Early-stage Peer Group Forming Now

The Chapter’s next early-stage peer group (ESP) starts January 28th.  This seven-week series is designed for individuals diagnosed with early-stage memory loss and their care partners.  The ESP group is based on research that suggests individuals with dementia can learn and adjust to their diagnosis, contribute to decision-making regarding their future, and live meaningful lives if provided with adequate information, resources, and support.

For more information and to schedule an January screening appointment, call Teri Miller at 713.314.1353.

Click here for a Fact Sheet that describes the early-stage peer group

Stigma cited as top concern for people living with Alzheimer’s disease
Report summarizes issues voiced by those living with early-stage memory loss

Recently, The Alzheimer’s Association released, “Voices of Alzheimer’s Disease: Summary Report on the Nationwide Town Hall Meetings for People with Early Stage Dementia”.  The report is a qualitative analysis based on the first dialogue of more than 300 people living in the early stages of significant memory loss.

“Voices of Alzheimer’s Disease”  illuminates the experiences of those in the early stage of dementia and shares their perspectives on how they wish to be viewed, respected, listened to, engaged, and treated by family, friends, physicians, health care professionals and the community at large.

The overriding theme influencing a great deal of the discussion during the town hall meetings is that people in the early stages of memory loss are misunderstood due to misconceptions and myths about dementia.  Many people are worried about sharing their diagnosis openly because of the negative stigma.  People with early-stage dementia repeatedly point out that they are “still here” and are fighting to remain engaged as contributing members of their communities.

Click here to read the full report