Some healthcare providers and researchers have a limited understanding of the barriers to care that exist for people who are members of populations that experience inequities. We needed to determine which approaches in rheumatology care are desired, effective and improve outcomes for all people with Rheumatoid Arthritis (RA) and put them into practice. The two years previous to this research, we explored the experiences of RA care of various populations: persons from rural and remote areas, those who are of Indigenous ethnicity, persons who are elderly with frailty, population groups who have immigrated to Canada, those who are homeless or have low income, and who are women pursuing motherhood. In speaking with people from these diverse communities and their healthcare providers, we developed guiding principles for RA treatment recommendations reflective of their unique circumstances. With this research, we sought to expand this work further.