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If you’ve never worked with patient partners or caregivers in your research before (or even if you have!), the CPN Patient Engagement Committee and Network patient partners have some ideas for you to consider. In this, you will find the definition of Patient Engagement and some thoughts about the way you might work with us so that we may bring our lived experience to your research project as collaborators or partners.
Text LinkThe Quebec Pain Research Network shares publications on this page that highlight researchers, research advances as well as their activities and that of student researchers, making everything accessible to the general public.
Text LinkA free, self-paced online program for health care providers who want to support people living with pain to move with more ease.
Text LinkThis practical, compact course allows learners to develop clinically relevant approaches to chronic pain management and develop a strong grounding in pain science.
Text LinkThis free online course for health care providers covers clinically relevant strategies for managing pain before and after surgery, with an emphasis on self-management strategies patients can use.
Text LinkThis is a free self-paced online program offered by Pain Canada and designed to help people undergoing surgery and their families better manage pain after surgery and decrease complications.
Text LinkThe Power Over Pain Portal aims to provide a one-stop shop for resources for people with pain, including articles, videos, podcasts, courses, workshops, and peer support. It also links to national and provincial services.
Text LinkPain BC's free-to-access video series that provides guided movement and relaxation for people living with pain from the comfort of their homes.
Text LinkMyCarePath is an online resource developed by BC Children's Hospital to support youth, young adults, and families across in understanding and managing chronic pain.
Text LinkPain BC's nine-week online program is designed to empower people with pain to improve well-being. The weekly 90-minute online group class is delivered by Pain BC's clinical support staff, and is free to access for people with pain living in BC.
Text LinkPain BC has numerous downloadable information sheets on accessing income supports, managing pain, choosing the right health care provider, and other commonly asked questions by people living with pain. The sheets are available in multiple languages, including English, French, Spanish, Traditional Chinese, Simplified Chinese, Punjabi and Arabic.
Text LinkLivePlanBe+ is Pain Canada's free online program that helps people with pain learn to make small changes that add up to big improvements in well-being. The program is now available in Arabic, French, Punjabi, Spanish, and Traditional and Simplified Chinese, in addition to English.
Text LinkPIPN's virtual Pain Self-Management Education and Support Groups help you find the support you need to acquire and apply self-management skills, reintroduce meaning and purpose into your life, and, most importantly, regain the confidence to establish your own "new normal."
Text LinkThis toolkit is designed for family physicians and other providers to help navigate the journey of care for patients with vulvodynia. From diagnosis to initiating management of symptoms for patients with vulvodynia, this toolkit is your go-to resource for step-by-step compassionate care.
Text LinkThis evidence-informed common core curriculum serves as a foundational resource for self-management programs within tertiary chronic pain programs and other clinical settings.
Text LinkThe CARD system provides strategies that can be used to help cope before and during vaccination and needle procedures for children. The system consists of resources such as videos, handouts and activities that will help to prepare parents and children for childhood vaccinations.
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