Select Committee on Health Written Evidence


Memorandum by the Disability Rights Commission (WP 91)

1.  BACKGROUND

  1.1  The Disability Rights Commission was created by the Disability Rights Commission Act 1999 (DRCA). Section II of the DRCA imposes the following duties on the Commission:

    —  To work towards the elimination of discrimination against disabled persons;

    —  To promote the equalisation of opportunities for disabled persons;

    —  To take such steps as is considered appropriate with a view to encouraging good practice in the treatment of disabled persons;

    —  To keep under review the workings of the Disability Discrimination Act (DDA) 1995 and this Act.

  1.2  The Commission's goal is a society in which all disabled people can participate fully as equal citizens.

2.  RESPONSE

Summary

  2.1  The DRC welcomes the Government's commitment to tackling health inequalities and the focus set out in the White Paper Choosing Health on removing the barriers to effective health care choice and access for all.

  2.2  We urge the Government to build on its current programme and make reducing the inequality gaps in health access and increasing healthy living options for disabled people one of the centrepieces of future health policy and part of a joined-up strategy across all Government departments.

  2.3  Providing high quality health services to disabled people can also play a crucial role in supporting them in other areas of their lives, like helping them to stay in work and participate in family life and other activities. It is important to relate to the person in the context of their whole life and to enable them to participate in society—not to focus on treatment alone.

  2.4  For our part the DRC has made the achievement of greater equality in health outcomes and choice one of our four strategic priorities for 2004-07. We aim to achieve this by promoting and implementing new rights under the DDA effectively, by using our enforcement powers as a catalyst for change, by strengthening the rights framework in health where evidence suggests policy gaps or weaknesses and by building major partnerships with the NHS and its regulatory bodies.

3.   Whether the proposals will enable the Government to achieve its public health goals?

  3.1  The DRC welcomes the government's broad commitment to tackling health inequalities. We also welcome that the white paper acknowledges there is a need to "step up action" on tackling the causes of ill health and health inequalities.

  3.2.  However we remain concerned that opportunities for good health are not shared equally by all people Evidence points to the fact that disabled people have higher mortality rates (ie die earlier) than the overall population—not always for reasons related to their impairment. Some deaths are preventable illnesses.[163] Disabled people have unequal access to health screening, treatment and assessment and—partly as a result—are more likely to die young from preventable "killer" diseases like coronary heart disease.

  3.3  For example, one piece of research has shown that people with learning disabilities risk of dying before the age of 50 is 58 times greater than the general UK average.[164] Another found that people who are psychiatric outpatients are nearly twice as likely to die as the general population.[165]

  3.4  Disabled people—people with physical, sensory, learning or psychiatric impairments or other long-term health conditions—make up about 22% of all adults and a far higher proportion of primary care service users. Therefore making disability equality central to the health service is essential to meeting national priorities. It is not possible to improve the overall quality of care and support, to deliver on patient choice or to meet service standards without meeting the needs of disabled people. Disabled people are a "target group" on which local action needs to be focused in order to make progress against targets to reduce health inequalities.

4.   Whether the proposals are appropriate, will be effective and whether they represent value for money?

Appropriateness

  4.1  The DRC welcomes the Government's outline proposals laid out in the white paper Choosing Health to support people in disadvantaged groups to make informed and healthy choices and take control of better access to healthier choices.

  4.2  Offering disabled people access to a health check and support on making healthier choices from a health trainer is a positive step in the right direction but further concerted action is required to close the gap in health outcomes between disabled and non-disabled people.

  4.3  We look forward to seeing more detailed proposals on the government's plans to equip people with the skills to look after their own health and provide individuals with appropriate local support and services to do this.

Effectiveness

  4.4  For the DRC, the provision of health and social care are not ends in themselves. They should be seen as a means of enabling disabled people to enjoy the same opportunities for participation as any other citizen could reasonably expect. If we want disabled people to be full and equal citizens this requires individuals ultimately to carry the same responsibilities and rights as others. However this has to be accompanied by the right to whatever support or additional requirements needed to enable such responsibilities to be met.

  4.5  It is important that debates about extending choice, rights and responsibilities are not defined in ways that disadvantage disabled people, but rather that disabled people are enabled to secure their rights and take on responsibilities as active citizens. Ensuring disabled people have "equal opportunity" to exercise choice and access health services or health promotional activities requires change at national, community and individual levels.

  4.6  Health and health promotional services and activities need to be accessible to all, including people with mobility, sensory or mental health impairments. Service providers need to ensure that disabled people have fair access to services and that disabled people are consulted when services are being developed.

  4.7  People cannot take a more active role in maintaining their own health unless they have access to information and other resources they need to make informed choices. Access to information is essential to enabling disabled people to exercise choice about their health. Equally important are how information is communicated and processed and—where applicable—the availability of advocacy to enable self-directed decision making.

