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100,000 Genomes Project: in conversation with Tess Lopez
For Jul/Aug 2021, ENT & Audiology News features several contributions from the 100,000 Genomes Project, and Tess Lopez very kindly agreed to talk to me about her involvement with the project, as well as sharing her personal experiences of having...Vulnerability in audiological care: insights from Brené Brown and Kristin Neff
Embracing emotional openness and self-compassion can improve outcomes and relationships in the often-overlooked emotional landscape of audiological care. Audiological care is a deeply personal and often emotional journey for individuals experiencing hearing loss or other auditory challenges. Beyond the clinical...Congenital cytomegalovirus causing deafness in children: an update
Congenital CMV is the leading non-genetic cause of sensorineural hearing loss in children. Keith Trimble draws our attention to this and gives a comprehensive guide on diagnosis and treatment. Congenital cytomegalovirus (cCMV) infection is common, affecting 1% of all newborns,...Developing ENT and audiology services in Southern Africa (Part 2)
In the last issue of ENT & Audiology News, we heard from retired Professor Christopher Prescott on the challenges faced and progress made made locally to address the inequity and inequality of access to ENT and allied health professional services...Getting the message right on hearing loss and dementia
Are we reaching a consensus on how hearing professionals should talk about hearing loss and dementia? In 2024, the British Society of Audiology (BSA), in collaboration with the British Academy of Audiology (BAA) and the British Society of Hearing Aid...Wilde and the foundations of medical epidemiology
William Wilde (father of Oscar) was renowned as an otologist, but less well known for his work in epidemiology. The bedrock of the modern discipline of public health is good data collection, and we hear from our good friend, Ray...Genetic foundations of Ménière’s disease: changing the game
Sydney researchers reveal genetic roots of Ménière’s disease. Familial patterns and gene discoveries highlight autosomal inheritance in rare cases, transforming molecular insights. Ménière’s disease (MD) is a chronic disorder of the inner ear defined by clinical criteria of episodic vertigo...EVOTION: Big data supporting public health policies for hearing loss
Big Data? Biosensors, smart hearing aids and smartphones? The EVOTION Project has it all and more! What will this project tell us about the future of hearing management? Doris-Eva Bamiou, Giorgos Dritsakis and Louisa Murdin, members of the EVOTION team,...Big data and the future of cochlear implant aftercare
With a million people using cochlear implants worldwide, the time is right for us to harness this vast data for patient benefit. Every day, cochlear implant (CI) processors quietly collect data: how long they’re worn, how often users switch programs...In conversation with Paul Lamb
Paul Lamb recently joined a team undertaking a hearing care mission to Armenia with the Starkey Hearing Foundation. Paul took time to discuss the aims and achievements of these missions through his personal experiences with the foundation. Paul Lamb. The...Prof Tanon of the Côte d’Ivoire and Stephanie Unterrieder of MED-EL: challenges and successes of a public-private partnership
The Côte d’Ivoire (RCI) is a large country on the West African coast. It has recently launched a pioneering neonatal hearing screening programme. Dr Cheka Spencer caught up with Prof Marie-Josée Tanon to discuss this and other recent developments which...
