Archive for the ‘Budget’ Category

Science funding is being threatened on an unprecedented scale. It’s so bad, scientists are leaving their benches and laboratories, and campaigning against the cuts. The Science is Vital campaign is encouraging everyone who cares about science to contact their MP, sign their petition, attend the demo, or lobby parliament.

Therefore, on 15th September I duly sent this brief email to Julian Sturdy MP, my constituency MP.

Dear Julian,

I hope you will sign EDM 707. Many of your constituents (myself included) work in science both in Universities in Yorkshire, and in related scientific industries. Please assure me of your commitment to science funding in the UK by signing this EDM.

Here is the reply I received from him. Disappointingly, he made no mention of the EDM I had asked him to sign. It was a boiler-plate response, incredibly similar to the speech made a few days earlier by Vince Cable.

Here is the reply I sent last week – I’m still awaiting a response.

Dear Julian,

Thank you for your reply dated 20 September 2010, regarding science funding. I’m pleased that you acknowledge the value that science makes to the economy, and that scientific research has its own merit.

I disagree with you about the need for the sector to do more, with less however. Scientific funding in the UK already gets less funding than many other OECD countries, and yet ‘punches above its weight’ with 10% of the best publications coming from the UK. The sector is deeply financially constrained, with funding levels at the same as they were, in real terms, in 1986. You argue that the output measure is what matters, not the input measure – but without that input, that investment from government, scientists will leave the UK, and internationally excellent scientists will not chose to come to the UK. The output measure depends on having excellent scientists carrying out excellent research, and without the appropriate input that will not happen. The reputation of the UK as a place to do science, will be immeasurably damaged by cuts that are out of step with the international consensus.

Research in the UK is already rationed by excellence. Speak to any member of a grant committee in any research council, and they will tell you that much excellent research is not funded. I suggest you investigate how many top rated grants were not funded in the last couple of years. In the RAE2008, 90% of the research submitted was rated as internationally recognized.

Finally, I would like to challenge you on the assertion that ‘there is no justification for public money being used to support research which is neither commercially useful nor theoretically outstanding’. What does this mean? It is not always clear in advance how research will come to be commercially useful. For example, research in pure maths concerning prime numbers could never have been anticipated to be as useful as it is – but without that research, we would have no secure transactions on the internet. If it is obvious that work will be commercially useful, shouldn’t it be funded by industry, rather than by the taxpayer? It also impossible to determine in advance if research will have an impact on theory – theory may be wrong, or the experiment may fail – how can you anticipate what will be theoretically outstanding?

Please engage with the scientific community within your constituency, and at Westminster, to form your own opinion on the importance of science. Please support the science is vital campaign (http://www.scienceisvital.com), and attend the lobby of parliament on 12th October. Please sign EDM 707 and EDM 767.

Thank you for your time,

Will he engage? Will he make his own enquiries, and form his own opinions, rather than simply supporting the party line? I’ll let you know when he replies!


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Because the Department of Health thinks you should! Here is a photo of a poster from an unnamed source at the Department of Health.
DH poster

I don’t know where to start with what is wrong with this. Patronising, sexist, a waste of money. Searching and tagging is better than folders anyway. And what category are the shoes in the open locker?!

Perhaps this sort of thing should be cut… anyone feel like a FoI request to see how much it cost?

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I n a previous life, I worked as a welfare rights adviser and eventually managed free legal advice services for carers and disabled people living in one of the poorest London boroughs.  Much, much of our work involved resolving problems with claims for Disability Living Allowance (DLA).

In my time I have been to tribunals for a woman with breast cancer who was undergoing chemotherapy (her condition fluctuated), a boy with ADHD who was in danger of causing significant harm to himself or one of his younger siblings if he wasn’t supervised all the time (his GP was an ADHD sceptic and gave him a vague report), a diabetic baby who needed blood tests every two hours and insulin injected accordingly (the decision maker argued that this was not significantly more care than you would have to give a baby of the same age), a housebound woman with arthritis and high blood pressure who used to pass out on her way to the loo at night (she had tried to put a brave face on during her medical assessment), numerous people with non-specific pain issues, numerous children with emotional and behavioural problems who don’t have a label (yet).

I also used to train volunteers in completing the forms.  Completing the forms was arduous, taking at least 3 hours at a time.  It was emotionally draining as it focused on what the person couldn’t do, not what they could.  It was repetitive.  The forms had to be signed by a professional, the professional would have to know the person well and the professional would need to know how to put things in the right way so that the decision maker would understand the extent of the difficulties.

