Emma DG
@e_grintYoga, art, travel, photography, spoken word & political debate. All views are my own.
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The contempt in which Britain's elite holds the public has never been more eloquently expressed than in the decision to award Tony Blair the highest order of knighthood. One million Iraqis dead, three million dispossessed, a trail of blood to 7/7. Rise Sir Tony!
Hard to tell if I recorded this 30 years or 10 minutes ago...
What a team, championing the rights of everyone with rare, genetic and undiagnosed conditions ❤️👏🏼
Thank you to everyone who took part in #RareDiseaseDay at Westminster, we had a great event! - from the @GeneticAll_UK team. #raredisease #rarereality
I can’t even...😂😂😂
this dog literally failed every single test thrown at him to become a service dog and i am scream laughing. but imho he’s still a very very good boy.
Unbelievable array of short films, truly inspiring. Cast your vote peoples! #RareDiseaseDay @rarediseaseuk #rarefilmfestival
People's Choice Award - Rare Disease UK - time to cast your votes! #rarefilmfestival #RareDiseaseDay raredisease.org.uk/rarefilmfestiv…
So sad to be missing the #rarefilmfestival tonight! Wishing all my colleagues and guests a wonderful evening as they shine a light on living with #raredisease
Right or left, I think we can we all agree, nobody needs or indeed asked for Tony Blair’s opinion on anything. Thanks pal, a decade was quite enough. #GeneralElection2019 #pipedownsir apple.news/AnOBzTdCYRpC-p…
Just my girl doing her funnies x
People's Choice Award - Rare Disease UK - time to cast your votes! #rarefilmfestival #RareDiseaseDay raredisease.org.uk/rarefilmfestiv…
Nothing like being woken up by a pneumatic drill in the road at 8am on a Sunday @Ameyplc when you're not supposed to start anything until at least 9am. When the workman are challenged, I'm told 'it's tough'. Good work! 👆🏼🤦♀️ Great service to the community. Thanks so much.
#RareDiseaseDay activity...why not test your #RareDisease knowledge and share to help illuminate the #RareReality buzzfeed.com/geneticallianc…
A powerful tribute to a wonderful woman in the field of #genetics #TSC theguardian.com/science/2019/f…
Organising events, suporting national health campaigns, getting stuck in to dynamic comms and developing training sessions and workshops...come work with us @GeneticAll_UK #CharityJobs #RareDisease #vacancies #patients #Genetics #thirdsector jobs.thirdsector.co.uk/job/439332/mem…
Please help support Illuminate the #RareReality, add a #Twibbon now! twibbon.com/support/illumi…
"This report helps to show the systemic failings in our decision-making systems for access to rare disease treatments" @GeneticAll_UK CEO @Jayne451 68 funded rare disease treatments in England vs 133 in German. #RareDisease #Genetics #RareReality pmlive.com/pharma_news/in…
Exciting opportunity to join us @GeneticAll_UK in a creative and central role, engaging and informing our membership. #charityjobs #charity geneticalliance.org.uk/news-event/we-…
"If it wasn't for them we'd all be speaking German now" is how I describe my school's exceptionally bad languages department
I’m supporting Rare Disease UK by sharing my rare disease experience, to offer comfort and hope to other patients and their families. Read my story and add your star for Rare Disease Day. #RareDiseaseDay #RareReality rarereality.raredisease.org.uk/star/33
Head over to our FB Live feed to join the discussion on genomics. #GAUKConf
Next up is @gm_jill - don’t forget to join us on Facebook live if you were unable to attend #GAUKConf m.facebook.com/GeneticAllianc…
So proud of the team I work with...I hope you're bringing home some glassware for the office 😍
We are so excited to be at the #TSAwards tonight! We’re up for Communications Team of the Year - fingers crossed! #raredisease #genetic #undiagnosed
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