes tasks, the details around ketone testing were easy to forget, especially during illness.
  • A heavy emotional load. Some participants did not see themselves as “sick” and hesitated to ask for help. Others described burnout and feeling overwhelmed by constant management.
  • Negative experiences in the health‑care system. Fear of stigma or feeling dismissed made some people reluctant to visit the emergency department.
  • Limited access to supplies and outdated educational tools. Ketone strips can be expensive, and many sick‑day resources were viewed as confusing or overly technical.

At the same time, the study highlighted strong enablers: reminders from clinicians or apps, supportive communities, simple visual resources, and tools that use clear language.

These findings point to practical, actionable improvements, especially as technologies such as continuous ketone monitoring continue to advance.

How Connect1d Strengthened This Research

Diabetes Action Canada is thrilled that Connect1d played a key role in this study.

Connect1d was designed to make it easier for people living with type 1 diabetes to participate in research that matters to them. By using Connect1d, the study team recruited participants directly from a national community of individuals who had already expressed interest in contributing their experiences to science.

This study demonstrates exactly why Connect1d exists:

  • to help researchers meaningfully involve people with lived experience
  • to ensure studies reflect real‑world challenges, not assumptions
  • to strengthen patient‑oriented research across Canada

Looking Ahead: What’s Next for Connect1d in Spring 2026

The insights from this study are already shaping next steps. The research team is now co‑designing an easy‑to‑use, visually engaging DKA prevention infographic with patient‑partners. This new resource will undergo testing and refinement to make sure it is clear, practical, and usable in everyday situations.

For Connect1d, Spring 2026 marks an exciting period of growth. While details will be shared closer to launch, major improvements are underway to make the platform even more intuitive and accessible. New capabilities will enhance how people connect with researchers, shape study priorities, and stay engaged in research that reflects their lived experience.

Preventing Lower-Limb Amputations with Explainable AI

Lower-limb amputations remain one of the most devastating complications of diabetes, yet many are preventable with timely screening and intervention. Through a collaboration with GEMINI, the Vector Institute, and Unity Health Toronto, Diabetes Action Canada researchers helped develop and validate a new artificial intelligence (AI) model designed to identify people at high risk for diabetic foot complications.

The goal is simple but critical: help clinicians intervene earlier and prevent avoidable amputations.

People living with diabetes face more than a 30% lifetime risk of developing foot complications, and even after a wound heals there is roughly a 40% chance of recurrence within one year. Evidence shows that routine foot screening significantly reduces amputation rates, but clinicians need better tools to identify which patients require the most urgent follow-up.

Most modern AI prediction models operate as “black boxes,” generating risk scores without explaining how they reached their conclusions. This lack of transparency can make it difficult for clinicians to trust the predictions or use them to guide conversations with patients.

To address this challenge, the research team developed an interpretable AI model designed specifically for clinical use. Rather than simply generating a risk score, the model shows how individual factors, such as age, kidney function, or blood glucose levels, contribute to a patient’s overall risk. This transparency allows clinicians to understand the reasoning behind each prediction and integrate it more confidently into care decisions.

The model was trained using health data from 107,836 adults with diabetes discharged from 29 hospitals across Ontario between 2016 and 2023. Unlike many traditional prediction tools, it also accounts for competing health events, such as in-hospital death, that may occur before a foot complication develops.

When evaluated, the model demonstrated competitive or superior accuracy compared with existing black-box AI approaches, while remaining fully transparent and auditable.

Most importantly, the tool can be used at the point of hospital discharge to flag patients who may need urgent follow-up foot screening in the community. This creates an opportunity to prioritize care for those at highest risk and strengthens provincial efforts focused on lower-limb amputation prevention.

The model’s analytical engine — Competing Risks Survival Prediction using Neural Additive Models: Fine Gray (CRISPNAM-FG) — was recently presented in a spotlight session at International Association for Safe and Ethical AI (IASEAI) 2026, an international conference on trustworthy AI held at UNESCO in Paris.

This work represents another step toward using responsible artificial intelligence to support clinicians, improve care pathways, and prevent avoidable complications for people living with diabetes.

