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Because your voice matters.

Respondents, Canadian Pain Task Force Public Consultation

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Open to Patients, caregivers and researchers across Canada

Last updated

The Canadian Pain Task Force launched a national public consultation to learn more about the issues, needs and priorities that matter most to Canadians in order to improve how pain is understood and managed in our country. The consultation provides a critical opportunity for Canadians to share their perspectives on chronic pain and is open to anyone with an interest in pain, including people living with pain, caregivers, health care providers, researchers, policy makers and the general public. The input received from this consultation will help inform the Task Force’s second report to Health Canada in June 2020, which will outline elements of an improved approach to pain in Canada.

The Canadian Pain Task Force was established by Health Canada in spring of 2019 to recommend an improved approach to pain care, education, research and data monitoring in Canada.

Learn more about the Canadian Pain Task Force.

From Our Community

Lucie Neliba

Patient Partner, Surrey

Lucie Neliba

The Patient Voices Network has connected me to a community with the same drive to bring person- and family-centred care to the forefront. I am grateful for all opportunities I have been a part of thanks to PVN, which positively impacts patients like my sister and their caregivers. No matter how small, all patient engagement will help shape the future of health care and that I can stand behind