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Resources for You and Your Practice


Clinical Practice Support

Find Doctors and Resources
Find Doctors and Resources helps people living with MS find healthcare providers and community resources.  If you're not currently listed or want to update your information, claim your profile now.  Learn how

Healthcare Appeals
Information and resources to help with submitting appeals and prior authorizations.

Literature Search Service
This time-saving service helps clinicians and researchers access the journal articles they need.

Resources and Tools
Access valuable resources and tools to support your clinical work.

Resources for Specific Populations
Find information, resources and support for Veterans, children with pediatric MS, and African American and Hispanic/Latino individuals.

Find professional publications to inform your clinical work.

Society-Branded Slide Decks

Slide decks with notes are available for training of physicians, nurses, rehabilitation professionals, mental health professionals and dentists, and for providing patient education about multiple sclerosis. To request a slide deck, email

Current Topics in MS

A collaboration between the VA MS Centers of Excellence and the National MS Society. This CME/CE webinar series provides a free, accessible educational opportunity for health care clinicians involved in the care of patients with MS with the aim of improving MS knowledge and patient outcomes.


ECHO MS increases the capacity of neurologists to diagnose and manage patients with multiple sclerosis.  The program establishes an innovative peer-to-peer professional knowledge sharing network through a six month 18 CME cohort.

Webinars and case calls

Free diagnosis & management healthcare professional app


Help Make a Difference in MS Research

MS affects African Americans and Hispanics in different ways compared with other ethnic groups. Symptoms may differ, the disease may progress faster, and treatments may have different effects. Yet African Americans and Hispanics are underrepresented in clinical research, making it difficult to identify the best treatments or wellness activities to help them.

The National MS Society is working with the MS Minority Research Engagement Partnership Network, a group of non-profit organizations, health care professionals, researchers, MS biopharmaceutical companies, and people with MS, to better understand why racial and ethnic minorities aren’t fully represented in research and to develop solutions to encourage participation. Download the Minority Engagement in MS Research Patient Recruitment Toolkit for Health Care Professionals for tools and resources to help you talk to patients about research. Learn more about the project at and follow Twitter posts on this topic with #MSResearch4All.

Partners in MS Care

Partners in MS Care are healthcare providers — such as neurologists, physical therapists and long-term care providers — who have demonstrated knowledge and expertise in treating people with MS. Centers for Comprehensive Care are a form of Partner in MS Care that provide coordinated multi-disciplinary care. These providers have a relationship with the National MS Society which helps connect their patients to the information, resources and support available to assist them in living their best lives.
Connect with the healthcare provider engagement team member in your area to learn more about becoming a Partner in MS Care.


Become a Research Champion

An MS Research Revolution

Support MS Research

Understanding and ending MS can’t come fast enough – it will take all of us working together. It’s easy to be a champion for MS Research – join us and proudly let everyone know that you’re helping to lead the MS Research Revolution.

Become a Research Champion

Become a Research Champion
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