Read the full study:
Explore how an interpretable deep survival model was developed to predict post-discharge diabetic foot complications using data from hospitals across Ontario here: https://arxiv.org/pdf/2511.12409

Why Patient Voices Matter Here: How Conferences Can Better Include Lived Experience

Written by: Brit Hancock. Brit is a disability and health equity advocate from London, Ontario. As someone living with type 1 diabetes and diabetes-related complications, she speaks openly about how stigma shapes healthcare experiences. She is a Research-to-Action Fellow with Diabetes Action Canada, focused on turning lived experience into action.

Returning to In-Person Diabetes Conferences

This past November, I attended the 2025 Diabetes Canada Professional Conference. I was genuinely excited. Being back in a shared space mattered more than I expected. After so much time connecting through screens, it felt meaningful to be together again, listening in real time and learning alongside one another.

As the week unfolded, I became more aware of where that sense of belonging was coming from, and why it mattered. Within our Fellowship group, patient voices felt valued and safe. We learned from one another in ways that were immediate and practical, through late night Zoom calls and early morning WhatsApp conversations.

It made something clear to me. There is a depth of knowledge within patient communities that does not always surface on conference slides or panels, even though it shapes the work in important ways. Conferences bring people together, and that creates an opportunity not only to share research, but also to surface knowledge that already exists within the communities living the reality being discussed.

I really felt this while watching other fellows present their scientific posters developed outside of the Fellowship. We often speak about lived and loved experiences, but standing there and listening to them walk through their work, I was reminded that patient partners bring far more than personal perspective. They are professionals working across research, policy, technology, education, and care. Once someone is labelled as a patient partner, that experience is not always fully heard.

I learned practical things from their projects, insights that I will carry into my own diabetes management and advocacy.

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Jeremy Auger, Matt Larsen, and DAC Team members pictured at the Low Priority film premier, Toronto 2025.

At one point while presenting, a fellow in our cohort, Anmol, said almost in passing, “I’ll be getting my PhD too.” It landed because it named something so many of us live every day. Patient partners are often understood as people who respond or react, while the work we do to lead, design, analyze, and teach is less visible. Standing there, it was clear how much expertise and effort can go unnoticed once someone is placed into a single category.

During the screening of Low Priority, fellows Jeremy and Matt spoke openly about their own experiences in front of a huge auditorium. They did not ask for sympathy, but asked for attention. The panel repeated a simple line: “We are the system.” As the room listened, the tone shifted in a quiet but very noticeable way. It was one of those moments where lived experience changes how people sit with what they think they know.


Learning Beyond the Sessions

Outside of the formal sessions, the learning continued in quieter moments.

Over lunch, fellow Maryann and I were managing dropping blood sugars after a busy morning. At the same time, Amanda was supporting her son from provinces away, guiding his diabetes care through an AID system while staying present in the room. It struck me how much she carries, and how easily that kind of work goes unseen — parenting, professional contribution, advocacy, and constant life-altering decision-making all at once.

That same kind of care showed up again on the final day when a few of us came down with a flu bug. We shared sick-day tips, talked through electrolyte options, and compared what helps when blood sugars are unpredictable and energy is low. In those conversations I learned more about my fellow Wajeeha’s work on ketones and sick-day management, not in a meeting but through care and mutual support.

What surprised me most was how natural all of this felt. I have only met most of my fellow Fellows twice in person as we live across Canada, and yet there we were supporting one another through illness, pump and CGM glitches, and fatigue. Community built through screens and long conversations had become something very real.

These moments might seem small, but together they show the kinds of practical expertise people living with diabetes share every day. Much of diabetes care happens between appointments, and peer learning is often where management strategies become usable in real life.


Why Patient Voices Matter in Conferences

This is why patient voices matter here. Not because they are symbolic, and not because they are there to react, but because they carry forms of knowledge that are difficult to find elsewhere. “Nothing about us, without us” is not just a slogan. It is a practice.

Conferences like this one matter because they create opportunities for learning to move in more than one direction. When patient voices are included meaningfully, research becomes more grounded and care becomes more responsive. The work benefits because it is informed by people who live within the realities being discussed.

Including patient voices is not about adding emotion to science. It is about strengthening it.

People living with diabetes ask different questions, notice different outcomes, and identify practical barriers that may otherwise remain invisible. That leads to more relevant research and more usable care.

In practice, this can look simple. It can mean inviting patient partners into program planning earlier, including them as presenters beyond lived-experience panels, and creating space for conversation rather than only presentation. When dialogue is intentional, the learning becomes shared rather than one-directional.


