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  • Lord Hylton – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    Lord Hylton – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    The below Parliamentary question was asked by Lord Hylton on 2016-02-22.

    To ask Her Majesty’s Government what representations they have made to the government of France about their plans for the refugee camp at Calais, known as The Jungle; in particular (1) whether the site will be forcibly reduced to 500 women and children in the Jules Ferry Centre, and 1500 others in container units; (2) what facilities for cooking and education there will be for the latter; and (3) what is to happen to current residents who are not willing to move to the semi-permanent units or to go to centres d’accueil.

    Baroness Anelay of St Johns

    The management of the migrant camp in Calais is the responsibility of the French government. The French authorities plan to reduce the size of the Calais camp and improve humanitarian conditions, and are encouraging migrants to move into the heated containers or to one of the reflection centres (centres d’accueil) across France. We do not have details of how many people will remain at the site nor further information of the facilities in the camp. We have however cooperated closely with the French in their efforts to improve conditions in Calais by: providing support and facilities elsewhere in the country; carrying out joint visits to the camps to inform migrants about their rights and responsibilities; putting in place a joint programme to identify the most vulnerable migrants and moving them to a place of safety; increasing the number of places in the French asylum system and encouraging those in Calais to claim asylum. Migration issues were discussed at the UK-France Summit on 3 March. The summit communiqué provides details of the further cooperation agreed.

  • Lord Hylton – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    Lord Hylton – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    The below Parliamentary question was asked by Lord Hylton on 2016-02-22.

    To ask Her Majesty’s Government whether they are discussing unemployment in Kasserine and other parts of Tunisia with the government of that country; and whether any steps are being taken to mobilise investment from the Arab Partnership Fund and other institutions to improve employment rates in those areas.

    Baroness Anelay of St Johns

    We have regular dialogue with the Tunisian government on a range of issues, including their economic development, particularly in marginalised areas like Kasserine.

    UK support to Tunisia has doubled in the last year to nearly £6 million, and we will continue this high level of support in the next financial year. Since 2011, working with international partners and using funds including the Arab Partnership, Arab Partnership Economic Facility and Conflict Security and Stability Fund, the UK has supported private sector development, vocational training, job creation, economic governance and transparency, including in marginalised areas. Partners such as Germany, the US, France, the EU, the European Reconstruction and Development Bank, the World Bank and the European Investment Bank are also involved in similar initiatives. It is also important that the Tunisian government sets out and implements its vision for economic and social development. This will help ensure that international support is sustainable.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Foreign and Commonwealth Office

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government whether they plan to hold an event on their Preventing Sexual Violence in Conflict Initiative at the sixth session of the Commission on the Status of Women in March.

    Baroness Anelay of St Johns

    At the current time, four UK Ministers (from the Department for International Development, the Ministry of Defence and the Department for Education) are planning to attend the Commission on the Status of Women (CSW) and promote UK objectives. The UK is not planning to host a specific event on the Preventing Sexual Violence in Conflict Initiative (PSVI) during the CSW. Ministers will be actively participating in the Review Theme and a number of side events focussed on tackling all forms of violence against women and girls, including sexual violence. As the Prime Minister’s Special Representative on Sexual Violence in Conflict, I am actively exploring future opportunities to engage with UN partners in 2016 to promote PSVI objectives on tackling stigma, supporting survivors and increasing accountability.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government what steps they are taking to increase public awareness and understanding of autism.

    Lord Prior of Brampton

    The number of children, young people and adults diagnosed with autism by the National Health Service is not collected centrally. Latest figures from the School Census (2015) state that there were 90,775 pupils with an autistic spectrum disorder at state funded schools and non-maintained special schools in England. This has increased from a total of 56,250 in 2010 who were recorded as having a primary need of autism, but it is not directly comparable to the 2015 figures because of a change in collection methodology. Local authority areas provide information for Public Health England’s annual self-assessment exercise on implementing the Autism Strategy. This includes the number of adults receiving an autism diagnosis but because information is submitted on a voluntary basis a complete total for England is not available.

    The Department has discussed with NHS England the difficulties that people on the autistic spectrum can have in getting an appropriate diagnosis and support in a timely manner. NHS England has commenced a programme to visit clinical commissioning groups to identify and share good practice in accessing autism diagnosis, and look at possible barriers. The Department is funding the Association of Directors of Adult Social Services to support this work. NHS England will complete a report on this by the end of April 2016.

    The Department is also encouraging the autism third sector to work together and the four charity representatives on the Cross Government Autism Programme Board, which oversees the implementation of the Autism Strategy, gave presentations at the meeting on 18 February on work they are doing to increase public awareness. The charities are the National Autistic Society, the Autism Alliance UK, Autism Plus and Ambitious about Autism. The Autism Alliance UK is also being funded by the Department to undertake work with national and local organisations, to make reasonable adjustments to services and to train staff to be aware of what autism can mean to individuals who have the condition and their families.

