COMMONWEALTH OF AUSTRALIA
INTRODUCTION COMMUNITY PARTICIPATION AND INCLUSION
In this unit we will be exploring the information and skills that a support worker needs to have to maximise the participation of a person with a disability into various community settings and activities to enhance their psychological and social wellbeing and lifestyle.
Areas that will be covered are:
WHAT IS COMMUNITY
The idea of ‘community’ probably came about where people gathered around a common area for their mutual benefit. Sharing a language, customs, ideas, skills, goods and services, or protection from enemies would be some of the advantages in being a part of a group.
Additionally communities often have other things in common: they may live in the same area; share common interests or characteristics; work or play together or just enjoy each other’s company. They provide something worthwhile to the members in as much as there is a value in being a part of the community.
Communities are about sharing and caring. There is this sense of supporting each other as well as being a part of something that is greater than us. We look to community to provide us with the skills and resources to meet our needs.
Generally, most people define themselves as a part of a community. It could be that they are part of a group, team or club which is a part of the wider community. You could probably list four or five communities that you are a part of where you give and take from one another:
As society and technology changes, the word ‘community’ continues to take on new meanings. New technology in communication and transportation means that a community is no longer where we live. While we may live in a suburb, town, city or some geographical location, they no longer define the communities that we are able to participate in. Internet cafés and forums could mean being part of a discussion group with people from all over the world.
Within society, we see all sorts of communities. There are ethnic communities, religious, living, sporting, educational, employment and even disability communities. These communities have all evolved to fulfil a social need and all have valued roles within society. People generally belong to more than one community and each is designed to fulfil a particular need.
We all have a deep need to belong and be a part of a community. It is one of the aspects of life that brings a sense of purpose, belonging, self-esteem and makes life worth living. Included and not excluded from life.
WHAT DO WE MEAN BY INCLUSION?
Community inclusion is the opportunity to live in the community and be valued for one’s uniqueness and abilities. When we talk about being included in society and community, we are including all areas of life such as:
? peer support
? health status
? valued social roles (e.g., marriage, parenting) ? citizenship and civic engagement.
Community inclusion or the opportunity to live like everyone else, should result in being ‘in’ community and the participation of people with disabilities similar to that of those without a disability. A research article on people with a disability says people are crying out to be included.
“I want to be included”, is being spoken, signed, facilitated, key-boarded, whispered and shouted by people of all ages, shapes, sizes, colours and cultures.
(http://www.inclusion.com/artbiggerpicture.html accessed 26-11-2012)
Think back on your life. Can you remember times when you were included and excluded from groups, discussion or ‘communities’? It is not a nice experience to be excluded. We all like to hear the words...
“Welcome! We want to include you.
Come and be a part of us and our community”.
When a person is excluded, words like these describe how they feel: awful, lonely, scared, sad, mad, unhappy, miserable, depressed, etc. When people are excluded, they feel ‘bad’.
However, when a person is included, words used to describe this are: happy, terrific, loved, great, wonderful, important, thrilled, warm, healthy, etc.
Your answers in activity 1 will probably mirror these words. That is because the responses are worldwide. The answers are the same for people of all ages, people of all lands, tall and short, old and young, male and female. When people are included, they feel welcome, they feel good and they feel healthy.
John O’Brien and his wife who are consultants, spend their time and lives supporting people with a disability to engage fully in life. John has outlined ‘five dimensions of inclusion’ which attempt to capture what makes a good life.
Contributing: We all have gifts and capacities. But ‘gifts aren’t gifts until they are given.’ Using our gifts and capacities are important parts of living a fulfilled life.
Being someone: We all want to be noticed, to be valued by others. We want people to notice if we’re missing, to want to know our opinions, to see us as equals.
Belonging: We all want to belong: to have friends; to be loved; to have people we want to have us around. It is about who we want to be around and who wants to be around us. Belonging is about personal, not professional relationships.
Choice and control: We all want to be allowed to strive for our own unique identity and future. We want to have as much power over our destiny as other people, not to have others making decisions for us – and when we need help we want to be in control of what happens, not to be carried along in the current. Our individuality, our person-hood, is not made up of just big things but also of our many tiny and seemingly insignificant decisions and preferences.
Sharing ordinary places: None of us like to be put away, kept apart from the real world. It is in ordinary places that belonging and contributing matter to us. We want to be free, not locked away, or put aside.
Of course these five dimensions of inclusion are all tightly interrelated. We get to be ‘someone’ because we’re giving our gifts or bringing something individual to an ordinary place. By doing this we get to belong there and we meet people who become friends or more. It is our individual dreams or ambitions, influenced by our gifts and capacities that drive us to want to be known and belong somewhere.
CONTEXT OF DISABILITY CARE
The disability sector has some guiding principles and legislation. You will see that Standard 2 is specifically about ‘Participation and Inclusion’. These standards along with the Disability Services Act 2006 provide the framework by which all service providers must deliver support.
AN OVERVIEW OF THE NATIONAL STANDARDS
The National Standards for Disability Services (NSDS) will help to promote and drive a nationally consistent approach to improving the quality of services. They focus on rights and outcomes for people with disability. The national standards were first produced in 1993. They have been revised to reflect current language, philosophies and service models, particularly the move towards individualised supports and person-centred service delivery.
THE SIX NATIONAL STANDARDS FOR DISABILITY SERVICES
The service promotes individual rights to freedom of expression, self-determination and decision-making and actively prevents abuse, harm, neglect and violence.
2. Participation and inclusion
The service works with individuals and families, friends and carers to promote opportunities for meaningful participation and active inclusion in society.
3. Individual outcomes
Services and supports are assessed, planned, delivered and reviewed to build on individual strengths and enable individuals to reach their goals.
4. Feedback and complaints
Regular feedback is sought and used to inform individual and organisation-wide service reviews and improvement.
5. Service access
The service manages access, commencement and leaving a service in a transparent, fair, equal and responsive way.
The service has effective and accountable service management and leadership to maximise outcomes for individuals.
To assist the client to know their rights, the easy read version of the National Standards for Disability services is available from www.dis.gov.au. Also,the web page www.dss.gov.au has an option to listen to the standards being read to them.
HISTORICAL TRANSITION OF MODELS OF DISABILITY SUPPORT
Over the past 100 years the lives of people with disability and their engagement with the broader community has changed dramatically.
Beliefs and practices
Beliefs and practices
Beliefs and practices
? Saw the person as a ? patient.
? Wanting to change the person with a ? disability.
? Give people ? segregated care in institutional settings. ?
? A protective, prisonguard attitude and
medical strategies. ?
? People kept in isolation, exclusion, jail-like environment. ?
? Aim: to meet the basic needs.
? Goal: to control or ? cure.
