HIDRADENITIS SUPPURATIVA RESOURCES:
For Your Practice and for Your Patients
View and download resources and tools for your practice or to provide your patients as they navigate life with hidradenitis suppurativa (HS).
For Your Practice
HS Foundation Website
Find a range of information and resources on HS education, management, and events on the HS Foundation website.
For Your HS Patients
No BS About HS: Website for Patients
Patients and families can learn about living with HS, get tips and tricks from others with HS, hear patient stories, sign up to receive emails, and more.
Hope for HS
Hope for HS is a non-profit patient advocacy organization providing in-depth HS education, support groups online and across the country, and news on the latest HS research.
Patient Handout Guide
This handout covers what HS is, how symptoms appear, and frequently asked questions.
Conversation Guides for your Patients
Talking with a doctor
Talking with a partner/spouse
Keeping positive
Talking with friends and family
Talking with bosses/coworkers
HS Events and Organizations
Discover professional and patient events and organizations providing more information on HS.
Co-managing HS With a Specialist
Partner with an experienced HS specialist in dermatology to co-manage your HS patients.