The Rhoda Goetz Foundation – Resources for Patients and Caregivers
The National MS Society is dedicated to supporting individuals affected by multiple sclerosis (MS) and funding research to find a cure for the disease. It provides resources, support services, advocacy, and educational programs to improve the lives of people with MS, and their families.
The Tom Sherak MS Hope Foundation is a game-changing, action-oriented, nonprofit organization that responds, with immediacy, to the needs of people with multiple sclerosis by supporting innovative, person to-person programs and services, and funding cutting edge research.MS Hope Foundation
The UCLA Health Multiple Sclerosis (MS) Program offers world-class care for patients with MS. Our team’s research focus allows us to provide novel, advanced MS treatments. Our dedicated specialists have decades of combined experience and training in the diagnosis and management of MS.
For Newly Diagnosed Patients
National MS Society – Newly Diagnosed
Comprehensive information for understanding your diagnosis, what happens next, and navigating early treatment decisions.
MSAA – What Does Newly Diagnosed Mean?
Educational videos and webinars specifically for those newly diagnosed or experiencing initial symptoms.
Healthline – Ultimate Guide for the Newly Diagnosed
Practical advice from medical professionals and people with MS on what you need to know right now.
Multiple Sclerosis News Today – Newly Diagnosed Guide
Information on treatments, lifestyle changes, and what to expect after diagnosis.
For Living With MS
National MS Society – Living Well with MS
Resources on diet, exercise, healthy behaviors, and wellness strategies.
Can Do MS
Free wellness programs including MS Moves® fitness, fatigue management, sleep coaching, and brain health resources.
Healthline – Living with MS
Guidance on fitness, daily living, symptom management, and maintaining quality of life.
MSAA – My MSAA Community
Peer-to-peer online forum for sharing experiences and finding support.
For Caregivers
MS Care Partner Connection
Comprehensive online resource specifically designed for MS caregivers, covering everything from diagnosis through long-term care.
National MS Society – For Care Partners
Support, resources, and information specifically for those caring for someone with MS.
Family Caregiver Alliance – MS Caregiver Resource Guide
State-by-state resources, self-care tips, and practical caregiving guidance.
Healthline – Caring for Someone with MS
Tips for providing care while maintaining your own health and well-being.
Financial Resources
National MS Society – MS Navigator
Free personalized help connecting to financial assistance, insurance navigation, and resources. Call 1-800-344-4867.
Patient Advocate Foundation – Co-Pay Relief
Co-pay assistance for medications and insurance premiums (up to 500% of Federal Poverty Level).
HealthWell Foundation – MS Medicare Access Fund
Financial assistance for eligible patients with Medicare coverage.
PAN Foundation – MS Medication Copay Grant
Up to $5,000/year assistance for MS medication copays.
The Assistance Fund
Copay assistance program for MS medications and treatments.
Community Connection
MyMSTeam
Social network with 206,000+ members – connect, share daily experiences, and get practical advice.
MSWorld
One of the largest all-volunteer MS communities with chat rooms, forums, and 220,000+ members worldwide.
National MS Society – Online Communities
Facebook groups, Discord channels, and peer support programs including MSFriends one-on-one connections.
My MSAA Community
Free online community for people with MS, families, and caregivers to share experiences and support.
The Mighty – MS Support Group
Online community with thousands of members sharing stories, coping techniques, and daily support.