THE SNOOTY GET SNOTTY

Well I have had a snotty email response.

I got a ticking off, would you believe, because they did not state that I had not got a greater then 51% chance of winning a court case ...

Umm ... except that is the second time I have been told exactly that and the fact that they said 'NO' to help in the same letter, well ... in my book that basically is stating that you did not get far enough over half a chance of winning a court case, lol.

Then there was a sarcastic comment about going through hours and hours of blog posts ... umm except for the fact it works the same a a Google search.

In other words this organisation meant to help the public just did not bother to look.

They must be helping so, so many people to not be able to spend a couple of hours doing some searching and listening to some tapes? LOL.

Also they do not seem to know anything about the fact a Doctor, or DOCTORS and a Specialist, falsified an ultrasound test result for a condition that is actually a killer?

My word, my Fibrofog from my Fibromyalgia must really be getting bad if I emailed  an organisation and did not actually state what I was emailing them about?!

LMAO!

ANYHOO ...

Here is the email response from AvMA, or confusingly called Action Against Medical Accidents, and my reply to them. I point out the sarcasm but I DO NOT bother to be sarcastic about her not telling me she was not prepared to search through my blog. I am stern about being spoken to like I posses an IQ below the score of 10.

Hmm, I hope they have not changed the name officially to Action Variable Against Medical Accidents, lmao, to cover themselves if they never do anything by stating that they clearly do not 'promise' anything. Cynical, much? Lol.

Or as it more likely sounds like ... making an excuse for why they did not look for it when I had actually asked them why they had not even bothered to ask me for it?

You with me?!

LMAO!

EMAIL ... BETTER INCLUDE THE SMALL PRINT FOR INFORMATION PURPOSES

Dear Mr Haswell

Thank you for your email.

I am afraid that AvMA has only limited resources in terms of staff and I am afraid that it is simply not feasible for us to read or listen to web-based information which can take several hours to look through and to listen to and it is for this reason that I was not able to do more than briefly look over your blog pages. If you are able to provide a concise, chronological, written account of your concerns about health care we would be able to look over this if you want specific advice on a  potential clinical negligence case but with the greatest respect your letter to us did not highlight that this was advice you were seeking. I also must say that I did not make an assessment that your case had a less than 51% chance of success, I simply told you that given that most cases now have to be undertaken by solicitors on a no win no fee basis, this is the benchmark chance of success that solicitors are looking for:-

I am afraid that changes in funding for claims means that increasingly solicitors are only able to take on cases where on initial assessment the chances of success are over 51% and there are no additional litigation risk factors such as the claim is well within the three year time limit for making a claim.

If you are able to submit further  information  in the format I have proposed we are happy to see if there is anything further  we can do.

Tracy

f o r   p a t i e n t   s a f e t y   a n d   j u s t i c e

Action against Medical Accidents (AvMA)

Freedman House  | Christopher Wren Yard | 117 High Street | Croydon  | CR0 1QG |  DX: 144267 / CROYDON 24 Fax: +44 (0) 20 8667 9065 | e-mail tracy@avma.org.uk  | http://www.avma.org.uk/

Please give feedback at:- http://www.avma.org.uk/help-advice/how-we-can-help/feedback-form/online-feedback-form/

Follow me on Twitter: @TracyMinns1

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Action against Medical Accidents is a registered charity in  England & Wales (number 299123), and in Scotland (number SCO39683) and is also a company limited by Guarantee (number 2239250). Registered offices: Freedman House, Christopher Wren Yard, 117 High Street, Croydon CR0 1QG.

EMAIL BACK ...

Dear Tracy Minns

First off it does not take several hours and I( do not appreciate your sarcasm.

I said ‘audio recordings’ and any other details you asked for, like name of the Doctor on the audio recording can be searched on the blog via the search function, you know it is like using Google search, it sis the same principal really.

Second of all ‘you did state as much’ to what your now denying.

The fact that you stated what you did about the 51% implies that I was under that for chances of success.

Your asking concise information of someone who is disabled and one condition affects memory. I am afraid that the recording of ...

Darren Francis admitting on tape he falsified the test result for an area of inguinal hernia repair as well as the new inguinal hernia I had, dictated a new letter to my GP at the time stating that I DID have an inguinal hernia and then did NOT send the letter he dictated in front of me.

I diagnosed myself with Fibromyalgia. Just prior to this I had been put on Gabapentin for a couple of years. I then asked to be put on Pregabalin, which is the same family as Gabapentin, but was refused and put on Amitriptyline, a totally different class of drug. I was then accused of first being ‘mad’ and then accused of being violent when I told them I had a recording of a Doctor from Chase Farm Hospital admitting he was lying.

