Monday, 19 September 2011

Paralympic Games


So the ticketing process for the Paralympics Games 2012 is now underway – I have submitted my choices and wait with bated breath to see if (a) I have been successful in securing some and (b) if so, for which events!

It is hoped that by using the same ticketing process as London Olympics 2012, the events will be a sell-out – the first time in their history. Increased television coverage (which in the past has been fairly lacklustre and made the event seem like an also-ran) will also bring the Paralympics Games 2012 to a much wider audience. But what do we truly know about the Paralympics Games? What events are included and more importantly what are the rules?

Over the coming weeks, I will be looking at the history of the Games, the individual events in detail and maybe one or two more unusual facts. After all, did you know that the last time the Paralympics were held in Britain was in 1984? Yes, that’s right the VII Summer Paralympics were held in both Europe and North America. After much wrangling about the event, it was decided that the American National Wheelchair Athletic Association (NWAA), an affiliated organization to the International Stoke Mandeville Games Federation (ISMGF), would hold its own Games for wheelchair athletes at a separate venue. As a result, the other three disability groups combined their efforts and chose New York as their Games venue. Amputee and les autres athletes, cerebral palsy athletes and visually impaired athletes competed in New York, USA, while athletes with spinal cord disabilities competed in Stoke Mandeville, right here in England.

The Games in Stoke Mandeville were held from 22 July to 1 August. The British Paraplegic Sports Society (BPSS) organized the Games at the Stoke Mandeville Stadium and more than 1,100 athletes from 41 countries competed in 14 events.

I do hope that as we look forward to next Summer you will join me in my journey to understand the Paralympics Games 2012 more.

Come back soon when I will be looking into the history of the Paralympics Games in more detail.............

Wednesday, 13 July 2011

Reform is needed for improved employment!















I have a keen interest in employment opportunities for disabled people so am encouraged by the recent consultations regarding how as a society we can move forward with increasing employment choice for disabled people. For far too long there has been a preconceived notion that disabled people cannot work and do not want to work. I have been further exasperated by the idea that disabled people are happy to fulfill mundane or menial roles. Yes some disabled people do want these roles but there are far more of us that want meaningful employment and career development.

Even worse, disabled people should not be used as some sort of “trophy” to employers. Yes it does happen! Daniel Biddle is a 7/7 survivor – his employers kept a position open for him but not the same role. He returned to work but found it difficult not to be in the same role and therefore decided to seek alternative employment. Daniel took on a number of positions but was unhappy with the amount of emphasis some employers put on him firstly being a 7/7 survivor and secondly being disabled. Fortunately, he is now employed with an organisation that is more interested in his skills and personal qualities.

Speaking at a meeting with Minister for Disabled People, Maria Miller MP, he said: “After the bombing I realised it wasn't the end of my life. I can still do the same as everyone else in my job and travel round the country visiting clients.

“There are real benefits of employing disabled people. We are good at problem solving skills, as we overcome different challenges in our everyday lives.

“I think the idea that disabled people are only capable of menial work is an outdated post-WWII view of disability. Why should we just do menial work because we are disabled when we are capable of so much more?”

It is interesting to note that at the current rate of progress it will be 2070 before the employment rate of disabled people catches up with that for non-disabled people. Disabled people's employment has crept up slowly – from 41% in 1998 to 47% in 2010. There are currently over 3 million disabled people in paid work but what about the 53% that are not?

Liz Sayce, chief executive of disability charity, Radar, has said that “a personalised approach to employment support be extended to disabled people, rather than subsidising separate work places. If the government implements my recommendations to support disabled people to "get in, stay in and get on" in employment, it would make a significant difference.

Disabled people's aspirations have changed. We want the opportunity to work in every sector from hairdressing to engineering, to "get in" through apprenticeships and work experience, and to "get on": progress in our careers and set up our own enterprises. We want to contribute to the economy. The only adjustment most of us need is a fair chance, or low cost flexibilities (such as not travelling in rush hour) – but some need support, extra training or equipment. The support must focus on the person so we can move from job to job and take our support with us”

I agree with Liz but reform in the broadest sense must take place to push forward this ideal. The Access to Work Scheme needs to be addressed. It needs to be publicized more broadly so that both disabled employees and potential employers are aware of the support that is available. There needs to be a more holistic approach to how the funding is allocated. Benchmarking everyone the same does not work and therefore Access to Work needs to focus more on the individual and their specific requirements. It should be easier to move your support with you should you change your employment. The uncertainty of whether the Access to Work Support will continue often results in disabled people being unconfident about seeking alternative employment opportunities.

Disabled people want to work – they recognise the value of being part of the working society and like all people they have personal aspirations. For us as a society to see better employment and career opportunities for disabled people, reform is imperative and must be something that is addressed sooner rather than later for us to see a serious improvement of employment rates of disabled people.

