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1715015
registered interest false more like this
date remove maximum value filtermore like thismore than 2024-04-30
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Coronavirus: Carers more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what assessment he has made of the potential merits of including carers in the eligibility criteria for the Spring 2024 Covid Vaccination Programme. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 24326 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-05-07more like thismore than 2024-05-07
answer text <p>The Government remains committed to protecting those most vulnerable to COVID-19 through vaccination, as guided by the independent Joint Committee on Vaccination and Immunisation (JCVI). On 7 February 2024, the JCVI published further advice on the United Kingdom’s COVID-19 vaccination programme. The JCVI advice is that a COVID-19 vaccine should be offered in spring 2024 to those at greatest risk of serious disease, and who are therefore most likely to benefit from vaccination. Those eligible are: adults aged 75 years old and over; residents in a care home for older adults; and individuals aged six months old and over who are immunosuppressed, as defined in chapter 14a of the UK Health Security Agency Green Book. The JCVI’s advice for spring 2024, including the approach to eligibility, is available via the following link:</p><p><a href="https://www.gov.uk/government/publications/covid-19-spring-2024-and-future-vaccination-programmes-jcvi-advice-4-december-2023/jcvi-statement-on-covid-19-vaccination-in-spring-2024-and-considerations-on-future-covid-19-vaccination-4-december-2023" target="_blank">https://www.gov.uk/government/publications/covid-19-spring-2024-and-future-vaccination-programmes-jcvi-advice-4-december-2023/jcvi-statement-on-covid-19-vaccination-in-spring-2024-and-considerations-on-future-covid-19-vaccination-4-december-2023</a>.</p><p>The Government has accepted this advice, and the spring 2024 COVID-19 vaccination programme is now in progress. The spring programme is targeted to those at highest risk of serious outcomes from COVID-19. Whilst carers as a group are therefore not recommended for vaccination in this programme, any carer who falls within one of the above cohorts will be eligible. Everyone who is eligible is encouraged to take up the offer of spring COVID-19 vaccination.</p>
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2024-05-07T16:24:29.797Zmore like thismore than 2024-05-07T16:24:29.797Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713223
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Diagnosis more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, if she will publish the waiting times from the point of a GP referral for a diagnosis of a patient with suspected Parkinson's Disease to the date of an appointment with a neurologist or geriatrician, by Integrated Care Board for the latest period for which that data is available. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23308 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-29more like thismore than 2024-04-29
answer text <p>Information is not held centrally on the waiting times from the point of general practice (GP) referral for a diagnosis of suspected Parkinson’s disease, to the date of appointment with a neurologist or geriatrician, by integrated care board.</p><p>Similarly, information is not held centrally on how many people with Parkinson’s disease are on waiting lists for a referral for diagnosis from a neurologist or geriatrician in each integrated care board area.</p><p>GP referrals are not classified by suspected diagnosis, so data is not available in the form requested. Not all patients referred to a neurologist or geriatrician with suspected Parkinson’s disease will go on to receive a diagnosis of Parkinson’s disease, while some receive other diagnoses.</p> more like this
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
grouped question UIN 23309 more like this
question first answered
less than 2024-04-29T10:59:08.39Zmore like thismore than 2024-04-29T10:59:08.39Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713224
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Diagnosis more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, how many people with Parkinson's Disease are on waiting lists for a referral for diagnosis to a neurologist or geriatrician in each Integrated Care Board area as of 23 April 2024. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23309 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-29more like thismore than 2024-04-29
answer text <p>Information is not held centrally on the waiting times from the point of general practice (GP) referral for a diagnosis of suspected Parkinson’s disease, to the date of appointment with a neurologist or geriatrician, by integrated care board.</p><p>Similarly, information is not held centrally on how many people with Parkinson’s disease are on waiting lists for a referral for diagnosis from a neurologist or geriatrician in each integrated care board area.</p><p>GP referrals are not classified by suspected diagnosis, so data is not available in the form requested. Not all patients referred to a neurologist or geriatrician with suspected Parkinson’s disease will go on to receive a diagnosis of Parkinson’s disease, while some receive other diagnoses.</p> more like this
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
grouped question UIN 23308 more like this
question first answered
less than 2024-04-29T10:59:08.437Zmore like thismore than 2024-04-29T10:59:08.437Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713225
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Diagnosis more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what guidance is provided to clinicians on advising patients recently diagnosed with Parkinson's Disease; and whether that guidance recommends that patients be given a leaflet from Parkinson's UK. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23310 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-29more like thismore than 2024-04-29
