Press Releases

Atlanta, GA--11/2/15—For the first time, an advocate for the Lewy body dementia (LBD) community, Angela Taylor, Director of Programs at the Lewy Body Dementia Association (LBDA), has been named a member of the U.S. Department of Health & Human Services (HHS) Advisory Council on Alzheimer’s Research, Care and Services.

Atlanta—November 4, 2015—Yesterday, Susan Williams, Robin Williams’ widow, spoke on Good Morning America (GMA) and in other media, about it taking the past year for her to learn that Robin was suffering from Lewy body dementia (LBD), which she believes led him to take his own life. Susan Williams explained that the original Parkinson’s diagnosis did not cover all of his symptoms, and he was unaware of the LBD diagnosis when he died.

ATLANTA (OCTOBER, 2015) — In its sixth year, during the month of October, the disease with the unusual name of Lewy body dementia (LBD) is being heralded as Lewy Body Dementia Awareness Month nationwide. Texas also recently designated October as Lewy Body Dementia Awareness Month for the Lone Star state. The Lewy Body Dementia Association (LBDA) is determined to keep sharing information until LBD rolls off the tongue as easily as other well-known diseases.

The Lewy Body Dementia Association (LBDA) mourns the passing of a special friend, Dorothy “Dottie” Mangurian.  The inspiration for the Harry T. Mangurian Jr. Foundation’s visionary commitment to the cause of Lewy body dementia (LBD), she died in Fort Lauderdale, Florida on March 28, 2015 after a 15-year battle with LBD.