Monday, 16 May 2011

Disabled People in Politics


I was not surprised recently to read that the number of disabled people in politics is extremely low and this does need to be addressed if we are to have a clear and true voice within our political system. I am sure that if you were to ask the everyday man in the street to name a disabled politician their answer would be either David Blunkett or Gordon Brown.

Why are so few disabled people actively involved in politics?

On current figures, the House of Commons would need to have at least 65 disabled elected representatives to truly reflect our society. However, those standing for election in local or national elections do not have an obligation to disclose a disability.

In research conducted by University of Plymouth and its elections centre, surveys in 2008 and 2009 showed very low numbers of disabled people – it even dropped in 2009! Their research showed that in 2008 out of 1,000 local election candidates only 2.8% described themselves as “permanently sick or disabled. This figure reduced in 2009 to just 1.3%.

Is it possible for disabled people to be included more within our political system? And if so, how?

Well at last the Government are looking to change this and have implemented The Access to Elected Office for Disabled People project which includes plans for a £1m fund to help disabled politicians meet costs. All political parties will be encouraged to improve their disability policies and to work closely with the Local Government Association, and disabled organisations to develop a cross-party network of disabled councillors and MPs. It is hoped that these will become role models for aspiring candidates.

David Blunkett has said "Obstacles arise out of fear or ignorance of disability, people not knowing what is possible or how best to help," he says, "with occasional paternalistic blips where individuals have been disquieted by the thought that someone with a major challenge could work not just on equal terms, but succeed in the same professional sphere that they are in. Much of this is covert rather than overt."

Lady Jane Campbell, a wheelchair user, says we need more imaginative ideas for overcoming problems. "Many disabled people would want to get out on the street and knock on doors and canvass but, for some, like me, it would be impossible. It might be that we find other ways of engaging the public." She further states “If you can change hundreds of years of tradition you can do anything, and we do need to change to include disabled people because it's not a democracy if we don't."

There is no doubt that disabled people need to be more engaged in our political system but the reality is that there is no short-term solution. Prejudices still exist largely within our society and until these fundamental attitudes are changed than the voters will just not be there in large enough numbers to make real differences.

So let’s get our message across – we want involvement, we can have involvement, we just need to make it happen!

Thursday, 12 May 2011

The Hardest Hit March & Lobby


Yesterday saw more than 8000 disabled people take part in the Hardest Hit March & Lobby. A direct demonstration against the Coalition austerity cuts that will affect disabled people far more harshly than any other group in our society. The message was clear – the proposed cuts are unjust and will take away real independence from many of the most vulnerable people in our communities.

The March was organised by the UK Disabled People's Council and the Disability Benefits Consortium, and was supported by many disability organisations including Mind, Mencap , RNIB and Sense.

Richard Hawkes, the chief executive of the charity Scope, said that he hoped the march would give disabled people a sense that they were not alone - "We know there's a deficit, but government has said we're in it together. Taking away the DLA mobility allowance for people in residential care, which means that they can't go out, is not a sign that we are all in it together."

In comparison to recent demonstrations, the turnout might have seemed quite low but we need to remember the barriers faced by all those that did attend; inaccessible transport links, practicalities of health issues and, more importantly, the high cost of rail travel for those dependent on disability benefits.

The March brought a uniqueness to demonstrating – there was no angry clashes, no fire-bombing or vandalism of prominent buildings and no reported arrests. Just a dignified showing of opposition to the proposed cuts.

The steady stream of wheelchairs users moving alongside cane users and other disabled people supported by their families, friends and carers with innovative placards in Braille held aloft and sign-language chants highlighted the real challenges disabled people face every day.

Let’s hope that the politicians take note of the concerns raised and address the real issue - "act now to make sure that disabled people are not the Hardest Hit”.

Monday, 9 May 2011

The Hardest Hit March & Lobby - 11 May 2011


On Wednesday of this week (11th March 2011), thousands of disabled people will be demonstrating at Westminster and Parliament to express solidarity and anger at the cuts threatening benefits, services, jobs and rights.

This demonstration is widely supported by many disabled groups and organisations and is being overseen by the UK Council of Disabled People, the Disability Benefits Consortium and the Disability Charities Consortium.

The march will begin on Victoria Embankment between Horseguards Avenue and Bridge Street and will assemble at 11.30am. There will be a rally on Victoria Embankment with speeches between 12 noon and 12.30pm before the march sets off. The march will then begin at 12.30pm taking in Victoria Embankment, Parliament Square and Millbank and will finish in Dean Stanley Street.

Following the march the group will be lobbying MPs as the Welfare Reform Bill reaches its critical stage in the House of Commons. The aim is to make sure that Parliamentarians understand the combined impact of the cuts on the lives and futures of disabled people.

