Showing posts with label Patient Claim Line. Show all posts
Showing posts with label Patient Claim Line. Show all posts

Monday, 25 April 2016

CITY OF SPIKING

Well this is odd.

The numbers to the last posts shot up, the NHS one most of all, then fell flat through Sunday and now, Monday morning, have spiked considerably.

The NHS breakdown post has shot past anything I have posted in the last few weeks, so maybe we are finally getting somewhere?

I have a couple of other posts I need to post up, one more to do with deep and philosophical kins of thoughts. Not supposed to marry up with science, philosophy that is, but I do not know why they say that. I have always been rather partial to both. Though I have a degree in one I did consider acquiring a degree in Philosophy too. In fact I was envious of a really nice woman I attended some lectures with at Middlesex University, called either Miranda or Melanie, as she did a joint degree in both Applied Computing and Philosophy.

Lost contact with her and so wish I had not.

Yeah so there is a deep thought like post coming up.

Had a rare visit from my sister and of course my house was a total mess, odd as I had this urge to rifle through everything like a nutter. While in her car started to feel that dreadful nausea coming on and was pressing hard into my neck into a tender region, as I have woken up finding myself doing on occasions. In fact I go through a period of doing that several mornings out of just a few and then I seem to stop for ages. Very weird and something to do with why I was sent for a DEXA scan due to Osteopenia a few weeks back.

Ooh yeah I forgot about that in my NHS breakdown. Well in fact there are over 100 symptoms to Fibromyalgia I did not go through but did not see the point. Can be so boring for a reader just to go through an inordinately long list of health symptoms.

I used to say it was around 120 but my right knee turned out to be a separate problem and at last some of my back is too, neck and thoracic. In fact that Dr Kirkham did look at my back and did a lot of 'hmm'ing' and 'ahhh'ing' so maybe the buggered back shows how bad the Fibromyalgia is?

Because Fibromyalgia Syndrome is to to a natural kink in your central nervous system taking a whack to some point and becoming even more kinked. This leads to not receiving non-restorative sleep which screws up your brain and without it cannot 'reset' itself each night and fires things off all over the place. You might call these signals 'red herrings' as there is nothing there, except the pain is exactly the same as if they ARE there. Hence why it can be classed as a disability.

The difficulty comes when you only have Fibromyalgia causing a few things and of course as I have already established, the NHS and GP's wanting to avoid diagnosing anything they can because they are obscure.

I long for the day with a Star Trek like 'tri-corder' that can diagnose you in an instant. No more lying and avoiding tricks, and hopefully by then much better was at ridding people of all of these obscure ailments and especially the 'syndromes'.

I hope this spiking is a sign because I could do with a bit of a boost. I have been lacking my mojo of late and it has been driving me nuts. I keep nodding off too, don't know what that is all about. I am even praying for dear life that acquiring this new camera is going to make my hyperactive again?!

This is the time of you I should be becoming more active and cycling a lot more and with a camera in tow. A decent camera and a decent zoom bridge camera at the very least. Because of photographing and filming birds, you see? Anything else animal wise at a distance too, so most mammals. Because of my knowledge I can normally identify a majority of things and at least know its something out of the ordinary. Well, if it stands still for 5 seconds! Lol.

I have people into animals, scientists even, that come along and use my location and recordings on YouTube to track animals and even study differences in bird song of the same species but different geographical locations. The Yellowhammer for example.

So I help keep a check on populations of given areas, something I would very much like to spread further afield.

I did used to drive an Alfa Romeo GTV 3.0V6 but thanks to illegally losing my Disability Living Allowance about 8 years back I was forced to sell it and lost £2,000 on it. This is fresh in my mind because my sister is trying to sell her Mitsubishi FTO 2.0 Manual and I was explaining that had I not lost my car my blogs and YouTube channel would have ten times as much content as they currently do.

With the visitors to everything passing the 300,000 mark some weeks ago you could guess that this number would at least have a zero on the end of it?

That is why I contacted all those people ... and then some I filmed the envelopes to that either claim to take people to court on your behalf or offer help to disabled people...


This was not all of them and was actually 'Wave 2' of possibly three, as some may have given me others to approach, cannot recall but was at least one, AvMA.



There was these but not included with the mentioned 'Wave 2' and these were letters to literary agents about 3 books (two corruption one amphibians) I approached them about prior to blogging, it seems that acquiring over 300,000 people across the blogs and YouTube channel does not amount to much.

Maybe you need to be a brain-dead TV, Film or radio celebrity to be taken seriously about getting published? Degrees, experience and knowledge do not count for much, just ask J.K Rowling who was rejected countless times for Harry Potter and I even read that her being accepted was actually a mistake on the literary agents part? Lol.

