Why am i not surprised by all this The DWP ARE CORRUPT and need firing an ordinary company such as Capita no way could they argue with a G.P .Neurosurgeon or what ever title they may hold can be argued by civilian staff who have no idea and are not allowed to read your medical reports its The professionals who should be in attendence with you at an assessment Mel Stride you need to watch these videos and hang your head in shame.I grew up in an NHS Background with 2 relatives who were charge nurses i spent 16 years as a qualified first aider i wanted to become a paramedic but a brain tumour stopped all that. even diagnose a holiday maker at a holiday camp with possible IBS Which proved accurate and my wifes bad lady problems again i was right.I took my late father to a G.P. And informed him my father had a urine problem i was wearing Med Fleece and the doctor asked me if i was a G.P. I said no but i have had a lot of training in First Aid
You are not qualified,certified or insured to diagnose...so why are you trying to do so?Medically there is no such thing as ' lady problems' .If you have no medical credentials stay put of it...before you're sued.....The term is gynecological issues...just stop.Anybody can get a First Aid certificate.You need a minimum 3 years Anatomy and Physiology to have any medical credentials .
@@keepitreal665 quite, and no GP is asking in all seriousness, if someone who speaks like that “is a GP”. It would have been sarcastic, it asked at all. Such embellishment simply doesn’t lend credibility - actual medic.
Why do you think the DWP are corrupt when they only follow the rules set by the current government? It is these ministers that set the bureaucracy and targets not the DWP, they are following the rules and regulations set by this fascist govt. I would have thought this was plainly obvious, there has been 14 years of austerity targeting the most vulnerable in society while their mates buy private jets and yachts from spunking away billions from private contracts. A prime example is Capita, put in place by the Tory cronies.
I get what he is saying about idiots applying for PIP I personnel think that your doctor or consultant should be the ones to recommend you for PIP as they know your medical condition better than anyone but the DWP can't control doctors
Yeh there does need to be more medical based stuff around it , they quote they use the evidence and I know others have said they've done it and requested it from their GP etc but I know personally speaking none of my evidence was ever used or requested when I filed a freedom of information.
I agree but unfortunately a fit note from your gp doesn’t hold that much weight in the DWP eyes…. I had a fit note and was told I had to come off esa and find a job basically…. Yet… if I was employed and handed a 2 week fit note into my employer but then went back to work after only having a week off, chances are, should I have an accident at work in that week, I wouldn’t be covered under my employers insurance as my doctor has deemed me NOT FIT for work.
@@DynamicDuoUK My GP doesn’t know me well at all. I have along and complex medical history and have only been registered there for a year. I can’t afford a £15 cab every time to go to the GP and most of what I say falls on deaf ears anyway. I supplied my own evidence after accessing my files medical record and took lots of photos of my mobility aids, my actual conditions, included reports from police, ambulance etc. and because it took 7 years for me to get PIP Imade a point the last time of highlighting all the evidence that wasn’t taken into account the last time around and put it in bold so they can’t ignore it again
I have lost my dwp/pip 4 times since being disabled every time I have done mandatory reconsideration and failed so gone to court and recieved it back its outrageous truly
I've been about 6-8 times over the years even though my back is tucked and I'm in pain 24\7. My medical records and x-ray speak for itself but I was still being told in as fit as everyone else
65% failure rate to save money! Just ask our GP’S they will save 100% of the fortune that they are paying people to torture the already suffering. This is a cruel system. People don’t want to be sick. That guy is telling the truth, no question about that.
I have a broken spine, a hole in my spine, Lung disease and arthritis on top of depression...they just stopped my money without notice.... ice cold winter and I had no heating...could only get by with loans just to live..17 months wait for court... finally I won.. I was awarded 10 years none stop PIP...i ve never been so humiliated/cold/ and low in all my life...But I won hey
I was awarded PIP in 2020 for fibromyalgia. Lower rate daily living, no mobility. In 2021 I started developing serious symptoms of POTS, I get dizzy when I stand, and I get breathless ahd blackout/faint when I stay standing up for longer than a few minutes. I'm seeing a cardiologist for diagnosis but that alone took 1 year to get an appointment! I have to now use crutches at home and a wheelchair outside my home as it is unsafe for me to walk because I get dizzy, blackout/faint. I can't cook a meal and getting in and out the shower is extremely dangerous so I have my husband help me. In my PIP renewal in 2023 I told them this. Nothing more awarded, lower rate daily living, no mobility (i scored 4 on mobility as i did in 2020). So I did a Mandatory Reconsideration detailing exactly my symptoms and they gave me no more points, didnt even give me a reason. Their scores are the same as before all this started, point for point the same and no mobility awarded, just the same 4 points! So now I'm taking it to tribunal. I will fight this every step of the way. The thing that gives me the fight is I already know they are incredibly biased against us and they know people won't fight it at a tribunal. I know there are some people like "Andrew" but most of them are not, they think we are lying. My life has been flipped upside down with chronic illnesses and I will not stop fighting to better my life. I currently cannot work (after being in fulltime work for almost 20 years) and the £270 a month that DWP gives me is no where near enough to survive. When I asked citizens advice what evidence am I supposed to provide if confirmation of my symptoms from my cardiologist and my very detailed explanation isn't enough and they were shocked because what I provided is enough "proof" and they think i should get higher rate awarded on both daily living and mobility. I filed my tribunal at the end of March so now is the waiting game. Please send me good vibes!
What you have gone through is extremely common they have denied people PIP entirely who are dying and sent them a letter denying them after appeal when the person had died from the conditions they were seeking PIP for in the first place. I was aware of this issue before I myself applied, so used my local welfare rights officer to help me fill out the forms as well as attend the assessment call…. because you will then get a fair assessment rather than a denial of you have a advocate with you that can dispute any lies they tell.
Sending vibrations of positivity, love and compassion to you. I also send healing frequencies for your journey of the PIP process and also for your emotional wellbeing. Anticipating your win over this obstacle ❤️🙏🏾
Sending you good vibes, and I hope you get a positive result, but more than any thing, I hope and pray you get healing, my stepdaughter has fibromyalgia and I have witnessed the impact on her life sending you love.
After being refused initially and then on appeal I wasn't going to stop and got referred to a welfare rights officer who then filled out my forms etc I took it to tribunal. I have numerous health conditions and at tribunal cried all the way through I got high rate of both daily living and mobility. I was told most people who do try to claim without an advocate/welfare rights officer will get refused. Don't give up and I wish you every success.
Any worker for the GOV, be it jobcentre staff etc has to sign the official secrets act, that in its self is bad news what they are quietly up to in the background!
we know we are despised, and hated. its good to know about the 45mins assessment time, as if they keep on at you through one question, they can only do it for so long, as they have to move on, or not do a complete job on your application. which gives you a good appeal argument. - (one point,) and it wont work for everyone, is a friend of mine, did their application through a specialist solicitor, and at the assessment end, he said "so will you notify me, ? or my solicitor"?, the guy hadn't read the bit where it was prepared and obviously read and filled in by the solicitor, - so he fumbled an answer to him, - and he passed. its not the cost, but the fact it had been completed beforehand by someone reputable.....when your on your own, your a little guy getting pushed around.....great video!!!
The whole dwp needs a shake up. If your an alcoholic or drug addict you get help but if your genuinely knackered you get no help. I remember a few year ago that poor lass who was a paraplegic and bed ridden was found fit for work..
My daughter has addicts living in flats near her,they get loads of money and cost of living payments. They’re always out shoplifting and selling goods. My daughter has two grown up children who’ve left home, she’s always worked and didn’t claim the paltry amount that she was entitled to off her council tax bill because they wanted to know the ins and outs of a cats arse. Her kids have both got good jobs because their mother had a work ethic that she got from her parents. I’m a carer still working age 69, most of my clients are in need of care but I have a couple who are playing the system and there’s nothing wrong with them. What am I supposed to do when I know someone who’s able to decorate and do their garden yet claims to be disabled!
I've entirely given up trying to get PIP, because as an autistic person, I am highly sensitive to the wording of questions, and realized very quickly that I was being asked the same question multiple ways, and being pressured towards a particular answer. I have trauma around this exact issue due to it being something that is done to me regularly by people who do not understand how autism works. Until the DWP ceases to exist, and is replaced with a system that actually works, it quite simply isn't worth the stress and trauma of going through a process that is designed to be harmful to the mental health of claimants. My mental health should not need to be destroyed in order to gain the benefits I am actually entitled to. And so, I am stuck living only on Universal Credit. That isn't living, it's surviving, but the alternative is that I don't survive because of the impact going through PIP assessment has on my mental health.
You can ask a professional help ypu fill out the form and be adamant on a paper based assessment so that they don't disturb you and can just ring the professional with any queries. The professional can guide you and be with you every step of the way .
You need to apply for ESA and they will put you in the support group that is extra income paid fortnightly especially if you can't work.I was medically retired for 11 years but now I'm retired claiming state pension and Pip good luck and take care
I have been claiming enhanced pip for approx 10yrs or so due to chronic illnesses. Few days ago I endured a 1hr 20min assessment of solid interrogation which has left me in a real dark place. The lady was really emotionless and my wife who is my carer also was with me and she was gobsmacked at how cold this assessor was to me. I was struggling to deal with it after 45mins and broke down telling her that this has made me feel worthless. My concentration levels aren't very good anyway but as this went on I was starting to struggle understanding questions but she kept pounding regardless. I just can't shake this feeling of emptiness I have now and can't think of anything else but the assessment. This has really really affected me bad.
So sorry you had to endure that. I lost my PIP a few years back. It took me 12 months to get it back, and they put me in the lowest bracket. I ended up living on 76 pound a week. It made me ill. JUST KEEP FIGHTING IT. ITS YOUR RIGHT.
Unfortunately when parts of services are sent onto private companies, it will be compromised! It’s disgusting the way vulnerable ill people are treated, so disrespectful. Thank you for this information
I'm in tears watching this . I had my assessment 2 years ago, it was the worst experience I have I have ever had . I have a rare blood cancer and anxiety told to apply for pips , my sister was with me for a phone interview as support . The assesser was 1 hour late from time scheduled, which made me start to panic then she said she would have to be quick so she could get back on track her end. I went to pieces my sister tried to explain what was happening the assesser was extremely rude to her and told her to shut up otherwise she would end the call. I tried my best to pull myself together the interview went on for 2 hours !! . I was awarded basic part of pips . When I got the letter through stating reasons for each bit she had lied changed what I had said . Tried to appeal but to no avail.
Thank you "Andrew" for finding the courage to speak out. As horrific as the PIP process is to go through, I'm glad that there's someone there who genuinely cares about us. I've spoken with a few condescending and abrupt assessors in the past and only one nice one. You guys are few and far between. I've met a few ex-assessors who said they quit because they couldn't handle the mental strain and toxic work environment as you described it. Thank you for trying your best to make a difference. Stay strong. ❤
You're very welcome and thank you for being here. It certainly seems like there is a lot more assessors starting to admit the truth now. Even the lady today clearly stated it's a stressful and sometimes horrible situation to be in with the work. She does take that as you will but it says to me they are starting to feel the strain. X
100% true. Thanks to your source and you for getting this made known. I say if you get refused appeal and ask for a Mandatory Reconsideration - even though it can take time. Maybe if enough people took a civil action against the department the numbers might count, like the Hillsborough case.
@@DynamicDuoUK True. Their goto reaction is usually offensive as defensive or stone walling. But writing to the department minister and secretary in email firstly then snail mail means by parliamentary law they are obligated to do something. Imagine getting 20k letters a week on constant basis. Plus forms of course, the department will have to process thousands, preferably millions or forms and calls to the lines. Good luck everyone
To be honest my sister had a telephone assessment, after sending in her PIP form with supporting evidence. The assessor was uninterested in anything she said, kept cutting her off mid sentence, and only spent 20 minutes on the phone. After the call she said to me “they’re going to take it off me, I know they are”. Then she received her award letter. The DWP case manager said they’d chosen to deviate from the assessors recommendations of a lessor award, based on the vast amount of supporting evidence received from medical professionals involved in her care. And had decided to award her the highest rate on both components. So I don’t think we can judge all people in one role or another. Some are excellent in their job and recognise the failings of others. As can be seen from my sister’s case. Where maybe another case worker maybe wouldn’t have. Or if she’d have gotten a more competent assessor it wouldn’t have been an issue at all.
That's the way it should be done !! ❤️ I'm hoping that with enough push now on the system people are starting to realise and I seriously hope we've had some sort of effect in some way or another, even if it's only minimal. A massive congratulations to your sister. Wishing you all the best. Thank you for your story ❤️❤️
What happened to me, I literally cried when the manager rang me with enhanced on both parts. For the first time in decades I have some quality of life now. My review wasn't due until Sept, but they made me do it in Feb which totally sent me in a panic, I'm being sick every day through anxiety can't stop thinking about it and so scared they will take it away from me. At least this man who emailed actually feels compassion, respect to him.
I had my assessment last week to continue my PIP after 5 years. They want to turn it into a new claim so they can fail me. If I lose I’ll be homeless and unable to use the medical equipment that helps me breathe so chances are I won’t be around for long. It took 8 attempts to get the assessment because every time I told them they were being recorded, they hung up the phone. I’m waiting for them to write to me with their decision…..
I fought for my PIP all the way to the tribunal and won was given a lengthy award by the judges the DWP didn't even want to send my award notice and money to me until I phoned up and warned them if they didn't I would see them in Court and well few days later I got my award notice + money.
