Multiple System Atrophy (MSA) is a rare disease that affects the brain and body, making it hard for patients to do everyday things. This study is testing a new program to help MSA patients and their caregivers learn and cope better. The program lasts for 12 months and includes both in-person visits and online activities. The goal is to see if this program can make life better for patients and their caregivers by teaching them about the disease and how to handle it.
- Program lasts 12 months with in-person and online activities.
- Open to early MSA patients diagnosed in the last 3 years and their caregivers.
- Participants must have internet access for online learning.