A Seahouses man due to have an operation to repair a ruptured Achilles has been left stranded by new transport to healthcare rules.
Health bosses have changed the transport criteria, meaning some patients are expected to spend over five hours a day on public transport to attend hospital appointments.
Mr Vickers from Seahouses was informed of the change when he phoned to book transport to an appointment ahead of his operation on the 28th of this month.
“I would usually get an ambulance taxi but they told me I couldn’t anymore. The whole thing is ludicrous. Now I’m stuck, I can’t get to Hexham unless I get a private taxi.
“I was even more upset when they said after I have the operation, am in plaster and on crutches, I’m still not entitled to transport to get home.
“We had no idea anything was going to change. They said a new criteria had been brought in and asked all these ridiculous questions like are you blind, are you in a wheel chair, do you get housing benefit. I don’t know how many others have operations booked and don’t yet know about this.”
Berwick’s Liberal Democrat MP Sir Alan Beith described the new rules as “grotesquely unfair”.
“People have been told to get from Berwick to North Shields and back on a series of buses with no certainty their treatment will be finished in time for the last bus back to Berwick. Another constituent was told to take a two-and-a-half hour bus journey from north Northumberland to the Wansbeck Hospital for regular injections.
“Elderly widows are being told if they can use a local bus for a 10 minute journey into Berwick they should have no difficulty travelling on several buses to get to the Freeman.
“This is simply not acceptable and creates a huge barrier to healthcare for people in north Northumberland.”
Sir Alan said the situation was “even more insulting” to local people when they are being told they cannot go to Borders General Hospital which has a direct bus link from the centre of Berwick to the door of the hospital.
“This chaos all results from decisions of the Northumberland Clinical Commissioning Group and the uninformed way the decisions are being implemented in rural areas,” he said.
“It’s clear that people sitting behind desks in urban parts of south east Northumberland have no idea how difficult it is for people without a car or someone to drive them to get to distant medical appointments.
“I have raised this issue with the Chief Medical Officer of the Clinical Commissioning Group and I will be raising it in Parliament, where I have already been taking up the restrictions on cross-border access to health services.”
A spokesperson for the Northumberland CCG said:
“From 20 October 2014, we implemented the Department of Health’s national policy where all new patient transport bookings are subject to a short assessment. The assessment includes asking a few questions about how you would normally travel for day-to-day activities and if friends or family normally take you to your appointments.
“The purpose of this assessment is to make sure that the people who require ambulance services are prioritised based on their health needs and that the NHS is making the best use of the funding it has available. We understand that this can be a frustrating experience and some people who have previously used this service may find that they are no longer entitled to patient transport.
“If this is the case, then the booking service is offering information and advice on alternative forms of transport.”
They added: “We are in the early stages of implementing this process and we would like to reassure everyone that we are continually reviewing issues and concerns raised to make sure a common sense approach is applied.
“We are committed to ensuring that patients who live in rural areas are not disadvantaged by the implementation of the criteria, however, we still need to ensure that this is applied fairly across the region.”
If patients have any concerns, queries, or you are unhappy with a decision, they can contact the Patient Advice and Liaison Service (PALS) via Freephone 0800 0320202, by text to 01670 511098 or by emailing firstname.lastname@example.org.
Source – Berwick Advertiser, 06 November 2014
By Helen Sims
As I write this I am recovering from what we campaigners call ‘Brown Envelope Disorder’ – or ‘White Envelope Disorder’ (since it applies in equal measures now). It is what happens to a disabled or ill [benefit claimant] when a brown or white envelope appears on the doormat, particularly those marked ‘DWP’ –Department for Work and Pensions.
I was upstairs, waiting for my painkillers to kick in, when the letterbox went. For an ‘everyday’ person, it is normality. It is part of life. However, if you are disabled or an ill benefit claimant, living under the constant threat of an ATOS assessment or benefit sanction, [the sound of the letterbox] immediately causes the blood pressure to rise, and panic to kick in.
