Welcome!

The Lupus Association of Tasmania is a self-funded non-profit organisation served by volunteers.

We are committed to understanding and supporting people with Lupus, Sjögren’s, Scleroderma, Fibromyalgia or any auto-immune disease in the following ways:

  • By educating and informing patients and their families.
  • By providing support in the form of encouragement and service.
  • By promoting and supporting research designed to discover the cause of, and a cure for, lupus and related auto-immune diseases. 
  • To read our Patron and President’s messages, please click here
  • For information on Lupus, Sjögren’s syndrome, Fibromyalgia syndrome, and Scleroderma, please click here.
  • To make a donation and support your local organisation and research, please click here.
  • To contact the Lupus Association of Tasmania, please click here.

Established 1st December, 1999.

It is with great relief our Organisation has managed to secure all the positions needed to successfully operate and continue to offer support and education for people with Lupus.
At the AGM, we were able to gather together a blend of old, recycled expertise of Murray, and the new I will give it a go, Leanne, and the very kind volunteer of Di Whiteley who has past experience as a club secretary and who is new to Lupus.
A group of members, Julie, John, Cheryl, Edna, and Heather also rallied to help as co-ordinators, editor and committee members. Thanks to all we will stay viable and continue the work to improve the lives of people with Lupus.
President
Lois Beckwith

It is my honour to serve the Lupus Association of Tasmania as its patron.