That's disgusting. At the end of the day a court is much higher up than the department for working pensions. They are not above the law and they need to keep realising this despite the fact they think they are. I'm glad you got your reward and it's a testament to other people. I actually cannot wait until the DWP collapse and something else takes over in its place because they are truly shocking and the staff that work for them at the moment are terrible and I don't care if that offends anyone. Well done to you. All the best
Well done for reading this out as i have just been refused my pip she defo did the same to me lied so i did not get it now waiting for mandorey reconsideration but i wont hold my breath i will keep u informed thank u so much people should no what they are doing to people who have disabilities
Your welcome, I'm fed up of them treating people like this I've been through the same thing you have been through and won! Not once but twice ! They do lie, they break rules and they don't shed a tear as they never know you as a person but rather a number, it's time we all joined together and showed them the person not the number. Best of luck to you with your process ❤️❤️
it certainly hits the nail on the head and seems to follow a process that the DWP and subsides follow, ive had similar reports but never fully in depth like this and it all matches seperate accounts so unless they all have a big what's app group together to discuss it then god knows! but i beleive it to be true.
THANK YOU RICH FOR THIS VIDEO, AS IT PUTS ME OFF CLAIM PIP, ETC OR ANY EXTRA MONEY ON TOP OF MY UNIVERSAL CREDIT, AS IF PEOPLE SHOW EVIDENCE THEY ARE SICK FROM THERE GP, THEN THEY SHOULD GET PIP, ETC, AS WHY DO THEY NEED TO BE ASSESSED BY THE DWP, WHO DO NOT LOOK AT MEDICAL EVIDENCE FROM YOUR GP AND HAVE ONLY TRICK QUESTIONS TO MAY YOU FEEL UNCOMFORTABLE.
Try not to be put off it's a hard process don't get me wrong but it can be won and achieved it's been proven it's a long process and hard. Your right assesment is a horrible process doctors should be able to recommend for it as they are more officially trained for identifying things.
You should try anyway. Go to Citizens/Community Advice for help with filling in the form. If you're are entitled to it, at least try. And if you get turned down appeal it. Just try. And I pray you are successful. It's very intimating, but you are allowed to have someone with you to support you during any calls.
@@DynamicDuoUK I agree. I was asked for a doctor's letter. Why do they ask for evidence yet not look at it or take it into consideration? It's really corrupt and underhanded and I hope it changes. I really pray it does🙏
This is all depressingly familiar. When my disabled wife was alive it was a constant battle with the DWP and included two tribunal hearings and an assesment by a dubious foreign doctor who was subsequently struck off for malpractice. They are a corrupt shower and should be closed down and replaced with a professional medically qualified system
I went to a PIP assesment once with my mate as a witness. They asked him to stand up, lift his arms up, asked if he could go to the shops in which he responded i drive when i need to. And that was the end of the assesment. He has fibromyalgia and is in remission from leukemia. He failed. Hes now on jobseekers looking for work that he can't physically do and now suffers mental health as a result of the stress and embarrassment. He has to actively look for work and attend job interviews, hes been rejected from every job interview. He hasnt been able to work in around 10 years due to health and he is close to 60. How is he going to find a job when he is in constant pain? The system is a joke. However i do also know of people who play the system and succeed, he just has morals and wont try to deceive.
They stopped my PIP last year based on a 2 MINUTE phone call. Didn't want to know whats wrong with me or how I'm affected. Reinstated it after 4 months and had the audacity to CONGRATULATE me.
I applied for a job several years ago with one of the third party companies who assess the PIP claimants & got offered an interview. While waiting they put me in the kitchen area & I sat listening to the "assessors" and other admin assistants sit having their break and taking the pee out of some of the applications. They were laughing and openly discussing things in front of a complete stranger (me). Thankfully I didn't get offered the job, but I would have turned it down anyway. It was disgraceful behaviour.
And this is what needs reporting more and more. I'd be interested to hear your story in detail because people do need to realise this is happening and shouldn't keep happening. It's pretty much them against us at the moment and that's horrible. Thank you for telling the world that we appreciate it and I'm glad you didn't set that job even if you didn't get offered it. X
The problme is they lie about what you tell them and when you prove they lied nothing happends to them because they are told they must fail as many as possible these scumbags are there to save the DWP money if it was a company you compline about them they would be disaplined sacked so on. But as its part of the plane to fail you there told do what you can .. why evertime you talk to them RECORDED THEM you can tell them or not its your right too . That's the only way you stop them from lying as when you fail and you appeal you talk to like judges NOT .DWP they are in the room but only to listen an ask some questions rest up to judges . When you show the transcript yours and there's you see the lies . Then you win . You get there transcript sent thro to you. So have yours printed out and.check word for words you see many missing (there'sor changed )
My family member has been on PIP since it was DLA from the age of 18...we had an appeal back in 2018..NOTHING has changed with them, however, we are now waiting for a court date for another appeal. Been waiting 5 months now!
I was sent for a medical by the job centre arthritis and mental health .was told I would never work again .told to put in for pip on my medical. I didn't get one point .mental health prevented me from putting in for a review
Thanks for speaking out Andrew you are just confirming what we already knew. Some good news here My daughter got her PIP again now I can sleep and no more worrying did I say the right thing for the next 5 years when it all starts again. I didn't agree with the scores they gave her but thankfully what they did award kept her getting the same amount. Now I wait for my interrogation which is due soon!!
They've done this to me and I've got a broken back. How the hell am I able to work when I can't even walk . Immigrants need funding and war of course. Sunak has offshore billions and could help this country but theyre so greedy
Yeah I can confirm, I've had Multiple Sclerosis for 23 years I did used to get DLA then got switched over to pip and unceremoniously told I didn't qualify for benefits I do a ten minuet walk to shop five days a week it's what stops me from ending up in a wheelchair because, that daily exercise is literally what stops what is left of my muscles from fading away completely, I cook for my daughter when she comes home from school and do the laundry, its not much but its about all I can do when its dry enough I cut the grass, this may sound strange to some but that can take up to 6 weeks to get over the pain of pushing a lawn mower round and raking moss, my record for moss raking is about 3 square meters! it tears my muscles and isn't easy to get over, but I have about 250 square meters of lawn! So I have a mossy lawn. In short I do as much as I can when I can. As for medication I literally cannot take things like anti depressants I wont take meds for my MS as the first time I tried the side effects almost killed me, the only response I got from my neurologist at the time was Anti depressants which I tried they also had a detrimental effect so I had to stop them also, SO my wife works full time to support the family and we live from paycheque to paycheque, every now and then we end up not being able to afford food shopping at the end of the month, But our daughter will always be fed. I can't put into words how broken and corrupt our government is! But I do know that bonfire night is a time for solemn reflection of what could have been.
The DWP are not just currupt, they are highly trained and conditioned to find any spurious reason to fail in any applicants application. Assessments should only be made with a claimants doctor and then assessed by a medical panel for final decision. Then and then only should the assessment be sent over to the DWP with a recommendation for acceptance of Pip. The DWP should have NO part in any assessment proccess whatsoever. There are completely untrustworthy and not medically trained to carry out any level of medical examination, period.
From what I am reading, it is the medical assessor who is biased, even though they are supposed to be impartial. They are the ones who write the report which gets sent to a decision maker. i.e. the decision maker can only make the decision based on the report they receive. So if that report is biased, lacks information, is only filled with positive abilities. That report is not a credible report, it is not actually the fault of the DWP decision maker. it is the assessors that are the problem.
As Promised to "Andrew" I didn't post the email or details as promised to not breach data, i read it as best as i could sorry the eyes arent great today!! Truly Shocking !!
My 53yrs daughter has been taken from enhanced rate to basic pip...she's got copd..advanced emphazima..loss of hearing Rheumatoid arthritis...can you please advise on how to get this investigated...thankyou for everything that you both do x
In court at the moment medical serve copd unable to work 5years ago yet still on esa poor system private company need to keep the numbers down I promised myself after my self-harm stay about long enough to win hopefully my lungs 🫁 hold out 😅 you man is right that's exactly what they do sent med records with all paperwork it give them less chance to coerce you 💪🏼👊🏽✌🏽❤️
I was told that by turning up to a PIP assessment and making an effort to dress properly (which anyone with self-respect would do) counts against you. But not making an effort proves you're not serious and counts against you.
When my husband died two professional ppl from my housing association insisted that I claim for pip. Id always suffered from mental health but with medication, I'm stable. I told them I'm not sick enough to claim and stated I didn't want to. But they insisted and a few months later they were on my case. Questions they were asking were to much, and I told them nothing. I didn't respond to letters, which the second one was pretty abrupt. I ignored that and then they started phoning me. They're just trying to get more information about you and I'm not willing to. I don't need pip. Simple
What is the point of sending in medical evidence if they don’t even read it! It clearly says on the forms that it’s your responsibility to provide medical evidence 🤷♀️
Shocking. Is this true? Yes, one thing DWP has done is extreme targets; they adapted the sales KPI technique to get people out of the system whenever they are disabled or not; it all depends on your character never back down to them.
I beleive this to be true i did respond to the indivudal but the email has since bounced back i can only assume it was an email address created to send the email? it does however fit in line with the practices that other DWP agents or staff have informed me about and is following a pattern also explained on other youtube content creators accounts
What this whistleblower says is 100% true, as I can attest from undergoing the PIP assessment every three years since 2007. The last time was last year, and it took me ALL of last year and a threat of tribunal to make them pay. I am Autistic, ADHD, have CPTSD, Delayed Sleep Phase Syndrome, Fibromyalgia, Interstitial Cystitis, Fibroids, Migraine, and Depression - yet they turn me down as a matter of course every time until I threaten to go to tribunal, at which point they magically call with an offer as if they never refused it in the first place. To top it all off, my dad has still not had his Pension Credit processed in over a year, and we’re threatening legal action. They are truly, utterly corrupt.
I went for a pip assessment and the guy had to google my condition because he didn't know what it was, how can he assess me when they don’t know what the condition is 😂
I was disabled and unable to walk. They stopped my money because they said if I was really as unwell as the Dr and I said then I would be more “ depressed “ . Apparently depression is completely visible
My friend and myself are Registered Nurses and applied for positions as PIP Assessors a few years ago now, we are Both in our 60’s and have 30 years plus experience as Nurses, we Both failed the interviews, we were told by someone anonymously that the company don’t want older experienced professionals as we wouldn’t ’do as we were told’ ie mark applicants down etc, it’s a disgrace that people who have worked for years and paid into the system and become disabled are being turned down, I was given 0 points and appealed and lost my appeal, the reason given was my conditions didn’t match the meds I was taking 🤷♀️ the whole system needs overhauled
I've applied for pip 3 times n got rejected on grounds I can walk from my bedroom to the bathroom a whopping 10 feet away, I suffer from hypertrophic cardiomyopathy, lymphodemia in my legs n severe migraines from all my meds it's just a waste of time applying at this point
I’m sorry to hear that. My godmother is the same. She’s 88 only has one lung has type 2 diabetes, thyroid, asthma, heart condition and uses a walker. Can’t walk up/down stairs and can’t do any chores but got knocked back coz she still holds a drivers Licence so they say she’s not disabled. These people are vile. I have more respect for a hooker on a street corner. At least they are providing a service, unlike these f&ckers !!!
OMG! Very interesting, it's worse than I thought! I'm now off to find out why my ESA payment has not reached my bank today! Will the problems ever end! Thank you for posting and please keep up your fantastic work.
if its like another subscriber then they would have stopped your payments, they did her and they used the excuse they are weeding out alot of them now and then when you call they sort it out basically closing claims down as they want you all on UC and not ESA.
Going back more than a decade ago, I know some one who applied for disability, a doctor was sent to assess them, and said they would have no problem, they would get the benefit. A couple of weeks later, they had a letter to say they had ‘lost the notes’ the original doctor wrote up. They would send another assessor out, needless to say the benefit was declined.
CHANGE OF CIRCUMSTANCES ... Firstly many thanks for all the valuable information you provide and all the hard work. I notified PIP or in my case ADP of a change of circumstance in Oct 2023, this is now 15th April 2024. I contacted ADP to see when my change of circumstances would be looked at. My answer from ADP was short simple and to be honest rude. "there is no deadline for a change of circumstances to be looked at and we are too busy still trying to get through ADP first claimants". The strange thing is I had to report the change of circumstance within a month or I could lose my entitlement altogether.
That is very rude response ! Should just have been more delicate and said we're very busy so sorry I can't give you a time frame, honestly I'd be better at customer services for the DWP 🤣!
My pip assessor lied throughout her report on me and I had to go through a tribunal. The tribunal spent 5 minutes talking to me then put me on hold then came back to me and said that your appeal is upheld. 45 minutes on an assessment, 5 mins for the tribunal to reverse the assessors report! I have a permanent disability, I’m never going to get better, and can have no more surgery, it would be too dangerous. I should never have to be assessed ever again. Thank God Scotland are changing this procedure to being medical based.
i provided my intire medical history at an appeal but it was ignored by the judge and the assessors as they are not interested in what the real doctors say about my disability that has no known cure .
It's true and a shame they ignore the majority of the evidence available to them, it just proves there more driven on a high failure rate to turn over as many as they can as it's easier. It's disgusting
Thank you for this scary video what DWP doing to their participants and staff working for them. I think corruption is all over the place with the DWP. You think the information between your work coach and advisors remains private and confidential, but trust me, it doesn't they don't even respect the claimant's confidentiality plenty rules and laws are broken.
