Hope For HS

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

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

1 IN 100

7 YEARS

10%

Because our organization is 100% volunteer, with no paid staff and very little overhead, any funds raised go directly toward our programs

Our founding directors realized there is a tremendous amount of work to be done for HS, so they banded together to do it

Every member of our Board of Directors is a patient themselves, or the spouse or parent of someone diagnosed with Hidradenitis Suppurativa

January 18, 2019

Keeping a positive outlook while struggling with pain, discomfort, isolation and all the negativity associated with HS…

January 10, 2019

A few short years ago, Suzanne Moloney was a pastry chef trying to manage daily life with…

January 9, 2019

Simply put, living with Hidradenitis Suppurativa is hard. It puts a tremendous burden on us physically and…

January 7, 2019

One of the most common Hidradenitis Suppurativa home remedies, recommended over and over again by patients, is…

January 3, 2019

Amber Taylor is back on TLC this season, in a "Where are they now?" episode of Dr. Pimple Popper: This…

January 2, 2019

On Wednesday, January 16th, join us at Penn State Medical Center in Hershey, Pennsylvania for a Hidradenitis…