This is a support group for New Yorkers coping with the painful, often-debilitating, and seldom understood condition of Hidradenitis Suppurativa (HS). This is an opportunity for us to network as a community and gain friendship as well as valuable information about our condition and treatment modalities. By requesting to join this group, you are acknowledging that you are a New Yorker over the age of 18 or have parental consent. This group is open to New York HS sufferers as well as their friends and familiFacebook Facebook Support Group
Facebook Group: Hidradenitis Suppurativa Empire State New York
reddit “Our Voice Forum for HS Sufferers – earn $20 a month in Amazon gift cards for sharing your experiences about HS! (self.Hidradenitis)” HS Personal Story, Social Media, reddit, 0
Our Voice Forum for HS Sufferers - earn $20 a month in Amazon gift cards for sharing your experiences...
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Photo album of HS on my arms (self.Hidradenitis)
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
Join our mailing list to learn more about the measurable results being made for the patients of rare and orphan disease communities.