Playground bullying...

Well written very relevant article:

http://www.parentdish.co.uk/kids/parents-playground-bullying/?icid=maing-grid7%7Cuk%7Cdl8%7Csec1_lnk1%26pLid%3D251089

The dreaded 'Bedroom Tax' rears it's ugly head again...

I was going to post this on an obscure 'news' site but thought it better here because I don't like to waste words...

The Welsh Assembly (Scotland and Northern Ireland equivalent), and, indeed, Westminster, in my view, are feeding private landlords' greed again...

All politicians should bow their heads in shame...

They should keep their heads bowed for the travesty they are continuing in the social housing sector knowing full well even if there were properties available it would cost far more for horrendously sub standard housing that private landlords can kick out tenants after only six months (if they're lucky):

"Unfortunately there is a glaring pink elephant in the room...

Social tenants affected adversely by the 'bedroom tax', particularly the most vulnerable, face yet another bill of between £14 and £23 per week (over £60 -  £100 per month out of the already MINIMUM the LAW says they need to live on).

It has been proved time and again that there simply are no suitable properties for those affected to move to.

Purely as an example, I moved 4 years and 9 months ago at the specific approach and request of another tenant with the same housing association, not at all expecting to become severely ill and permanently disabled 7 months later...

The move cost over £3000 just in removal expenses and flooring. My home has been substantially adapted at great cost to the Welsh Assembly yet I face again another 'fight' for DHP (Discretionary Housing Payment) which I 'won' last year due to health grounds.

For myself, and I'm sure everyone affected, the stress, anxiety, uncertainty etc. is horrible.

I thought last year that I would feel safe and secure, even 'settled'. That isn't the case".

Even a year; I really do know how fortunate I was to get that; is not enough...

When the 'occupancy' rules were brought in for private tenants all existing tenants were protected. Anyone moving to private rentals after that date knew exactly where they stood...

Social tenants should, at the very least, be afforded that consideration.

There will always be exceptions, not least people needing an extra room for genuine reasons, but, for goodness sake, give the rest of us with no option the same chance as was given to private tenants...xxx

Collateral damage...

Collateral damage I think is the phrase...

A trade; a barter; bought and sold...

Money cannot buy it because it has no monetary value...

It cannot be touched unless it is exchanged for mere physical treasure...

Experience is abject because it means many things; individual...

Today someone I know paid a very heavy price...

A price that was, it would seem, brokered long ago...

A betrayal if you like...

Worse than a broken promise...

An innocent caught in a web of deceit; a piece in a game; no hope of breaking free, even though freedom was, in a fair game, within a soft touch...

TBC...

Lady Justice...

A glimmer of justice shines no more this day,
She was murdered in a cold courtroom;
So now I pray,
That the light that comes ahead has a chance to shine,
And Lady Justice will reign free again...

Lynda Phillips, 13 March 2014...xxx

Dear IDSIOT...

PLEASE READ AND SPREAD!!!

(I have never seen or heard about a mass first class mailing by any government department in an effort at damage limitation such as the following)

Dear DWP,

For the attention of IDSIOT

Thank you for your letter dated 10 March 2014, which I received via first class post on 11 March 2014, the contents of which have been duly noted.

On Friday 7 March I called your offices because I received a letter from ESA regarding my benefit rates from next month. The letter included all the little bits and pieces that certain severely disabled claimants automatically qualify for when getting certain levels of DLA when claiming ESA.

After the shock of reading the letter I had a little think. My first reaction, naturally, was to assume they’re processing the DLA to PIP quickly on the straight forward or obviously worse to save time and money. How wrong I was.

I’m one of a group of claimants whose award of DLA is due for renewal next month and, late last year I received a letter from DLA asking me to ring their offices urgently, which I did. The gentleman that I spoke to assured me that this was a short call of 45 minutes duration and would be the first step in my migration from DLA to PIP. He asked me lots of questions which I answered as fully as possible and then said that I would shortly receive a claim pack with all the details I had provided him with already on it. He said that it wouldn’t be a problem as the form wasn’t very long and that I’d have plenty of time to get help filling it in if needed.

