There are a wide range of disabilities in society. These range from the physical and very obvious, to those that are not physical and certainly not so obvious. Apparently, such disabilities are not obvious even to the so-called professionals that are hired especially to engage and help such people into employment.
My sister has autism. She got diagnosed as being on the autistic spectrum when she was about 12 years old but long before that it was known she had special needs. She was given a statement saying that she was a child with special needs when she was in primary school and the diagnosis of autism was a much later diagnosis. All through primary school she was not given the support she was entitled to.
She was meant to be provided with a classroom support assistant throughout school; this person was meant to help her through her work as my sister has always been slower than others in her classwork. This assistant was meant to be there on a daily basis but in both primary and secondary school she was rarely provided with the necessary support.
In primary school, there was support. The problem was that the support was never in. It took the school long enough to find someone to support my sister, then that person was always ‘ill’. This woman was getting paid to help my sister and in the end, the only support she received consistently was off another classmate. He helped her because the seating plan just happened to put that kind soul next to her. Otherwise, I dread to think how far behind her classmates she would have become. The point is it should never have come to the point where it was down to another child to provide the help my sister needed. If the woman being paid to help my sister and was consistently off sick, common sense should say that someone else should be put in that job. The person that was being paid to do the job was off for weeks at a time, surely this should have meant someone else should have been able to help my sister.
In secondary school, there was support. It was limited. My sister was told that students in wheelchairs took precedence over her needs. My sister needed constant support in the classroom. She was mocked and teased and lost concentration without having a classroom assistant present. Isn’t it disgusting how the department in my school dedicated to special needs told my sister that her needs were not as important as that of others? I agree that people in wheelchairs needed help getting around but my sister actually needed help in the classroom. My sister was also given a laptop to use by the school. At least, for a while she was allowed the use of a laptop. This was for the purpose of work. My sister’s handwriting has never been particularly great, and the premise was that she should have the laptop to be able to type quickly and hopefully keep up with the class. Eventually, the staff within the department decided that a child with a more obvious (a physical disability) needed it more.
The message the Special Education Needs (SEN) department, always sent was that if it wasn’t physical it was not important. The classroom assistants were always being switched over- that was on the days she actually had an assistant. My family have kept records on how many times a week she had an assistant and it was very rare if she had help on a daily basis. I should also describe another instance when my sister thought she wanted to be a beautician.
My sister was going through a phase where she wanted to be a beautician. We suspect it had something to do with another girl in her class who wanted to be a hairdresser but that is not the point. My sister told the school about this desire to work in the beauty industry and they seemed to want to support her. They even told her of courses that were available and that one was in Catford. They told her a start date and time but there was something slightly off about it all. So my Dad phoned the place where she was meant to be attending. They had never heard of my sister. She had no place there and her hopes were dashed.
That was just another thing in a long line of disgraces. There is very little help available for people who have disabilities. There is even less help available for those who have a disability that isn’t immediately obvious. My sister can walk and talk but if you spend a little longer with her you will realise that she is affected on a daily basis by her disability. The lack of help available during school was just the start of a long battle. To get anything for my sister we have always had to fight.
We should not have to fight so hard to get the necessary support. It should be readily available. The reality is very different. No government in recent years has done anything that has had any impact on improving the position of my sister. In fact, with the cut backs things have only been made worse for people with disabilities. With funding cuts, various agencies that have been created and funded by government are now running on a skeleton of staff. Many of these agencies also have to find private support funds because government is not helping.
The staff working for these agencies are not fully trained in the nuances and needs of those with autism. Many are just young people who work with people with disabilities to get that ‘I’ve done work with the some of the most vulnerable people in the community’ tick on their CV. It is work they deign to take on but not many actually want to do. For many it is a stepping stone to further employment. Truth be told, I can’t blame these people who do this type of work for those reasons. It can be hard to be around people with autism but more training and understanding is needed. Sometimes the simple ability to listen is needed.
My sister is now looking for work. She has done various BTECs and other courses to make her more employable. She is getting help from some of the few agencies that exist to help people with disabilities but even though these agencies have been set up to help people with disabilities, they seem to not hear the needs of those they are working for.
There are two recent examples where they have sent my sister for job interviews at the wrong time. I will not name the organisation in question at this present time. I am hoping my family will file a formal complaint against them soon. To send someone to an interview at the wrong time makes that person look foolish. The same organisation has also applied for jobs on my sister’s behalf. This means they have not asked her permission. This alone infuriates me. To not ask my sister’s permission is to deny her a very simple right- the right to choose. They have been applying for jobs that are inappropriate. Equality is not applying for a job for a disabled person on the basis that an able person could do it. My sister has her limitations. Shift work that starts at 6 in the morning is one of them. My sister is scared of the dark. The time she would have to leave the house would mean she is always travelling in the dark. She also has difficulty in travelling. She would have to remember the names of the stops and be awake enough to hear them as that is her only chance of getting off the bus at the right stop.
I understand that many people do early morning shift work. I do understand that. However, not everyone is suited to those types of jobs. Some people are better suited to working day time hours. That decision was taken from my sister when a junior office member applied for this job, obviously without reading what the job entailed and my sister’s file.
It would appear that the people who are employed to work with those with disabilities are not as conscientious as we would like. There are some who know their jobs inside out. There are many that do not know what they are doing in the workplace. They do not have the necessary understanding of the people they are meant to be working for. This disgusting trend needs to stop. Listening to the needs of people with disabilities would be a great start.