Monday, 27 February 2012


Spartaci – we need you – to get the message out…

Posted by Jane on 27/02/2012

… that our PIP Consultation Guidance is available

Sometimes you come across something that inspires and uplifts you. I have struggled all day to write something uplifting, something inspiring that would spur you into action, not only to respond to the Government’s consultation on PIP but to take it further and inspire others too.
I was shattered and ready to go to sleep after nearly 15 hours of hard slog, preparing to launch the documents on which the small but dedicated team of volunteers have been beavering away, when I stopped to read a post. The bone weary tiredness vanished and I was inspired by this:
Please, please, please, please, please, please…. let this be the way for advocacy. We have waited so long for a consolidated effort.
How true. Each of us has our own reason for being involved or wanting to make our voice count. Perhaps this is the first you’ve heard about what’s happening and can’t quite believe it; maybe like many you’re scared and feel so powerless that fear translates into a worsening of your condition.
The internet gives access to information, support, friendship and a sense of community, in a way that perhaps you only appreciate if your life is spent within narrow confines, even while your enthusiasm and passion transcends your limitations. You feel reduced to a label, a diagnosis that cannot possibly show that you once sailed the seven seas, created art or had a degree in maths.
This is the next chapter in the Spartacus story – it’s our story, one we write together, inspired by a few and supported by many. It’s hard, we know that, but the truth is on our side. Never again should we be made to feel any less than the brilliant, talented unique individuals that together achieve great things.
Have a look at the documents here or join us in the forum – we have 8 weeks to respond. Let’s see if we can get to 10,000 responses; that would be amazing. Why not aim high? The more we succeed the louder our voices become. We are Spartacus!
For more information, please go to http://wearespartacus.org.uk and HUGE aplause, congratulations and love to all who worked so hard. 

Sunday, 26 February 2012

Responsible Reform report, Fundraising

I have been meaning for some time to outline the costs of producing the Responsible Reform report. I'm sorry it's taken so long, I literally just threw all the receipts in a box and dealt with the madness of 18 hour days as they happened. Then, as most of you know, I had to go into hospital soon after producing the report and have been extremely unwell and in and out of hospital ever since.

Printing Costs : 1856
Envelopes : £100
Couriers : £114
Phone Bills (landline) : £390 (On top of normal costs over 4 months)
Phone Bills (mobile) : £261 (On top of normal costs over 4 months)
Parking Ticket : £70 *See anecdote
Petrol £182

Bank / Credit Card charges : £292 - (Paypal error over Xmas left my personal account carrying the printing costs for 10 days, then transfer delayed following month too)
Cheapest laptop I could find (mine broke in late December, leaving me unable to finish report) : £339
New Landline phones (mine had died by December too! By Xmas I was using two home phones, a mobile and a computer all with dead batteries!) £39

Childcare 6 x £36 : £216 (When I had to drop everything to get to interviews etc)
Train Fares : £267
Taxi Fares : £162
Expenses while in London on various trips (PA to accompany, meals, drinks etc) £313
Expenses for volunteers (envelope stuffing weekend, snacks, drinks etc) £72
Printer ink, paper,stamps (covering letters) : £177
Fund/PayPal fees : £737

Food and personal expenses gifted to me personally at end of campaign to cover miscellaneous costs I had incurred producing the report, ie debt, take aways/food for children when too exhausted/away from home to cook etc : £827

Money still in fund : £956

Total Donations : £7370


Today, I have closed the fund. Many, many supporters and friends have wanted to donate funds to me personally, and I have repeatedly asked that they don't.
http://diaryofabenefitscrounger.blogspot.com/2012/02/why-i-write-this-blog.html
http://diaryofabenefitscrounger.blogspot.com/2011/12/fighting-fund.html
http://diaryofabenefitscrounger.blogspot.com/2012/01/consultation-way-forward.html

Despite being enormously touched and grateful, it is simply not right that you give your money to me - many people have campaigned on the welfare reform bill, many have given their time, I'm sure many have incurred personal costs they can ill afford.

Thank you for making the Responsible Reform report possible, for trusting me to complete it, to produce it and to pay for it on your behalf. It was however, a specific fund for a specific reason and thanks to your goodwill and a huge heap of luck, we achieved our goal. 


I will keep the £956 in the fundraising account for future potential fundraising, or donate it to a charity of your choice - please make suggestions in the comment thread. 


When I discussed whether or not to raise money with other campaigners, no-one was either prepared or able to set up an account. In the end, after much discussion with my family, I did so. I may have risked my own security and that of my family, but I did it because it had to be done and frankly, no-one else would do it. Any changes to the fund were made after consulting widely through my blog.

