Welcome to the

Hidradenitis Suppurativa Society of South Africa (HS3A)

The Hidradenitis Suppurativa Society of South Africa (HS3A) is a non-profit organisation dedicated to improving the lives of individuals affected by Hidradenitis Suppurativa (HS). 

doctor-talking-patient-medium-shot
Who We Are
We bring together dermatologists, surgeons, nurses, researchers, patients, and advocates with the common goal of raising awareness, advancing education, promoting research, and improving access to care for HS in South Africa.

HS is a chronic, painful, and often under-recognised skin condition. In South Africa, where awareness and resources remain limited, HS3A provides a platform for education, advocacy, and collaboration to ensure patients receive the care and support they deserve.

What is Hidradenitis Suppurativa (HS)?
Hidradenitis Suppurativa (HS) is a chronic inflammatory skin disease

It causes recurrent, painful nodules, abscesses, and tunnels (sinus tracts) in areas such as the armpits, groin, buttocks, and under the breasts. These lesions can lead to significant scarring, disability, and reduced quality of life

Prevalence:

HS affects about 1–4% of the global population, but is often underdiagnosed.

Causes

The exact cause is not fully understood, but HS is linked to immune dysregulation, genetic predisposition, lifestyle factors, and comorbid conditions such as obesity and metabolic syndrome.

Impact:

Beyond the skin, HS has a profound psychological and social impact. Patients frequently face stigma, depression, anxiety, and challenges in daily activities.

Early recognition and multidisciplinary care are key to preventing complications and improving outcomes.
Our Mission

Awareness:

Increase public and professional knowledge about HS across South Africa.

Support:

Provide resources, advocacy, and community for patients and their families.

Education:

Increase public and professional knowledge about HS across South Africa.

Research:

Promote and support scientific studies into the causes, treatments, and outcomes of HS.

Access:

Work with stakeholders to improve access to diagnosis, medical care, and advanced treatments for South African patients.

Why HS3A Matters

Hidradenitis Suppurativa has long been under-recognised and under-treated in South Africa. Many patients suffer in silence for years before receiving a diagnosis. HS3A strives to change this by:

Reducing stigma and misconceptions about HS
Improving standards of care in both public and private sectors
Advocating for access to modern therapies, including biologics
Supporting patients through education and community outreach

What We Do

Patient Advocacy

Amplify the voices of those living with HS.

Educational Events

Host congress sessions, workshops, and awareness campaigns.

Research Collaboration

Partner with local and international experts to advance HS knowledge.

Resources

Provide patient-friendly information and guidance for navigating care.

Networking

Connect healthcare providers, researchers, and patients to foster a supportive community.