Written questions by Collins.

Communities and Local Government, whether his Department plans to (a) amend planning policy and (b) issue guidance on (i) the sequential test and (ii) flood-risk management in the context of recent (A) appeal and (B) other judicial decisions.

The National Planning Policy Framework makes clear that inappropriate development in areas at risk of flooding should be avoided by directing development away from areas at highest risk (whether existing or future). Where development is necessary in such areas, the development should be made safe for its lifetime without increasing flood risk elsewhere. To ensure a proportionate, pragmatic and constituents approach to surface flood risk, we published updated planning practice guidance to clarify how the sequential test should be applied in September 2025. We will consider whether any further changes are required to national planning policy for flooding as part of the new suite of national policies for decision making that we intend to consult on later this year.

Communities and Local Government, what assessment he has made of the potential impact of Section 106 obligations on developer funding for the (a) long-term maintenance or (b) adoption of sustainable drainage infrastructure where those assets fall outside the red line boundary of new housing developments.

The National Planning Policy Framework makes clear that developments of all sizes should use sustainable drainage techniques where the development could have drainage impacts. This is supported by National Planning Guidance which sets out that local authorities should be satisfied that all Sustainable Urban Drainage Systems (SUDS) have maintenance and adoption arrangements in place for the lifetime of the development.It is the responsibility of local planning authorities to consider whether otherwise unacceptable development could be made acceptable through the use of conditions or planning obligations when determining applications. All section 106 contributions must comply with the three tests in regulation 122 of the CIL regulations (necessary to make the development acceptable in planning terms, directly related to the development; and reasonable in scale and kind). Infrastructure such as SUDS, which can lie outside the red line boundary of new housing developments, can be capable of being funded by section 106 contributions where it meets the statutory tests.National design guidance, which is part of the Planning Practice Guidance, also explains that well-designed places are designed and planned for long-term stewardship, and well-managed and maintained by their users, owners and other stakeholders.

What assessment his Department has made of the adequacy of mandatory training requirements for food handlers in businesses serving the public on increasing awareness of (a) allergens, (b) gluten-free diets and (b) other food hygiene regulations for people with coeliac disease.

Under United Kingdom law, food business operators must ensure that staff training is appropriate to the type of food handled, including high-risk foods such as those containing allergens or gluten. While there is no standalone legal requirement for allergen-specific training, the Food Standards Agency provides free online allergy training, allergen guidance for food businesses, and technical guidance on food allergen labelling, which includes gluten-free considerations.While food allergen training is the responsibility of the food business operator, local authorities assess its adequacy during inspections to ensure compliance with allergen management requirements.

Communities and Local Government, when his Department plans to publish the Community Cohesion Strategy; and what recent progress he has made in developing the Strategy.

The Ministry for Communities, Housing and Local Government is leading cross-Government efforts to develop a longer-term, more strategic approach to social cohesion - working in partnership with communities and local stakeholders to rebuild, renew and address the deep-seated issues. On 25 September, MHCLG published the Pride in Place Strategy, which sets out how we will deliver £5 billion funding and support over ten years to 339 neighbourhoods experiencing the highest levels of deprivation. This funding can be used to support community cohesion interventions. Our strategy is a significant step change in how we support communities. It focuses on three overarching objectives: building stronger communities; creating thriving places; and helping communities to take back control of their own lives and areas.

Communities and Local Government, whether he is taking steps to help tackle the practice of subdividing agricultural land into multiple small plots for onward sale without an accompanying (a) planning and (b) change of use application; and what assessment he has made of the potential impact of such practices on (i) planning enforcement capacity and (ii) local communities.

It is for individual local planning authorities to take enforcement action where development, including change of use of land, is undertaken without planning permission.

What estimate her Department has made of the travel costs to families for their child to meet their (a) educational, (b) pastoral and (c) mental health needs where the local school is unable to meet those needs; and whether she plans to review support for home-to-school transport in such cases.

The government’s ambition is that all children receive the support they need to achieve and thrive. Our home-to-school travel policy aims to make sure no child is prevented from accessing education by a lack of transport.A child is eligible for free home-to-school transport if they are of compulsory school age (5 to 16), attend their nearest school and would not be able to walk there because of the distance, their special educational needs, disability or mobility problem, or the safety of the route. If they have an education, health and care plan, the school named in that plan will usually be considered their nearest for home-to-school transport purposes. There are extended rights to free travel for children from low-income households.We have committed to improving inclusivity and expertise in mainstream schools so fewer children need to travel long distances to a school that can meet their needs and will bring forward a White Paper with plans to improve the special educational needs and disabilities system.

