who we are
About Us
The South African Psoriasis Association (SAPSA) aims to:
- Support people with psoriatic disease
- Encourage connections with others also affected by the disease
- Offer credible information to assist in managing this chronic condition
We are a group of volunteers who want others to know that they are not alone and that each patient journey is different. Understanding the disease and how to manage it can lead to improved quality of life.
Learn about psoriasis, treatments, and self-care tips to manage symptoms and improve your quality of life.
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Our story
The South African Psoriasis Association (SAPSA) was established in 1986 by a group of individuals passionate about helping others affected by psoriatic disease. The SAPSA community continues to provide support and raise awareness about the disease through sharing personal stories and relevant resources that offer credible information. Our non-profit organisation celebrates World Psoriasis Day annually on October 29th with other similar support groups worldwide to draw attention to the health needs of this largely hidden disease. Through our online resources and the efforts of our volunteers, SAPSA aims to educate, inform, and engage people to foster greater understanding and support for individuals affected by psoriatic disease. We are a member of the IFPA (International Federation of Psoriasis Associations) community and greatly value their support.
Our mission
We are committed to empowering individuals living with psoriatic disease through education, awareness, and support. Our mission is to provide the tools and resources needed to manage this condition with confidence. By fostering a compassionate and understanding community, we aim to reduce the stigma around psoriatic disease, ensuring everyone affected can lead a healthier, more fulfilling life.
Our vision
We envision a world where those with psoriatic disease are understood and supported. Our goal is to provide access to the knowledge, care, and tools needed to live confidently without stigma. Through advocacy, education, and support, we aim to ensure a future where every person with psoriatic disease can thrive in an inclusive, informed society.
YOU ARE NOT ALONE!
If you or a loved one is dealing with psoriatic disease, remember that you are not alone. It’s essential to seek medical attention for proper diagnosis and treatment. Reach out to a healthcare professional, and don’t hesitate to connect with our community for support and resources. We’re here to help you navigate this condition with shared experiences.