Showing posts with label Disability Living Foundation. Show all posts
Showing posts with label Disability Living Foundation. Show all posts

Monday, 25 July 2016

I AM NOT WRONG AND YOU ARE NOT RIGHT

I get that attitude I have in the headline soo many times. People do not look over emails properly as was clear this time around from the fact that several emails had been exchanged by 9.30am to 10am.

I wont ever claim about a late response ever again ... unless it is as bad as this one is, lol.

How have I not got a job?

How on Earth have I not got a job with a help & advice organisation?!

There beside manner is non existent.

I had an answer one of my my emails way, way early ... like a little after 8am I think it was?

I cannot tell which of the organisations he is from but shows his complete naivety and lack of the understanding of simple English, Christ I did a short version (see below) and people still do not read?!

He actually tells me that I should attend an assessment, it is long gone, and tat the DWP would be sympathetic, what planet as he been living on?

When I tell him that they are never sympathetic and that I have proof of it and that proof was used by Machael Meacher MP, still have the email, he still wont simply say he was wrong but then annoyingly stating 

"However, as you do not agree with me ..."

Umm it was not a case of agreeing ... you were wrong .. mate! It is as simple as that. I admit it when I am wrong but so few people are able to do it. They have to twist and say things in a way tat makes them look like they were right and that I was wrong.

Of course my immediate reaction was to email the guy back and tell him it is not about disagreeing and that he was simply wrong and to have some gonads to admit it.

I also wanted to ask him if he was really in the business of helping disabled people as his knowledge was utter crap, he got things well and truly wrong, only advised by stating the absolute obvious which was way too late to use anyway and ... his bedside manner was shite.

He could have gotten some pretty rude responses from a great many of frustrated disabled people but in the end I thought 'what's the point in having a go?' so I did not.

Both emails to and fro are below but his email did not give away which of the 5 organisations I contacted he worked for, there were two solicitors too but I do not think it was them.

I did think Masis for some reason but could have been Disability Living Foundation or SEAP, none of which I had heard of until today. Funny that. God elp their clients of that was a solicitor!

Why do people state the obvious? More specifically why do people not pick up tat they do not have to state the obvious?

Hmm I see the time '9.13am' and I thought it was earlier than that, hmm oh well do not know why I thought that.

Oh and notice I kept it short only to not explain what I wanted ... which is funny as I tell them the facts and expect them to tell me what they can do or who next to speak to. You give them most o it, you are wrong and complained at, you give them minimal amounts ... you are wrong again.

If the DWP were so understanding why did I not get a second appointment with a taxi arranged or a Home Visit? They have come here in the past ... or rather they claim to have done so and the letters are on this blog for all to see, the dates and times as well as the letters explaining why they did not arrive which was so full of shit it was untrue.

Anyway here are the emails ...


Hello Martin,
I was trying to suggest the most beneficial way forward to be of assistance to you. However, as you do not agree with my suggestions I do not know what more I can advise you to do.
As you have stated that you are due to see a Neurologist in August, perhaps he or she can make a more constructive suggestion as far as your future needs are concerned.
I cannot become involved in personal disputes with the DWP or the decisions they make.

Regards,

Peter Lyne.


========================================
Message Received: Jul 25 2016, 09:13 AM
From: "Martin Haswell"
To: "Peter Lyne"

Cc:
Subject: RE: Cheated by All

Dear Peter Lyne



No sorry, you seem to be unaware that the DWP lie, have done for a number of years and cheat people with disabilities.



I did say my email was very, very, very short...



I recorded every meeting and appointment I had with everyone over 7 years ... I even have a Specialist at Chase Farm Hospital admitting he falsified my ultrasound test results on my groin all available on my blog



Just remaining in the world of the DWP I have them lying several times, lying about not turning up for Home Assessments and various other things. Indeed, if you looked at enough of my blog, enough of the recordings are there, you will see this and see that I easily proved it.



IN fact if there was anything in the way of Legal Aid left, which is why I strongly believe they removed it, I would have taken them to court years ago.



Added to this and your insinuation that the DWP would be in any way helpful ...



Back in January 2013 the late Michael Meacher MP found my site, data and asked if he could use it in the House of Commons to attack Iain Duncan-Smith over Atos and the DWP..



As for getting to an assessment ...



I have pains in heels, legs, ankles, back and added to this I do not tolerate warm temperatures and sweat way, way too much and have recently had a series of blackouts, full seizure and other symptoms of a brain tumour I am seeing Neurology about in August. I am in pain all day every day in one way or another or several at once.



So you can imagine I was a little surprised at your response?



Thanks anyway.