Whether he will ask the Pensions Commission to consider the potential merits of allowing people of working age living with a terminal illness to claim state pension.

The government recognises the importance of ensuring that individuals who are terminally ill are treated with compassion and dignity. The Terms of Reference for the Pensions Commission, which set out the scope for the Commission, were published on the 21st July. The Commissioners will consider what is required in the long term to deliver financial security in retirement through a pensions framework that is stronger, fairer and more sustainable. The Commissioners will engage with a wide range of issues relevant to their terms of reference and will publish their findings in due course.

Whether he has made an assessment of the implications for his policies of the recommendations of the All Party Parliamentary Group on Hospice and End of Life Care’s report entitled Inquiry into the financial impact of a terminal diagnosis, published on 9 September 2025; and what steps he will take in response to those recommendations.

The Department supports people nearing the end of life through the Special Rules for End of Life. These enable people who are nearing the end of their lives to get faster, easier access to certain benefits, without needing to attend a medical assessment or serve waiting periods, and in most cases, receive the highest rate of benefit. The Universal Credit Act 2025, ensures that all Special Rules for End of Life claimants will receive the higher LCWRA rate, no matter when they make their claim. The Department values the insights and perspectives provided by the All-Party Parliamentary Group on Hospice and End of Life Care and has noted the recommendations made in the report.

What assessment he has made of the adequacy of access to specialist psychological support for parents following pregnancy or baby loss in each region; and what steps his Department is taking to ensure that all bereaved parents can access such support through the NHS regardless of where they live.

The Government is determined to ensure all women and babies receive the high-quality care they deserve, regardless of their background, location or ethnicity. That is why the Secretary of State has set up a rapid, national, independent Investigation into National Health Service maternity and neonatal services to understand the systemic issues behind why so many women, babies and families experience unacceptable care. The Investigation will deliver interim recommendations in December 2025, ahead of further findings in spring 2026. The Secretary of State will chair a Maternity and Neonatal Taskforce that will develop an action plan based on the Investigation recommendations and oversee implementation and improvement in outcomes. Bereavement services that are available seven days a week are also being set up in every area in England to support women and families who experience pregnancy loss or neonatal death.  These services are in place in 115 out of 120 trusts with maternity services in England. All NHS trusts in England are also signed up to the National Bereavement Care Pathway which is designed to improve the quality and consistency of bereavement care for parents and families experiencing pregnancy or baby loss.

Whether his Department plans to update information on the commissioning framework within the NHS England guidance entitled Prescribing Gluten Free Foods in Primary Care: Guidance for CCGs, published on 28 November 2018.

No recent assessment has been made by the Department. However, a review was undertaken in 2019, which confirmed that the position in England remains that gluten free (GF) bread and mixes can be provided to all eligible coeliac patients on a National Health Service prescription. A wide range of these items continues to be listed in Part XV of the Drug Tariff.NHS England developed guidance on Prescribing Gluten Free Foods in Primary Care in 2018 which states that NHS commissioners can restrict the prescribing of GF foods to bread and mixes only. Under the current legislation, integrated care boards may choose to further restrict product choice, or end prescribing of GF foods altogether, if they feel this is appropriate for their population, whilst taking account of their legal duties to advance equality and having regard to reducing health inequalities. NHS England currently has no plans to update the guidance.

What steps he is taking to help improve the financial security of people with a terminal diagnosis.

This Government is committed to providing a financial safety net for those who need it. The primary way the Department supports people nearing the end of life is through special benefit rules which are known as the Special Rules for End of Life (SREL). These enable people who have 12 months or less to live to get faster, easier access to certain benefits, without needing to attend a medical assessment or serve waiting periods and, in most cases, receive the highest rate of benefit. The Special Rules apply across Attendance Allowance, Disability Living Allowance, Employment and Support Allowance, Personal Independence Payment and Universal Credit. The rules are also used elsewhere, for example the Early Access to Financial Assistance Scheme, administered by the Pension Protection Fund.

Whether the Government intends to review the effectiveness of the special rules for end of life.

The primary way the Department supports people nearing the end of life is through special benefit rules which are known as the Special Rules for End of Life (SREL). These enable people who are nearing the end of their lives to get faster, easier access to certain benefits, without needing to attend a medical assessment or serve waiting periods and in most cases, receive the highest rate of benefit. The system is kept under review to ensure it is meeting its objectives. The latest figures show new claims to Personal Independence Payments (PIP) in Great Britain) under the Special Rules are being cleared in 3 working days on average. The Government is committed to ensuring that the fast-tracked access to benefits via SREL is maintained, while keeping under review how we can continue to improve the effectiveness and efficiency of the delivery of the current system.