Onwards and SIDEWAYS.

Looking outside ... grey and being outside ... COLD!

Marvellous!

I start to wonder if I want to buy an expensive camera as things go so wrong and so sideways soo often that I tell myself 'You will buy this camera and it will be SHITE weather all summer, just you watch!'. Lol.

Short range shots and filming and the Sony is still OK for ... umm I think?

I digress.

Yes so that is the film of most of the help agencies, charities and organisations advertising legal representations. Hmm, when did I post that I wonder?

It was posted on the 23rd March and I probably posted the letters 24 to 72 hours earlier? SO well over a month since I have posted them.

On the legal front I got three 'NO's' with some serious changing of the goalposts without seeing, listening or even asking for any evidence. That was Patient Claim Line.

On another I have got a 'NO' and then this changed to a 'Maybe' for the same reply that Patient Claim Line got which they then got snooty and insulting about while also moving the goal-posts.

I cannot recall if there were any others.

So I spent a number of years gathering the best evidence in the world while helping someone close to me for three years with a case that judges said was the biggest they have ever seen and for someone with short term memory issues too.

So registered disabled, buggered feet, back, ankles, knee and memory and a mountain of data, helping with someone else's case so that they win and I get ... nothing. Lol.

But wait? Did I not say this is what would happen?

In all honesty if I ever got someone to act on my behalf legally I would have a fit and then pass out. I tell you it would literally be such a shock to me it would take me days to get over it. Even weeks later I know I would stop and think ... 'blimey, this is actually happening?!'

I just did a search for 'medical negligence no win no fee' and the top three in the search results are 

  • Slater Gordon
  • Patient Claim Line
  • Irwin Mitchell

All of which I have contacted about my evidence.

  • No answer, which is rude
  • No, rude and moving the Statute of Limitation from 3 years to 2 (their own rules)
  • No answer, which is technically, once again, rude

Just contacted ... EDITED

  • http://www.medicalnegligenceassist.co.uk/contact-us
  • http://www.theclaimsconnection.co.uk/contact
  • http://www.medical-solicitors.com/contact-us/

Let us see how they respond? Instead of what I did last time I sent the chronological list that made AvMA to go from 'No' to 'Maybe', though I have not heard back from them. Lol.



I have always maintained that everything is corrupt or false and was my suspicion that these companies just advertise on TV to make us think, while they do away with Legal Aid and any rights you have left, that there is still an avenue to traverse should anything go awry.

That was my suspicion.

I have approached a number of them with the best evidence in the world, already proved for them that I did have something wrong with me three times over, which they failed to help me with three years ago. I have also managed to do all this within the three years Statute of Limitation but I have short term memory issues anyway. Plus the other court case I helped with.

So I have legitimate reasons for taking as long as I have.


  • Getting enough evidence
  • Getting recording of Doctors lying and one admitting falsifying test results
  • Helping daughter with her legal case for several years
  • Having short term memory issues
  • Keep going to these people, who say no, and forced to move ojnto the next one

There you go, four things I can think of, off the top of my head. Lol.

I remember once before someone being narky because they found out I had contacted several others ... errr there is a Statute Of Limitations on these things, as much as I disagree with them!

SO many people have a vastly overrated view of their own intellect and all because of a job position they hold. SO very funny, lol.

Saturday, 23 April 2016

OMBUDSMAN WILL SAY LIKE COMPUTER

Well I have made an official complaint now to the Legal Ombudsman about Patient Claim Line and there members of staff.

Oddly I had completely forgot, as is so often the case, to also mention I had previously contacted The Law Society about all this a few days back. No reply as yet, wow now there's a surprise!

Anyhoo just for sake of record and as always I am posting up the email I sent to the Legal Ombudsman.

EMAIL ...

Dear Sirs

Patient Claim Line/British Law/Legal System

I want to mainly complain about Patient Claim Line but the other listed above too.

I have been trying to get legal representation for several years now for medical negligence.

Now initially, as I was telling the truth, I thought this would be a simple act of acquiring a private medical report and then taking the NHS to court, but no. Everyone I contacted said I had less than a 50% chance.

Now with my many areas of pain I also suffer from memory lapses in a bad way.

So what I did was start out on a lengthy course of action to prove what I had wrong with me, acquire Doctors lying and to render this incontrovertible I had to not do this once, as it may well not have been enough judging from the initial response, but several times.

·         Prove my SEVERAL conditions
·         Prove they were lying SEVERAL TIMES
·         Re-approach organisations that talk themselves up like they can sue anyone

I did all of the above and then some.

