Our Mission is:
To support advances in research and treatments; to create public awareness; to provide education and support to people affected by lupus.
Our Vision is:
- That early diagnosis and optimal treatment will be available to everyone with lupus
- That the public at large will be aware of lupus
- To ensure community based support networks and services
Where we came from:
In 1977 a group of lupus patients, with the support of three rheumatologists, formed a support group, known as the Lupus Erythematosus Group (L.E.G.). With an increasing membership and expanding representation throughout the province, the name was changed to the B.C. Lupus Association in 1980. In January 1993 the group was incorporated as an official non-profit society in accordance with the Society Act, and the name was changed to the B.C. Lupus Society. In 2007 the BC Lupus Society celebrated 30 years of working together to conquer lupus.
Who we are:
The Lupus Society is the only BC organization dedicated solely to providing lupus education and support services. We are committted to sponsoring research and providing hope for those affected by lupus.
The Lupus Society is incorporated province-wide, with members residing across the country and internationally, as far away as Singapore and Hong Kong. An extensive volunteer network of 8 support groups and 33 provincial contacts, we provide a wide variety of services which link the Lupus Society to thousands of people touched by lupus.
The Lupus Society sponsors and assists in the development of location support groups and provides access to literature on lupus and coping with this chronic illness. The Society also organizes education meetings and seminars where medical and professional resource people discuss all aspects of lupus including new trends in research.
There are many dedicated volunteers throughout the province. Their continued dedication, enthusiasm and support is integral to the success of the Lupus Society. Our support groups, provincial contacts and chapters provide information and support to those in their communities, actively participating in public awareness campaigns and initiating fundraising efforts. As well, there are other valued and committed volunteers who generously donate their time to various on going and special projects.
The Board of Directors is comprised of up to ten volunteers, who are elected into their position at the Annual General Meeting. Their responsibilities and activities range from reviewing and assessing the needs of the Lupus Society membership; sourcing, researching, developing and implementing programs and services to best fulfill these needs; initiating fundraising activities and grant application funding; liaising with the medical community and government regarding advocacy and education; assisting in the development of national programs and campaigns; liaising with other lupus organizations throughout the world.
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