Our partners are leading advocates, researchers, clinical experts, and champions on the issue of chronic pain in Canada.
Pain Canada creates new opportunities for action from coast to coast to coast. We do this by connecting people, ideas, organizations and resources. We help researchers find clinicians; we help clinicians find patient-partners; we help care providers access education and information; we help pain organizations interact and share ideas; and we help people living with pain access help closer to home.
We also mobilize resources to build capacity throughout Canada towards a common goal: dramatically improved systems of care and support for people with pain. We’re building a movement and seek to unite a national community to develop country-wide standards, encourage relevant research, promote equity, amplify diverse voices, and champion the rights of people living with chronic pain to live the best possible life, free from stigma and discrimination.
Pain BC is the largest pain-specific charity in the world and an active participant in both British Columbian and Canadian pain initiatives. It was founded by a group of health care providers who were determined to improve the lives of people with chronic pain. They worked to develop a broad group of professionals and people with lived experience and incorporated the charity in 2008.
Since then, Pain BC has increasingly provided backbone support for a growing network, supporting national pain initiatives and campaigns and developing regional, provincial, national and international partnerships. Pain BC’s leadership has helped drive provincial and national policy change, including creation of Health Canada’s Canadian Pain Task Force and the resulting 2021 Action Plan for Pain in Canada.
The Atlantic Mentorship Network builds capacity for primary care providers in the management of pain, addiction and related chronic illnesses. Its innovative programs include the first interprovincial mentorship launched in 2010, a monthly discussion series, annual workshops on key pain and addiction topics, monthly online discussions, mentor training workshops and a safe opioid prescribing course.
The Canadian Pain Society brings together scientists, educators, health care professionals, and patients to foster education and research on pain mechanisms and management, and to improve access to high-quality care with the goal of preventing and treating pain more effectively.
The Centre of Excellence works as a research centre to improve the understanding of Veteran-specific chronic pain and how best to manage it. Its mission is to foster a national network of interdisciplinary pain management centres using research and evidence-based strategies to improve care for CAF Veterans and their families.
The Chronic Pain Network is one of five networks to receive funding through the Canadian Institutes of Health Research’s Strategy for Patient-Oriented Research (SPOR). Working with patients as partners, the Network supports, coordinates and synchronizes leading innovative and high-impact research with the ultimate goal of removing barriers to better chronic pain management.
Health Canada is responsible for helping Canadians maintain and improve their health. It ensures that high-quality health services are accessible, and works to reduce health risks.
The Global Alliance of Partners for Pain Advocacy (GAPPA) Task Force’s brings together patient advocates, patient organizations, scientists, clinicians, healthcare providers, and policymakers to create better outcomes in the awareness, understanding, research, teaching, assessment, and management of pain throughout the world.
Since 2004, the mission of the Association québécoise de la douleur chronique (AQDC), a non-profit charitable organization, has been to improve the well-being of people with chronic pain in Quebec and reduce their isolation. It provides pain support groups and a help line.
The Ontario Chronic Pain Network is a partnership between the Ontario Ministry of Health and Long Term Care (MOHLTC), health care professionals working in chronic pain programs, and people living with pain. The network has pediatric and adult subnetworks, with integrated activities and overlap in committee structure. The committees include Clinical Care, Communication/Outreach/Knowledge Translation, and Research. The OCPN and its Executive Committee are working to strengthen Ontario’s network of chronic pain health care providers and evolve models of care for chronic pain management to best serve.
Pain Ontario is a community-based nonprofit organization transforming the way pain is understood and managed throughout the province. Their work makes positive change for everyone who is impacted by the devastating consequences of pain, including people with pain and their loved ones, health professionals, researchers, and the broader community.
People in Pain Network is a non-profit organization that promotes well-being for people living in persistent pain and those who care about them, by strengthening self-management programs, access to resources, and community support.
The Quebec Pain Research Network contributes to the improvement of the quality of life of Quebecers who live with pain through basic, clinical, evaluative and epidemiological research. It leads cohesive efforts between a group of more than 170 researchers associated to the four University Health Networks in Quebec. QPRN ensures knowledge mobilization, interactions between stakeholders and responses to the needs and concerns of people living with chronic pain
SaskPain promotes improved understanding of pain, Saskatchewan-based pain research, and clinical practice improvements that impact people living with pain
Solutions for Kids in Pain (SKIP) is a national knowledge mobilization network incorporated as a not-for-profit organization. SKIP's mission is to improve children's pain management by mobilizing evidence-based solutions through coordination and collaboration.
