Canadian Care Library
Sponsored by
Hidradenitis & Me Resources
HS Basics
The basics of hidradenitis suppurativa (HS), including symptoms, prevalence, severity guidance and known treatments.
Canadian Healthcare Provider Directory
A curated directory of Canadian healthcare providers to help individuals living with Hidradenitis Suppurativa connect with informed and supportive care.
Accessing Treatment
Clear, Canada-specific information on public and private drug plans to help you navigate your way to care.
Finding the Words
A collection of words and phrases that help describe the lived experience of hidradenitis suppurativa (HS), making it easier for us to express what we’re feeling and for others to better understand the impact of the condition.
Clinical Trials
Explore trusted resources to find hidradenitis suppurativa (HS) clinical trials in Canada and learn how research studies help advance new treatments and care.
National Organizations & Advocacy
Canadian HS Foundation
A national organization advancing awareness, research, and improved care for Canadians living with Hidradenitis Suppurativa.
Canadian Skin Patient Alliance
A national patient advocacy organization working to amplify the voices of Canadians living with skin conditions and improve access to equitable, patient-centered care.
Canadian Dermatology Association
The Canadian Dermatology Association (CDA) is the national organization representing dermatologists in Canada and promotes skin health through education, research, and advocacy.
Reports & Research
The Health Policy Partnership’s Canadian Call to Action Report (2022)
A national policy report outlining key recommendations to improve care, access, and health outcomes for people living with HS in Canada.
