be seen for who you are.
not for what you have.
who we are
a tax-exempt national patient advocacy organization & non-profit at the forefront of Hidradenitis Suppurativa (HS) research, health equity, diversity, inclusion, awareness, education, art, film, & wellness.
An Organization
by & for HS Warriors
Founded in 2020 by Hidradenitis Suppurativa (HS) warrior & advocate Jasmine IVANNA Espy, The Association of Hidradenitis Suppurativa & Inflammatory Diseases (AHSID)’s goal is to continue developing ways to increase education, advocacy, and awareness to close gaps, ensure adequate care, and empower people in the communities we serve to feel supported emotionally, spiritually, mentally, and physically.
Join our Movement!
AHSID is dedicated to changing the landscape of Hidradenitis Suppurativa (HS) and associated comorbidities. We believe that there is exponential power when members of the community unite to spread awareness and share important information with our larger patient community and stakeholders.
Whether as a volunteer, ambassador, or advocate, you can help us make a difference. Explore opportunities to partner with AHSID and support our mission to uplift the HS community.
HS warrior & AHSID volunteer Gloriel V. shares our educational resources about HS with an attendee at SHSA 2024.
2025 Hidradenitis Suppurativa Summit
Join us June 6-8, 2025 at College for Creative Studies, Detroit, MI
The I Reclaim Hidradenitis Suppurativa (HS) Summit, born in 2020, is a transformative, patient-centered event that brings together individuals living with HS in a journey of education, advocacy, and healing.
What began as a virtual gathering has blossomed into a vibrant, three-day hybrid summit held during HS Awareness Week. This soulful event connects participants with leading HS specialists, creating a safe, nurturing space for personal growth—physically, mentally, and emotionally. It empowers individuals to embrace their condition, discover meaningful solutions, and break free from isolation, fostering deep connections within a community that understands, supports, and values them.
"I've dealt with HS since I was 11 but just got diagnosed early this year at the age of 25! I learned about HS through a TikTok & cried because I realized I wasn't alone. It's been such an amazing journey learning and connecting with other HS warriors! Thank you for creating a platform for us to feel seen, heard & valued. Changed my life for real!”
alyse
online community member
