Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether his Department has made an assessment of the potential merits of funding research into the (a) causes of and (b) potential cures for Myalgic Encephalomyelitis.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
As indicated in the interim delivery plan for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), the Government is keen to increase and improve research in this area. ME/CFS can have a devastating effect on the lives of those who suffer from it, and those close to them, and research can hold the key to improving the quality of life for people with ME/CFS.
The Government funds ME/CFS research through the National Institute for Health and Care Research (NIHR) and the Medical Research Council (MRC). Funding is available and we welcome funding applications for research into ME/CFS. These applications are subject to peer review and judged in open competition, with awards being made based on the importance of the topic to patients and health and care services, value for money and scientific quality.
In areas, like ME/CFS, which are underserved by research, we work with other relevant funders to develop strategic solutions. For example, the MRC and NIHR co-funded the DecodeME project. The NIHR, Scottish Chief Scientist’s Office, and the MRC also funded the James Lind Alliance PSP for ME/CFS, facilitated by the charity Action for ME. We will outline further research actions as part of the Final Delivery Plan.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what estimate his Department has made of the average (a) distance travelled and (b) cost incurred by children and young people when attending cancer appointments in North Cornwall constituency.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Department knows that the cost of travel is an important issue for many young cancer patients and their families. NHS England and the integrated care boards are responsible for commissioning and ensuring the healthcare needs of their local communities are met, including providing support for travel.
The National Health Service in England runs the Healthcare Travel Costs Scheme (HTCS) to provide financial assistance for travel to a hospital or other NHS premises for specialist NHS treatment or diagnostics tests, when referred by a doctor or other primary healthcare professional.
Patients who do not qualify for the HTCS and who are on a low income may be able to claim the costs from the Department for Work and Pensions through Universal Credit or a Personal Independence Payment. There are also a number of charities in the United Kingdom who provide support, including financial support, for patients with cancer.
The Department of Health and Social Care has not made an estimate of the average distance travelled and cost incurred by children and young people when attending cancer appointments in the North Cornwall constituency.
On 4 February 2025, the Department relaunched the Children and Young People Cancer Taskforce to identify tangible ways to improve outcomes and experiences for young cancer patients. The taskforce will explore opportunities for improvement, including detection and diagnosis, genomic testing and treatment, research and innovation, and patient experience. The taskforce will also ensure that the unique needs of children and young people with cancer are carefully considered as part of the National Cancer Plan.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, whether his Department has made an assessment of the potential merits of introducing a Young Cancer Patient Travel Fund.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Department knows that the cost of travel is an important issue for many young cancer patients and their families. NHS England and the integrated care boards are responsible for commissioning and ensuring the healthcare needs of their local communities are met, including providing support for travel.
The National Health Service in England runs the Healthcare Travel Costs Scheme (HTCS) to provide financial assistance for travel to a hospital or other NHS premises for specialist NHS treatment or diagnostics tests, when referred by a doctor or other primary healthcare professional.
Patients who do not qualify for the HTCS and who are on a low income may be able to claim the costs from the Department for Work and Pensions through Universal Credit or a Personal Independence Payment. There are also a number of charities in the United Kingdom who provide support, including financial support, for patients with cancer.
The Department of Health and Social Care has not made an estimate of the average distance travelled and cost incurred by children and young people when attending cancer appointments in the North Cornwall constituency.
On 4 February 2025, the Department relaunched the Children and Young People Cancer Taskforce to identify tangible ways to improve outcomes and experiences for young cancer patients. The taskforce will explore opportunities for improvement, including detection and diagnosis, genomic testing and treatment, research and innovation, and patient experience. The taskforce will also ensure that the unique needs of children and young people with cancer are carefully considered as part of the National Cancer Plan.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, if his Department will make an assessment of the potential merits of taking additional steps to improve the quality of life of people living with Myalgic Encephalomyelitis.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
We are committed to improving care and support for people with myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS). We recognise how devastating the symptoms can be, and the significant impact they can have on patients and their families.
We aim to publish the final ME/CFS delivery plan by the end of June 2025, where one of the key themes is bettering the lives of those living with this debilitating disease, as well as boosting research, and improving attitudes and education.
The responses to the interim delivery plan consultation, along with continued close engagement with the Government, National Health Service and external stakeholders, will inform the development of the final ME/CFS delivery plan, which will include actions to improve quality of life.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to increase accessibility of GP appointments in rural areas.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
We acknowledge the urgent challenge of ensuring that rural areas have the resources to continue serving their patients. To address this, we are increasing capacity in general practice (GP) by recruiting more GPs, ensuring rural areas have the necessary workforce to provide integrated, patient-centred services.
We have invested £82 million into the Additional Roles Reimbursement Scheme, which has enabled the recruitment of over 1,500 recently qualified GPs across England since October 2024. This will increase the number of available appointments, secure the future pipeline of GPs, and alleviate the pressure on those currently working in the system.
We’ve also delivered the biggest boost to GP funding in years, an £889 million uplift, with GPs now receiving a growing share of National Health Service resources. For the first time in four years, the General Practitioners Committee England backed the new 2025/26 contract, which includes key reforms to improve access to GPs, like making sure patients can request appointments online throughout core hours.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what steps his Department plans to take to help increase the availability of GP appointments in North Cornwall constituency.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
We are committed to improving capacity and access to local services across the country, including in the North Cornwall constituency. North Cornwall sits within the NHS Cornwall and Isles of Scilly Integrated Care Board. Since June 2024, there has been an 18.2% increase in appointments delivered, higher than the national average increase of 17.8% in the same period.