Except Patient Claim Line were first both rude and patronizing and then when I pointed out a few things they insinuated I was lying and stupid.

However the one funny thing is I have a blog and on that I have maintained for 3.5 years that I was suspect that despite the adverts on radio, TV and newspapers no one has ever any intention of doing anything and that the whole British legal system is a farce and nothing but lies.

Asaintcalledallnights.blogspot.com (or .co.uk does not matter).

It is absolutely shocking that no matter how long I am at this, how much I acquire as evidence on the NHS, and I have many other public services besides and am well known even with MP’s one of which used my data to attack Iain Duncan-Smith in January 2013, no one seems to appreciate the gravity of this and the highly serious nature of the crimes, almost like they are both known and accepted.

How can you wriggle out of acting after everything I have done? This makes most organisations, I am still looking, look like a front to make the British public believe that there are still avenues to take that do not actually exist!

Now I am going to copy and paste their last email to me, when I give them a breakdown of the times and dates.

I also need you to ask me that ...

Why is it then when I have explained to ombudsman, GMC, NHS England and organisations such as these that I have all this proved several times over and have all these recordings that highly suspiciously no one has EVER asked me for them.

So decisions made, like the recent I have less than a 50% chance, are done without viewing any documents at all or listening to a shred of my recordings and that when I challenge them on this they get even more rude and snooty than they did previously and move the goal posts for Statute of Limitation to 2 years instead of 3.

Three years is hardly fair when it applies to the public and not organisations and when there is no legal aid and no organisations to truly help you or even understand that after spending several years I am disappointed and angry that with all my efforts and helping other for nearly four years, no one wants to get off their arses and help in any way at all?!

I will send you copies of the emails with the follow up email, as I cannot copy and paste

Yours faithfully


Martin Haswell BSc

COMPUTER SAYS NO ... AGAIN!

Well here we go.

Another rude and patronizing email and my reply regarding Patient Claim Line.

Notice how they have now managed to move the goal posts and stating that with Statute of Limitation it is now 2 years and not 3? They act as a go between but completely failed to take into account that I had to decide WHEN I had enough proof, as they said no previously, how LONG it took to get all the proof and if they had bothered to look up Fibromyalgia, plus I FUCKING WELL TOLD THEM, I have memory issues that is well catalogued on my blog.

But no, according to them the best evidence in the world and all those reasons are not worth a Rat's arse!

Now remember these are Doctors I am going up against, normally the ones you trust to give evidence in court cases? I am also up against the entire NHS too.

But without money, as I would not be fucking approaching these incompetent idiots, I am supposed to gather and acquire all the evidence with a year?! Are they fucking joking?!

LMFAO!!

They really need to stop speaking in a patronizing manner as normally to have the right to do that you first need to be intelligent! Lol.

Remember I said nothing will ever happen? ;)


Dear Mr Haswell

Your recent email dated 20th April 2016 timed 18:12 has been passed to myself to review.

Following your approach, and wish to become a client, a full assessment of all of the information that you provided to us was completed.  As per your email dated 25th March 2016 timed 17:52 you advised that you had 'provided (us) with all the details' of the intended case. 

The decision was made, based upon this information supplied, that you had knowledge of any potential negligence in excess of 2 years prior to your approach to us.  When reviewing cases we usually need a minimum of 1 year until limitation expires to allow at least basic investigations to be made.  In one of your contacts with us you suggest that you have been asking about the condition for 13 years.  In another contact you suggest that you have been blogging for 3.5 years to help other perceived victims.  You also suggest that you have been recording consultations for the last 6 to 8 years.  This would suggest that any date of knowledge, from which limitation of 3 years would run, is more than 2 years ago; and in fact I believe much more than 3 years ago. 

As a result of this your case does not fulfil our criteria in respect of an approach that we would accept.

As suggested previously, you are entitled to a second opinion, and as such I would suggest that you contact another firm of solicitors who may be able to assist.

Yours sincerely


Dawn Bowdler
Complaints and Compliance Solicitor
Patient Claim Line


Phone
03300 080 352
Fax
0871 971 1622
Email  
Web  
Patient Claim Line
Dukes House
34 Hoghton Street
Southport
Merseyside
PR9 0PU


Dear Dawn Badler

First off you seem to be implying that I am lying ... oops, no.

You could have asked for the documents and proof yet again, but you did not. ...


They are now all there with the dates. I did state that I have Fibromyalgia and that with that comes memory problems as well as all the pain? Did you miss that part? Not a valid reason, a medical fact, for the amount of time it took for me to gather all the evidence because organisations were too stupid, lazy or had no intention of acting on anyone’s behalf the first time around?

