To match an exact phrase, use quotation marks around the search term. eg. "Parliamentary Estate". Use "OR" or "AND" as link words to form more complex queries.


Keep yourself up-to-date with the latest developments by exploring our subscription options to receive notifications direct to your inbox

Written Question
Parkinson's Disease: Nurses
Wednesday 24th April 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps she is taking to ensure that there are sufficient numbers of Parkinson’s specialist nurses.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

Under the NHS Long Term Workforce Plan, backed by more than £2.4 billion over the next five years, the National Health Service will focus on expanding the number of clinicians, including nurses, who train to take up enhanced and advanced roles, and work as part of multidisciplinary teams with the right skills to meet the changing needs of patients. The ambition is to train at least 3,000 advanced practitioners in 2024 and 2025 across all specialties, and to increase the number in training to 5,000 a year by 2029. The Long Term Workforce Plan also sets out actions and reforms needed to improve workforce supply and retention.


Written Question
Parkinson's Disease: Nurses
Wednesday 24th April 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps she is taking to ensure that Parkinson’s specialist nurses are retained in the profession.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

Under the NHS Long Term Workforce Plan, backed by more than £2.4 billion over the next five years, the National Health Service will focus on expanding the number of clinicians, including nurses, who train to take up enhanced and advanced roles, and work as part of multidisciplinary teams with the right skills to meet the changing needs of patients. The ambition is to train at least 3,000 advanced practitioners in 2024 and 2025 across all specialties, and to increase the number in training to 5,000 a year by 2029. The Long Term Workforce Plan also sets out actions and reforms needed to improve workforce supply and retention.


Written Question
Parkinson's Disease: Health Services
Tuesday 23rd April 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps her Department has taken to improve care for people with Parkinson's disease.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

I would like to thank my Honourable friend who is a tireless campaigner on this issue.
NHS England’s RightCare toolkit and Getting It Right First Time programme aim to improve care for people with Parkinson’s by reducing variation and delivering care more equitably across England.
A new treatment for advanced-stage Parkinson’s was rolled out in the NHS earlier this year. Tomorrow, the Secretary of State is also meeting the Movers and Shakers, a group of broadcasters and public figures living with Parkinson’s, to discuss their ‘Parky Charter’.
Written Question
House of Lords: Reform
Thursday 28th March 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Cabinet Office:

To ask the Minister for the Cabinet Office, what assessment he has made of the potential merits of reducing the number of sitting peers in the House of Lords.

Answered by Alex Burghart - Parliamentary Secretary (Cabinet Office)

The House of Lords has a key role in scrutinising the executive and as a revising chamber. The Government has made no assessment of the merits of reducing the number of sitting peers and notes that unlike the Commons, peers are not full-time salaried legislators. It is important to focus on the number of peers who attend, and not just the number eligible to sit. Existing mechanisms allow sitting peers to retire or resign.


Written Question
Pupils: Transgender People
Wednesday 27th March 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department for Education:

To ask the Secretary of State for Education, what recent steps her Department has taken to help protect trans children from bullying and harassment in schools.

Answered by David Johnston - Parliamentary Under-Secretary (Department for Education)

The government has sent a clear message to schools that bullying, including cyberbullying, for whatever reason, is unacceptable.

The department has provided over £3 million of funding, between 10 August 2021 and 31 March 2024, to five anti-bullying organisations to support schools to tackle bullying, this includes projects targeting bullying of particular groups.

In addition to this, on 19 December 2023 the department published the draft guidance for schools and colleges in relation to gender questioning children, along with a consultation, which was clear that bullying must never be tolerated. The consultation closed on 12 March 2024 and the responses will support the department to finalise the guidance for schools and colleges for final publication later this year.


Written Question
Alcoholic Drinks: Excise Duties
Monday 25th March 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the HM Treasury:

To ask the Chancellor of the Exchequer, if he will make an assessment of the potential merits of reducing alcohol duty for independent wine merchants.

Answered by Gareth Davies - Exchequer Secretary (HM Treasury)

At Spring Budget 2024, the Chancellor announced that alcohol duty will be frozen until 1 February 2025 to support alcohol producers, pubs, and consumers with cost of living pressures. This extends the six month freeze the Government announced at Autumn Statement 2023 to give businesses time to adapt to the new duty system introduced on 1 August 2023.

As with all taxes, the Government keeps the alcohol duty system under review during its yearly Budget process.


Written Question
Postural Tachycardia Syndrome
Wednesday 20th March 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps she is taking to increase (a) awareness of and (b) research investment in postural tachycardia syndrome.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

To improve awareness of postural tachycardia syndrome (PoTS) amongst healthcare professionals, and specifically general practices (GPs), the Royal College of General Practitioners provides training on PoTS as part of its Syncope toolkit, which is available at the following link:

https://elearning.rcgp.org.uk/mod/book/view.php?id=12386&chapterid=247

The National Institute for Health and Care Excellence has also produced a clinical knowledge summary, last revised in November 2023, which outlines the method healthcare professionals should follow for diagnosing PoTS. This summary is available at the following link:

https://cks.nice.org.uk/topics/blackouts-syncope/diagnosis/assessment/

GPs are asked to investigate symptoms to ensure that it is not misdiagnosed. Following referral, patients are treated within National Health Service cardiology and neurology services. Where more specialist advice is required, a referral will be made to an appropriate clinician.

