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“I WILL NOT HIDE” Hidradenitis Suppurativa (HS) Patient Personal Stories

Everyone has the opportunity to publish their story within the Organization. Although we all share the same orphan disease, each story can be different and unique. Learning about other existing co-morbidities associated with HS/AI can lead to proper treatment for patients that do not have awareness or are currently at risk. ( More Info )

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Obtaining knowledge of how others handle their pain can be useful – the mental health implications for all patients are the most debilitating aspects of this chronic disease. Online publishing on AMAZON is a focus. Our self publishing book project, with your contribution, will be available in libraries, schools, book stores, online vendors and homes. The endless series and collection of patient stories will foster general awareness for a disease, and sales will directly benefit awareness programs such as these.


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Hidradenitis suppurativa (HS) Support Group, a humble special project of HSAWARENESS.ORG ©2017 | This website does not provide medical advice, diagnosis or treatment. Your use of this website constitutes your explicit agreement to our Terms of Use and Privacy Policies.

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