On World Lewy Body Dementia Day
Date
1/28/2025 8:45:49 PM
(MENAFN- PR Newswire)
Sue's Story: A Journey with Lewy Body Dementia has been presented in Continuing Medical Education programs offered by Kaiser Permanente and other health systems; in nursing programs offered by University of California, California State University, and California Community College systems; and in community education programs offered by organizations such as AARP.
Now on YouTube, the film centers on Sue Berghoff who was diagnosed with LBD in 2017. As Sue explains in the film, she decided to transform her diagnosis into something positive to help others living with LBD, starting with advocacy. Also in the film: Sue's husband/caregiver Chuck Berghoff; and neurology and neuroscience experts Dr. Kathleen Poston (Stanford Medicine), Dr. Geoffrey Kerchner (Roche), and Dr. Elena Call (Kaiser Permanente).
Lewy body dementia (LBD) is an umbrella term encompassing two different but related diagnoses: Dementia with Lewy bodies (DLB) and Parkinson's disease dementia (PDD). Historically, LBD has not been sufficiently prioritized, described or supported in research funding; Continuing Medical Education; public health initiatives; or the general media.
The Berghoff's established the Sue Berghoff LBD Research Fellowship at Stanford (2019), formed the Susan and Charles Berghoff Foundation (2021), and launched an LBD caregivers support group (2024). Sue's Story: A Journey with Lewy Body Dementia won "Best Documentary Film" at the Poppy Jasper International Film Festival (2018).
About LBD
Lewy body dementia is the second most common neurodegenerative dementia, a leading cause of mortality in the U.S. LBD is characterized by cognitive decline, behavioral changes, hallucinations, sleep and movement problems and autonomic system dysfunction. LBD has two diagnoses: Dementia with Lewy bodies (DLB) and Parkinson's disease dementia (PDD). Currently there is no cure for LBD.
About the Susan and Charles Berghoff Foundation
We provide dementia education, funding for research, and caregiving resources for families living with LBD. Watch the film on YouTube . Connect with us: berghoff-foundation , LinkedIn , Facebook or Twitter/X .
SOURCE Susan and Charles Berghoff Foundation
MENAFN28012025003732001241ID1109140961
Legal Disclaimer:
MENAFN provides the information “as is” without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the provider above.