The disabled person would have to include the name of any other specialists they had seen and the DWP would often write to them to get a report from them.  Disabled people would have to photocopy reams and reams of paperwork including statements from school, cardiology reports, psychology reports etc.

Most disabled people would have a home visit from a Dr working on behalf of the DWP.  I have seen it written on such a report: ‘Mrs  X was able to make me a cup of tea’!!!  The Dr would spend a very short amount of time with the disabled person before submitting their report and would often make judgemental statements about the housing conditions and so on.  In my experience, they often got it very, very wrong.

Ordinarily, I would be dancing a jig at the news that the government are planning on getting rid of the forms (although it seems this is now vague, and the initial forms are likely to remain as the first ‘filter’ for claims).  Those bloody forms are the bane of the lives of any disabled person, or any person caring for a disabled person.

I’m not dancing a jig though.  I’m really worried.  I find George Osborne’s words chilling:

That brings me to another universal benefit, Disability Living Allowance.

Mr Deputy Speaker, it is right that people who are disabled are helped to lead a life of dignity.

We will continue to support them, and we will not reduce the rate at which this benefit is paid.

But three times as many people claim it today than when it was introduced eighteen years ago.

And the costs have quadrupled in real terms to over £11 billion, making it one of the largest items of government spending.

We will introduce a medical assessment for Disability Living Allowance from 2013, which will be applied to new and existing claimants.

This will be a simpler process than the complex forms they have to fill out at present.

That way we can continue to afford paying this important benefit to those with the greatest needs, while significantly improving incentives to work for others

This is so breathtakingly ill-informed I’d be disgusted if a backbencher said it, never mind the Chancellor of the Exchequer during  a budget!

First off, DLA was introduced as a compensation to disabled people because they have a higher cost of living (and quite honestly, often ends up going to straight back into the coffers via charging for social services).  It is not an earnings replacement benefit, it stands alone!  It is not means tested or taxable and disabled people who work are able to continue getting payments.

Given that The Shaw Trust found out that between January and March 2009:

  • There are currently 1.3 million disabled people in the UK who are available for and want to work, that only half of disabled people of working age are in work (50%), compared with 80% of non disabled people
  • Employment rates vary greatly according to the type of impairment a person has; only 20% of people with mental health problems are in employment
  • 23% of disabled people have no qualifications compared to 9% of non disabled people
  • Nearly one in five people of working age (7 million, or 18.6%) in Great Britain have a disability
  • The average gross hourly pay for disabled employees is £11.08 compared to £12.30 for non disabled employees.

I think it would be fair to assume that disabled people are still experiencing a degree of discrimination in the workplace.  This needs to be tackled before cutting off disabled people’s money.

Further, the only benefit which is available to full time carers, Carers Allowance – paid at a woeful £53.90 per week, hinges on the disabled person getting either the middle or higher rate of the care component of DLA or Attendance Allowance (DLA for the over 65s).  Carers save the treasury the equivalent of a second NHS. If carers are forced back to work because their benefits stop, who provides the care to the disabled person?  The state.  I can assure you that this will cost far more than £53.90 per week.

According to Carers UK research, it takes carers an average of two years to identify themselves as a carer.  Carers are often isolated, and their own health suffers as a result of their caring responsibilities.  They are not caring for the sake of a bit of extra cash, many of them have to chose between food and heating.  They are caring because they love the person they care for.

It has since been reported that George Osborne is hoping that 1 in 5 claims for DLA will stop as a result of the new regime.  As he said in his budget speech, payments of DLA have quadrupled since it first began.  What he didn’t say is that the Disability Rights Commission estimate that between 40-60% of people who are entitled to DLA do not make a claim!  They either have not heard of it or do not think they would be eligible.

Around 50% of DLA claims are turned down.  Of these, around 50% go to tribunal, and most people win tribunals.  What does that tell you?

Of course there are people who claim benefits that they are not entitled to, but in the case of DLA, the bar is set so high, that it is actually really difficult to fake entitlement!  Unlike Incapacity Benefit, which by the way, does have a personal capability test, it is extremely rare to find cases where the DWP have wrongly assessed someone as needing DLA who doesn’t.

The new approach to DLA is going to hit some groups of disabled people much harder than others.  The mentally ill, those whose conditions fluctuate, those with hidden disabilities, those in denial about their condition.  I know this because I have seen it. I know it, so why doesn’t the cabinet?

Osborne closed his speech with these words:

The richest paying the most and the vulnerable protected. That is our approach.

I don’t believe that.  Do you?

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