A Housing Benefit Item on Channel 4 News. AND Where Paul Rutherfords case is mentioned.

 The news slot where Paul Rutherford's Bedroom Tax case is spoken about Thanks Channel 4 ! >>>> Will you support Paul and sign #wowpetition ? SIGN WOWPETITION HERE

WOW Dont just email your mates try these too...

Some other emails to think about to send reason why you signed #wowpetition.

If enough send there may be inclusions/ more publicity. 

Please do 

EMAIL CONTACTS:
(You need to copy and past these links into your email client / browser)


TV PROGRAMMES


1 BBC mike.sergeant@bbc.co.uk


2 Have your say bbc.co.uk/haveyoursay


3 ITV Tonight mailto: tonight@itv.com


4 Channel 4 News news@channel4.com


5 Five studio@five.tv


6 Sky news@sky.com & newsonline@bskyb.com


7 Newsnight newsnight@bbc.co.uk


8 Politics Show politicsshow@bbc.co.uk


9 Andrew Marr show http://news.bbc.co.uk/1/hi/programmes/andrew_marr_show/
8379560.stm (Leave comment)


10 form for This week with Andrew Neal http://news.bbc.co.uk/1/hi/programmes/
this_week/contact_us/default.stm


NEWSPAPERS:


11 The Independent News:newseditor@independent.co.uk
letters@independent.co.uk


Letters:


12 The Guardian
News: home@guardian.co.uk
Letters: letters@guardian.co.uk


13 The Morning Star
News: lettersed@peoples-press.com


14 The Evening Standard
Letters: letters@standard.co.uk


15 The New Statesman
editorial@newstatesman.co.uk


16 The Telegraph
Letters: dtletters@telegraph.co.uk


17 The Mirror
Letters: mailbox@mirror.co.uk


18 The Times
News: editor@the-times.co.uk
Letters: letters@the-times.co.uk


19 The Sun
News: editor@the-sun.co.uk
Letters: talkback@the-sun.co.uk


20 The Daily Mail
News: editorial@dailymailonline.co.uk
Letters: letters@dailymail.co.uk


21 The Observer
editor letters@observer.co.uk


If you want to contact your MP and why not? Here’s a useful link to find your MP’s
email address: http://www.parliament.uk/mps-lords-and-offices/mps/

Heres A reason to sign #Wowpetition NOW - 2015 is too late.

#Wowpetition I think this response to a petition calling for a general election should be a very good reason to sign #wowpetition. 2015 is too late for many.

Here it is:

Your Government writes :

The Government will not seek to dissolve Parliament before 2015. We came together at a time of crisis to fix the country and ensure our long term prosperity. We intend to secure a country in a better state than when we came into office. Although we know that not everything we do is popular, we know it is necessary for Britain to rebuild and compete in the world. We are making progress and keeping our promises by cutting the deficit, cutting crime and immigration, reforming our welfare and education systems to help people work hard and get on. We have cut corporation tax and are slashing red tape to make Britain a good place to do business, and have increased the personal allowance to cut taxes for millions of low and middle income earners, frozen council tax and cut fuel duty to help families with the cost of living.

Practically, the Fixed- term Parliament Act 2011 abolished the Prime Minister's prerogative power to dissolve Parliament. The Act provides that Parliament can only be dissolved early if a Government is unable to secure the confidence of the House of Commons within 14 days of a no-confidence vote, or where at least two thirds of all MPs vote for an early general election. The legislation established five year fixed terms for the UK Parliament. The next General Election is therefore planned in law for 7 May 2015, and polling day will ordinarily be the first Thursday in May every five years. A debate in Parliament on an e-petition is unlikely to result in legislation to undo this legal lock.


So I ask you after consideration of the above... PLEASE SIGN #wowpetition

Click and Sign #Wowpetition  

Wow petition asks this : 

We call for a Cumulative Impact Assessment of Welfare Reform, and a New Deal for sick & disabled people based on their needs, abilities and ambitions

Responsible department: Department for Work and Pensions

We call for:

A Cumulative Impact Assessment of all cuts and changes affecting sick & disabled people, their families and carers, and a free vote on repeal of the Welfare Reform Act.

An immediate end to the Work Capability Assessment, as voted for by the British Medical Association.

