Did you want to take a boxing class for Parkinson’s but couldn’t because it was too expensive for you? Do you need a piece of equipment that your insurance doesn’t cover? Where can you get help with the expenses that keep piling up because of PD?

The Parkinson’s Wellness Fund was created in 2009 specifically to fill in the financial gaps. Founder Russell Meyerowitz’s father has Parkinson’s. He had been going to physical therapy, but stopped. Meyerowitz asked his father why he stopped going. The answer: Medicare would not pay for any more PT sessions. Russell, who was in his twenties at the time with a young family, decided that he had to do something so that People with Parkinson’s (PwP’s) would have the money to continue with physical therapy or other needs not covered by insurance.

A bridge between service providers and individuals living with Parkinson’s

Russell, along with his wife, Amy, have worked hard to make sure that there are funds available to all who need help. They review every application they get from PwP’s in need of assistance. All of the revenue is either from direct donations to the website or from their annual golf tournament in Southern California.

Today, The Parkinson’s Wellness Fund serves as a bridge between service providers and individuals living with Parkinson’s who otherwise could not afford access to the services they need to live a life with Parkinson’s.

This year, Russell will be particpating in an Iron Man Race for Parkinson’s on December 3 to raise money for PWF. Please consider making a donation to ensure that they can continue to help all who need it.

Finally, the PWF is the fiscal sponsor for Twitchy Woman, enabling us to raise funds for programs such as our Peer to Peer Mentoring program for Women and the Sunday morning Zoom webinars Sunday Mornings with Twitchy Woman. You can donate to Twitchy Woman through the PWF website

Thank you Russell and Amy for your continued support to the Parkinson’s Community!


Twitchy Woman Gift Guide Roundup

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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. Each month I host a free Zoom webinar exclusively for other “Twitchy Women” with Parkinson’s Disease.

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

Let’s connect

A Son’s Journey

A new book by super Parkinson’s Advocate George Ackerman

Just out “A Son’s Journey from Parkinson’s DIsease Caregiver to Advocate. I am looking forward to reading this new book today.

Recent Posts

Sunday Mornings with Twitchy Woman

Sunday May 19, 2024

Time for Ping Pong!

Maureen and Trent will talk about Ping Pong for Good – a program for people with PD.

If you live in Los Angeles and want to participate in the live Ping Pong demo, please contact Sharon for details.

Click here to register.

This program is open to everyone.

Want to practice Ping Pong at home but don’t have room for a Ping Pong table?Click on the image to learn more.

Clinical Trials Corner

LIGHTPD

The University of Rochester and Dr. Ray Dorsey have an interesting new clinical trial in which you participate from the comfort of your own home, doesn’t involve changes to your current meds, and you can earn $500.00!  All interactions with the medical  team will be via Zoom and phone. 

Read more here