Yesterday was bad news day.
It started early when I rang the Department
of Works and Pensions (DWP) to check if my second appeal had been received as I’ve
had no acknowledgment. After waiting 15mins, I finally got through to be told
none was on the computer file. They would ring back later when they’ve had
chance to check the post.
Sure enough, later in the morning they
rang. The letter hadn’t arrived. It didn’t matter they assured me as I couldn’t
have a second tribunal as it was regarded as all part of the one application on
which I am already appealing. I pointed out I had filled in a second form &
filled it in differently from the first form. Surely a different set of
evidence would therefore be placed in front of the tribunal. It makes no
difference they said. They had already reviewed the decision on the first
application & had not changed their opinion.
I couldn’t help wondering why they had
enclosed the booklet on how to appeal with the second decision if it isn’t available
to me. I’ve even read the act putting the legislation into force in which it
specifically states a person can reapply at any time. Surely that is what is
what I had done in filling in a second form.
The chap went on to suggest that even if I
was dying with cancer I would not be entitled to being part of the Support
group. I pointed out I accepted that some of my conditions are hopefully
temporary, but the underlying condition, the reason why I am unable to work, is a deteriorating one that can only worsen.
My chances of ever being able to look for work are nil.
He also added the only thing that would
change the decision is if I can get written evidence from the various medical
people involved in my treatment, confirming my prognosis of continued
deterioration. I just don’t see it’s fair to put pressure on my GP etc to get
such letters. Or to waste my time & their time, going to see the various hospital
specialists to obtain such letters, when they could use that time better
treating others who need help. And I certainly don’t see why I should have to
pay for all those letters, especially when at the end of the day I suspect they
will just be ignored on the basis that I’ve put undue pressure on the various
doctors, therapists etc.
Whenever I tell people of my situation, or
tell them I am now expected to indulge in work related activity, they stare at
me in horror. Even the DWP’s staff at the Jobcentre reacted similarly. However,
the people who make the decisions never talk to me directly, only through forms
& letters. They don’t see the days it’s taken to fill those forms, write
those letters, or the toll it takes on me.
As far as I can see, it’s all about saving
them money. If they want shot of me, I wish they would just use the Athenian
government’s method of getting rid of Socrates. I would drink the hemlock
draught willingly. But I’m told that’s just my depression talking & the NHS
is there to keep me going whether I want to or not.
As if all that wasn’t bad enough, come
lunchtime, the phone goes again. This time it’s one of my cousins ringing to
tell me that her sister, another of my cousins, has been told she has a lump in
her lungs, almost certainly cancerous. She will have to have a course of chemo
& radiotherapy to reduce the lump as a bear minimum. And that’s on top of
my cousin Ann having treatment for her cancer. Ann is only just out of hospital
having had to have two pints a blood as she had become so anaemic. Even with
the new blood she still is very breathless, possibly not helped by the fact she
has a “patch” on her chest. As for the cousin who rang, she is having problems
with her kidney, her high blood pressure, her heart (she had a massive bypass a
couple of years ago) and her eyes.
Maybe after all, I’m doing better than
some. We will be able to continue to afford to live reasonably comfortably even
if our income is virtually cut off for a while. The Fox will be 65 in another
couple of year so we will be able to get his pension then. It just means the
state is likely to have to pay for our care as we grow older, as we will have
had to spend our savings on living now, rather than on our care needs later. I
can’t help feeling sorry for those in a worse financial position.
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