* Anecdote : To produce the Responsible Reform report in time for the ESA votes in the House of Lords (11th Jan) we had incredibly tight deadlines. Everything had a day on which it simply had to be completed or we would have missed those deadlines. Everything rested on the printers - closed over Xmas, they opened on 3rd Jan and our order HAD to be in by 10am on that date.

I took my 3 yr old to nursery that morning and as I started my car and pulled onto the main road it ran out of petrol! It was icy cold and raining.

Thankfully, two good Samaritans stopped and pushed my car onto the kerb. It was 9.05. I could call my breakdown service and wait - missing the print deadline - or I could attempt to walk home, put in the order, then arrange to rescue my car, hoping it would be OK. I did the latter.

I stumbled the mile or so to my flat, rain dripping off my nose, staggering and weaving with pain by the time I got there, vomiting twice on the way, walked in the door, picked the phone up and got the order in by 9.45. Then, I arranged for a neighbour to drive me to a petrol station and went to rescue the car. By this time, despite leaving a note in the window, I'd incurred a parking ticket. I am appealing the ticket, but have to assume they will make me pay it.



Wednesday, 22 February 2012

They don't like it up 'em

Well, well, well.

Diddums Dunky-Smith (So named after this Mail rant : http://www.dailymail.co.uk/debate/article-2104022/The-delusions-X-Factor-sneering-job-snobs-betray-young.html ) is NOT happy.

It seems some serfs dared to question the wisdom of his Great Reforms. It seems that slavery was a step too far for "ordinary folk" who quite like a bit of X-Factor, and that a department used to getting their own way with absolutely everything - sending cancer patients to the jobcentre, halving support for disabled children and conducting a programme of disability denial I am not allowed to make any comparisons with (*cough* Nazi Germany *cough*) - do NOT like the masses having opinions.

This has made ministers Very Cross.

They have accused their critics of being "A small group of anti-capitalist extremists" (Grayling) "Luddites" "liars" and "elitist snobs" (IDS)

For daring to suggest that forced, unpaid, work, might be a teeny-weeny bit like slavery.

Gracious!! And there was me being so awfully, excruciatingly, polite with all that Spartacus Report stuff!!

So apart from the obvious retort : Pot. Kettle. Black . I just wanted to say one thing.

This department (DWP) have used politicised press releases, media bias, misleading statistics & misrepresentation at EVERY stage, as they tried to push through changes that will hurt millions. It has set neighbour against neighbour, poor against wealthy, sick against healthy. It has knowingly and purposely used the most damning spin and the most cruel angles.

Watching them stamp their feet in a frenzy of entitlement has given me much pleasure. Watching their outrage whilst keeping one eye on the Daily Mail comments - unanimously against the scheme on votes - has been delicious.

Reap what you sow Dunky, reap what you sow.




Tuesday, 21 February 2012

Anyone for Disability Ping-Pong?

I'm too tired to explain to anyone who doesn't read my blog why this is funny, so dear regulars, look on this as a private joke :)

Courtesy of the saucy, heart-lifting, belly-achingly funny @MargoJMilne




Why I write this blog

Pssssst! I'm home! *looks around furtively*

We haggled ;) Lovely consultant agreed to a kind of in-patient-at-home arrangement where he will order all the tests I need as urgent, and I will schlep up and down the M11 to get them done.

I know it sounds fairly bonkers, but of all the options available - abandoning poor little broken 3 year old, pushing Dave further into a stress frenzy, squatting in the middle of my Mother-In-Law's life, crumbling under the horror of an in-patient stay etc it was my "preferred option" and Addenbrookes are my "preferred provider." (See what I did there Mr Lansley!!)

The utterly unstoppable Kaliya Franklin folded her indomitable arms (no doubt popping a few joints as she did so) and squared up to Social Services on my behalf. Apparently they weren't mean at all and didn't laugh at her. They phoned back within the hour and a nice lady is going to go through all the options for some support with me today.

Finally, my Mother folded her equally indomitable arms and will be terrifying GPs and dentists all around Sussex once surgeries open. I'd stay indoors if I were you.

Soooo, as usual we have "a plan" or at least a "plan for a plan."

I started writing my blog because I thought that by telling my story, day in, day out, it would give a picture of life with a "fluctuating condition". My life has been a fairly constant basket case for as long as I can remember. You're not just ill - if only!! Noooo, the being ill bit means that everything else in your life is affected. Your finances, your time, your partner and family. I'm sure it can't just be me. Dave and I just sort of lurch from one crisis to the next, trying to manage everything as best we can.

My Dad is 89 and has Parkinson's. Dad's get old. They just do. He needs a lot of care now and has his own crises every month or so - midnight ambulances, pneumonia over Xmas.

But I'm still ill. So then there are two crises to deal with.

We had to move in November. Tenancies expire, they just do.

But I'm still ill. So then there are three crises to deal with.