From Presence to Partnership

There is also so much I have not even touched upon here. I did not speak about the Diabetes Action Canada breakfast, where we presented work created alongside our partner organizations and sparked conversations long after the session ended. That moment mattered to me because it showed how collaboration allows ideas to travel between researchers, clinicians, and people living with diabetes.

Even writing this, I am aware that naming only parts of the experience still feels incomplete, which in many ways reflects the Fellowship itself. It is not defined by a single project or panel. It is built through relationships that continue to grow and shape the work.

That is what stayed with me this week, and why patient voices matter here.

Stem-Cell Therapy for Type 1 Diabetes: Why Measuring What Matters Is the Next Frontier

A new commentary published in Nature Medicine
“Adults with type 1 diabetes define what matters to them in stem-cell derived islet cell therapy” — calls for a shift in how emerging therapies are evaluated.

The science behind stem-cell–derived islet cell therapy is advancing quickly. Clinical trials are showing promising results, including insulin independence for some participants.

But as this publication argues, the question is not only whether these therapies lower A1c. The question is whether they change people’s lives in ways that matter.

Read the full publication here. 

Stem-Cell–Derived Islet Therapy and the Limits of Traditional Diabetes Outcomes

Stem-cell–derived islet therapies aim to restore endogenous insulin production. Larger trials are underway, and regulatory review is on the horizon.

Historically, diabetes treatments have been evaluated using metrics such as:

  • Hemoglobin A1c
  • Time in range
  • Severe hypoglycemia

These measures are important. But they do not capture what many adults living with type 1 diabetes describe as transformative.

Lower glucose variability matters.

But so does sleeping through the night without fear.

So does no longer planning every meal, every trip, every swim around insulin dosing and device management.

When therapies evolve, evaluation frameworks must evolve with them.

What Adults Living With Type 1 Diabetes Say Matters Most

The PROMISE workshop brought together clinicians, researchers, regulatory experts, and adults living with type 1 diabetes to define meaningful outcomes for stem-cell–derived islet therapy.

Participants described changes that extended far beyond glycemic control:

  • Freedom and spontaneity in daily life
  • Reduced cognitive burden
  • Relief from constant decision-making
  • Fewer visible devices
  • Less fear during sleep
  • Reduced impact on family members

One participant described post-transplant life as “the freedom I never dreamt of.”

These are measurable experiences. But they require intentional tools to capture them.

Without fit-for-purpose person-reported outcome measures, these dimensions risk being invisible in regulatory and reimbursement decisions.

Peter Senior, Linxi Mytkolli and Kitty Shephard pictured at ATTD 2025 PROMISE workshop. 

Diabetes Action Canada’s Role in Advancing Patient-Engaged Cell Therapy Research

Diabetes Action Canada has played a direct role in shaping this work.

Linxi Mytkolli, Director of Patient Engagement at DAC, co-facilitated the PROMISE workshop and is a co-author on the publication.

Peter Senior, DAC member and clinician-scientist, was a leading driver for the workshop and is also a co-author.

Kitty Shepherd and Kathleen Gibson, both DAC patient partners, contributed directly to the discussions at the ATTD Conference in Amsterdam. 

In addition, fourteen DAC patient partners who have received cell transplants submitted written testimonies ahead of the workshop. Their reflections informed the facilitation design and were synthesized into a one-page insight summary distributed to all attendees. These lived experience narratives anchored the conversation in real-world impact.

This patient-engaged approach did not begin or end with a single meeting.

DAC presented this work at d-Data in Chicago last summer.

It was also featured through our Research-to-Action Fellowship at the Diabetes Canada conference in November.

We have dedicated an entire Fellowship project to cell therapy and lived experience, led by Alex St John and Emily Burke-Hall, with knowledge mobilization outputs forthcoming.

Peter Senior and Esther Latres, SVP of Research at Breakthrough T1D, authors of the PROMISE workshop and paper, pictured at dData 2025 in Chicago. 

Why Patient-Reported Outcomes Matter for Stem-Cell Therapy Approval and Access

Regulators must determine whether benefits outweigh risks. If the benefits that matter most to people living with type 1 diabetes are not measured rigorously and consistently, they may not carry weight in formal decision-making.

