Just 2 more days.... - Twitchy Woman: My Adventures with Parkinson's

Just 2 more days….

Until Giving Tuesday.

As a PWP I see me in each of those words. I’m not sure yet if I’ll wear it, hang it “loudly” a flag for all to see, or cuddle it quietly while I muse.

Pam

Dear Twitchy Followers,

It has been a pleasure writing this blog for the last 11 years and I hope to continue to be able to keep it going for a long time. I have gotten to know so many of you over the years, either on-line, at the World Parkinson Congress or other events.

I hope that something I wrote or something I said has helped you on this journey together with Parkinson’s Disease. Or at least made you smile. 🙂 I would love to hear from you, either in the comments below, or by email to me, some little thing that you learned or something that made a difference for your life with PD.

As we approach the end of the year, there are several ways that you can support Twitchy Woman so that we can continue providing our webinars, blog posts, online support groups and more at no charge to the participants.

A woman wearing a white t-shirt featuring colorful text related to Parkinson's disease and community support for women.

Our new t-shirts are still available, but like Cinderella’s coach, they will disappear at Midnite on Tuesday, December 2. Click here to order yours today.
Shop on Amazon. Cyber Monday deals continue until Tuesday night. You can support Twitchy Woman by clicking here to shop on Amazon.*
Donate to Twitchy Woman at GiveButter.com. Our fiscal sponsor, The Meyrow Foundation will ensure that all donations will benefit Twitchy Woman.

Next Sunday Morning with Twitchy Woman

We will be back next Sunday, December 7 with Samantha Elandary, MA, CCC_SLP, Founder & CEO of Parkinson’s Voice Project. You won’t want to miss the program, which is open to everyone. People with Parkinson’s have more control over Parkinson’s than they might think. The key is INTENT. Learn about the impact of dopamine loss on automatic movements, such as walking, talking, swallowing, and writing. Discover how to override the automatic motor system by being intentional and deliberate.
Register here

With much gratitude for your ongoing support for our community.

A digital signature displaying the name 'Shawn' in a cursive font.

*As an Amazon Associate, Twitchy Woman earns from qualifying purchases.

I’m Sharon

Welcome to Twitchy Woman.

I started Twitchy Woman as a way to exchange ideas and solutions with other whose lives have been affected. It has been recognized by Everyday Health, Healthline, Stanford University and more as one of the top Parkinson’s blogs to follow.

Feel free to explore the site – there are goodies on every page to help you live your best life with Parkinson’s Disease.

Twitchy Woman named to Top 50 Parkinson Influencer list

Thank you Feedspot for recognizing Twitchy Woman on this new list. Check it out here. Twitchy Woman is #44. I am amazed to be included with so many young onset people who actually know how to use Instagram and TikTok!

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Youupport is Appreciated

Sunday Mornings with Twitchy Women

Sunday, April 12 @ 1:00 PM ET

Robert Cochrane, PhD introduces his film The Boys of Summer: Short Stop, followed by a discussion of the film

Support Twitchy Woman

Shop on Amazon*

Do you need headphones for sleeping?

Do your air buds fall out while listening to a sleep meditation? Check out these Headphone Headbands. Click on either image to see what is available on Amazon.

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*As an Amazon Associate, Twitchy Woman earns from qualifying purchases.

The latest video from Sunday Mornings with Twitchy Woman

Clinical Trials Corner

SEPTEMBER 2025

I’ve been hesitant to feature new clinical trials as a few that I had on my list to include in future columns have either been removed from the site or marked as withdrawn. Keeping my fingers crossed that the trials I feature continue to recruit and maintain their funding. Click here for the rest of the report from Jen

Thank You!

All Twitchy Women programs are free to all who participate. However, they are not without cost. It takes resources to continue our work and we cannot do it without your help. Through our partnership with the Parkinson’s Wellness Fund, those who want to provide support can do so. Thank you to all of you who have contributed. It is really appreciated.