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- Arthritis Society Canada
AR
Arthritis Society Canada
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À propos de nous
Arthritis Society Canada is a national Canadian charity focused on improving the lives of people living with arthritis and ultimately working toward a cure. It’s one of the main organizations in Canada dedicated specifically to arthritis research, support, and advocacy.
Opportunités de Bénévolat
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Position Overview The Government of Prince Edward Island is seeking input from Islanders living with chronic pain, as well as those who support someone experiencing chronic pain, to help shape PEI’s first Chronic Pain Strategy. As arthritis is a leading cause of chronic pain, this is an important opportunity for our community to share lived experiences and help improve how chronic pain care and support are delivered across the province. Participation is through focus groups or an online survey. These opportunities are intended for individuals with lived experience and are not clinical appointments or treatment sessions. Important note This opportunity is not being hosted by Arthritis Society Canada. It is an initiative led by the Government of Prince Edward Island. Our advocacy team felt it was important to share this with the public, as it represents a valuable opportunity for Islanders living with chronic pain, or those supporting someone who is, to provide input and help shape PEI’s first Chronic Pain Strategy. Time Commitment Focus groups: 2-hour session (in person or virtual, depending on date selected) Survey: approximately 10–15 minutes to complete The survey will remain open until June 12, 2026 Participation is voluntary and one-time (unless you choose to engage in more than one format) Key Areas of Participation Participants will be invited to share their lived experience and perspectives on topics such as: Living with chronic pain and its impact on daily life Accessing care and support services Experiences with healthcare systems and community supports Gaps in resources or services Suggestions for improving chronic pain care in PEI Participation Options Focus Groups (In-person and Virtual) June 2 (6–8 pm) – Microtel Inn & Suites, Summerside June 3 (4:30–6:30 pm) – Stratford Town Hall June 15 & 16 (6–8 pm) – Virtual sessions To register for a focus group, please use: Chronic Pain Focus Group Sessions. Online Survey The survey is open to Islanders living with chronic pain, as well as family members, friends, and caregivers supporting someone with chronic pain. English: Community Survey ENGLISH French: Community Survey FRENCH Estimated completion time: 10–15 minutes Closing date: June 12, 2026 Major Contacts Government of Prince Edward Island – Chronic Pain Strategy team Community members and participants with lived or caregiving experience For questions or additional information, please contact: ChronicPain@gov.pe.ca Working Environment Focus groups are held in-person at designated community locations or virtually online The survey is completed online at a time convenient to participants Participation can be done from home or community settings, depending on format Applicant / Participant Notes Participation is voluntary and intended to gather community input to inform provincial planning for chronic pain services. We thank all Islanders who choose to contribute their experiences and perspectives to this important initiative.
Court terme (moins de 6 mois)
Flexible
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Coordonnées
- Lieu
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220 Bay St, Suite 300, 416.979.7228 ext. 3355
Toronto, Ontario
M5J 2W4