I know how the readers well see it.

I was diagnosed with Fibromyalgia in April, 2014. The argument and refusal of the drug I attended Guy’s Hospital for was weeks later, so two years but now your moving the goal posts.

Secondly I could not approach solicitors again until I had enough proof. I happen to know this because I tried before.

Knowing in my head and having the actual proof are not one and the same thing.

Also your now moving the goal posts...now it is two years because you need a year, well that is convenient, is it not?

Lastly a blog is an online diary. Something that many, especially patronizing ones, seem to miss. SO guess what is getting posted on the blog within seconds of reading this? Obviously you failed to pick up on my stating that my recent posting on my blog with the recorded evidence is going to hurt a lot of people.

Like I said .... my statement and my entire blog is based on the premise that no matter what you have ... no one does or indeed has any intention of doing anything for anyone.

But I guess you missed that too?

Yours

Martin Haswell BSc

Sunday, 10 April 2016

ONCE MORE UNTO THE SOCIETY

Well I heard back from Patient Claim Line, replied to them and have heard back from them again.


  1. I emailed them the details of what I have suffered and what I had on mainly the NHS
  2. They emailed me back with the same thing I was getting 5 years ago
  3. I replied to their ... err reply asking how they had come to this conclusion without seeing, or rather HEARING, the audio recordings and why they or the solicitor did not even request them
  4. I got fuck all from those two questions and told to email The Law Society so I did
EDIT: Hmm, starting to think that these organisations are just out there by the government to make it appear to ... mere mortals that there IS an avenue to which you can obtain justice but when in fact there is not.

I mean, what more do I have to do? Get the culprits to accompany me into their offices and them fully admitting it?

LMAO!


EMAIL REPLY ..

Dear Mr Haswell 

Re: Your Medical Negligence Enquiry 

We write with reference to our recent telephone conversation in relation to a potential clinical negligence case. 

We write to confirm that having reviewed your potential case we are unable to act for you under a conditional fee or “no win no fee” basis as we do not believe that the chances of success with your case are greater than 50%.  

We must advise you that if you do wish to pursue this claim, court proceedings must be brought against the defendant or defendants within 3 years of either the date of negligent treatment or the date you became aware of the negligent treatment. 

This is only our view of the chances of success and a different firm of solicitors may take a different view on the chances of success. Should you wish to obtain further advice you may wish to search for solicitors who specialise in this area on the Law Society website, which is www.lawsociety.org.uk

Yours faithfully  

Grace Mawdsley
Patient Claim Line

So ... here we go again ...lol...


EMAIL TO LAW SOCIETY ..

Dear Sirs

Medical Negligence

It has been suggested by someone, think it was Patient Claim Line, that I email you. I did this some years back.

I tried to get legal representation some years ago because I knew that the NHS were lying to me through GP’s.

Since then I have been through no less than 5 GP Surgeries, locally, an not only did I have these surgeries and five hospitals lie to me but I recorded them on an audio file as they did.

I had one admit that the NHS get GP’s to lie to patients and another admitting that they falsified an ultrasound scan, then sent off the original falsified scan results after re-dictating a letter to my GP to say something WAS found. Subsequent letter stated ultrasound was clear.

These are just two of many recordings I have.

In this time I also managed to diagnose myself, something the NHS managed to miss then lie about for well over a decade, and then had my diagnosis confirmed by Guy’s Hospital. While being diagnosed the Doctor also spotted a problem with my right knee I had asked the NHS about for also close to a decade, possibly more. He did a test on my right knee without warning me that if I experience pain then I failed the test. Surprised while experiencing said pain he then declared that I had a physical problem with said knee.

When the letter came back from the hospital it the knee problem was not mentioned at all, or the test or the experiencing of pain. Also the drug I was promised, which was Pregabalin, was also not mentioned and I was set up for the umpteenth time just to save money. But saving money is not the only thing this behaviour has en effect on.

Obviously there is the problem of being left and dealing with pain and also subsequent support and financial help from local councils and the DWP. I warned both of these and the NHS that I knew they were lying as well as setting me up and I knew both how and why.

Everything I ever state is recorded.

I spent several years doing this because when I tried to get legal representation previously I was told I could not get it because I did not have a good enough chance of winning?! It would appear that telling the truth and having witnesses was not enough, along with a simple exam by a Doctor NOT associated with the NHS.

So can you imagine my confusion when I send my details, and a lot more than I put here, off to the Patient Claim Line only to get told the exact same thing?!

Also are you able to explain to me that whenever I have tried to get help and told them I have recordings proving this that I deliberately did not send the recordings because I suspect every one, including every single ombudsman.