In October 2024, we injected £82 million into the Additional Roles Reimbursement Scheme to enable the recruitment of 1,000 newly qualified general practitioners (GPs) across England, which will increase the number of appointments delivered, and care for thousands of patients
The Government has delivered the biggest boost to GP funding in years, an £889 million uplift, with GPs now receiving a growing share of National Health Service resources. For the first time in four years, the General Practitioners Committee England backed the new 2025/26 contract, which includes key reforms to improve access, for instance by making sure patients can request appointments online throughout core hours.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what assessment his Department has made of the adequacy of the availability of specialist (a) paediatric and (b) transitional healthcare services for teenagers in the South West.
Answered by Ashley Dalton - Parliamentary Under-Secretary (Department of Health and Social Care)
The Government is committed to raising the healthiest generation of children ever. This involves ensuring that children receive the appropriate care and support whenever they need it.
Supporting children and young people as they transition into adulthood, especially those with long-term or complex conditions and/or vulnerabilities, including those with mental health issues, is a priority in the South West, and work is underway in some National Health Service trusts.
Currently, the Royal Cornwall Hospitals NHS Trust’s paediatric department delivers care to children up to the age of 16 years old. Work in some pathways, such as eating disorders and diabetes, has started to address transitional arrangements. A review of the transition arrangements in place for children over 16 years old is underway with the local community and acute hospital trust, as this has been identified as an area for improvement by the Cornwall and Isles of Scilly Integrated Care Board.
In the NHS Long Term Plan, NHS England committed to delivering a service model for zero to 25 year olds where appropriate, to enhance children and young people’s experience of health, continuity of care, and outcomes, and their experience of the transition between services.
A national transition framework is currently awaiting publication to help local areas set up this model, or to strengthen an existing one. The principles of age-appropriate services set out in this document apply to young adults receiving care for the first time, as well as those already on a transition pathway.
While this framework focuses on the broad principles of transition, future work will focus on specific considerations and conditions. Training is also being developed for healthcare staff to develop their skills in providing the best standard of care.
Improving transitional care for young people is a South West regional priority, and the national transition framework and core competencies, once published, will support integrated care boards with implementation.
The Government’s 10-Year Health Plan, set to be published later this year, will outline the broader measures to shift England’s health and care systems toward preventing ill health. The Department will also publish a refreshed Long Term Workforce Plan to ensure the NHS has the right people in the right places, with the right skills to deliver the care that patients, including teenagers, need when they need it.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
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 of including mental health waiting lists in the targets outlined in the Plan for Change.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
Waiting lists for those referred for support are too high across England, including in rural communities. People with mental health issues are not getting the support or care they need, which is why we will fix the broken system to ensure we give mental health the same attention and focus as physical health, so that people can be confident in accessing high quality mental health support when they need it.
Nationally, we plan to recruit an additional 8,500 mental health workers across child and adult mental health services in England to reduce delays and provide faster treatment. We will also introduce access to a specialist mental health professional in every school and roll out Young Futures hubs in communities.
We recognise the unique challenges for mental health services across England, the growing treatment gap, and the spectrum of interventions required, from prevention to early intervention and treatment for mental ill-health. Early engagement from our 10-Year Health Plan has indicated that early mental health support and community-based interventions are critical in delivering substantial long-term health benefits to the public.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, if he will take steps to ensure that waiting times for mental health treatment are no longer than waiting times for treatment for physical health conditions.
Answered by Stephen Kinnock - Minister of State (Department of Health and Social Care)
Too many people with mental health issues are not getting the support or care they need when they need it, which is why we are committed to ensuring we give mental health the same attention and focus as physical health, so that people can be confident in accessing high quality mental health support when they need it.
This includes recruiting 8,500 more mental health workers, introducing access to specialist mental health professionals in every school, rolling out Young Futures hubs, and modernising the Mental Health Act.
We have also committed £26 million in capital investment to open new mental health crisis centres, reducing the pressure on busy emergency mental health and accident and emergency services and ensuring people have the support they need when they need it.
Asked by: Ben Maguire (Liberal Democrat - North Cornwall)
Question to the Department of Health and Social Care:
To ask the Secretary of State for Health and Social Care, what discussions his Department has had with NHS England on reducing delays in referrals for specialist treatment in the South West.
Answered by Karin Smyth - Minister of State (Department of Health and Social Care)
Too many people have been left in limbo waiting for National Health Service treatment. The waiting list in the South West region stands at 642,756, with 63% of those having waited less than 18 weeks, compared with the 18-week standard of 92%, and with a median waiting time of 12.8 weeks from referral to treatment.
The Department and NHS England are supporting a range of efforts, nationally and in the South West region, to reduce the time patients are waiting from being referred for specialist care, and to return to the 18-week constitutional standard. We have delivered an additional 2.5 million operations, scans, and appointments across elective services nationally since July 2024. We will support further progress in the South West region and across the United Kingdom, with approximately £1.5 billion of capital funding in 2025/26 for new surgical hubs and diagnostic scanners across England.
The Elective Reform Plan, published in January 2025, sets out the productivity and reform efforts needed to return to the 18-week standard, including reforms to outpatient care to ensure care is delivered in the right clinical setting and unnecessary appointments are reduced. In addition, the plan commits to diagnostic transformation, including investment in new and expanded community diagnostic centres and the rollout of straight to test pathways. Significant transformation across high priority specialities with waiting list challenges will also bring down waiting times for patients who have been referred for specialist treatment.