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UCB at AAN 2021: A patient-led analysis on the experience of living with MG

Posted by Kenza Seddik, Rare Disease Patient Experience Lead 19-Apr-2021

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Our commitment to innovative technology in Rare Disease

Posted by Chris Clark, Patient Value Neurology & Europe/International Solutions 23-Nov-2020

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Our focus on Myasthenia Gravis at AANEM 2020

Posted by Ahmad Alrawi, Neurology Patient Value Unit 07-Oct-2020

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Going Virtual – Supporting the MG Community Online

Posted by Tyler Story, Patient Value Neurology & Europe/International Solutions - Medical Affairs 25-May-2020

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