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.

The Department of Health is preparing for further cases of novel coronavirus (COVID-19) in Tasmania, and healthcare workers are on high alert for potential cases. At the moment there are 15 people who have COVID-19 in Tasmania and one Tasmanian in isolation on the mainland.
One of the requests from the government is that “Non-essential organised indoor gatherings of greater than 100 people (including staff) are no longer permitted.” Our support meetings may not have 100 people attending but for the welfare of each member we need to protect them.
Lupus Association of Tasmania Inc. committee are adhering to the new rules set in place by the government and advise all members that there will be NO support meetings conduct throughout Tasmania until after May 31st 2020.
If you would like further information, please log on to the Department of Health website - https://www.dhhs.tas.gov.au/publichealth/communicable_diseases_prevention_unit/infectious_diseases/coronavirus
We apologise for any inconvenience.
Please stay safe and protect yourself and your family.

Lois Beckwith - President