28 February 2017 marks the tenth international Rare Disease Day coordinated by EURORDIS. On and around this day hundreds of patient organisations from countries and regions all over the world will hold awareness-raising activities based on the theme of research.Rare Disease
Rare Disease Day® 2017
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Pfizer has reported positive results from a trial of its monoclonal antibody PF-06410293, which the firm is developing as...
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SANTA BARBARA, Calif. – Santa Barbara has a new singing sensation. Jackson Cocciolone was crowned 2016 Teen Star Champion...
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Tiffanie’s patient interview and webinar discusses her HS story, journey, and frustrations along the way.Hidradenitis Suppurativa “#iwillnotHIDE” Patient Personal...
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Guideline on Hidradenitis suppurativa Developed by the Guideline Subcommittee Several studies aimed to assess frequency of HS using...
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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