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Advanced stage and end-of-life care – Webinar notes

May 21, 2020 By Lauren Stroshane

In early May, the UCSF Memory and Aging Center (MAC) presented the fifth and final webinar in its series on caregiving for those with Lewy body dementia (LBD), a discussion of advanced-stage and end-of-life care topics. While the webinar was geared towards those caring for individuals with LBD, we felt the content would also be helpful for others with cognitive impairment or Parkinson’s disease dementia. The speaker was Maya Katz, MD, a movement disorders specialist with the UCSF Weill Institute for Neurosciences. She covered what caregiving is like in advanced LBD, end-of-life care, indicators of the individual’s prognosis, and advance care planning. We at Stanford Parkinson’s Community Outreach viewed the webinar and are sharing our notes.

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Filed Under: Webinars - Announcements & Notes

Ask the Expert: Parkinson’s and Hospitalization – Webinar notes

May 19, 2020 By Lauren Stroshane

In early April, the Parkinson’s Foundation offered a Facebook Live presentation on hospitalization and Parkinson’s disease (PD), featuring Dr. Michael Okun, a movement disorders specialist at the University of. He answered questions about PD and hospitalization, provided tips about what to do if you or your loved one with PD is hospitalized, and discussed how to get the best care possible during an anticipated or emergency hospital stay. We at Stanford Parkinson’s Community Outreach viewed the webinar and are sharing our notes.  

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Filed Under: Webinars - Announcements & Notes

Advocacy in healthcare and community settings – Webinar notes

May 15, 2020 By Lauren Stroshane

In late April, the UCSF Memory and Aging Center (MAC) presented the fourth webinar in its series on caregiving for those with Lewy body dementia (LBD). The topic was how to be an advocate for your loved one with LBD in both a healthcare setting and a community setting. While the webinar was geared towards those with LBD, we felt the content would also be helpful for others with cognitive impairment or Parkinson’s disease dementia. The speakers were Sarah Dulaney, Clinical Nurse Specialist with the MAC, and Helen Medsger, an LBD family caregiver, advocate, and support group leader. We at Stanford Parkinson’s Community Outreach viewed the webinar and are sharing our notes. 

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Filed Under: Webinars - Announcements & Notes

Is a Parkinson’s pandemic coming? – Webinar notes

May 12, 2020 By Lauren Stroshane

In mid-March, the Davis Phinney Foundation offered a webinar on the rise of Parkinson’s disease (PD) worldwide, featuring Michael Okun, MD, a movement disorders specialist at the University of Florida who is a co-author of the new book, Ending Parkinson’s Disease. Dr. Okun discussed the current knowledge about how to prevent PD and what actions individuals can take to try to impact the increase of PD long-term. There was a Question and Answer session as well. We at Stanford Parkinson’s Community Outreach listened to the webinar and are sharing our notes.  

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Filed Under: Webinars - Announcements & Notes

Insight into Parkinson’s 2020, Day 3 – Conference notes

May 8, 2020 By Lauren Stroshane

Insight 2020 is the largest online conference for people with Parkinson’s disease (PD), their caregivers, and those who work with the PD community. It took place this year on April 1-3, and covered a wide range of topics, from living positively to the latest PD research. We at Stanford Parkinson’s Community Outreach attended all three days of the virtual conference and took notes on some of the talks that seemed most interesting or relevant to our audience. Highlights from Day 3 of the conference are below.

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Filed Under: Webinars - Announcements & Notes

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Stanford Parkinson’s Community Outreach provides vital resources and support to individuals living with Parkinson’s disease (PD), caregivers, family members, and friends. We curate a comprehensive list of PD-related webinars and virtual meetings, sharing insightful summaries through our blog and dedicated email lists. Whether you seek online support groups, educational webinars, or access to helpful blogs and podcasts, we are here to empower you with the knowledge and connection you need on your Parkinson’s journey.

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