Living with HS can be stressful—and managing your HS symptoms can take a lot out of you. UCB is committed to partnering with the medical community and patient advocacy groups to support everyone with HS—here’s how to get help.
is a national patient advocacy group focused on education and awareness.
offers information on HS and other skin conditions.
is a volunteer organization focused on raising HS awareness and advocacy.
is an online hub for HS support and education led by real people living with HS.
offers support, resources, and education for those living with HS.
connects individuals with chronic health conditions to supportive communities and resources for better management and understanding of their health challenges.
was created by people with HS to track HS symptoms with prompts, a journaling section, and an area to house photos. Plus, it shares the latest HS research and can help locate nearby healthcare providers.