Consultation between the Depts of Health & Education to improve support into work for sick & disabled people, and an end to forced work under threat of sanctions for people on disability benefits.

An Independent, Committee-Based Inquiry into Welfare Reform, covering but not limited to: (1) Care home admission rises, daycare centres, access to education for people with learning difficulties, universal mental health treatments, Remploy closures; (2) DWP media links, the ATOS contract, IT implementation of Universal Credit; (3) Human rights abuses against disabled people, excess claimant deaths & the disregard of medical evidence in decision making by ATOS, DWP & the Tribunal Service.

That Fear of too sick for JSA too well for ESA ?

VERY IMPORTANT!!! 

The fear is of that for some, should an error occur.

But then the Mandatory Reconsideration on appeal they fear NO INCOME. 

There is this though via an FOI 

>> DOWNLOAD LINK <<    <possible income support in interim?

Read and apply it where you need to. 

Its a download pdf link. hope the resource is useful to people. 

(Link courtesy of Jenny Clarke I believe [no relation ] ) 

The Forgotten Aspects of Same Sex Couples - The Children

When Peter Ferguson said he was going to write something on this subject , I asked him about it... What I heard back was quite insightful and so I waited for his article on this.

I do like these crowdsourced sorts of analysis, and so I share the start of it and a link to read more should you wish to.

Children of same-sex couples send equal marriage opponents a message.

There is an argument prevailing among equal marriage opponents that equal marriage will somehow violate a child’s natural right to a mother and a father. For instance .... CLICK TO READ ARTICLE

Appeal and get no money? Disgusting.

Cross posted... 

New rule will leave ESA appellants without ANY income indefinitely

I've been away for a long time - basically being very ill. I'll update you all on my personal travails another time but my first post in over a year will be dedicated to the extraordinary logical brain of Ian Duncan Smith.

He has been lambasted today for the horrendous mess that is Universal Credit - which is over budget, under target, poorly managed, and with no solution in sight on how to get it back on track. But while this central plank of IDS's welfare reform receives all the attention, other smaller, but arguably more costly changes are being introduced with little attention.

On October 28th his department of Work and Pensions introduced.....

Read more ... From nhsbuff.blogspot. 

--------------------------------------------------------

So please join people who are asking for complete review of these damaging and messy Welfare Reforms and Sign #WOWpetition here... http://epetitions.direct.gov.uk/petitions/43154 

Disability doesn't discriminate

This a guest blog from Jane. ... 

How often have I said "Disability doesn't discriminate"?

Some of you know I have been terribly upset and worried this week because my sister has been unwell and in hospital. Thank you for your support through this, frankly it's been awful and without my family, friends and "virtual" friends I don't know how I'd have coped. We've been waiting for the diagnosis, it's come.

Let me start at the beginning.
My sister is healthy, has decided to take early retirement from the #DWP (yes, stop booing) because of the tremendous stress she is under. So with just one year to go she decided to bring to an end nearly 30 years of work for the DWP. My sister was really looking forward to finishing because she has a new grandson,her first, just 8 weeks old. My sister already has a swimming session booked in with him, has changed her car to accommodate all the paraphernalia that goes with having a baby these days. My sister was looking forward to the retirement she and her husband have worked hard for. The round Europe in a camper van type holiday. The round the world trip etc etc.

So. My sister was getting ready to board a plane for Vietnam on Wedsnesday. She "fell" - she cracked her head open and has four staples in it. She started to "fit" - she had eight "episodes" in an hour and continued to have episodes every hour or so, she still is. I knew immediately from what she said that it was Epilepsy, however the hospital have done many, many tests - a lumber puncture, taken bloods, monitored her for 24 hours, a CT scan etc etc (thank god for our #nhs), all this time she has been losing consciousness, at one time the crash team were called and my brother in law stood by thinking he was about to lose his wife. Finally today at 6pm, the consultant came, finally today the diagnosis came...."you have epilepsy". Let me tell you being at the receiving end of that statement is horrendous. The clock stops. Time stops. Then it hits you. The enormity of that diagnosis.
The enormity for my sister. She won't be able to drive her new car to pick up her new grandson. She won't be able to go swimming with him (on her own), she won't be able to ride her scooter round Europe..... the ramifications are enormous.

