Making deaf children matter

Musings and blogs from a deaf campaigner

Posts Tagged ‘Personal Independence Payment’

Pushing the disability ministry to take disabled access seriously

Posted by Ian Noon on July 17, 2013

A minor little campaign victory achieved at NDCS the other week: the Department for Work and Pensions (DWP) accepted that deaf people should not be forced to use the phone to make a claim for the new Personal Independence Payment (PIP) benefit. Usually, I do a little jig and get the Bucks Fizz out when a campaign victory has been achieved. But this was a very small, unsettling one and which left an unpleasant taste in the mouth.

How come? Because the only real concession is that deaf people have been given a postal address that they can write to to ask for a paper form instead.

And why is it an unsettling one? Because it was such a small issue that should absolutely never have been an issue at all. And because it’s revealed some rather interesting things about how the Department for Work and Pensions, which has responsibility for disability issues across Whitehall, seem to approach issues around access for disabled people.

For example, who at DWP thought it was OK to propose that the only way that a disabled person could make a claim was via a telephone?

If an online system is being created, why not wait until this is developed before rolling out the new benefit so that more people can access?

And, the worse one of all for me, who on earth thought it was acceptable to suggest that if a deaf person couldn’t use the phone, it didn’t matter too much because they could ask a family member to call DWP for them?

Something has gone very horribly wrong when the Minister and officials responsible for disability have to be hectored at some length and for some time to take a tiny step to improve access.

Official were seemingly operating in ignorance of the Equality Act 2010 and its central tenets to remove discrimination and promote access for disabled people. Throughout the whole exchange with DWP, it was abundantly clear that the needs and the convenience of their ‘system’ was far more important than the physical access needs of disabled people.

And this is before we’ve got to the raft of spending and welfare cuts that are going to impact on disabled people (and which the Government refuses to assess the impact of – another legal requirement). This was a small issue. But it said big things about the Government’s wider attitude towards disabled people.

I despair. It makes me angry and depressed. But equally it makes me more determined to keep challenging the Government. And I hope others do too.

P.S. If you’re not sure what this new PIP benefit is all about, both the National Deaf Children’s Society and Action on Hearing Loss have recently produced some information resources on PIP for deaf young people, parents and deaf adults.

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Welfare cuts targeting deaf people?

Posted by Ian Noon on December 17, 2012

Well, it’s official. The Government thinks that deafness is just a ‘minor’ disability. A piffling little thing of no consequence or cost.

Last week, the Government confirmed the arrangements for the new Personal Independence Payment (PIP) benefit which is replacing Disability Living Allowance (DLA) for disabled people over 16 (DLA is safe for children – for now). In doing so, they confirmed that deaf people will be among those hardest hit. Here’s a National Deaf Children’s Society (NDCS) story on it.

The older lower rate for DLA is out which will hit a lot of deaf people.

And the criteria has been worded in such a word that basically you have to be a sign language user reliant on interpreters all the time to get even basic standard rate of PIP. Some estimates suggest around 90% of deaf people don’t use sign language as their main form of communication in the home.

To add insult to injury, the entire claim process is predicated on the basis that all disabled people can use the phone to request a form. Forget about such quaint things like webforms or email.

From next April over 600,000 disabled people will start to see their DLA cut or removed. That’s over half a million. And yet the announcements got hardly any coverage.

MPs and Lords will have to approve the changes at some point early in the new year. If you’re angry about the fact the Government doesn’t seem to understand deafness or think that it carries any significant extra costs, then get in touch with your MP and ask him or her to oppose the changes. If you get DLA now, explain to your MP what you use it for and what life would be like if you didn’t get it.

And don’t forget, if the Government thinks they can get away with this, deaf children and their families will be next.

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