Caregiver Resources for Parkinson’s
Spouses, family members, and friends very often serve as caring partners to individuals with Parkinson’s disease.
Though they do not have the diagnosis of PD themselves, the lives of care partners are also greatly affected by the disease. Being the caring partner of a person with PD requires a major transition of roles and adjustment of expectations about the future.
PCLA is here to support the open communication, education, and teamwork that are vial elements in the relationships among you and your caregiving partners.
Publications on Parkinson’s Caregiving
Parkinson’s Care Partner Rulebook, from the Davis Phinney Foundation (request a free digital copy by email)
UPCOMING EVENTS FOR CAREGIVERS
Parkinson's disease can change your loved one's life in many ways and can also change yours. How your relationship will grow depends on your outlook as a care partner. However, the weight is not entirely on your shoulders, and you must also care for yourself. Being an...
As people living with Parkinson’s disease navigate their diagnosis, they’ll encounter various physicians and specialists with education and experience specific to PD. One of these is a movement disorder specialist (MDS). Let’s explore the role of a movement disorder...