So. My oft spoken & written words "disability doesn't discriminate" are proven true again. It didn't discriminate against me, it didn't discriminate against my sister.

What if it doesn't discriminate against you? What if your comfortable lifestyle is all of a sudden hit by disability? Maybe you'll realise then that you should have signed http://wowpetition.com ......

I'm not writing this to make mileage from my sister, or to make a dramatic difference to the signatures, I'm writing this to show you it happens, it really does happen. There are for of us, four siblings. Two have diabetes, two have epilepsy. What are the odds of that happening?

Please protect your future and the futures of those you love, sh*t happens - believe me, it does, and when the sh*t hits the fan wouldn't you like to think the state will be there to provide for you? Think again!!

Please sign & share http://wowpetition.com NOW, TODAY!

There are just 40 days till the petition closes. 40 days for us to make a fairer, better, safer future for all of us.

My sister is aware I am writing this and fully supports me with all I and all the WOWteam, followers and supporters are doing to make #WOWpetition a success. In fact just 2 weeks ago, to help me in my "traipsing" around the country for WOW, trying to raise awareness and signatures, my sister drove me to Bangor so I could help @TenPercent. Most of my family have met Rick. All my family support#WOWpetition. All of my family know the urgency to succeed and the need/importance to sign http://wowpetition.com ......because all of my family know DISABILITY DOESN'T DISCRIMINATE .......

Ever asked "Am I wrong?"

Last blog i did was about realising people lose stuff. Real Lives. Affected by sickness and disability.

There are a few of us in this nation that can see quite clearly that we need to stand, suggest, do. Its tough when All the people doing it themselves are doing it at person cost, and cost to health.

i do.

I have had four emails recently saying "Are you okay" like that meeting you were there but looked very tired, not well, affected by what you are doing.

I just had a chat with another campaigner who said dont just hear your body, listen to it.

I suppose I really should.

Its hard to do.

And when I blogged what people have lost, it was hard to write. I cried. Ive lost stuff too.
This is the blog > THIS IS NOT A LIFESTYLE CHOICE

And as I type this, I have an open tab, and read another plaintive plea for a wake up within a sanitised non responsive pressure driven system.

If people can think enough, then we can change things.
If they dont engage what can people like myself and others do of any worth?

I would like you to read this and comment here. THIS needs reading > AM I WRONG?

Comments here are open. feel free.

Sickness and Disability is not a Lifestyle Choice.

When your world changes....

You know that a stones throw, a coin toss, can put you in need of support and help? a need for Social Security?
When your life changes beyond recognition, because of a sickness or disability... it takes stuff AWAY.
You dont Volunteer for removal of vocation, job, business, lifestyle.

ITS NOT A LIFESTYLE CHOICE.


SIckness and disability isnt something "Over there" that happens to other people.

This is a list of real people, what they did before they could no longer work.

Just think, all of it, taken away. And this govt wants to remove as much support as it can from these people. Real people.

And so we begin...

"What did you do before you could no longer work? "

"We both worked in engineering, last project 2006-07 abu dhabi port project. had a brilliant life now life is shit."

"IT manager. Prior to IT work I was a mobile phone salesman"

"taxi driver for 10 years self employed in diff things b4 that and joined army at 16 "

"senior features co-ordinator for a magazine"

"international retail consultant "

"Lecturer for the Unemployed and CAB Volunteer. They were the days when I could go out/do whatever I wanted...."

"Police officer for almost 10yrs, always employed since leaving school at 16"

"Chief Financial Officer"

"Volunteer Coordinator / Project Management in voluntary sector."

"I was a baroque viola player and violin, viola and music theory teacher. Also worked as an usher at concert hall."

"I was a Property Valuer & Manager for the high end rental market. I had a portfolio of properties over 2 million quid. Good sal, bonus, car"

"Fundraiser, yoga teacher, youth worker. Working full-time since 15."

"Housing Officer. Gave up to become a carer"

"I was a checkout manager with 130 staff working 37 hrs a week. Now bedbound /housebound."

"I was a Community MH Nurse with specialist training to help people with severe/enduring MH Problems"

"Brought up my kids, once an acceptable thing, so now long-term unemployed & seemingly unemployable."

