Tag: Lord Bassam of Brighton

The below Parliamentary question was asked by Lord Bassam of Brighton on 2014-05-07.

To ask Her Majesty’s Government why European Union solidarity funding was not sought to assist with damage caused in the recent floods and cliff falls.

Lord Deighton

EU Solidarity Fund money is available to eligible States suffering from large-scale natural disasters but is subject to a number of eligibility requirements, including on the level of direct damages.

Comparing the recent damage in the UK to the 2007 floods, and following contact with the Commission, the Government’s assessment is that we did not meet these conditions.

However, the Government continues to explore external mechanisms, including through discussions with EU institutions such as the EIB, to support the existing package of UK Government support, which includes £130 million for flood recovery in the South West.

The below Parliamentary question was asked by Lord Bassam of Brighton on 2014-05-06.

To ask Her Majesty’s Government how many neurofibromatosis sufferers they estimate to be in the United Kingdom, broken down by (1) county, and (2) type.

Earl Howe

NHS England commissions neurofibromatosis type two (NF2) services and complex neurofibromatosis type 1 (NF1) services as part of its remit to deliver specialised services.

NHS England has published service specifications for both types of neurofibromatosis. These estimate that in England there are 11,267 individuals with NF1 and 862 with NF2.

The Department does not have specific guidance relating to the special travel needs of neurofibromatosis sufferers. Domestic equality legislation makes it unlawful for transport operators to discriminate against a disabled person simply because they are disabled, treat disabled people less favourably or fail to make reasonable adjustments in the way they provide their services, depending on the type of vehicles and the services they offer to the public.

Furthermore, an extra level of protection is provided by recently implemented European regulations on passenger rights across all transport modes. These provide a set of rules for the treatment of disabled people and people with reduced mobility.

The below Parliamentary question was asked by Lord Bassam of Brighton on 2014-05-06.

To ask Her Majesty’s Government what diagnostic training general practitioners receive with regard to neurofibromatosis.

Earl Howe

The content and standard of medical training of trainee general practitioners (GPs) is the responsibility of the General Medical Council, which is an independent statutory body. It has the general function of promoting high standards of education and co-ordinating all stages of education to ensure that medical students and newly qualified doctors are equipped with the knowledge, skills and attitudes essential for professional practice.

In the specific area of genetics in primary care, the curriculum designed by the Royal College of General Practitioners (RCGP) requires GPs to understand that while some genetic conditions always present with the same signs and symptoms, others can show variability between family members, particularly some autosomal dominant conditions (such as neurofibromatosis type 1).

The Government has mandated Health Education England (HEE) to provide national leadership on education, training and workforce development in the National Health Service. This mandate includes a commitment that HEE will ensure that GP training produces GPs with the required competencies to practise in the new NHS. Consequently HEE will work with stakeholders to influence training curricula as appropriate.

The below Parliamentary question was asked by Lord Bassam of Brighton on 2014-05-06.

To ask Her Majesty’s Government what financial support is provided to carers of neurofibromatosis sufferers.

Earl Howe

We are very much aware of and greatly value the significant contribution which unpaid carers make to the care of disabled people.

If a disabled person has neurofibromatosis and qualifies for a ‘gateway’ benefit, then their carer could be entitled to Carer’s Allowance, which is currently £61.35 per week. This will depend on certain conditions of both the disabled person and the carer being satisfied. Universal Credit includes a carer element where an eligible adult in the household provides regular and substantial care for a person with a long-term health condition or disability. The element is awarded where that person satisfies the conditions of entitlement of Carer’s Allowance.

Support for carers is an integral part of social care. Under current legislation, local authorities have a duty to assess carers who are providing substantial care on a regular basis, when requested to do so. The assessment and any eligible services to follow that are designed to support a carer to continue their caring responsibilities, are for the local authority to determine.

Carers are also central to the Government’s proposals for improving care and support, and there are significant improvements in the Care Bill for carers. The Bill extends carers’ rights to an assessment, which will be based on an appearance of need and will include consideration of the impact of caring on the carer, and the outcomes they wish to achieve. For the first time, there will be a duty on local authorities to meet carers’ eligible needs for support, putting them on an equal footing to the people they care for.

We have also provided £400 million to the National Health Service over four years from 2011 for carers to have breaks from their caring responsibilities. In the 2013 Spending Review, we announced the £3.8 billion Better Care Fund, which includes £130 millionfunding for carers’ breaks for 2015-16.