Crucially, they will be asking MPs to challenge policies that will push disabled people further into poverty and isolation. The lobby will take place in Westminster Hall and Methodist Central Hall between 1.30pm and 5.30pm.

I fully support this demonstration and hope that the policymakers not only listen to, but actively embrace, the true concerns of disabled people.

Thursday, 10 March 2011

Disabled Children let down by NHS


Disabled children across the UK are being left in pain and the need for operations due to ill-fitting wheelchairs and the excessive waits experienced within the NHS. Many children have to wait for over a year for a new wheelchair whilst undergoing an average of 32 assessments. Those in East Lancashire have to wait an average of two years – the longest in the UK – for specialist electric wheelchairs.

At present there are 70,000 disabled children in the UK waiting for wheelchairs and the NHS currently only provides the most basic models due to lack of resources. Many parents are being forced to look away from the NHS in order to meet the needs of their children. Many rely on charities, who’s funds are being stretched to the fullest, whilst others take out huge loans to buy the correct equipment themselves.

A report by Whizz-Kidz and Barnados recommends that the Government should:-

* End the "postcode lottery" of wheelchair provision for children
* Make sure that the forthcoming spending review specifically addresses the issue of wheelchairs for children
* Establish and enforce a set of standards for wheelchair provision
* Work with partners to commission services more strategically
* Act on the recommendations contained in the Prime Minister's Strategy Unit Report -Improving the Life Chances of Disabled People - to provide disabled children and their families with appropriate equipment without undue delay

The Department of Health says its 2004 10-year plan for child health services advocated designing and delivering services around the needs of children.

"The plan includes a chapter devoted to children with disabilities and stresses the Primary Care Trusts need to consider a child's needs and their future development when deciding what equipment they provide," a spokesperson said.

"We expect health, social and educational services to meet the core standards in the plan and offer the best possible solutions for all children by 2014."

As a wheelchair user I know from experience that an ill-fitting wheelchair impacts greatly on your day-to-day life. Living in constant pain and losing your independence is intolerable. However, the right wheelchair can transform your life; providing you with greater mobility, more independence and greater self-confidence.

Provision of a wheelchair should not be detrimental to the health and well-being of anyone especially children. Early intervention is paramount to how a child goes on to live their life. This outrageous situation needs to be addressed now and the bureaucracy and red-tape should be lifted to ensure that our children have the proper care they rightly deserve.

Monday, 7 March 2011

Can you afford to be ill if you live in England?


From 1st April 2011 the cost of prescriptions in England will rise by 20 pence to £7.40 per item! Whilst on the same day, Scotland will scrap all prescription charges to fall in line with Wales and Northern Ireland which already see free prescriptions.

Can this be fair to those living in England?

Surely as a nation, all prescription charges within the UK should be standard for all. Why do we have this postcode lottery whereby you can only truly afford to be ill if you live in certain areas of the country? Why should one area pay for the luxury of all other areas to be exempt from charges?

This can only be seen as inequality within our NHS service.

The Department of Health said removing charges in England would cost too much. A spokesperson from the Department of Health said: "The extensive exemption arrangements we have in place mean that in England, around 90% of prescription items are already dispensed free of charge.

"The price of the 12 month prescription pre-payment certificate will be frozen for the second year running. This allows people to get all the prescriptions they need for an average cost of £2 per week.

The government went on to say that the NHS would be left with a shortfall of more than £450m per year if prescription charges were removed altogether in England.
"This is valuable income - equivalent to the salary costs of nearly 18,000 nurses, or 15,000 midwives, or over 3,500 hospital consultants. This income helps the NHS to maintain vital services for patients," the Department of Health said.

Dr Hamish Meldrum, chairman of BMA Council, which has been asking the government to abolish prescription charges, said: "Patients in England have to pay, while those in Wales and Northern Ireland do not. From 1 April Scotland will completely scrap its charges, a move that further exaggerates the absurd postcode lottery that exists in the UK".

"The bureaucracy needed to administer prescription charges is cumbersome, many of the exemptions are confusing and unfair. Patients with disabling long-term conditions still have to pay them despite a recent report recommending they be phased out."

Dr Meldrum added that the principle of charging for prescriptions runs counter to the founding principle of an NHS that is free at the point of use.

"The BMA understands that we live in financially difficult times, but this is a tax on the sick that contributes only a modest amount to the NHS budget and does not offset the unfair disadvantage of asking the ill to pay for their medicine," he said.

I personally think it is ridiculous that we have a system which discriminates on the grounds of where you happen to live!

There are two fair systems for these charges; all prescriptions are free or the cost is reduced and levied equally across the whole of the UK.

I know which option I support..................