Select Committee on Health Minutes of Evidence


Memorandum by the Maternity Alliance (MA 3)

MOTHERS IN EXILE: MATERNITY EXPERIENCES OF ASYLUM SEEKERS IN ENGLAND

  In 2001, the Maternity Alliance carried out a qualitative study of women's experiences during the asylum process. The study found that most of the women were satisfied with their antenatal care and half also had positive experiences during labour and the postnatal stay in hospital. However, half of the women experienced indifference, rudeness and racism from the health professionals caring for them during delivery or on the postnatal ward. These women felt powerless to challenge hostile attitudes and fearful of the consequences if they attempted to do so. Offensive remarks went unchallenged by other health professionals.

  Interpreters were generally provided when necessary during pregnancy and labour, except in antenatal classes, which prevented many non-English speaking women from attending. In one case, however, a decision was made, without an interpreter present, to perform a Caesarean section on a woman who did not speak English.

  Many women had not been given any information about what services and support were available to them.

Key recommendations relating to healthcare and the maternity services

    —  All agencies in contact with asylum-seeking pregnant women, new mothers and babies should recognise and meet their social, psychological and physical needs. The new support system should provide specifically for the needs of pregnant asylum seekers, new mothers and their babies.

    —  Anti-racism training for NHS staff should be strengthened. Management should take a more proactive role in ensuring that staff do not exploit the vulnerability of asylum-seeking clients with racist abuse.

    —  Pregnant asylum seekers should be given clear and accessible information on GP, maternity, health visiting and child health services. There should be a clear explanation in advance of what their choices and rights are, potential complications and treatment options, and of what support will be available.

    —  There should be better communication between maternity and child health services and accommodation providers during dispersal, to ensure that staff are forewarned of the arrival of asylum seekers who will need their services, and test results and notes are forwarded.

    —  Funding for interpreting services, and in particular for advocates and link workers, should be expanded. Out-of-hours advocacy services should be developed and more female interpreters and advocates should be recruited to them. It should be a clear target to provide interpreting or advocacy support for antenatal classes and for postnatal visits.

    —  Staff must ensure that genuine informed consent is obtained for any interventions.

A CRYING SHAME: PREGNANT ASYLUM SEEKERS AND THEIR BABIES IN DETENTION

  This briefing paper highlights the specific problems associated with the detention of vulnerable women and babies. Despite Immigration Service instructions that pregnant women "normally only considered suitable for detention in very exceptional circumstances . . .", this study found that pregnant asylum seekers (and their babies) are amongst those currently detained, sometimes for many months, even where there is no prospect of early removal.

  Generally the health care centres within the detention centres did not provide the type of care or support that women wanted. The detention centres were required to escort the women to hospital appointments and in one instance, failed to do so. Being moved between detention centres disrupted continuity of care and, in one case the centre had failed to forward the results of blood tests to a pregnant woman who had been released. One of the detainees did not speak English and had no access to an interpreter while in detention, including during her appointment with the midwife. In one case medical treatment had been withheld from a premature baby and immunisations had not been provided.

Key Recommendations

    —  The user of prolonged detention for pregnant women and mothers with young children inflicts physical and psychological harm disproportionate to the policy aim of immigration control, and should be stopped immediately. Alternatives to detention, such as regular reporting, should be used where there are evidence-based concerns about an individual absconding.

    —  Pregnant women and young children should not be placed in accommodation centres, if the institutional regime and segregation from normal sources of social support found in detention centres are replicated.

    —  Where brief detention (for a few days) of pregnant women and mothers of young children is genuinely unavoidable, no woman or baby should be detained in a place where physical conditions (including food) or medical care are inadequate. Detailed Operational Standards covering the needs of pregnant women, new mothers and babies should be established.

LIVES ON HOLD: HOMELESS FAMILIES IN TEMPORARY ACCOMMODATION

  Low income is known to be a risk factor for poor health status, as well as for homelessness, and living in poor quality accommodation also has an adverse effect on health. Evidence suggests that becoming homeless and living in temporary accommodation may put families at further risk of ill health. Research has consistently shown that exposure to poor material conditions in early life, including in utero, is detrimental to health in the short term but the effects also extend into adult life, independent of adult socio-economic status.