Saw the person as ?
client or consumer (a user of the service). Wanting to change disability services. ? A community based specialist services. A developmental, behavioural approach.
Individualised planning, care plans, ? rehabilitation.
skill development, ? behaviour managed. Goal: to change behaviour, skills and competencies.
See the person as citizen makes decisions about their own life.
Wanting to change the community, environment,
attitudes to disability (people no longer view disability as a negative affliction).
Supported in home, neighbourhood, local communities. Community development to integrate local area planning and coordination.
Aim: the person is enabled and included communities.
Goal: social inclusion and community membership.
A brief summary of this history shows that over 100 years ago people with disabilities were most likely to be living with their families. Those with severe impairments would be unlikely to survive and those who experienced catastrophic injury also did not live long or were reliant on relatives to provide care. From the late 1800s people with intellectual disability, acquired brain injury, and multiple disabilities were highly likely to be put into institutions for the insane, or expected to be institutionalised. For 30 years, the institutional model for ‘disabled care’ has been disappearing across Australia. (Disability: Local, National and International Trends, Prepared by Samantha Jenkinson (2008))
In this model of the institutional approach the needs that were met were basic:
This approach looks after the lowest two needs on Maslow’s Hierarchy of Needs. What about the other needs that are important? What about love, belonging, achievement, becoming the unique individual that was created.
CASE STUDY: MICHAEL’S STORY
Michael grew up in institutions and had become ‘institutionalised’.
In the institution ‘patients’ were ‘given’ their meals, their medications, told when to get up, when to go to bed, etc. If they ‘played up’ they were contained or secluded (placed in an isolation room). Even clothing was handed out daily. There were no choices and no chance to make any personal decisions.
In this setting, the basic human needs were considered to be met – food, water, shelter. There were no meaningful activities for ‘patients’, in other words, there were no opportunities to ‘better oneself’ or to learn new skills. In this type of environment the people did not have any sense of self-worth or self-esteem.
Each day was pretty much the same as the one before and routines were strictly adhered to. ‘Patients’ never left the institution and they were effectively isolated from society and the everyday life that we take for granted.
They were all placed together because they had a disability.
The questions and concerns expressed by society led to a deinstitutionalised approach.
In the 1980’s and 1990’s deinstitutionalisation saw people moving from institutions to more community engagement. Group homes, cluster housing and support in the family home became the generally accepted ways of supporting people with disability.
Many people with disabilities began to attend mainstream education, worked in open or supported employment and participated in community activities. Many also worked in business services (previously known as sheltered workshops), or attended disability specific day services or groups and special schools.
(Disability: Local, National and International Trends Prepared by Samantha Jenkinson (2008))
In this model of the deinstitutionalisation approach, the basic needs of the person were being met but additionally other needs were beginning to be understood and were being addressed somewhat. For example:
This approach began to address higher needs for work and family, however services were still able to limit and dictate the choices people had regarding their care.
Funding was given to service providers who were required to offer a range of services that people with a disability had to choose from.
CASE STUDY: MICHAEL’S STORY
Michael now lives in a hostel where he is learning to make choices in his everyday life, such as what to prepare for dinner, what to wear, how to budget and how to interact with others.
Michael is learning to prepare his own meals, how to wash his own clothes, and he is gaining confidence and self-esteem.
Michael sometimes finds this hard as waiting to be told what to do is ingrained into his mind. For Michael this will be a potential barrier which he is determined to overcome.
He enjoys being able to get up each morning at the time that suits him and go to the local newsagent to buy a paper, a freedom he never knew before. He has even learnt how much money to count out for the purchase of the paper.
He has made some friends in the hostel and they like to watch footy on the television or go for walks in the local park.
Michael’s long term goal is to live fully independent and get a part time job. He is half way toward his goal of work by currently volunteering for two half days per week to gain work skills.
(This is a true story – name changed to protect privacy).
Even though this is so much better than the institutions, there is a newer model that has been implemented.
SOCIAL INCLUSION APPROACH
Social inclusion is about allowing people to participate fully in the social and economic life of the nation – by having a job, receiving a secure and adequate income, and being closely connected to family, friends and the local community.
There has been a policy shift in Australia in recent years towards individualised or person-centred approaches. Since 2014 NSW, Victoria and WA had pilot programs where people with disability and their families receive their funding allocation as a direct payment.
All states now have funding individually allocated although this does not automatically mean that the supports received are person centred or selfdetermined by people with disability. There seems to be recognition of the need to give people with disability a level of control over their lives and services but with it also a concern for the level of risk and need for safeguards which can often swing
the balance back to inflexible and restrictive practices. (Disability: Local, National and International Trends Prepared by Samantha Jenkinson (2008))
“I’d like to have friends. It’s really hard. I’ve tried lots of groups but none have worked out. I get really worried about if anyone is going to like me and if anyone is going to have things in common with me and it goes around in my mind and it’s hard to decide to go, so a lot of times I don’t”.
(O’Connor and Fowkes, 2000)
Most people think that people with intellectual disability have a lot of family assistance or that they have support from service providers or other community organisations, but the truth is that many people living with a disability still experience extreme levels of social isolation. This is both a cause and a consequence of a range of difficult life situations that many people living with a disability commonly experience.
Many people with a disability grow up with limited family support and they may also have limited capacity and resources to advocate for themselves, or to develop supportive connections with others in their local community. Social exclusion is an important factor in explaining the social isolation of individuals. While many people with intellectual disability might be highly visible in the community and be seen to access services and community resources, opportunities for meaningful engagement and the full range of human relationships with others outside of the ‘disability service system’ are limited. They are often socially restricted to organisationally-based social activities with other people with a disability. (Craig and Bigby, 2010)
The first experiences that people without disability have of people with a disability are crucial in setting their personal attitudes and these experiences will encourage them to either exclude or include people in their social networks. Prejudice against people living with a disability is common, and there are often major challenges to the inclusion of people with disability especially in the social networks of people without disability. (Craig and Bigby, 2010).
People with a disability often identify numerous personal and social barriers to community inclusion, such as:
events. (Abbott and McConkey, 2006).
Social isolation can be described as having two components:
CASE STUDY: INCLUDING BILLY AND HIS MUM IRENE
Shortly after birth, Billy was diagnosed with Down Syndrome. Billy’s mother Irene was a single mother from a low socio-economic background. She knew very little about Down Syndrome, had very little support and often felt alone. She longed for understanding friends to share life with.
When Billy was three years old, Irene was put in contact with a local family who also had a child with Down syndrome. From this contact Irene and Billy joined a local support group for families living with children with Down syndrome. At the weekly support group, the children played while their mothers chatted and discussed the ‘difficulties’ experienced with raising a child with special needs. Irene often left the group feeling anxious and depressed about what the future may hold for her and Billy.
