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Alumni Angles: In conversation with Professor Sir Andrew Pollard

Queen Mary University of London Perrin Lecture Theatre, Blizard Building, Faculty of Medicine & Dentistry, 4 Newark Street, London, United Kingdom

Join QMUL for a special in conversation event with vaccine expert and alumnus Professor Sir Andrew Pollard (Medicine MBBS, 1989), who leads the team behind the Oxford-AstraZeneca vaccine for COVID-19. You will also hear from the Principal, Professor Colin Bailey CBE, Professor Sir Mark Caulfield, Vice-Principal (Health), and our chair, Dr Vanessa Apea, Consultant Physician […]

Not All Genes are Equal (Pint of Science)

Espresso Library 210 East Road, Cambridge, Cambridgeshire, United Kingdom

Every person has two copies of each gene, one inherited from each parent. Most genes are the same in all people, but a small number of them are slightly different. These tiny differences contribute to each person’s unique physical features. Let’s explore rare imprinted genes, a special class where one parental copy is switched off,  […]

Curing with Kindness: Rare Childhood Brain Tumours (Pint of Science)

Espresso Library 210 East Road, Cambridge, Cambridgeshire, United Kingdom

Researchers developing new treatments for children with rare brain tumours know that it’s not a case of treating children like tiny adults and that surviving the disease isn’t enough. Reducing the damage done by treatments is just as important to the survivor. Discover how researchers are minimising damage and why they think studying rare children’s […]

Online workshop: Understanding access and reimbursement

ONLINE

Getting wider access to drugs for as many patients a possible is a clear priority in the drug development process, especially for patient groups who are working to secure research into and treatments for their rare conditions. However, understanding how to secure access to newly developed treatments is an often-neglected challenge. The processes involved in […]

Understanding Rare Disease: Communicating with Patients

Sign up to learn about the role of communication in rare disease from those affected directly, in an interactive FREE virtual event! About this event The event will kick off with a session from our guest speaker, who will explore the value of effective and sensitive communication skills when it comes to handling complex conditions, […]

The genetics of intellectual disability: Episode 15

LIVE STREAM

This webinar is part of the popular Genetics of webinar series and will provide an interesting update on the genetic origins of intellectual disability, as well as explore what challenges remain in this area.  Our speakers will explore what research is required after a genetic diagnosis of intellectual disability and what families would value the most from the […]

Hypermobility syndrome: A practical guide to assessment, management and care

Royal Society of Medicine 1 Wimpole Street, London, United Kingdom

Join the RSM at this multidisciplinary event which will provide a valuable overview and a broader understanding of hypermobility syndrome and the care of these patients. Experts in their field will present a series of talks that will inform delegates about practical guides for the assessment and management of this condition and will explore how […]

11th European Conference on Rare Disease & Orphan Products (ECRD)

ONLINE

The European Conference on Rare Diseases & Orphan Products (ECRD) is recognised globally as the largest, patient-led rare disease event in which collaborative dialogue, learning and conversation takes place, forming the groundwork to shape goal-driven rare disease policies and allow for important and innovative discussions on a national and an international level to take place. ECRD 2022 will take […]

Facing up to the genomic gap: Tackling equality and diversity in genomics on

LIVE STREAM

This webinar is part of the popular Genetics of webinar series and will discuss the challenge of equality and diversity in genomic research and clinical settings and strategies to address this.  Genomic research has traditionally been focused on caucasian populations, which leads to inherent biases in genomic findings translated into clinical research. Underrepresentation of other populations in […]

Showcase of Genomics across North Thames

UCL Gower Street, London, United Kingdom

Join the North Thames Genomic Medicine Service showcase to find out how genomic medicine is transforming healthcare in their region. Genomic medicine is coming into every-day-practice for multi-disciplinary healthcare professionals across the NHS, improving how we diagnose and treat patients of all ages with cancer and rare or inherited diseases. In North London, Essex and […]