Save Our Sons (@SOSsaveoursons) header
Save Our Sons (@SOSsaveoursons) profile picture

Save Our Sons

@SOSsaveoursons

SaveOurSons is a collaboration of 3 families raising money for research into fighting Duchenne Muscular Dystrophy

 Yorkshire and The Humber, England
Joined May 2016
  • Tweets20
  • Following625
  • Followers196
1Media
Photo by Save Our Sons (@SOSsaveoursons)
Save Our Sons retweeted
Brian Cox (@ProfBrianCox) profile picture
Brian Cox
@ProfBrianCox15 Jun 2016
It's possible to get people to vote to abolish gravity, but there will be a constitutional crisis when they discover they aren't floating
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Dont miss @DiscoveryUK 'The Challenge' 7:30pm June 19th, Fathers Day... vimeo.com/103366112 #IronManDad Please RT
The Challenge - Trailer

The Challenge - Trailer

A documentary feature film, The Challenge tells the story of Alex Smith, who, in June 2015, completed an Ironman, known as the toughest single day challenge you can undertake, carrying his 40kg...

vimeo.com
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Thanks Louise and Sharon.In training for the London 26 mile walk. @ActionDuchenne @BeverleyBS @SOSsaveoursons
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Thanks Bec and Sharon. sky diving and swim with sharks as part of Dive for Duchenne @BeverleyBS @SOSsaveoursons @ActionDuchenne
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Save Our Sons retweeted
STAT (@statnews) profile picture
STAT
@statnews24 May 2016
Senators urge the FDA to approve a controversial drug to treat Duchenne muscular dystrophy bit.ly/20vQPEX
Image from STAT (@statnews)
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Save Our Sons retweeted
CureDuchenne (@CureDuchenne) profile picture
CureDuchenne@CureDuchenne24 May 2016
The Procko family shares their story about living with Duchenne muscular dystrophy. Evan, 12, is on the clinical... fb.me/87Bz9EgMp
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Save Our Sons retweeted
STAT (@statnews) profile picture
STAT
@statnews25 May 2016
In closely watched case, FDA delays decision on whether to approve drug for Duchenne muscular dystrophy. bit.ly/1WSJX6A
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.@UCLA Stem Cell Gene Therapy Could Treat Duchenne Muscular Dystrophy Patients Using CRISPR/CAS9. (@UCLAstemcell) ow.ly/44Sx300zhUx
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F.D.A. is said to delay a decision on Duchenne muscular dystrophy drug nyti.ms/1WSStCJ

F.D.A. Is Said to Delay Decision on Duchenne Muscular Dystrophy Drug (Published 2016)

The news caused a sharp rise in the stock of Sarepta Therapeutics, the maker of the drug, as some investors saw a hint of approval in the development.

nytimes.com
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Two Scientists Fight to Cure Their Son's Duchenne Muscular Dystrophy #RareDisease @People 1jp.cc/s/08mXF
Image from Rare Genomics (@RareGenomics)
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JUST OUT: Lab-grown muscle cells mimic Duchenne muscular dystrophy @CellPressNews bit.ly/1sAJRmX
Image from Hopkins Med News (@HopkinsMedNews)
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