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SUPPORTING PATIENTS

Our support groups relieve some of the
tremendous isolation and emotional burden that accompanies a life with Hidradenitis Suppurativa.

ADVOCATING FOR CHANGE

We empower the HS community to interact with payers, researchers, and their government to bring about the change needed to someday find a cure.

RAISING AWARENESS

Raising awareness of Hidradenitis Suppurativa is vital in promoting compassion, understanding, and a correct, timely diagnosis.

ABOUT US

Hope for HS is a 100% volunteer, grass-roots, patient and caregiver directed non-profit organization, supporting and advocating for Hidradenitis Suppurativa patients since 2013.

We first came together at a local support group and realized that there is so much work to be done! Who better to do it, and be sure that it is done right, than the people that live with this disease every day?

Since 2013 we have successfully launched several new chapters for in-person support groups, creating a bridge between HS doctors and patients in their area. Our perennial efforts to raise awareness through events, speaking engagements, and national proclamation campaigns empower members of the HS community to get involved and create change for patients everywhere.

TESTIMONIALS