The Hidradenitis Suppurativa Patient Advocacy Coalition is dedicated to providing outreach to the HS community, promoting HS awareness, and moving HS forward together. We are a coalition of patient advocates and patient advocacy groups. We understand the unique needs of the HS community because we all live with HS. We are moved to help others with HS and raise awareness with the goal to earlier diagnosis, earlier treatment, and better long term outcomes.  ​

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The Hidradenitis Suppurativa (HS) Patient Advocacy Coalition (PAC)’s mission is to educate physicians about the patient experience and facilitate joint awareness campaigns and collaboration amongst patient advocates, patient advocacy groups, and nonprofits supporting the HS community with an overall goal to raise awareness of HS. The HS PAC members have been collaborating since 2022 and became a 501(c)(3) nonprofit organization in 2024.

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