"Engineer, quality, process"

"Ward receptionist in neuro disability hospital"



Has that made you think enough yet? THESE ARE REAL PEOPLE .

And in my belief these people are being treated as scroungers, less than human, even bordering on implication that they are Shirkers, not trying hard enough. Shouts of Fraudster, Scrounger, Waster, Feckless all abound quite virulently through the media and society. Sickness/ Illness/ Disability has hit these people. ITS NOT A LIFESTYLE CHOICE.

Its not as simple as one or the other...

When speaking about broken WCA, i was thinking of my own situation when a lot of the mental stuff is caused by the physical stuff.

The insomnia by the tablets. The naturally resultant anxiety of illness, etc etc. The displacement, the fears, a whole raft of mental health issues exist directly resultant of physical ill.

For the DWP / ATOS to separate these in the WCA and say either or with no link, as it APPEARS to do is a complete fallacy.

Its well documented and thought widely that mental health issues are dealt with appallingly in the WCA.

So I decided to think on how people cope with a diagnosis of chronic illness. What it does, what it means to their life, things that those without might understand the way it weaves a different pattern to your life, changes things, transmutes into places you have never been. And how difficult yet often invisible that side of things are.

I know. Because its changed me radically. Some of you reading this will identify and have a cloud of understanding from these basic words.

To highlight it from an individidual's own perspective , a lady called Penny has given permission to share HER story of this life changing impact.

Without more words, here it is:

Coming to terms with this disease has been and continues to be the hardest thing I have ever had to do.
My life has changed beyond recognition from the self assured, independent, professional woman I was up to a few years ago. I studied, qualified and worked as a Dr of Psychology for many years, firstly within organisations and then when I could no longer work out of the home I ran my own private practice from home. My work was a very big part of my life but since this condition has progressed these last few years my concentration has been affected and I am no longer able to be reliable for clients, I also find it impossible to sit for the hourly sessions that are required.
I have had to adapt each time another part of my independence has been eroded, I can no longer drive, I am no longer capable or safe to go out of the home alone. This has caused isolation and depression recently and I have had many discussions with my GP about my emotional well being.
As well as socially my life has changed beyond recognition personally, I am no longer able to cook or prepare food for myself or even a simple cup of tea when I want one, I can not bathe or keep myself clean and need physical help to do this and so my dignity has suffered.
I can not simply decide I wish to do something and be able to do it so have had to come to terms with my daily limitations.
Stress is one thing that aggravates the Psoriasis and the arthritis but life as me is very stressful much of the time as asking for and accepting the constant help of another person/people is very hard, also the constant forms and need to continually prove to yourselves and others that I have actually got what is a recognised medical condition brings the whole sorry process to the front of my mind again and again.
I get very upset very easily, partly due to frustration with myself I suspect and wanted to write this statement to show you that a physical condition also impacts on a persons mental health.

Now that shows a personal impact in such a lucid way, and I hope reading that, you can see if someone says they have a chronic illness, its so much more than the physical. 

I stated earlier that the WCA seeks to separate, or mitigate these effects as irrelevant. The BMA state the WCA is broken. They voted for its cessation. 

Theres something you can to to help this happen. Sign Wowpetition.  Many thanks. 

CLICK TO SIGN WOWpetition

__________________________________________________ 

Facts on claimants with mental health conditions Cross posted from http://ilegal.org.uk

Did you know?

(1) Of 1,609,430 claimants coming off Employment & Support Allowance between March 2010 and February 2013, 566,250 (35%) had a mental health condition. 


(2) Of 2,699,780 claimants taking up a claim for Employment & Support Allowance between March 2010 and February 2013 (including those converted from pre-existing incapacity benefits), 1,0930,330 (40.5 %) had a mental health condition.



(3) Out of a total of 1,591,040 claimants on Employment & Support Allowance in the February 2013 quarter:


724,150 (45.5%) had a mental health condition, of which (percentages relating to the 724,150 figure)


24,890 (3.4 %) were of 'unknown' claim status 


214,090 (29.6 %) were in the Assessment Phase


252,250 (34.9 %) were in the Work Related Activity Group


232,910 (32.3 %) were in the Support Group


(4) Of the 724,150 ESA claimants with a mental health problem in February 2013, 401,390 were new claims and 322,760 were claims which had been 'converted' from pre-existing incapacity benefits claims.



