Policy and Advocacy

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The policies governing the receipt and/or delivery of infertility treatment entail equality in accessing the treatments for all, irrespective of individual differences and to provide a wider approach in speeding the availability of infertility treatment or services. They also recommend a balancing in the charges pertaining to the same and should not be varied from one zone to the other. Given the availability of the available resources, the differences should not be of wide margins.

Nonetheless, these policies are insufficient of surveillance requirements at the state level while at the same time lack proper coordination, therefore posing absence of appropriate strategies diagnosing and treating infertility. This is same for services, care and insurance tariffs which are not consistent with the other states. In addition, there is lack of procedures concerning the relevant information that should be given and the form of counseling which should be accorded the infertile people. The counseling (as guided by the policies) should promote the merits of getting infertility treatment, adopting of children and how to live as childless couple, but these lack in them, (Gnoth et al 2005).The policies are inadequate in giving detailed plan to tackling infertility problem even though they dwell much on the essence of managing infertility amongst the nationals.

The policies are not focused on the prevailing evidence and is not in agreement of the stakeholders who should be the ones developing and implementing the plans designed. Policies on the infertility treatment should facilitate approaches towards prevention and managing the situation. However, there are implications on the policies as they are not appropriately acted upon along with the failure of health care insurance to concentrate on treatment, prevention and diagnosis, (Skakkebæk, N.E. & Lutz, W. 2006). These policies on the other hand recommend adherence to the current approaches for checking infertility for instance, examination and treatment of infections arising from sexual contacts which have a potential of contributing to infertility and encouraging of basic methods of prevention to all the stakeholders.

The stakeholders here include the state residents – with infertility problems, the existing community and non-community organizations, clinicians and health care providers, industries, agencies affiliated to the federal state, insurance care providers, advocacy units, the employers and scientists-cum-researchers. These assist in achieving the best outcomes necessary.

On the demands and features of infertility heath care services, there is need for increased and improved distribution and use of those who provide assisted reproduction treatment (ART) and the basic care to help in the debate on the application of using ART in the treatment of infertility, as Jensen et al (2008) suggest. Apart from this, there is demand for the installation of databases for collecting data concerning the use and funding of public services on both treatment and prevention of infertility amongst the stakeholders. This comes along with the need for relevant information regarding infertility and how it is treated especially with clear assessment on the outcomes.

Last but not least, there is demand for the improvement on the accessibility of facilities for diagnosing and treating infertility, alongside checking on discrepancies on the same. The other demands are need to enhance efficacy and safety in the treatment of infertility, and enhancing life quality of the infertile persons. Access to infertility treatment services should enhance the effort to curb by adopting the most appropriate infertility prevention health plan, and management of the situation. Identifying initiatives is useful and should focus also on the funding of health care programs.

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