Martin Haswell BSc



Sent from Mail for Windows 10



From: Peter Lyne
Sent: 25 July 2016 08:43
To: Martin Haswell
Subject: RE: Cheated by All



Hi Martin,
Thanks for your reply.
If I may make a constructive suggestion, as it is clearly apparent from within your very detailed first e-mail that your mobility is worsening. I would advise you to attend an assessment.
I have discussed issues with many disabled people on matters relating to Personal Independence Payments (PIP) which is what I believe you are referring to rather than Independent Living Allowance.
DLA was replaced by PIP for people aged between 16 and 65. The higher rate of the mobility component of PIP (which allows people to receive Motability) means that if an individual can walk more than 20 metres they lose their entitlement to Motability.
However, if a qualified medical practitioner or assessor were to see the difficulties you are experiencing, then you may find that the DWP will be more sympathetic to your specific needs.
Remaining within the guidelines and stipulations set by the DWP is perhaps the only way in which you can protect your future independence. If you do not agree with the results of your assessment then you have the right to appeal. However, this can take in excess of 6 months which causes many disabled people considerable anxiety and distress.

I hope that this response has been of some assistance to you.

Regards,

Peter.


========================================
Message Received: Jul 25 2016, 08:19 AM
From: "Martin Haswell"
To: "Peter Lyne"

Cc:
Subject: RE: Cheated by All

Hi Peter



Sorry ... so much information sometimes forgot the relevant things.



Two things really I need to find a way around...



The DWP have cancelled my Incapacity Benefit and this is going to make things hard. They are also being dicks about it because I did not go to an assessment, I have NEVER been at an assessment and not gone to four in the last five years without issue.



It begs belief how they can state your fit when you have failed to do something so simple and travel several miles, simple for someone without anything wrong with them that is.



Also I am getting near to not being able to get around even in my home town and difficulty with housework and silly things, not to mention the depression and anxiety that comes with it. Yet each time I ask my GP he just looks at me blankly and changes the subject. The last time he told me to ask the Citizen’s Advice, who I shall meet in a couple of days time and all everyone says is that the Citizen’s Advice are useless as all they do is advise.



I cannot see how they can help in this regard.



I had been making remarks and trying to think how to get some help for a number of months when suddenly the DWP decide to broadside me with more off their deceitful crap.



All I ever get is organisations that tell you to go to one of half a dozen others and eventually you start getting told to go to organisations you have already been to



Many thanks for replying I was not expecting something back so fast and so early in the morning.



Yours sincerely



Martin Haswell BSc



Sent from Mail for Windows 10



From: Peter Lyne
Sent: 25 July 2016 08:10
To: Martin Haswell
Subject: RE: Cheated by All



Hello Martin,
Many thanks for contacting me and for the detailed summary of your many medical conditions as well as the numerous barriers you are facing or have experienced.
However, you have not stated as to how I could prove to be of assistance to you and what your present dilemma is.

I do have links with various legal experts but am unsure as to whether it is a legally related matter that you want to discuss.

Could you please send further details so that I can consider a way in which I may be able to be of assistance.

Thank you,

Peter Lyne.

Founder of Mobility and Support Information Service (MASIS).


========================================
Message Received: Jul 25 2016, 07:36 AM
From: "Martin Haswell"
To: "info@masis.org.uk"
Cc:
Subject: Cheated by All

Dear Sirs

I have a situation that the CAB are helping me with but I am not filled with confidence by them.

I have contacted others too but one turns out has no advocacy or legal people, despite saying they did on their website.

Instead of droning on for 7 pages or so,, as there is a hell of a lot and that’s without anyone else I have been involved with in public services, which involves two Police Forces and four local councils for instance, I will be brief with a short report.


· Twenty years of life screwed up

· Currently and for years suicidal thoughts out of anxiety or boredom

· Have Fibromyalgia which causes pains or embarrassment

o Heels, Arches, Ball of feet

o Ankles

o Left knee

o Hips

o Anxiety

§ So bad now loss use of legs

§ Tingling arms

o Depression

o Body Temperature and Over Sweating

o Skin Conditions 3 areas

§ Ignored by NHS 14 years plus

§ Diagnosed myself 2013

§ Confirmed Guy's Hospital 2014

§ Then realised they knew as I was on only two drugs for FMS for 2 years

o Bad short term memory loss most of the day every day

· Collapsed Vertebrae (x-rays private)

o Back pain that lasts for weeks on end

o NHS deliberately x-rayed so collapse would not show, foetal position

o Had for around 8 years plus

· Possible Brain Tumour or Epilepsy

o Seizure lasting ten minutes

o Frequent Blackouts

o Irritation on forehead

o Irritation Right Eye Socket

o Forgetting Words

· Damaged Right Knee

o Not full diagnosis

o First spotted by Orthopaedic Surgeon Dr Saksena at Chase Farm Hospital

o Was supposed to be seen by Barnet Hospital

o Barnet tried to refuse to see me under violent conduct (were unsuccessful)

o Then they ignored knee and look at feet

· Inguinal Hernia

o Pain from one repair

o On inspection found second hernia left and painful black lump right

o Then tried to say nothing showed up, I challenged and he admitted lying about result

o That conversation is recorded

· As the last remark 95% of NHS and others recorded by me over 7 years plus

Got so fed up with so many disability,, help & advice organisations that did not help with this or many other things I started blogging and publishing my evidence …

· BLOGS ..

o asaintcalledallnights.blogspot.com

§ I have a back up blog, in case government managed to close me down, where I am thanked by a man of the cloth (he and his family made to feel like liars by NHS)

o Another on CPUs and Computing

o Another on Orchids

o Another on Reptiles, Amphibians & Fish

o Another on British Wildlife

o Several others

o A YouTube Channel

o At last look I had tipped over 330,000 visitors

I would be grateful for any help and advice you could provide.

