September Staying Connected Newsletter

This Month’s Events:

Let’s Talk about the Uncomfortable Side of Parkinson’s – Part II

Tuesday, September 10
10:00am – 11:30am ET
(9am CT, 8am MT, 7am PT)

We will continue the discussion we started earlier this year. There are some aspects of Parkinson’s disease that can be uncomfortable to live with or watch someone you love live with. The goal of this program is to provide a safe space to discuss these challenges, both in a large group and in smaller breakout groups.

Click Here to Register for this Event


Watch & Discuss: 2024 Emerging Therapies and Parkinson’s

Wednesday, September 18
10:00am – 11:30am ET
(9am CT, 8am MT, 7am PT
)

Watch and Discuss

We will Watch and Discuss this webinar recording by the Davis Phinney Foundation, in this video, Dr. Soania Mathur interviews Dr. Michael Okun about emerging therapies for Parkinson’s, including continuous infusion levodopa, cell replacement research, repurposed diabetes medication, and more! After watching the video, there will be a facilitated discussion of the video.

Click Here to Register for this Event

Why is it so hard to get a good night’s sleep with Parkinson’s disease? with Dr. Lawrence M. Stein, MD, FACP, FCCP

Tuesday, September 24
12:30pm – 1:30pm ET
(11:30am CT, 10:30am MT, 9:30am PT)

Dr. Stein will share his knowledge and expertise helping those living with Parkinson’s disease to find a better night’s sleep. Dr. Lawrence M. Stein, MD, FACP, FCCP has over 40 years experience working in Sleep Medicine, Pulmonary Disease, Critical Care Medicine, Internal Medicine for PMA Health. He is also Director of the Virginia Hospital Sleep Lab.

Click Here to Register for this Event

Happening In Our Parkinson’s Community…

GIVE BACK TO THE COMMUNITY – BE A PSN BUDDYsm
Would you be willing to help a fellow Person-with-Parkinson’s Disease?  We hope you will.
 
Frequently PSN receives inquiries from those newly diagnosed with Parkinson’s Disease, as well as people who are not newly diagnosed, seeking to speak with a fellow Parkinsonian on a one-on-one basis.
 
If you wish to help your fellow Parkinsonians by engaging in a telephone conversation, please let the PSN Board know.  With your permission, we will provide your telephone number and email address on request.  We will, of course, let you know each time we share this information.
 
To participate, kindly email board@parkinsonsocialnetwork.org, or call our office at 571-286-5000.