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Move it for MS: Personal stories
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Move it for MS: neuro-pilates circuits
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Childhood MS stories
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A gift in your will
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Latest
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Latest
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My Vespa adventure for the MS Trust
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"Cycling on closed roads with fellow enthusiasts is amazing!"
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"I can’t remember what a healthy body feels like, but that’s ok, because I love my body and all it can still do"
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"MS doesn"t stop me, it just makes me do things a little differently"
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"Starting a podcast in lockdown helped us take ownership of the situation"
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"Where you lose something, it makes you appreciate what you have"
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15 minutes with paediatric neurologist, Dr Evangeline Wassmer
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A personal interest in psychological support
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A sticky situation
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Amy"s story
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An update on staffing at the MS Trust
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Ask the expert: Cognitive problems
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Ask the expert: Disease modifying drugs
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Ask the expert: Dizziness and balance
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Ask the expert: MS pharmacists
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Ask the expert: MS relapses
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Ask the expert: Sex and MS
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Ask the expert: heat sensitivity
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Ask the expert: palliative care
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Ask the expert: pregnancy and MS
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Ask the expert: stem cell transplantation
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BMA award honours for MS Trust resources
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Back to school? Guidance for young people with MS
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Cabbages and an MS King
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Call for national neurology plan following largest ever survey of people with neurological conditions
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Can"t take the heat?
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Challenged myself to walk 150 miles throughout May
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Christmas cards are here!
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Cocoa improves MS fatigue
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Coffee Break: Five minutes with MS specialist nurse Michelle Meehan
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Coming out of lockdown - slowly. But what do the new rules mean for people with MS?
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Continuing to support health professionals as far as we can
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Coronavirus COVID-19 and multiple sclerosis - update 13 March
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Coronavirus COVID-19: what does it mean for people with multiple sclerosis?
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Covid boosters and shielding changes for people with MS
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Covid-19 vaccine and MS: Your questions answered
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Covid-19 vaccines and MS: Part two
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Covid-19 vaccines and people with MS: side effects and the second dose
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Covid-19 vaccines: what they mean for people with MS
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Cycling 1,000km for the MS Trust
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Cycling for my sister
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David"s Diary - An afternoon volunteering with Cards for Good Causes
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David"s Diary: Inclusion and Diversity
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Designing a robot to help people with MS
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Disappointing topline results from high dose biotin study
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EMA warns that Gilenya must not be taken during pregnancy
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End of life planning: starting difficult conversations
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European drug regulator recommends restricted use of Lemtrada
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Fampyra approved for use on the NHS in Scotland
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Fampyra approved for use on the NHS in Wales
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Five top tips for improving your lung health
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Flu season 2020
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Flu season 2021
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Focus on: fact or fiction?
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Focus on: self-compassion and resilience
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Focus on: sleep problems in MS
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Focus on: using orthoses to improve walking difficulties
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Gabapentin and pregabalin - new rules for prescriptions
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Good news! NICE approves Ocrevus (ocrelizumab) for primary progressive multiple sclerosis
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Healthy hobbies
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Heath Technology Wales guidance for AHSCT
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Here we are again!
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How could Brexit affect you, if you have MS?
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How fundraising for the MS Trust helps me to help my daughter
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How people react to my MS - Ian"s story
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How to get the most out of virtual appointments
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I adore "the Proclaimers" and 500 miles was a fitting tribute to them
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I would like to say how proud I am of all of them
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If we could raise money to help other people in need of support for the sake of a few blisters, then we will!
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If you are thinking of supporting the MS Trust in these difficult times, we would encourage you to do it!
