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Written Question
Leukaemia
Tuesday 26th May 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

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 improve timely access to haematology specialists for patients with (a) suspected and (b) diagnosed leukaemia.

Answered by Sharon Hodgson

The National Cancer Plan for England, released on 4 February 2026, sets out a commitment to diagnose cancers earlier and ensure people receive timely, effective treatment.

The Government is committed to helping the NHS England detect cancers, including blood cancers, earlier and provide faster treatment to improve outcomes.

NHS England uses non‑specific symptom pathways for people presenting with symptoms such as unexplained weight loss, fatigue or general illness that do not point to a particular cancer type. These pathways are especially important for detecting blood cancers, which often present with vague or non‑specific symptoms.

In addition to ongoing investment in diagnostic capacity, including new magnetic resonance imaging (MRI) and computed tomography (CT) scanners, we will support NHS England to diagnose all cancers, including blood cancers, earlier and ensure patients can begin treatment as quickly as possible.

The Department will work to end the postcode lottery to ensure that access to the best cancer diagnosis, treatment and care is available for everyone, including leukaemia patients.

The Department is working with partners such as the Royal College of Pathologists, Cancer Alliances, and genomics programme leads to strengthen diagnostic workforce capacity across cancer services, including pathology and cancer genomics. This includes investment in new training pathways, digital pathology, and genomics education, all of which support timely and accurate diagnosis for people with blood cancers, including leukemia.

NHS England is investing in expanding specialty training posts in high-demand disciplines, including haematology, and is supporting local systems to retain and develop multidisciplinary teams. This includes increasing medical training posts in haematology and enhancing the scientific workforce supply through initiatives such as the Scientist Training Programme and Higher Specialist Scientist Training.

As of February 2026, there are 2,318 full-time equivalent (FTE) doctors working in the specialty of Haematology in National Health Service trusts and other core organisations in England. This is 130, or 6%, more than a year ago. This also includes 1,082 FTE consultants, which is 51, or 4.9%, more than a year ago.

We will publish a 10 Year Workforce Plan later this spring to put the NHS workforce on a sustainable footing so staff can deliver the transformed service set out in the 10-Year Health Plan.


Written Question
Leukaemia: Blood Tests
Wednesday 20th May 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, with reference to the National Institute for Health and Care Excellence's NG12 guideline document entitled Suspected cancer: recognition and referral, updated on 15 April 2026, what steps he is taking to tackle phlebotomy capacity issues to ensure full blood count testing occurs for patients in primary care presenting with non-specific symptoms which may indicate leukaemia within 48 hours of referral, as recommended in the NG12 guidelines.

Answered by Sharon Hodgson

The National Cancer Plan for England, published on 4 February 2026, sets out a commitment to diagnose cancers earlier and ensure people receive timely, effective treatment. The Government is committed to helping NHS England detect cancers, including blood cancers, earlier and provide faster treatment to improve outcomes.

NHS England uses non‑specific symptom pathways for people presenting with symptoms such as unexplained weight loss, fatigue, or general illness that do not point to a particular cancer type. These pathways are especially important for detecting blood cancers, which often present with vague or non‑specific symptoms.

In addition, ongoing investment in diagnostic capacity, including new magnetic resonance imaging and computed tomography scanners, the Government will support NHS England to diagnose all cancers, including blood cancers, earlier to ensure patients can begin treatment as quickly as possible.

The National Institute for Health and Care Excellence (NICE) has a guideline on suspected cancer called Recognition and referral, which aims to support the identification of children, young people, and adults with symptoms that could be caused by cancer. The guideline provides guidance on appropriate investigations in primary care, and the selection of people to refer for a specialist opinion. The guideline recommends that people with specific symptoms should be offered a very urgent full blood count to assess for leukaemia. Local National Health Service organisations are expected to take NICE guidelines fully into account in ensuring that their services meet the needs of their local populations. The NHS is held to account to deliver guidelines, which include all NICE directions, at a local and regional level.


Written Question
Electronic Cigarettes: Retail Trade
Monday 18th May 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what plans he has to introduce regulations under the Tobacco and Vapes Act to require vaping products in retail premises to be stored (a) out of sight, (b) behind the counter, (c) in closed or locked cabinets and (d) in such a way as to reduce their attractiveness and visibility to children.

Answered by Sharon Hodgson

The Tobacco and Vapes Act received Royal Assent on 29 April 2026. The Act contains powers to introduce future regulations on where and how vapes and nicotine products can be displayed within shops.