Irene’s neighbour Mary who also had preschool children invited Irene to bring Billy along to the local playgroup. Irene was reluctant at first as she had already experienced negative reactions (pitiful glances) from the local community at the baby clinic. With Mary’s gentle persuasion, Irene went along and was warmly welcomed by the rest of the group. After initial apprehension Irene soon settled in and was delighted to watch Billy interact with the other children. Although Billy had not reached many of the developmental milestones of his peers, he was gentle and happy and spontaneously attracted playmates. Irene, for the first time began to see the similarities between Billy and the other children, not the differences.
Irene thought of the other children in the support group and organised a get together at the local park. The day was a resounding success and resulted in the merging of the two local groups as parents realised how much they could benefit from each other’s experiences and the sharing of resources.
As a support worker it is important to advocate for your client against exclusion and advocate for inclusion. This also involves assuring that all support systems are available to those who need such support: ? Inclusion is about ALL of us.
WHAT IS COMMUNITY PARTICIPATION?
Being in the community is not the same as being part of the community.
It is important to think about the difference between ‘being in the community’ and ‘being part of the community’. Being in the community means only having a physical presence, but being part of the community means having the opportunity to interact and form relationships with other community members. We can see that this has a direct connection to the word inclusion that was just outlined.
Participation is an action word, the act of sharing in the activities of a group. There are certain elements that help us understand being part of a community. Let’s consider these now.
Being part of the community:
Since the Commonwealth Government signed the United Nations Convention on the Rights of People with Disability in 2008, a profound shift has occurred in our community. Now that the rights of people with disability have been placed firmly on the agenda, the voices of people with disability are being heard louder than ever before.
The trend in disability care is opening up choices in personal living arrangements and supports enabling active citizenship in communities. It is time that government and the community sees people with disability not for what they cannot do, but for who they are and what they can achieve as citizens.
(Strong Voices a blueprint - https://www.dcsi.sa.gov.au/__data/assets/pdf_file/0004/13567/strong-voices-a-blueprint.pdf)
Active citizenship means people getting involved in their local communities and democracy at all levels, from towns to cities to nationwide activity. Active citizenship can be as small as a campaign to clean up your street or as big as educating young people about democratic values, skills and participation. Active citizenship is one of the most important steps towards healthy societies. Watch this short YouTube clip describing active citizenship.
Active Citizenship https://www.youtube.com/watch?v=kiZNO_Lca8k
ACTIVE CITIZENSHIP AND DISABILITY
The concept of active citizenship is not new, however it is new language in the disability sector. This new language is replacing the language of ‘needs and services’ with ‘concepts of active citizenship’. There is a move from:
Watch this short You Tube video on the European project called DISCIT.
DISCIT - Active Citizenship and Disability https://www.youtube.com/
Across Australia all states and territories are addressing more choice and community inclusion. For example in March 2006, the Disability Services Commission (WA) implemented a series of projects with different service models and strategies to increase the opportunities for community inclusion. The aim was to provide actual inclusion and/or increase the capacity of community networks to include people with disabilities in a natural and mutual way.
Feedback from participants has been that volunteering has provided a sense of worth and giving back to the community in a meaningful way bringing about a sense of having a valued role. Through volunteering, participants have had the opportunity to develop skills and gain confidence that can be transferred into formal employment opportunities and some participants have since gained paid
employment positions. (Review Report: Alternatives to Employment Demonstration Project 2006-2008)
The Quality Framework for Disability Services (Department of Human Services 2007) identified 16 life areas which are important to most people and are directly associated with the way wellbeing is measured. These can be used as a guide to help identify and address some of the barriers and circumstances that prevent might otherwise people with a disability from being fully included in local community life. The areas of life important to people are:
Guide to the National Quality Standards 2013
CASE STUDY: MANDY GETS AN AWARD
Mandy loves her local community. Everyone at the local shops knows her by name and takes the time to ask how she is today. They rarely complain that she takes too much time to count her money and check her change. They help her to select a purchase when the many options confuse her.
Every Saturday morning, while it’s still dark, Mandy arrives at the local newsagents to help ‘sort’ the newspapers with Mr Benson. They always have a cup of tea and chat afterwards before he opens the shop.
On special occasions like Easter, Halloween and Christmas, Mandy will dress up and hand out treats to the local children at the local shops, promoting business. All the children love her. Mandy feels proud to participate in her local community and has been photographed for the local newspaper so many times she has lost count.
Today, the local councillor presented Mandy with a plaque with her name on it, thanking her for her 10 years contribution to the community. It will be fixed to the bench outside the newsagents. Mandy feels proud to participate in her local community and can’t wait to see her photo with the councillor and all her community in the local newspaper.
Remember, being in the community is not the same as being part of the community. The role of a support worker is to continually look for ways to include your client in areas of interest, strength and capacity. There may be skills that need to be developed or maintained in order to meet the client goals for their life.
Organisations and support workers must continue to use best practice in developing plans for inclusion of a person with a disability into the community. In your studies you will have already developed an understanding of the main practices that will be used:
We are artists, musicians, actors, poets and athletes, just like everyone else.
We have talents to give to the world.
We find arts give meaning to life.
Arts and sports are a key part of our belonging to society.
We have the right to play sports with others who have disabilities.
We also have the right to play sports that are open to everyone. Source:
“Whatever the speed of our feet or the power of our arms, each of us is capable of the highest virtues. Intelligence does not limit love, or wealth produce friendship.”
“Every person, regardless of whatever different abilities they may have, can contribute, can be a source of joy, and can beam with pride and love.”
(Source: Eunice Kennedy Shriver (http://www.dhs.state.il.us Community Inclusion accessed 3-12-2012)
SECTION 1 ENGAGE WITH SOCIAL NETWORKS
IN THE COMMUNITY
INTERESTS TO ENGAGE THE CLIENT
The starting point is to identify interests, abilities and requirements of person with disability in order that they may engage with a social network.
CASE STUDY: A LOVE FOR HORSES
David has a diagnosis of Autism. He is legally blind but retains some peripheral vision. David is 14 years old. He communicates with gestures which his parents interpret. David had always shown a keen interest in animals, horses in particular and would draw accurate pictures of them. At a recent planning day with David and his parents, it was decided to enlarge this interest and engage David in local horse riding lessons for people with disabilities.
David was enrolled in classes and initially appeared really happy when he saw the ponies. He looked at them intently. It took months of hard work and a lot of perseverance to finally get David onto the horse and for David to tolerate being led gently around the paddock. Everyone was pleased with his progress.
By chance an uncle of David’s came to visit and presented David with another option regarding his interest in horses. A day at the local races. David was enthralled and on his return home began to sketch what he had seen. The team evaluated David’s responses and changed his plan to include regular days at the races.