  All of the pregnant women interviewed felt that their pregnancy had been negatively affected by their experience of being in temporary accommodation. Health service provision was patchy and fragmented. There was no consistency as to the type and level of service provision the families in different parts of different boroughs had access to. The services a family received were generally determined less by need and more by luck with respect to the level and quality of what was available in the locality in which they were living. Over half of the women did not have a GP in the area where they were temporarily housed. In every case this was because the women had chosen to remain registered with their GP in the area where they had last been securely housed. They were, therefore, often travelling considerable distances, paying the costs of public transport, to see their doctor. One woman, who was hoping to be rehoused in her original neighbourhood, had been told she would not be accepted back onto her GP's list if she left the practice and registered elsewhere, even on a temporary basis. Women experienced considerable difficulties in finding out about local services.

  The pregnant women in the study were generally satisfied with the monitoring aspect of antenatal care, however, their expectations were low. They did not expect any social support or continuity of care, yet their concerns for their pregnancy all related to their social circumstances.

  The hospital midwife interviewed described discharging homeless women who had just given birth, with their new baby, to the local Homeless Persons Unit (HPU). She spoke of the frustrations and anxieties for ward staff of trying, often over several days, to get information on a woman's new address from the HPU. Beds were regularly being blocked by delaying the discharge from hospital of new families, either because the women gave birth at the weekend when the HPU is closed, or because a few extra days care might help protect them a little from the inevitable stress associated with leaving the hospital without a home to go to.

Key Recommendations Relating to Healthcare and the Maternity Services

    —  Consistent, reliable and sufficient access to a network of primary health care services should be available in all boroughs.

    —  Health visitors and midwives should keep in contact with families in their care that become homeless. When the family's next temporary or permanent address is known, their care must be transferred immediately to local teams.

    —  Training should be provided to raise awareness of health related causes and effects of homelessness on family members.

    —  Staff have a responsibility to be well informed about all local services that may be of use and interest to homeless families, and to offer this information to families as appropriate.

    —  The most intensive home visiting service possible should be offered, with the emphasis being on building positive relationships with clients, using a family centred, social model of care.

    —  Practitioners should prioritise involvement in existing professional networks such as the CPHVA's Special Interest Group on Homelessness (SIGH) as a means of giving and receiving professional support, sharing good practice and acting as a pressure group.

AS GOOD AS YOUR WORD: A GUIDE TO COMMUNITY INTERPRETING AND TRANSLATION IN PUBLIC SERVICES

  Statutory agencies are still reluctant to recognise both that there is a valid and ongoing need for interpreting and that its provision is their responsibility.

  In-house lists of bilingual staff are still being used as a substitute for properly resourced and co-ordinated interpreting services with trained, paid staff.

  Attitudes to bilingualism are as misguided as ever. People who speak two languages do not necessarily know how to interpret. Service providers and clients alike do not always appreciate the importance of using properly trained interpreters, and the dangers of using unskilled ones.

  Clients whose first language is not English are still being encouraged to bring their own unpaid and often unskilled interpreters, including children, other relatives and friends.

  Although there is more talk of consultation and user involvement, linguistic minority communities still face difficulties in raising these issues and lobbying for resources owing to their lack of representation on policy-making bodies inside the services and the absence of real commitment—financial and political—to equal access.

  There is still no recognised pay structure for interpreting work within the health service, nor a national umbrella organisation to represent and co-ordinate the activities of language support service providers. This means the work suffers from low pay, where it is paid at all, and abuse of the goodwill of volunteers from local communities.

  Where paid interpreting facilities exist, they are usually poorly resourced and the function and role of the interpreter is unclear and unsupported.

  Despite the obvious advantages of a seamless service and economies of scale, there is still reluctance to work in partnership with pooled funds to provide joined-up language services across agencies, e.g., health and local government.

