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Meet Dr. Stephan Grimaldi: an APDA-funded Researcher Working to Use MRI Imaging as a Possible Biomarker for Early Parkinson’s Disease

May 22, 2023 By Parkinson's Community Help

Stephan Grimaldi, MD, PhD
Dr. Stephan Grimaldi

The American Parkinson Disease Association’s (APDA’s) A Closer Look blog is designed to educate, inform, and inspire you through a variety of topics and insights about Parkinson’s disease (PD). One way the APDA does that is through our Interview with APDA Researchers series within this blog so you can get a closer look at some of the dedicated APDA-funded researchers who are working tirelessly to understand this disease.

… Full Story>

Filed Under: News

Family Caregiver Alliance Webinar, May 31: Trust it or Trash It? Techniques for Evaluating Health News Stories

May 22, 2023 By Parkinson's Community Help

FCA Webinar logo

Too often health and medical news reporting is unreliable, at best – ten years ago one study found nearly 90% of all health news stories contained inaccurate information, and it’s only gotten more difficult since then to sort out the useful information from hype, advertisements, or genuinely fake news. In the effort to make their stories catch readers’ eyes, journalists frequently mistake, exaggerate, or spin reports. Often reporters also miss details that make all the difference when it comes to transforming research findings into useful medical treatment.

… Full Story>

Filed Under: Webinars - Announcements & Notes

Anxiety and Parkinson’s Disease: What to Do if You’re Feeling Anxious

May 19, 2023 By Stanford Parkinson's Community Help

Anxious woman
source: APDA

Anxiety is a very common non-motor feature of PD, and symptoms of PD can worsen in the presence of stress and anxiety. Unlike stress which is fueled by external sources (such as work, family tension, finances, etc.), anxiety is fueled by internal forces and can persist when all external causes of stress have been resolved. Anxiety in PD may need to be treated with medication in order for a person to regain his/her quality of life. But there are also a number of lifestyle modifications that may be very helpful. Check out more of this blog post, including a list of resources, from the American Parkinson Disease Association.

… Full Story>

Filed Under: News

APDA Webinar: Let’s Keep Moving With APDA: FAQs About Exercise & Physical Therapy

May 16, 2023 By Parkinson's Community Help

With special guest Teresa Baker, PT, DPT

Let’s Keep Moving With APDA Logo

Join us May 23  at 1:00 pm ET / 10:00 am PT for Let’s Keep Moving With APDA: FAQs About Exercise & Physical Therapy.  In this new episode, hosted by special guest Teresa Baker, PT, DPT, Clinical Research Physical Therapist, from Boston University and the APDA National Rehabilitation Resource Center for Parkinson’s Disease, we will answer some of the most common questions about physical therapy as a treatment for PD symptoms as well as some of the challenges they most frequently see among their PD patients. Teresa will answer audience questions live during the program.

… Full Story>

Filed Under: Webinars - Announcements & Notes

SUNDAY MORNING – Michael J. Fox on Parkinson’s and how he finds “optimism is sustainable”

May 1, 2023 By Parkinson's Community Help

Michael J Fox with Jane Pauley
source: CBS Sunday Morning

……In a revealing interview, the actor Michael J. Fox spoke about his own mortality and the challenges of living with Parkinson’s disease for more than 30 years, including his experiences with falling and breaking bones.

The interview, with Jane Pauley of “CBS Sunday Morning,” was to promote his new documentary “Still,” to be released May 12.

… Full Story>

Filed Under: News

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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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