You are not alone in living with lupus
Find practical guidance, emotional support, and a community that understands what daily life with lupus really feels like.
By Lupus Association (Singapore)
Supporting the lupus community through education, support, and advocacy since 1992.
Member of National Council of Social Service (NCSS)
Living with lupus can feel overwhelming and isolating. Many people go through it quietly, without knowing where to turn.
What is lupus
Lupus is a chronic autoimmune condition where the body’s immune system mistakenly attacks its own tissues. It can affect different parts of the body in ways that are often invisible and unpredictable.
For many people, this can feel confusing, overwhelming, and difficult to understand, even for those living with it every day.
What we do
60-minute education session featuring live demonstrations of low-impact exercises at the LAS Empowerment Talk 2026 held in March. Photo by David Fong
Lupus Association Singapore (LAS) works with healthcare professionals, volunteers, and partners to support people living with lupus through every stage of their journey.
We focus on raising awareness, encouraging early diagnosis and treatment, and building a supportive community where people can connect and feel understood.
Through support groups, public education, and wellness initiatives, we aim to make sure no one has to face lupus alone.
Embrace
Connect with others who understand
Educate
Access support and resources
Empower
Stay informed and supported
Join us
Together, we work to make invisible illness visible and support individuals with lupus to live with dignity, strength, and confidence.