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Education Cuts & Protecting the Vulnerable – Budget 2011/2012 – Aberdeen

 

10th November was the day that the council in Aberdeen voted once again on the budget  cuts.

The statement is here for anyone local to Aberdeen http://www.aberdeencity.gov.uk/council_tax_benefits/council_tax_home.asp

As with the other statements which will be being released up and down the country, they make for quite light reading, touching on issues, and promising to deliver on what looks like good practice.

Some of the main priorities in Aberdeen are :

  • providing services for the most vulnerable people;
  • ensuring all schoolchildren reach their potential;

Initially, the council were planning to remove 50% of the PSA (Personal Support Assistants)  in classrooms across the city, in both primary and secondary provision, and that is in an area where inclusion has been heavily carried out with PSA support.  This was after already losing 300 at the last round of cuts.

There are children being excluded for not being able to cope now.   How much is that going to increase when more support is taken away, is anybody’s guess.  Excluding is easy where the staff cannot, and will not take responsibility for the issues that arise from placing children inappropriately.

Our children in mainstream schools now share classes with the ASN children who would, probably in our generation have attended the stand alone special schools, or childrens institutes in the area.  We have a high PSA ratio in our schools, as they are now there supporting the children who need help.  I have heard many excuses surrounding why they should be cut, from people outraged that they are pinning up things to make classes look pretty, to sitting “babysitting” children with bad behaviour.

Both of these arguments are irrational.  Yes, teachers could pin up the sticker charts, the projects, the work that the children are doing, but then we are eating into teaching time.  What do you really want??    And as for the “babysitting……..    From my perspective, in a school where there are children not coping, there will be bad behaviour.

The other options for those children struggling without support are limited to quietly not receiving much of an education, and exclusion.  With the right support, they are living a full life, and integrating with the school.  I thought that was the whole point!!!!!!!   Maybe I misunderstood the point of integration / exclusion all these years.   Any arguments, or issues people have with PSA’s should be taken up with the individual headteachers who allocated them, and they should not be not used to denigrate PSA’s overall.

One of the options tabled was to cut music in schools and another was to amalgamate two secondary schools, which was sensible in terms of the school roll.   Both of these options raised high profile campaigns, that parents AND the children themselves fought.   The councillors very quickly decided that these options were going to cause them some problems, and might likely affect their future election prospects.  Both issues were taken off the table.

Taking those issues off the table, meant that for education, there needed to be cuts from somewhere.   The other potential eduction cuts that run deep in Aberdeen included

  • Increasing special school class size from 1:7 to 1:10  (this means losing approx 27 ASN specialist teachers)
  • Cutting PSA’s between 50 – 100%  in mainstream  (we are talking possibly 300 more support staff)
  • Not fulling educational psychologist positions (so reduced access to support for additional support needs)

Now, I am not being unreasonable to say, that doing all of this up front, without the training of the staff who are left to cope, is madness.  All I can see are the unsupported children struggling, and with no prospect of assistance.  These children then add to the social care system, but sorry, that is being cut as well.

And in the process, hundreds of thousands of people up and down the country are being made redundant in the name of paying back the debt our banks got us into).

Now who, in the cutting process, is going to be left to pay the debs off?

The demand on benefits is increasing with the redundancies.  With less money to spend, more people are having to give up their small businesses – oh wait, that means yet more on benefits again.

Now forgive me for being pessimistic, but the people making these decisions don’t live in the real world.  They live in their comfortable, well paid little bubbles, with their comfortable and well paid little friends, living their perfect little lives, with nannies, cooks, cleaners and bottle washers on tap.

Those of us in the general public can’t fight the upper classes, but we have  to live with their bad choices.  I have nothing but respect for the parents in the constituencies who decided to boycott school for a day in protest at the education cuts.    All power to them.

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Cuts to Services for and of the Disabled

With one special needs child, and two others who need some assistance at school, but who cope with a little extra support, it fills me with horror to read the stories of what is going on around Scotland this year.  The support staff from different authorities seem to be targetted.  The cuts are savage, and directed at the welfare of the disadvantaged population. 

When other cuts, such as music have been mentioned, people have been up in arms and complaining about it in huge numbers.  It is sad that ASN children are not seen as an attractive enough issue to warrant the public rising up to protect them.

I am ashamed of my country, my government, and my local council.

There, I’ve said it.

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Disability Injustice and Cuts to Services

I was absolutely astounded to read the case of  Riven Vincent, but not surprised.

In case you have not yet heard of her, or read the news over the last couple of days, she has asked social services for residential care for her daughter, as she can no longer cope at home.    She asked for additional respite to help her, and it was refused. 

For one, I am not surprised that this has happened, and I do believe that it is going to happen more and more often as the cuts that the Government send down to local councils bite.  In my own local council, there are several cuts to disability and ASN childrens services which have been given the green light for swathing cuts.

People who have never lived with severe disability, or mental illness, have actually no idea of what stresses they and their carers are often under.   The long term effects of people who do not access help are far reaching.

1.  On average, it can take years for requested services to come into effect.  Thats if they are offered at all.  Contrary to popular belief, it is quite difficult to be allocated a social worker for a disabled child, even if you ask for one.