There is evidence that display has played a role in the growth of youth vaping and that regulating the point-of-sale display of vapes will reduce their appeal to children. It is unacceptable that vapes in some shops have been displayed alongside confectionery and toys.

This is why we will soon consult on proposals for regulating the display of vapes and nicotine products to reduce the appeal and accessibility of vapes to children.


Written Question
Hydrocortisone
Tuesday 28th April 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, whether he is taking steps to licence ACT-O-VIAL containing 100mg hydrocortisone sodium succinate (powder) and 2ml of water (diluent), in the context of the discontinuation of the liquid form of hydrocortisone sodium phosphate.

Answered by Zubir Ahmed

The Medicines and Healthcare products Regulatory Agency (MHRA) recognises the concerns raised about the withdrawal of the previously marketed liquid hydrocortisone injection.

Following a review of our current regulatory position, we can confirm that any marketing authorisation application for a liquid hydrocortisone injection product submitted to the MHRA will be rapidly progressed. A licensed hydrocortisone sodium succinate powder for solution for injection remains authorised.

ACT-O-VIAL containing 100 milligrams hydrocortisone sodium succinate, as a powder, and two millilitres of water, as a diluent, does not have a United Kingdom licence. Should a company choose to submit an application for such a product, the MHRA would prioritise its assessment, recognising the clear clinical importance. However, decisions regarding the development, manufacture, and marketing of medicines rest solely with the companies that hold, or seek to hold, the relevant product licences. The MHRA cannot compel companies to supply a medicine.


Written Question
Breast Cancer: Medical Treatments
Tuesday 7th April 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, how much funding he plans to provide for treatments for secondary breast cancer in each of the next three years.

Answered by Sharon Hodgson

Decisions about the funding and provision of health services are the responsibility of local integrated care boards. Further details and allocations will be set out in due course. The National Cancer Plan, published 4 February 2026, has set out actions aimed at supporting people with secondary breast cancer.

To improve outcomes for breast cancer patients, NHS England funds the National Audit of Breast Cancer Treatment, covering both primary and metastatic disease. By analysing routine clinical data from National Health Service settings, these audits identify regional variations in care quality and establish best practices. This will benefit all breast cancer patients, including secondary breast cancer patients.

The plan highlights the Government’s ambition to ensure that every person with secondary breast cancer has faster diagnosis and treatment, access to the latest treatments and technology, and high-quality support throughout their journey, while driving up cancer survival rates.


Written Question
Gynaecology: Waiting Lists
Monday 9th February 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

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 reduce gynaecology waiting lists, which include those who need a diagnosis of, and treatment for, endometriosis.

Answered by Karin Smyth - Minister of State (Department of Health and Social Care)

Reducing waiting lists is a key part of the Government’s Health Mission. We are committed to putting patients first by ensuring that they are seen on time and that they have the best possible experience of care. Our Elective Reform Plan (ERP), published in January 2025, sets out reforms we are making to improve gynaecology waiting times across England. This includes:

- innovative models of care that offer care closer to home and in the community;

- piloting gynaecology pathways in community diagnostic centres for patients with post-menopausal bleeding; and

- increasing the relative funding available to incentivise providers to take on more gynaecology procedures.

We are also introducing an “online hospital”, NHS Online, which will give people who are experiencing menstrual problems which may be a sign of endometriosis the choice of getting the specialist care they need from their home.

Lastly, the National Institute for Health and Care Excellence updated their guidelines on endometriosis in November 2024, and two new treatments have been approved.


Written Question
Chronic Fatigue Syndrome: Research
Monday 19th January 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

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 put in place a long term funding strategy for research into Myalgic Encephalomyelitis.

Answered by Zubir Ahmed

As set out in the Government’s final delivery plan for myalgic encephalomyelitis, also known as chronic fatigue syndrome (ME/CFS) that was published in July 2025, the Department has taken action to strengthen research capacity and capability for ME/CFS to support the long-term future of the research field.

These actions include hosting a research showcase event, a new development award to evaluate repurposed pharmaceutical interventions, and announcing newly funded studies in health and care services, research infrastructure, and capacity-building.

We are determined to accelerate progress in the treatment and management of ME/CFS and will continue working with the community to identify and address barriers to research.

The Department funded National Institute for Health and Care Research welcomes funding applications for research into any aspect of human health and care, including ME/CFS.


Written Question
Chronic Fatigue Syndrome: Health Services
Monday 19th January 2026

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

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 ensure consistent application of NICE guidelines across Integrated Care Boards for the diagnosis and access to specialist care for the treatment of ME/Chronic Fatigue Syndrome.

