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

February 17, 2019

According to Dr. Elizabeth Kubler-Ross, there are Five Stages of Grief: denial, anger, bargaining, depression, and acceptance.…

February 12, 2019

Due to hazardous road conditions, tonight's Hidradenitis Suppurativa support group meeting in Detroit has been rescheduled for…

January 29, 2019

Due to the extreme cold and wind chill, the Minneapolis meeting scheduled for January 30th has been…

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…