The Multiple System Atrophy Coalition offered a two-day conference in late-October on various aspects of multiple system atrophy (MSA), which is a disorder similar to Parkinson’s disease (PD) (MSA is called an atypical parkinsonism disorder). One of the talks, presented by Tom Chelimsky, MD, a neurologist at Wisconsin Medical College, focused on blood pressure issues in multiple system atrophy patients, but his advice applies to Parkinson’s patients.
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This recently published research article in the journal Nature demonstrates the importance of “belonging” to a social network, such as a support group, if you have Parkinson’s Disease (PD). This is especially true during the pandemic of isolation within the larger pandemic of COVID-19. The data suggest that people who have regular opportunities for socialization do better with PD, and that it is “neuroprotective,” just like exercise. No doubt this applies to us all — whether we have PD or not!
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In his fourth memoir, “No Time Like the Future,” the actor and activist opens up about his newfound, uniquely upbeat brand of pessimism.
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The Parkinson Association of Northern California (PANC) hosted a day-long conference on Parkinson’s disease (PD). One of the talks was a fireside chat on living with Parkinson’s. The moderator was Suketu Khandhar, MD, movement disorder specialist at Kaiser Permanente. The keynote speaker was Soania Mathur, MD, who was diagnosed with Parkinson’s at 28 years old and has been living with Parkinson’s for 21 years.
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This two-day virtual symposium features speakers from the upper midwest. On Thursday, November 19, speakers address what’s new in PD treatment; challenging non-motor symptoms; and hallucinations and delusions. On Friday, November 20, speakers address thriving with purpose in this uncertain world; exercise research; and the what/why of PD medications. Register now.
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