    The Health and Social Care Information Centre’s publication Estimating the Prevalence of Autism Spectrum Conditions in Adults – Extending the 2007 Adult Psychiatric Morbidity Survey (APMS) gave the overall prevalence of autism in England as 1.1% (95% confidence interval 0.3% to 1.9%). Among adults with learning disabilities living in private households whose learning disability was sufficiently severe that they could not have taken part in the 2007 APMS, the prevalence of autism was 35.4% (95% confidence interval 24.7% to 46.2%). Among adults with mild or severe learning disabilities living in communal care establishments, the prevalence of autism was 31% (95% confidence interval 23.9% to 38%). Detailed supporting information regarding the underlying data and how figures have been derived is found within the detail of the report, a copy of which is attached.

    The APMS was repeated in 2014 and findings are scheduled to be published in September 2016.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government what steps they are taking to reduce waiting times for autism diagnosis.

    Lord Prior of Brampton

    The number of children, young people and adults diagnosed with autism by the National Health Service is not collected centrally. Latest figures from the School Census (2015) state that there were 90,775 pupils with an autistic spectrum disorder at state funded schools and non-maintained special schools in England. This has increased from a total of 56,250 in 2010 who were recorded as having a primary need of autism, but it is not directly comparable to the 2015 figures because of a change in collection methodology. Local authority areas provide information for Public Health England’s annual self-assessment exercise on implementing the Autism Strategy. This includes the number of adults receiving an autism diagnosis but because information is submitted on a voluntary basis a complete total for England is not available.

    The Department has discussed with NHS England the difficulties that people on the autistic spectrum can have in getting an appropriate diagnosis and support in a timely manner. NHS England has commenced a programme to visit clinical commissioning groups to identify and share good practice in accessing autism diagnosis, and look at possible barriers. The Department is funding the Association of Directors of Adult Social Services to support this work. NHS England will complete a report on this by the end of April 2016.

    The Department is also encouraging the autism third sector to work together and the four charity representatives on the Cross Government Autism Programme Board, which oversees the implementation of the Autism Strategy, gave presentations at the meeting on 18 February on work they are doing to increase public awareness. The charities are the National Autistic Society, the Autism Alliance UK, Autism Plus and Ambitious about Autism. The Autism Alliance UK is also being funded by the Department to undertake work with national and local organisations, to make reasonable adjustments to services and to train staff to be aware of what autism can mean to individuals who have the condition and their families.

    The Health and Social Care Information Centre’s publication Estimating the Prevalence of Autism Spectrum Conditions in Adults – Extending the 2007 Adult Psychiatric Morbidity Survey (APMS) gave the overall prevalence of autism in England as 1.1% (95% confidence interval 0.3% to 1.9%). Among adults with learning disabilities living in private households whose learning disability was sufficiently severe that they could not have taken part in the 2007 APMS, the prevalence of autism was 35.4% (95% confidence interval 24.7% to 46.2%). Among adults with mild or severe learning disabilities living in communal care establishments, the prevalence of autism was 31% (95% confidence interval 23.9% to 38%). Detailed supporting information regarding the underlying data and how figures have been derived is found within the detail of the report, a copy of which is attached.

    The APMS was repeated in 2014 and findings are scheduled to be published in September 2016.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government what assessment they have made of the proportion of people with autism who have a learning disability.

    Lord Prior of Brampton

    The number of children, young people and adults diagnosed with autism by the National Health Service is not collected centrally. Latest figures from the School Census (2015) state that there were 90,775 pupils with an autistic spectrum disorder at state funded schools and non-maintained special schools in England. This has increased from a total of 56,250 in 2010 who were recorded as having a primary need of autism, but it is not directly comparable to the 2015 figures because of a change in collection methodology. Local authority areas provide information for Public Health England’s annual self-assessment exercise on implementing the Autism Strategy. This includes the number of adults receiving an autism diagnosis but because information is submitted on a voluntary basis a complete total for England is not available.

    The Department has discussed with NHS England the difficulties that people on the autistic spectrum can have in getting an appropriate diagnosis and support in a timely manner. NHS England has commenced a programme to visit clinical commissioning groups to identify and share good practice in accessing autism diagnosis, and look at possible barriers. The Department is funding the Association of Directors of Adult Social Services to support this work. NHS England will complete a report on this by the end of April 2016.

