A study analyzed data from the 2017 Aboriginal Peoples Survey to assess pain-related disabilities (PRDs) among Inuit in Canada. Collaborating with an Indigenous Advisory Committee, researchers collected self-reported data from Inuit aged 15 and older, defining PRDs as experiencing activity limitations due to pain from a long-term condition lasting six months or more. The study found that 11.1% of Inuit reported PRDs, with higher rates among females (13.4%), individuals aged 55 and older (23.7%), and those living outside Inuit Nunangat (17.1%). The prevalence of PRDs also increased with the number of co-existing disabilities, particularly among those with physical disabilities. Additional factors linked to higher PRD rates included lower education levels, attendance at residential schools, and difficulties related to food, housing, employment, and health. These findings highlight the need to communicate risk factors associated with PRDs to Inuit stakeholders to inform awareness, advocacy, and service interventions.