Hope for HS is fortunate to collaborate with a number of dedicated HS specialists. We asked them why they are passionate about treating HS. I am passionate about HS because I am passionate about the patients and their caregivers. I am passionate about their love of life and resilience. I am thankful to be witness…
For Awareness week Hope for HS asked medical providers, caregivers, and those with HS their top tips for living with HS. Add your top tips in the Comments! Try to connect with other people living with HS. You’re not alone, and people can share ways to navigate everyday life with HS. Steve Daveluy, MD Be…
Hope for HS is a 100% volunteer, grass-roots, patient and caregiver directed non-profit organization, supporting and advocating for HS patients since 2013. All of the work we do is accomplished through volunteers who freely give their time to advance our mission. We asked our volunteers to share why they are passionate about Hope for HS.…
Sometimes we need some uplifting words to get us through the rough patches. Add your uplifting messages to the comments! HS affects patient’s quality of life in many ways. Together, we can make a difference with community education, specialty HS clinics, top-notch research and the most amazing group of volunteers. Our patients are not alone.…
Written by Helen Bui and medically reviewed by Chris Sayed, MD and Tara Jaleel, MD Hidradenitis Suppurativa is not a rare disease The prevalence of HS ranges from 0.1 to 2% of the US population.1 Since HS is often out of sight and not talked about it may seem like it is uncommon, but you’ve…