Dave suffers from depression. He's a carer, he's exhausted, it'd be a miracle if he didn't have depression.

But I'm still ill. So then there are four crises to deal with.

Little one smashed his arm last week. Toddlers hurl themselves off things, they just do.

But I'm still ill. So then there are 5 crises to deal with......

You get the idea. And I KNOW many of you reading this will have lives that are just the same. Because the illness part makes everything else a much bigger crisis.

I write my blog to show my life, but by doing that, it's so that I can show YOUR lives. You know what we don't say often enough? In our quest to be reasonable and convincing and rational?

IT'S BLOODY HARD!

You need endless positivity to be ill. Endless resilience. You have days where gritting your teeth against the pain or fear just isn't enough. In quiet, desperate, exhausted moments where it seems there is nowhere to turn, no answers, we all crumble. Just getting out of bed can be a major task with an endless string of tasks stretching on towards the horizon.

So, to all the wonderful people who wanted so much to give me money yesterday, to help me out of a fix and make things just a bit easier "Thank you" (If you didn't see the comments on the articles yesterday, do read them. I promise it will restore your faith in human nature http://diaryofabenefitscrounger.blogspot.com/2012/02/reality-of-disability-denial.html )

But this is just my life. If you all give me money you can't afford, (yes, I know some of you were fibbing outrageously when you said it was fine) you'd be paying for me until the kids leave home!!

Nope, other options must be found. I will just have to get my head down, look at our budget and make some big decisions. If I can't earn money now, after the year I just had, the trolls really would have cause to criticise wouldn't they? You'll see, I have no advertising on my site and I always declined any offers from organisations to fund me. Who could I take money from that wouldn't compromise the campaigning I do?

But now, with the bill practically law, I'll just have to find someone who wants to pay me for all this work I've been doing for free. I'm not quite sure who yet, but "something will come up"

Of course, there's still the illness. Always the illness. So it has to be something I can do when I like. It has to pay enough that Dave and I don't miss the tiny support left that we do still get, but that ought to be possible - after all, I'm practically running the DWP already and Dunky-Smith earns a huge wedge ;)

So when I write about my life, I'm always hoping that I'm writing about writing about our lives. I don't need sympathy or glory, I don't need any more help than I always need. I don't want you incredible people to hurt for me I want you to be heard. Hurt for your own losses, your own crises - believe me, I know that they take up most of your strength, every day. Mine are just another story, another life, another utter failure of the system.

It's that failure I want to expose - for all of us. Enough is enough. By telling the world how the state and the systems and the structures fail me I am simply showing how they fail us all.



**By the way, later I will put up another post outlining what the Research Fund was spent on and how much is left. I've been meaning to for weeks. As the fund still looks as though it has £6,000 in it (It definitely doesn't, lol) I'd better lay out how the money was spent.





Monday, 20 February 2012

What WILL I do?

I'm going up to hospital today. They might keep me in.

The "might" part of that sentence is that they will almost certainly want to and I will do my best to wriggle out of it.

Oh, I'm not well. No doubt about that. I'm less unwell than my last admission, but unwell enough not to be able to get through a day. I can't look after my own children, my Mother-In-Law has been here for about a month doing school runs and making the dinner. She can't stay much longer - her own life urgently needs attention.

It's not the crohn's. Nope, this time it's some unspecified immune oddness. I've lost a shocking amount of weight, I'm weak and frail, I'm getting constant low grade fevers, I've had a cough since May and every few weeks it flares into some kind of full blown infection/flu.

My local hospital weren't interested. At all. Too complicated. Sent me home muttering something about it all being something for my consultant to look into (My consultant is 130 miles away in Cambridge and my local hospital still use carrier pigeon.) They didn't even recognise my chemo-shots until I told them the generic name.

That was 3 weeks ago. 3 more weeks of shuffling around the house, coughing, trying not to pass out when anyone's looking, aching and paining, basically cluttering up the place like a great heap of patheticness.

So the only option is for Cambridge to take me as an in patient and run all of the tests my local hospital should be running but haven't heard of yet. (**See why I think NHS localism is a really, really, bad idea?)

So why on earth wouldn't I want to go into hospital? Why wouldn't I want to find out what's wrong and get it treated?

Oh, you know, it's that little thing called "life" again.

Who will look after my children? While I brew a nice few PTSD attacks in a hospital bed 130 miles away, who will do the school run? Wipe away tears? Pack lunches and do cuddles? My 3 year old broke his arm pretty horrifically on Wednesday and is still getting used to the cast and the pain - who will help him up when he get's stuck on his back? Or make sure he has his medicine in the nice Toy Story cup that means he takes it? Seriously? Who?

How will I afford it? Dave will have to visit (only at weekends though) and that costs £60 a time in petrol, £70 for overnight stays, £15 or so in hospital parking and £70 here and there every time he has to take a day off for compassionate leave.