I’m sat on the bottom of the stairs, shaking and looked at the brown envelope (marked DWP) on the mat. Even though I know (rationally) that ATOS assessment envelopes are usually white, and that I am not due to be assessed for Personal Independence Payment (PIP) – the government’s replacement for Disability Living Allowance – for at least a year, the effect on me (and so many other ill and disabled people) is a reaction of pure fear. I sat there, unable to move, almost as if I was frozen to the spot. Rationality doesn’t come into it anymore. They play games, change dates, change criteria; so even if you think you know what’s what, (and when), for me (and so many others) the fear is still there. My heart begins to pound so loudly that I can hear it in my ears, and my palms begin to sweat. The rational part of me says ‘pick it up and open it. It’ll be fine’. The vulnerable, anxiety prone, part of me knows it is coming.
If I want to keep my life the way it is, I will have to go through a Disability Assessment for PIP, which is stacked against me. I will have to justify my right to the small amount of support I get. I will have to justify myself, my existence, my attempt at as normal a life as I can. I will have to sit there while someone judges me, and asks me leading, (unfair) questions, that are designed to deprive me of support and the things that able-bodied people take for granted.
I was born with Cerebral Palsy, and cannot walk or stand unaided. I suffer more or less constant pain, anxiety and depression – not to mention a few other things. The anxiety and depression have been made worse by this government and the media’s portrayal of disabled people as ‘scroungers’ and fakers. They have deliberately misled the public on the levels of benefit fraud, and we are paying the price.
I continued to sit on the bottom of the stairs, with all this going through my head. I feel worthless, and I know that I will be stripped of my Disability Living Allowance by the transition to Personal Independence Payment. I know that I am luckier than some. I have my husband (and his Pension Credit) to help us live, but for me it’s about independence. It’s about being able to behave like a ‘normal’ wife.
As things stand, I can help my husband pay the bills, I can take myself to the doctors or hospital appointments, I can go out (when I feel well enough), and see friends. I can feel like a ‘normal’ person. If they take my DLA, they take all that too – and I have spent years fighting to keep self-esteem and independence and to build a life for myself. I can’t lose it!
At this point, I am beginning to hyperventilate. ‘Be rational,’ I try to tell myself – ‘be RATIONAL!’ I fear the assessment itself even more than the consequences of it. Sitting on the stairs, I’m imagining all sorts of things. The assessor’s eyes look at me, and judging me. She looks tidy, she looks together, she tells herself. Yes I can, and I’m so lucky. What isn’t so lucky, is that I can’t sleep due to pain and anxiety….even though I’m so very tired.
I’m tired by life, and I’ve been made even more tired by government lies, and persecution, and the feeling that I have to struggle even more than I do already. Why is this happening to me? Why is this happening to any of us? Haven’t we been through enough? I start to cry. Eventually, mid panic attack, I ring my sister, who tells me to breathe deeply, and reminds me that whatever this government says or does, I am a person…and I am worth something. She tells me that if it is the assessment, I’ll handle it, and that they have no right to make me feel like this…in my own home. I tell her I’ll open the envelope and call her back, which I do.
It turns out, that is just a letter confirming my benefit amount, and my level of claim. I curse myself, knowing that I should have checked with a fellow campaigner before panicking, but like I said rationality doesn’t come into it anymore; and besides, there are so many other people like me (and worse off) that don’t have the campaigners to turn to, and don’t have the information at hand. Who cares about how they feel? This government certainly doesn’t!
As my heavy breathing subsides, I go back upstairs, and I’m physically sick in the toilet bowl. No one should be going through this. It is psychological torture, and I’ve had enough. This government needs to be held to account for its actions. There needs to be a proper impact assessment done on the Welfare Reform policy, because what I went through today is only a small part of it. It is causing pain, suffering, panic, malnutrition, isolation, homelessness, and even suicides. Somebody, somewhere, needs to make it stop… Now!
Source – Welfare News Service, 22 March 2014