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The Lupus Society of Alberta is a non-profit organization formed to provide education and support for lupus patients, their families and friends. Funds are raised to further lupus research, promote public awareness and provide education to the community at large. The Lupus Society of Alberta was established in August of 1972 and has the distinction of being one of the first lupus organizations organized in the world. Support Services:One-on-one telephone peer/crisis support; One-on-one in-person support; A Self-Help workbook; Support Groups in various regions; Public Awareness Initiatives; Education Programs: The Lupus Library (lending library); distribution of lupus information packages at no charge; Sale of videos, books, articles and other literature; Annual Education Days; LSA Web Page (www.lupus.ab.ca); Quarterly Newsletter: The Lupus Courier; Research:The Lupus Society of Alberta provides research grants and has developed a Grant Application Protocol for this purpose.
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