Wider benefits of participation

  4.8  There is a link between poverty and poorer health outcomes, and disabled people make up a disproportionate percentage of those who live on Social Security benefits. Providing high quality healthcare services to disabled people is crucial in supporting them in other areas of their lives, like helping them to stay in work and participate in family life and other activities. This in turn helps to support a healthier and fitter population.

  4.9  In reality, disabled people are customers, workers, students, parents, taxpayers and voters, and community members. The purpose of any form of support should, therefore, be to enable people to overcome the practical barriers they face to participating in all of these roles and activities. By meeting the health and social care needs of disabled people appropriately, and gearing services to their rights to choice, independence and inclusion, disabled people can have improved opportunities to participate in employment, public life and service delivery. Increased participation not only benefits disabled people themselves but also produces economic benefits to governments, businesses and communities.

  4.10  Improving services for disabled people can also bring about improvements in services for all service users. Disabled users may have impairments which can make it particularly difficult for them to exercise choice and access appropriate services—and if services can be responsive to their needs and wishes, then they will also be responsive to people who face less significant obstacles. For example, providing information in ways that are accessible to people with learning disabilities may also help people whose first language is not English; and improving physical access for wheelchair users can help parents with pushchairs.[166]

5.   Whether the necessary public health infrastructure and mechanisms exist to ensure that proposals will be implemented and goals achieved?

  5.1  We remain concerned that despite compelling evidence of inequalities in health outcomes between disabled and non disabled people, government policy to date has concentrated on health inequalities due to geographic area, deprivation level and ethnicity.

  5.2  The DRC believes specific measures are required to address health inequalities experienced by disabled people. Differences in how disabled people access and experience health services need to be fully understood and systematic action taken to close the gap in health outcomes between disabled and non-disabled people.

  5.3  On our part the DRC has decided to use its powers of formal investigation to instigate a comprehensive inquiry into physical health inequalities experienced by people with long term mental health problems and people with learning difficulties. Launched In December 2004 the formal investigation will run for 18 months. The investigation will look at both health inequalities and potential solutions with the aim of proposing practical solutions to tackle inequality that can be taken forward at primary care level. The work will include recommendations for national policy and implementation.

  5.4  The DRC is committed to working in partnership with the Government to ensure that Disabled people are able to routinely access the full range of health and health promotion services with the same ease as anyone else. Over the past 12 months the partnership framework between the Commission and the Department of Health has started to deliver a number of tangible products that will help raise awareness about disability equality among staff in the health service and equip them to make real changes on the ground.

  5.5  The new Public Sector Duty (PSD) to promote equality for disabled people offers a real opportunity for local authorities to provide a strong lead on disability equality and to help drive forward a culture change across the public sector. The PSD will require all public bodies to produce action plans to tackle discrimination and improve outcomes and to monitor the impact on the lives of disabled people.

  5.6  Mainstreaming disability equality and anti-discriminatory practice into national standards for health and social services is a key means of transforming services. The DRC looks forward to working with partner organisations the Healthcare Commission and the Commission for Social care Inspection to develop a framework of standards that better support and promote participation and independent living.

6.  CONCLUSION AND RECOMMENDATIONS

  6.1  While we welcome proposals to offer disabled people support to make healthier choices we urge the Government to:

    —  Develop demonstrable leadership on the issue of disability equality.

    —  Develop PSA (Public Services Agreements) targets to reduce health inequalities experienced by disabled, as compared to non-disabled, people.

  6.2  The agreed compact between the DRC and the Department of Health and planned partnerships with inspection and health promotion agencies offer major opportunities for strategic change in key areas such as promoting inclusion and equality, tackling access and communication barriers for disabled people and through greater representation of disabled people in NHS employment changing attitudes and approaches on the ground.

  6.3  Disabled people being able to routinely access the full range of health services with the same ease as anyone else isn't just a matter of equity. It makes a real difference to people's chances of living happy and healthy lives and, in many cases, to how long they will live.

February 2005









163   For more evidence on inequalities in health outcomes for disabled people see the Background evidence paper for the DRC's formal investigation into health inequalities experience by people with learning disabilities or mental health problems, available online at http://www.drc.org.uk/newsroom/healthinvestigation.asp, accessed January 2005. Back

164   Sheila Hollins et al "Mortality in People with Learning disabilities: risks, causes and death certification findings in London" 1998. Back

165   Harris EC, Barraclough B. "Excess Mortality of Mental Disorder". British Journal of Psychiatry 1998; 173; 11-53. Back

166   For more information on making health services accessible for disabled people see the DRC/DH You can make a difference leaflets Available online at http://www.dh.gov.uk/assetRoot/04/08/92/84/04089284.pdf Back


 
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