Well done Neil Bradley for riding 400km to Amsterdam in aid of Muscular Dystrophy UK!

Muscular Dystrophy UK BGC Charity Day so excited about Wednesday KIRSTY GALLACHER is coming too.....

I am a very excited girl looking forward to representing Muscular Dystrophy UK at BGC Charity Day Really looking forward to a repeat office floor football re-match with Sam Alladyce inbetween trading. I'm not sure if he knows my skills have improved since I started powerchair football ⚽⚽⚽

I am so looking forward to seeing this legend Monty Panesar representing Muscular Dystrophy UK at#BGCCharityDay

Looking forward to attending the BGC Charity Day on behalf of Muscular Dystrophy UK always great fun getting money from the BIG players for a great cause! Xxxx

Proud to be here BGC Charity Day Muscular Dystrophy UK

I think we did all right, didn’t we?Muscular Dystrophy UK BGC Charity Day

Thank you Hayley Lloyd for speaking so honestly about what it means having a child diagnosed with #musculardystrophy. We will not stop fighting. A whooping amount raised at the #MicroscopeBall in aid of Muscular Dystrophy UK

Last night Muscular Dystrophy UK was at Puccini’s Restaurant. Its owner Michele Pucci is a true philanthropist. Thank you for organising another great fundraiser, a room full of famous faces, football legends and genuine generosity. To date Michele raised over £100K for the charity.

Today, breakfast really is the most important meal of the day. Exciting to share knowledge and inspiration with colleagues across the sector and help our charities, day after day and pound after pound #BreakfastClub #EveryDayCounts

“I try to keep positive and live for the present”. Hayley talks about how important emotional support is for parents like her and young people like her son Tommy, who has #LGMD. Read her story here >> bit.ly/2WOzHip #WorldMentalHealthDay #EveryDayCounts

I woke up with major #FOMO on #MDUKConf19 so I visited my local @SOHO_Coffee_Co where Lucenea welcomed me with a delicious chocolate and cherry muffin with 20p going to Muscular Dystrophy UK. Now off to follow the conference on Facebook Live!

Live from our corporate partners chapmanbdsp office. This is how you #BakeADifference . £400 raised and counting!

This kid and his mum ❤️

What a great Christmas party celebrating our business and our people! We also raised more money for our charity of the year Muscular Dystrophy UK taking us to a total of £14,000 for this great cause! Thank you to everyone who donated 🎄🎉 #christmasparty #charity #chapmanbdsp

Breaking News: VYONDYS 53™, Sarepta Therapeutics’s exon skipping drug has been approved by the U.S. FDA. The drug could be a potential treatment for about 8% of people with #Duchenne. Read more >> bit.ly/2BmYBwX

Thank you DLA Piper for having me today to talk about Muscular Dystrophy UK and thanks to Jen for sharing her story of living with the condition. I didn’t tell her so (I should have done) but today she is my hero #musclesmatter

Undoubtably the fun and rewarding bit of the job, collecting big generous cheques from long terms partners. Thank you Redevco since 2002 supporting Muscular Dystrophy UK

We’re excited to be at BT today for their #BeyondDisability event with @emma_vogelmann and @NuraMDUK

Huge thanks to the- visionary Garfield Weston Foundation for donating £5 million to our UCL Queen Square Institute of Neurology new world-leading neuroscience centre building | UC⁦UCL Brain Sciences⁩ ⁦UCL Queen Square Institute of Neurology⁩ ⁦UCLH⁩ ⁦Medical Research Council⁩ ucl.ac.uk/campaign/news/…