Stephanie Duguez
@sduguez_lab
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Working on #MND & #NMD and the of role muscle communication - Senior Lecturer in Stratified/Personalized Medicine @StratifiedMedicineNI @UlsterUniversity
Northern Ireland
Joined January 2015
Bill's interview with @MDUK_News. About his brother James, and his research career. @UlsterUniMed @PersonalMedNI @NI_RDP @BillDuddy
"James was always smiling and playing, even when other children tried to knock him down" Dr Duddy's brother James was diagnosed with Duchenne muscular dystrophy aged 7. He was motivated to follow a career in research after the diagnosis. Read his story: https://t.co/omgcqda0Cf
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New @CellReports paper: Efficient exon skipping by base-editor-mediated abrogation of exonic splicing enhancers.
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Fantastic talk from Dr Duguez and Dr Rene at the ALS and MND research meeting #ALS @sduguez_lab @UlsterUniMed @ARSLA75
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On Duchenne awareness week - stories from 1 in 17 impacted by rare conditions
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.@PersonalMedNI One week to our Personalised Medicine Centre 10th Anniversary Event. Really looking forward to this amazing showcase including speaker and poster sessions and guest speaker @WaterfordMafia
#10YearsOfResearchExcellence #BeMore #WeAreUU #ProudOfUU #1weektogo
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“I’m putting MND Over Matter by sharing my story. If I can help just one newly diagnosed person feel less alone, then I’ve done my job.” Jennie is a mother-of-four and a PhD student. When she was diagnosed with #MND, very few around her knew what it was. She felt really lonely.
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The @ALSMNDAlliance are looking to find out more about the experience of the global #MND #ALS community regarding fundamental rights. Have your say by taking part in the survey below ⬇
We have had 748 people living with ALS/MND and 837 caregivers give us their feedback on whether their fundamental rights are respected. Can you spread the word and see if we can get over the 1000 mark for both? The survey link is: https://t.co/2BbipvLqvS
#ALSMNDWithoutBorders
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Calling community organisations in the Northwest of Northern Ireland. Have your say on the training of new doctors in Derry-Londonderry. Check the details and contact us to participate.
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Yesterday, the skybridge on our Belfast campus was lit up for #GlobalMNDAwarenessDay. To all those battling with Motor Neurone Disease, you're not alone in this fight. Your strength and resilience inspire us all. 💙
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We had a fantastic awareness raising and fund raising event at @UlsterUni today for @mndni @Marie_MNDANI on #GlobalMNDAwarenessDay. Special thanks to @UlsterSDN, to the presenters, to everyone who attended and to all who have kindly donated to our Just-giving page @sduguez_lab
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I am pleased to facilitate the lighting of Council buildings blue to raise awareness of Motor Neurone Disease #MNDAwareness Day is celebrated globally and aims to highlight the condition Full details: https://t.co/ZcbK96f94a
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Today is Global MND Awareness Day. A dreadful illness which has been brought home to us through the recent diagnosis of a well-respected colleague. Today we host an event to raise awareness supported by @UlsterSDN @MNDA_NI @UlsterUniMed’s @sduguez_lab #WeareUU #MNDOverMatter
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Have you heard of motor neurone disease (#MND)? It’s a disease that kills a third of people within a year, and more than half within two years of diagnosis. It kills six people a day. It has no cure. On #GlobalMNDAwarenessDay, put #MNDOverMatter and help us raise awareness!
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“I put MND Over Matter by taking part in research for a future without motor neurone disease.” Dani is the fifth member of her family to have MND. She’s had over 70 lumbar punctures as part of a clinical trial to find a treatment for people with #MND. Dani is bravery
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Today is #GlobalMNDAwarenessDay & buildings across NI will be lighting up blue. Please send photos to marie@mndani.com
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Today is #MNDAwarenessDay and it's an opportunity for all of us to help to raise awareness of motor neuron disease. We've created this infographic to help educate people about MND - please share it as increasing awareness is vital 🤝 More about MND: https://t.co/OxM5kC7Ryr
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Today is World ALS Day. As a part of the International Alliance of ALS/MND Associations, ALS TDI celebrates June 21st as the Global Day of Recognition of ALS/MND. Please help share to spread awareness of ALS/MND and the work being done to end this disease. #ALSMNDWithoutBorders
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“I’m putting MND Over Matter by using my wheelchair to follow my passion for photography and help other people living with MND find accessible days out.” Ken struggled with his mental health following his diagnosis of #MND. The idea of being a full-time wheelchair user made
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Big thanks to @YvetteCooperMP for speaking with people living with and affected by #MND at our event in Parliament today! #GlobalMNDAwarenessDay.
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