Question to the Home Office:

To ask the Secretary of State for the Home Department, what steps she is taking to help prevent bicycle theft in Twickenham constituency.

Answered by Sarah Jones - Minister of State (Home Office)

The central aim of our police reforms is to protect and revitalise neighbourhood policing. We are lifting national responsibilities from local forces so they can focus on tackling issues of key concern to communities, such as dealing with bike theft. The Neighbourhood Policing Guarantee will ensure that every community in England and Wales will have named and contactable officers dealing with local issues, and that neighbourhood teams spend the majority of their time in their communities providing visible patrols and engaging with local communities and businesses.

In addition, we are also providing the police with new powers to support their response. The Crime and Policing Bill, now at Committee Stage in the House of Lords, will ensure that Officers can enter and search premises where stolen items – such as GPS-tracked bicycles – are reasonably believed to have been stolen and located, and where it is not reasonably practicable to obtain a court warrant. This will significantly enhance the ability of the police to act swiftly and effectively in recovering stolen property.

Question to the Department for Transport:

To ask the Secretary of State for Transport, if the consultation on the draft ANPS will include community engagement events across a) London and b) the wider regions.

Answered by Keir Mather - Parliamentary Under-Secretary (Department for Transport)

Engagement during the consultation on any revised Airports National Policy Statement (ANPS) draft will be proportionate to the amendments that are made. This will be considered as part of the ANPS review process.

In line with the Planning Act 2008, any consultation on a revised ANPS will be appropriately publicised ensuring that affected communities and authorities are properly notified and able to engage in the consultation.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, if he will make an assessment of the potential merits for every stroke survivor to have a 6 month review post-stroke.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England’s national Stroke Programme has undertaken work to understand the value and impact of six‑month post‑stroke reviews, particularly through the development of the Integrated Community Stroke Service (ICSS) model and the Stroke Quality Improvement in Rehabilitation (SQuIRe) programme.

Overall, the emerging evidence demonstrates that six‑month reviews are likely to provide a positive mechanism for identifying unmet need, enabling personalised care, and supporting longer‑term recovery and self‑management. The learning from SQuIRe continues to inform the national ICSS model and future commissioning guidance.

The ICSS model includes tailored, patient-centred reablement care. As part of this, through the SQuIRe programme, NHS England has funded several projects testing models of delivery of six month reviews, working closely with third sector partners, such as the Stroke Association. Analysis of these projects is pending.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what estimate he has made of the cost of ensuring every stroke survivor receives a 6-month post-stroke review.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England’s national Stroke Programme has undertaken work to understand the value and impact of six‑month post‑stroke reviews, particularly through the development of the Integrated Community Stroke Service (ICSS) model and the Stroke Quality Improvement in Rehabilitation (SQuIRe) programme.

Overall, the emerging evidence demonstrates that six‑month reviews are likely to provide a positive mechanism for identifying unmet need, enabling personalised care, and supporting longer‑term recovery and self‑management. The learning from SQuIRe continues to inform the national ICSS model and future commissioning guidance.

The ICSS model includes tailored, patient-centred reablement care. As part of this, through the SQuIRe programme, NHS England has funded several projects testing models of delivery of six month reviews, working closely with third sector partners, such as the Stroke Association. Analysis of these projects is pending.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to help support people with Motor Neurone Disease.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England commissions the specialised elements of motor neurone disease (MND) care that patients may receive from 27 specialised neurology centres across England. Within these specialised centres, neurological multidisciplinary teams ensure patients can access a range of health professionals and specialised treatment and support, according to their needs.

At the national level, there are a number of initiatives supporting service improvement and better care for patients with MND, including the Getting It Right First Time Programme for Neurology and the RightCare Progressive Neurological Conditions Toolkit.

Baroness Casey has set out that the Government must take immediate action on MND. Where someone has a severe, reasonably predictable, and life-limiting condition, it is essential that we provide rapid access to the support they need, and we will take forward immediate work to develop a fast-track process, or “passport”, that speeds up assessments and access to care for people diagnosed with MND. We will consider how best to safely implement a process that expedites assessments and gets people with MND the care and support they need more quickly.

The Government has provided £6 million in funding for the MND Translational Accelerator, which aims to speed up the development of treatments for MND, and £2 million in funding for the MND Data Catalyst, to accelerate the discovery of new diagnostics, treatments, and support better care for MND patients. Twelve projects have been funded through the accelerator, and all aimed at speeding up the development of treatments for MND.

The Government has also invested £8 million through the National Institute for Health and Care Research for the EXPERTS-ALS study, a pre-clinical study which is designed to accelerate the identification and testing of the most promising treatment candidates for treating amyotrophic lateral sclerosis, the most common form of MND.

Local authorities have duties to support people caring for their family and friends. The Care Act 2014 requires local authorities to deliver a wide range of high-quality care and support services, including support for unpaid carers.