What steps her Department is taking to ensure children with Developmental Language Disorder receive appropriate support within the education system.

The government is committed to ensuring that every child has the best start in life. This includes all children and young people with special educational needs and disabilities (SEND), including speech, language and communications needs such as Developmental Language Disorder.We know that continuing to build the pipeline of speech and language therapists (SaLT) is essential. The department is working closely with the Department of Health and Social Care and NHS England to improve access to community health services, including speech and language therapy, for children and young people with SEND.In addition to the undergraduate degree route, SaLTs can now also train via a degree apprenticeship. This route is entering its fourth year of delivery and offers an alternative pathway to the traditional degree route into a successful career as a SaLT.In partnership with NHS England, the department has extended the Early Language and Support for Every Child programme, trialling new ways of working to better identify and support children with speech, language and communication needs in early years settings and primary schools.

If he will make an assessment of the potential impact of recent (a) disability benefit and (b) social care policy changes on (i) polio survivors and (ii) people with post-polio syndrome.

Any changes to Personal Independence Payment eligibility will come after the Timms Review, an ambitious and inclusive review that aims to ensure we have a system that supports disabled people to achieve better health, higher living standards and greater independence, including through employment.To ensure lived experience is at the heart of its work, the review will be co-produced by disabled people, the organisations that represent them, and other experts. We are committed to concluding the review by autumn 2026, when it will report to the Secretary of State for Work and Pensions for a final decision.Under Section 18 the 2014 Care Act, local authorities are required to meet the needs of adults in their area who meet the eligibility criteria, which would include polio survivors and people with post-polio syndrome with eligible needs. The Care Quality Commission is assessing how well local authorities are meeting their duties under Part 1 of the Care Act.

What assessment his Department has made of the potential merits of reviewing the regional disparities of access to (a) therapy and (b) rehabilitation services for people living with (i) the long-term effects of polio and post-polio syndrome and (ii) the long-term effects of polio.

Although there is currently no cure for post-polio syndrome, a range of treatments and support is available to help manage the symptoms and improve quality of life. Treatment will depend on the severity of a patient’s condition, but care may involve pain-relieving medication, physiotherapy, dietary and exercise advice, and/or counselling or cognitive behavioural therapy. It is for commissioners, providers, and clinicians, supported by relevant clinical practice, to determine the best treatment for people with post-polio syndrome.Ongoing rehabilitation for polio survivors is commissioned at a local level by integrated care boards (ICBs) as it is unlikely they would require the complex rehabilitation services commissioned by NHS England.It is the responsibility of ICBs to make available appropriate provision to meet the health and care needs of their local population, including services for people with polio and post-polio syndrome, as they are best placed to make decisions according to local need.The 10-Year Health Plan commits to a health system that is inclusive and equitable. While polio survivors are not named explicitly, the plan’s shift from hospital to community care is particularly relevant for polio survivors, many of whom require ongoing rehabilitation and support to live independently. The 10-Year Health Plan outlines the expansion of community-based services and neighbourhood health models, which will bring care closer to home and reduce reliance on hospital-based services, and investment in digital tools and assistive technologies, which can enhance independence and access to services for those with mobility challenges.While the Department has not made a specific assessment of the potential merits of reviewing the regional disparities of access to therapy and rehabilitation services for people living with the long-term effects of polio and post-polio syndrome, addressing healthcare inequity is a core focus of the 10-Year Health Plan, to ensure the National Health Service is there for anyone who needs it whenever they need it, including people with polio and post-polio syndrome.

What data her department holds on the number of pupils in England requiring gluten free meal provision in schools.

The department does not hold data on requirements for gluten-free meal provision in schools. The government sets out required minimum standards for school food in the School Food Standards. Headteachers, governors and their caterers are best placed to make decisions about their school food policies that take into account local circumstances and pupil needs, including the provision of gluten-free meals.Additionally, Section 100 of the Children and Families Act 2014 places a duty on governing bodies of maintained schools, proprietors of academies and management committees of pupil referral units to make arrangements for supporting pupils at their school with medical conditions, which may be food-related. Schools must therefore take appropriate action in supporting such pupils to access food provision.

What steps his Department is taking to ensure that post-polio syndrome is (a) recognised, (b) diagnosed, and (c) treated though (i) access to specialist neuromuscular clinics, (ii) appropriate care pathways and (iii) other means.

