The MS Register is a ground-breaking study designed to increase our understanding of living with MS in the UK. Let's make sense of MS.

Swansea University
Joined June 2011
We are currently taking a break from X, but you can find us on lots of other platforms! We would love to connect with you on LinkedIn, Threads, YouTube, Instagram and Facebook 👋🫂 You can also sign up to our mailing list by contacting: [email protected] 📩
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The UK Multiple Sclerosis (MS) Register helps research into this condition by gathering data to answer fundamental questions and giving researchers safe access to this information. Find out more - popdatasci.swan.ac.uk/centre… @SwanseaMedicine @SwanseaUni @UKMSRegister @mssocietyuk
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It's nearly the end of Brain Awareness week! 🧠 Are you aware of Multiple Sclerosis (MS) and did you know about UK MS Register? The MS Register is a ground breaking study designed to increase our understanding of living with MS in the UK. Find out more: bhtresearchandinnovation.org…
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📽️Watch MS Register analyst, Sarah Knowles discuss the findings and impact of her new paper on late onset MS, published in Annals of Neurology👉youtu.be/UwEfhkI2AAc?si=dCk9… #Lovedataweek @UKMSRegister @SwanseaUni @SwanseaMedicine @mssocietyuk @mscymru
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✍️@UKMSRegister blog - Late Onset MS Newly published research by Sarah Knowles found that MS looks different when it develops in the later stages of life. Read more about the findings of this study here👉popdatasci.swan.ac.uk/uk-ms-… @mssocietyuk #msresearch #lateonsetMS
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The @UKMSRegister is definitely a useful tool if you have MS.
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Thank you very much to the @UKMSRegister Team for the Christmas card and chocolates. We hope all of the team have a lovely Christmas and New year, and we look forward to continuing to work with you throughout 2024.
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🎉@UKMSRegister Highlight from the Year!🎉 The Register facilitates recruitment for the 'Octopus' trial,revolutionising progressive MS testing - this is a pivotal moment in global #MS research and could speed up life-changing results. mssociety.org.uk/research/ex… #PDShighlights2023
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A lot of questions that require answers but how to #prioritise & rank your #MS #registry questions🤯 💡Everyone wants to ask ALL questions but it's important to assess questions in the core data set ➡️ Are they 🔴 impossible to answer 🟢 easy to answer 🟡 complex, but possible
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MSDA @msdataalliance and EMSP now leading on a lively workshop with MS societies from Western Europe on setting up #MS #registries to ensure updated and relevant #data is available for improved care and advocacy and informed #decisionmaking. #DataSavesLives #MultipleSclerosis
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🎉We're @QAPrizes winners! 🏆For our groundbreaking work with the @SAILDatabank! 🌍From vital COVID-19 research to global initiatives, SAIL's achievements offer crucial insights for informed decisions & positive societal outcomes bit.ly/47e782f @SwanseaUni
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Great to see the fantastic work from the @UKMSRegister @mssocietyuk @SwanseaUni at the @ADRUK2023 @adr_uk 🎉
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Well done to our intern Deepak who is featured here discussing his internship 👏 It was great having Deepak working with us over the summer months. Before he finished he was able to share his work at the showcase event 👇
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New video podcast from @shiftms focusing on #MultipleSclerosis and women's health, including: ☑️Medical gaslighting ☑️Awkward conversations with HCPs ☑️A lack of research on women with #MS ☑️Changing HCPs This is the 1st episode in a 6 part series ⏯️youtube.com/watch?v=skfc8gPs…
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