    The Department is also encouraging the autism third sector to work together and the four charity representatives on the Cross Government Autism Programme Board, which oversees the implementation of the Autism Strategy, gave presentations at the meeting on 18 February on work they are doing to increase public awareness. The charities are the National Autistic Society, the Autism Alliance UK, Autism Plus and Ambitious about Autism. The Autism Alliance UK is also being funded by the Department to undertake work with national and local organisations, to make reasonable adjustments to services and to train staff to be aware of what autism can mean to individuals who have the condition and their families.

    The Health and Social Care Information Centre’s publication Estimating the Prevalence of Autism Spectrum Conditions in Adults – Extending the 2007 Adult Psychiatric Morbidity Survey (APMS) gave the overall prevalence of autism in England as 1.1% (95% confidence interval 0.3% to 1.9%). Among adults with learning disabilities living in private households whose learning disability was sufficiently severe that they could not have taken part in the 2007 APMS, the prevalence of autism was 35.4% (95% confidence interval 24.7% to 46.2%). Among adults with mild or severe learning disabilities living in communal care establishments, the prevalence of autism was 31% (95% confidence interval 23.9% to 38%). Detailed supporting information regarding the underlying data and how figures have been derived is found within the detail of the report, a copy of which is attached.

    The APMS was repeated in 2014 and findings are scheduled to be published in September 2016.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government what assessment they have made of long-term trends in the prevalence of autism in the UK.

    Lord Prior of Brampton

    The number of children, young people and adults diagnosed with autism by the National Health Service is not collected centrally. Latest figures from the School Census (2015) state that there were 90,775 pupils with an autistic spectrum disorder at state funded schools and non-maintained special schools in England. This has increased from a total of 56,250 in 2010 who were recorded as having a primary need of autism, but it is not directly comparable to the 2015 figures because of a change in collection methodology. Local authority areas provide information for Public Health England’s annual self-assessment exercise on implementing the Autism Strategy. This includes the number of adults receiving an autism diagnosis but because information is submitted on a voluntary basis a complete total for England is not available.

    The Department has discussed with NHS England the difficulties that people on the autistic spectrum can have in getting an appropriate diagnosis and support in a timely manner. NHS England has commenced a programme to visit clinical commissioning groups to identify and share good practice in accessing autism diagnosis, and look at possible barriers. The Department is funding the Association of Directors of Adult Social Services to support this work. NHS England will complete a report on this by the end of April 2016.

    The Department is also encouraging the autism third sector to work together and the four charity representatives on the Cross Government Autism Programme Board, which oversees the implementation of the Autism Strategy, gave presentations at the meeting on 18 February on work they are doing to increase public awareness. The charities are the National Autistic Society, the Autism Alliance UK, Autism Plus and Ambitious about Autism. The Autism Alliance UK is also being funded by the Department to undertake work with national and local organisations, to make reasonable adjustments to services and to train staff to be aware of what autism can mean to individuals who have the condition and their families.

    The Health and Social Care Information Centre’s publication Estimating the Prevalence of Autism Spectrum Conditions in Adults – Extending the 2007 Adult Psychiatric Morbidity Survey (APMS) gave the overall prevalence of autism in England as 1.1% (95% confidence interval 0.3% to 1.9%). Among adults with learning disabilities living in private households whose learning disability was sufficiently severe that they could not have taken part in the 2007 APMS, the prevalence of autism was 35.4% (95% confidence interval 24.7% to 46.2%). Among adults with mild or severe learning disabilities living in communal care establishments, the prevalence of autism was 31% (95% confidence interval 23.9% to 38%). Detailed supporting information regarding the underlying data and how figures have been derived is found within the detail of the report, a copy of which is attached.

    The APMS was repeated in 2014 and findings are scheduled to be published in September 2016.

  • Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    Baroness Hodgson of Abinger – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Baroness Hodgson of Abinger on 2016-02-22.

    To ask Her Majesty’s Government how many (1) children under 9 years of age, (2) children aged between 9 and 16 inclusive, and (3) adults over 18, have been diagnosed with autism in each of the last five years.

    Lord Prior of Brampton

    The number of children, young people and adults diagnosed with autism by the National Health Service is not collected centrally. Latest figures from the School Census (2015) state that there were 90,775 pupils with an autistic spectrum disorder at state funded schools and non-maintained special schools in England. This has increased from a total of 56,250 in 2010 who were recorded as having a primary need of autism, but it is not directly comparable to the 2015 figures because of a change in collection methodology. Local authority areas provide information for Public Health England’s annual self-assessment exercise on implementing the Autism Strategy. This includes the number of adults receiving an autism diagnosis but because information is submitted on a voluntary basis a complete total for England is not available.