answer text <p>The National Institute for Health and Care Excellence’s (NICE) guidelines on Parkinson’s disease in adults include recommendations for communication with people with Parkinson's disease, and their carers. The guidelines do not specify a particular leaflet, such as the one from Parkinson’s UK, but they do recommend that: communication with people with Parkinson's disease should aim towards empowering them to participate in judgements and choices about their own care; discussions should aim to achieve a balance between providing honest, realistic information about the condition, and promoting a feeling of optimism; because people with Parkinson's disease may develop impaired cognitive ability, and communication problems, they should be provided with both oral and written communication throughout the course of the disease, which should be individually tailored and reinforced as necessary, in a consistent manner; family members and carers should be advised about their right to a carer assessment, assessment for respite care, and other support; people with Parkinson's disease should have a comprehensive care plan agreed between the person, their family members and carers as appropriate, and specialist and secondary healthcare providers; and people with Parkinson's disease should have an accessible point of contact with specialist services, such as a Parkinson's disease nurse specialist.</p><p>The exact information that is provided to a newly diagnosed Parkinson’s patient will vary, but would usually include referral to a Parkinson’s nurse. Information about local support groups would usually be provided by the Parkinson’s nurse. The Department will explore whether anything further can be done to improve the provision of post-diagnosis patient information for those with Parkinson’s disease.</p>
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
grouped question UIN 23311 more like this
question first answered
less than 2024-04-29T11:04:22.39Zmore like thismore than 2024-04-29T11:04:22.39Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713226
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Diagnosis more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, whether advice given to a newly diagnosed Parkinson's Disease patient contains (a) contact details for a local Parkinson's nurse, (b) a date for a first appointment and (c) information on local support groups. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23311 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-29more like thismore than 2024-04-29
answer text <p>The National Institute for Health and Care Excellence’s (NICE) guidelines on Parkinson’s disease in adults include recommendations for communication with people with Parkinson's disease, and their carers. The guidelines do not specify a particular leaflet, such as the one from Parkinson’s UK, but they do recommend that: communication with people with Parkinson's disease should aim towards empowering them to participate in judgements and choices about their own care; discussions should aim to achieve a balance between providing honest, realistic information about the condition, and promoting a feeling of optimism; because people with Parkinson's disease may develop impaired cognitive ability, and communication problems, they should be provided with both oral and written communication throughout the course of the disease, which should be individually tailored and reinforced as necessary, in a consistent manner; family members and carers should be advised about their right to a carer assessment, assessment for respite care, and other support; people with Parkinson's disease should have a comprehensive care plan agreed between the person, their family members and carers as appropriate, and specialist and secondary healthcare providers; and people with Parkinson's disease should have an accessible point of contact with specialist services, such as a Parkinson's disease nurse specialist.</p><p>The exact information that is provided to a newly diagnosed Parkinson’s patient will vary, but would usually include referral to a Parkinson’s nurse. Information about local support groups would usually be provided by the Parkinson’s nurse. The Department will explore whether anything further can be done to improve the provision of post-diagnosis patient information for those with Parkinson’s disease.</p>
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
grouped question UIN 23310 more like this
question first answered
less than 2024-04-29T11:04:22.42Zmore like thismore than 2024-04-29T11:04:22.42Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713227
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Medical Records more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, if she will make an assessment of the potential merits of implementing a Parkinson's Passport that would give automatic access to clearly defined benefits. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23312 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-05-01more like thismore than 2024-05-01
answer text <p>The Department is currently exploring the feasibility of this, and the other asks within the charter.</p><p>The Department for Work and Pensions offers Personal Independence Payments (PIP) to individuals with health conditions or disabilities. However, there is currently no automatic entitlement to PIP in relation to specific health conditions, except in cases of people nearing the end of life, specifically the last year of life. The Government understands that there are people with severe and lifelong health conditions which will not improve. Guidance ensures that those on the highest level of support, whose needs will not improve, receive an ongoing award with a light-touch review at the 10-year point.</p><p>The primary focus of the Department for Transport’s Blue Badge scheme is to help those with the greatest mobility needs. Eligibility is not based on the type of disability. There are several automatic qualifying criteria for a Blue Badge, such as being in receipt of PIP because you cannot walk more than 50 metres. People who do not automatically qualify for a Blue Badge may still be eligible for a badge through further assessment.</p><p>With regards to free prescriptions, approximately 89% of prescription items are currently dispensed free of charge, and there is a wide range of exemptions from prescription charges already in place. People with Parkinson’s disease who are 60 years old or over are entitled to free prescriptions. For those that have to pay for prescriptions, the cost can be capped by purchasing a pre-payment certificate, which can be paid for in instalments. Additionally, the NHS Low Income Scheme can provide help with health costs on an income-related basis.</p>
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
question first answered
less than 2024-05-01T16:48:48.773Zmore like thismore than 2024-05-01T16:48:48.773Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1713228
registered interest false more like this
