Now available for viewing everywhere: “Shake With Me”

A documentary by Zack Grant

Image result for movie reviews 5 stars
190310_SWM_IND_rev5.png

Last March I went with Parkinson’s friends to a screening of the documentary short film “Shake with Me”, the story about artist and designer Debra Magid, who was diagnosed with Parkinson’s Disease in 2012. We all loved the movie and gave it an enthusiastic 5 stars for its portrayal of a woman – wife, mother and designer – and her family as they all learned to cope with the aftermath of her diagnosis and her re-emerging skills as an artist. I interviewed Debra afterwards about the film, life with Parkinson’s, family and more. You can read about it at Shaking with Debra Magid, which I posted last July.

The story that Debra’s son Zack tells in the film is not just a wonderful tribute to Debra but is also about her family and how they have met the challenges that Parkinson’s presents to all them. The documentary has been making the film festival circuits and has not had wide distribution. However, beginning today, it will be available to everyone on Vimeo.

From Zack:

SWM_hero_still2.jpg
Debra and Zack

After a nearly four year journey, I’m very excited to release the film and give everyone the chance to find their own way to relate to my family’s story..

Shake With Me is a documentary short about Debra Magid, an artist and designer who was diagnosed with Parkinson’s disease (PD) in 2012. In the fall of 2016, Debra agreed to let her son, Zack Grant, document the relationship between her art and her condition. What started as an exploration of Debra’s growth as an artist in the face of PD grew into a larger story of creativity, health, family and the will to cope.

You can view the entire film on Vimeo here beginning December 4, 2019. I highly recommend it.

Image result for movie reviews 5 stars
SWM_hero_still6.jpg
Debra in her studio

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!



Sunday Mornings with Twitchy Women

Sunday, June 28 @ 1:00 PM ET

Jim O’Connell will join us to discuss his new book Incurable Gifts 

Register here



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.

*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.

Discover more from Twitchy Woman: My Adventures with Parkinson's

Subscribe now to keep reading and get access to the full archive.

Continue reading