Mike Matters (@MikeMattersDMD) header
Mike Matters (@MikeMattersDMD) profile picture
Scotland, United Kingdom
Joined May 2015
Photo by Mike Matters (@MikeMattersDMD)Photo by Mike Matters (@MikeMattersDMD)Photo by Mike Matters (@MikeMattersDMD)Photo by Mike Matters (@MikeMattersDMD)Photo by Mike Matters (@MikeMattersDMD)
#standwithlewis #Translarna Lewis and his family on TV tonight asking for medicine that is available in 22 European countries. tv3.ie/news_sub_page.php?vid…
Replying to @theSNP
@theSNP @MikeMattersDMD Michael Young (age11) is still walking and living life to the full after the SNP ensured he got Translarna, a life enhancing medicine. #SNP17
Please sign this petition. Little Lewis Harte is being denied Translarna. He is five years old and desperately needs this life enhancing medicine as quickly as possible. change.org/p/simon-harris-pl…
Managed Access Programme announced for Exondys51 by Sarepta Therapeutics. Suitable for deletions amenable to exon 51 investorrelations.sarepta.co…
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Cross Party meeting for Muscular Dystrophy on Wednesday focused on Adult Services @markichapman @h0pefulmummy @ActionDuchenne @jackiebmsp
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Please support Duchenne families in Ireland Here’s the link: change.org/p/hse-ireland-ple…
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A big Thank You to Fiona Fitzpatrick and Susan Dickson who, with help from Lloyd's Bank, raised £630 today for Mike Matters. WOW!!
Delighted that Michael won Pride of Forth Valley 'Young Person of the Year Award' for all his campaigning for Translarna.
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Replying to @NicolaSturgeon
@NicolaSturgeon Big congratulations from me and all my team. Looking forward to seeing you again with mum and dad x
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Replying to @MathesonMichael
@MathesonMichael congratulations and thank you for the awesome support. See you soon x
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Replying to @jackiebmsp
@jackiebaillie16 we are delighted for you and appreciate all you do for MD. look forward to battling on with your amazing support.
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@JimEadieSNP very disappointed for you and thank you for everything you have done for Duchenne. We hope to keep working with you in future.
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We cannot believe Craig is making his year so itchy for Duchenne! xitter.gq/gillespie_fiona/status…
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This could be SMC or FDA, different countries, same story... #makeduchennehistory xitter.gq/theracetoyes/status/72…
Pat Furlong: @ParentProjectMD urges for flexibility for rare disease assessments. #MakeDuchenneHistory
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Team UK speaking with conviction ❤️👍 #MakeDuchenneHistory
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Austin tells us "I can now feed myself". This isn't about breaking records, just living life. #MakeDuchenneHistory
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