I had to go to court after 2 years for my partner, she was turned down twice, so went to court and won, keep pushing to go court you'll be heard by an impartial judge,dwp did'nt even turn up. Back dated payment for two years was awarded. 😊
Big thank you to Andrew for emailing you and confirming what disabled suspected. I myself am a housebound disabled and have not received any disability money since DWP stopped by DLA (over 8 years ago) and deleted all medical info they had for me after they where informed my medical notes where among that 700,000 lost. Andrew stay safe and thank you from the bottom of my heart for the email you sent to Dynamic Duo UK.
I ended up homeless and it took me 7 years to get PIP after my DLA award ended. They don’t just transfer your information or award anyway you have to start from scratch a) you need to go online and go into your medical record and take screenshots of anything relevant that talks about your conditions and b) you need to use their descriptors when explaining how your condition affects you so there is no ambiguity
@@SobrietyandSolace wow if ur homeless how can u do all that! everywhere is shut!!! all the council buildings are shut down since convid... and the rents have gone up as well as the council tax.. and all the houses are all falling apart!!... most houses are over 100 years old ... they should be giving them away for free... ots an utter joke!!
Yes social housing tenants paying 7% rent increase for black mould infested or asbestos filled "homes" black mould and asbestos cause lung diseases followed by death
If you can walk 50 meters you are fit for work, if you are fit for work and unemployed you will be required to travel up to 90 minutes from home for work. Big difference between 50m walk and 90 minutes travel. Carers allowance is also a scam, carer gets £320 a month but they take £160 from the care recipient, so it cost the DWP less to pay someone carers allowance than universal credit. When you factor in inflation, carers allowance payment today is equivalent to living on hardship allowance in the 1990's
And if the person getting the care is on housing benefit, that, that gets cut down because someone is getting carers allowance to look after them! Beggers belief. 😮
Yeah that makes no sense to me. My CFS/ME is more that just my inability to walk. i.e. not all conditions can be fit into those boxes as to why I am LCWRA. I suffer with brain fog, extreme tiredness, but you have to translate that into mobilizing. Which does not fully capture why I can't work. It is looking like they might change that to say, "they cant walk, but they can WFH".
I commented on another post This is how it has been for me: Pip declined at tribunal , no assessment or consultation . ( amputated finger & bone misdiagnosed as a laceration , turned away from treatment 6 times because of original diagnosis, causing whole hand to claw & severe pain .. N H S admitted fault of misdiagnosis after an investigation) I’m a full time carer & lost my part time job because of it, living on carers allowance & £160 UC a month . Council tax department also admitted to mistaking my identity and deducted £8,000 of my UC for six years & still rising ! . Mistaken identity goes back 34 years ! If I didn’t have the documented evidence of admittance from N H S and council tax no one would believe me . I have PTSD because of both issues and receiving therapy. Diagnosed CRPS , arthritis & dupytrens contracture . At my tribunal they told me they used my application forms as their assessment, with no need for a consultation!!!
that all sounds very distressing and im so sorry you was put through that, its rare for them to use just applications forms and not an assesment, ive known it to happen but normally only in sucessful claims, all very odd and its like they just tried to brush you under the carpet !?
@@DynamicDuoUKthey did brush me under carpet . I was asked if I buy china cups or get my haircut with money left over each month . I just sat there open mouthed . I wish ☹️
@@Dinadino994 disgraceful 😞😞 have you thought of sharing your story to the big issue or some publication like this? They might print it. More exposure on the disgusting way disabled people are treated in this country.
@@colourfulcrafts5492 I’m up for it getting out there definitely. I didn’t know who best to contact. After my therapy session this week I started seeing the headlines regarding the same . I now know I’m not alone in the carers scandal. Thankyou
PIP absolutely unfit for purpose. Have just this week been turned down a 4th time after suffering a dozen heart attacks 12 years ago, ongoing heart disease, mobility terrible and painful most days. Have received 0 help in all that time. Beyond disgraceful.
Is there a way to find out if decision makers are actually health ‘professionals’ or not? It would be very interesting to find out, and be able to throw it in the face of the tribunals if they aren’t!
I believe you could request in a freedom of information, however requesting it during an assessment doesn't go down well someone tried it before and they ended the assessment there and then!
Decision makers are not medically trained. Most of us have already established this, but if you need confirmation, see below. Taken from the government website: "Decisions on benefit entitlement are made by non medical decision makers." If you want to verify this information for yourself, copy and paste the quoted sentence into Google, and you'll find the source.
A PiP DM cross references everything that was submitted by the customer alongside the report from the AP.. Their job is to find anomalies, what I mean by that is, if the AP says they can grip.... Whatever it is, but the customer indicated otherwise, they then amend the score accordingly, based upon all the evidence they have available to them. That's it in a nutshell.
I am reading the WCA handbook. They are not experts, and the handbook specifically says it is the assessors who are "experts" and they are not to use jargon in their reports. Essentially the decision maker is using the evidence in the report to judge if you meet the LCWRA criteria. From what I undestand, they can recommend an award for LCWRA, but in their report they are not allowed to say "cannot walk 50m" they are only supposed to say "claimant claims they cannot walk 50m". they make a descriptive report and not a "proscriptive" one. The problem is when their report is BS.
Some years ago my good friend Cath got a job at a DHSS Dole office in Newcastle. On her first day she found the doors locked, and a bunch of people standing around waiting for them to open. When they did, she asked where she should go. She was taken to her supervior, who guffawed, and said "Oh dear, I see you didn't come to the Staff Entrance, and all this time you've been out in the cold with the Great Unwashed!!" Lovely 🤨
@@DynamicDuoUK My Mam and Granma used to always tell me that wherever you go... school, job etc. there will always be ONE.... one person who, today we would call a sociopath. They are always passive aggressive..... which is very sly. Grrrrrr...🤐
Theyve turned me down 4 times and i suffer mental health plus copd and osteoarthritis but still turn me down, thanks for what you are doing. They made me feel like a liar, i work full time as i have no choice but i struggle so much and the pain gets unbearable. So much so i have days i cannot walk but its a case of plod on. They are so cruel but yet pay alcoholics when i have to work to live, i really shouldn't be working but ive always worked
I am In the same boat as you Karen suffer from chronic osteoarthritis due to breaking my legs in a RTA when. I was a child nearly 50 now and always worked trying to do the right thing they obviously hold it against you for working because you want to try and live a normal life I can't even score one point even though I have the medical history to prove I'm not making it up please don't let it get you down stay strong maybe one day things will improve for people like us who suffer in silence👍
There are obviously ppl who play the system but there are many who do not and are refused their entitlement having paid into the system all their lives. The biggest issue for me is the disproportionate attention placed on ppl with disabilities V’s the BILLIONS we spend on wars around the world, foreign aid and lately, the millions spent on the Rwanda scheme whereby a foreign govt has received countless millions and we’ve sent 3 ppl there! all who have been Foreign Secretary’s. If you arrive on our shores illegally, you are guaranteed a room & board with pocket money for yrs…unquestioned. Will somebody please make this makes sense to me?
I've recently had something about PIP, I'm due for another assessment and I am fearful that they are going to deny me even though I was diagnosed with Asperger's when I was 7 years old and do struggle with day to day life. This country is getting worse and worse and it is heading for a very dark place if things keep on they way they have been going.
I will teach you a trick learn to turn people off that upset you (I call it light switch turn off) as soon as you have done talking to them turn them off and think of anything else, have a treat waiting after a call is over and thank yourself for doing well with it..
The Govt taking Medical doctors out of the equation is so they can reduce the numbers of people claiming benefits. A Doctor is MORE qualified than a Nurse who are usually the ones carrying out those assessments, Furthermore Nurses, Physiotherapists etc are NOT qualified to make a Medical Diagnosis. , The Govt is Happy to pay a PRIVATE company taxpayers money to do these “alleged” assessments. Q1. HOW much is the Govt paying these companies. Q2. What is the qualifications of the assessor. Q3, HOW MUCH are they paid in commission for EACH rejected claim? Q4. Does ANY MP have interests in these private companies. Q5. HOW were the contracts awarded. and what are the Terms for these contracts?
Not to mention some of the nurses seem to have been struck off. Happened in my work capability assessment after getting serious post thrombotic syndrome after a dvt at 21. Nurse who did the assessment said in the notes that no such thing existed and marked me up. Saw a video where someone had found that their assessor was struck off, so checked and found the same. But why, I couldn't find out. Think there needs to be some sort of independent oversight committee or organization with investigative powers alongside the appeal process who should keep tabs on what is going on, because there needs to be some sort of standards held and also to check the assessors backgrounds and make sure the DWP has actually got an ironclad checks system for assessors to ensure members of the public who do apply for a disability benefit, aren't at any health risk from the assessor themselves.
Well that has happened before, Atos did not consult your GP when you had an assessment and if you got a sick note they ignored it. The relied on their own "experts", but the pubic got wind of it and went nuts so they had to include doctor's medical diagnoses. Now the DWP are going back to their own experts.
After a work related injury in 2021, resulting in 300 stitches, 50 staples, a skin graft, skin flap, and amputation, my mobility and balance are extremely limited. I've had dealings with PIP and ESA. Can i walk to the shop? Not without a cane. Can i pick up a 2pint bottle of milk? Not by bending my legs. Can i walk up 2 steps? Not without a banister and doing it sideways. Sorry, ZERO points! The questions they ask are made for you to fail. Every day is a painful fight simply getting to the bathroom, and then I'm made to feel like I'm feigning injury from these so-called assessors. How do you fake an amputation? I've yet to find any organisation that'll help properly either. Even the CAB were useless. It's gotten to a stage that there's no fight left as each rejection is just another blow to an already shattered confidence. I understand that there are people that play the system, but where's the help and empathy for those of us that have genuinely had life changing accidents? Where confidence is so low and anxiety so high that even making a phone call is met with dread and panic. I feel completely let down and left to rot by these organisations.
You must fight this because you know they purposefully fail you because they know you won't fight it in court. Fight, go to court, don't give up! We have to stick together and support each other! You can do this! I filed my tribunal case in March this year. I'm terrified, I'm exhausted, I'm so stressed but I will fight damn it and so should everyone. Please fight this, you are not alone.
I had a bloke who worked at running an ambulance station before he went to atos 🤡 lied through his teeth, said he see me for an hour when it was 20mins I even supplied my work clockings & Google map to show his lies for the MR but no one cared so I took them to tribunal & won most of it back but that was a year from hell
When people have mental impairment the application and assessment is hell, having to go from your notes because of your memory issues and lacking a working memory then the result declines you on being 'perfectly functioning memory etc' because you talked to someone about the issues you face on the phone. It really is appalling and a totally unfair system.
this is spot on, i suffer with memory issues and have done for a while due to mental health issues and im not afraid to admit it, i had to do the same and because i was refering to notes they said " your capable of reading so cognitive function is intact " they then said the exact same copy and pasted sentance in relation to a mobility question, they are getting lazy and finding any reason to remove the benefit.
Oh I believe it! I know a claimant who was awarded zero points after applying. The denial letter stated they could drive in spite of suffering seizures! Applied a second time and was afforded full benefits.
12 years ago after an accident I was off work for 14 months. I was denied any sick/disability after home assessment. One part the assessor claimed he had observed me climbing the stairs. I lived in a ground floor flat and had my leg in long term plaster.
Well said. The PIP assessment is designed to assess someone's practical abilities to look after themselves and get around. A diagnosis of any particular medical condition is important medical evidence which supports the difficulties the claimant reports. It's important for people to understand that a diagnosis in itself does not mean an award of PIP will be made (and similar rules apply to other health-related benefits). An explanation or diary of good days Vs bad days is very helpful, particularly if it covers say a week or two to give the PIP assessor a more rounded picture of how the person manages, or rather doesn't manage, to do things like cook wash, pay bills, walk, etc.
I hate people like you who just keep repeating bad advice you've heard written somewhere. The first step to obtaining PIP is a diagnosis. Any condition that you put in your claim form needs to be backed up by a diagnosis. Secondly, you should always explain your worst day to them, never your good days. Otherwise, they will write in your reports that your good days are your majority of days. You giving out bad advice when you failed your assessment and having to go Tribunal. If you give the assessors an inch, they will take a mile. So always give them your bad days.
This is like a filter system.. imagine each level trying to get rid of 50% of applicants at each level... each level doesnt know what the previous one has already rejected, and has the sole system set up to end up with about 20% success and 80% failure.. which stacks up to why 70% of refused applicants win on appeal in court.
I applied 4/5 times & zero points. 5-6 years stress of repeating sending evidence etc talk talk about every issue. I approached CAB & had a fantastic woman specialised in it, we finally went to Tribunal & won my case, 3 year back payment on top! So my advice is get the right help with people who know the law. Good luck everyone
I have bipolar been sectioned 5 times been refused pip 3 times. I am not well enough to appeal it causes too much stress to think about it. Every day, I struggle to stay out of hospital going to a tribunal would tip me over the edge.