Although there is currently no cure for post-polio syndrome, a range of treatments and support is available to help manage the symptoms and improve quality of life. Treatment will depend on the severity of a patient’s condition, but care may involve pain-relieving medication, physiotherapy, dietary and exercise advice, and/or counselling or cognitive behavioural therapy. It is for commissioners, providers, and clinicians, supported by relevant clinical practice, to determine the best treatment for people with post-polio syndrome.Ongoing rehabilitation for polio survivors is commissioned at a local level by integrated care boards (ICBs) as it is unlikely they would require the complex rehabilitation services commissioned by NHS England.It is the responsibility of ICBs to make available appropriate provision to meet the health and care needs of their local population, including services for people with polio and post-polio syndrome, as they are best placed to make decisions according to local need.The 10-Year Health Plan commits to a health system that is inclusive and equitable. While polio survivors are not named explicitly, the plan’s shift from hospital to community care is particularly relevant for polio survivors, many of whom require ongoing rehabilitation and support to live independently. The 10-Year Health Plan outlines the expansion of community-based services and neighbourhood health models, which will bring care closer to home and reduce reliance on hospital-based services, and investment in digital tools and assistive technologies, which can enhance independence and access to services for those with mobility challenges.While the Department has not made a specific assessment of the potential merits of reviewing the regional disparities of access to therapy and rehabilitation services for people living with the long-term effects of polio and post-polio syndrome, addressing healthcare inequity is a core focus of the 10-Year Health Plan, to ensure the National Health Service is there for anyone who needs it whenever they need it, including people with polio and post-polio syndrome.

What steps his Department is taking to ensure (a) polio survivors with post-polio syndrome and (b) other polio survivors have equitable access to specialist treatment centres providing (i) physiotherapy, (ii) hydrotherapy, (iii) pain management and (iv) rehabilitation across the country.

Although there is currently no cure for post-polio syndrome, a range of treatments and support is available to help manage the symptoms and improve quality of life. Treatment will depend on the severity of a patient’s condition, but care may involve pain-relieving medication, physiotherapy, dietary and exercise advice, and/or counselling or cognitive behavioural therapy. It is for commissioners, providers, and clinicians, supported by relevant clinical practice, to determine the best treatment for people with post-polio syndrome.Ongoing rehabilitation for polio survivors is commissioned at a local level by integrated care boards (ICBs) as it is unlikely they would require the complex rehabilitation services commissioned by NHS England.It is the responsibility of ICBs to make available appropriate provision to meet the health and care needs of their local population, including services for people with polio and post-polio syndrome, as they are best placed to make decisions according to local need.The 10-Year Health Plan commits to a health system that is inclusive and equitable. While polio survivors are not named explicitly, the plan’s shift from hospital to community care is particularly relevant for polio survivors, many of whom require ongoing rehabilitation and support to live independently. The 10-Year Health Plan outlines the expansion of community-based services and neighbourhood health models, which will bring care closer to home and reduce reliance on hospital-based services, and investment in digital tools and assistive technologies, which can enhance independence and access to services for those with mobility challenges.While the Department has not made a specific assessment of the potential merits of reviewing the regional disparities of access to therapy and rehabilitation services for people living with the long-term effects of polio and post-polio syndrome, addressing healthcare inequity is a core focus of the 10-Year Health Plan, to ensure the National Health Service is there for anyone who needs it whenever they need it, including people with polio and post-polio syndrome.

What steps her Department is taking to ensure that SEND reforms under development (a) take account of the needs of children with (i) coeliac disease and (ii) other medical conditions and (b) ensure that pupils with dietary requirements are supported in school.

The government sets out required minimum standards for school food in the School Food Standards. Headteachers, governors, and their caterers are best placed to make decisions about their school food policies that take into account local circumstances and pupil needs.Additionally, Section 100 of the Children and Families Act 2014 places a duty on governing bodies of maintained schools, proprietors of academies and management committees of pupil referral units to make arrangements for supporting pupils at their school with medical conditions, which includes coeliac disease and other food-related conditions. Schools must therefore take appropriate action in supporting such pupils to access food provision.In doing so, schools must have regard to the 'Supporting pupils with medical conditions at school' statutory guidance issued by my right hon. Friend, the Secretary of State for Education. This guidance can be accessed at: https://www.gov.uk/government/publications/supporting-pupils-at-school-with-medical-conditions--3.

What steps his Department is taking to reduce the processing times for disability benefit (a) applications, (b) reviews and (c) mandatory reconsideration requests.

Managing customer journey times for PIP claimants is a priority for the department and we are working constantly to improve our service.Our aim is to make an award decision, including on an award review decision, as quickly as possible, taking into account the need to review all the available evidence, including that from the claimant, and ensuring that the decision is robust.