Today David can be seen at all the local races, sketching and selling his works of art to proud horse owners.
It is necessary to accurately identify the interests and abilities of your client so they can start to build and develop a social network. In the case study above the team explored David’s interests and some options were suggested to David and his parents. They were monitoring David’s involvement in horse riding over a few months and saw he was making some progress, but still very frightened.
When the other suggestion proved to be much more enjoyable and rewarding for David his community access plan was changed. The care team need to continue to check with the client and their carers to evaluate if the strategies are meeting the goals. Changes to support the plan will often need to be made.
Monitoring and evaluating goals and plans is a normal part of life and it is essential when working with any client. We will now look at a sample activity plan to demonstrate what a plan could look like and the documentation required to show ongoing evaluation of the plan.
Description of activity:
Method: (This is how you will accomplish the goals, objectives and the activities that you plan to implement.)
(How was this activity effective? How did you know it was effective?)
What was the outcome?
(Was the activity successful? Are there any learnings for next time?)
Staff name Signature Date
An individual lifestyle plan is a first place to look to know the interests of your clients. This document has been developed with the client, their close contacts and the service team. This will give you lots of helpful information to continue to provide for the changing needs of your client.
The other main source of information should be the client, whenever possible. The case study above highlighted how difficult it can be at times to understand what a client wants. If their disability effects their communication and self-expression, then there can be some guess work and creativity needed.
Look for ways to build communication with each individual client. Sometimes by watching them closely in different settings, you can get clues as to their interests and likes and may be able to try some options.
Things you could observe in everyday life can be the key to discovering an interest or opportunity to develop community participation:
Combining all this information with further discussion with the support team and carer or family is a way of continuing to develop ongoing interests for your client.
If you cannot get clear information directly from the client then others will be able to help. Remember, it is a team effort. Many people can be helpful for resources regarding the possible interests of a person with a disability. Anyone who knows the person well, interacts with them regularly or has an interest in people with this type of disability can offer great ideas: ? The family, close friends, advocates
It is important to try options but not get stuck on thinking that one option is the only way. As in the case with David, they tried one thing - horse riding, which was a great start, but David was an observer and not a participant. The team also tried something else (horse races) which was even better. David now fully participates in his community rather than just being an observer.
Being creative and looking for options to connect people with their interests is very rewarding for all involved. As you see a client open up and develop meaningful relationships, you have a sense of achievement and satisfaction that this client is now enjoying a full and happy life.
CASE STUDY: MATT’S PASSION IS NOW ALSO HELPING OTHERS
Matt is a 19 year old male with a diagnosis of mild cerebral palsy. He left school two years ago and although he had many friends during his school years and was an integral part of the school community, his friends seemed to have dropped off one by one as they pursued careers and relationships. Matt was spending more and more time isolated in his unit with his computer for company.
Matt had funding for five hours of support three times a week but this seemed to be swallowed up with personal care, banking, shopping and swimming or Hydrotherapy. His support workers seemed to change all the time too.
He grieved for the days when he was part of the school community. He had a purpose in life back then. He remembered the day he became “editor’ of the student newsletter. He wondered if it was still going.
One of Matt’s support workers noticed Matt’s collection of old school newsletters and read Matt’s name as editor. The support worker began to see that while he had been taking care of Matt’s physical needs, he had never looked beyond that.
With a few phone calls and a change in routine, Matt visits his old school twice a month to resurrect the student newsletter, advocating strongly for the student with special needs. The local newspaper got hold of the story and did an interview with Matt who now writes a weekly article for the community services section of the paper. Other schools in the area have approached Matt to start a similar student newsletter in their school communities to enhance the relationship between mainstream students and their peers with special needs. Matt now does his banking and shopping online.
We can see in this case study that Matt’s needs were not assessed very well from the start. They focused on his physical needs and did not address his holistic needs. There was also a failure by this disability service to review Matt’s goals or follow-up on Matt’s satisfaction. There are many ways to get feedback from a client and their carers. Surveys, questionnaires, interviews and case meetings are just a few options.
OPTIONS TO SUIT THE CLIENT
Once the clients’ interests and abilities have been accurately identified, the next step is to research and identify options available to the client within their community. Remember, the aim is person-centred care. The client is actively involved in the process from the beginning to the end. You may help your client to explore options and research things for themselves or you may be asked to develop some options to present to the client and the care team.
Just as the phrase ‘person-centred’ suggests, a person-centred approach is about ensuring a person with a disability is at the centre of decisions which relate to their life. The ultimate aim is to understand what each individual person wants and needs to live their own, personally defined, good life.
A person-centred process is the cornerstone of individualised support and involves listening, thinking together, coaching, sharing ideas, and seeking feedback. This process is ongoing to ensure each person is supported towards their personal goals, even as they evolve and change.
Person-centred practice also recognises and involves other people who make a difference in a person’s life – family, friends, and the community. Relationships are important in person centered care because friends and family can support the process and help identify and develop the person’s strengths.
Ultimately though it is:
Be careful not to rule out options before the person/client has had time to consider everything and make their own decision remembering a decision may take some time. Respecting a person with a disability involves allowing them the time and space and information they need to make a decision themselves. All of us like to consider choices and process information before making a decision and we usually do not like to be rushed.
CASE STUDY: FROM SPECTATOR TO STAR PLAYER
Jordan has just celebrated her 50th birthday at the local sporting club with her family, friends and colleagues.
It wasn’t always like that. As far back as she can remember, her birthday was always celebrated at home with her mum and dad. Her gifts were always personal care items, talc, bath salts and sometimes perfume.
Jordan had no idea there was another way to celebrate. Although she went out in her local community, it was always with her Mum and Dad. She would sit and watch as they played lawn bowls.
One day, five years ago, a staff member asked Jordan if she would like to have a go. Mum and Dad said “No, no she’s happy to watch”. But the staff member insisted and the rest is history. Jordan was a natural and years of being a spectator paid off as Jordan became the star player.
As you start to explore options related to your clients goals you need to make sure you are aware of your organisation’s policies and protocols that will guide you in identifying and accessing appropriate resources. Options that you may need to explore could include:
? educational opportunities
? recreational pursuits
? religious bodies
? drama and the arts
? generic community groups
? job prospects
? health and fitness
? social clubs
? support groups
? specialised groups.
The list could go on forever because we are talking about the interests of each unique individual.
A support worker and the organisation they work for will have developed networks with many organisations within the community. Be aware though that you will need to be open to developing more community networks as each individual client expresses their own individual goals and objectives. Taking this into consideration, there could also be specific cultural needs and resources required.
You can continue to explore options and opportunities and make suggestions to your coordinator if you have seen something that may suit some of the clients in your service.