Measurement influences:

  • Regulatory approval
  • Reimbursement and coverage
  • Health technology assessment
  • Access and equity

This commentary calls for:

  • Consensus-driven conceptual models of what matters to adults living with type 1 diabetes
  • Modern, strengths-based person-reported outcome measures
  • Reduced response burden
  • Global collaboration to ensure validity and comparability

Innovation in stem-cell biology must be matched by innovation in evaluation science.

Linxi Mytkolli facilitating at ATTD 2025 PROMISE workshop. 

Looking Ahead: Continuing the Conversation on Cell Therapy and Lived Experience

This work continues.

This spring, insights from DAC’s patient-engaged cell therapy initiatives will be shared at the End Diabetes Stigma Global Summit, where Alex and Linxi will present findings from our Fellowship project.

As stem-cell–derived islet therapies move closer to clinical reality, DAC remains committed to ensuring that lived experience shapes how these therapies are assessed, approved, and implemented.

Progress in diabetes care should not be defined by glucose metrics alone.

It should be defined by whether people can live more freely, safely, and fully.

At the Table: Youth, Diabetes, and Canada’s Global Health Voice

This piece was written by Linxi Mytkolli, Director of Patient Engagement at Diabetes Action Canada. Linxi brings deep expertise in patient partnership and knowledge mobilization, and her appointment as Canada’s Youth Delegate on Global Health is a meaningful opportunity to extend that work onto the international stage. We are proud to see her leadership helping bridge lived experience, research, and global policy dialogue.

Why youth consultation and lived experience belong in global health governance

Living with diabetes feels, to me, like a stereo that does not turn off.

The music is grief. Sometimes it is quiet, just a background hum. Sometimes it swells when stress rises. Sometimes it layers with joy or achievement. It changes tone, but it never fully stops.

That constancy has shaped how I understand health.

Diabetes is not an event. It is an environment. It is the ongoing recalibration of numbers, risk, emotion, and identity. It is calculating insulin under fluorescent lighting. It is waking up to alarms. It is building a life while the stereo keeps playing.

For a long time, global health felt far from that reality. The World Health Assembly. Multilateral negotiations. Diplomatic briefings. Acronyms and formal statements.

This year, those worlds meet.

I will serve as Canada’s Youth Delegate on Global Health.

When I received the news, I felt the weight of what this role carries. Because I know the stereo does not turn off for other young people either.

From Community to Committee Rooms

As Canada’s Youth Delegate, I serve as an Advisor within the Canadian Delegation to multilateral health meetings, including the World Health Assembly at the World Health Organization and the Directing Council of the Pan American Health Organization.

In practice, this means conducting youth consultations across Canada on key health priorities and bringing those perspectives forward to help inform how Canada engages internationally.

In parallel, I continue to serve as Director of Patient Engagement at Diabetes Action Canada.

These roles are not separate. They are extensions of one another.

At DAC, we have embedded patient partnership into the foundation of how research and policy engagement are designed. We work alongside patient partners and fellows across the country to co-design projects, mobilize knowledge, and ensure that research is shaped by the communities it aims to serve.

Through this delegate role, I am especially committed to opening consultation and co-design opportunities to our patient partner community and fellowship network. Not as a symbolic exercise, but as a natural continuation of the work we already do.

When Canada enters global health discussions, it should do so informed by the lived realities of the people most affected.

Why This Matters for Diabetes

For young people living with diabetes, the issues debated in global health forums are not abstract.

Non-communicable diseases.
Digital health and artificial intelligence.
Universal health coverage.
Mental health.
Access to medicines and innovation.

These themes shape how care is delivered, how devices are regulated, how data is governed, and how stigma is acknowledged or ignored.

Global health governance influences research priorities, funding streams, and national implementation strategies. It shapes the conditions in which we manage our conditions.

If youth perspectives are absent from those conversations, the distance between policy and lived experience widens.

One consultation theme I expect to hear clearly — especially from young people living with diabetes — is the layered reality of affordability and stigma.

Affordability is not only about the price of insulin or devices. It is about aging out of parental coverage. It is about navigating early career jobs without benefits. It is about provincial variation in access to technologies that are framed as “standard of care” but remain unevenly funded.

