Im trying to find as many aussie ppl whom suffer from HS so hopefully next year we can organise...
Hidradenitis suppurativa (HS) Facebook
Bienvenue dans ce groupe de discussion désormais privé, créé et géré par l’AFRH (Association Française pour la Recherche sur...
This Group is to help people who suffer with HS and their families. No one should ever feel alone...
This is a support group for New Yorkers coping with the painful, often-debilitating, and seldom understood condition of Hidradenitis...
Welcome all HS sufferers!!! This page is specifically for New Zealand and Australia HS sufferers I myself am a...
Hidradenitis Suppurativa is a rare and painful illness, and there are people in this community who suffer with it,...
Este é um grupo de apoio para pessoas com HS (hidradenite supurativa). Este grupo serve para darmos apoio uns...
A hidradenite supurativa é uma doença dermatológica inflamatória crônica, caracterizada pela presença recorrente de lesões (nódulos ou caroços) dolorosos...
Je schamen voor je aandoening is absoluut nergens voor nodig! Je bent ziek geworden en dat is je overkomen....
HS is een chronisch huidziekte die gepaard gaat met pijnlijke, terugkerende, onderhuidse ontstekingen in oksels, liezen, billen en andere...
Akne Inversa … auch Acne inversa, Hidradenitis suppurativa, Aknetetrade, Aknetriade, apokrine Akne, Morbus Verneuil, Pyodermia fistulans sinifica, Schweißdrüsenabszess, Perianalfistel...
Support group for people living in Ireland and suffering (yes suffering!!) with HS. The aim of this group is...
I am a stage 4 HS survivor, who has relied a lot on God & my faith to keep...
This group is a discussion page for people struggling with Hidradenitis Suppurativa and using or considering using Humira as...
Este grupo es para personas que padecen Hidradenitis Supurativa familiares y amigos de quienes lo padecen aquí podremos compartir...
Our programs and projects seek to improve the quality of life for Hidradenitis suppurativa (HS) patients.
Hidradenitis suppurativa (HS) Non-Profit (501c3) 2017 Registration
We are currently fundraising for the Non-Profit (501c3) registration of HSAWARENESS.ORG and our growing NGO at large. We cannot realize this next and essential step for our critical work without you.
“I WILL NOT HIDE” Hidradenitis suppurativa (HS) Patient Stories Book Series
The “I WILL NOT HIDE” Hidradenitis Suppurativa book series is now available. These patient story volumes tell the stories of Hidradenitis Suppurativa (HS) patients in vivid and personal narrative. Told by HS patients themselves.
HSAWARENESS EMAIL UPDATES
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