Having initially carried out accurate assessment with the client and their carers about the resources required for the client to participate in community, issues such as cost limits, time required, support needed and accessibility need to be discussed. The options need to be realistic for the client’s abilities and affordable.
Brainstorming the likes, interests and needs with the client, family and support network as discussed previously.
Check out lots of options with your support team, other organisations, community groups and ask the following questions:
ORGANISE AND PRESENTING THE INFORMATION
If the client has not been able to research with you, then you will need to provide clear information in a presentation to the client. You could present information in lots of ways, remembering to be creative in the way you format your research in order for it to be easily understood. Some formats could be:
Presenting information in a suitable format empowers the client in the decision making process and can encourage them to choose to try an option.
Once the options are presented the client needs to be given time to choose. Remember, it is ultimately the client’s choice and you cannot make them participate in something they do not want to. We want to support and empower the individual.
SECTION 2 STRATEGIES FOR COMMUNITY PARTICIPATION
There are still widespread misconceptions and stereotypes about people with a disability. These include that they are a danger, a burden, and a threat. It is not uncommon to hear people express the view that people with a disability would be better off in institutions with people of their own kind. There also appears to be a common belief that people with a disability are not able to make a significant contribution to the community and that they are somehow not of equal value as human beings and members of the community.
Many people have low expectations of people with a disability, believing that they cannot learn or are not able to do anything useful. They are often denied opportunities to experience life, to explore their potential and achieve success, because it is assumed that their potential is limited. It is often stated that people with a disability are tolerated in the community. It should be noted however, that tolerance is not acceptance and genuine inclusion and so denies people with disabilities their rights.
Additionally in a society where the values that predominate are power and wealth, physical prowess, beauty, intelligence, competition, autonomy and self-control, many people with a disability are marginalised and devalued.
It could well be that, as a result of a lack of knowledge, many people are fearful about engaging with and including people who live with a disability and therefore they are treated as ‘the other’ rather than involved. (SHUT OUT 2012 www.dss.gov.au)
Let’s summarise again the powerful successes and benefits of people being able to engage and participate in the community in which they live.
First: Community inclusion is a success when people:
Second: The benefits of inclusion to the individual:
Thirdly: The benefits of inclusion to the community:
We have already discussed the general community’s misconceptions, stereotypes and devaluing of people with a disability, now we will explore different strategies to support your client to participate in their community. As you know, all stages of providing support is in full consultation with the clients, their carers and the support team. The client gets to run the show.
Some areas we will consider in this section are:
Let’s begin by looking at what Standard 2 of the National Standards for Disability Services states:
You can take part in the community and feel included when you use disability services.
People with a disability have the same rights, interests and needs as every other member of the community. They want to be involved, included, belong, have fun and love life. The main difference is simply the level of support each individual may require to achieve these goals. It is part of the role of the support worker to provide appropriate support and use various strategies to help these goals and dreams to become a reality. The key point to remember with community inclusion is that everyone has the right to participate in their community and as such, participation should be positive and based on the persons’ individual interests and wishes.
People with disabilities are all too aware of the impact of their impairment. They live with it every day. But what they clearly struggle with is the way that impairment affects their interaction with the social and physical environment. They do not want mountains to be moved, but they do want to be able to go to the library or the
movies. (SHUT OUT 2012 www.dss.gov.au)
How society views impairment and disability has changed dramatically over recent years. The impairment a person has is a reality however the disablement is still caused by environmental and social barriers.
CASE STUDY: I JUST WANT TO GET INTO THE LIBRARY
I do not expect to get access to the pyramids or Uluru but I do want to get into all of the library and all of the community centre.
Access and inclusion means different things to different people. Processes and outcomes for access and inclusion cannot be prescriptive. One size does not fit all and one program will not suit everyone. It can be a complex, challenging and yet rewarding journey to meet the individual client where they are, identify their goals and dreams and work with them to plan to achieve those goals. There are also times where the goals are not too difficult to reach, yet barriers can still exist as demonstrated the following case study.
CASE STUDY: LITTLE GIRL AT THE GYM
The gym offered a separate class for kids with disabilities. I asked one of the teachers whether it would be possible for my daughter to attend one of the other mainstream classes.
She frowned and looked concerned and said that was why they had created the separate class. I said she was perfectly capable of joining in with the other girls. The teacher said “Well that’s okay for your daughter but if we let her in we will have to let everyone else in.”
These are not elite gymnasts. They are little girls jumping around in leotards having fun on a Saturday morning.
The attitude this mother faced from the gym teacher created a barrier for her daughter to experience a ‘normal place’ and activity that her daughter was very capable of participating in.
Planning for community inclusion and access must take into account the diverse needs of individuals and the nature, strengths, priorities and resources of a community. The common elements of access and inclusion are removing or reducing barriers to participation. By ensuring that information, services and facilities are accessible to people with a variety of disabilities.
A person’s ability to access information, services and facilities is affected by a number of factors, including the degree and type of disability.
(Planning for access and inclusion for people with disability. www.disability.wa.gov.au/)
CASE STUDY: ACCESS AND INCLUSION MATTERS
To appreciate the various aspects of access and inclusion, imagine that you are a person who uses a wheelchair and you wish to visit your local community centre. You are able to drive your own car and therefore do not have to use public transport.
When visiting your community centre:
You ring to check the accessibility of the venue and are assured that it is accessible. You arrive and park in an accessible parking bay, however you cannot get to the footpath as there is no ramped kerb from the parking bay to the footpath.
You make a long detour through the parking area and when you get to the front door find it is too heavy for you to open. You wave and someone opens the door for you.
You get to the reception counter. It is high. The receptionist sees you and comes out from behind the counter and answers your query.
You are directed to the enrolment desk for community courses. Your chair cannot fit under the desk, however the receptionist comes to your side of the counter and provides you with a clipboard so you can fill in your form.
You prepare to pay your enrolment fee. The cashier’s desk is upstairs and as there is no lift. You have to wait while the receptionist arranges for the cashier to come to you with a receipt book.
You wait in the foyer for the cashier and look at the noticeboard. You see a flyer and pamphlets promoting a community consultation about proposed changes to zoning in your district. As a resident you are interested and are pleased that the pamphlet holder is located where you can reach it. You notice the venue for the consultation and know that it is not wheelchair accessible.
This case study identifies fairly common barriers to information and services that would be in many communities.
BARRIERS TO INCLUSION
It is understood that people’s engagement with their community enhances their feeling of wellbeing and forges stronger community spirit. This is as much the case for people with disabilities as for the broader population. People with disabilities may be restricted in participation in some areas because of their particular activity limitation or impairment. But factors in their living environment, such as the attitudes of the people among whom they live, the constructed environment and the framing of social institutions may also act as barriers to participation.