83.244.183.180/100pc/esa/icdgp/esa_phase/a_carate_r_icdgp_c_esa_phase_feb13.html


(5) Of 918,560 claimants still on the older incapacity benefits (not all have been transferred or assessed for ESA conversion) in the February 2013 quarter:


389,580 (42.5%) had a mental health condition. Of the 389,580 claimants, 29,750 have been claiming between 2 and 5 years and 355,520 have been claiming over 5 years. Claimants who claim on mental health grounds constitute by far the largest percentage of the total claimants followed by 143,560 claiming with diseases of the Musculoskeletal system and Connective Tissue and 75,120 claimants affected by diseases of the nervous system. 


83.244.183.180/100pc/ibsda/icdgp/ctdurtn/a_carate_r_icdgp_c_ctdurtn_feb13.html


(6) Geographical breakdown of the 389,580 claimants with a mental health condition on pre-existing incapacity benefits by region (this does not include ESA claimants but the longer term breakdown is likely to be similar when the reassessment programme is completed in 2014):

Region	Number of claimants
London North West Scotland South East West Midlands South West Yorkshire & the Humber East of England East Midlands Wales North East Living abroad Unknown	56,090 53,820 42,470 39,750 33,410 32,110 31,140 29,100 25,820 25,720 18,760 1,380 10

(7) Taking just one quarterly set of figures covering the period between December 2012 and February 2013, out of a total number of 155,180 ESA claimants coming off the benefit, 57,670 (37%) had a mental health condition.  


Of the 57,670 coming off ESA in the February 2013 quarter:


14,110 were of 'unknown' claim status  

34,010 were in the Assessment Phase 

6,340 in the Work Related Activity Group  

3,190 in the Support Group


(8) Of the 724,150 ESA claimants with a mental health condition in the February 2013 quarter, the age breakdown is as follows:

Age group	Claimants
Under 18 18 - 24 25 - 34 35 - 44 45 - 49 50 - 54 55 - 59 60 +	1,940 76,270 145,780 185,430 109,360 97,260 80,490 27,630

205,380 is the total number of ESA claimants aged 50+ (but not exceeding 65) affected by a mental health condition.  

JSA , lambasted by this govt......

EXCLUSIVE!




Theres a massive focus on tiny sections of expenditure by this govt.

And then this happens......

A fella on JSA goes to Jobcentre
Is put on a course.
The course says "Research a subject, and do a presentation to the people on the course"
Now this sounds all fair. However the presentation chosen by Benjamin here was RESEARCH on JSA and Jobcentres. Ironic. No. Brilliant? Yes.

The following I got from Benjamin:
=====================
(Dear Jules, Via email ) 
In June I was forced to go on a course by the Jobcentre as I'd been unemployed for six months. I say forced because if I hadn't gone on the course, they would have sanctioned my benefits. The course wasn't as painful, embarrassing, and demeaning as I expected it to be.. A constituent part of the course was that I had to do a presentation. I decided, given the resources and audience that I'd research the true impact of Job Seekers allowance on society. It busted myths and made people feel a lot better about their situation. When questions pop up, ask yourself those questions. Share it, and ask and show others. The presentation makes a compelling case.

I was happy to keep the presentation to myself and put it away having only shown it to the group. That changed though. The myths need busting, and I'll tell you why. Every time I hear about a bedroom tax suicide, I realise as many people as possible need to see this, to debunk myths. Every time I hear about yet another person dying after being found "fit for work" I realise it needs to be seen. We need to be heard, that's why I need people to see it.

Benjamin
====================
Did I tell you also he showed me MSM emails not wanting to particularly extract info from slides 40ish onward? No? Ah. Thats what they did.they didnt wanna show anyone.

The presentation is in powerpoint.I've hyperlinked it to microsoft on line. There should be no compatibility / viewing problems.

                                          < Click here to see the presentation >

A bit of myth busting eh?

Nice one Benjamin.


PS . ALSO CAN YOU LOOK OVER TO THE RIGHT, A LITTLE LOWER DOWN, CLICK AND SIGN WOWPETITION. THANKS