Year End Giving to Parkinson’s Organizations

Giving is not just about making a donation, it’s about making a difference

Kathy Calvin, CEO and President of The United Nations Foundation

Support Your Favorite Local Causes on Giving Tuesday - Only In Arkansas

Yes, it is that time of year again.

Giving Tuesday is next week on November 30 and I have already received numerous reminders from Parkinson’s organizations to give to them. So how do you decide who to give to and why?

Start Local

Let’s start with the local organizations. Is there a local organization in your community that supports people with Parkinson’s. If so, that should be a priority, especially if you are participating in any of their programs and support groups. These organizations are usually grassroots and need your support.

Do you attend local or online classes for People with Parkinson’s? Consider donating to them as well for the same reason. Many have struggled since the Pandemic began, offering classes on Zoom for a very small fee or for free.

National Organizations

There are many national and international organizations for Parkinson’s Disease. In an ideal world, we should support all of our national organizations, but given the limited resources many people with PD have, that may not be an option.

So how do you decide who to give to? There is some overlap in what many of them do, but each has its own niche. What are their missions? Do they provide something for you that you cannot get elsewhere? Do you volunteer for any of them?

Last summer I held two Sunday Morning with Twitchy Woman webinars devoted to learning about what the different organizations are and what they do. Representatives joined us from American Parkinsons Disease Association (APDA), Brian Grant Foundation, Davis Phinney Foundation, Michael J Fox Foundation, Parkinson’s Foundation, PD Avengers, PMD Alliance and the European Parkinson’s Disease Association(EDPA). You can watch the recordings for July 11 and July 25 to hear what leaders of each organization had to say. You can also read my summary of the different organizations at Parkinson’s Organizations (August, 2021)

I hope that this helps you make some decisions about year end giving.

A Personal Thank You

Finally, thank you to everyone who participated in the Twitchy Woman T-shirt fundraisers this year. Your generosity and support during this past year has helped to keep all of the Twitchy Woman programs, webinars and this blog, free for everyone.

With much gratitude,

Sharon Krischer (Twitchy Woman)

No one has ever become poor by giving

Anne Frank

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3 responses to “Year End Giving to Parkinson’s Organizations”

  1. Nessa Barrad Weinman Avatar
    Nessa Barrad Weinman

    Sharon, PCLA, Parkinson’s Community Los Angeles is also a local nonprofit serving the Parkinson’s community. I’ve been active in the Los Angeles Parkinson’s Community for about 20 years. I’ve worked with APDA, and have run 2 local support groups for many years. PCLA is focused 100% locally and provide many free services to the community. This organizations should definately be among those that you have chosen to highlight. Please check out https://pcla.org/

    1. Nessa, I only highlighted organizations with a national or international reach. I could not start listing local organizations because there are so many of them and it would be impossible to list all of them.

      1. Nessa Barrad Weinman Avatar
        Nessa Barrad Weinman

        Your blog did not just highlight national/international programs. your blog “Start Local

        Let’s start with the local organizations. Is there a local organization in your community that supports people with Parkinson’s. If so, that should be a priority, especially if you are participating in any of their programs and support groups. These organizations are usually grassroots and need your support.” That’s why I’m upset.

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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.