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Introducing our new Advanced MS Champion for Cumbria
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Introducing our new Advanced MS Champion for Swansea
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Jenna"s treatment story: Mavenclad
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Kenny"s remarkable journey
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Kesimpta (ofatumumab) approved for relapsing remitting MS in Scotland
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Lara’s story: “You can emerge in a new way”
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Laura"s story: my Covid-19 vaccine experience
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Letisha"s story
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/news/views-and-comments/letishas-story
Letisha"s story: Work and MS
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Living with primary progressive MS: Yvonne"s story
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MS Trust funded nurses in Lanarkshire have improved support and care for people with MS
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MS and the menopause
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MS in the Media - 1 June 2018
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/news/views-and-comments/ms-media-1-june-2018
MS in the Media - 1 May 2020
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/news/ms-media-1-may-2020
MS in the Media - 1 November 2019
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/news/ms-media-1-november-2019
MS in the Media - 10 January 2020
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MS in the Media - 10 May 2019
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MS in the Media - 11 October 2019
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MS in the Media - 12 April 2019
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MS in the Media - 12 July 2019
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MS in the Media - 13 December 2019
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MS in the Media - 13 July
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/news/views-and-comments/ms-media-13-july
MS in the Media - 14 February 2020
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MS in the Media - 15 January 2021
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MS in the Media - 15 June 2018
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MS in the Media - 15 March 2019
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MS in the Media - 15 November 2019
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MS in the Media - 16 August 2019
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MS in the Media - 16 October 2020
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MS in the Media - 17 April 2020
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MS in the Media - 17 January 2020
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MS in the Media - 17 May 2019
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MS in the Media - 18 December 2020
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MS in the Media - 18 September 2020
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MS in the Media - 19 July 2019
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MS in the Media - 19 June 2020
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MS in the Media - 2 August 2019
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MS in the Media - 2 October 2020
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MS in the Media - 20 December 2019
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MS in the Media - 20 July 2018
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MS in the Media - 20 November 2020
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MS in the Media - 21 August 2020
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MS in the Media - 21 June 2019
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MS in the Media - 22 June 2018
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MS in the Media - 22 May 2020
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MS in the Media - 22 November 2019
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MS in the Media - 23 August 2019
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MS in the Media - 24 April 2020
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MS in the Media - 24 January 2020
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MS in the Media - 24 May 2019
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MS in the Media - 25 September 2020
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MS in the Media - 26 July 2019
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MS in the Media - 27 November 2020
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MS in the Media - 27 September 2019
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MS in the Media - 28 August 2020
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MS in the Media - 28 February 2020
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MS in the Media - 29 January 2021
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MS in the Media - 29 November 2019
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MS in the Media - 3 April 2020
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MS in the Media - 3 May 2019
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MS in the Media - 30 August 2019
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MS in the Media - 31 May 2019
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MS in the Media - 4 October 2019
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MS in the Media - 4 September 2020
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MS in the Media - 5 April 2019
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MS in the Media - 5 July 2019
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MS in the Media - 6 December 2019
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MS in the Media - 6 July 2018
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MS in the Media - 6 November 2020
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MS in the Media - 6 September 2019
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MS in the Media - 7 August 2020
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MS in the Media - 7 February 2020
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MS in the Media - 7 June 2019
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MS in the Media - 8 November 2019
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MS in the Media - 9 August 2019
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MS in the Media - 9 October 2020
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MS in the Media - ECTRIMS 2019
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MS nurse takes on 2020 London Marathon
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Mission:100 Orkney vs Shetland
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Multiple sclerosis and disease modifying drugs, what are my options?
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My fundraising challenge to support my son and daughter-in-law
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NICE recruiting people living with MS and health professionals to update the MS Clinical Guideline
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NICE rejects Sativex in draft guidance on cannabis-based medicinal products
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New guidelines for pregnancy in multiple sclerosis
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Ocrevus (ocrelizumab) for primary progressive MS – NICE confirms approval in final guidance
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Ocrevus approved for primary progressive MS in Scotland
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Ocrevus: What you need to know
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Ofatumumab (Kesimpta) approved for relapsing MS in England and Wales
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Ofatumumab (Kesimpta) gets UK licence for relapsing remitting MS
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One Cat and her dog
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Ozanimod (Zeposia) - NICE says no in final decision
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Ozanimod (Zeposia) approved for relapsing remitting MS in Scotland
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Ozanimod (Zeposia) for relapsing remitting multiple sclerosis rejected by NICE
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Ozanimod (Zeposia) recommended for European licence
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Pass on something wonderful
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Plegridy approved for relapsing remitting MS in England
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Poetry and MS
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Ponesimod (Ponvory) for relapsing remitting multiple sclerosis rejected by NICE
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Preliminary research on Covid-19 in people with MS in Italy offers some reassurance
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Providing the best service we can for people affected by MS
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Questions about shielding from 1st June
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Regan"s treatment story: Lemtrada
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Remembering my sister with a 50-day cycle ride
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Remyelination research: what it means for people with MS
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Researchers develop mRNA vaccine to treat MS-like condition in mice
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Reset and reform
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Restarting our specialist nurse and advanced MS champion programmes
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Sativex cost-effective in final NICE guideline on cannabis-based medicines
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Sew-cially distancing fundraising ideas!
