Posts Tagged ‘Disability’

Who Cares for the Carer?

Sunday, February 6th, 2011

Carers suffer more illness and disability, survey shows

Carers protest outside Hammersmith town hall, London, about the closure of a carer centre

Carers protest outside Hammersmith town hall, London, about the closure of a carer centre.

A new study shows that carers’ responsibilities often bring them ill-health. Photograph: Jethro Bradley-Firth for the Guardian

Carers are twice as likely to be suffering long-term illness and disability as the rest of the population, a study reveals today.

The survey, for Carers Scotland, found that 96% of unpaid carers had experienced a negative impact on their health because of their responsibilities, with more than a quarter rating their own health as poor or very poor. More than half had a long-term illness or disability, and two-thirds had experienced a range of physical problems.

The report, Sick, Tired, and Caring (pdf), which is published today, comes amid continuing publicity over the role of carers prompted by the case of Riven Vincent, who asked social services to take her severely disabled daughter Celyn into care because she could no longer cope with the demands of looking after her child.

Carers Scotland said the study had shown the human cost that caring can place upon individuals and is calling for a range of services to be made available to carers, including early intervention by GPs and other professionals, regular health checks, practical training and concessionary rates for sports and leisure services.

Almost half of those questioned for the study suffered from a significant illness, including diabetes, depression, or cancer. More than a third were suffering from arthritis, osteoarthritis or osteoporosis, and a third had high blood pressure. A total of 70% suffered from stress, and 34% suffered from exhaustion. Almost half reported that their conditions had started after they began caring. Of those whose condition predated their caring role, a quarter said it had worsened since they took on the extra responsibilities.

Patrick Begley, director of Carers Scotland, said health and social services relied heavily on the support provided by unpaid carers. In Scotland, there are some 660,000 carers, and Carers Scotland said the economic value of the work they do is around £7.6bn a year in Scotland, and £87bn across the UK as a whole.

“Despite this irreplaceable contribution, this study shows the real human cost that caring can place upon carers – stress, poor health and long-term illness and disability,” said Begley.

“Information and support provided at an early stage is critical. This is often overlooked as carers do not have the time or backup to look after their own needs. This cannot be good for the carer and risks a breakdown of care, with the subsequent need for intervention by health and social care.”

Fiona Thomson, 41, from Irvine in Ayrshire, is the sole carer for her 17-year-old son, Dean, who has ADHD and autism.

“I’ve had major stress. I also suffer from depression and anxiety because of my caring role,” she said. “My health has deteriorated over the years and, unfortunately, they now think I may have lupus as well, which could be to do with the stress of caring for Dean.”

Thomson used to get nine hours of respite care a month, but that was recently cut to six hours after Care Partners, the local charity that has supported her, had their funding cut by North Ayrshire council. Thomson is now spearheading a protest group against further cuts in public money to the charity, which could affect more than 100 families.

Anne*, 41, from central Scotland, cares on her own for her two daughters, aged 20 and 16, who have severe learning difficulties and require 24-hour care. Stress and exhaustion brought her almost to breaking point last year.

“It was at the point where if I didn’t get more help, then something serious was going to happen. It was a really serious cry for help.” Anne’s respite care was increased from the three nights a month she was receiving. Now carers come every week from Friday to Sunday.

“I would say I’m feeling a bit better,” she said. “It has given me a chance to think and focus on different aspects of the girls’ lives now.”

• * Not her real name

When Disability IS the story- a thought provoking piece!

Sunday, August 22nd, 2010

When Disability IS the story!

 I’m all for remarkable stories about remarkable people, from the historical and the famous to heroes next door. In fact, much of my free time is spent studying great people, where I’ve learned that we can discover much of our own potentials through the examples of others. Yet, what’s discouraging is all of the mainstream-distorted disability fribble that we must wade through to get to great stories that involve disability. Sure, there are lots of so-called “inspiring” stories about disability on the newswire and television every day; but, very few are actually newsworthy when you take out the disability aspect. For example, there’s nothing newsworthy about a 17-year-old kid with a great smile and lots of friends. But, if we give that young person a disability, then you have a feel-good cover story for your local paper, where, …Jimmy may not have all of his limbs, but he still has a smile that lights up the neighborhood. Or, there’s nothing remarkable about two parents with four kids who live on a farm. But, if those two parents have a disability – dwarfism – now it becomes a sensational reality TV show, Little People, Big World. Why is that? Why do we, as a 21st-century, westernized culture still see disability, in itself, as newsworthy and sensational, without requiring any real substance?

Unfortunately, the answer is, because our culture still doesn’t recognize the fact that many with disabilities live strikingly “normal” lives, where we work and raise families like most others. People still buy into the myth that disability, in itself, somehow makes every day “different” – and it’s captivating and mysterious to those readers and viewers who don’t know any better. It’s really tying into stereotyping and ignorance in the name of newsworthy. Nevertheless, some with disabilities argue that such news stories and television shows about strikingly average people who happen to have disabilities are positive and educational, showing them in a “normal” light. However, that doesn’t prove true, as if that was the case, those with disabilities wouldn’t be profiled in the first place. The network, TLC, would never produce a show about an “average” family on a farm – that is, because no one would watch such a mundane subject.

