Musings from a deaf campaigner

A man with a mission, a soapbox AND a placard…

Archive for December, 2011

My “Campaigning for Deaf Children” Christmas wish list

Posted by Ian Noon on December 21, 2011

As a campaigner, what would I like Santa Claus to give deaf children for Christmas?

1) Greater focus on making sure deaf children start primary school on a level playing field with other children. The newborn screening programme is now over 5 years in and every child born deaf should be being diagnosed within the first few weeks of life. Late diagnosis was a major barrier, now removed. And deafness isn’t a learning disability. Yet government figures suggest little change in the early years attainment gap. So what’s going on? And what needs to change to close this gap? In my view, there’s lots of theories and lots of best practice suggestions but no concrete answers or explanation of why the gap isn’t closing. I’d like Santa to bring us closer to some solutions.

2) Local authorities stop picking on deaf children’s services for cuts. It’s a false economy; denying deaf children support the help they need now means a generation of deaf adults failing to achieve their potential and make a full contribution. It also means parents of deaf children will push for statements for special educational needs, and the legal entitlements this brings. NDCS’s Save Services for Deaf Children campaign has information on campaigning to protect services. There’s lots of ways councils can make savings without impacting on services: such as working with neighbouring council’s to share and pool resources. I’d like Santa to knock heads together in council offices. Or at least make sure they get no presents this year.

3) And something for the stocking. The BBC, ITV and other programme makers stop using live subtitles for pre-recorded programmes. Charlie Swinbourne’s blog explains the fury caused when the final of the Young Apprentice had subtitles out of sync with what was being said. “Technical problems” are often cited. More likely, the programme editors were too busy faffing about with last minute changes that there wasn’t enough time to prepare subtitles. This denial of access is just not on. I’d like Santa to say to whoever is responsible for these kind of “technical problems”: you’re fired.

It’s a pretty modest list of requests, I think. What else do you think we should ask Santa for?

Otherwise, all that remains is to wish everyone who reads my blog a very happy Christmas and prosperous 2012. I hope you’ve enjoyed reading the 2011 blogs and see you next year.

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How I started to lose faith with the Government on deaf children

Posted by Ian Noon on December 16, 2011

I can’t really pinpoint the moment when it happened. I started with really high hopes. But slowly, I’ve personally been getting more and more exasperated with the Government. The trickle of inconsistencies. Assumptions. And, above all, the lack of urgency on protecting help for deaf children when 1 in 5 councils are making cuts to the vital services on which deaf children rely.

My main gripe is the increasing tendency for the Government to say it’s a “matter for local authorities” to arrange provision for deaf children. That councils are expected by the Government to protect funding for “vulnerable learners”. If deaf children are not getting the help they need from specialist support services for deaf children and/or where massive cuts are taking place, it’s the nasty councils’ fault. Don’t blame the Government.

The Government can’t do everything, obviously. But at the end of the day, where else does the buck stop? The Government has the legal powers to intervene in specialist support services for deaf children. But even when faced with evidence of councils making swingeing cuts to vital services and not following legal processes, it has seemed quite relaxed about the impact on deaf children. Whenever asked to intervene, we hear that the Government can only intervene in “limited circumstances”. What those circumstances are remain a mystery – the Government has refused to be drawn, despite several attempts.

I wouldn’t mind so much if this was a principled approach on not intervening. But it isn’t. Instead, there’s a rather arbitrary way of categorising what’s for local authorities to sort out and when local authorities can’t be trusted. For example, the Government appear quite unapologetic about apparently imposing academies on poor performing schools, regardless of the views of the local community – if this article is anything to go by.

The Government’s main defence is that they have a massive programme of reform underway with the Special Educational Needs and Disabilities Green Paper. But many of the proposals will only benefit the quarter of deaf children that have a statement. The proposals come with a lot of risks that haven’t yet been properly assessed or mitigated. Throughout it treats children with special educational needs as a homogeneous group; there’s little in it that is directly focused on the unique needs of deaf children. But most importantly, if so many councils are making cuts, what’s going to be left by the time the Green Paper is implemented?

The article I mentioned earlier includes this quote from a Department for Education spokesperson:

“We can’t just stand by and do nothing when schools are sub-standard year after year.”

It’s a shame they seem content to stand by and do nothing for deaf children when their services are being slashed.