Answered by Ashley Dalton

National Institute for Health and Care Excellence (NICE) guidelines are evidence-based, informed by clinical expertise, and represent best practice. Healthcare professionals and integrated care board (ICB) commissioners are expected to take NICE guidelines fully into account when designing and delivering services, including for the diagnosis and treatment of myalgic encephalomyelitis, also known as chronic fatigue syndrome (ME/CFS). NHS England ensures that ICBs follow NICE guidance through a combination of statutory oversight frameworks, annual performance assessments, and local clinical governance requirements.

We published the final ME/CFS delivery plan in July 2025, which is available at the following link:

https://www.gov.uk/government/publications/mecfs-the-final-delivery-plan

The plan focuses on boosting research, improving attitudes and education, and bettering the lives of people with this debilitating disease. It also sets out a series of actions, which will help address the key challenges and drive forward improvements to outcomes and quality of life for people living with ME/CFS in England.


Written Question
Palliative Care: Aylesbury
Thursday 30th October 2025

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what recent assessment he has made of the adequacy of palliative care services in Aylesbury constituency.

Answered by Stephen Kinnock - Secretary of State for Wales

Palliative care services are included in the list of services an integrated care board (ICB) must commission. To support ICBs in this duty, NHS England has published statutory guidance and service specifications.  The statutory guidance states that ICBs, including the Buckinghamshire, Oxfordshire and Berkshire West ICB, must work to ensure that there is sufficient provision of care services to meet the needs of their local populations. NHS England has also developed a palliative care and end of life care dashboard, which brings together all relevant local data in one place. The dashboard helps commissioners understand the palliative care and end of life care needs of their local population.

The Department and NHS England are currently looking at how to improve the access, quality, and sustainability of all-age palliative care and end of life care in line with the 10-Year Health Plan.

We will closely monitor the shift towards the strategic commissioning of palliative and end of life care services to ensure that services reduce variation in access and quality, although some variation may be appropriate to reflect both innovation and the needs of local populations.

Officials will present further proposals to ministers over the coming months, outlining the drivers and incentives that are required in palliative care and end of life care to enable the shift from hospital to community, including as part of neighbourhood health teams.

We are supporting the hospice sector with a £100 million capital funding boost for eligible adult and children’s hospices in England to ensure they have the best physical environment for care. The Hospice of the St Francis and Rennie Grove Peace Hospice Care, which both serve people in the Aylesbury constituency, are receiving £486,476 and £1,114,316 from this funding respectively.


Written Question
Coronavirus: Vaccination
Thursday 23rd October 2025

Asked by: Laura Kyrke-Smith (Labour - Aylesbury)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, whether he will take steps to extend the eligibility criteria for the covid-19 booster vaccination for winter to include those who are clinically vulnerable in winter 2025-26.

Answered by Ashley Dalton

The Government is committed to protecting those most vulnerable to COVID-19 through vaccination, as guided by the independent Joint Committee on Vaccination and Immunisation (JCVI). The primary aim of the national COVID-19 vaccination programme remains the prevention of serious illness, involving hospitalisations and deaths, arising from COVID-19. Population immunity to COVID-19 has been increasing due to a combination of naturally acquired immunity following recovery from infection and vaccine-derived immunity. COVID-19 is now a relatively mild disease for most people, though it can still be unpleasant, with rates of hospitalisation and death from COVID-19 having reduced significantly since COVID-19 first emerged.

The focus of the JCVI’s advised programme has therefore moved towards targeted vaccination of the two groups who continue to be at higher risk of serious disease, including mortality. These are the oldest adults and individuals who are immunosuppressed.

On 13 November 2024, JCVI published advice on who should be offered vaccination in autumn 2025. On 26 June 2025, the Government accepted the JCVI’s advice, and in line with that advice, in autumn 2025, a COVID-19 vaccination is being offered to the following groups:

  • adults aged 75 years old and over;
  • residents in care homes for older adults;  and
  • individuals aged six months old and over who are immunosuppressed, as defined in the ‘immunosuppression’ sections of tables three or four in the COVID-19 chapter of the UK Health Security Agency’s Green Book, which is available at the following link: https://www.gov.uk/government/publications/covid-19-the-green-book-chapter-14a

The Government has no plans to change eligibility for autumn 2025. It has accepted the JCVI’s advice for this campaign in full. As for all vaccines, the JCVI keeps the evidence under regular review.