Take a Pain Check Foundation is a non-profit organization led by youth for youth. Its mission is to empower youth and young adults impacted by rheumatic diseases to advocate for themselves and create a supportive, safe, and inclusive community where individuals feel understood. Through several youth-led initiatives such as the Take a Pain check podcast hosted by Natasha Trehan, blog posts, as well as their new Joint Chat Rheum program and ambassador program, their vision is that all youth and young adults feel supported in their journey when living with a chronic illness.
Canadian Pain Society Representative
He is the Knowledge Translation Chair for the University of Toronto Centre for the Study of Pain and an Associate Professor in the
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Lead for the Alberta Pain Strategy
Dr. Elena Lopatina is a health services and policy researcher, whose embedded research program focuses on the design
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Ontario Ministry of Health representative
Annette Guillemette is a Senior Program Consultant with the Contract Management Unit, Physician Relations
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Quebec Ministry of Health representative
Lucie Beauregard is an advisor for the Chronic Pain Continuum at the Ministry of Health and Social Services
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Clinical Exercise Specialist at Government of Yukon
Annie Worth, BScKin, is a certified exercise physiologist with over 15 years of front-line experience working with chronic pain clients.
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Executive Director for Pain Care BC
Within her 10 years at Fraser Health, she led multiple programs at multiple tertiary and community sites in the areas of emergency, surgery,
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Pain BC Board of Directors liaison
Dr. Chawla is a physiatrist and pain medicine specialist. He is the co-founder of Canadian Pain & Regenerative Institute and holds...
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Person living with pain representative
Desmond Williams is a community healer and TRE practitioner, stand-up comedian and writer whose work is grounded in ...
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Person living with pain and IASP Global Partners for Pain Advocacy representative
Keith has lived with persistent neuropathic pain for over 35 years following a near-fatal car accident. After years of health care...
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Solutions for Kids in Pain Knowledge Mobilization Centre of Excellence representative
Dr. Kathryn Birnie, PhD RPsych is a Clinical Psychologist and Assistant Professor in the Departments of Anesthesiology...
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SaskPain representative
Dr. Susan Tupper is the Manager of Professional Practice for Pain Strategy and Research with the Saskatchewan Health...
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Canadian Pain Task Force “legacy” representative
Dr. Jaris Swidrovich is an Assistant Professor, Teaching Stream, in the Leslie Dan Faculty of Pharmacy at the University of Toronto...
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Person living with pain and youth representative
Natasha Trehan is a student at the University of Ottawa in the Biomedical Sciences Program in the French Immersion Stream...
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Chief Scientific Officer for the Centre of Excellence for Chronic pain in Canadian Veterans
Dr. Abhimanyu Sud is an Assistant Professor at the Temerty Faculty of Medicine, University of Toronto and Research Chair, Primary Care...
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Ontario Chronic Pain Network – Tertiary care representative - Pain Ontario representative
Dr. Deepa Kattail is a pediatric anesthesiologist and pain physician at The Hospital for Sick Children (SickKids) as well as an...
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Chronic Pain Network representative
Dr. Norm Buckley is a Professor Emeritus in the Department of Anesthesia at McMaster University. Dr. Buckley’s interests are pain...
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Québec Pain Research Network representative
A researcher in the pain field since 2006, Dr. Hélène Beaudry is currently the Executive Director of the Québec Pain Research...
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L’Association québécoise de la douleur chronique (AQDC) representative
Alice is a member of the Association Québécoise de Douleur Chronique (AQDC) since 2018. She served as a facilitator...
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Atlantic Mentorship Network for Pain and Addictions representative
Dr. Joshua Rash is an Assistant Professor in the Dept. of Psychology at Memorial University of Newfoundland, Director of...
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Person with pain and People in Pain Network representative
Virginia McIntyre is the President and Executive Director of People in Pain Network (PIPN). She developed persistent pain in...
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