“It is really important to me and the HidraWear team to make sure we are doing our part to raise awareness of Hidradenitis Suppurativa. More awareness will mean faster diagnoses and fast diagnosis is key to being able to manage the condition.”
CEO & FOUNDER OF HIDRAWEAR
Our story begins with our Founder & CEO, Suzanne Moloney.
Suzanne has been living with HS since she was 13 years old. She has had a long journey with HS and felt that the HS community was often underserved by the healthcare industry. As her frustrations with this terrible skin condition grew, so did her need to do something about it.
As an active member of many online HS communities, Suzanne knew she wasn’t alone in her frustration. She talked to other HS patients and interviewed multiple dermatologists and HS specialists. Two things became very clear to Suzanne:
- There is no established cause of HS or how lesions initiate. This meant the likelihood of a pharma, topical or procedural based solution was unlikely to happen in the near future.
- One of the biggest challenges for people living with HS is the daily management of their wounds.
From this, the idea for HidraWear was born.
Suzanne, along with the HidraMed Solutions team, works to make wound care management for HS patients less strenuous. HidraWear is comfortable to wear, kind to your skin and ensures you have no leakages throughout the day.
Our goal is simple: Help you spend less time thinking about HS so you can get back to living life to the fullest.
We believe in support
Would you like to become an HS warrior and help us raise awareness?
If so, follow us on social media and help spread the word.