Then I was lied to by my next GP, being told there were no NHS Fibromyalgia specialists/Doctors in the whole of the UK and also lied to me about there being no drugs for overs-weating. I then found out about Guy’s Hospital and had to force them to refer me where after 13 years I had my Fibromyalgia finally confirmed.

Referring back to the second paragraph in bold, I then read in Black’s Medical Dictionary in around 2014 that Fibromyalgia only had two drugs that had any effect, the two totally unrelated drugs of Gabapentin and Amitriptyline which I was given consecutively, despite wanting Pregabalin. I was also told by the Pain Consultant that the Gabapentin being prescribed would NOT work on my back.

Odd as despite asking for several years my back has NEVER been diagnosed while they have x-rayed and scanned the WRONG part of my back several times.

I am currently going through this with my back all over again and now they have quite deliberately x-rayed me several times but in the completely wrong way so that my real diagnosis does not show and have had this confirmed by a Osteopath in Potters Bar my current GP promised to refer me to 6 months ago but keeps making excuses why he has not, along with excuses as to why he has not looked at the private x-ray I gave him showing the two back problems 6 months ago too.

That above in bold is only a small fraction. I have recordings in the absolute dozens and many of the most shocking ones, probably a dozen or two, have been posted on my blog over the past 3.5 years.

As to the length and amounts to anything ... I am sorry but it is not I that is responsible for the amount of corruption and the number of organisations ... ‘at it’.

Also if my knowledge of law was ‘that good’ I would not need a solicitor and would represent myself in court, which is why people go to advice organisations in the first place.

I am an expert on herpetology, batrachology, ichthyology, astronomy and astrophysics, orchidaceae, have knowledge of quantum mechanics and a single honours degree in applied computing and am a kung fu expert among several other skills.

Despite all that I cannot be expected to also know the intricacies of legal areas and know hat is relevant to a solicitor and what is not ... oh ... and I was a Personal Assistant to a solicitor right here in Enfield. Not in this area, before you ask. Conveyancing mostly with Wills & Probate.

So to summarise ...

·         Fibromyalgia I have had 14 years plus, discovered about three years ago and then when I finally got diagnosed, 2 years ago, I started to realise certain things but was already long since recording

·         I was lied to 3 years ago but I have spent the last two years being messed around by NHS England and the PHSO, the latter I have half a dozen to a dozen letters and compliments slips from them and now they say that they have never heard of a member of staff called Jonathan White, I still hold the emails for (digitally) and no record of my case.

·         So therefore sounds like a deliberate time waste by a government organisation so I go beyond a Statute Of Limitation, yes I know what they are called, which is totally unfair as it applies to people that have no expertise in such areas and with not a single organisation, please do not mention CAB, to go to, to actually get any genuine help at all.

·         In fact over 300,000 people that will soon be in the millions on my blog, all agree or have now realised this is the case and why the blogs exist

·         There is far, far more than one blog, fifteen to be precise and my YouTube channel backs them all up with 0ver 1,500 videos and around 160,000 views of my videos and rising

If I did not explain this clearly previous, I thought I had, then I apologise for that.

But you have to understand that it is bloody annoying when I have spent several years at my own expense collecting all this data and evidence while helping closing on on half a million people for no money whatsoever while having a several disabilities and pain and an organisation that actually receives money to help us says ‘oh we have no money and they are cutting this, that and the other’.

Help is help. Words mean something. Start changing this and you change the meaning to one that is misleading.

As for me ... I got on with the job at hand. It matters not to me that I do not get paid. I research, work things out, plan, by the tools, approach and capture and then spend years telling others so that they can help themselves.

Yours

Martin Haswell BSc

AN ORG LONG FORGOTTEN

I remembered an organisation today that I have contacted previously but not for a couple of years.

In fact the first time I contacted these people was actually quite some time ago when I first realized I was being screwed over by public offices and this was over 4 and maybe 5 years ago!

So as I recalled them today I thought it would be a good idea to send them an email and explain to them what I had managed to achieve in the time since I contacted them!

The first time they stated they had been inundated with people stating their money had ceased, I was expecting as much and remember this was 5 years ago now. The second time I cannot recall if they even answered me.

This time I have exhausted every avenue, as many of you are aware, and I have acquired a great deal of evidence.

So let us see what the Disability Law Service says this time around?

LOL, here is the email I sent them...

EMAIL

[address omitted]

Dear Sirs

NHS & DWP

Do you know I actually forgot all about your organisation?!

Now I have recalled it I have a couple of groups of points I wanttomake to you...

