Posts Tagged ‘human rights’

More room for rich foreigners as government cuts Disabled Students Allowance

Some readers may find the above headline a bit strong, but please be assured – this is what it means.

Vox Political became aware of this story in two contrasting ways, as follows.

Firstly, from The Guardian: “From September 2015 [the government] will only pay for support for students with specific learning difficulties, such as dyslexia, if their needs are ‘complex’, although the definition of this, and who decides it, remains unclear.

“It will no longer pay for standard computers for disabled students, or for much of the higher specification IT it now subsidises.

“And it will no longer fund non-specialist help, likely to include note-takers and learning mentors. The costs of specialist accommodation will be met only in exceptional circumstances.”

Paddy Turner, of the National Association of Disability Practitioners (NADP) is quoted: “This is going to have a disastrous effect on students with specific learning difficulties because it looks very clear that [universities minister David Willetts] is trying to remove them from the DSA. It looks like a knee-jerk reaction to recent reports that specific learning difficulties and dyslexia aren’t really disabilities at all.”

Thanks to Vox Political

I wonder if UKIP’s policies or even the 3rd Reichs policies will/would differ?

This will make for an interesting court case.

UKIP logo

From other socially responsible people who shall remain valued.

Irene Sendler verses Al Gore

irena

M.E. awareness month

The month of May is “ME Awareness Month”, with May 12th being the particular day, and I have also seen the week starting May 11th designated as ME awareness week.

ME is classified by the World Health Organisation as a neurologically-based disease. It is of unknown cause, although there are several theories including viral and environmental agents. There is no known cure.

Unfortunately, in the UK the NHS seems to have ignored the WHO’s classification of ME as a specifically neurological illness, and has lumped ME together with any and all unexplained tiredness and fatigue, which can in fact be caused by a number of things, including Lyme Disease, Lupus, vitamin B12 deficiency and Pernicious Anaemia, Thyroid and adrenal problems, Sjögren’s, PCOS and other endocrine diseases, MS, fibromyalgia, depression and more, and has called the whole collection CFS, MEcfs or cfsME.

Within the umbrella of CFS there is obviously a vast spectrum of symptoms which range in severity, from those who are experiencing a mild loss of ‘get up and go’ to those who are in constant pain and utterly bedbound and unable to care for themselves, and since it is an umbrella term, treatments that may be helpful for mild types of CFS, such as GET – graded exercise and CBT – cognitive behavioural therapy, are wholly inappropriate and can be harmful for those who actually have ME.

CBT can be useful for people not coping well with any long term chronic illness but should not be touted as a main treatment for ME in the way that it is, based on the faulty assumption that CFS is inevitably linked to caused by psychological factors, and GET is harmful to PWME who have the key symptom of Post exertional malaise.

This situation has been exacerbated by the psychiatric establishment which has greedily claimed all ‘CFS’ patients as their own, baselessly alleging that all CFS must be related to mental and emotional factors.

Thus the tendency is to treat all CFS patients as though they are all suffering from an unexplained, probably psychologically-based, rather than neurologically-based illness, regardless of the severity, and further to fail to investigate thoroughly or adequately in order to rule out any other cause (such as those listed above).

There is no definitive test for ME yet (largely because genuine research has been so scarce), and so ME should never be diagnosed until every other possible cause has been eliminated.

The classification of ME together with any unexplained CFS is a nonsense which means that people who actually have curable and treatable diseases aren’t getting the help they could and should be able to expect, while those with ME are simply treated with disdain instead of receiving the palliative care they need.

This is a wholly unacceptable situation for everybody involved, which helps no-one, except those few outspoken psychiatrists who like to gain notoriety by making the psychological case and denying the reality of the suffering.

A friend has also pointed out that MS, asthma, duodenal ulcers and other illnesses were all considered psychiatric problems before biomedical caught up.

Thanks to “life for beginners” for the reminder and the post.

Freepost!

All freepost mail is paid for by UKIP.

bricks to UKIP

Lies, Dam Lies and Statistics

With many thanks to the brilliant Benefits And Work.

Benefits and Work has obtained documents via the Freedom of Information Act that may undermine claims by Atos that its staff were the subject of nearly two thousand episodes of assault or abuse, including death threats, by claimants in 2013 alone. Atos used the claim to justify wanting to exit early from the contract to carry out work capability assessments (WCAs).

Atos claimed that they were experiencing around 1,956 incidents throughout the year.

This was, by any standards, a very serious accusation.

Characterising thousands of sick and disabled claimants as violent thugs that Atos could no longer expose its staff to is likely to have increased the level of prejudice against benefits claimants. It may even have contributed to a rise in the number of violent hate-crimes committed against disabled people.

Three of the most important figures from our point of view, are:

Security called/police called’ 215

Threat made to staff direct or implied 110

Staff assaulted 5

Readers can decide for themselves whether they believe Atos’ claims by downloading the whole year’s figures here.

Thanks to “same difference” for the original post.

Pilgrimage to Capitalism!

Thanks to “Kicking the Cat”

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