Our medical advisory panel helps to ensure our charity is communicating correct and relevant information on vascular EDS.
We are extremely grateful for their support and also their commitment towards the planning of our vascular EDS conference in May 2017.
Dr Tim Clayton is a consultant dermatologist based in Manchester. He practices at Salford Royal NHS Foundation Trust and the Royal Manchester Children’s Hospital and is fully trained in both adult and paediatric dermatology.
Dr Clayton is listed on the dermatology specialist register by the General Medical Council in London.
Dr Clayton was named in the top 100 children’s doctors in the Times, one of only three dermatologists recognised in the UK. Tim is an official spokesperson for the British Skin Foundation and has been interviewed regularly on TV and radio.
Dr Clayton is a member of the Royal College of Paediatrics and Child Health and a fellow of the Royal College of Physicians (Edinburgh). He is also a member of the British Association of Dermatologists, the European Academy of Dermatologists, the British Society for Cutaneous Allergy and an executive board member of the British Society for Paediatric Dermatology.
Dr Burrows is a Consultant Dermatologist at Addenbrooke's Hospital NHS Trust Cambridge and also an Associate Lecturer, University of Cambridge Clinical School, Cambridge.
He graduated from St Thomas's, London and trained as a dermatology registrar in London and as a senior registrar in Cambridge. Prior to taking up his consultant post Nigel spent two years at Strangeways Research Laboratories, Cambridge, investigating the molecular genetics of inherited connective tissue diseases. This work culminated in an MD. He continues to see both regional and supraregional referrals for patients with these disorders.
Following a period of clinical and genetic research into EDS with Professor Mike Pope in the mid-1990’s Dr Burrows continues to look after patients with Ehlers-Danlos syndrome. Dr Burrows is also on the medical advisory panel for EDS UK and is involved in clinical research writing several book chapters, as well as lecturing on national courses on EDS. He also runs an EDS clinic in Cambridge and has recently set up a multidisciplinary team approach for our vascular EDS patients
Dr Burrows is committed to raising the profile of EDS amongst dermatologists and other health care professionals.
Dr Sobey is a consultant dermatologist with extensive expertise and experience in medical and surgical dermatology.
Dr Sobey sees adults and children of all ages. Her practice is based in Yorkshire with consulting rooms at BMI Huddersfield Hospital and Spire Elland Hospital.
Dr Sobey also runs the EDS National Diagnostic Service and is Honorary Senior Lecturer at the University of Sheffield.
Dr Sobey is a fully qualified and accredited Consultant Dermatologist on the Specialist Register of the General Medical Council, she has published and presented many academic papers and lectures nationally and internationally.
Jessica Bowen is a genetic counsellor based at the EDS diagnostic clinic at Sheffield Children’s Hospital. Jessica provides essential counselling to give people information about genetic conditions and how they are inherited, and they work very closely with clinical geneticists.
Jessica’s role is to help a family to understand better the implications of a diagnosis of a genetic condition in a family. This includes helping the family to understand who else in the family might be at risk and how the condition is inherited. Jessic provides support to our charity with the education of vascular EDS ensuring the content and information we provide is accurate and relevant.
Judith Tocher is on our medical advisory panel to help ensure that all information regarding vascular EDS is accurately communicated by our charity.
Working closely with Judith we will soon be planning a strategy to help identify individuals affected by vascular EDS who are not currently on the national EDS database.
Judith and the team work at the UK national EDS diagnostic service which is a specialist service for individuals and families who are suspected to have complex Ehlers-Danlos Syndrome (EDS). The two branches of this service are based at The North West London Hospitals Trust and at Sheffield Children’s Hospital.
Dr Diana Johnson is a consultant clinical geneticist working with the EDS national diagnostic service and has expertise in vascular EDS.
Dr Johnson has joined our medical advisory panel to help the charity further its objective in providing education of vascular EDS to the medical profession and general public.
Rebecca is currently the Lead Scientist for the Connective Tissue Disorders Service and is a member of the
Sheffield Diagnostic Genetics Management team working with the EDS Diagnostic Service based at Sheffield Children's NHS Foundation Trust.
Rebecca joined Sheffield Diagnostic Genetic Service in January 2004 as part of the re-configuration of the Genetic Services in Sheffield. Prior to this she was a Senior Biomedical Scientist at Sheffield Teaching Hospitals.
Rebecca is an Honorary Research Associate at The University of Sheffield and a facilitator for the 'Health Challenge – Local Engagement Global Citizenship' module provided by the Faculty of Medicine, Dentistry and Health.
Rebecca is registered with the Health and Care Professions Council and is a member of the British Society for Human Genetics, the Association of Clinical Genetic Science and the South Yorkshire Institute for Innovation and Research in Child Health. She is also an assessor for the Osteogenesis Imperfecta scheme offered by the European Molecular Quality Network.