People with disabilities are less likely to be employed than people in the broader population, are more likely to have lower income and may rely on a carer. Personal networks are particularly important in supporting the integration of people with disabilities into the wider community.
(Community Participation of People with a Disability ABS 2006)
Each person with a disability will face unique physical and intellectual challenges. They can also face many barriers to inclusion in the community.
In the case study Access and inclusion matters the barriers were as follows:
If a person with a hearing or vision impairment was visiting the same local community centre as the one used in the above example, they would have faced different barriers.
People with a disability can be non-verbal or have mobility challenges. They may be unable to control their own movements. This may be true even to the point of being unable to move away from painful or unpleasant sounds, smells, sights, or other sensations.
Barriers can be in any shape or form related to the type of disability or to cultural perceptions and misunderstandings or fear of asking for help. A barrier could be a carer or family member who does not believe the client is capable of achieving their goals and says “No, he can’t do that.”
At times issues will arise that you must refer to your coordinator according to organisational protocol and because they will be the best person to deal with your concern. In a case such as a carer causing barriers to the client plan to be carried out, some delicate discussions may be required between your coordinator and the carer.
Always contact your coordinator if you feel a client’s choices are being ignored or treated as unimportant. Reporting concerns is essential and the whole team must work together to make sure the client gets the best possible support. Saying “No”, shuts people down.
One residential service that cares for people with disabilities states at their orientation to new staff, “You must never say ‘You can’t do that’ when a client dreams of something they would like to try.”
They went on to give the example of an 80 year old man in a wheelchair that said he would like to sky dive. The response in this organisation would be “Wow that sounds like fun. How long have you wanted to do that? We can check out that activity together.” In this case the person may choose to explore jumping out of a plane or they may just like to go and watch or want to go up in the plane.
Overcoming people’s barriers to inclusion includes understanding and being able to describe and promote the person’s gifts and strengths. This will make the process of inclusion easier.
Remember the common mistake of thinking ‘being physically in the community’ is community participation. The fact that a person is physically present in a community environment does not make it community participation – ‘being an active part of community’ means community participation.
CASE STUDY: BARRIER OF FEAR OF PEOPLE
Bob was very anxious about strangers and the outside world and he had not been out of the house for six months. He was more and more lonely and missed being able to do things.
He wanted to re-join the community but was frightened to leave the house and his social skills had been slowly deteriorating as he spent more and more time alone.
The disability service team met with Bob and put a plan together to help him begin the process of re-entering life and enjoying being an active part in the community. The service plan objectives included the following:
? Building rapport: visit Bob at his house twice per week and engage in rapport building activities for thirty minutes, for four weeks.
? Ascertain his past interests.
? Do activities of interest.
? Start outings at one hour per week: explore other options such as recreation, work experience. (For three to six weeks depending upon how Bob was dealing with the social anxiety.)
? Extend outing to two hours per week: explore other options, recreation, work experience and volunteer work.
Once these were achieved more options were discussed and introduced including visiting possible work experience opportunities, visiting the office and visiting some of the group activities that were already in operation.
Three months later and Bob now participates on a one-to-one basis three times per week for approximately three hours each and two more have been introduced to his program. This has expanded the potential for further opportunities and for meeting his goals as they develop.
In this case we see the goal of the client established (re-joining community), then the team addressed the possible barriers to that goal (helped him identify his fears) and set a plan in place with the client to help him achieve his goals over time (slow integration and support).
The support team helped Bob, bit by bit, over time to overcome his fears, develop social skills and engage in the community. Overcoming the barriers and achieving goals had a big impact on Bob’s quality of life.
CASE STUDY: SUPPORT TO ENGAGE IN TRADITIONAL CULTURE
Namatjiri is a member of the Yankunytjatjara people. He was born with Spina Bifida and as is the custom, having a disability did not separate him from the clan. He is included within their extended families and able to assume kinship roles and responsibilities where possible. Namatjiri is now 16 years old and uses a wheelchair for mobility but due to the structure of his house, requires two men to lift him up and down the steps. The family would like to take Namatjiri on family outings, especially to take him out bush to learn culture. As Namatjiri grows, this has become more difficult due to the lack of accessible transport.
Support workers in the region understand how important it is for Namatjiri to be involved in family outings and helped the family overcome their reluctance to deal with government and other agencies by organising a yarning session to introduce the Yankunytjatjara people to disability services.
As a result, Namatjiri’s community were provided with an all-terrain, wheelchair accessible vehicle, the first of its type in the region. It is used regularly by Namatjiri and by frail and elderly members of his community.
ACCESS TO TRANSPORTATION
It is preferable that a person with a disability utilise public transport where possible as opposed to specialised transport services. The simple act of using public transport engages a person with a disability with the community and the community with the person with a disability.
Transportation however, can be a significant barrier as when we say accessibility it is meant to be applied to the whole journey from starting point to destination. Many clients will require support with mobility or accessing public transport such as: assistance getting up a few stairs; stepping over the gutter to steps; trying to manage a walker; impatience of driver; need for assistance from carer.
It may seem easier to call for a taxi, and it can seem easier for both the person with the disability and the support worker to use specialised transport services (Star Transport, wheelchair vans) even though they are capable of using the public transport system. Mainstream services however, should be accessed first and then disability services as required.
TRANSPORTATION IN METROPOLITAN AREAS
There are benefits to living in metropolitan areas in that most buses on the city networks have low floors or ramp systems. Stations along busways— roads dedicated to buses—have lifts, ramps and pathways. Additionally, tactile paving for people with vision impairment and hearing augmentation for people with hearing impairment are also in place in busway stations.
Many city councils have low-floor buses to allow easier access for all passengers. The low floor buses have:
New buses will also feature stability devices to improve the comfort of passengers in wheelchairs. For more information regarding travelling with wheelchairs and mobility scooters, visit your local council website. It could be possible to arrange for a low-floor bus to arrive at your client’s stop at an agreed time.
Train travellers using a wheelchair or mobility aid will find priority seating just inside the train’s doors. Some Queensland Rail stations have platforms that are slightly higher or lower than the train entry. If you need a portable ramp or help to board or disembark, wait at the assisted boarding point-indicated on the platform by a white wheelchair on a blue background and where there is a mat with a raised, tactile surface.
As a disability support worker you will develop local knowledge of the available transport options for the clients you work with. Each state rail authority have a mandate to make their services accessible. Here are a few examples you may wish to check out:
The Queensland Rail website also has useful information on travelling: www.queenslandrail.com.au The website specifically states that Queensland Rail is committed to providing rail services that enable all their customers to carry out their journey without barriers. Through their station upgrade program, they continue to improve their facilities and services to provide independent access for all. Customers with a disability, those who have walking difficulties or use a mobility aid can read access information under the following headings:
You will notice that the third last point is Accessibility Reference Groups and customer engagement. The Queensland Rail’s Accessibility Reference Group was established in 2003 and it aims to provide a forum to obtain community input into the development of non-discriminatory and accessible procedures, design work, construction and customer service.