And stigma compounds that burden. Young people are often expected to self-manage perfectly while proving they are capable students, employees, partners, and leaders. When blood sugars fluctuate, it is read as irresponsibility. When devices are visible, it invites commentary. When mental health falters, it is framed as weakness rather than chronic strain.

If we want better outcomes, we have to name the conditions around the condition.

The 4Ls at the Global Level

At Diabetes Action Canada, we speak about the 4Ls framework: Lived, Loved, Learned, and Laboured experience all belong at the table.

Science is stronger when it is informed by lived experience.
Policy is more durable when it reflects caregiving realities.
Health systems are more responsive when they integrate frontline insight.

Extending that philosophy into global health governance is not symbolic. It is structural.

Canada’s engagement at WHO and PAHO shapes technical guidance, global strategies, and shared commitments that cascade into national systems. The work we do nationally does not sit outside that architecture. It is shaped by it.

Bridging grassroots co-design with multilateral diplomacy is not a contradiction. It is necessary infrastructure.

Carrying Both Worlds

The stereo will still be playing when I walk into those rooms.

I will still manage insulin doses. I will still respond to device alarms. I will still live inside the constancy of chronic disease.

And I will sit in spaces where global health priorities are debated and negotiated. Spaces where language becomes strategy, and strategy becomes lived reality for millions of people.

As Director of Patient Engagement at Diabetes Action Canada, I have seen what happens when lived experience is integrated early and meaningfully into decision-making. Research improves. Trust strengthens. Outcomes shift.

As Canada’s Youth Delegate on Global Health, I carry that same commitment forward.

Youth deserve more than symbolic inclusion.

They deserve influence.

And lived experience does not belong on the margins of policy.

It belongs in the rooms where decisions are made. 

An Invitation 

If you are under 40 and living with diabetes, or if you work with young people navigating this condition, I invite you to help shape what Canada carries into those rooms.

Over the coming months, we will be hosting consultation opportunities through Diabetes Action Canada. We are starting with a very short survey to identify the priorities and questions that matter most to youth and young adults with diabetes.

Your input will help set the agenda for what is elevated in consultations and what is brought forward into global health discussions.

If youth and diabetes perspectives are not named early, they are often missing later.

Let’s name them.

Diabetes Action Canada Secures Two-Year Renewal to Advance Patient-Oriented Research and Systems Impact

Diabetes Action Canada (DAC) has secured two additional years of funding through the Canadian Institutes of Health Research (CIHR) Strategy for Patient-Oriented Research (SPOR) program.

This renewal supports the next phase of DAC’s national work to ensure patient-oriented research delivers measurable impact in policy, in practice, and in communities across Canada.

Three Pathways to Impact

At DAC, research is designed to move.

To people — where lived experience shapes priorities and knowledge returns to communities in ways that are usable and meaningful.

To policy — where evidence informs funding decisions, standards of care, and health system planning.

To practice — where research translates into scalable equitable models that strengthen prevention, care, and outcomes.

This means scaling what works, embedding lived experience in governance and design, and ensuring evidence moves into health systems where it can improve care.

Core Platforms and Implementation Programs

Over the next two years, DAC will continue advancing four cross-cutting platforms that anchor the Network’s national impact:

  • Patient Engagement, embedding lived experience across governance, research design, implementation, and evaluation.
  • Digital Health, enabling registries, data governance, and responsible AI to support real-world implementation and system improvement.
  • Knowledge Mobilization, translating evidence into community-ready resources, policy guidance, and scalable models of care.
  • Indigenous Health, advancing Indigenous-led priorities through sustained partnership, Indigenous governance, and action on policy and systems change.

These platforms enable implementation-focused programs addressing some of the most pressing challenges in diabetes care:

  • Diabetic Retinopathy Screening, improving early detection and access to prevention.
  • Lower Limb Preservation, strengthening coordinated pathways to prevent avoidable amputations.
  • Older Adults with Diabetes, scaling interdisciplinary community-based care pathways to promote aging in place.
  • Mental Health and Diabetes, scaling a Patient Partner co-designed model integrating structured mental health support and digital tools for young adults experiencing diabetes distress.

Together, these initiatives move prevention and complication reduction upstream, address inequities, and are designed from the outset for real-world implementation and scale.

Indigenous Health: Integrated, Indigenous-Led Partnership

Indigenous Health remains foundational to DAC’s mandate.

