The Scottish Alliance for Hidradenitis Suppurativa is a support group aimed at providing support and awareness to HS patients. The group are members of the SCVO and GCVS as a voluntary organisation. It is our aim to lobby on behalf of patients to medical professionals and elected members to provide continuity of treatments and better patient care.Facebook Facebook Support Group
Facebook Group: Scottish Alliance for Hidradenitis Suppurativa
reddit “I’m willing to share my scars and story. Here is my blog, I will update more photos as well! (klmaphis.blogspot.com)” HS Personal Story, Social Media, reddit, 0
I'm willing to share my scars and story. Here is my blog, I will update more photos as well!...
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“Chapter Two. Doctors. Depression.Desperation” Hidradenitis Suppurativa Personal Stories and Support Groups Online Public Domain Source: MDJunction activity for “Hidradenitis...
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I've got a blog about HS (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 organization 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.
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