Prior and proper preparation and proactive planning for participation prevents poor performance!
Accessible transport and physical access to places makes inclusion possible, however this is still identified as one of the major barriers to people with a disability accessing their community. Designing for inclusion is known as barrier free design or universal design and includes everyone regardless of age, ability or resources.
There are a lot of resources for people to research regarding public transport. Knowing where to access this information and passing it on to your client and their carers is part of your role. They can plan trips, timetables and know the costs all by some research and internet access either with or without support.
CASE STUDY: JOHN IS A DRAMA KING!
John, a 32 year old male with a diagnosis of Autism has always expressed an interest in drama as far back as his family can remember. John was very knowledgeable on the subject and joined the local review club.
As time went on he was invited to join the amateur drama group. This was based on the other side of town and presented John with transport issues. Using public transport was a confusing, frightening and expensive exercise for John.
A support worker linked him up with a local transport service who agreed to take John to and from the Amateur drama group each week. Soon John was required to attend rehearsals for an upcoming play twice a week. The local transport service could not accommodate John’s requirements.
By this time John had become an integral member of the group and by voicing his issues it was discovered that a member of the group lived in the next street and was more than happy to pick John up as necessary.
Setting goals too low for a person with a disability is limiting and can be patronising. To the other extreme, setting unachievable goals or very high goals will lead to disappointment and failure that could also be devastating to a person’s self-esteem. As a support worker it is important to assist the person with disability and where appropriate, their family, to select activities that will enhance successful integration
Like other Australians, people with a disability join clubs, go to the movies, do voluntary work, learn life skills, attend church and go on holidays. Selecting appropriate activities will enhance successful integration, participation, sense of accomplishment and worth as well as a sense of purpose.
BE A POSITIVE ROLE MODEL
The support worker needs to demonstrate a positive appreciation of their client as a person of worth. We demonstrate our valuing of a person in the way we assist and relate to the individual and in the way we talk to others about that person. Our actions and words communicate our attitudes.
The support worker can be an incredible asset or a hindrance and barrier to the development of their client’s own selfconcept and self-esteem. Likewise, the actions and words of a support worker can influence the attitudes, values and behaviour of people in the community.
Support workers need to provide support in a way that provides a positive role model and promotes development and maintenance of the person’s skills physically, emotionally and relationally. This is demonstrated in many simple things that a support worker does. For example the way we dress, interact and treat other models what is appropriate in community. How we communicate to the person with a disability and how we communicate to others about the person with a disability has a direct impact on how that person learns to view themselves and also interact with others.
The community provides opportunity for role modelling and imitation to occur. The person with a disability will be watching the support worker and learning from them:
Read the case study below about a woman who started an art class for people with a disability and the challenges she faced with some support workers.
CASE STUDY: SUPPORT WORKERS NOT VERY SUPPORTIVE
It was the first day of the new art workshop I had worked so long and hard to start. There were very few opportunities in the local community for people with complex disabilities to be creative and spontaneous through art. No one would be excluded; we would be an inclusive group welcoming the diversity of people.
The start time was 10 am and by 10 past 10, there were seven people and their support workers settling themselves into a circle for welcome and introductions. Some of the participants could introduce themselves by name and say a little bit about why they had come and what they like best about art. In other cases the support worker would introduce the participant.
We talked a little about the different mediums we would use and invited the participants to take a look around at the work stations set up around the room and see which medium they were most drawn too. Support workers enthusiastically assisted their clients to explore. Two support workers had engaged in conversation and their clients sat silently and patiently in their wheelchairs waiting for them to finish. “In a minute John,” one support worker said impatiently.
At 10.45am, two more participants joined the group; I welcomed them and their support workers warmly and listened as they complained long and loud about the difficulties they experienced getting here. I explained where we were up to and one of the support workers said, “Oh Peter wouldn’t be interested in any of that, it’s just so difficult to find anywhere to take him for community access.”
It occurred to me that the support worker could be the difference between a happy, successful outcome for the client or an unpleasant experience in their local community. When I advertise my workshops now, I add a little piece about the support workers role and how they might enhance the client’s experience.
The attitude and actions of some of the support workers in this case study were negative role models. The clients were not treated as valued people and there were negative impacts on the client and the whole group of people attending the art class. If this was your child, parent, brother or friend how would you respond?
Standard 2 and 3 of the National Standards for Disability Services states:
Standard 2: Participation and inclusion
You can take part in the community and feel included when you use disability services.
Standard 3: Individual outcomes
Your service supports you to make choices about what you want to do. You can work toward your goals.
These standards require service providers to implement policies and practices to ensure that:
ACCESSING COMMUNITY OPTIONS
A person’s level of participation in a particular activity may be influenced by their disability status. But it may also reflect the preferred activities of people of a certain age.
Going out to a cafe, restaurant or bar, attending a movie, theatre or concert and visiting a library, museum, art gallery, park, botanic gardens, zoo or theme park are other activities for which increased severity of disability is associated with reduced participation.
Yet increased severity of disability is not associated with markedly lower rates of participation in group activities such as recreational, cultural, community and special interest group, church or religious activities.
(Community Participation of People with a Disability ABS 2006)
Technological change over the past decade has created new ways to participate in community activity from home. Home computers, e-mail, chat sites and a range of other Internet sites offer potential for fresh modes of community interaction.
The disability support team is there to assist the person and where appropriate their family, to identify and access community options that will meet needs identified in the individualised plan and to establish connections through shared interests. Once an option has been decided upon, then it is time to establish strategies to make the option a reality. This needs to be done in a timely and efficient manner. The aim is for the person with a disability to develop the skills that will enable them to access their community as independently as possible.
This may include assisting people overcoming barriers in skill deficit areas by developing skills in:
These skills enable people with a disability to feel part of their community and to gain the confidence and ability to access community services.
CASE STUDY: VOLUNTEERING IS GREAT BUT WHERE?
Sal Jessop is 22 and she has Cerebral Palsy. Sal initially expressed an interest in assisting in a hospital or aged care facility. She was not particular about the type of work she would like to do but said that she got along well with older people.
Sal is very independent and lives alone with support from her family and a home support service. Sal and the disability service worker visited a local hospital and two aged care facilities. She was offered a position assisting in the hospital gift shop but was unable to take advantage of this due to physical limitations, e.g. lifting, bending etc. Sal accepted a volunteering position in one of the aged care facilities, reading to residents and assisting with craft and games.
At the end of the trial period, Sal continued to volunteer at the aged care facility and has now been there for nine months. Sal expressed that she “finally feels she belongs somewhere and is important to people”. She was recently awarded a certificate of appreciation by the facility which she proudly displays in her home.