date less than 2024-04-23more like thismore than 2024-04-23
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Parkinson's Disease: Research more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what estimate she has made of the amount of funding allocated to the research of Parkinson's disease over the next five years. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23313 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-05-01more like thismore than 2024-05-01
answer text <p>The National Institute for Health and Care Research (NIHR) welcomes funding applications for research into any aspect of human health, including Parkinson’s disease. Future funding allocated to research into Parkinson’s disease, and into other aspects of human health, will depend on the volume and quality of proposals received from the research community, with the level of spending outlined in the end of year accounting.</p><p>The Department, through the NIHR, invested £12.2 million into Parkinson’s research over five financial years, ending in 2022/23. The NIHR has supported a broad portfolio of Parkinson’s research and, in the last year alone, supported the conduct of 114 studies relating to Parkinson’s disease through the NIHR Clinical Research Network. For example, the NIHR is investing £3 million in the PD MED clinical trial, which investigates the efficacy of different drugs in the treatment of Parkinson’s disease. The usual practice of the NIHR is not to ring-fence funds for expenditure on particular topics.</p>
answering member constituency Pendle more like this
answering member printed Andrew Stephenson more like this
question first answered
less than 2024-05-01T16:38:30.863Zmore like thismore than 2024-05-01T16:38:30.863Z
answering member
4044
label Biography information for Andrew Stephenson more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1712885
registered interest false more like this
date less than 2024-04-22more like thismore than 2024-04-22
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Infant Mortality: Certification more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, pursuant to the Answer of 26 March 2024 to Question 19419 on Infant Mortality: Certification, what her planned timetable is for extending the scheme to pregnancy losses before 1 September 2018. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23040 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-25more like thismore than 2024-04-25
answer text <p>On 22 February 2024, we launched the Baby Loss Certificate service, fulfilling our commitment in the Women’s Health Strategy. We recognise that some people will wish to obtain a certificate for a baby loss that happened in the past. It is currently open to pregnancy losses since 1 September 2018, and we will extend this to earlier losses as soon as we can.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2024-04-25T16:52:28.513Zmore like thismore than 2024-04-25T16:52:28.513Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1712886
registered interest false more like this
date less than 2024-04-22more like thismore than 2024-04-22
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Gender Dysphoria: Health Services more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, what assessment she has made of whether the NHS workforce plan should be updated by NHS England to reflect the staffing needs of the eight new children and young people's gender services regional centres. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23041 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-04-25more like thismore than 2024-04-25
answer text <p>No specific formal assessment has been made. Gender medicine is a highly specialised field of medicine, and NHS England are actively working to recruit more staff for the new regional children and young people gender identity services. NHS England has also been working closely with other professional bodies to develop tailored training for these professionals. NHS England will commission the required professional training curriculum and competencies framework, not just for staff working in the new gender services, but also for clinicians working in secondary, primary, and community care. It is expected that this will also help to increase the support for children and young people, ensuring they receive a more holistic model of care.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2024-04-25T16:57:05.947Zmore like thismore than 2024-04-25T16:57:05.947Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4769
label Biography information for Daisy Cooper more like this
1712887
registered interest false more like this
date less than 2024-04-22more like thismore than 2024-04-22
answering body
Department of Health and Social Care more like this
answering dept id 17 more like this
answering dept short name Health and Social Care more like this
answering dept sort name Health and Social Care remove filter
hansard heading Gender Dysphoria: Health Services more like this
house id 1 more like this
legislature
25259
pref label House of Commons more like this
question text To ask the Secretary of State for Health and Social Care, whether she plans to develop waiting time targets for receiving treatment in the eight new children and young people's gender services regional centres. more like this
tabling member constituency St Albans remove filter
tabling member printed
Daisy Cooper more like this
uin 23042 more like this
answer
answer
is ministerial correction false more like this
date of answer less than 2024-05-01more like thismore than 2024-05-01
answer text <p>There are no plans to develop tailored waiting time targets for receiving treatment in children and young people's gender services regional centres. NHS England has made significant progress on its overhaul of children’s gender identity services. NHS England closed the Tavistock Gender Clinic last month and opened two new, regional services operating under a fundamentally differing service model earlier this month. A third clinic is set to open in Bristol this Autumn, and NHS England has committed to a further three services by 2026. These new services will increase service capacity and reduce waiting lists.</p> more like this
answering member constituency Lewes more like this
answering member printed Maria Caulfield more like this
question first answered
less than 2024-05-01T10:56:17.287Zmore like thismore than 2024-05-01T10:56:17.287Z
answering member
4492
label Biography information for Maria Caulfield more like this
tabling member
4769
label Biography information for Daisy Cooper more like this