Tag: UK
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