ACTIVE IN LOCAL NEIGHBOURHOOD
Assisting the person, if appropriate, in becoming an active member of their local neighbourhood is very rewarding for the client as they see people they know and can interact in a much more personal and everyday manner.
Often the local neighbourhood presents a person with a disability with many opportunities to develop and increase their confidence to access the wider community.
Volunteering their services has been identified as an ideal opportunity to develop skills such as time management and teamwork that they can transfer to paid employment at a later time if that opportunity arises.
Something as simple as getting to know the neighbours and taking the time and effort required to make the connection can reap many benefits. Offering to look after the neighbour’s cat while they are away may lead to a request from others in the neighbourhood to look after their pet while they are away. Then maybe walking the dog while the neighbour is at work … the progression can be endless!
Local smaller shops where you are known by name are often ideal for a person with a disability to develop their money handling skills and develop relationships. Local organisations such as the Rotary Club or Lions club can provide information and support regarding the local community.
SEEKING SUPPORT FOR THE SUPPORT WORKER
Sometimes, the best laid plans go wrong. This doesn’t mean give up but the situation needs to be reviewed to establish what went wrong and what measures can be implemented to ensure success next time. The service coordinator will need to know what happened and be involved in planning how to move forward.
CASE STUDY: JOHN GETS A FRIGHT
John has started going to a music group on Thursdays. His support worker Karen has been travel training John so he can catch the train independently. John likes to plan his day and is meticulous about what time he should leave the house to walk one kilometre to the train station. Karen has been watching John from afar to ensure he gets on the correct train and so far John has been spot on.
Today however, John was bailed up by a big barking dog when he was walking to the train. John is afraid of dogs as he was bitten as a child. He freezes up then becomes very agitated. Karen sees that the dog is leaving and recognises that the fear (dog) is gone. She steps in to assist John to continue with his routine. By the time John arrives at the music group, he is calm and enjoys the session.
By sticking to John’s usual routine, Karen ensures that John still enjoys his music group despite a small unforeseen setback. But what if the setback could have been foreseen?
CASE STUDY: FORGETTING A TASK
The next week John continues to the train station to attend his music group. When he arrives to the turnstiles and tries to swipe his Go Card it is declined due to insufficient funds. John has no money on him and cannot board the train.
Karen has already left after seeing John enter the station. John has no option but to go home and calls Karen very distressed. She did not remind him last week to top up his Go Card. John is upset for the rest of the day and is angry that he has missed out on music.
Karen apologised to John and organised a meeting with the coordinator, John and Karen to discuss with strategies to put reminders regarding his Go Card somewhere that will increase John’s independence. The discussion was recorded and some more goals for independence were established.
Some issues must be reported to your coordinator straight away, such as:
There will be other issues that you will also need to refer on to others. You need to be able to identify aspects of involvement in the individualised plan outside your scope of knowledge, skills and job role and seek appropriate support. The type of issue that will fall outside the role of the support worker include:
Attitudes: A big barrier to the participation of people with developmental disabilities in community activities and organisations is a problem of attitude. Read the following extract from a support worker supporting an Aboriginal adult:
“I provide support to an Aboriginal adult living independently in a flat. He has had difficulty getting a taxi as he appears drunk (due to his disability). He has also been arrested by police as he appears violent (due to his disability).”
This man has significant difficulty participating in the community because of assumptions, negative attitudes and stereotypes. As a support worker these attitudes are something we can influence for the good over time, but cannot be changed quickly.
If your client is having issues make sure you raise this with your team leader and team so there can be discussions on how to best assist and support inclusion for that individual. Sometimes a solution can be found simply by consultation with the client themselves. Other times it may be necessary to refer the issue to your supervisor, another agency or specialised service.
CASE STUDY: NO WOMEN ALLOWED
Christine is a 16 year old lady with a diagnosis of Cerebral Palsy. Her speech is difficult to understand and very slow. She uses a wheelchair for mobility.
Basketball has recently been identified as her favourite sport.
To date Christine has been content to be a spectator but lately has expressed an interest in participating.
The local sports centre advertised wheelchair basketball - “A great way to keep fit, develop new skills and meet new friends. Players of all ages and abilities welcome.”
Upon inquiry, it was found that the wheelchair basketball team was made up entirely of males and, although they did not say so directly, it was implicated that a female would not be welcome, especially a female with no experience.
REPORTING CONCERNS AND SUGGESTIONS
Almost every area of community participation will result in maintaining and developing the existing attributes and skills of the person with a disability. For this reason it is necessary to continually update and review the strategies employed. A support worker is in the best place to review and notice changes in the client or if a plan is not working. This plan can have various names including a support plan, skill plan, client plan or an action plan.
Variations in support requirements must be identified and reported to your coordinator. It is essential for your safety and the safety of the client, that you observe your client before proceeding and contact your coordinator if you have any concerns about the their ability to participate, as identified in the plan.
The care cycle shown here identifies the step of reporting change or raising concerns. This is part of evaluation and receiving feedback from your clients.
People with increased dependence often need the opportunity to have disabilities reduced through effective review and the implementation of strategies to maximise their independence. (Shaw1998 pg120)
When the support worker identifies a change or concern, they will work with the person, their family and the disability support team to identify processes and aids requiring alteration. By overcoming problems you are reducing their disability because they have more ability to be involved and active in life.
EVALUATING THE ACTIVITY
The prime goal underpinning any monitoring and evaluation exercise in relation to person-centred planning must be to establish whether its overall aim of ‘good planning leading to positive changes in people’s lives and services’, is being achieved. (Ritchie et al, 2003)
Each activity should be evaluated in terms of both objective effectiveness and how it has been experienced by the person.
The quality of a plan can be evaluated in terms of:
Programs, processes and supporting structures can be evaluated in terms of whether:
Any concerns noted should be reported to the coordinator and also documented in the client notes as well as any other documentation as identified by the organisation. Having contacted the coordinator you might be asked to suggest that the client contact their doctor or you might be instructed to contact the client’s doctor or family member.
The sample provided of the weekly log is another type of report a support worker may need to fill in to evaluate programs and progress. Many organisations will have computerised versions of reporting tools that make reporting that much easier and accessible to people in a variety of different locations.
Always follow organisational policies and procedures of who to contact in the event of a client change of concern. After reporting your concern, you will need to monitor the client’s condition and evaluate the effectiveness of the change to the service delivery plan. Keep reporting information until the concern has been addressed with a successfully working strategy/strategies.
All written reporting should be:
Client name: Date:
My main goals this week:
Tasks and activities:
Meetings or special activities:
What went really well this week?
What did not go as planned?
Ideas to raise in my next meeting:
Staff name Signature Date
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