Mission MSA
Leading the Charge to Cure Multiple System Atrophy.
Mission MSA is a 501(c)3 dedicated to support, education, advocacy, and research funding for multiple system atrophy (MSA), a rare and fatal neurodegenerative disorder.
Navigating Self-Care, Recognizing Burnout, and Caring Through the Holidays
Autonomic Dysfunction in MSA
How to Use NOVA: Mission MSA's AI Chatbot Demo
Building a Care Team for MSA
Customizing Your MSA Connect Profile
Creating Your MSA Connect Profile
Living Better at Home: Adapting Your Space for Life with MSA
Considerations For Future Care
Kids and MSA: Support Strategies
Mind Matters: Energizing Mental Health for Patients and Care Partners
Physical Therapy and Exercise for MSA Patients
Nutrition and MSA: Dietary Strategies for Symptom Management
Mission MSA has been featured on Viewpoint with Dennis Quaid - Raising Awareness in Rare Diseases
Skin Testing for Early Diagnosis of Rare Autonomic Diseases
MSA Movement Revolution Fitness Class
Patient Panel: MSA Awareness Month (2024)
Clinical Trial Roundup
Family’s Journey with MSA: Dane’s Story of Resilience & Hope
Discovering Products for Accessible Living
Pain in people with Multiple System Atrophy
From Referral to Care: Navigating Home Health for MSA
Patient & Family Conference (2023) - Planning Ahead
Patient & Family Conference (2023) - Handling MSA Symptoms
MSA Awareness Month: Patient Panel (2024)
Patient & Family Conference (2023) - MSA Research Update
Patient & Family Conference (2023) - Coping with Grief
Patient & Family Conference (2023) - Organization Update
Patient & Family Conference (2023) - Voices of the MSA Community
Patient & Family Conference (2023) - Welcome Remarks