🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

A great opportunity to engage in the discussion about the use of WGS for newborn screening in the NHS Genomic Medicine Service

Join experts at #iDR24 discussing the present and future of #DrugRepurposing, including: 👉Getting repurposed drugs to patients 👉The challenge of translation 👉The LoDoCo case 👉Challenges & opportunities Learn more & book tickets here: remedi4all.org/international-…

Meet the rare disease path speakers at #iDR24! 🗣️ Tim will discuss his experience searching for a repurposing candidate through to the closing stages of a clinical trial, without support from pharma. Find out more: ow.ly/r3CO50QHTsh

‘Survival capitalism’ and the Big Bang doi.org/10.7765/978152… My book, 'Survival capitalism' and the Big Bang is now published with Manchester University Press. New insights into #Thatcherism and the 1980s financial revolution. Fascinating oral histories with government and City insiders.

#RareDiseaseDay #unibirm_MDS Wolfram Syndrome UK Birmingham Health Partners #IcgsUob BWC NHS Trust Birmingham making a real-world impact on rare diseases, with a multi-facility infrastructure for research to help find new treatments for PLWRC healthawareness.co.uk/rare-diseases/…

Our #RareDiseases24 campaign is here 🧫🔬 Grab your copy in today's The Guardian and online at bitly.ws/3ecCm featuring Nick Meade with Genetic Alliance UK #RareDiseaseDay #geneticresearch #healthcare

AS Global Conference Films and Graphics are out NOW! We hope you all enjoyed the AS Global Conference in January as much as we did. Don't worry if you missed any of the sessions, as you can now find them all on the website. #AlstromSyndrome alstrom.org.uk/as-global/#ASG…

#REMEDi4ALL Drug repurposing conference building an international multidisciplinary community

#REMEDi4ALL Helpful talk from Catriona Crombie of LifeArc about upcoming research funding opportunities for translational research, and repurposing toolkit-LifeArc - available via their website

On #IWD we celebrate our Institute Director Pam Kearns. Her extensive research into children’s #cancer research & fundraising activities have been praised by Little Princess Trust Birmingham Cancer Research UK Clinical Trials Unit @unibirm_MDS rb.gy/ds2wo0

How do we improve outcomes for children & young people from Black and ethnic minority backgrounds? Session led by ⁦⁦Barnardo’s⁩ with their young ambassadors and ⁦NHS Race & Health Observatory. #KFTimeForAction

Just heard Dr Lauren M Quinn present at #DUKPC on elsadiabetes, a project #screening children for #Type1Diabetes which is co-funded by @JDRFUK and Diabetes UK Research 🤝💙 Learn more and sign up: jdrf.org.uk/research_proje…

#DUKPC great talk by Dr Jess Wheeler highlighting inequalities in diabetes outcomes for children of different heritage

Really helpful aide memoir when talking with children with diabetes from diverse populations - thanks May! Prof May Ng OBE 吳 诗 梅 #DUKPC

LifeArc CEO Stephane Maikovsky announces launch of Rare Disease Translational Research Centres, including consortium Uni Birmingham, Belfast and Newcastle to speed up delivery of clinical trials LifeArc @unibirm_MDS Cancer and Genomic Sciences Genetic Alliance UK

Thankyou Jenny Prigg and all rare disease team at UoB and our partner hospitals BWC NHS Trust University Hospitals Birmingham Birmingham Health Partners and patient support groups Alström Syndrome UK Wolfram Syndrome UK Bardet-Biedl Syndrome UK (BBS UK) this award will be a step change for West Midlands rare disease translational research

Today is World #AlströmSyndrome Day! Celebrate the Birthday of Carl Henry Alström who first discovered the Syndrome. Why not donate to one of the rarest conditions in the world, and help support families with this complex condition. justgiving.com/alstromsyndrom…

Imagine getting life-saving drugs to sick people without relying on big pharma? We may have found a way theguardian.com/commentisfree/…

Rare Disease Research U.K. brings together rare disease researchers- rd-research.org.U.K. And first newsletter

#WHFEvents Westminster Health Forum on rare diseases great presentation by Prof Santosh Kings College London addressing mental health problems in rare diseases