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MS International
  • About MS

    About MS

    • What is MS?
    • Who gets MS?
    • Types of MS
    • MS in Children
    • Causes of MS
    • Diagnosing MS
    • Symptoms of MS

      Symptoms of MS

      • Bladder and bowel
      • Emotion and cognitition
      • Fatigue
      • Movement and coordination
      • Pain
      • Sexual problems
      • Vision
  • Living with MS

    Living with MS

    • Find MS support near you
    • MS, COVID-19 and vaccines – updated global advice
    • What influences quality of life with MS?

      What influences quality of life with MS?

      • Seven principles to improve quality of life
    • Treatments and therapies
    • Complementary and alternative therapies
    • Caregivers
    • Rehabilitation
    • Family life
    • Relationships and intimacy
    • Telling people you have MS
    • Ageing and MS
    • MS and menopause
    • Keeping healthy
    • Smoking and MS
    • Education and employment
    • International MS awards

      International MS awards

      • Award for people with MS
      • Award for caregivers
    • My story of MS

      My story of MS

      • Access to MS healthcare
      • Hanin, Jordan
      • Ling, Malaysia
      • Alexia, Cyprus
      • Christelle, South Africa
      • Hao, China
      • Sean, UK
  • Research

    Research

    • AtlasofMS.org
    • Key topics in MS research

      Key topics in MS research

      • Clinical research and trials
      • MS registries
      • Patient Reported Outcomes for MS
      • Research into Progressive MS
      • Stem cell therapy for MS
      • Quality of life research in MS
    • Awards, grants and fellowships

      Awards, grants and fellowships

      • Du Pré Grants
      • McDonald Fellowships
      • Charcot Award
      • Young Investigator Award
      • Global MS research fellowships
    • The Progressive MS Alliance webcasts
  • Access & advocacy

    Access & advocacy

    • Improve access to MS treatment
    • Improve MS diagnosis
    • Getting the healthcare I need
    • Get the evidence
    • How to get started in advocacy
    • Learn from others
    • MSIF work on access
  • Resources
  • News & events
  • About us

    About us

    • Who we are and what we do
    • Our strategy
    • Our members
    • Our progress
    • Our staff
    • How we are governed

      How we are governed

      • Board of trustees
      • Committees
      • International Medical and Scientific Board
    • How we are funded

      How we are funded

      • Our income in 2023
      • How we work with the healthcare industry
      • MSIF COVID-19 Response Initiative
      • Our supporter promise
    • Annual accounts
    • MSIF statement: War and Conflict

      MSIF statement: War and Conflict

      • People affected by MS in Ukraine
    • Contact us
  • Get involved

    Get involved

    • Fundraise for a world without MS
    • Join MSIF (MS organisations)
    • Sign up for our newsletters
    • World MS Day
    • Cykelnerven
    • Our fundraisers
  • Get involved
  • Fundraise for a world without MS
  • Join MSIF (MS organisations)
  • Sign up for our newsletters
  • World MS Day
  • Cykelnerven
  • Our fundraisers
  • MSIF statement: War and Conflict
  • People affected by MS in Ukraine
  • How we are funded
  • Our income in 2023
  • How we work with the healthcare industry
  • MSIF COVID-19 Response Initiative
  • Our supporter promise
  • How we are governed
  • Board of trustees
  • Committees
  • International Medical and Scientific Board
  • About us
  • Who we are and what we do
  • Our strategy
  • Our members
  • Our progress
  • Our staff
  • How we are governed
  • How we are funded
  • Annual accounts
  • MSIF statement: War and Conflict
  • Contact us
  • Access & advocacy
  • Improve access to MS treatment
  • Improve MS diagnosis
  • Getting the healthcare I need
  • Get the evidence
  • How to get started in advocacy
  • Learn from others
  • MSIF work on access
  • Charcot Award
  • Charcot Award winners
  • McDonald Fellowships
  • McDonald Fellowship recipients
  • Du Pré Grants
  • Du Pré Grant recipients
  • Awards, grants and fellowships
  • Du Pré Grants
  • McDonald Fellowships
  • Charcot Award
  • Young Investigator Award
  • Global MS research fellowships
  • Key topics in MS research
  • Clinical research and trials
  • MS registries
  • Patient Reported Outcomes for MS
  • Research into Progressive MS
  • Stem cell therapy for MS
  • Quality of life research in MS
  • Research
  • AtlasofMS.org
  • Key topics in MS research
  • Awards, grants and fellowships
  • The Progressive MS Alliance webcasts
  • My story of MS
  • Access to MS healthcare
  • Hanin, Jordan
  • Ling, Malaysia
  • Alexia, Cyprus
  • Christelle, South Africa
  • Hao, China
  • Sean, UK
  • Award for people with MS
  • James D Wolfensohn Award winners
  • International MS awards
  • Award for people with MS
  • Award for caregivers
  • What influences quality of life with MS?
  • Seven principles to improve quality of life
  • Living with MS
  • Find MS support near you
  • MS, COVID-19 and vaccines – updated global advice
  • What influences quality of life with MS?
  • Treatments and therapies
  • Complementary and alternative therapies
  • Caregivers
  • Rehabilitation
  • Family life
  • Relationships and intimacy
  • Telling people you have MS
  • Ageing and MS
  • MS and menopause
  • Keeping healthy
  • Smoking and MS
  • Education and employment
  • International MS awards
  • My story of MS
  • Symptoms of MS
  • Bladder and bowel
  • Emotion and cognitition
  • Fatigue
  • Movement and coordination
  • Pain
  • Sexual problems
  • Vision
  • About MS
  • What is MS?
  • Who gets MS?
  • Types of MS
  • MS in Children
  • Causes of MS
  • Diagnosing MS
  • Symptoms of MS
  • About MS
  • Living with MS
  • Research
  • Access & advocacy
  • Resources
  • News & events
  • About us
  • Get involved
  • Home
  • Investigación

Investigación

Information on MS research in Arabic, English and Spanish

Desafíos a los que se enfrentan las investigaciones en EM

La EM es una enfermedad extremadamente difícil de investigar

Learn more

Awards, grants and fellowships

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The Atlas of MS is live!

The 3rd edition of the Atlas has been released

Learn more

Patient Reported Outcomes for MS

Putting the experience of people affected by MS at the heart of research, care and health policy

Learn more

Clinical research and trials

Research and clinical trials are taking place around the world, trying to find and improve treatments for MS

Learn more

Terapia con células madres para EM

Para las personas con EM, es importante tener la mejor información disponible acerca de la terapia con células madres con el fin de tomar decisiones relacionadas con esta cuestión compleja.

Learn more

Progressive MS research

The International Progressive MS Alliance works to speed up the development of treatment for progressive MS

Learn more

Investigación en EM y calidad de vida

La EM puede influir sustancialmente en la capacidad de un individuo a la hora de participar en la sociedad, conservar su puesto de trabajo y tener relaciones

Learn more
Contact us

Multiple Sclerosis International Federation
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