Ok, listen, this is not correct to think this way - the Tribunal people are NOT just ‘yet another hurdle’ to climb. They are impartial and fair in my experience, and MOST PEOPLE WHO GO TO THESE TRIBUNALS FOR PIP ACTUALLY ARE AWARDED THEIR PIP AS APPLIED FOR, OR BETTER. Please view the Tribunal as finally, a fair hearing, after the logs thrown at your legs the DWP have as a process. You’ve reached a fair crack of the whip, when you get to a Tribunal. Better still, THE DWP USUALLY GIVE IN THE WEEK BEFORE THE TRIBUNAL IS DUE TO SIT. None of this is concrete, not a certainty, but it is statistically the way these matters generally go. The DWP are not happy about Tribunals, the Tory government keeps trying to clip the wings of the Tribunal system, therefore, you know you should do it. Get the ‘marking scheme’ for the PIP, fill in the form with this as your guide, be honest, and just stick with that line for the Tribunal. The tribunal, also will pay attention to the hardship endured by you in this process. Don’t give up, don’t let the bullies win, give yourself the chance you deserve. Steady away, plod on, you will get there.
100% i even beleive this to be the case now with appointments for GP's and mental health as a lot of things said are lies or twisted in reports in favour for them and not you as a person.
I’m quite pissed that apparently 2million plus people are signed of permanent for mild anxiety , I have permanent disability that could possibly get worse with nerve pain ,I had to reapply 3 times they put me through hell one accessor took away 10 points for giving him my mobile number, like I have a limb that doesn’t work but my mobility points is a 0 😅 I’ve met junkies on the highest pip because of self induced problems from drugs so they give them more money to go buy more
You should ask yourself why they're junkies though. My mums got a friend who was raped repeatedly and she self mediates with drugs and alcohol. I can't speak for others but alot of users are hurting.
@@HillbillyYEEHAA I couldn’t care of there past we all have not to be blunt look at the guys who’s wife strangled there kids just finished a marathon , I managed to save a deposit while homeless on 162 a month ? I’d watch a pair of junkie couple get 1500 a week on joined uc and pip claims spend it all in a night after having a homeless meal too after getting paid would turn up to the homeless breakfast in the morning crying they had no money 🤣🤓 and these people were on the highest pip rate for coke induced skitzo
@@calamcouzens2090 So you want fair and just treatment yet you say you don't care about the past of someone on drugs? By "skits" do you mean schizophrenia? If so, do you know how serious and dangerous that is?
I have just experienced of this statement or time allocated. A cailm that has to go to court because the assessor failed it. In this report asseser has copied and pasted an answer in the wrong box, time allocated was different from report snd phone record. This has caused the cailmant to appeal decision.
Another calm, which I am aware of in which the calmant stated she could only 15 -20 metres with aid of sticks, Assessor write 20 metres in one box and then 200metres in another box. Typo or deliberately failing claim. What is more annoying this calment has renewed the calm three times in the past and had to appeal everytime getting the calm reinstated.
They certainly have the money for illegal boat men, NHS Dentist,pocket money,rent paid.How dare they treat our disabled in this manner.Thank you Andrew for this information,we need more people like you to inform us all of what they do in the background.
I have a face to face assessment this month and i’m dreading it. Thanks so much for ur videos, i feel i’ll be much better prepared now & i’ll certainly have my wits about me.
I have to fight for my son's PIP and ESA every 3 years and can take up to 1 year fighting for him to keep it after being assessed as fit for work and having to go to mandatory reconsideration each time. His benefits are usually denied each time, hence the year of fighting for him to keep them. He was born with hydrocephalus, which wasn't diagnosed until he was 3 despite me expressing my concerns numerous times, and autism. I was told I was an over anxious first time mother. As a consequence of the late diagnosis his head was well above average size and I couldn't get clothes over his head, his first scan showed his brain had been squeezed to a ring inside his skull and they was amazed he had lived with such damage let alone walk and talk. He's since had many, over 20, operations to the extent he has no viable scalp skin left for a further operation so after his 5th craniotomy during covid, due to the titanium plate breaking through his scalp, he now hasn't enough for them to put yet another plate in to cover his brain. He's suffered greatly during his life and at 45 cannot carry out a normal life of other adults. He gets depressed and upset that he can't do what other adults do like go on the bus alone and has a carer twice a week as well as myself to help him cope with simple tasks. He used to be on DLA, care and mobility and AA and had a lifetime award until they brought in PIP and ESA, at that time he lost the mobility part of the allowance because he can walk. He had mobility as he cannot go anywhere alone and we have had to go searching for him a few times after he got upset and left his flat. Once was in the middle of winter and he had no coat or phone with him, his body thermostat doesn't work so he wears inappropriate clothing for the weather. The DWP are cruel heartless people who just think about the targets the government set for them. On his last ESA work capability assessment we found out that the assessor from the previous round recommended he keep his benefits but the DWP still stopped them. Sorry for the rant but the DWP truly isn't fit for purpose.
I have been through two tribuinals,too anyone waiting for a court date hang in there ,you have a good chance of an award, my second tribuinal was with same judge and panel, my case lasted 9mins, half of it was the judge roasting the d.w.p rep awarded more points and a five year award, 4.5k repayment....take it all the way.....
I had my benefit stole many yrs ago on a Christmas Eve with NO warning or prior correspondence, I had to wait for 11 months for the tribunal so within those 11 months I received nothing!! If it wasn’t for my loving mom and Dad I don’t know what we would of done…😢 if I was caught moving the lawn or doing a marathon I would understand, but was not given any particular reason, I can’t begin to explain the immense stress and anxiety and pain I went through in those months. I attended my tribunal and was awarded my benefit back, with 11 months backdated….what does make my blood boil 😡😡 is the amount of fraudsters out there, I went for an assessment once and hubby dropped me and mom off at door, while he parked car, I saw young man run down the road to a parked car open the boot grab pair of crutches and hobble into the building….I was so dam angry 😡 but couldn’t find him inside….but to me the most important part of peoples claims has got to be medical evidence, as that can’t be faked…X-rays, MRI results etc
Well done and good for you 🙏🏻💜 I'm having to take it to a tribunal now, they told me I had 6 weeks to resend information they "hadn't received", I called them a week later to check if they'd received it only to be told a decision had been made! The date at the top of my mandatory consideration was 21st Feb but I didn't receive it until the 2nd April! It's making me incredibly ill as have mental/emotional and physical chronic issues that have a domino effect on each other. I am so happy that you finally won! Thank you for sharing this, it's helped a lot. God bless you 🙏🏻🙏🏻🙏🏻💚💚💚
@@memyselfandgod5550 ,please remember ,although it feels personal ,its not just a blanket policy of giving everyone zero points,another tip when you win youre tribuinal keep youre award documents safe,for god forbid you have too appeal again, take a friend with you too the tribunal,its nothing too be anxious about the court staff are unbiased and helpful x
Brilliant video. We knew it, we know it. They knew it, they know it. Profit only based system. Tax payer money to these ngo's. Simple, and no accountability.
@@DynamicDuoUK I believe him. But he's going to need actual evidence. Like recorded converations. Anyone calling any dodgy, contracted out entity like PIP really MUST record the conversations themselves!!! Don't let them know, and be cool. They may or may not make their own recordings of interviews, considering the amount of deeply stressed and jaded assessors have to do. I am currently in a contretent with my PIP swag.... Wish me luck! And good luck to you all 🥰
@@RachaelMorgan-om4xw wishing you the best of luck ! You got this 😁! Apparently they don't record when you request it , but then suddenly its available weird lol!
The snoring part is true. Some friend of my mum's seems to think she can apply for snoring . But this explains why so many of my service users fail. A GP and a Consultant Psychiatrist vouches for them as well as OTs and social workers and nurses but the DWP still want to fail them. If they can fail someone with severe mental illness, they will fail everyone .
It's so odd because the DWP themselves state you can apply for this benefit for sleep apnea and it's like okay snoring is a part of it, I snore myself a lot and I always wake up with a closed throat and struggling to swallow or breathe through it, I sit up and usually it's fine, if that's the case then myself I qualify according to their guidelines. But I wouldn't do it because at the end of the day I'm fat so its bound to happen and snoring etc. I certainly wouldnt be phoning them tomorrow saying I snore lol
@@DynamicDuoUK Yes, you can definitely apply for sleep apnea. But , on Tiktok, it says you can apply for simply snoring. By that token, I could apply, and I don't have sleep apnea, which is ridiculous. The system is completely flawed. It is indeed a scam. I have fought for people on more than one occasion. If you have a disability/ health problem, any disability/ health issue, you can apply for PIP. They are supposed to look at how that disability affects your day to day activities and quality of life. The problem is that they make people who deserve it think that they don't, even when they have a formidable person like me strongly advocating for them .
But no-one will take them to court because it will cost a fortune in court costs and all public services have a policy of taking court cases right to the very end including as many appeals as they can get no matter what the cost. They will not award damages they would rather spend the money on court costs. I took The Pensions Regulator to court and this was explained to me by the judge
I recently just had a pip assessment via phone call . I have had my large bowel removed due to ulcerative colitis and wear a ileostomy bag . I still bleed and get chronic flare ups still , in my lower part of my bowel which makes me anemic and constantly fatigued. I’ve worked all my life as a flooring installer since I was 16 I’m now 45. The woman who was the pip assessor was completely unemotional. Robotic script reader . Cut me off lots of times when I was trying to give details of my condition ( I thought they wanted as much info as possible! Not to cut you off half way through your sentence) It just felt as if she wanted to get it over and done with with zero empathy or professionalism and get onto the next application as soon as possible . Just wasn’t interested one iota . I have 6 weeks for the result but I know I will get knocked back .
So absolutely despicable! The DWP management must be brought to task in the courts to determine who is responsible for such despicable 'guidelines' and face criminal prosecution!
I am going through this right now, diagnosed with bipolar and bps 15 years ago, have emphysema and coronary artery disease…I take meds etc like I have too! I have given the dwp all the evidence proof they have asked for and they have just failed me! I have been lied to by 1 assessor then guy on phone doing reconsideration and just failed that, been told the guy who just did the reconsideration also lied! Now I have to wait for a letter to go to a tribunal which will take months, I told them on the phone they have made me out to be a liar and suicidal..My doctor wrote a report and left out important info so I asked her why? She was adamant she did not write a report, I phoned dwp and they gave me the date she wrote a report, what she I feel purposely left out and was told her full name and they seemed to enjoy telling me she also got paid for it! Ok for her to get paid by dwp tho! I am hoping to speak to her tomorrow and see what lies she comes up with now, probably ban me from the practice as I am angry with bipolar!
You can see your medical records and will be able to find out when and what date and who wrote said report, it will be on your drs file at your surgery, how can a doctor say they didn’t write up a report? When there is always paper trial and backed up data!! Also I would advise anyone to photocopy or screenshot ANY and ALL correspondence you get sent or send personally….. When I got my assessment notes sent I read through and also noted points made which were totally false!! 😡 but as I had screenshot my forms I looked back and found where the lies were manipulated. I made a complaint against said person and was sent apologies and papers on was reprimanded and given a warning…should not be allowed to make up stories when people’s well being and emotional state are not taken into consideration….should be ashamed of themselves… I hope all goes well with your tribunal…😁 Take Care 😁😁
@@marieparrott7944 Thank you....Spoke to my doctor the next day and says she did not write a report, so i asked her to write a letter to the dwp which she is doing and also giving me a letter too explaining details...i don't think she would do this if she was lying because it would back track on what they said she wrote and got paid for?
I was interviewed by ATOS and I recorded it. I then made a transcript that was accepted by the Appeals Tribunal (Scotland). Their was 14 factual 'inconsistencies' between what ATOS declared and what I submitted. The Tribunal saw right through it and awarded my appeal and increased it a bit.
There is a good reason why they say that you are not allowed to record interviews...they lie so much and ignore information to suit their purposes and then say you have no proof. Fortunately for me I have memory issues so they had to let me record.
Had a re-assessment when went from life time award from,DLA to Pips ..dunno why they bothered coming to my house , had a bad chest infection, she took lots of notes, and basically said I lied about everything had all the relevant paperwork for her , but she didn’t wanna take it , when I appealed got a very shirty if not rude response from them , but she still lied ..she told me nothing wrong with my hands, yet have had a op on each hand , and that don’t suffer from depression despite showing all the paperwork to the contrary …she doesn’t know me , but decided was lying about everything…as a result lost my car …karma awaits those that are not nice people ..tribunal time was 6 months wait , and was so distressed , my two sons dissuaded me from appealing as was falling off my perch at the time . There was a lot of bad stuff going on in my life .
I failed PIP twice i have a spinal disorder and can hardly move, i got disability through UC but still failed PIP until it changed to ADP and passed with no assessments and got full mobility and medium care within 5 weeks! When i applied for PIP it was all lies produced by the assessors and people really struggle because of these liars and causes hellish mental health problems!
You have highlighted fraud on the part of the DWP, under instruction from H M Government. Individual civil servants need to go to their trade unions and take a collective stand against the Government. All employees have the right to refuse to comply with any instruction from an employer which they know or reasonably believe is unlawful or illegal. And DWP managers need to realise that if they continue to push the fraud, there is only one place they will be going. The Civil Service unions have got to take a stand on this and put the Government in its place.
I used to receive dla at higher rate but since pip replaced it i have had nothing but trouble with them and had to fight my corner, i have daily epileptic seizures with no warnings and have received many head, facial and body injuries which have left me with arthritis, i am also partially sighted yet my award is basic, they even said i could work in a factory where there is machinary, been there done it many years ago in my 20s and near broke my spine having a seizure. from what i have learned over the years, they the dwp and pip hate anyone with epilepsy.
