Canadian Migraine Society

The Canadian Migraine Society (CMS) is a patient-led organization dedicated to empathy, education and empowerment for Canadians living with migraine. Since our inception in 2021, CMS has been improving the quality of life for Canadians living with migraine by offering educational support, peer support and advocacy. It has been fully operated by volunteers, beginning with our founder and president, Maya Carvalho. Volunteers are essential partners in fulfilling the mission.

Please peruse our website for in-depth information.