Through partnership with the Indigenous Diabetes Health Circle and the First Nations Health and Social Secretariat of Manitoba, DAC participates in Indigenous-led policy priorities and systems change.

This work includes contributing to the National Public Policy Circle, advancing efforts to address anti-Indigenous racism in health systems, supporting engagement with Elders and community leaders, and expanding collaboration in Northern and Arctic communities.

Partnership and Leadership

This work is powered through strong and sustained partnership, research leaders advancing implementation science, Patient Partners embedded as true collaborators, and staff leaders innovating across patient engagement, knowledge mobilization, digital infrastructure, governance, and national coordination.

We are grateful to the Canadian Institutes of Health Research’s Strategy for Patient-Oriented Research (SPOR) program. We are also grateful to our partners, the UHN Foundation, Research Manitoba, the Children’s Hospital Research Institute of Manitoba, and the Alberta Diabetes Institute for their continued support and collaboration.

This continued funding from CIHR sustains the backbone of the Network; protecting equitable engagement, bilingual capacity, Indigenous partnership continuity, and the paid involvement of diverse communities. These commitments cannot be built on short-term funding alone.

Looking Ahead

The next two years represent an opportunity to demonstrate how coordinated, equity-driven patient-oriented research can create lasting systems impact.

DAC will continue to strengthen partnerships, advance responsible digital innovation, and ensure research informs policy and practice in real time.

Because research only matters if it moves — and at DAC, it does.

Amplifying Patient Voices: Reflections after ISPAD 2025

Last November, I had the opportunity to attend the annual international conference of the International Society for Pediatric and Adolescent Diabetes, held this year in Montreal. As DAC’s Francophone Engagement Coordinator, my goal was to learn about new clinical, policy, and advocacy developments, while proudly representing and championing Francophone voices. Accompanied by my colleague Linxi Mytkolli, we took part in numerous meetings, discussions, and learning opportunities around a shared theme: improving the quality of life of children, adolescents, and their families affected by diabetes. As this was my first international conference, I was particularly impressed by the richness and diversity of the exchanges that took place. It is by being exposed to different ideas and approaches that new avenues for reflection emerge and practice changes can take shape.

Learning more about barriers to care in other countries prompts reflection on our own system and highlights areas for improvement that still need to be explored to optimize access to care and services in an international context. One example that stood out to me was the moving session by Ms. Fauzia Moyeen from Pakistan, titled “What to do when there is no glucagon,” a reality that may seem far from ours but is very relevant in several remote and central regions of Canada.

Among the conference highlights, I was particularly touched by the session that immediately followed the opening lecture, titled “Advocacy is for All of Us.” Seeing the emphasis on advocacy right at the start of the conference sent a strong message: the engagement of people with lived experience of diabetes is not optional; it must be at the heart of ALL initiatives, whether clinical, research, or organizational. Decisions that are not made with the people directly affected are disconnected from reality. Too often, patient and family participation remains symbolic, sporadic, or restricted to rigid questions that do not impact their quality of life.

This reality was illustrated by several inspiring sessions: the practical workshop “Making the Case: Advocacy Strategies to Secure Funding for Pediatric Diabetes Care” presented by Didier Jean Pierre, whose talk was both inspiring and concrete: We are not anti-government, we are pro-impact. The session “#DEDOC: Advancing Diabetes Care in Complex Settings: Evidence, Experience, and Advocacy: What we wish you knew and why,” which included Linxi Mytkolli’s presentation on the co-created project with an Indigenous partner within the Research to Action Fellowship at Diabetes Action Canada, was also particularly impactful. Additionally, Ana Alvarez Pagola’s presentation “Adjunct therapies: beyond glucose therapies” highlighted several needs of people living with diabetes by integrating the patient perspective into therapeutic innovations. The conference “Advocacy meets Science: The Advocate’s Role in Advancing Diabetes Research with Patient-Centric Insights,” presented by diabetes advocates from the DAC and DEDOC communities, excellently showcased examples of co-created projects incorporating lived experience. Finally, I would like to mention the session “Are we ready to introduce DIY to a broader audience,” which included the perspective of people with lived experience of diabetes presented by Marie-Laurence Brunet. DIY systems are appreciated by patients but are sometimes a taboo topic in healthcare, and this session highlighted their benefits.

