Is there a link between Ashkenazi Jews and Parkinson's? - Twitchy Woman: My Adventures with Parkinson's

Is there a link between Ashkenazi Jews and Parkinson’s?

While browsing my Facebook feed, I came across the following post from the Michael J Fox Foundation: Find out if you may be eligible to participate in a clinical study investigating the link between Ashkenazi ancestry and Parkinson’s. The Parkinson’s Progression Markers Initiative (PPMI) is The Michael J. Fox Foundation’s flagship biomarkers study seeking to learn more about the genetics of Parkinson’s disease. PPMI is currently studying the connection between PD and having a mutation in either the LRRK2 or GBA gene — both are promising targets of PD research. https://www.michaeljfox.org/page.html?ppmi-genetics I have participated in a number of clinical studies for both PD and Breast Cancer. I encourage you to participate as well. Most studies have trouble recruiting enough people to actually do the study, even if they are fully funded. If you have not already done so, sign up for Fox Trial Finder so that you can take an active part in finding a cure for PD. In addition, please go to the 23 and Me website and sign up to be tested. There is no charge for the kit if you sign up for the PD research study. Here is the link: https://www.23andme.com/pd/ They do not give you medical information.. Privacy is very important, and you have to sign a release for the company to share your results with researchers. They do give you your Ancestry composition. Mine, as expected, was 97.8% Ashkenazi. The surprising part was the 2.8% Neanderthal!!!

WATCH: The Parkinson’s Minute on PD Genetics

2 responses to “Is there a link between Ashkenazi Jews and Parkinson’s?”

PDinAZ

June 26, 2015

I am of that heritage and getting tested was the first study I participated in. It was easy and educational. However, I do not carry the mutated gene. Secretly, I was hoping to have it as a reason behind my PD. BTW, those who do not have PD but are from Eastern European decent may be tested as well. I am currently in 2 web-based studies–Fox Insight (monitors your health, changes, etc.) and will be using a wearable device to track meds, movement, etc. for at least 6 weeks. The other study focuses on CAM Care in PD–complimentary & alternative medicine. It’s the least I can do!

Reply
1. skrischer
  
  June 26, 2015
  
  I don’t have the mutated gene either. And I am in the CAM study, too. I just got a notice about The Women in PD Initiative, which sponsored by the Parkinson’s Disease Foundation. They are having a conference in NJ in September. I will send you info about it.
  
  Reply

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!

Join the fun!

Stay updated with our blogs and other information by joining our newsletter.

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.

A colorful headband featuring butterfly designs, shown in use by a woman exercising and another woman lying down, showcasing its versatility for fitness and relaxation.

*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.