    The Department has discussed with NHS England the difficulties that people on the autistic spectrum can have in getting an appropriate diagnosis and support in a timely manner. NHS England has commenced a programme to visit clinical commissioning groups to identify and share good practice in accessing autism diagnosis, and look at possible barriers. The Department is funding the Association of Directors of Adult Social Services to support this work. NHS England will complete a report on this by the end of April 2016.

    The Department is also encouraging the autism third sector to work together and the four charity representatives on the Cross Government Autism Programme Board, which oversees the implementation of the Autism Strategy, gave presentations at the meeting on 18 February on work they are doing to increase public awareness. The charities are the National Autistic Society, the Autism Alliance UK, Autism Plus and Ambitious about Autism. The Autism Alliance UK is also being funded by the Department to undertake work with national and local organisations, to make reasonable adjustments to services and to train staff to be aware of what autism can mean to individuals who have the condition and their families.

    The Health and Social Care Information Centre’s publication Estimating the Prevalence of Autism Spectrum Conditions in Adults – Extending the 2007 Adult Psychiatric Morbidity Survey (APMS) gave the overall prevalence of autism in England as 1.1% (95% confidence interval 0.3% to 1.9%). Among adults with learning disabilities living in private households whose learning disability was sufficiently severe that they could not have taken part in the 2007 APMS, the prevalence of autism was 35.4% (95% confidence interval 24.7% to 46.2%). Among adults with mild or severe learning disabilities living in communal care establishments, the prevalence of autism was 31% (95% confidence interval 23.9% to 38%). Detailed supporting information regarding the underlying data and how figures have been derived is found within the detail of the report, a copy of which is attached.

    The APMS was repeated in 2014 and findings are scheduled to be published in September 2016.

  • Baroness Goudie – 2016 Parliamentary Question to the Ministry of Defence

    Baroness Goudie – 2016 Parliamentary Question to the Ministry of Defence

    The below Parliamentary question was asked by Baroness Goudie on 2016-02-22.

    To ask Her Majesty’s Government whether any Burmese Army soldiers from Infantry Battalions 213 or 217 have received any form of training from the UK.

    Earl Howe

    I refer the noble Baroness to the answer given by my hon. Friend, the Minister of State for the Armed Forces (Penny Mordaunt MP), on 14 January 2016 to Question 21564, which stated that we do not provide combat training to the Burmese Army. We do however provide educational training, as well as English Language Training. We have no information to indicate that participants on these educational courses were Burmese Army soldiers from Infantry Battalions 213 or 217.

  • Lord Freyberg – 2016 Parliamentary Question to the Department of Health

    Lord Freyberg – 2016 Parliamentary Question to the Department of Health

    The below Parliamentary question was asked by Lord Freyberg on 2016-02-22.

    To ask Her Majesty’s Government why it was decided to use an 18-month period for patient reported outcomes in the next Prostate Cancer Audit rather than a six-month period, as used in Germany.

    Lord Prior of Brampton

    The proportion of men diagnosed with locally advanced prostate cancer between 2010 and 2013 (the Audit period) who had radical treatment, and the proportion who had a hospital length of stay over three days and who required an emergency readmission within 90 days following an operation, are presented by health region in the attached headed Table 1.

    It should be noted that the results presented are based on an analysis of data from the English Cancer Registry linked to the Hospital Episode Statistics. These data were collected before the start of the National Prostate Cancer Audit (NPCA) in April 2013.

    The number of radical prostatectomies undertaken in men diagnosed between 2010 and 2013, and the proportion of men who had a hospital length of stay over three days and who had an emergency readmission within 90 days following an operation, are presented in the attached headed Table 2. The results of 56 men included in the data set used to generate Figure 8 in the NPCA Annual Report 2015 could not be included in Table 2. Of these men, 37 were treated in National Health Service trusts that treated fewer than five patients during the Audit period; and for 19 patients it was not possible to identify the NHS trust where they had undergone treatment without incurring disproportionate cost.

    The first results for the patient-reported outcomes of men who were diagnosed with prostate cancer between 1 April 2014 and 30 September 2014, and who underwent radical treatment (prostatectomy, external beam radiation, brachytherapy, cryotherapy, and high-intensity focused ultrasound), will be included in the NPCA’s Annual Report 2016, which is due to be published in the last quarter of 2016. These results will include incontinence rates.

    Men who had radical prostate cancer treatment were invited to complete a questionnaire about their experiences of care as well as about treatment outcomes, 18 months after the date of diagnosis. It was decided that questionnaires should be sent out at this time after diagnosis because it can take more than one year for men who have radiotherapy, in combination with androgen deprivation therapy, to complete their treatment. Subsequently, it will take at least three months for men to fully recover from the transient side effects of the radiotherapy. In order to include all men and to measure the final treatment outcome – rather than outcomes still affected by the transient side effects – an 18-month period was chosen.