The discussions initiated at ISPAD are encouraging: the importance of patient and family participation is increasingly recognized. However, concrete implementation remains uneven, and many contexts could benefit from more systematic and structured involvement. While the lived experience of adults, the support networks of parents, and the expertise of healthcare professionals are often highlighted, the perspectives of children and adolescents remain too rare. Living with diabetes through a child’s eyes is not the same experience as what adults recall today. Why not find ways to include them in these discussions? For example, for future conferences, co-creating youth panels that create space for discussion of issues that matter to them.

As I left downtown for the greater Montreal area, I did so with a full heart, carrying new connections, new learnings, and new ideas that will meaningfully shape my work at DAC over the coming year. For example, in the recruitment of patient partners for your Patient Circles, we are intentionally strengthening inclusive leadership by appointing two co-chairs, one of which is specifically reserved for a youth representative. This structure aims to move beyond symbolic engagement and create meaningful space for youth voices in decision-making processes that directly affect them. 

ISPAD was an incredible experience for me and reinforced my conviction that every initiative gains relevance and impact when people with lived experience are fully involved in its design and implementation.

Tom Weisz: A Patient Partner Who Kept Us Moving from Knowing to Doing

For nearly a decade with Diabetes Action Canada, Tom helped push foot care forward, asked the hard questions, and reminded us that real impact takes teamwork and persistence. As he retires from the Network, Tom sat down with DAC Executive Director Tracy McQuire to reflect on what he’s learned, what he’s helped shape, and the questions he’s carrying into this next chapter.

Some people change a network with a big, sweeping idea. Tom Weisz changed ours by doing something quieter and often harder: showing up, staying curious, and refusing to let important work stall at “good conversation.”

Tom has been part of Diabetes Action Canada (DAC) since the early days. As he steps back from his formal Patient Partner role, we wanted to pause and say thank you not just for what he contributed, but also for how he contributed: with humour, honesty, and a steady insistence that knowledge only matters if it leads to action.

“Knowing without acting is effectively meaningless.” – Tom Weisz

What brought Tom to DAC

Tom did not come to patient partnership looking for a title. He came because someone challenged him not to waste what he had learned.

Just before he retired from his professional career as a podiatrist, a nurse colleague offered a piece of advice Tom still carries: do not stop contributing just because you are retiring. Around that same time, he was publishing and presenting on diabetic foot care work that put him in rooms where policy, practice, and lived experience collided.

One moment still makes him laugh: attending a conference, hearing a speaker reference “a small article that sums it up nicely,” and realizing the article on the screen was his. That speaker was Dr. Charles de Mestral, and it sparked a connection that brought Tom into DAC’s growing community.

“Next thing I know, I was involved in this, that, and the other,” Tom said — a classic understatement.

A champion for foot care and the long game of change

Many people across DAC know Tom through his contributions to foot care and lower limb preservation work. He has helped keep the reality of complications on the agenda; not to scare people, but to be clear-eyed about what prevention can protect.

Tom’s approach is direct, grounded, and shaped by experience. He understands how easily diabetes complications can be minimized until they become urgent and how hard it can be to shift systems before that moment arrives.

But he also understands something else: change is rarely a single event. It is often a slow build.

Tom described it like this: you can chip away for a long time and only see tiny changes — until one day, you hit the right point and a whole section finally moves. For anyone who has worked on policy, funding, or practice change, the analogy lands.

A learner by nature — and a connector by instinct

If you ask Tom what stood out most over the years, he does not start with accomplishments. He starts with people.

“Without fail,” he said, “there’s not an individual who I’ve come across… that I wouldn’t love to break bread with.”

Tom talked about how much he learned through DAC, not only about different types of diabetes, but about broader realities that shape health outcomes: the health inequities experienced by Indigenous Peoples, stigma, access, and the everyday barriers people face navigating care. His default setting is curiosity, and he treats “I don’t know” as an invitation, not a weakness.

“Everybody knows something you don’t know.”

That mindset made him a steady presence in patient partnership spaces where DAC teams bring ideas, tools, and drafts to be tested, not just for whether they are “good,” but whether they will actually work in real life.

The role Tom played: the question-asker who sharpened the work

Tom often described himself as not being part of the “organizational” side.  He was not seeking to run processes. Instead, he was the person you brought something to when you needed it pressure-tested.