He didn't specify he just refers to it as snoring, because there's a lot of advertising in Google etc and news saying you can claim up to £790 a month for snoring or the following conditions etc. Snoring can be a part of sleep apnea , I snore badly doctor says it's weight related I do wake up struggling to breathe or swallow through the mouth the nose is okay but it clears once I've awoken so could be something similar, no point in me telling my GP he doesn't give a dam none of them do anymore now
@@DynamicDuoUK I got "possible" narcolepsy and sleep apnea. You wake up with the most horrific headaches. You don't need to be overweight or snore for sleep apnea. I don't snore. I snort myself awake and I gasp 😂 I laugh because I'm a female who's 5ft 2. Stress can bring sleep apnea on. You'd be suprised how many people with ptsd have severe sleep apnea. It worries me that these assesors are looking at these applications and thinking xyz condition isn't as bad as they think.. Sleep apnea and kill you while you sleep. Have you had a sleep study? What was it like? Mines not for another year. The hospital they'd send me too has a really long waiting list.
@@HillbillyYEEHAA Cara firstly shouted Your a girl ?!??? I thought it was a man !! 🤣🤣 So apologies for that she was like shocked 😧 lol. She's also five foot nothing ❤️❤️🤣 I had a sleep trial thing done about 2 years ago from castle hill hospital in Hull. I took the machinery home for the night and returned it and never heard anything back. Never contacted me. Never got in touch with my GP. Nothing so to this day I still don't know what the hell happened. I do wake up with severe headaches sometimes and I am awake several times during the night needing a toilet etc as well. Stress does certainly bring it on more that's true! Getting my doctor to listen to any concerns I have is difficult all I get is "it's mental health"
@@DynamicDuoUK 😆 🤣 😂 don't worry, not offended lol I'm like a chihuahua who bites likes a staffy lol Those drs suck. I'm making it a point to ask the dr or nurse, what thier differential diagnosis is when they blame mental health on everything. And magically ,ill get somewhefs. I had to beg for bloods . If you go again to the Dr about sleep apnea, make sure to tell them if you have super vivid dreams, any sleep paralysis ect I get sleep paralysis nearly every night . My dreams feel real. I can't distinguish them from real life. I fell asleep riding my bike once lol I'll never get better having cptsd with narcolepsy and sleep apnea. They play into each other. You'd think drs would want everyone to be healthy by referring them what they need.
Why am i not surprised by all this The DWP ARE CORRUPT and need firing an ordinary company such as Capita no way could they argue with a G.P .Neurosurgeon or what ever title they may hold can be argued by civilian staff who have no idea and are not allowed to read your medical reports its The professionals who should be in attendence with you at an assessment Mel Stride you need to watch these videos and hang your head in shame.I grew up in an NHS Background with 2 relatives who were charge nurses i spent 16 years as a qualified first aider i wanted to become a paramedic but a brain tumour stopped all that. even diagnose a holiday maker at a holiday camp with possible IBS Which proved accurate and my wifes bad lady problems again i was right.I took my late father to a G.P. And informed him my father had a urine problem i was wearing Med Fleece and the doctor asked me if i was a G.P. I said no but i have had a lot of training in First Aid
Corruption is spreading like wild fire throughout our land and the world.
You are not qualified,certified or insured to diagnose...so why are you trying to do so?Medically there is no such thing as ' lady problems' .If you have no medical credentials stay put of it...before you're sued.....The term is gynecological issues...just stop.Anybody can get a First Aid certificate.You need a minimum 3 years Anatomy and Physiology to have any medical credentials .
@@keepitreal665 quite, and no GP is asking in all seriousness, if someone who speaks like that “is a GP”. It would have been sarcastic, it asked at all.
Such embellishment simply doesn’t lend credibility
- actual medic.
This is a great example of where a bit of knowledge can be dangerous
Why do you think the DWP are corrupt when they only follow the rules set by the current government? It is these ministers that set the bureaucracy and targets not the DWP, they are following the rules and regulations set by this fascist govt.
I would have thought this was plainly obvious, there has been 14 years of austerity targeting the most vulnerable in society while their mates buy private jets and yachts from spunking away billions from private contracts. A prime example is Capita, put in place by the Tory cronies.
I get what he is saying about idiots applying for PIP I personnel think that your doctor or consultant should be the ones to recommend you for PIP as they know your medical condition better than anyone but the DWP can't control doctors
Yeh there does need to be more medical based stuff around it , they quote they use the evidence and I know others have said they've done it and requested it from their GP etc but I know personally speaking none of my evidence was ever used or requested when I filed a freedom of information.
I agree but unfortunately a fit note from your gp doesn’t hold that much weight in the DWP eyes…. I had a fit note and was told I had to come off esa and find a job basically….
Yet… if I was employed and handed a 2 week fit note into my employer but then went back to work after only having a week off, chances are, should I have an accident at work in that week, I wouldn’t be covered under my employers insurance as my doctor has deemed me NOT FIT for work.
@DynamicDuoUK hi Richard 👋🏽 I'm Richard to don't can't do telgram when I have an update soon hopefully 😂 keep you in the loop best of luck 💪🏼👊🏽✌🏽
@@DynamicDuoUK My GP doesn’t know me well at all. I have along and complex medical history and have only been registered there for a year. I can’t afford a £15 cab every time to go to the GP and most of what I say falls on deaf ears anyway. I supplied my own evidence after accessing my files medical record and took lots of photos of my mobility aids, my actual conditions, included reports from police, ambulance etc. and because it took 7 years for me to get PIP Imade a point the last time of highlighting all the evidence that wasn’t taken into account the last time around and put it in bold so they can’t ignore it again
Sadly I can't even trust GP's anymore
I have lost my dwp/pip 4 times since being disabled every time I have done mandatory reconsideration and failed so gone to court and recieved it back its outrageous truly
That's so dehumanising and cruel
I've been about 6-8 times over the years even though my back is tucked and I'm in pain 24\7. My medical records and x-ray speak for itself but I was still being told in as fit as everyone else
Yes I won a tribunal and was made to do a a completely new application 8 months later
65% failure rate to save money! Just ask our GP’S they will save 100% of the fortune that they are paying people to torture the already suffering. This is a cruel system. People don’t want to be sick. That guy is telling the truth, no question about that.
I have a broken spine, a hole in my spine, Lung disease and arthritis on top of depression...they just stopped my money without notice.... ice cold winter and I had no heating...could only get by with loans just to live..17 months wait for court... finally I won.. I was awarded 10 years none stop PIP...i ve never been so humiliated/cold/ and low in all my life...But I won hey
How the evil cronies in the DWP treat vulnerable persons in this country is an absolute disgrace
I was awarded PIP in 2020 for fibromyalgia. Lower rate daily living, no mobility. In 2021 I started developing serious symptoms of POTS, I get dizzy when I stand, and I get breathless ahd blackout/faint when I stay standing up for longer than a few minutes. I'm seeing a cardiologist for diagnosis but that alone took 1 year to get an appointment! I have to now use crutches at home and a wheelchair outside my home as it is unsafe for me to walk because I get dizzy, blackout/faint. I can't cook a meal and getting in and out the shower is extremely dangerous so I have my husband help me. In my PIP renewal in 2023 I told them this. Nothing more awarded, lower rate daily living, no mobility (i scored 4 on mobility as i did in 2020). So I did a Mandatory Reconsideration detailing exactly my symptoms and they gave me no more points, didnt even give me a reason. Their scores are the same as before all this started, point for point the same and no mobility awarded, just the same 4 points! So now I'm taking it to tribunal. I will fight this every step of the way. The thing that gives me the fight is I already know they are incredibly biased against us and they know people won't fight it at a tribunal. I know there are some people like "Andrew" but most of them are not, they think we are lying. My life has been flipped upside down with chronic illnesses and I will not stop fighting to better my life. I currently cannot work (after being in fulltime work for almost 20 years) and the £270 a month that DWP gives me is no where near enough to survive. When I asked citizens advice what evidence am I supposed to provide if confirmation of my symptoms from my cardiologist and my very detailed explanation isn't enough and they were shocked because what I provided is enough "proof" and they think i should get higher rate awarded on both daily living and mobility. I filed my tribunal at the end of March so now is the waiting game. Please send me good vibes!
What you have gone through is extremely common they have denied people PIP entirely who are dying and sent them a letter denying them after appeal when the person had died from the conditions they were seeking PIP for in the first place.
I was aware of this issue before I myself applied, so used my local welfare rights officer to help me fill out the forms as well as attend the assessment call…. because you will then get a fair assessment rather than a denial of you have a advocate with you that can dispute any lies they tell.
Sending vibrations of positivity, love and compassion to you. I also send healing frequencies for your journey of the PIP process and also for your emotional wellbeing. Anticipating your win over this obstacle ❤️🙏🏾
It's mallum inse ....we haven't caused rape theft and murder... make sure you tell them there causing you mallum then it becomes mallum inse ❤
Sending you good vibes, and I hope you get a positive result, but more than any thing, I hope and pray you get healing, my stepdaughter has fibromyalgia and I have witnessed the impact on her life sending you love.
After being refused initially and then on appeal I wasn't going to stop and got referred to a welfare rights officer who then filled out my forms etc I took it to tribunal. I have numerous health conditions and at tribunal cried all the way through I got high rate of both daily living and mobility. I was told most people who do try to claim without an advocate/welfare rights officer will get refused. Don't give up and I wish you every success.
Any worker for the GOV, be it jobcentre staff etc has to sign the official secrets act, that in its self is bad news what they are quietly up to in the background!
Very true !!
we know we are despised, and hated. its good to know about the 45mins assessment time, as if they keep on at you through one question, they can only do it for so long, as they have to move on, or not do a complete job on your application. which gives you a good appeal argument. - (one point,) and it wont work for everyone, is a friend of mine, did their application through a specialist solicitor, and at the assessment end, he said "so will you notify me, ? or my solicitor"?, the guy hadn't read the bit where it was prepared and obviously read and filled in by the solicitor, - so he fumbled an answer to him, - and he passed. its not the cost, but the fact it had been completed beforehand by someone reputable.....when your on your own, your a little guy getting pushed around.....great video!!!
The whole dwp needs a shake up. If your an alcoholic or drug addict you get help but if your genuinely knackered you get no help. I remember a few year ago that poor lass who was a paraplegic and bed ridden was found fit for work..
My daughter has addicts living in flats near her,they get loads of money and cost of living payments.
They’re always out shoplifting and selling goods.
My daughter has two grown up children who’ve left home, she’s always worked and didn’t claim the paltry amount that she was entitled to off her council tax bill because they wanted to know the ins and outs of a cats arse.
Her kids have both got good jobs because their mother had a work ethic that she got from her parents.
I’m a carer still working age 69, most of my clients are in need of care but I have a couple who are playing the system and there’s nothing wrong with them. What am I supposed to do when I know someone who’s able to decorate and do their garden yet claims to be disabled!
What exactly would a physiotherapist know about PTSD? The answer is nothing but they still assess for it.
Exactly.
I've entirely given up trying to get PIP, because as an autistic person, I am highly sensitive to the wording of questions, and realized very quickly that I was being asked the same question multiple ways, and being pressured towards a particular answer. I have trauma around this exact issue due to it being something that is done to me regularly by people who do not understand how autism works. Until the DWP ceases to exist, and is replaced with a system that actually works, it quite simply isn't worth the stress and trauma of going through a process that is designed to be harmful to the mental health of claimants. My mental health should not need to be destroyed in order to gain the benefits I am actually entitled to. And so, I am stuck living only on Universal Credit. That isn't living, it's surviving, but the alternative is that I don't survive because of the impact going through PIP assessment has on my mental health.
You can ask a professional help ypu fill out the form and be adamant on a paper based assessment so that they don't disturb you and can just ring the professional with any queries. The professional can guide you and be with you every step of the way .
You need to apply for ESA and they will put you in the support group that is extra income paid fortnightly especially if you can't work.I was medically retired for 11 years but now I'm retired claiming state pension and Pip good luck and take care
I have been claiming enhanced pip for approx 10yrs or so due to chronic illnesses. Few days ago I endured a 1hr 20min assessment of solid interrogation which has left me in a real dark place. The lady was really emotionless and my wife who is my carer also was with me and she was gobsmacked at how cold this assessor was to me. I was struggling to deal with it after 45mins and broke down telling her that this has made me feel worthless. My concentration levels aren't very good anyway but as this went on I was starting to struggle understanding questions but she kept pounding regardless. I just can't shake this feeling of emptiness I have now and can't think of anything else but the assessment. This has really really affected me bad.
So sorry you had to endure that. I lost my PIP a few years back. It took me 12 months to get it back, and they put me in the lowest bracket. I ended up living on 76 pound a week. It made me ill. JUST KEEP FIGHTING IT. ITS YOUR RIGHT.
I am so sorry for you. These people are heartless. Bless you x
Unfortunately when parts of services are sent onto private companies, it will be compromised!
It’s disgusting the way vulnerable ill people are treated, so disrespectful.
Thank you for this information
You're welcome and we whole heartedly agree. We're hopeful for some sort of change ❤️❤️
I'm in tears watching this . I had my assessment 2 years ago, it was the worst experience I have I have ever had . I have a rare blood cancer and anxiety told to apply for pips , my sister was with me for a phone interview as support . The assesser was 1 hour late from time scheduled, which made me start to panic then she said she would have to be quick so she could get back on track her end. I went to pieces my sister tried to explain what was happening the assesser was extremely rude to her and told her to shut up otherwise she would end the call. I tried my best to pull myself together the interview went on for 2 hours !! . I was awarded basic part of pips . When I got the letter through stating reasons for each bit she had lied changed what I had said . Tried to appeal but to no avail.
And if you had missed that phone called you would have been sanctioned for not attending the phone call assessment.
