Caregivers

As a caregiver to someone with a PS or ET movement disorder, you are intimately involved in their daily life and the decisions that have to be made, from testing to diagnosis to treatment. It's a responsibility that comes with unique challenges and rewards.

In this section, we share ways you can help your loved one at home, during appointments with their healthcare team, and during recreational activities that can benefit you both. Remember that it's important for both you and your loved one to eat right, get enough sleep, and enjoy physical activity.

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