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Is the Prime Minister keeping his promises on help for disabled children?

Posted by Ian Noon on December 13, 2011

One of my favourite campaigning organisations, Every Disabled Child Matters, have launched a new campaign action. They are asking people to write to the Prime Minister to give some good news to families with disabled children for Christmas.

In the days before David Cameron was busy pulling hissy fits in Europe, he promised that he would “never do anything that would hurt disabled children.”

This begs the question why the Government is pushing ahead with changes to disability benefits that effectively amount to a 50% cut in help for families with disabled children. As Every Disabled Child Matters explain, currently, low income and out of work families who claim DLA on behalf of their child are entitled to a ‘disability addition’ worth £53.62 per week. Families with a child in receipt of the high rate care component of DLA also receive a ‘top up addition’ worth an additional £21 per week. Proposals under the Universal Credit will see lower benefit ‘additions’ drop by over 50%. It might not seem much but to families already struggling without support, this may push them over the edge.

The worse thing? By the Government’s own admission, this change won’t have any impact on the overall benefit bill. That’s right, the cuts are completely unnecessary.

I’m fast becoming somewhat disillusioned about the widening gap between what the Government say and do on help for deaf and other disabled children. If there’s ever a time for cynicism to be dashed, it’s just before Christmas. So fingers crossed, the Government come up with a better gift for disabled children in the UK today.

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What are auxiliary aids and why do they matter?

Posted by Ian Noon on December 6, 2011

I was having a rummage around the attic in my parents’ house over the weekend and came across a blast from the past: my old radio aids from school.

My radio aid clipped onto my belt and had a wire that plugged into my hearing aid. My teachers or my mum would wear a microphone around their neck. And hey presto, everything said would be amplified remotely into my hearing aids.

They weren’t perfect. I could only hear what the teacher was saying, not my best friend sitting next to me. They sometimes amplified wider background noises. And, of course, the teacher would sometimes forget to turn the microphone off. Let’s just say I’ve been subject to conversations in the staff room that I really shouldn’t have.

But it did the job. I could follow lessons in the classroom. And my Mum could do her job and help me develop language. And other children loved the fact I could give them a 5 minute warning of when the teacher would be back from the staff room.

Radio aids like mine are often cited as an example of an “auxiliary aid”. It sounds like something from Star Trek but they are basically things that help disabled children in the classroom. They could also include, for example, communication support workers. Lots of deaf children get this kind of support because they have a statement of special educational need that says this help is needed. But most deaf children don’t have a statement and therefore no entitlement to this help if they need it.

Around 18 months ago, the previous Government passed a law, with cross-party support, that would legally require schools to provide auxiliary aids as a “reasonable adjustment”. In other words, schools better have a very good excuse if they didn’t provide it, if needed. A consultation has just closed on whether the Government should go ahead and bring this law into force. Better late than never.

It’s a really important change to the law and will introduce a new safeguard to help sure deaf children get the help they need. I needed it 20 years ago and deaf children today need it now. If the Government don’t hurry up and bring it into force, I’m going to seriously question their commitment to helping deaf children.

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Speaking to media about NDCS’s Save Services campaign

Posted by Ian Noon on December 1, 2011

Image courtesy of Remark!

Sometimes I wonder if the N in NDCS stands for nagging, judging by the persistence with which some people have been trying to get me to resume blogging about campaigning for deaf children. Well, NDCS is nothing if not determined.

Where have I been? It’s been a busy few months. Lots of councils across England still seem intent on slashing the services upon which deaf children rely on to do well. Depressingly, a few have joined my list in the past few weeks, and I’m not talking about my Christmas card list.

I also lost my media virginity by doing my first TV interview, for the Hub, a programme commissioned by the innovative British Sign Language Broadcasting Trust. Thanks to lots of patient prepping from NDCS’s media team, I was allowed to answer a few questions about NDCS’s Save Services for Deaf Children campaign and managed to slip in the key messages that sum up the issues. Hopefully, the answers helped spread the word about the campaign and motivated a few more people to support the campaign. And thankfully I managed to get through the interview without splurting out some expletive about councils making cuts.

Should I be allowed in front of a camera again? Judge for yourself online – I’m on programme 8.

I promise not to leave it too long before my next blog about campaigning at the Nagging Deaf Children’s Society.

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