Unfortunately, the gentleman’s idea of ‘not very long’ differs quite drastically from my own. When the claim pack arrived it was a book. It would appear that DWP are competing for some sort of award as to which government department can stretch the meaning of various words and phrases to encompass the broadest possible spectrum.

(Some very good examples of this are ‘form’ meaning book, ‘not very long’ meaning one of DWP’s own nice visiting officers having to attend my house twice for separate appointments because it took her nearly three hours to complete it for me).

Alarm bells started ringing straight away because I didn’t receive the pack until 19 December 2013 and of course, everything’s closed until at least 6 January because of the way the very long Christmas break was, and, of course, civil and public servants take almost all of that off on leave. The letter included stated that the form had to be completed, as much medical evidence as possible copied and sent with it at the claimant’s own time and expense and had to be returned to DWP by 6 January 2014.

A very kind friend advised that quite a lot of people had been treated in the same way and that the only thing that could be done was to call DWP on 6 January and tell them my concerns.

When I called I spoke to a nice lady and I explained that one of my severe disabilities is that I can’t fill in forms because I can’t write legibly much more than a few words without suffering extreme discomfort and pain. She advised that DWP could send one of their own visiting officers to fill it in for me. The book example above meant that she had to attend my house twice for separate appointments because it took her nearly three hours to complete it for me.

She was very nice by the way and didn’t mind at all having to return so that I didn’t miss vital care. She even copied the limited medical evidence I had, the whole form and returned it all to me the following day by hand so it didn’t get lost in the DWP alternate paperwork universe. Apparently, there are letters, medical certificates, forms etc. roaming endlessly around in there destined never to be collated with the rest of some poor soul’s paperwork.

She put my forms and evidence in to the correct pile and DWP received it in late January.

The call last Friday did not go at all well. The lady I spoke to was very rude and insisted that, even though DWP are aware of the massive backlog they, ATOSsers and Crapita have, my benefits would all be sanctioned if the paperwork wasn’t all completed, including a home visit face to face interview by Crapita.

Fortunately, before ending the call and grabbing the Kleenex, I had just enough composure left to ask her to log a formal complaint. I was fully expecting to be told I had to go through a lengthy process but she said she’d logged a complaint and that a complaints manager would contact me in due course.

On Monday 10 March I received a telephone call from a Complaints Resolution Manager who straight away apologised for the horrible way I was spoken to last Friday, assured me that she’d already listened to the call, the information I was given was totally wrong and that my DLA has been extended until at least October or until everything has been processed properly. She said that all staff were supposed to be fully aware of the way the department are handling the backlog, extending everyone’s claims that are nearing the renewal deadlines and that the staff member would be strongly advised of her mistakes, manner, the totally unnecessary way she’d upset me for a whole weekend and would face the appropriate disciplinary procedures.

I received another telephone call on 11 March from another Complaints Resolution Manager almost duplicating the previous day’s call only differing to say that he was from a different team. He kindly gave me all the information I need to make a written formal complaint and advised that he would listen to the call as well and that there is no charge for me to get recordings of all three calls under a Data Subject Access Request which, of course, I fully intend to do.

Thank you DWP for giving me the most fun I’ve had in a long time but please be assured I will take this one all the way because, not all to do with this, but greatly aggravated by it, I’ve been very poorly lately and the added misery was needless. There is also the very great concern that many people will be extremely upset, scared and more ill unless this is brought to national attention.

Yours faithfully,

Lynda Phillips

My reply to some comments:

I was having problems posting it and the pics. last night... Probably FB having a wobbly I expect... Just thought it needs to get out there, because, obviously, sheer numbers would dictate that it can't be a small isolated incident... The backtracking with the letter and two phone calls from senior managers indicates that DWP have made a very big mistake indeed... They obviously didn't count on me posting it all over the place as soon as I got my head around exactly what they'd done... Still having to read it back, read the notes I managed to make about the two managers phoning me and the letter... I copied, uploaded and posted the letter, envelope, and my thoughts in reply letter form to prove that this is indeed happening... I feel an FOI is needed before they try to bury this one... Am surprised that no one else has come forward, or was I maybe right in stating that perhaps others are more frightened than me of putting such private info. in the public domain because they fear any possible reprisal, sanction or backlash when posting such. My view on it is 'get it out there, you have it in black and white'... Let them try to silence me... Knowledge is free and this knowledge is priceless... I give it in the spirit that's meant in order to help show others exactly what DWP are up to and what thy can legally do about it... Formal complaint, LBA and put my 'money' where my words are 

Price tag...