How will Dave manage? Will his boss understand? Again? Or will this be the time he loses his job? Will he make it through yet another bout of stress and worry or will he have another breakdown?

The only answer anyone has ever managed is "Well, you have to. Your health is at stake."

Hospital stays trump everything. Getting "better" always comes first. If I object, I get the "look" - "concern mixed with frustration mixed with impatience. It's so easy when it isn't you. It's so easy to say "something will come up" about money. It's so easy to say "Oh, people will all pitch in with the kids" (They won't and don't) It takes just seconds to say "You'll be fine" (I won't and it will show as I crumble daily, trapped in a Kafkaesque in-patient system I have come to loathe)

But actually what do I do? There is no nice number to ring, no-one I can appeal to. Social Services would just laugh, I'm so far away from needing a care package according my local authority, I might as well be an Olympian. I got refused DLA, which would at least have paid for some petrol and childcare. Soon, I will lose my ESA too.

Dave and I have been in this situation many times. Our parent's are getting older and less able to step in, take over, run a family popping with the boundless energy of two small boys. What do you do? There is nothing. I'm no longer classified as "disabled" I'm no longer classified as "unwell" I never was classified as in need of care or local support.

Which is odd, because I know that the next 4 or 5 weeks will cost us thousands of pounds. Money we don't have. If there is no-one to pick my child up, he just has to stay at nursery - and we have to pay for it. If I can't walk to the school gate, we just have to get a taxi. When I'm in hospital I just have to buy extra food - or I'll lose more weight and get more ill. You can die if you lose too much weight you know Mr Dunky-Smith. The petrol money will have to come from somewhere, but where? Who will pay for the B&Bs?

It's not just about the money though. Who will look after my children? Do the school runs? Get the shopping in and cook dinner? Who?

"It'll all work out" is no answer at all.


Saturday, 18 February 2012

Eternal Slavery for Sick and Disabled

Well, I'm awfully sorry, I did always say the welfare reform bill was very, very, long and very very complicated.

We did our very best to make sure we'd noticed all of the evil, opposed all the of the disgusting nasties. We pored over plans to send cancer patients to the jobcentre and leave disabled children to starve. They tried to make profoundly disabled adults prisoners in their own care homes, but we noticed that and got it dropped. When they tried to "re-classify" paraplegics as "fully mobile" because they have wheelchairs, we screamed about it - they dropped that too.

We made quite a noise about socially cleansing all of the poor people out of London and evicting pensioners and foster parents for daring to have a spare room. As for letting the Government decide how long you are able to be unwell, we made a dreadfully big fuss over that, but sadly, they remained convinced that their DWP magic wands would make 1 year enough.

Well, it turns out, we missed the "Eternal slavery for sick and disabled people" Clause. (Clause 54) You know, it was busy, we had a lot on our plate, we had to keep taking naps. It was obvious we would miss something - possibly enforced euthanasia for puppies or the National rollout of a new eugencis programme, so in a way, it's a relief it's only eternal slavery. At least if we're lucky "Masser" might let us have a drink now and then, a bit of nice balm for the chaffing of the chains.

The satire urge is just too strong for me, so @latentexistence has done an excellent job of telling everyone what this actually means here : http://www.latentexistence.me.uk/government-taps-sick-and-disabled-people-as-source-of-free-labour/#comments
The Guardian broke the story here : http://www.guardian.co.uk/society/2012/feb/16/disabled-unpaid-work-benefit-cuts
And updated it here : http://www.guardian.co.uk/politics/blog/2012/feb/17/disabled-unpaid-work-benefit-cuts-documents

Basically if you are sick or disabled and an assessment has found that you may be capable of some work at some point in the future, with the right support, you can now be forced to take part in the Government's "Workfare" scheme, working for free to make more profit for Tesco and Asda and Poundland! Yay! With Lupus or Schizophrenia or Leukaemia or waiting for a kidney transplant or.... well anything really. You're probably exempt with less than 6 months to live, but only if you can be sure it's not a day over 6 months.

On top of this, although unemployed healthy people can be forced to take part for 8 weeks only; lazy, feckless cancer, MS and Parkinson's patients can be forced to work forever. For free. 

Now, it's OK cos  as with every last detail of the bill we opposed their answer is "But we wouldn't really do that, it's "just in case". We only want to the power to force sick and disabled people into eternal slavery for a rainy day! Of course we'd never make someone work forever for nothing!! Now off you go (pat on head) and trust us.........



**The satire is too strong. Even the Guardian cartoon today is about this : http://www.guardian.co.uk/commentisfree/cartoon/2012/feb/18/martin-rowson-welfare-disability-cuts-cartoon?CMP=twt_gu