Top Tweets for #AtlasofMS
π The #AtlasofMS was everywhere at #ECTRIMS2025!
From MRI availability, to barriers in diagnosis & access to treatment, Atlas data shaped key discussions across the congress.
Itβs clear: global evidence is essential to improve MS care worldwide. π‘
#MSResearch #GlobalHealth
π Global access to diagnostic tests at #ECTRIMS2025
In a session on MS diagnosis and the impact of the revised 2024 McDonald Criteria, Dr Andrew Solomon presented findings from the #AtlasofMS Topical Survey on diagnostic tests.
π Full data will be published this year.
π Next week at #ECTRIMS2025 MSIF is looking forward to sessions on MS diagnosis, including the impact of the updated McDonald Criteria, and insights from the #AtlasofMS on diagnostic tests.
#MSResearch #McDonaldCriteria #MSDiagnosis #AtlasofMS
π Over 2.8 million people live with MS around the world β each with a unique journey to diagnosis. Yet, many have faced the same challenges along the way. The #AtlasofMS identified seven major barriers that delay early & accurate diagnosis. π Learn more: https://t.co/HdODp1jr2t
π Did you know? At least twice as many females (69%) live with MS compared to males (31%). The #AtlasofMS highlights the vital need for any gender inequalities and healthcare access barriers to be identified and addressed. Join the #WorldMSDay campaign: https://t.co/1EsRXlWs5Y
οΏ½οΏ½ Based on data submitted to the #AtlasofMS during 2020-2022, we estimated that there are over 31,000 children and adolescents living with MS worldwide. π This data has recently been analysed in greater detail, Learn more about the findings here: https://t.co/CUg8hpk4Sg
The #AtlasofMS reveals the many global barriers to accessing MS healthcare. Get a snapshot of the key findings. ππ https://t.co/MsqlqDH4s1
Everyone with MS deserves to access quality healthcare. Read more about improving access to MS healthcare here: https://t.co/n28VqAY4HJ
π‘ Le saviez-vous ? Dans 57 % des pays, les personnes atteintes de #MS doivent payer une partie ou la totalitΓ© des coΓ»ts des traitements de fond, selon le #AtlasOfMS β¦Nous devons continuer Γ plaider pour un accΓ¨s Γ©quitable aux traitements ! πͺ
#ECTRIMS2024
π‘ Did you know? In 57% of countries, people with #MS have to pay some or all of the costs for DMTs, according to the #AtlasOfMS. This varies globally from 39% in Europe to 76% in the Americas. We need to continue advocating for equitable access to treatments! πͺ
#ECTRIMS2024
π‘ Did you know? In 57% of countries, people with #MS have to pay some or all of the costs for DMTs, according to the #AtlasOfMS. This varies globally from 39% in Europe to 76% in the Americas. We need to continue advocating for equitable access to treatments! πͺ
#ECTRIMS2024
In 2023, we updated the #AtlasofMS data. π New data from 125 countries showed there are now more than 2.8 million people with MS worldwide. π Some countries saw increased prevalence, others highlighted the ongoing need for accurate data. Learn more: https://t.co/5P2Q8PNR7l
The #AtlasofMS found that 70% of low-income countries have no licensed DMTs available for people with MS. A range of MS treatments should be available in all health systems at all times. π Read more about improving access to MS treatments here: https://t.co/NUfd57jAbn
Data from the #AtlasofMS can be a powerful tool for change. You can use it to raise awareness, support your advocacy efforts, and engage with governments and decision makers. Learn how the Atlas data can be used to support advocacy work in this video. π https://t.co/nuhL88Vyds
The #AtlasofMS reveals the many barriers and inequalities that exist in getting a diagnosis, and accessing treatments and rehabilitation. Find evidence, tools and case studies, to support your national efforts to improve access to MS healthcare. π https://t.co/n28VqAY4HJ
The #AtlasofMS shows that in 70% of low-income countries there are no licensed MS Disease Modifying Therapies (DMTs) available for use.
#GlobalHealth #MSTreatmentForAll
@MSIntFederation I was a database developer for 14 years before MS ended my career. #AtlasOfMS is impressive!
The perfect tool for highlighting regional disparities in care.
The Middle East and North Africa (MENA) region large and diverse, comprising of more than 20 countries. An in-depth analysis of #AtlasofMS data from the MENA region, focusing on access to treatments in each country, is now available. πLearn more here. π https://t.co/yPYx7sADj3
Psychological support is a vital part of MS care, but the #AtlasofMS shows that therapies to treat mood symptoms are only available in 69% of countries worldwide. π The theme of #WorldMentalHealthDay 2023 is βMental health is a universal human rightβ. We could not agree more.
The #AtlasofMS is the most comprehensive worldwide study of the epidemiology of MS. π In 2022, we sent a request for any new national data. New data shows that the prevalence of MS has increased in many countries. Read more on the latest figures. π https://t.co/5P2Q8POoWT
βIn order to be able to afford the cost of treatment, we are forced to deprive ourselves of our basic daily needs.β
The #AtlasofMS showed that the main barrier for accessing MS treatments across the world is cost. Oumaima, like many others living with MS, knows this well.
The Atlas of MS is the most comprehensive worldwide study of MS epidemiology. π The data can be used to raise awareness, support advocacy efforts, and engage with decision makers. Learn how to make the most of the #AtlasofMS website and tools here. π https://t.co/Wqu7T4cEnT
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