Care Partner Month 2023

This year, and every year, the Fixel Institute joins the Parkinson’s Foundation in recognizing our care partners for the National Family Caregivers Month.

We want to show our thanks and appreciation for those who give their all to ensure their loved one living with Parkinson’s disease (PD) is healthy, productive and living a happy life.

Care partners and caregivers deserve to be recognized and celebrated.

Being a care partner for a loved one with PD can be an emotional roller coaster. To help you along the way, the Parkinson’s Foundation and other programs across the country have pulled together resources to ensure that you have the tools you need to stay healthy and feel supported.

This year, the Parkinson’s Foundation wanted to empower and remind care partners of how much they are valued for everything they do in their daily caregiving roles. This year’s theme is #Take6forPD. In this campaign, the Parkinson’s Foundation encourages everyone to take six minutes to spend time learning about PD and support a care partner in their lives.

Thank you From Fixel

Letter FRom Dr. HEss

Parkinson’s Foundation Resources

Virtual- November 11, 2023

Care Partner Summit 2023

The Care Partner Summit brings care partners together to provide resources to make life better for themselves and their loved one with Parkinson’s disease. This year’s Summit will focus on how to communicate through difficult topics and find supportive connections. Join the Parkinson’s Foundation online at-home via Zoom!

care partner summit 2023

Care Partner Online Courses

The Parkinson’s Foundation Care Partner Program is a series of self-paced online courses designed with care partners in mind.  This course is recommended for anyone caring for someone living with PD, including spouses, partners, parents, children, friends or other family members. They encourage you to use this program in the way that best suits your needs and your schedule. Start with the course that you’re most interested in and progress through the others as you feel you are able.

Care Partner Program

Fixel Support

Fixel Institute Patients & Caregivers

C.A.R.E.S. Program

C.A.R.E.S (Caregivers Accessing Resources for Emotional Support) is free, 1-on-1 counseling to caregivers of patients in the Fixel Institute who are currently experiencing emotional and mental strain while caring for a loved one. Can be provided by Zoom online. To schedule this FREE service, call our office at 352.733.2410 or email Alana McKay.

CARES program

Parkinson’s CareGiver Resources

Practicing Self-care

Davis Phinney Foundation

Every Victory Counts Manual

Whether you are the spouse, partner, child, parent, sibling, or friend of your person with Parkinson’s, you are an invaluable part of their team. Your role as a care partner will evolve throughout the years, but in each stage, it is essential to equip yourself with tools, advice, strategies, and support to ensure that you and your loved one live well. Davis Phinney Foundation designed a new Every Victory Counts® Manual for Care Partners to give you just that.

davis phinney

PMD Alliance

Care Partner Roadmap

Being a care partner to someone with Parkinson disease often involves taking care of the immediate while thinking ahead to the future. In this program, Mindy Bixby, DO, movement disorder specialist, and Amy O’Rourke, certified care manager, will discuss: * symptoms and planning needs care partners can expect at each stage of PD, * ways to proactively manage the most challenging aspects of caregiving, * and how to utilize the Roadmap to Care as a planning tool.

care partner road map

Parkinson’s Foundation

My PD Story- Care Partners

Looking for inspiration? These stories are written by those in the Parkinson’s disease community who are helping bring awareness to this life-changing disease.

Also, find out how to share your story.

daughter caregiver

Davis Phinney Foundation

Care Partner’s Digital Toolbox for Parkinson’s

Often times as a care partner to someone with Parkinson’s, you need a solution to a problem, but you don’t have hours on end to search for it. That’s what this toolbox from the Davis Phinney Foundation is all about. It includes a few worksheets, a few apps, a few websites and a few nuggets of wisdom from people who have been caring for someone with Parkinson’s for long enough to know how valuable time is. And how time-consuming and emotionally and physically taxing being a care partner can be when you don’t have the formal training or resources you need.

caregiver computer

Parkinson’s Foundation

Caregiver Experience Podcast

In this podcast, a care partner relates her journey with her husband, who received a PD diagnosis at age 51. She tells about her initial shock and fears and how she came to terms with the disease, and about their journey together, using information and knowledge to help them deal with changing situations.

Parkinson's Podcast

Finding Support

PD Conversations

Join online discussion groups where you can connect with others who are sharing similar experiences to you and your loved one.

Male hand holding megaphone with Need Help speech bubble. Loudspeaker. Banner for business, marketing and advertising. Vector illustration.

November 15, 2023 at 12:30 P.M.

Getting Real- for Newly Diagnosed Care Partners

Join PMD Alliance and Fixel’s own Ashley Rawls, M.D. for this virtual workshop. This free workshop is your chance to learn from and ask your most pressing questions of a leading expert in the movement disorders community. As an adult child or care partner of someone with a movement disorder, you may feel overwhelmed or uncertain about how to plan for what’s ahead. The experts have practical advice and resources to best support you in your unique needs and concerns.

This program is for care partners and adult children of someone with PD at the newly diagnosed stage. Newly diagnosed is considered 0 – 5 years from diagnosis.

caregiver son

Davis Phinney Foundation

Care Partner Monthly Meetup

If you could use some extra support as a care partner, please join the Davis Phinney Foundation for our monthly Care Partner Meetup. During these one-hour sessions, Connie Carpenter Phinney and Davis Phinney Foundation Ambassadors and care partners Pat Donahoo and Gail Gitin discuss the concerns, challenges, and questions that many Parkinson’s care partners have today.

Meets the first Tuesday or every month at 2 P.M. EST

caregiver hands