Its not just dwp , its banks, insurance companies, energy providers et al......you are being ripped off wholesale EVERYWHERE!
Thank you "Andrew" for finding the courage to speak out. As horrific as the PIP process is to go through, I'm glad that there's someone there who genuinely cares about us. I've spoken with a few condescending and abrupt assessors in the past and only one nice one. You guys are few and far between. I've met a few ex-assessors who said they quit because they couldn't handle the mental strain and toxic work environment as you described it. Thank you for trying your best to make a difference. Stay strong. ❤
You're very welcome and thank you for being here. It certainly seems like there is a lot more assessors starting to admit the truth now. Even the lady today clearly stated it's a stressful and sometimes horrible situation to be in with the work. She does take that as you will but it says to me they are starting to feel the strain. X
100% true. Thanks to your source and you for getting this made known. I say if you get refused appeal and ask for a Mandatory Reconsideration - even though it can take time. Maybe if enough people took a civil action against the department the numbers might count, like the Hillsborough case.
The more overwhelming numbers against them shows something is up and they won't like that.
@@DynamicDuoUK True. Their goto reaction is usually offensive as defensive or stone walling. But writing to the department minister and secretary in email firstly then snail mail means by parliamentary law they are obligated to do something. Imagine getting 20k letters a week on constant basis. Plus forms of course, the department will have to process thousands, preferably millions or forms and calls to the lines. Good luck everyone
To be honest my sister had a telephone assessment, after sending in her PIP form with supporting evidence. The assessor was uninterested in anything she said, kept cutting her off mid sentence, and only spent 20 minutes on the phone. After the call she said to me “they’re going to take it off me, I know they are”.
Then she received her award letter. The DWP case manager said they’d chosen to deviate from the assessors recommendations of a lessor award, based on the vast amount of supporting evidence received from medical professionals involved in her care. And had decided to award her the highest rate on both components.
So I don’t think we can judge all people in one role or another. Some are excellent in their job and recognise the failings of others. As can be seen from my sister’s case. Where maybe another case worker maybe wouldn’t have. Or if she’d have gotten a more competent assessor it wouldn’t have been an issue at all.
That's the way it should be done !! ❤️ I'm hoping that with enough push now on the system people are starting to realise and I seriously hope we've had some sort of effect in some way or another, even if it's only minimal. A massive congratulations to your sister. Wishing you all the best. Thank you for your story ❤️❤️
What happened to me, I literally cried when the manager rang me with enhanced on both parts. For the first time in decades I have some quality of life now. My review wasn't due until Sept, but they made me do it in Feb which totally sent me in a panic, I'm being sick every day through anxiety can't stop thinking about it and so scared they will take it away from me. At least this man who emailed actually feels compassion, respect to him.
You *Andrew* are one in a million and I feel for you and what you have to do to able to look after your family. DWP have a lot to answer to !
I had my assessment last week to continue my PIP after 5 years. They want to turn it into a new claim so they can fail me. If I lose I’ll be homeless and unable to use the medical equipment that helps me breathe so chances are I won’t be around for long. It took 8 attempts to get the assessment because every time I told them they were being recorded, they hung up the phone. I’m waiting for them to write to me with their decision…..
I fought for my PIP all the way to the tribunal and won was given a lengthy award by the judges the DWP didn't even want to send my award notice and money to me until I phoned up and warned them if they didn't I would see them in Court and well few days later I got my award notice + money.
That's disgusting. At the end of the day a court is much higher up than the department for working pensions. They are not above the law and they need to keep realising this despite the fact they think they are. I'm glad you got your reward and it's a testament to other people. I actually cannot wait until the DWP collapse and something else takes over in its place because they are truly shocking and the staff that work for them at the moment are terrible and I don't care if that offends anyone. Well done to you. All the best
Well done for standing your ground!
Well done for reading this out as i have just been refused my pip she defo did the same to me lied so i did not get it now waiting for mandorey reconsideration but i wont hold my breath i will keep u informed thank u so much people should no what they are doing to people who have disabilities
Your welcome, I'm fed up of them treating people like this I've been through the same thing you have been through and won! Not once but twice ! They do lie, they break rules and they don't shed a tear as they never know you as a person but rather a number, it's time we all joined together and showed them the person not the number.
Best of luck to you with your process ❤️❤️
@tt_widowmaker4838 ❤️❤️❤️
Wow again not surprised, totally believe everything he said. Thank you to Andrew for exposing the truth of disgusting DWP.
it certainly hits the nail on the head and seems to follow a process that the DWP and subsides follow, ive had similar reports but never fully in depth like this and it all matches seperate accounts so unless they all have a big what's app group together to discuss it then god knows! but i beleive it to be true.
THANK YOU RICH FOR THIS VIDEO, AS IT PUTS ME OFF CLAIM PIP, ETC OR ANY EXTRA MONEY ON TOP OF MY UNIVERSAL CREDIT, AS IF PEOPLE SHOW EVIDENCE THEY ARE SICK FROM THERE GP, THEN THEY SHOULD GET PIP, ETC, AS WHY DO THEY NEED TO BE ASSESSED BY THE DWP, WHO DO NOT LOOK AT MEDICAL EVIDENCE FROM YOUR GP AND HAVE ONLY TRICK QUESTIONS TO MAY YOU FEEL UNCOMFORTABLE.
Try not to be put off it's a hard process don't get me wrong but it can be won and achieved it's been proven it's a long process and hard. Your right assesment is a horrible process doctors should be able to recommend for it as they are more officially trained for identifying things.
You should try anyway. Go to Citizens/Community Advice for help with filling in the form. If you're are entitled to it, at least try. And if you get turned down appeal it. Just try. And I pray you are successful. It's very intimating, but you are allowed to have someone with you to support you during any calls.
@@DynamicDuoUK I agree. I was asked for a doctor's letter. Why do they ask for evidence yet not look at it or take it into consideration? It's really corrupt and underhanded and I hope it changes. I really pray it does🙏
And now sunak is talking about removing doctors powers to give out fit notes alltogether,this is gonna make getting pip even harder
This is all depressingly familiar. When my disabled wife was alive it was a constant battle with the DWP and included two tribunal hearings and an assesment by a dubious foreign doctor who was subsequently struck off for malpractice. They are a corrupt shower and should be closed down and replaced with a professional medically qualified system
I went to a PIP assesment once with my mate as a witness. They asked him to stand up, lift his arms up, asked if he could go to the shops in which he responded i drive when i need to. And that was the end of the assesment.
He has fibromyalgia and is in remission from leukemia.
He failed.
Hes now on jobseekers looking for work that he can't physically do and now suffers mental health as a result of the stress and embarrassment. He has to actively look for work and attend job interviews, hes been rejected from every job interview. He hasnt been able to work in around 10 years due to health and he is close to 60. How is he going to find a job when he is in constant pain? The system is a joke. However i do also know of people who play the system and succeed, he just has morals and wont try to deceive.
Fair play to Andrew for letting us all the the truth
100% !! I got your email as well Kim but I'll respond when I can tomorrow as we're having a TV night on the sofa with the dogs chilling xx
They stopped my PIP last year based on a 2 MINUTE phone call. Didn't want to know whats wrong with me or how I'm affected. Reinstated it after 4 months and had the audacity to CONGRATULATE me.
Congratulate you ?...... Really ?
I applied for a job several years ago with one of the third party companies who assess the PIP claimants & got offered an interview. While waiting they put me in the kitchen area & I sat listening to the "assessors" and other admin assistants sit having their break and taking the pee out of some of the applications. They were laughing and openly discussing things in front of a complete stranger (me). Thankfully I didn't get offered the job, but I would have turned it down anyway. It was disgraceful behaviour.
And this is what needs reporting more and more. I'd be interested to hear your story in detail because people do need to realise this is happening and shouldn't keep happening. It's pretty much them against us at the moment and that's horrible. Thank you for telling the world that we appreciate it and I'm glad you didn't set that job even if you didn't get offered it. X
The problme is they lie about what you tell them and when you prove they lied nothing happends to them because they are told they must fail as many as possible these scumbags are there to save the DWP money if it was a company you compline about them they would be disaplined sacked so on. But as its part of the plane to fail you there told do what you can .. why evertime you talk to them RECORDED THEM you can tell them or not its your right too . That's the only way you stop them from lying as when you fail and you appeal you talk to like judges NOT .DWP they are in the room but only to listen an ask some questions rest up to judges . When you show the transcript yours and there's you see the lies . Then you win . You get there transcript sent thro to you. So have yours printed out and.check word for words you see many missing (there'sor changed )
My family member has been on PIP since it was DLA from the age of 18...we had an appeal back in 2018..NOTHING has changed with them, however, we are now waiting for a court date for another appeal. Been waiting 5 months now!
DWP told me in a letter that my GP would say whatever I told them to say don’t think they have met my GP
I was sent for a medical by the job centre arthritis and mental health .was told I would never work again .told to put in for pip on my medical. I didn't get one point .mental health prevented me from putting in for a review
That's horrific especially when they tell those with mental health to keep applying, it's an unfair system
Thanks for speaking out Andrew you are just confirming what we already knew. Some good news here My daughter got her PIP again now I can sleep and no more worrying did I say the right thing for the next 5 years when it all starts again. I didn't agree with the scores they gave her but thankfully what they did award kept her getting the same amount. Now I wait for my interrogation which is due soon!!
They've done this to me and I've got a broken back. How the hell am I able to work when I can't even walk . Immigrants need funding and war of course. Sunak has offshore billions and could help this country but theyre so greedy
Yeah I can confirm, I've had Multiple Sclerosis for 23 years I did used to get DLA then got switched over to pip and unceremoniously told I didn't qualify for benefits I do a ten minuet walk to shop five days a week it's what stops me from ending up in a wheelchair because, that daily exercise is literally what stops what is left of my muscles from fading away completely, I cook for my daughter when she comes home from school and do the laundry, its not much but its about all I can do when its dry enough I cut the grass, this may sound strange to some but that can take up to 6 weeks to get over the pain of pushing a lawn mower round and raking moss, my record for moss raking is about 3 square meters! it tears my muscles and isn't easy to get over, but I have about 250 square meters of lawn! So I have a mossy lawn.
In short I do as much as I can when I can.
As for medication I literally cannot take things like anti depressants I wont take meds for my MS as the first time I tried the side effects almost killed me, the only response I got from my neurologist at the time was Anti depressants which I tried they also had a detrimental effect so I had to stop them also, SO my wife works full time to support the family and we live from paycheque to paycheque, every now and then we end up not being able to afford food shopping at the end of the month, But our daughter will always be fed.
I can't put into words how broken and corrupt our government is!
But I do know that bonfire night is a time for solemn reflection of what could have been.
The DWP are not just currupt, they are highly trained and conditioned to find any spurious reason to fail in any applicants application. Assessments should only be made with a claimants doctor and then assessed by a medical panel for final decision. Then and then only should the assessment be sent over to the DWP with a recommendation for acceptance of Pip. The DWP should have NO part in any assessment proccess whatsoever. There are completely untrustworthy and not medically trained to carry out any level of medical examination, period.
Wow you have hit the nail on the head there!
From what I am reading, it is the medical assessor who is biased, even though they are supposed to be impartial. They are the ones who write the report which gets sent to a decision maker. i.e. the decision maker can only make the decision based on the report they receive.
So if that report is biased, lacks information, is only filled with positive abilities. That report is not a credible report, it is not actually the fault of the DWP decision maker. it is the assessors that are the problem.
As Promised to "Andrew" I didn't post the email or details as promised to not breach data, i read it as best as i could sorry the eyes arent great today!! Truly Shocking !!
My 53yrs daughter has been taken from enhanced rate to basic pip...she's got copd..advanced emphazima..loss of hearing
Rheumatoid arthritis...can you please advise on how to get this investigated...thankyou for everything that you both do x
In court at the moment medical serve copd unable to work 5years ago yet still on esa poor system private company need to keep the numbers down I promised myself after my self-harm stay about long enough to win hopefully my lungs 🫁 hold out 😅 you man is right that's exactly what they do sent med records with all paperwork it give them less chance to coerce you 💪🏼👊🏽✌🏽❤️
I was told that by turning up to a PIP assessment and making an effort to dress properly (which anyone with self-respect would do) counts against you. But not making an effort proves you're not serious and counts against you.
You're right. At one of my tribunals they discussed whether they should continue to deny my claim because I'd filled in the form.
It's so sick. The DWP are like the Stazi back in East Germany. They literally make you sick.
When my husband died two professional ppl from my housing association insisted that I claim for pip. Id always suffered from mental health but with medication, I'm stable. I told them I'm not sick enough to claim and stated I didn't want to. But they insisted and a few months later they were on my case. Questions they were asking were to much, and I told them nothing. I didn't respond to letters, which the second one was pretty abrupt. I ignored that and then they started phoning me. They're just trying to get more information about you and I'm not willing to. I don't need pip. Simple
What is the point of sending in medical evidence if they don’t even read it! It clearly says on the forms that it’s your responsibility to provide medical evidence 🤷♀️
Keep us informed Andy good man to expose the truth ❤
& thanks to Rick & Cara & sausage doggies ❤
Your very welcome !
Shocking. Is this true? Yes, one thing DWP has done is extreme targets; they adapted the sales KPI technique to get people out of the system whenever they are disabled or not; it all depends on your character never back down to them.