The Government recognises the vital role of unpaid carers and is committed to ensuring they have the support they need. Through measures in the 10-Year Health Plan, we are equipping and supporting carers by making them more visible, empowering their voices in care planning, joining up services, and streamlining their caring tasks by introducing a new ‘MyCarer’ section to the NHS App.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to help expand access to treatment for those with Motor Neurone Disease.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England commissions the specialised elements of motor neurone disease (MND) care that patients may receive from 27 specialised neurology centres across England. Within these specialised centres, neurological multidisciplinary teams ensure patients can access a range of health professionals and specialised treatment and support, according to their needs.

At the national level, there are a number of initiatives supporting service improvement and better care for patients with MND, including the Getting It Right First Time Programme for Neurology and the RightCare Progressive Neurological Conditions Toolkit.

Baroness Casey has set out that the Government must take immediate action on MND. Where someone has a severe, reasonably predictable, and life-limiting condition, it is essential that we provide rapid access to the support they need, and we will take forward immediate work to develop a fast-track process, or “passport”, that speeds up assessments and access to care for people diagnosed with MND. We will consider how best to safely implement a process that expedites assessments and gets people with MND the care and support they need more quickly.

The Government has provided £6 million in funding for the MND Translational Accelerator, which aims to speed up the development of treatments for MND, and £2 million in funding for the MND Data Catalyst, to accelerate the discovery of new diagnostics, treatments, and support better care for MND patients. Twelve projects have been funded through the accelerator, and all aimed at speeding up the development of treatments for MND.

The Government has also invested £8 million through the National Institute for Health and Care Research for the EXPERTS-ALS study, a pre-clinical study which is designed to accelerate the identification and testing of the most promising treatment candidates for treating amyotrophic lateral sclerosis, the most common form of MND.

Local authorities have duties to support people caring for their family and friends. The Care Act 2014 requires local authorities to deliver a wide range of high-quality care and support services, including support for unpaid carers.

The Government recognises the vital role of unpaid carers and is committed to ensuring they have the support they need. Through measures in the 10-Year Health Plan, we are equipping and supporting carers by making them more visible, empowering their voices in care planning, joining up services, and streamlining their caring tasks by introducing a new ‘MyCarer’ section to the NHS App.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps he is taking to help support families with someone suffering from Motor Neurone Disease.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

NHS England commissions the specialised elements of motor neurone disease (MND) care that patients may receive from 27 specialised neurology centres across England. Within these specialised centres, neurological multidisciplinary teams ensure patients can access a range of health professionals and specialised treatment and support, according to their needs.

At the national level, there are a number of initiatives supporting service improvement and better care for patients with MND, including the Getting It Right First Time Programme for Neurology and the RightCare Progressive Neurological Conditions Toolkit.

Baroness Casey has set out that the Government must take immediate action on MND. Where someone has a severe, reasonably predictable, and life-limiting condition, it is essential that we provide rapid access to the support they need, and we will take forward immediate work to develop a fast-track process, or “passport”, that speeds up assessments and access to care for people diagnosed with MND. We will consider how best to safely implement a process that expedites assessments and gets people with MND the care and support they need more quickly.

The Government has provided £6 million in funding for the MND Translational Accelerator, which aims to speed up the development of treatments for MND, and £2 million in funding for the MND Data Catalyst, to accelerate the discovery of new diagnostics, treatments, and support better care for MND patients. Twelve projects have been funded through the accelerator, and all aimed at speeding up the development of treatments for MND.

The Government has also invested £8 million through the National Institute for Health and Care Research for the EXPERTS-ALS study, a pre-clinical study which is designed to accelerate the identification and testing of the most promising treatment candidates for treating amyotrophic lateral sclerosis, the most common form of MND.

Local authorities have duties to support people caring for their family and friends. The Care Act 2014 requires local authorities to deliver a wide range of high-quality care and support services, including support for unpaid carers.

The Government recognises the vital role of unpaid carers and is committed to ensuring they have the support they need. Through measures in the 10-Year Health Plan, we are equipping and supporting carers by making them more visible, empowering their voices in care planning, joining up services, and streamlining their caring tasks by introducing a new ‘MyCarer’ section to the NHS App.

Question to the Department for Transport:

To ask the Secretary of State for Transport, if she will make an assessment of the potential impact of Heathrow Airport expansion on the number of flights from a) London Gatwick, b) Manchester Airport, c) London Stansted, d) London Luton, e) Edinburgh Airport, f) Birmingham Airport, g) Glasgow Airport, h) Bristol Airport and i) Cardiff Airport.

Answered by Keir Mather - Parliamentary Under-Secretary (Department for Transport)

The Government supports airport expansion where it is in line with the UK’s legal, climate and environmental obligations.

The Government has requested proposals for expansion at Heathrow to provide the capacity boost needed to support connectivity and growth. As part of this we are undertaking a review of the Airports National Policy Statement (ANPS), the modelling for which will consider the impacts of expansion at Heathrow, including on other UK airports. Any updates to the ANPS will be consulted on in the summer.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what discussions he has had with Cabinet colleagues on supporting people with Long Covid.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

The Government is aware that post-acute infection conditions, such as Long Covid, can have a devastating effect on those who suffer from them. We are committed to taking a comprehensive and compassionate approach to supporting individuals with post-acute infection conditions such as Long Covid, recognising the unique challenges these conditions present.