Everything has a price, even this:

http://www.wsandb.co.uk/wsb/news/2332645/exclusive-uk-should-discuss-prioritising-nhs-treatment-for-workers-dame-carol-black

Did I spend the last four years in an alternate universe? If the NHS had continued where ITU put me I wouldn't be sitting here painfully typing now... Four years after a coma and I have spent every possible moment chasing for every little scrap of vital health care; actually lack of... There have been numerous opportunities for proper timely intervention and treatment, but did I get it? No I did not! Why you might ask? I ask that question way too often... I was 41 in the prime of my life and career, got struck down by meningitis and a catastrophic series of life threatening/limiting illnesses, conditions and permanent severe damage and disabilities. Not just once, TWICE! The second time was the result of a complete farce of the most disgraceful (alleged) medical negligence... To get anywhere, anything done, anything properly at all you have to have means. I watched other patients not nearly as severely ill as I was get much better and timely treatment simply because they could pay private and even in a high dependency ward and a rehabilitation ward learning to walk etc. again, because I didn't have money or anyone to shout loudly enough for me, I was and am very lucky to have my life, let alone any quality which was obviously attainable as I found out after leaving long term hospital 'care' twice in the last four years. Sent home without a care plan TWICE! No follow ups, no hand over back to my GP... Nothing! Four years down the line and I am heartbroken whenever I read or hear about someone being mis treated, neglected, or even dying simply for lack of care or, actually, no one to pay private to jump queues, waiting lists, get essential early diagnosis, medication etc... On two different wards nursing staff regularly took medication out of my locked med. box to give to other patients when I couldn't even get decent pain relief or help cutting my food!!!

Unfinished...

Stupidity...

My reply to this:

http://www.huffingtonpost.co.uk/2014/03/05/toni-duggan-england-_n_4902588.html?icid=maing-grid7%7Cukt1%7Cdl1%7Csec1_lnk1%26pLid%3D247912

"This is stupidity in extremis... It's this kind of thing that makes me question what ISP, homepage, media et al I use and am exposed to... I'm a serious journalist and this stuff makes me cringe... I know better, but, sadly, others don't. Grow up, get a life and come back to the game of reality when you have something worth saying... The danger with one even unintentional wrong word/context/spelling etc. these days, especially, is that it can and will be jumped on by the 'PC brigade' and used for very wrong reasons including, but not limited to, arguments, bullying, community unrest and even war... We know this... Do we really have to keep repeating and revisiting the cyclical nature of destruction that our species knows no bound?"

Cost of the disabled...

Forgive me for being stupid, but I thought health care professionals are responsible for just that (my health)... 

It is not my job to do that for them, or, indeed, any other professional involved with my care for me to do/and/or/remind them of what exactly they are paid to do... 

For over four years I have been doing just that and more... 

Does that mean I can draw a salary in reflection of the amount their varying fields quite handsomely pay themselves?

Should I present invoices at a rough estimate of at least £5000 per week (time, expertise, research, costly administration; 100 civil servants don't come cheap these days; etc.)?

The kind of things I've been doing/continue to do/will have to continue to do in order for me to at least survive?

My cost to the government in so called benefit scrounging is approx. less than £300 per week which includes my 'scrounged benefits', care in the community, prescriptions and everything else I fight to get to remain in the community.

Perhaps I should send IDSiot, georgy nit, camcarrot, nick (off to oblivion with his personal millions after the next GE) et al a cheap calculator, along with realistic figures that even they can add up, to allow disabled people with proper support to remain in their homes at a fraction of the cost to tax payers and the betterment of our lives...

Which would the voters go for?

£300 per week or the horrific £2500?