Save Our Sons

A big thank you to this gentleman who generously donated in branch to our #charity partner @ActionDuchenne.

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

@ProfBrianCox brilliant

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

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

Dont miss @DiscoveryUK 'The Challenge' 7:30pm June 19th, Fathers Day... vimeo.com/103366112 #IronManDad Please RT

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

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

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

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

Please like and share

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

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

Senators urge the FDA to approve a controversial drug to treat Duchenne muscular dystrophy bit.ly/20vQPEX

The Procko family shares their story about living with Duchenne muscular dystrophy. Evan, 12, is on the clinical... fb.me/87Bz9EgMp

In closely watched case, FDA delays decision on whether to approve drug for Duchenne muscular dystrophy. bit.ly/1WSJX6A

.@UCLA Stem Cell Gene Therapy Could Treat Duchenne Muscular Dystrophy Patients Using CRISPR/CAS9. (@UCLAstemcell) ow.ly/44Sx300zhUx

F.D.A. is said to delay a decision on Duchenne muscular dystrophy drug nyti.ms/1WSStCJ

Two Scientists Fight to Cure Their Son's Duchenne Muscular Dystrophy #RareDisease @People 1jp.cc/s/08mXF