The Lupus Association (Singapore) is a self-help group dedicated to provide support for patients and their families. The group aims to assist lupus patients by providing practical support and by giving people the opportunity to share experiences with others who have lupus. The Lupus Association (Singapore) is committed to research on the disease and in improving understanding of the disease especially among people with lupus and their families.
Annual General Meeting
Minutes of the 31st LAS Annual General Meeting held on 27th August 2022
Annual Report Year 2022 (Finalise)
LAS YE 31.12.2022 Audit report v4-5 signed
Our Constitution
The Constitution of the Lupus Association (Singapore) is presented here. Please note that any mistakes found here, if any, were made in the process of transmission and one should refer to the original document for any purposes.
Our Role
Raising Public Awareness
This is done through talks to various interested parties. The illness has also been highlighted in the media regularly. A quarterly newsletter “LUPUS LINK” is distributed to patients and the members of the Singapore Medical Association.
Patient Education
Educational talks are given bi-monthly on topics related to SLE. These topics cover medical issues as well as practical ones such as buying insurance and improving self-image. A comprehensive pamphlet on SLE is given out to newly diagnosed patients.
Patient Support
There are weekly hospital visits carried out by members who are well to encourage those who have been warded. At the monthly talks. there are psychotherapy sessions led by psychiatrists. Every Wednesday afternoon, members meet for a handicraft session or just have tea together.
Interaction Among Patients
Regular social functions such as barbecues are held to strengthen bonds between patients who often become good friends. Many keep in regular contact with each other.
Interaction with Foreign Lupus Group
Our association participates in regional and international patients’ conferences to learn from and share our experiences with these like-minded organizations in other parts of the world.
Assisting Patients
With increasing health costs, many patients face a considerable financial burden. Most need regular check-ups. Some need expensive forms of treatment. Our association has a well-organized Welfare Subsidy Scheme to help deserving patients cope with health costs.
Supporting Lupus Research
Our association actively supports research in SLE, hoping that the treatment of this illness will continue to improve as it has done so in the last ten years. Most patients nowadays can survive beyond ten years and many lead normal lives. We look forward to the day when a permanent cure can be found.
How can you help?
We would appreciate your help in the following ways:
We look forward to your support.
Please feel free to address your enquiries to the Lupus Association (Singapore).
Alternatively, you may e-mail Dr. Leong Keng Hong (Vice-President, Lupus Association) directly.
Financial Statements