We are an organization for the provision of education and support to those in our communities living with, and/or caring for a loved one with Alzheimer’s disease or another form of dementia.
Therefore, we are a "working" organization and our meetings consist of determining needed education based on our day-to-day work with the dementia population and their families; and then working out the numerous details that go with planning educational events. Because we are a working group, we ask that members commit to attending the majority of meetings every year.
Numerous committees distribute the work required to implement the education; all Members are asked to take part in at least one of the committees. Typically, we have our annual caregiver conference in August as well as a few other educational programs. (See listing for descriptions of the committees.)
For the benefit of our membership, we have dementia-related education at three meetings per year for our members. And we have the opportunity to network with other agencies and individuals who are dedicated to the same mission.