Yet, once disability is brought into it, then there’s sensationalism that sells. The X-factor is disability, and it reflects poorly upon everyone involved, including those of us with disabilities at large. The consequence is this: When people see those with disabilities applauded for living ordinary lives, it actually diminishes our equality, where if the ordinary is seen as our peak, then our true potential is lost in the message. Interestingly, those of us with disabilities can likewise be falsely drawn into seeing the disability experience of others as inspirational, when it’s truly not inspirational at all. We can look at a story on television, just like everyone else, and say, Wow, isn’t it inspiring that a guy who’s a quadriplegic can play rugby, get tattooed, and pick up chicks? Yet, if you remove the disability, there’s no inspiration in that story – it’s every jock at your local bar. What we should do is remove the disability from the story, and see if true inspiration remains? For example, a 27-year-old preacher who travels the world speaking to millions is an amazing story, especially when you realize that he’s done it on his own, starting when he was 19, where religion is only part of his message, where he is also dedicated to speaking to youth about staying on positive paths, no matter the temptations or challenges that one faces. The fact that this amazing individual, Nick Vujicic, was born with no arms or legs simply adds to the story. The inspiration to look for, then, isn’t in the fact that one simply has a disability, but that he or she is truly impacting others in extraordinary ways.

 Of course, worst of all is when the media portrays those with disabilities as inspirational when, in fact, the individuals’ lives are absolute train wrecks. TLC recently debuted a documentary on “Kenny,” the gentleman known from the Jerry Springer Show, who has no legs and walks on his hands. As the documentary showed, Kenny, a high school drop-out, caught the attention of some in show business, landing a decade-long career on the Jerry Springer Show, where he would sneak-up on guests and “freak them out” as “the man with half of body.” However, as the documentary chronicled, Kenny left the Jerry Springer show, and was living in a transient motel with his fiancée and her two children, one of whom Kenny thought might be his biological child because he had slept with his fiancée seven years earlier when she was still married to her husband, the legal father of the two children. Kenny and his fiancée’s goal was to have a paternity test, but Kenny insisted that no matter what, he would be there for the two children – and they even called him ”Dad.” Well, the paternity test came back negative – Kenny was not the father – and the documentary ends with an update that Kenny left his fiancée and the two children, and is now living with his parents. Now, where the documentary crossed the line was in perpetually stating what a remarkable, inspiring individual Kenny is, seemingly oblivious that his life and choices are horrendous at best, devastating to others at worst – after all, how does a man of any moral fiber whatsoever vow to raise two children, have them living in poverty in a transient motel, then split? That may be a Jerry Springer episode, but it certainly isn’t inspirational, as TLC insisted.

Surely some reading this might argue that disability defines my own life story, asking the question of, Mark, if you remove disability from your own story, is there anything left to your merit beyond a guy with cerebral palsy? It’s a valid question, and I believe that the answer is, absolutely there’s more to my life story than cerebral palsy. See, my roles – through the mobility industry, writing, speaking, and charity – aren’t centered so much around my own disability, but are ultimately centered around serving others. Yes, my disability adds to the story, but it’s ultimately my larger efforts in life that create what I hope is a legacy of positively effecting the lives of others in many different ways. And, that’s how we should all assess the merits of our own lives if we end up in the public light in any way, where we candidly ask ourselves, Am I being acknowledged solely based on disability, or because of the larger merits and accomplishments in my life? Again, individuals like Nick Vujicic are great examples, where disability, by nature, may be part of the story, but it’s not the whole story – and I strive to follow their leads by making my own life less about disability and more about making a difference in the world around me. Indeed, I applaud mainstream media stories about those with disabilities, but only when they’re warranted. I don’t want to read about how 17-year-old Jimmy’s smile cheers up the neighborhood as one with a disability – it patronizes and reduces Jimmy to less than his potential, as it ultimately does everyone else with a disability. Nor do I want to see absolute train wrecks with disabilities presented as inspirational, making the inexcusable, excusable based solely on disability. However, what I do enjoy seeing are stories like when 17-year-old Jimmy, who happens to have a disability, gets a summer internship on Capitol Hill – that’s a great news story, as it would be about any 17-year-old with such accomplishment. Put simply, let us find inspiration in stories about the sum of one’s humanity and accomplishments, not the singularity of disability, where stories don’t patronize but honor.

 

Taken from a Wheelchair Junkie .com production

When Disability is the Story Posted on April 7, 2010 by Mark E. Smith|

Higher Education now more accessible for students with disabilities

Wednesday, December 16th, 2009

The Disability Access Route to Education (DARE), aimed at all school leavers with disabilities, was launched on the 6th of October by the seven Universities, Athlone IT,DIT,National College of Ireland, and the Mater Dei Institute of Education. This supplementary admissions scheme recognises the impact of disability on educational attainment and on progression to higher education. The eleven participating colleges aim to greatly increase the number of students with disabilities applying for college in 2010 by offering a quota of places on a reduced points basis. – see www.accesscollege.ie for further details on this very worthwhile initiative.