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Should I be preparing now in case I catch coronavirus?
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Should I be wearing a face covering during the COVID-19 outbreak?
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Sign up to Miles for MS for FREE
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Siponimod (Mayzent) approved for active secondary progressive MS in England and Wales
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Siponimod (Mayzent) approved for active secondary progressive MS in Scotland
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Siponimod for active secondary progressive MS rejected by Nice
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Siponimod for secondary progressive MS: help us make the case to NICE
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Siponimod granted European licence for active secondary progressive MS
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Siponimod recommended for secondary progressive MS by European Medicines Agency
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Staying connected
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Support the MS Trust this April through Discount Promo Codes
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Taking on Miles for MS for the MS Trust
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Temporary restriction on use of Lemtrada
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Thanks to MS, I am learning to ride!
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The Walkie Talkies team conquer 100km of the Jurassic Coast for the MS Trust
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The challenges of choosing a DMD as a new mother
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The group of MS nurses covering 1,000 miles to say thank you for their education
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Trial reports myelin repair success
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Under-the-skin injection of Tysabri gets licence in UK and Ireland
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Update on coronavirus COVID-19 and multiple sclerosis
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Using creativity to cope with long-term conditions like MS
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Walking difficulties: getting your walking back on track after lockdown
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We are planning to make it an annual event!
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What does the future look like for community MS support?
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What led Trishna to become a health and disability advocate?
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When will people with MS get a covid vaccine?
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Who gets MS and why?
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Would having children be impossibly hard for me, my partner, and the children themselves?
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Research
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Brain training: a cognitive rehabilitation programme evaluated
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Can standing frames improve mobility in progressive MS?
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Coronavirus COVID-19 and multiple sclerosis
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Daytime sleepiness and driving in MS
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Do disease modifying drugs affect life expectancy?
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Do medicines reduce fatigue in MS?
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Effect of vitamin D supplements on MS activity
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Exercise is good for your brain
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How do families affected by MS manage health information?
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How does multiple sclerosis affect dating and romantic relationships?
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How long does it take for an MS drug to be fully effective?
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Learning a second language improves brain structures in MS
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MRI reveals smouldering MS lesions
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MS onset in childhood: do disease modifying drugs delay long term disability?
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MS research update - Exercise early in the course of MS and FES effects on bladder symptoms - 31 July 2018
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MS research update - The right word won"t come to me... A study looking at slowed word retrieval in MS - 21 October 2013
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MS research update – Abdominal massage for constipation – 4 December 2018
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MS research update – Cell therapy targeting Epstein-Barr virus tested in progressive MS – 20 December 2018
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MS research update – Could cocoa help MS fatigue? – 15 October 2018
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MS research update – Factors affecting DMD prescribing in the UK – 21 January 2019
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MS research update – Walking improves with mental rehearsal – 8 November 2018
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Machine learning identifies new subtypes of MS from MRI scans
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Microaggressions at work; more than just hurt feelings
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New report highlights barriers to accessing Sativex across the UK
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Remyelination – what progress has been made?
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Stem cell transplants in the news
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Temelimab: early clinical trial suggests potential for remyelination
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Testing iStep-MS, a new programme to encourage physical activity
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Treatments for foot drop compared
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Tysabri risk of PML with extended interval dosing
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