The World Parkinson Coalition (WPC) hosted a session in early December 2020 for care partners of people with Parkinson’s disease (PD). In this combined presentation, panel discussion, and question and answer session, four speakers talked about creative, non-medical approaches to managing care partner wellness as they support their person with Parkinson’s (PWP). The panelists included a movement disorder specialist, a social worker, a person with Parkinson’s, and his care partner.
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The webinar “YOPD Women, Diagnosis, and Symptoms” was presented by the YOPD Women Council at the Davis Phinney Foundation. YOPD is Young Onset Parkinson’s Disease, where Parkinson’s is diagnosed earlier in life. This was the first in a new webinar series for YOPD women, to be held the first Wednesday of every month. The panelists spoke of their experience with Parkinson’s, how they came to be diagnosed, unique symptoms they’ve had, and recommendations for how women can advocate for themselves.
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On February 10th and 11th Dementia Alliance of North Carolina hosted the first Dr. Daniel Kaufer Memorial Caregiver Conference. The theme of the conference was Behaviors: Awareness, Attitude (Day 1), and Action (Day 2). I attended three sessions on Day 1. These notes have relevance for those dealing with Parkinson’s Disease and dementia.
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On February 10th and 11th Dementia Alliance of North Carolina hosted the first Dr. Daniel Kaufer Memorial Caregiver Conference. The theme of the conference was Behaviors: Awareness, Attitude (Day 1), and Action (Day 2). I attended three sessions on Day 1. This session is relevant for those dealing with Parkinson’s Disease and dementia.
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In December 2020, Parkinson and Movement Disorder (PMD) Alliance hosted a panel discussion on people living alone with Parkinson’s disease (PD). It featured two speakers, an aging life care specialist and a social worker, who talked about the importance of having a care system around you even if you are living independently from family or a caregiver.
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