As a member of the DAC Collective Patient Circle, he valued this group as a safe place for people to disagree, to speak up, and to improve ideas early before they became finished products that were harder to change.

And he noticed something important: over time, people got more comfortable naming what didn’t work, not just what did.

That ability to surface what is missing, to ask the question that unlocks the next step, is one of Tom’s gifts. It shaped projects in visible and invisible ways, including DAC’s Research to Action Fellowship (where his feedback helped strengthen the program design) as well as the Patient Partner Recruitment process.

Tom’s “secret sauce” for patient partnership

When asked what makes patient engagement work, Tom did not give a slogan. He gave a practical recipe:

  • Be clear on your target — know what you are actually trying to change.
  • Do not insist on one route — there are “a bazillion ways” to get there.
  • Do not “hear” the word no — expect it, and keep going anyway.
  • Build up the team — you will not do it alone.

He compared it to sport: a good play only works when everyone does his or her part. The “stars” might get the spotlight, but the outcome depends on the whole team.

And he named the truth that patient partners often know best: this work takes time and sometimes progress arrives in bursts after long stretches of slow effort.

Life shifts — and why Tom is stepping back (for now)

Tom is retiring from his formal DAC role due to a shift in health priorities. He shared openly that he and his wife have been navigating long COVID, and that energy is now the limiting factor, not commitment.

As Tom steps back, he is not stepping away from questions that matter. He is turning his attention to a growing and complicated intersection: diabetes and long COVID. For him, the tension is practical—diabetes care often emphasizes exercise, while long COVID can make physical activity unpredictable or impossible. It is a gap he is actively trying to understand, and one he hopes the research community will take seriously and study in depth.

“As someone with diabetes, you’re always told exercise matters for blood glucose. But with long COVID not everyone can exercise. That’s where I’m looking now: what does good care look like when diabetes guidance and long COVID realities don’t line up?”

For Tom, the question is ultimately clinical: what can physicians actually offer; what can they say or do when a person is living with both diabetes and long COVID, and the usual tools (like exercise) don’t apply? He’s hopeful for practical guidance that improves day-to-day health and he is candid about the urgency: he doesn’t want it to take 15 years for emerging evidence to reach the clinic door.

Even as he steps back, Tom’s identity as a contributor has not changed. He still reads widely, follows emerging evidence, and shares articles when something feels important, especially when it connects diabetes with broader health issues.

And while he’s stepping away from committee responsibilities, his message to DAC was simple: he’ll miss the people, and he hopes to re-engage when he can.

Thank you, Tom

Tom, thank you for nearly a decade of partnership, for helping elevate foot care and prevention, for asking the questions that made our work better, and for reminding all of us that progress is only progress when it turns into action.

We are grateful — and we’re keeping a seat open for you.

Calls to action


Congratulations to DAC Researchers Funded Through Diabetes Canada Awards

Strong ideas rise to the top in competitive funding rounds and this year’s Diabetes Canada competition was no exception. With 13 awards funded from 135 applications, the bar was high. Against that backdrop, five of the 13 funded awards (38%) were led by DAC members.

DAC supported 14 of the submitted applications, with three funded, representing a success rate of more than 21% for DAC-supported submissions. Congratulations to David Campbell, Annalijn Conklin, and Mahavir Agarwal, whose projects were supported by DAC.

Projects funded:

  • Does impaired brain insulin action underlie the shared risk of depression and diabetes? A neuroimaging clinical trial
    • Led by Mahavir Agarwal
  • Can social connections help protect against the risk of diabetes and its physical and mental health complications?
    • Led by Annalijn Conklin
  • Enhancing food skills among people exiting homelessness
    • Led by David Campbell

We also celebrate DAC members Bruce Verchere and Dylan MacKay, who were funded through this competition as well.

Projects funded:

  • Can type 2 diabetes remission be achieved with the help of a diabetes medication that works for weight loss
    • Led by Dr. Dylan MacKay
  • Fixing insulin production in type 1 diabetes 
    • Led by Dr. Bruce Verchere

Every project funded through this competition addresses an important aspect of diabetes research. We congratulate all of this year’s award recipients and are proud to see DAC members contributing to such a strong and diverse portfolio of work.

Learn more about Diabetes Canada’s funded research: https://www.diabetes.ca/research/research-funding/currently-funded-research