I beleive this to be true i did respond to the indivudal but the email has since bounced back i can only assume it was an email address created to send the email? it does however fit in line with the practices that other DWP agents or staff have informed me about and is following a pattern also explained on other youtube content creators accounts
What this whistleblower says is 100% true, as I can attest from undergoing the PIP assessment every three years since 2007. The last time was last year, and it took me ALL of last year and a threat of tribunal to make them pay.
I am Autistic, ADHD, have CPTSD, Delayed Sleep Phase Syndrome, Fibromyalgia, Interstitial Cystitis, Fibroids, Migraine, and Depression - yet they turn me down as a matter of course every time until I threaten to go to tribunal, at which point they magically call with an offer as if they never refused it in the first place. To top it all off, my dad has still not had his Pension Credit processed in over a year, and we’re threatening legal action. They are truly, utterly corrupt.
Look out for med beds free for all 6000 will help I also get spiritual healing very helpful
I went for a pip assessment and the guy had to google my condition because he didn't know what it was, how can he assess me when they don’t know what the condition is 😂
🤣🤣 that's an instant fail on the dwps behalf straight away! 🤣 Take that to tribunal and your laughing all the way to the bank 🤣🤣
@@crichardson4789Yep, what it is is irrelevant.
I was disabled and unable to walk. They stopped my money because they said if I was really as unwell as the Dr and I said then I would be more “ depressed “ . Apparently depression is completely visible
They are truly delusional!
Thanks
Thank you so so much for this!!!! we really appreciate all the support and the kind gift thank you once more xx
My friend and myself are Registered Nurses and applied for positions as PIP Assessors a few years ago now, we are Both in our 60’s and have 30 years plus experience as Nurses, we Both failed the interviews, we were told by someone anonymously that the company don’t want older experienced professionals as we wouldn’t ’do as we were told’ ie mark applicants down etc, it’s a disgrace that people who have worked for years and paid into the system and become disabled are being turned down, I was given 0 points and appealed and lost my appeal, the reason given was my conditions didn’t match the meds I was taking 🤷♀️ the whole system needs overhauled
I've applied for pip 3 times n got rejected on grounds I can walk from my bedroom to the bathroom a whopping 10 feet away, I suffer from hypertrophic cardiomyopathy, lymphodemia in my legs n severe migraines from all my meds it's just a waste of time applying at this point
I’m sorry to hear that. My godmother is the same. She’s 88 only has one lung has type 2 diabetes, thyroid, asthma, heart condition and uses a walker. Can’t walk up/down stairs and can’t do any chores but got knocked back coz she still holds a drivers Licence so they say she’s not disabled. These people are vile. I have more respect for a hooker on a street corner. At least they are providing a service, unlike these f&ckers !!!
OMG! Very interesting, it's worse than I thought! I'm now off to find out why my ESA payment has not reached my bank today! Will the problems ever end! Thank you for posting and please keep up your fantastic work.
if its like another subscriber then they would have stopped your payments, they did her and they used the excuse they are weeding out alot of them now and then when you call they sort it out basically closing claims down as they want you all on UC and not ESA.
@@DynamicDuoUK UC being a pilot for Universal Basic Income, right?
Going back more than a decade ago, I know some one who applied for disability, a doctor was sent to assess them, and said they would have no problem, they would get the benefit. A couple of weeks later, they had a letter to say they had ‘lost the notes’ the original doctor wrote up. They would send another assessor out, needless to say the benefit was declined.
its a total f*k up isnt it!
We already knew this anyway, but the more whistle-blowers come forward with the truth, the better in my view.
Exactly!
CHANGE OF CIRCUMSTANCES ... Firstly many thanks for all the valuable information you provide and all the hard work. I notified PIP or in my case ADP of a change of circumstance in Oct 2023, this is now 15th April 2024. I contacted ADP to see when my change of circumstances would be looked at. My answer from ADP was short simple and to be honest rude. "there is no deadline for a change of circumstances to be looked at and we are too busy still trying to get through ADP first claimants". The strange thing is I had to report the change of circumstance within a month or I could lose my entitlement altogether.
That is very rude response ! Should just have been more delicate and said we're very busy so sorry I can't give you a time frame, honestly I'd be better at customer services for the DWP 🤣!
My pip assessor lied throughout her report on me and I had to go through a tribunal. The tribunal spent 5 minutes talking to me then put me on hold then came back to me and said that your appeal is upheld. 45 minutes on an assessment, 5 mins for the tribunal to reverse the assessors report! I have a permanent disability, I’m never going to get better, and can have no more surgery, it would be too dangerous. I should never have to be assessed ever again. Thank God Scotland are changing this procedure to being medical based.
i provided my intire medical history at an appeal but it was ignored by the judge and the assessors as they are not interested in what the real doctors say about my disability that has no known cure .
It's true and a shame they ignore the majority of the evidence available to them, it just proves there more driven on a high failure rate to turn over as many as they can as it's easier. It's disgusting
Thank you for this scary video what DWP doing to their participants and staff working for them.
I think corruption is all over the place with the DWP.
You think the information between your work coach and advisors remains private and confidential, but trust me, it doesn't they don't even respect the claimant's confidentiality plenty rules and laws are broken.
I had to go to court after 2 years for my partner, she was turned down twice, so went to court and won, keep pushing to go court you'll be heard by an impartial judge,dwp did'nt even turn up. Back dated payment for two years was awarded. 😊
Well done 👍
Good on you Sean 👍
Big thank you to Andrew for emailing you and confirming what disabled suspected. I myself am a housebound disabled and have not received any disability money since DWP stopped by DLA (over 8 years ago) and deleted all medical info they had for me after they where informed my medical notes where among that 700,000 lost. Andrew stay safe and thank you from the bottom of my heart for the email you sent to Dynamic Duo UK.
I ended up homeless and it took me 7 years to get PIP after my DLA award ended. They don’t just transfer your information or award anyway you have to start from scratch a) you need to go online and go into your medical record and take screenshots of anything relevant that talks about your conditions and b) you need to use their descriptors when explaining how your condition affects you so there is no ambiguity
@@SobrietyandSolace wow if ur homeless how can u do all that! everywhere is shut!!! all the council buildings are shut down since convid... and the rents have gone up as well as the council tax.. and all the houses are all falling apart!!... most houses are over 100 years old ... they should be giving them away for free... ots an utter joke!!
Yes social housing tenants paying 7% rent increase for black mould infested or asbestos filled "homes" black mould and asbestos cause lung diseases followed by death
If you can walk 50 meters you are fit for work, if you are fit for work and unemployed you will be required to travel up to 90 minutes from home for work. Big difference between 50m walk and 90 minutes travel. Carers allowance is also a scam, carer gets £320 a month but they take £160 from the care recipient, so it cost the DWP less to pay someone carers allowance than universal credit. When you factor in inflation, carers allowance payment today is equivalent to living on hardship allowance in the 1990's
And if the person getting the care is on housing benefit, that, that gets cut down because someone is getting carers allowance to look after them! Beggers belief. 😮
Can I just say @Kevharkins1 it's not 50meters anymore it's 20. Meters they changed it
Yeah that makes no sense to me. My CFS/ME is more that just my inability to walk. i.e. not all conditions can be fit into those boxes as to why I am LCWRA. I suffer with brain fog, extreme tiredness, but you have to translate that into mobilizing. Which does not fully capture why I can't work.
It is looking like they might change that to say, "they cant walk, but they can WFH".
I commented on another post
This is how it has been for me:
Pip declined at tribunal , no assessment or consultation .
( amputated finger & bone misdiagnosed as a laceration , turned away from treatment 6 times because of original diagnosis, causing whole hand to claw & severe pain .. N H S admitted fault of misdiagnosis after an investigation)
I’m a full time carer & lost my part time job because of it, living on carers allowance & £160 UC a month .
Council tax department also admitted to mistaking my identity and deducted £8,000 of my UC for six years & still rising ! . Mistaken identity goes back 34 years !
If I didn’t have the documented evidence of admittance from N H S and council tax no one would believe me .
I have PTSD because of both issues and receiving therapy.
Diagnosed CRPS , arthritis & dupytrens contracture .
At my tribunal they told me they used my application forms as their assessment, with no need for a consultation!!!
that all sounds very distressing and im so sorry you was put through that, its rare for them to use just applications forms and not an assesment, ive known it to happen but normally only in sucessful claims, all very odd and its like they just tried to brush you under the carpet !?
@@DynamicDuoUKthey did brush me under carpet .
I was asked if I buy china cups or get my haircut with money left over each month .
I just sat there open mouthed .
I wish ☹️
@@Dinadino994 disgraceful 😞😞 have you thought of sharing your story to the big issue or some publication like this? They might print it. More exposure on the disgusting way disabled people are treated in this country.
@@Dinadino994 id of been like who da f*k do you think i am a prince ? china cups or hair good lord lol they havent got a clue do they
@@colourfulcrafts5492 I’m up for it getting out there definitely.
I didn’t know who best to contact.
After my therapy session this week I started seeing the headlines regarding the same .
I now know I’m not alone in the carers scandal.
Thankyou
PIP absolutely unfit for purpose. Have just this week been turned down a 4th time after suffering a dozen heart attacks 12 years ago, ongoing heart disease, mobility terrible and painful most days. Have received 0 help in all that time. Beyond disgraceful.
Im sorry dude. Im too afraid to claim. At least you have tried.
Is there a way to find out if decision makers are actually health ‘professionals’ or not? It would be very interesting to find out, and be able to throw it in the face of the tribunals if they aren’t!
I believe you could request in a freedom of information, however requesting it during an assessment doesn't go down well someone tried it before and they ended the assessment there and then!
Well said 😊
Decision makers are not medically trained. Most of us have already established this, but if you need confirmation, see below.
Taken from the government website: "Decisions on benefit entitlement are made by non medical decision makers."
If you want to verify this information for yourself, copy and paste the quoted sentence into Google, and you'll find the source.
A PiP DM cross references everything that was submitted by the customer alongside the report from the AP.. Their job is to find anomalies, what I mean by that is, if the AP says they can grip.... Whatever it is, but the customer indicated otherwise, they then amend the score accordingly, based upon all the evidence they have available to them. That's it in a nutshell.
I am reading the WCA handbook. They are not experts, and the handbook specifically says it is the assessors who are "experts" and they are not to use jargon in their reports.
Essentially the decision maker is using the evidence in the report to judge if you meet the LCWRA criteria. From what I undestand, they can recommend an award for LCWRA, but in their report they are not allowed to say "cannot walk 50m" they are only supposed to say "claimant claims they cannot walk 50m".
they make a descriptive report and not a "proscriptive" one.
The problem is when their report is BS.
Some years ago my good friend Cath got a job at a DHSS Dole office in Newcastle. On her first day she found the doors locked, and a bunch of people standing around waiting for them to open. When they did, she asked where she should go. She was taken to her supervior, who guffawed, and said "Oh dear, I see you didn't come to the Staff Entrance, and all this time you've been out in the cold with the Great Unwashed!!" Lovely 🤨
That's horrible !! Not all those on benefits don't wash or can't, why do those who work for the DWP look down on others ? Baffles me !
@@DynamicDuoUK My Mam and Granma used to always tell me that wherever you go... school, job etc. there will always be ONE.... one person who, today we would call a sociopath. They are always passive aggressive..... which is very sly. Grrrrrr...🤐
Theyve turned me down 4 times and i suffer mental health plus copd and osteoarthritis but still turn me down, thanks for what you are doing. They made me feel like a liar, i work full time as i have no choice but i struggle so much and the pain gets unbearable. So much so i have days i cannot walk but its a case of plod on. They are so cruel but yet pay alcoholics when i have to work to live, i really shouldn't be working but ive always worked
I am In the same boat as you Karen suffer from chronic osteoarthritis due to breaking my legs in a RTA when. I was a child nearly 50 now and always worked trying to do the right thing they obviously hold it against you for working because you want to try and live a normal life I can't even score one point even though I have the medical history to prove I'm not making it up please don't let it get you down stay strong maybe one day things will improve for people like us who suffer in silence👍
There are obviously ppl who play the system but there are many who do not and are refused their entitlement having paid into the system all their lives. The biggest issue for me is the disproportionate attention placed on ppl with disabilities V’s the BILLIONS we spend on wars around the world, foreign aid and lately, the millions spent on the Rwanda scheme whereby a foreign govt has received countless millions and we’ve sent 3 ppl there! all who have been Foreign Secretary’s.
If you arrive on our shores illegally, you are guaranteed a room & board with pocket money for yrs…unquestioned. Will somebody please make this makes sense to me?
I've recently had something about PIP, I'm due for another assessment and I am fearful that they are going to deny me even though I was diagnosed with Asperger's when I was 7 years old and do struggle with day to day life. This country is getting worse and worse and it is heading for a very dark place if things keep on they way they have been going.
As soon as the process was contracted out to a third party with incentives for targets attached it was gonna take a wrong turn.
Exactly that!
Quite often now I wish I was dead rather than deal with DWP/PIP and the unbearable stress it causes …
So sorry sue to hear this xx 😞
@@DynamicDuoUK Thank you 🙏🏻. I’m not alone sadly …
I will teach you a trick learn to turn people off that upset you (I call it light switch turn off) as soon as you have done talking to them turn them off and think of anything else, have a treat waiting after a call is over and thank yourself for doing well with it..
