The Other Side of Self-Care: Feeling Worn Out

Originally published by Parkinsonsdisease.net
By Sharon Krischer · June 19, 2020

Put yourself at the top of your to-do list every single day and the rest will fall into place. -Unknown

I met with my movement disorders specialist recently, and she asked me if I thought that we, people with Parkinson’s (PwPs), are spending too much time on self-care at the expense of everything else. It is a valid question that I admit I have also thought about. Many PwPs will say that they are not defined by our Parkinson’s disease (PD). However, these same people spend an awful lot of time just taking care of themselves to help manage their disease. And I am one of them. I often say that since my PD diagnosis, I spend more time taking care of myself than anything else. And I often feel worn out.

Read the rest of the story at Parkinsonsdisease.net

Sunday Mornings with Twitchy Women

This Sunday, June 28 at 10:00 am Pacific Time, Movement Disorders Specialist, Indu Subramanian, MD, will be joining us to talk about Living well with PD in Covid-19 era, including the importance of social connections, mindfulness and yoga to alleviate some of the stress we are all feeling during this unsettling time. Click here to see her recent talk on PMD Alliance with Dr. Ray Chaudhuri

To register for this meeting, click here

These programs are for Women with Parkinson’s Disease. To maintain privacy for this group, we ask that care-partners and family members not attend unless an event states that registration is open to all. If you have any questions, please contact twitchywoman18@gmail.com.

Healthline Best Parkinson’s Blogs

This week I was honored once again by Healthline to be on their list of Best Parkinson’s Blogs of 2020

Advertisement

Leave a Reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

A Note To My Readers


I love to see your comments and get your emails as we share our collective experiences. But based on a couple of private questions from some of you, remember, I am just a lay person and a patient like the rest of you. For medical and similar advice, you need to talk to your own doctor

Twitchy Woman

Twitchy Women partners with the Parkinson’s Wellness Fund to ensure we have the resources to offer peer support for women with Parkinson’s.