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Evidence of how knowledge and awareness of DM is becoming consolidated amongst professionals working in the field comes from a report of the 1st Myotonic Dystrophy Workshop held at the Queen Square, London, Centre for Neuromuscular Diseases last December.
With MDSG represented by Margaret Bowler, Elycia Ormandy, Mike Walker and John Kelly, the event brought together clinicians, scientists, and patient organisations. Amongst topics presented by speakers from UK and the USA, were plans for a UK National Register of DM patients in a presentation by Dr Mark Rogers.
Readers will hear more of MDSG’s plans to support such a UK National Register in the coming weeks.
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