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

Hidradenitis Suppurativa Foundation, Inc. logo

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 icon

HS Events and Organizations

Discover professional and patient events and organizations providing more information on HS.

co-managing HS with a specialist icon

Co-managing HS With a Specialist

Partner with an experienced HS specialist in dermatology to co-manage your HS patients.