Saturday, June 22, 2019

Iris Publishers-Open access Journal of Current Trends in Clinical & Medical Sciences | Comparative Study of Supporting Services for Children with Down’s syndrome and Their Families: Perspective of United Kingdom and Bangladesh


Authored by Mohammad Kamrujjaman

Background: A comparative study of supporting services which are available in United Kingdom and Bangladesh for the children with Down syndrome (DS) and their families were explored in the present research by doing literature review based on documentary research methodology.
Purpose: The aim of the study was to identify the gaps, discrepancies, merits and demerits between these two countries service providers for the children with DS and their families.
Methods: Bangladesh and United Kingdom were selected for the literature review. The literatures were collected from many sources such as websites, international or national organizations, public and private organization’s published report, provision and strategies, e-books, journals, articles and books. The Literatures reviewed were key sources of evidence to justify findings. Gaps, discrepancies have also been found in the Government and private sector providing services.
Discussion: There are some similarities, merits and demerits have also identified by exploring services which are available in United Kingdom and Bangladesh for proving services for the children with DS and their families. Some recommendations have been suggested for the authority who deals with the children with DS and their families.
Conclusion: It has been stated that except accessible roads, schools and transportation for the children with DS, without trained and enough professionals and staffs who can deal with DS children and their families properly, and improper management among stakeholders can make very challenging for DS children and their families to get proper services.
Keywords: Down syndrome; Literature review; Supporting services; Public & private organization

Introduction


Down syndrome (DS) is a genetic condition that results in some level of learning disability and a particular range of physical characteristics. Learning disability can affect a person to learn very new things into their every aspect of their life including at school [1]. Therefore, children with DS can have difficulty in learning new things, understanding information, communicating properly, confronting a complex situation, and/ or coping independently. In addition of learning disabilities, children with DS may have various kinds of health-related problems such as CHD (Congenital Heart Disease), vision problems, hearing loss, infections, hypothyroidism, blood disorders, poor muscle tone, sleep disorders, gum or dental problems, epilepsy, digestive problems, mental and emotional problems, and so on [2]. Hence, a different type of supporting services like educational, emotional, financial, recreational rather than medical services is needed for dealing with DS children. DS can be detected from mother’s womb to after birth. There are many screening programmes which can be carried out during pregnancy. During this screening programme, every mother should get proper guidelines and idea about what to do if the outcome is positive or negative. Education can be provided to the children with DS either at special school or mainstream school according to the parent’s desire or the present condition of that child. As children with DS have associated health problems as well as they require special care, their parent’s may face financial problem to look after them. Therefore, children with DS require supporting services from being their mother’s womb till lifelong. United Kingdom is a country of 63,136,000 populations. Among them, almost 60,000 people are living with DS as every year one in every 1000 babies are born with this condition [3]. Unfortunately, Bangladesh does not have studies to say how many people are suffering from the chromosomal disorder like a DS. But some organizations who work with children with DS has estimated that about 200,000 individuals are suffering from DS in Bangladesh, this estimation has been made based on the global trend that one in every 800 children born with this chromosomal abnormality though. The children with DS begin to get their services from a different type of health care providing institutions as prenatal screening and diagnostic test. Supporting health care services can be public funded and/ or private hospital, clinic, and diagnostic centre. As the prenatal screening or diagnostic test is to be done on the pregnant woman, therefore proper, realistic, unprejudiced knowledge about the test should be provided to them before going to test. Thus, prenatal screening and diagnostic test is related to health care providing institutions, health care providers, professionals and services provided information about test and DS, and government policies. Therefore, this study will be looked at all the services regarding prenatal and diagnostic test both in UK and Bangladesh in order to compare their services. Mother of a child with DS may face various problems when she noticed that she has given birth a child with DS. Yildirim et al. [4] state that this situation exposes mothers to intense stress and emotional problems such as denial, anxiety, anger, guilt, unexpected crisis, avoidance of facing external world’s attitude, disappointment, decrease in selfconfidence and self-respect. As individuals with DS have associated medical problems, so referral and getting access to specialized professionals according to their problems need to be done. Supporting services may take useful steps to do this. Specialized education and interventions can greatly benefit children with DS [5]. All children place a financial burden upon their parents because of their special needs for therapy, toy, medical procedures, and additional care. Except for financial supporting services, it may be difficult for a nation without universal health care systems in order to raise a child with DS. The research will explore the services for the children with DS and their families which are provided by the both UK and Bangladesh in order to get a comparison study. By exploring the services, the research will be looked at the gaps, advantages, disadvantages, similarities between these two countries’ services and trying to find out the potential reasons which are lie to know the present condition of the supporting services which are mostly used and accessed by the children with DS ages from 0 to 18 years and their families. 


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