HSAWARENESS.ORG Presents Hidradenitis Suppurativa Patients Paige and Ron

Paige’s accounts of how our work got started and how it is has changed her life, as well as discussion on what we patients need, and a call for awareness for Hidradenitis Suppurativa.

Hidradenitis Suppurativa “#iwillnotHIDE” Patient Personal Stories Published Online and In Print:

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. Obtaining knowledge of how others cope with HS can be useful – the mental health implications for all patients is also a debilitating aspect for this potentially life long chronic disease.

Learn more at http://hsawareness.org.

Pronounced: HID-ra-den-EYE-tis SUP-you-rah-TEE-vah:
Hidradenitis,Suppurativa,Hidradenitis Suppurativa,Hidradenitis Suppurativa Comorbidity,HS Skin Disease,Hidradenitis Suppurativa Support Group,Hidradenitis Suppurativa Cure,Hidradenitis Suppurativa Treatment,Hidradenitis Suppurativa Diet,Hidradenitis Suppurativa Diagnosis,Hurley classification system,Chronic Gluteal Hidradenitis Suppurativa,Prepubertal Hidradenitis Suppurativa Organizations,Hidradenitis Suppurativa Personal Stories

Otherwise known as:
Acne Conglobata; Acne Inversa; Apocrine Acne; Apocrinitis; Fox-Den Disease; HS; HS Skin Disease; Pyodermia Significa Fistulans; Velpeau’s Disease, Verneuil’s Disease

*HSAWARENESS.ORG does not provide medical advice, diagnosis or treatment.


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HSAWARENESS.ORG | Fighting for Hidradenitis suppurativa (HS), a.k.a Acne Inversa Patient and Doctor Awareness ©2019 hidradenitissuppurativaawareness.org  All Rights Reserved. Your use of this website constitutes explicit agreement to our Terms of Use and Privacy Policies. This website does not provide medical advice, diagnosis or treatment.

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