NHS England has invested significantly in supporting people with Long Covid. This includes setting up specialist post-COVID, or Long Covid, services nationwide for adults, and children and young people, and investing in ensuring general practice teams are equipped to support people affected by the condition.

Since April 2024, in line with the National Health Service operating framework and the establishment of integrated care systems, commissioning of post-COVID services has been the responsibility of local integrated care boards to meet the needs of their population, subject to local prioritisation and funding.

Where referral into a Long Covid service is not possible, for example because a service has closed or is due to close, general practitioners can refer patients into other appropriate existing NHS pathways, depending on their clinical needs.

To support clinical leadership in this area, NHS England worked in partnership with the British Society of Physical and Rehabilitation Medicine to establish the International Post Covid and Post Infection Conditions Society to facilitate the ongoing sharing of best practice to support people affected by Long Covid.

Officials routinely engage with other government departments on Long Covid-related issues which span departmental boundaries.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what assessment he has made of the level of support needed for those suffering with Long Covid.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

The Government is aware that post-acute infection conditions, such as Long Covid, can have a devastating effect on those who suffer from them. We are committed to taking a comprehensive and compassionate approach to supporting individuals with post-acute infection conditions such as Long Covid, recognising the unique challenges these conditions present.

NHS England has invested significantly in supporting people with Long Covid. This includes setting up specialist post-COVID, or Long Covid, services nationwide for adults, and children and young people, and investing in ensuring general practice teams are equipped to support people affected by the condition.

Since April 2024, in line with the National Health Service operating framework and the establishment of integrated care systems, commissioning of post-COVID services has been the responsibility of local integrated care boards to meet the needs of their population, subject to local prioritisation and funding.

Where referral into a Long Covid service is not possible, for example because a service has closed or is due to close, general practitioners can refer patients into other appropriate existing NHS pathways, depending on their clinical needs.

To support clinical leadership in this area, NHS England worked in partnership with the British Society of Physical and Rehabilitation Medicine to establish the International Post Covid and Post Infection Conditions Society to facilitate the ongoing sharing of best practice to support people affected by Long Covid.

Officials routinely engage with other government departments on Long Covid-related issues which span departmental boundaries.

Question to the Department for Education:

To ask the Secretary of State for Education, what statutory time limits will apply when SEND Tribunals quash local authority decisions under the proposed Specialist Provision Package framework; and what safeguards will be put in place to prevent cycles of reconsideration impacting on provision.

Answered by Georgia Gould - Minister of State (Education)

The government set out its proposals for reforming the special educational needs and disabilities (SEND) Tribunal in its ‘SEND Reform: Putting Children and Young People First’ consultation document.

The department proposes that the SEND Tribunal will make binding judgments on local authority decisions to not undertake an education, health and care (EHC) needs assessment, whether a child or young person meets the threshold for a specialist provision package or whether the package(s) offered is suitable. The Tribunal will also consider whether a local authority’s decision about the placement named in an EHC plan is reasonable and, if they find against the local authority, it will have the power to require the decision to be retaken.

The SEND reform proposals are subject to consultation and further details will be set out in the government’s response to the consultation.

Question to the Department for Education:

To ask the Secretary of State for Education, if she will set out the requirements councils must meet to be eligible for the write-off of 90% of their historic SEND-related deficits.

Answered by Georgia Gould - Minister of State (Education)

As set out in the final Local Government Finance Settlement, all local authorities with a special educational needs and disabilities (SEND) related High Needs deficit will be eligible in 2026/27 to receive a High Needs Stability Grant that will cover 90% of their accumulated High Needs‑related DSG deficit up to the end of 2025/26. This is conditional on each local authority securing my right hon. Friend, the Secretary of State for Education’s approval of their Local SEND Reform Plan, as confirmed in the government’s announcement on managing accumulated SEND deficits.

Each local area will be required to set out credible and deliverable actions that support a more inclusive and financially sustainable system, consistent with the vision for earlier intervention, stronger mainstream inclusion and improved outcomes for children and young people as set out in the Schools White Paper.

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what assessment he has made of the economic cost of working-age stroke survivors not receiving suitable stroke rehabilitation.

Answered by Sharon Hodgson - Parliamentary Under-Secretary (Department of Health and Social Care)

The Government is committed to ensuring that stroke survivors receive high quality rehabilitation, recognising the economic, personal and wider impacts of strokes.

The National Stroke Service Model provides best practice for stroke care, including post-discharge, which should include comprehensive rehabilitation and personalised care and support. The model sets that that local stroke systems need to ensure that all stroke survivors are appropriately offered a comprehensive holistic and person-centred six-month post-stroke review.

The National Stroke Quality Improvement in Rehabilitation programme is helping to transform community-based care by increasing access to specialist stroke rehabilitation at home.

100th anniversary of the birth of Her late Majesty Queen Elizabeth II

King's Guard's ceremonial bearskin caps

Closure of Al-Aqsa Mosque during Ramadan

Financial Support for the Music and Dance Scheme

Meta and YouTube and legal liability for addictive design and online harms