Steering Committee

About the Steering Committee

The committee is responsible for reviewing all requests for data from the registry. This is intended to be a streamlined and rapid procedure in order not to delay approval.

 

Members

Chiara Marini-BettoloDr Chiara Marini-Bettolo

Principal Investigator & Steering Committee Chair

The John Walton Muscular Dystrophy Research Centre, Newcastle

Dr Marini-Bettolo completed her medical degree and training in Neurology at the University of Rome Sapienza, and has always had a special interest in neuromuscular disorders. During her training in Neurology she was awarded with a Scientific Fellowship by the European Federation of Neurological Societies which gave her the opportunity to join the Neuromuscular team at Imperial College London, working on a lab-based project on inflammatory myopathies. In 2015 she completed her PhD in neuromuscular disorders at Imperial College London. Since joining the John Walton Muscular Dystrophy Centre at Newcastle University, Chiara has been leading the Clinical Team and the Highly Specialised Service for Limb-girdle muscular dystrophies (LGMDs). She runs adult and paediatric neuromuscular clinics, and more recently has led the implementation of a novel treatment currently available under various access schemes in Newcastle.

Jassi SodhiJassi Sodhi

Steering Committee Vice-Chair

The John Walton Muscular Dystrophy Research Centre, Newcastle

Jassi is a Neuromuscular Research Physiotherapist and has worked at the John Walton Muscular Dystrophy Research Centre, at Newcastle University, since March 2017. Jassi currently works with both paediatric and adult patients with myotonic dystrophy which has provided him with a comprehensive understanding of their health and social care needs. Clinically, he has updated both clinical assessment and referral pathways for the cohort of DM1 and DM2 patients. From a research perspective, he has been involved in year 2 and 3 of the PHENO-DM1 natural history study and will be a clinical evaluator for a forthcoming CTIMPS study in Newcastle. 

Chris TurnerDr Chris Turner

National Hospital for Neurology and Neurosurgery, London

Chris Turner has been working as a consultant at the MRC Centre for Neuromuscular Disease, Queen Square and UCLH since 2007. He has a specialist interest in muscle disease and runs a twice monthly Myotonic Dystrophy clinic at Queen Square.

 

Kate AdcockKate Adcock

Muscular Dystrophy UK

Kate became Director of Research and Innovation Muscular Dystrophy UK in 2018. She works with Trustees, clinicians, researchers and – most importantly – MDUK’s supporters to deliver research that is meaningful to patients living with neuromuscular conditions. There are over 110,000 adults and children living with over 60 different types of neuromuscular conditions the UK. These are rare and very-rare conditions many of which have no treatment, although several advanced therapies are coming through the pipeline for a number of them.

Kate has over 15 years’ experience of research funding and strategy through senior roles at the Medical Research Council, Wellcome Trust and latterly, MDUK. Kate has a PhD in Neuroscience from the University of Cambridge. She worked as a post-doctoral assistant at the University of Basel and in the Department of Diagnostic Imaging at the University Children’s Hospital in Zurich before taking up a post at Wellcome in 2005.

 

Emma-Jayne AshleyEmma-Jayne Ashley

Cure Myotonic Dystrophy UK Charity

Emma-Jayne Ashley is co-founder of Cure Myotonic Dystrophy UK Charity. She became involved with all things DM after her son Dregan was diagnosed with paternally inherited Congenital Myotonic Dystrophy, giving her a personal insight into the day-to-day challenges which are faced by the community. The delay in diagnosis, and the years of difficulty leading up to it, instigated a dedication to help others and improve diagnosis and widespread understanding of the condition. Cure DM is committed to raising awareness, facilitating research and supporting families affected by DM, particularly those with congenital and childhood onset.

 

Michael WalkerMichael Walker

Myotonic Dystrophy Support Group (MDSG)
 

Michael has worked with the Myotonic Dystrophy Support Group for over 20 year, since one of his twin boys, Nathan, was diagnosed at birth with Congenital Myotonic Dystrophy, and his wife Sharon was also found to have the faulty gene, with adult onset.

 

 

Mark HamiltonDr Mark Hamilton

West of Scotland Clinical Genetics Service, Glasgow

Mark is a newly appointed Consultant in Clinical Genetics with the West of Scotland Genetics Service. He has a longstanding interest in myotonic dystrophy, having recently completed a clinical PhD research project exploring central nervous system effects of the condition. In his current role, Mark supervises the delivery of the DM1 management clinic for the West of Scotland and sits on the subgroup committee of the Scottish Muscle Network responsible for producing and auditing evidence-based national guidelines for DM1.

 

Channa HewamaddumaDr Channa Hewamadduma

Sheffield Teaching Hospitals Foundation Trust, Sheffield

Channa currently works as a Consultant Neurologist with specialist interests in neuromuscular disorders (NMD) and motor neurone disease (MND) at the Sheffield Teaching Hospitals Foundation Trust. He is passionate about improving care for the DM1 cohort which is the largest group of adult muscular dystrophies. In his current work he manages over 120 DM1 patients with a large neuromuscular team. Channa has also conducted a large audit in the regional cohort of 114 DM1 patients he works with in line with published care recommendations and is conducting research into assessing fatigue and quality of life in DM1 patients and other neurodegenerative conditions.

 

Darren MoncktonProf Darren Monckton

Institute of Molecular Cell and Systems Biology, University of Glasgow, Glasgow

Darren Monckton is Professor of Human Genetics and Director of the University of Glasgow’s Wellcome Trust four-year PhD programme. His research group is investigating the basis of genetic instability in disorders such as Myotonic Dystrophy and Huntington disease, with the aim of providing improved diagnostics, treatments and cures. He has published numerous scientific papers and book chapters, and has presented his research in many invited seminars and lectures and is also a Scientific Advisor to the Myotonic Dystrophy Support Group (UK) and the Myotonic Dystrophy Foundation (USA).