Global MS research fellowships

A selection of fellowships and grants open to MS researchers around the world

Vacaciones inclusivas y accesible para todos

Examples of accessible resorts and services shared by our members

Committees

The MS International Federation draws on the expertise of its members, people with MS and others

Du Pré Grant recipients

These researchers have received Du Pré Grants to enable them to work in established MS research centres outside their own country

Progressive MS research

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

Stacey’s story

Stacey Black ran a half-marathon in memory of her grandmother

Teresa’s story

Teresa was diagnosed with MS 24 years ago. To celebrate World MS Day 2015 she walked a mile for each year she’s had MS.

Young Investigator Award

The award is given for the best presentation of a translational project by a young researcher

Registros de EM: hacer que las personas con EM sean el centro de la investigación

MS affects people all over the world. MS registries are one of the many advances in MS research that are bringing us closer as a global MS community and closer to ending MS.

Los daños en la médula cervical y la discapacidad en la EM

Cord lesion load and spinal cord atrophy may contribute to disability in people with progressive MS

La leyenda de la música Masta Ace: hip-hop, EM y creatividad

The UK MS Society met up with Brooklyn rapper and record producer Masta Ace to talk about music and life with MS

Más de 20.000 personas firman la petición de la Sociedad Británica de EM para mejorar la prestación por discapacidad para personas con EM

The UK MS Society’s campaign calls on the government to change criteria of Personal Independence Payments (PIP), a vital disability benefit for people with MS.

Los voluntarios de la Asociación Británica de la EM crean conciencia sobre la EM en un evento internacional

Volunteers from the UK MS Society’s English Council worked with the Rotarian Action Group for MS Awareness (RAGSMA) to attend the event and share information about MS.

James D Wolfensohn Award winners

Winners of the James D. Wolfensohn Award come from all over the world

Sean Hegarty

Sean Hegarty from the UK is in his mid-forties and lives with relapsing progressive MS

El 45 % de las personas con EM en Reino Unido han sido víctimas de prejuicios.

A recent survey by the UK MS Society has shown that 45% of people with MS have experienced prejudice because of their symptoms

¿Qué ha pasado en ECTRIMS?

Our highlights from the world’s largest scientific conference on multiple sclerosis

La línea de asistencia para la EM cumple 25 años ayudando a las personas afectadas con EM en el Reino Unido

This year marks the 25th anniversary of the UK MS Society’s helpline.

Eficacia de la rehabilitación de la memoria en las personas con EM

Review shows previous measures of memory rehabilitation were not reflective of daily life

Nuevo objetivo para entender la progresión secundaria de la EM

Chemical in the brain involved in signaling may play a role in progressive MS

La médula espinal se ve afectada en la fase temprana de la EM primaria progresiva

Study suggests that early spinal neurodegeneration may underlie clinical impairment

Becas de prácticas profesionales remuneradas para personas con EM

Believe and Achieve is a programme of paid internships for young people with MS

Alliance anuncia becas de investigación para la EM progresiva

The Progressive MS Alliance has awarded its first round of 22 research grants to investigators in nine countries

La campaña “Treat Me Right” cambia las directrices en el Reino Unido

The UK MS Society’s campaign calls for the right treatment at the right time

Progressive MS meeting in Milan

The first scientific meeting of the International Progressive MS Collaborative took place in Milan, Italy

MS International Federation announces first wave of 2014 Du Pré Grants

The MS International Federation has announced its first six Du Pré Grants for 2014

Un nuevo informe muestra una mayor prevalencia de la EM de lo que se pensaba

The Atlas of MS is the most extensive worldwide survey of the disease