  Services for ethnic minority groups rely on tokenistic funding, usually from government. Eventually the funding runs out and services evaporate. Tokenistic funding leads to a lack of interest and a growth of unprofessional attitudes. The powerlessness that surrounds ethnic minority groups seems to permeate through the NHS. For services to be equitable, someone has to make a commitment that lasts a lifetime and not just until "the money runs out".

Key Recommendations

    —  Health services (and other agencies) should establish a policy on language and communication for all services.

    —  Health services should allocate permanent mainstream resources to all services to set up properly structured and supported interpreting services.

    —  Health services should ensure real consultation with linguistic and ethnic minority communities.

MATERNITY SERVICES FOR WOMEN WITH LEARNING DIFFICULTIES: A REPORT OF A PARTNERSHIP OF MIDWIVES, COMMUNITY NURSES AND PARENTS

  The "Right from the Start" project looked at ways to improve maternity services for people with learning difficulties. For women with a learning difficulty, the possibility of motherhood is often discouraged, active decisions to become a parent are unsupported and resources to prepare and support the future parent are unavailable. The project aimed to find ways of involving women with learning difficulties which gave them a real say and did not treat them as token participants.

MOTHERS' PRIDE: A SURVEY OF DISABLED MOTHERS' EXPERIENCES OF MATERNITY

Recommendations

    —  More care and understanding from medical and allied staff.

    —  A change in attitude towards disabled people from staff.

    —  An end to discrimination at an institutional level, not just on an individual basis.

    —  Assessment of womens' needs as an individual, and an acknowledgement of their particular needs arising from their condition.

    —  Staff should have the time and patience to listen and be more understanding of disability.

    —  Staff should be ready to admit a lack of knowledge and take advice from the disabled woman herself.

CONSUMER EMPOWERMENT: A QUALITATIVE STUDY OF LINKWORKER AND ADVOCACY SERVICES FOR NON-ENGLISH SPEAKING USERS OF MATERNITY SERVICES

  The contribution of linkworkers and advocates to the empowerment of non-English speaking users of maternity services is considerable. Women were able to make fuller use of the maternity services. They felt more confident and reassured, able to ask questions and make maternity services. They felt more confident and reassured, able to ask questions and make choices and generally expressed satisfaction with their experience of maternity care when supported by a linkworker or advocate. However there are a number of constraints and weaknesses that limit the effectiveness of linkworker and advocacy services. A number of recommendations detail how linkworker and advocacy services can be best developed and utilised in order to improve the maternity experiences of non-English speaking users.

TRAVELLER MOTHERS AND BABIES: WHO CARES FOR THEIR HEALTH?

  This report looks at some of the ways in which health authorities and local authorities can take action to promote the health of Traveller mother and babies. Travellers often face acute problems with access to health care. A woman who is moved on from one official stopping place to another has little chance of consistent or even continuous antenatal or postnatal care. After every move, she must seek out local health services and begin again, with health professionals who don't know her and who may have no access to her medical records. The hostility which Travellers often face from the settled population raises yet another barrier in the route to health care.

Recommendations

  Local health services should include in their strategic plans a statement on their proposed action on the health care of Travellers and should be encouraged to give evidence that they are attempting to work with Travellers.

    —  Local health services should liaise with local authorities and other agencies to update information about sites within their districts. There should also be opportunity to all agencies to meet for discussion with user representatives.

    —  Local health services should identify a named person to co-ordinate information relating to Travellers, including transfer of health records when Travellers move across health authority boundaries and notifying relevant health professionals when the local authority is planning an eviction from an unauthorised site.

    —  Before embarking on initiatives in service provision, there should be careful collaboration and consultation with representative of the main Traveller organisations and of local Traveller communities who may not be represented by official organisations.

    —  A national system of personal health records should be developed which Travellers keep and take with them on visits to different health professionals in different health authorities, so helping to maintain continuity of record keeping. An evaluation exercise should be set up to establish the most useful format and content of such personal records.

    —  Health services should review their policies with regard to Travellers in order to identify and eliminate discriminatory practices. They should provide specialist induction and in-service training for all staff working with Travellers.

May 2003





 
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