GROUP A

1. I have contacted you previously and several times too
2. Secondly as no one seemed to believe me I have spent the last couple of years ACQUIRING MY OWN PROOF!
3. Thirdly what I have done is already helping many people and tens of thousands are already aware of my endeavours

I will now add at this juncture and all I will say for now because I cannot trust anyone and until I do better to be safe than sorry is that every single appointment I had with Doctors, Orthopaedics, Neurologists, Physiotherapists, Pain Management Consultants, Pain Support Groups (which were really recruitment drives to get people to work for Chase Farm Hospital for free), Biomechanics, Podiatrists and even including my GP were RECORDED.

This was purely because I have been refused diagnosis, MRI scans, help, support, the drugs I needed and many other things for over 12 years. I also have every letter going back to 2003 including some prior to this! I suspected I was being fobbed off and possibly even lied to, so in a short a space of time as I could I recorded every department I was referred to and then some! What I can show to the world is that the NHS: Lie, Cheat, alter test results, contradict each other, keep giving a string of different diagnosis and stating the previous peron was wrong.

I did not only do this with Medical Professionals but also included 90% of public offices as well as some private companies too. All I will state right now is that I have a BLOG and it has been going for a year. I am heading towards 100,000 visitors, not looked since it hit 55,000 a few weeks previous. Also my victims include most QUANGOS you can imagine and a vast majority of Ombudsman.

I will also add that you many note that in recent times many of what I have talked about has been in the News Media? Well back in January a backbench Labour MP of a household name was told of my blog and emailed me asking if he can use my data against Iain Duncan-Smith in the House of Commons as well as handing it to the media. Of course I keep all correspondences if linked to any of my endeavours.

I can tell you now that my entire data collection of evidence alone will be over 50GB most likely and certainly over 40GB.

GROUP B

1. I have been falsely accused of using language that insinuates I will be violent towards a GP
2. The GMC and the PHSO are both aware of the above, as are sections of the NHS who now claim they will help me
3. I was lied to about an Ultrasound on both sides of my groin, being told it was totally clear when one side had a black hard patch that causes the pain I was THERE for and he unwittingly scanned the other side which revealed I had ANOTHER hernia
4. This is not the only thing they lied about and others include Neurologist, Back Specialists and other all of which I have proof of as I stated above.
5. ICE,the Independent Case Examiners of the DWP are nothing of the kind and as far as I can tell all complaints procedures will go nowhere and exist to waste time until the plaintiff becomes bored and gives up.
6. Also while their investigation was crawling along I also pointed out to them that I had a current claim that I had an initial letter about but suddenly nothing happened and I forgot all about it. They never asked the DWP WHY this current claim had NOT been dealt with.

The one thing I had forgotten about while explaining the truth about the UK is that I had forgotten all about you. When I contacted you previoulsy I did not have anything in the way of all this proof and it was down to losing my Disability Living Allowance. Well I went through all the procedures and now I can tell you something ELSE I have as proof.

1. Atos and the DWP agreed to perform a Home Visit.
2. Only they arranged this three times and each time came up with an excuse as to why they failed to turn up, two were LIES...
3. One time they said they knocked but I was not in and yet I was
4. Another time they stated that a big STEEL BIN was in front of my street door and they could not reach the door to KNOCK?!
5. This is also a lie and I do not have a street door as the street is fifity yards away down a very narrow alley. The steel bins are also communal and 50 yards from my house and do not FIT inside the alley-way! There are also three other paths that lead to my house and I have no bins outside.
6. I filmed myself walking from my street to my house and and walking inside and showed how small my house is plus how from my living room settee I can SEE my street doors!
7. When given all this ICE stated it was INCONCLUSIVE, after 20 months of investigating?! Nothing in the way of a visit, not even asking questions they should have done like what Is the widths of the bins and alley-way?!

So this is just a brief description of what I have collected. Believe me when I state BRIEF and I am quite literal when I speak or type.

Now as I remembered your organisation today I thought it a good idea to email you about everything I have beendoing and see what you have to say?

After all I have proved many things that can be highly beneficial to any organisation that exists to help people who have had injustices against them, including disabled people.

Also I would like to finally add something that I MAY have mentioned before...

It is my belief that a nasty little setup was created some years previous whereby if the NHS do not diagnose you this therefore prevents you from getting the necessary help and money from other so called public services like the DWP and Local Councils.

I had initially thought that GPs and Doctors where naïve to all this but it seems that in my endeavours to start conversations to get them to reveal bits of information it turns out that every one I met is not only well aware of it but aid it by lying.

I look forward to any correspondence I may receive.

Yours sincerely

Martin Haswell BSc