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The NARCOMS Registry is a project of the Consortium of Multiple Sclerosis Centers. 

© NARCOMS 2017 ​

Welcome to the

NARCOMS Registry

for Multiple Sclerosis

NARCOMS is a global registry for Multiple Sclerosis research, treatment, and patient education. 

NARCOMS Now

Our Quarterly Magazine.

A resource for collaboration.

Click here to learn more about improving care and quality of life.

Individuals with MS

Researcher & Providers

Our Vision

NARCOMS is a global registry for Multiple Sclerosis research, with links to other collaborative organizations and patient education.  

 

The Registry has enrollment data for over 38,000 persons with Multiple Sclerosis, many of whom share their on-going experience with the disease, so researchers can use it to better understand the disease, improve clinical care and quality of life. The more people who share their anonymous experience, the more we know about this disease that impacts so many lives, and the better we can handle it. 

Please Join Us.

Request registration materials and survey

Phone:      1-800-253-7884 (toll free US)

Email:        MSregistry@narcoms.org

                   

Mail:         NARCOMS Coordinating Center
                Washington University School of Medicine

                Campus Box 8067
                660 S. Euclid Ave.

                St. Louis, MO 63110-1093

Contact Us

Directory

Robert Fox, MD

Managing Director

Ruth Ann Marrie, MD, PhD

Scientific Director

Amber Salter, PhD

Director of Data Coordinating Center

Gary Cutter, PhD 

Advisor

Tuula Tyry, PhD, MAEd

Program Manager