2.  DLA to which disabled people are entitled, make applicants jump through hoops, and expect people with disabilities to manage to complete a novel sized application form intelligently.   Many give up trying to get it. 

3.  Parents with disabled children are often not in a position to fight for their children, as they are exhausted by the day to day caring.  They are an easy target.

4.  If services, respite and additional care is not offered when it is needed, suicide rates and passing off to care services will increase as people cannot cope in their homes.

The fact that Riven Vincent has asked for her daughter to go into care is not surprising.  She has other children to look after, a huge workload with Riven, and being denied enough support for her to be able to nurture her family properly.  

I do not pretend to understand how hard it is for her with a doubly incontinent child, not enough incontinence pads, and insufficient support to allow her to care for her other children.  I know how hard it is for me with my family, and my heart goes out to her, and those like her.

She gets no sleep, and it cannot carry on like that.  I have huge respect for her, and the fact that she has asked for help shows how strong a lady that she really is.  

Leave the political stuff aside.  This is a family that is struggling, who asked for help and were denied. 

I wish Riven Vincent all the luck in the world, and I hope that she gets all the help she deserves. It sounds like an awful situation that she can neither move forward, nor backwards from, unless someone takes charge to help her.

Moving the blame back onto local government is a disgraceful cop-out.

Thats my opinion.

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Saving Education Services in Aberdeen – Cuts for ASN affect ALL Children

I’ve become aware of a campaign running to save services for ASN in Aberdeen.  What I have read so far is almost unbelievable.    Being a parent of ASN, this is something that affects me daily, and is an issue that affects all children in every class when PSA’s are taken away.

I am not yet sure of the full extent of the cuts, but I will be planning to find out by tomorrow.  In the meantime, I am aware that even such a small thing as putting a link up to the petition being run, might in some small way, help with this campaign.

Here it is:

Save ASN Services Petition

http://www.gopetition.com/petition/41203.html

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Communications Shutdown – Autism Awareness – Not for me.

Today you might have seen lots of posts, or information about the communication shutdown.
It is an appeal to raise awareness of autism and how it affects those affected.  Unlike those of us who are neuro-typical, many children on the autistic spectrum have difficulty communicating their feelings and thoughts in an appropriate manner, and in an appropriate fashion.

The idea of the communication shutdown is to have people who have no experience of autism feel the frustration that communicating with the world entails, by not logging onto facebook or twitter.  They also support the campaign by using the application which will post their involvement to their accounts, and donating to the campaign.

 The truth is, that simply not being in contact with social media is not even a quarter of the way to feeling the frustration that people on the autistic spectrum feel every second of every day of their lives.  The people who are taking part in the shutdown have the luxury of being able to carry on with daily life and take enjoyment from doing the most basic of tasks, and will more than likely simply replace their online activities with something else productive at home or at work. 

A good idea of how frustrating it can be for some of these children is to try reading a book, and imagine that someone is placing a black sheet of paper over the paragraph every 5 seconds as you try to read it, and then see how frustrated you get with it.  I am all for autism awareness, and the money that is raised by the people who take part in the shutdown will be a welcome addition, although I suspect the ones who take part are those who are already involved with autism on some level.

The National Autistic Society in the UK is not an official partner of the project, but wishes them every success.   http://www.autism.org.uk/get-involved/campaign-for-change/campaign-actions/communication-shutdown.aspx

As a parent with two children on the spectrum, and looking like the third is as well, I rely on the NAS for much information and support.   Locally, a group of parents decided to take action on the fact that there were no clubs to take our children to, and we began a local parent led group which provides a play club for up to 36 special needs children.   

While I wish the campaign all the success in the world, the dangers of  large scale campaigns like these,  is that those of us who struggle to provide suitable playschemes and groups on the ground may find it difficult to source funds to help these children on a practical level.   The flip side of the coin is that every pound raised is another pound spent on helping our children indirectly.  It really is a double edged sword. 

My other reason for not directly supporting the communications shutdown is that the internet is my lifeline.  Living with children on the spectrum (or indeed any child with significant special needs), may be a difficult existence.  Twitter, for me, means the freedom to indulge in general chitter chatter that is not practical in daily life. 

Often parents, guardians and carers have little or no outlet for their own frustrations and difficulties.  Friends often fall by the wayside one at a time as their children get older and become more demanding on time and ability to socialise.  If taking away the communications network for even a day could have a potentially devastating effect for even one family, then the campaign is not for them.

On a day to day basis, life here is not easy.  One of my sons is struggling at his new school and may need moved to a more suitable environment.  Being in crowds causes anxiety which translates to disruptive behaviour.   Meltdowns occur on a regular basis, but we are used to those.

Would I change my children if I could.  Yes and no.  I have been asked in the past, and have sometimes heard parents of special needs children say that they would not change them for the world.  I would not part with my children, no matter how hard work they are, but at the same time, there is always a point in every day where I wish that they could have the type of life that a neuro-typical child has.  

You have to excuse the use of the words neuro-typical as I am not really sure how to refer to the children who do not have special needs.  The use of the word “normal” would seem to imply that special needs children are “not normal”, and this is simply not true as they are indeed “very normal” in their world.

I will leave you with that last thought as this is indeed a very tricky subject and one which has raised much talk and discussion today.