Lupus Association of NSW Inc

National Accredited Education for GPs

AVAILABLE ONLINE - This accredited GP Education Module will allow GP's to learn more about the key diagnostic and management features of systemic lupus erythematosus
Entertainment Books available now!Save money at a variety of local businesses including restaurants and entertainment venues and you will be helping to support people living with lupus. $13 from every book sold goes to the Lupus Association of NSW Inc.
Become a Member

Receive quarterly newsletters, telephone counselling, support groups, library facilities and more. Membership is just $35 per year.
Join us on Facebook!Find support through our Facebook groups and chat about tips on lifestyle, medication, diet and how to cope with this condition in general. NOTE: The Young Adults group is a private group. You must be logged in to Facebook first.
THANK YOU for making City to Surf a huge success

The Lupus Butterflies were a bright scene of orange amongst the crowds at the City to Surf and we raised over $19,000 for lupus! There's still time to donate!

The Lupus Association of NSW Inc.

Welcome to our brand new website!

The mission of the Lupus Association is to work towards a world without Lupus and associated connective tissue diseases through support education and research into a cure.

The Lupus Association has over 1100 members Australia-wide and provides services to those newly diagnosed, as well as those who have been living with lupus for some time.

Please explore our website and discover as much as you can about this life-changing disease. For further information you can contact the Association direct and speak with someone who can guide you to a more detailed understanding. With your help and continued financial support we can assist researches and practitioners with developing better and more effective diagnosis and treatment programs for lupus patients, as well as support research efforts to find a cure for lupus.

The Lupus Association provides this website to allow users to gather information. The opinions and statements expressed by the authors or contributors to this website do not necessarily reflect the opinions or positions of the Lupus Association.

Welcome to our brand new website!

The mission of the Lupus Association is to work towards a world without Lupus and associated connective tissue diseases through support education and research into a cure.

Stay in touch