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Proceeding contribution from Ann Keen (Labour) in the House of Commons on Tuesday, 17 July 2007. It occurred during Adjournment debate on Epilepsy Services.


Epilepsy Services

I thought the hon. Gentleman would be able to relate to that. Decisions, however, on the skill mix required for patient care are best made at a local level. It is for local health economies to determine how many specialist nurses they require and to prioritise the resources needed for the necessary work force development. Nevertheless, we want to ensure that local health economies are encouraged to fully utilise the skills and experience of specialist nurses. In May, the Under-Secretary of State for Health, my hon. Friend the Member for Bury, South (Mr. Lewis), held a summit with the MS Society, Epilepsy Action, the Parkinson’s Disease Society and the Royal College of Nursing to discuss those very concerns. There was an agreement to produce best practice guidance and to encourage PCTs to advocate the role of specialist nurses across the country. Having enough staff with the right skills and experience, who are well led and well supported, is of course key to implementing the national service framework for long-term conditions. The national service framework is now our key delivery mechanism for improving services for people with neurological conditions across England. The hon. Member for Romsey asked about the number of neurologists. I believe that the answer is 437. So we have areas to look at concerning the number of neurologists. However, people with neurological conditions will get a faster diagnosis, more rapid treatment and a comprehensive package of care. In addition, all people with long-term conditions will be supported so that they can live as full and independent a life as possible. Those are some ambitious plans. I am very aware of the implications of saying them; implementation is a different matter. The hon. Member for Chesham and Amersham (Mrs. Gillan) invited me to see work being done in her constituency, and I acknowledge the work that she has done and the spirit in which she made her comments. It is important that the Government and the all-party epilepsy group reflect on that matter and look at how we can work together to bring about the necessary long-term changes. Successful implementation of the national service framework is of vital importance to us. We are working with a range of key stakeholders to identify and develop practical tools and advice that can help local services and organisations to deliver the NSF. That means that services for people with neurological conditions from diagnosis to the end of life will progressively improve. My hon. Friend the Member for Calder Valley has been successful not only in securing this debate, but in bringing to it the enthusiasm that she brings to everything that she has done since she has been a Member of the House. I know that in the work that she has done through listening to witnesses for the report, she has not pushed the matter to one side. She has approached it with the commitment that she has brought to everything else since she has been a Member of the House. At this point, it is particularly important that we raise the good practice taking place already. It is easy to place too much emphasis on what is not working rather than reflecting on and celebrating what is working well. Yes, there are problems and yes, the case for improving the quality of services overall is compelling, but that should not overshadow the good work that is currently taking place. For one example of good practice, I would like to mention King’s College hospital, which is providing a comprehensive service from diagnosis to treatment. High quality care is being provided also through the community-based service in east Kent. That is an example of the direction of travel in which we want to see services going, which would embrace networks of general practitioners, with a special interest, and epilepsy nurses working in collaboration with the local neurology service. Through the national service framework, NICE guidance and the epilepsy action plan we have set out very clearly what the expectations are for the pattern of services for people with epilepsy. We have mentioned, in this debate, the services to prisoners and those in our prison care service. Much work has to be done, and I give another commitment to work with colleagues in the Ministry of Justice to ensure that that takes place. I might not have managed to answer other questions, in particular those concerning new light bulbs and the Olympic logo, but they are serious issues. It is important that we really assist those with neurological symptoms and problems, under a diagnosis of epilepsy, and that they are seriously catered for, as they would be if they had any other condition causing alarm to them and their families.


Secondary information

Type
Proceeding contribution
Reference
463 c40-2WH 
Session
2006-07
Chamber / Committee
Westminster Hall
Subjects
Health services Diseases Epilepsy NHS
Link
View this Proceeding contribution on www.publications.parliament.uk