Services for PoTS are locally commissioned and, as such, it is the responsibility of the local commissioning teams within integrated care boards to ensure that their locally commissioned services meet the needs of their local population.

The Department invests over £1 billion per year in health research through the National Institute for Health and Care Research (NIHR). The NIHR funds research in response to proposals received from scientists rather than allocating funding to specific disease areas. The NIHR welcomes funding applications for research into any aspect of human health, including PoTS, although it is not usual practice to ring-fence funds for particular topics or conditions. Applications are subject to peer review and judged in open competition, with awards made on the basis of the importance of the topic to patients and health and care services, value for money, and scientific quality.


Written Question
Postural Tachycardia Syndrome
Wednesday 20th March 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps she is taking to support people living with postural tachycardia syndrome.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

To improve awareness of postural tachycardia syndrome (PoTS) amongst healthcare professionals, and specifically general practices (GPs), the Royal College of General Practitioners provides training on PoTS as part of its Syncope toolkit, which is available at the following link:

https://elearning.rcgp.org.uk/mod/book/view.php?id=12386&chapterid=247

The National Institute for Health and Care Excellence has also produced a clinical knowledge summary, last revised in November 2023, which outlines the method healthcare professionals should follow for diagnosing PoTS. This summary is available at the following link:

https://cks.nice.org.uk/topics/blackouts-syncope/diagnosis/assessment/

GPs are asked to investigate symptoms to ensure that it is not misdiagnosed. Following referral, patients are treated within National Health Service cardiology and neurology services. Where more specialist advice is required, a referral will be made to an appropriate clinician.

Services for PoTS are locally commissioned and, as such, it is the responsibility of the local commissioning teams within integrated care boards to ensure that their locally commissioned services meet the needs of their local population.

The Department invests over £1 billion per year in health research through the National Institute for Health and Care Research (NIHR). The NIHR funds research in response to proposals received from scientists rather than allocating funding to specific disease areas. The NIHR welcomes funding applications for research into any aspect of human health, including PoTS, although it is not usual practice to ring-fence funds for particular topics or conditions. Applications are subject to peer review and judged in open competition, with awards made on the basis of the importance of the topic to patients and health and care services, value for money, and scientific quality.


Written Question
Syria: Earthquakes
Wednesday 28th February 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Foreign, Commonwealth & Development Office:

To ask the Minister of State, Foreign, Commonwealth and Development Office, what support his Department is providing to Syria following the earthquake in that country last year.

Answered by David Rutley - Parliamentary Under-Secretary (Foreign, Commonwealth and Development Office)

In 2023, the UK committed up to £43 million to support the response to the earthquakes in Northwest Syria and Turkey, including £28 million for Syria. The UK also committed up to £150 million to support Syrians at the Brussels Pledging Conference in June 2023. In financial year 2022/23 UK aid in north west Syria supported the provision of over 203,000 health consultations and nutrition support to over 27,000 women and children.

Since 2012, the UK has spent over £3.8 billion to provide lifesaving and life-sustaining assistance to those in need, both inside Syria and to refugee hosting countries.


Written Question
Motor Neurone Disease
Tuesday 27th February 2024

Asked by: Julian Sturdy (Conservative - York Outer)

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps she is taking to support people living with motor neurone disease.

Answered by Andrew Stephenson - Minister of State (Department of Health and Social Care)

The National Institute for Health and Care Excellence has published a clinical guideline on the assessment and management of motor neurone disease (MND), to support its diagnosis. The guideline recommends coordinated care for people with MND, using a clinic based, MND specialist, multi-disciplinary team approach. The core multi-disciplinary team should consist of healthcare and other professionals with expertise in MND, and should include specialist nurses.

The Government has committed to delivering at least £50 million to support MND research over five years, from 2022 onwards, as part of a package of £375 million for research into neurodegenerative diseases. In June 2023, the Government announced that more than £35 million of the £50 million pledged to cutting-edge MND research has now been allocated, just two years into a five-year funding commitment. Work continues at pace to support MND researchers in submitting high-quality bids for open funding calls. Further information is available at the following link:

https://www.gov.uk/government/news/government-continues-delivering-on-50-million-funding-pledge-for-motor-neurone-disease-research

NHS England commissions specialised services to support people living with MND, as set out in the published service specification for specialised neurology services. The support provided includes the provision of multi-disciplinary care from specialist clinicians, including neurologists, specialist nurses, speech and language therapists, dietetics and nutrition support, and physiotherapy, depending on individual clinical need. The service specification for specialised neurology services is available at the following link:

https://www.england.nhs.uk/wp-content/uploads/2013/06/d04-neurosci-spec-neuro.pdf

In addition, NHS England commissions a specialised communication aid service known as Augmentative and Alternative Communication, as set out in the published service specification. This service supports and prioritises individuals with rapidly degenerative conditions, including MND. The service specification for Augmentative and Alternative Communication, is available at the following link:

https://www.england.nhs.uk/commissioning/wp-content/uploads/sites/12/2016/03/aac-serv-spec-jan-2016.pdf