Thank you for your time.

Yours faithfully

Martin Haswell BSc

Sent from Mail for Windows 10



THE UNRELENTING HEAT

I am definitely having a hot day today.

Recently I thought I was doing well but I am not so this morning. My typing is all over the place too and with this playing up I get from this crap keyboard sold to me by PC World it is already a pain after just two sentences and a little YouTube searching.

I feel like I am almost burning.

I am going to do a quick search, never thought it would quite get like this especially as it is supposed to be cooler, going to check the temperatures too. Nope, 23 celsius so I should not be feeling this bad, it feels more like it is 40 Celsius or more and there has not even been any sun that I have seen!

Aha … hmm my system is refusing to copy an paste! I thought it did this previously but thought it was me forgetting to select 'copy'. May be I am not going mad?

Hmm going to close this and start it up again.


Aha!

There is a page of Fibromyalgia sufferers speaking about heat … going to see if there is anything I can buy or get from my GP for this … it is very, very uncomfortable today.

I like this line …

Typically, a person with fibromyalgia may see more than 10 healthcare providers, including multiple specialists, before being properly diagnosed,”Argoff told Healthline. “Who wouldn't be frustrated under those circumstances?”


Every year I feel like I can pull through and normally it is just feeling hot while sweating an incredible amount. But I feel like I have been sunburnt today, God damn it!

Ooh I have a sofa pillow with a different material, ribbed, and I have just used that behind my back as the sofa feels as it it has central heating going on inside it. Yeah the material of my sofa prbably not the best with my condition, like the rest of my house.

I have been diagnosed with Fibro for at least 15 years I would say the devil caused it if anyone”


That above is another good quote by a lady in Tennessee, Texas, USA. If, of course, you ignore all the religious crap where they argue which God created Fibromyalgia and whether there is a God or not, lol.

Hours of discomfort and tingling arms feeling as if they were burning but it has finally died down … probably because I moved my ig velocity fan around to blast at me. I still feel heated in places.

Nope … getting hot again. Does not seem to be an easy fix for this and though beta-blockers were suggested in the past the ones I am taking, Propranalol, are not doing anything. Funny that these things are happening after what the DWP did?

I have not posted this and now it is the next morning.

I was looking up to see who is out there to help people wit disabilities and in my experience thus far there seems to be a hell of a lot but none of which actually do anything. I try to feel confident that I have the advice of the Citizen's Advice but every time you ever mention them to anyone you only ever get one single response from people They are useless, all they do is advise” and to be honest this was all that I had form them in the past … only they did not even give advice on the trouble I found myself in. They told me they knew nothing about bailiff law, even though it consists of a couple of A5 pages, as it turned out.

I find it funny when you go t sites for help and all they seem to do is list everyone else, including several you have just been to or told they do not help other than to give advice. How many organisations giving advice do you bloody need?

Even after finding out that Mind have their own advocacy and legal people they have since written to me and told me that they do not.

As I was looking around I saw this page whereby a similar thing that happened to me between the Citizen's Advice and Jobcentre Plus. The CAB tell me to go to the Jobcentre Plus to do something and the Jobcentre Plus tell me I can't, or they can't, do it! I am even more confused because it states on the web-page that the Jobcentre Plus have disability advisors and I am wondering why this is the first time I have heard about this. Though quite bizarrely according to a Jobcentre member of staff the disability advisors only apply to disabled people that are working?!

The other funny thing is the remark about finding someone that knows what they are doing and I think this shows up the British public's naivety at large. I get the same thing from people but no one seems to realise two things …
  • No one seems to know what they are doing so you wasting your time
  • The fact that no one seems to know what they are doing means they are up to something and damn well know it
How nice it would be if you could have just one advice organisation and if you went there and you needed help they would put you onto the only help organisation. I mean, how hard is that?

To me there are a lot of cheats out there taking donations for faux jobs and careers doing basically nothing.

I just added someone called Masis and the Disability Living Foundation to my lists of people I have contacted that claim to help those with disabilities. That takes the total up a few to around two dozen I think it is?

Oops, add someone called SEAP to that list.

If I am to become homeless once again and with a bonafide disability diagnosis after 14 years of asking and twenty years of having it I am going to make sure that everyone that is useless and a waste of tax or donation money is seen as just that.


Lol.