HS Resources

https://www.hs-foundation.org/ - research, information on speciality HS clinics, support groups, and clinical trials

https://www.nobsabouths.com/hs-patient-stories/hidradenitis-suppurativa-resources - website from Abbvie, makers of Humira (a biological treatment for HS)

http://hidradenitissuppurativaawareness.org/ - support and advocacy organization for HS patients, providers, and caregivers

https://hopeforhs.org/ - support groups (monthly Zoom meetings), local support groups in several locations across the US, advocacy and awareness building around HS

https://www.aad.org/public/diseases/a-z/hidradenitis-suppurativa-self-care - dermatological information about HS

https://www.hstrust.org/ - UK support and awareness for HS, in-person and online support groups, HS support phone line, and leaflets with basic info about HS

Facebook support groups:

•  #HSGLOBAL - Hidradenitis Suppurativa (HS) International 

• The HS Support Group

• HS Fighters

• Hidradenitis Suppurativa (HS)