Hidradenitis Suppurativa (HS) Patient Personal Stories Volume 1 & 2 are available
Everyone has the opportunity to publish their story within our growing Organization. Although we all share the same orphan disease, each story can be different and unique. Learning about other existing comorbidities associated with Hidradenitis Suppurativa can lead to proper treatment for patients that do not have awareness or are currently at risk. Obtaining knowledge of how others cope can be useful – the mental health implications for all patients is also a debilitating aspect of this potentially life long chronic disease.
Our new Book Program kicks off with the releases of I WILL NOT HIDE,Hidradenitis Suppurativa (HS) Patient Personal Stories Volume 1 and Volume 2. Our Amazon and Kindle series of book releases for #HSAWARENESS tell the stories of Hidradenitis Suppurativa (HS) patients in a vivid and personal narrative. Told by the patients themselves.
PUBLISHING IN PRINT: Our self-publishing book program with patient contributions is available in libraries, schools, book stores, online vendors, and homes. The endless series and collection of patient stories will foster general awareness for Hidradenitis Suppurativa and sales will directly benefit awareness programs such as these.
A HSAWARENESS.ORG special project for HSSUPPORT.ORG. Published both online and in print for patient and physician awareness and for fundraising that supports the sustainability of our hard work. 15 to 20 patients per volume will be featured.
All profits from sales will go directly to establish and grow our organization. Into our 3rd year as a NGO, we are finally fundraising to realize our Non-Proft (501c3) status. Click here for details.