Can you therefore explain to me just how it is that not only did each and every one of them NOT ask for the recordings but also when I point out that they made decisions on NOT hearing the recordings but did not even ask for them I do not get an answer as to why?

I will also add that unlike previously when I tried to get help to prove I had something wrong with me, since found three things, and that the NHS was lying I have managed to do this over and over and over again and while doing so I have published each and every step of the way along with my findings and evidence to a series of blogs and a YouTube channel that is proving to be very popular.

In the 3.5 years since I started publishing my findings I have had over 300,000 visitrors, in just 3.5 years with no promoting of any kind, had many, many likes followers and even a comment of thanks from a man of the cloth who realised his family had been lied to as well!

This has also had an extremely detrimental affect on my relationships, family, friends and a love life has been off the cards for well over a decade too!

My depression as a result of all this is on medical file and has been for well over ten years.

So for me, not forgetting my readers who follow my plight for justice and against corruption in the UK from all over the world, can you please explain to me what the hell everyone is getting paid for, including you?!

Because just like everyone else these past 3 years I am also expecting the same old crap from you too ... YET ANOTHER BLANK! I have not been wrong these 3.5 years as my visitors have noted.

Also so much so that the late Michael Meacher MP requested in January 2013 if he could use my data, of the DWP & Atos, against Iain Duncan-Smith in the House of Commons and it was I that got rid of Atos and produced evidence against them and NOT the Tory Party! I still have his email request.

I look forward to hearing from you as I am sure my readers will.

Yours

Martin Haswell BSc



Screenshots of EMAILS ..



Wednesday, 6 April 2016

WADING THROUGH THE SEA OF HELP (Patient Claim Line)

Write well I have had some responses to those thirty odd letters I sent off, the ones from the videos ..



Oh? It seems I did not film the other letters, or at least not uploaded them to YouTube?

Anyway ... I have spent a couple of years getting evidence and in that time I have proved that I did indeed have something ailing me, in fact I proved three things, and that I was lied to about the existence of NHS departments, drugs available and drug types as well as lying about other things and admitting they falsified ultrasound tests.

Now you would think that with all that, and who the fuck else would do what I have done, that this evidence I have that acquiring legal representation would be easy?

The fact is that I had a feeling that the answer would always be no. Hence now that I amassed all that I did I would start asking once again, knowing that the answer would be no only THIS TIME to the viewers and repeat visitors this would like highly suspect.

In fact just like everyone else they did not even ask for a listen to the evidence, or any of the letters I have had that are contradictory to what I proved.

In fact it seems that legal idiots are gifted with divine intervention?!

They said no, that I had LESS than a 50% chance, utter bullshit, pulled the statute of limitations on me and never asked for a single piece of evidence.

So here are the last two emails of Patient Claim Line saying no and me pointing out the deliberate mistakes to see quite how they react?


EMAILS ..


Dear Grace Mawdsley

That is quite amazing that you come to the conclusion that my chances are no greater than 50% without asking or listening to the evidence.

How did you do that, as I would like to know?

Secondly you said some bad words ...

A statute of limitations is hardly something you can enforce when I have been asking for months on end for help and being lied to by a bunch of incompetent people.

I look forward to your response.

Something else to post onto my blog ... I did state it was about the truth, how corrupt the Uk and all its companies and public offices are and how quite impossible it is to get justice, even with the evidence laid out for people on sound files.

Because part of my plan is to show what an awful state the legal industry is in and that new laws announced by Prime Ministers in the House of Commons are not worth a wet ... weekend. AS there is no way for the majority of the British public to enforce them.

I did state my blogs are very popular, there is a reason for this. Also I reason I do occasionally get thanked and liked, not forgetting followers.

Martin Haswell BSc

Sent from Mail for Windows 10

From: Grace Mawdsley
Sent: 06 April 2016 11:40
To: s
Subject::Mr M Haswell


Dear Mr Haswell

Re: Your Medical Negligence Enquiry

We write with reference to our recent telephone conversation in relation to a potential clinical negligence case.

We write to confirm that having reviewed your potential case we are unable to act for you under a conditional fee or “no win no fee” basis as we do not believe that the chances of success with your case are greater than 50%.

We must advise you that if you do wish to pursue this claim, court proceedings must be brought against the defendant or defendants within 3 years of either the date of negligent treatment or the date you became aware of the negligent treatment.


This is only our view of the chances of success and a different firm of solicitors may take a different view on the chances of success. Should you wish to obtain further advice you may wish to search for solicitors who specialise in this area on the Law Society website, which is www.lawsociety.org.uk.