Results 1–20 of 600 for myalgic

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Research (23 Jul 2020)

Paul Beresford: To ask the Secretary of State for Health and Social Care, how much Government funding was allocated to biomedical research into myalgic encephalomyelitis in the financial years (a) 2017-18, (b) 2018-19 and (c) 2019-20.

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome (22 Jul 2020)

Helen Whately: Holding answer received on 14 July 2020 No specific assessment has been made. Funding for services for people with myalgic encephalomyelitis is a local matter and is the responsibility of clinical commissioning groups (CCGs). CCGs are best placed to ensure NHS services are commissioned to meet local population need, taking into account best practice guidance such as the National...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Exercise (21 Jul 2020)

Olivia Blake: To ask the Secretary of State for Health and Social Care, whether the NICE guidance on chronic fatigue syndrome/myalgic encephalomyelitis will be updated to remove graded exercise in response to the increasing numbers of patients with fatigue symptoms after a diagnosis of covid-19.

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Coronavirus (7 Jul 2020)

Jo Churchill: Public Health England has made no assessment on the effect of the COVID-19 outbreak on trends in the level of post-viral complications in relation to people with myalgic encephalomyelitis.

Written Answers — Department of Health and Social Care: Coronavirus (6 Jul 2020)

Helen Whately: ...2020 Public Health England has advised that they have made no assessment on the effect of the COVID-19 outbreak on the potential for increases in post-viral complications, symptoms and myalgic encephalomyelitis.

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Health Services (18 Mar 2020)

Helen Whately: ...care, taking into account best practice guidance, such as that produced by the National Institute for Health and Care Excellence (NICE). The NICE clinical guideline, ‘Chronic fatigue syndrome/myalgic encephalomyelitis (or encephalopathy): Diagnosis and management of CFS/ME in adults and children’ sets out best practice in the referral of people the with condition to specialist...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Research (10 Feb 2020)

Stephen Morgan: To ask the Secretary of State for Health and Social Care, how much money from the public purse has been allocated to funding research on myalgic encephalomyelitis since 2010.

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome (30 Oct 2019)

Caroline Dinenage: General practice is where most patients with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) are likely to be managed, and the condition is identified as a key area of clinical knowledge in the Royal College of General Practitioners (RCGP) Applied Knowledge Test (AKT) content guide. The AKT is a summative assessment of the knowledge base that underpins general practice in the...

Scottish Parliament: Motor Neurone Disease (Blue Badge Scheme) (26 Sep 2019)

Finlay Carson: ...for, including those in my region, where the numbers are stark. It is not yet known why Dumfries and Galloway has a higher-than-average rate of diagnosis for conditions such as multiple sclerosis, myalgic encephalomyelitis and MND, but we know that those conditions have a profound impact on people’s way of life. I pay tribute to former SNP MP Richard Arkless for all the work that he has...

Written Answers — Department for Transport: Blue Badge Scheme (22 Jul 2019)

Stephen Morgan: ..., what assessment he has made of the effect of the use of the term non-physical to refer to people with hidden disabilities in the new Blue Badge guidance on the well-being of people with (a) myalgic encephalomyelitis and (b) Parkinson's disease.

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome (2 Jul 2019)

Seema Kennedy: General practice is where most patients with chronic fatigue syndrome/myalgic encephalomyelitis are likely to be managed, and the condition is identified as a key area of clinical knowledge in the Royal College of General Practitioners (GPs) Applied Knowledge Test (AKT) content guide. The AKT is a summative assessment of the knowledge base that underpins general practice in the United Kingdom...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Exercise (2 Jul 2019)

Seema Kennedy: The National Institute for Health and Care Excellence (NICE) guideline for ‘Chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) (or encephalopathy): Diagnosis and management of CFS/ME in adults and children’, was published in 2007 to support clinicians in the diagnosis, treatment, care and support of people with ME. This sets outs evidence-based best practice for the management of...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Health Services (25 Jun 2019)

Seema Kennedy: As with the vast majority of National Health Service care, the design and delivery of services for people with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) is the responsibility of local clinical commissioning groups. The National Institute for Health and Care Excellence guideline ‘Chronic fatigue syndrome/myalgic encephalomyelitis (or encephalopathy): Diagnosis and...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome (24 Jun 2019)

Stephen Morgan: To ask the Secretary of State for Health and Social Care, what assessment he has made of the effectiveness of the existing NICE guideline on myalgic encephalomyelitis.

Written Answers — Department for Work and Pensions: Employment: Chronic Fatigue Syndrome (24 Jun 2019)

Stephen Morgan: To ask the Secretary of State for Work and Pensions, what recent steps she has taken to support people with Myalgic Encephalomyelitis in the workplace.

Written Answers — Department for Work and Pensions: Employment: Chronic Fatigue Syndrome (24 Jun 2019)

Stephen Morgan: To ask the Secretary of State for Work and Pensions, what steps she is taking to ensure that job centre staff are aware of the effect of myalgic encephalomyelitis on an individual's ability to work.

Invisible Disabilities and Accessibility Challenges (5 Jun 2019)

Sharon Hodgson: ...people have hidden impairments not immediately obvious to others—neurodiversity, Crohn’s disease, colitis, dementia, arthritis, or mental distress and energy impairment conditions such as myalgic encephalomyelitis, or ME, and chronic fatigue syndrome, to name but a few. According to Scope, nearly half the British public are not aware that they even know someone who has a disability....

Written Answers — Department of Health and Social Care: Medical Treatments: Children (5 Jun 2019)

Baroness Blackwood of North Oxford: The Lightning Process (LP) is not offered as a part of the chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) standard treatments on the National Health Service. Subject to the nature of the safeguarding concerns, issues should be directed to the relevant professional regulator, should the practitioner be a member of a registered profession; the local authority (trading standards...

Written Answers — Department of Health and Social Care: Chronic Fatigue Syndrome: Greater London (3 May 2019)

Seema Kennedy: Services for people with myalgic encephalomyelitis; including those provided by the voluntary sector, are commissioned by local clinical commissioning groups. It is the responsibility of the local National Health Service commissioners to ensure NHS services are commissioned to meet local need and that they address any shortfalls in provision.

Ten Years of the Work Capability Assessment — [Sir Henry Bellingham in the Chair] (24 Apr 2019)

Alex Chalk: The hon. Gentleman mentions compassion, but is it not also correct that there must be professionalism? Linda Hending in my constituency set up a support group for people with myalgic encephalomyelitis. She found that, while 10 of those 11 people had either been found fit for work or had insufficient points for PIP, all those decisions had been overturned on appeal. While it is inevitable that...


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