Care partners play a major role in the well-being of a person with Parkinson's disease. Within these sessions, people experiencing PD and their care partners have the opportunity to share information for newly diagnosed people and their care givers, share tips for managing a loved one's care, navigating a relationship with a Parkinson's diagnosis and making time to care for oneself. Real people sharing real experiences!
We will also have special events by inviting speakers, and information on access to special events regarding information on managing symptoms, updates on the search for a cure, etc.
A care partner is an essential member of a person's medical and care teams. While most care partners are spouses, children, siblings, and parents, even friends can be part of the care team.
The role of a Parkinson's care partner will evolve over the years; therefore, we want to offer you resources and action plans to help YOU live well while also while providing the best care possible for your loved one.” Thank you to our Care Partner Support Group Leader and Host - Peggy Hubbell
As Parkinson’s disease progresses over time — so does your role as a care partner. Build a support system with people who understand.
The caregiver support group is presented by the Alzheimer's Association and conducted by trained facilitators. This is a safe place for people experiencing living with dementia brought on by ALS or PD. These support groups allow people living with dementia to:
Please join us for an in-person caregiver support group each month on the 2nd Thursday from 2:00 pm - 3:00 pm at the Pickaway County Library located at 1160 North Court St., Circleville, Ohio 43113. To register, please call 800.272.3900
Parkinson’s disease progresses over time — so does your role as a care partner. Explore all stages of the care partner journey and practical tips that can help along the way.
The American Parkinson Disease Association works tirelessly every day to support and empower anyone who is impacted by Parkinson’s disease (PD). Our nationwide network provides information and referral, education and support programs, health and wellness activities, and other events to facilitate a better quality of life for the PD community, while also funding vital research. It is this grassroots structure that distinguishes APDA from other organizations serving people with PD.
Care partners play a major role in the well-being of a person with Parkinson's disease. Here we share tips for managing a loved one's care, navigating a relationship with a Parkinson's diagnosis and making time to care for oneself.
As a Parkinson's care partner, you are an essential member of your person's medical and care teams. While most care partners are spouses, children, siblings, and parents, even friends can be part of the care team. Your role as a Parkinson's care partner will evolve over the years; therefore, we want to offer you resources and action plans to help YOU live well while also providing the best care possible for your loved one.
The Secret Life of Parkinson's is a podcast created by Parkinson's patients, sharing their stories
and interviewing others, on things we deal with on a daily basis. It's hard for people with PD to
talk to others about the disease because sometimes it's difficult for the patient themselves to
describe what they are feeling. Talking to other PD patients helps us express what we are going through in ways we might not be able to express to family and friends. (Subscription Available)
A big part of making life better for people with Parkinson’s disease (PD) is taking care of the people who care for them. The Parkinson’s Foundation Care Partner Program is a series of self-paced online courses designed with care partners in mind and is recommended for anyone caring for someone living with PD, including spouses, partners, parents, children, friends or other family members.
A big part of making life better for people with Parkinson’s disease (PD) is taking care of the people who care for them. The Parkinson’s Foundation Care Partner Program is a series of self-paced online courses designed with care partners in mind and is recommended for anyone caring for someone living with PD, including spouses, partners, parents, children, friends or other family members.
All information on This website is intended to inform the reader of recent developments in the Parkinson Community. Any advice or recommendations contained herein should not be taken without first consulting your own medical provider. always consult your medical team/doctor regarding all matters pertaining to your health.
We thank everyone for making the 2024 event the biggest ever, showing unity and support for those families in Pickaway county and the surrounding area with loved ones experiencing Parkinson's disease.
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