Save Our Sons

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

[Save Our Sons @SOSsaveoursons]

@hulldailymail is 'chaos' too strong? 3 weeks to PL season, no team, no manager, no buyer. No, 'chaos' is about right

[Save Our Sons @SOSsaveoursons]

@ProfBrianCox brilliant

[Brian Cox @ProfBrianCox]

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

[Save Our Sons @SOSsaveoursons]

The next SOS charity ball has been confirmed for Saturday 28th October 2017 at Lazaat Hotel, Cottingham

[Harrison's Fund @HarrisonsFund]

Dont miss @DiscoveryUK 'The Challenge' 7:30pm June 19th, Fathers Day...
https://t.co/B2Vqvb3fwM #IronManDad Please RT

[Lesley - FPL ⚽️🎶 @Weggster]

Thanks Louise and Sharon.In training for the London 26 mile walk. @ActionDuchenne @BeverleyBS @SOSsaveoursons

[Lesley - FPL ⚽️🎶 @Weggster]

Thanks Bec and Sharon. sky diving and swim with sharks as part of Dive for Duchenne @BeverleyBS @SOSsaveoursons @ActionDuchenne

[Save Our Sons @SOSsaveoursons]

@KTHopkins because they are making a great personal sacrifice in order to better understand the plight of those in desperate need?

[Save Our Sons @SOSsaveoursons]

Planning is underway for the third Save Our Sons charity ball in 2017. Watch this space for an announcement later this week. Please RT

[Save Our Sons @SOSsaveoursons]

Please like and share

[Save Our Sons @SOSsaveoursons]

Save Our Sons Charity Masked Ball 30th September 2017 at Mercure Grange Park Willerby. Put it in your diary

[Save Our Sons @SOSsaveoursons]

@beverleybs.co.uk. Thanks for choosing @ActionDuchenne as Charity Partner

[Save Our Sons @SOSsaveoursons]

https://t.co/FwXviO0d1i

[STAT @statnews]

Senators urge the FDA to approve a controversial drug to treat Duchenne muscular dystrophy https://t.co/Un5U6vLkDJ

[CureDuchenne @CureDuchenne]

The Procko family shares their story about living with Duchenne muscular dystrophy. Evan, 12, is on the clinical... https://t.co/5tHa6PZBJg

[STAT @statnews]

In closely watched case, FDA delays decision on whether to approve drug for Duchenne muscular dystrophy. https://t.co/NDgn742Vz8

[World Stem Cell Summit @WSCSummit]

.@UCLA Stem Cell Gene Therapy Could Treat Duchenne Muscular Dystrophy Patients Using CRISPR/CAS9. (@UCLAstemcell) https://t.co/hts1lPdpjC

[NYT Business @nytimesbusiness]

F.D.A. is said to delay a decision on Duchenne muscular dystrophy drug https://t.co/czHNKarZqI

[Rare Genomics @RareGenomics]

Two Scientists Fight to Cure Their Son's Duchenne Muscular Dystrophy #RareDisease @People https://t.co/sgzu4ckpKt

[Hopkins Med News @HopkinsMedNews]

JUST OUT: Lab-grown muscle cells mimic Duchenne muscular dystrophy @CellPressNews https://t.co/cnW3yfhAv4