The Govt taking Medical doctors out of the equation is so they can reduce the numbers of people claiming benefits. A Doctor is MORE qualified than a Nurse who are usually the ones carrying out those assessments, Furthermore Nurses, Physiotherapists etc are NOT qualified to make a Medical Diagnosis. , The Govt is Happy to pay a PRIVATE company taxpayers money to do these “alleged” assessments. Q1. HOW much is the Govt paying these companies. Q2. What is the qualifications of the assessor. Q3, HOW MUCH are they paid in commission for EACH rejected claim? Q4. Does ANY MP have interests in these private companies. Q5. HOW were the contracts awarded. and what are the Terms for these contracts?
Not to mention some of the nurses seem to have been struck off. Happened in my work capability assessment after getting serious post thrombotic syndrome after a dvt at 21. Nurse who did the assessment said in the notes that no such thing existed and marked me up. Saw a video where someone had found that their assessor was struck off, so checked and found the same. But why, I couldn't find out. Think there needs to be some sort of independent oversight committee or organization with investigative powers alongside the appeal process who should keep tabs on what is going on, because there needs to be some sort of standards held and also to check the assessors backgrounds and make sure the DWP has actually got an ironclad checks system for assessors to ensure members of the public who do apply for a disability benefit, aren't at any health risk from the assessor themselves.
Well that has happened before, Atos did not consult your GP when you had an assessment and if you got a sick note they ignored it. The relied on their own "experts", but the pubic got wind of it and went nuts so they had to include doctor's medical diagnoses. Now the DWP are going back to their own experts.
After a work related injury in 2021, resulting in 300 stitches, 50 staples, a skin graft, skin flap, and amputation, my mobility and balance are extremely limited.
I've had dealings with PIP and ESA. Can i walk to the shop? Not without a cane. Can i pick up a 2pint bottle of milk? Not by bending my legs. Can i walk up 2 steps? Not without a banister and doing it sideways. Sorry, ZERO points!
The questions they ask are made for you to fail.
Every day is a painful fight simply getting to the bathroom, and then I'm made to feel like I'm feigning injury from these so-called assessors. How do you fake an amputation?
I've yet to find any organisation that'll help properly either. Even the CAB were useless.
It's gotten to a stage that there's no fight left as each rejection is just another blow to an already shattered confidence.
I understand that there are people that play the system, but where's the help and empathy for those of us that have genuinely had life changing accidents? Where confidence is so low and anxiety so high that even making a phone call is met with dread and panic.
I feel completely let down and left to rot by these organisations.
You must fight this because you know they purposefully fail you because they know you won't fight it in court. Fight, go to court, don't give up! We have to stick together and support each other! You can do this! I filed my tribunal case in March this year. I'm terrified, I'm exhausted, I'm so stressed but I will fight damn it and so should everyone. Please fight this, you are not alone.
I had a bloke who worked at running an ambulance station before he went to atos 🤡 lied through his teeth, said he see me for an hour when it was 20mins
I even supplied my work clockings & Google map to show his lies for the MR but no one cared so I took them to tribunal & won most of it back but that was a year from hell
When people have mental impairment the application and assessment is hell, having to go from your notes because of your memory issues and lacking a working memory then the result declines you on being 'perfectly functioning memory etc' because you talked to someone about the issues you face on the phone. It really is appalling and a totally unfair system.
this is spot on, i suffer with memory issues and have done for a while due to mental health issues and im not afraid to admit it, i had to do the same and because i was refering to notes they said " your capable of reading so cognitive function is intact " they then said the exact same copy and pasted sentance in relation to a mobility question, they are getting lazy and finding any reason to remove the benefit.
Oh I believe it! I know a claimant who was awarded zero points after applying. The denial letter stated they could drive in spite of suffering seizures! Applied a second time and was afforded full benefits.
12 years ago after an accident I was off work for 14 months. I was denied any sick/disability after home assessment. One part the assessor claimed he had observed me climbing the stairs. I lived in a ground floor flat and had my leg in long term plaster.
Cant stress this enough
IT'S NOT YOUR DISABILITIES, its how it affects you on a daily basis
Explain a good & a bad day
Well said. The PIP assessment is designed to assess someone's practical abilities to look after themselves and get around. A diagnosis of any particular medical condition is important medical evidence which supports the difficulties the claimant reports. It's important for people to understand that a diagnosis in itself does not mean an award of PIP will be made (and similar rules apply to other health-related benefits).
An explanation or diary of good days Vs bad days is very helpful, particularly if it covers say a week or two to give the PIP assessor a more rounded picture of how the person manages, or rather doesn't manage, to do things like cook wash, pay bills, walk, etc.
I hate people like you who just keep repeating bad advice you've heard written somewhere. The first step to obtaining PIP is a diagnosis. Any condition that you put in your claim form needs to be backed up by a diagnosis. Secondly, you should always explain your worst day to them, never your good days. Otherwise, they will write in your reports that your good days are your majority of days. You giving out bad advice when you failed your assessment and having to go Tribunal. If you give the assessors an inch, they will take a mile. So always give them your bad days.
This is like a filter system.. imagine each level trying to get rid of 50% of applicants at each level... each level doesnt know what the previous one has already rejected, and has the sole system set up to end up with about 20% success and 80% failure.. which stacks up to why 70% of refused applicants win on appeal in court.
I applied 4/5 times & zero points. 5-6 years stress of repeating sending evidence etc talk talk about every issue. I approached CAB & had a fantastic woman specialised in it, we finally went to Tribunal & won my case, 3 year back payment on top! So my advice is get the right help with people who know the law. Good luck everyone
I have bipolar been sectioned 5 times been refused pip 3 times. I am not well enough to appeal it causes too much stress to think about it. Every day, I struggle to stay out of hospital going to a tribunal would tip me over the edge.
By a dingy then come from France you'll be quids in!
Ok, listen, this is not correct to think this way - the Tribunal people are NOT just ‘yet another hurdle’ to climb. They are impartial and fair in my experience, and MOST PEOPLE WHO GO TO THESE TRIBUNALS FOR PIP ACTUALLY ARE AWARDED THEIR PIP AS APPLIED FOR, OR BETTER. Please view the Tribunal as finally, a fair hearing, after the logs thrown at your legs the DWP have as a process. You’ve reached a fair crack of the whip, when you get to a Tribunal. Better still, THE DWP USUALLY GIVE IN THE WEEK BEFORE THE TRIBUNAL IS DUE TO SIT. None of this is concrete, not a certainty, but it is statistically the way these matters generally go.
The DWP are not happy about Tribunals, the Tory government keeps trying to clip the wings of the Tribunal system, therefore, you know you should do it. Get the ‘marking scheme’ for the PIP, fill in the form with this as your guide, be honest, and just stick with that line for the Tribunal. The tribunal, also will pay attention to the hardship endured by you in this process. Don’t give up, don’t let the bullies win, give yourself the chance you deserve. Steady away, plod on, you will get there.
Whenever at an appointment make sure you record your interaction as proof of what was said
100% i even beleive this to be the case now with appointments for GP's and mental health as a lot of things said are lies or twisted in reports in favour for them and not you as a person.
@@DynamicDuoUK very true ,they only have themselves to blame
Always take somebody with you.
I’m quite pissed that apparently 2million plus people are signed of permanent for mild anxiety , I have permanent disability that could possibly get worse with nerve pain ,I had to reapply 3 times they put me through hell one accessor took away 10 points for giving him my mobile number, like I have a limb that doesn’t work but my mobility points is a 0 😅 I’ve met junkies on the highest pip because of self induced problems from drugs so they give them more money to go buy more
You should ask yourself why they're junkies though.
My mums got a friend who was raped repeatedly and she self mediates with drugs and alcohol.
I can't speak for others but alot of users are hurting.
@@HillbillyYEEHAA I couldn’t care of there past we all have not to be blunt look at the guys who’s wife strangled there kids just finished a marathon , I managed to save a deposit while homeless on 162 a month ? I’d watch a pair of junkie couple get 1500 a week on joined uc and pip claims spend it all in a night after having a homeless meal too after getting paid would turn up to the homeless breakfast in the morning crying they had no money 🤣🤓 and these people were on the highest pip rate for coke induced skitzo
@@calamcouzens2090 So you want fair and just treatment yet you say you don't care about the past of someone on drugs? By "skits" do you mean schizophrenia? If so, do you know how serious and dangerous that is?
I have just experienced of this statement or time allocated. A cailm that has to go to court because the assessor failed it. In this report asseser has copied and pasted an answer in the wrong box, time allocated was different from report snd phone record. This has caused the cailmant to appeal decision.
Another calm, which I am aware of in which the calmant stated she could only 15 -20 metres with aid of sticks, Assessor write 20 metres in one box and then 200metres in another box. Typo or deliberately failing claim. What is more annoying this calment has renewed the calm three times in the past and had to appeal everytime getting the calm reinstated.
The country is fuked
never even got the chance to use lube first either!
They certainly have the money for illegal boat men, NHS Dentist,pocket money,rent paid.How dare they treat our disabled in this manner.Thank you Andrew for this information,we need more people like you to inform us all of what they do in the background.
I have a face to face assessment this month and i’m dreading it. Thanks so much for ur videos, i feel i’ll be much better prepared now & i’ll certainly have my wits about me.
Best of luck with your assessment! You've got this!
I have to fight for my son's PIP and ESA every 3 years and can take up to 1 year fighting for him to keep it after being assessed as fit for work and having to go to mandatory reconsideration each time. His benefits are usually denied each time, hence the year of fighting for him to keep them. He was born with hydrocephalus, which wasn't diagnosed until he was 3 despite me expressing my concerns numerous times, and autism. I was told I was an over anxious first time mother. As a consequence of the late diagnosis his head was well above average size and I couldn't get clothes over his head, his first scan showed his brain had been squeezed to a ring inside his skull and they was amazed he had lived with such damage let alone walk and talk. He's since had many, over 20, operations to the extent he has no viable scalp skin left for a further operation so after his 5th craniotomy during covid, due to the titanium plate breaking through his scalp, he now hasn't enough for them to put yet another plate in to cover his brain. He's suffered greatly during his life and at 45 cannot carry out a normal life of other adults. He gets depressed and upset that he can't do what other adults do like go on the bus alone and has a carer twice a week as well as myself to help him cope with simple tasks. He used to be on DLA, care and mobility and AA and had a lifetime award until they brought in PIP and ESA, at that time he lost the mobility part of the allowance because he can walk. He had mobility as he cannot go anywhere alone and we have had to go searching for him a few times after he got upset and left his flat. Once was in the middle of winter and he had no coat or phone with him, his body thermostat doesn't work so he wears inappropriate clothing for the weather. The DWP are cruel heartless people who just think about the targets the government set for them. On his last ESA work capability assessment we found out that the assessor from the previous round recommended he keep his benefits but the DWP still stopped them. Sorry for the rant but the DWP truly isn't fit for purpose.
This is so sad. He's genuinely disabled, the system is so unfair. Thinking of you x
I have been through two tribuinals,too anyone waiting for a court date hang in there ,you have a good chance of an award, my second tribuinal was with same judge and panel, my case lasted 9mins, half of it was the judge roasting the d.w.p rep awarded more points and a five year award, 4.5k repayment....take it all the way.....
I had my benefit stole many yrs ago on a Christmas Eve with NO warning or prior correspondence, I had to wait for 11 months for the tribunal so within those 11 months I received nothing!! If it wasn’t for my loving mom and Dad I don’t know what we would of done…😢 if I was caught moving the lawn or doing a marathon I would understand, but was not given any particular reason, I can’t begin to explain the immense stress and anxiety and pain I went through in those months. I attended my tribunal and was awarded my benefit back, with 11 months backdated….what does make my blood boil 😡😡 is the amount of fraudsters out there, I went for an assessment once and hubby dropped me and mom off at door, while he parked car, I saw young man run down the road to a parked car open the boot grab pair of crutches and hobble into the building….I was so dam angry 😡 but couldn’t find him inside….but to me the most important part of peoples claims has got to be medical evidence, as that can’t be faked…X-rays, MRI results etc
Well done and good for you 🙏🏻💜 I'm having to take it to a tribunal now, they told me I had 6 weeks to resend information they "hadn't received", I called them a week later to check if they'd received it only to be told a decision had been made! The date at the top of my mandatory consideration was 21st Feb but I didn't receive it until the 2nd April! It's making me incredibly ill as have mental/emotional and physical chronic issues that have a domino effect on each other. I am so happy that you finally won! Thank you for sharing this, it's helped a lot. God bless you 🙏🏻🙏🏻🙏🏻💚💚💚
@@memyselfandgod5550 ,please remember ,although it feels personal ,its not just a blanket policy of giving everyone zero points,another tip when you win youre tribuinal keep youre award documents safe,for god forbid you have too appeal again, take a friend with you too the tribunal,its nothing too be anxious about the court staff are unbiased and helpful x
Brilliant video.
We knew it, we know it. They knew it, they know it. Profit only based system. Tax payer money to these ngo's. Simple, and no accountability.
100% its coming out now, id love to see them have a pop at me for telling what we already knew! fools they are.
Thank you for the update and information and its a real situation and l do believe him .its takes the guts to send you a email
It does yeh hopefully it's real and it would seem so as I've been in the situation he describes their staff doing etc.
@@DynamicDuoUK I believe him. But he's going to need actual evidence. Like recorded converations. Anyone calling any dodgy, contracted out entity like PIP really MUST record the conversations themselves!!! Don't let them know, and be cool. They may or may not make their own recordings of interviews, considering the amount of deeply stressed and jaded assessors have to do. I am currently in a contretent with my PIP swag.... Wish me luck! And good luck to you all 🥰
@@RachaelMorgan-om4xw wishing you the best of luck ! You got this 😁! Apparently they don't record when you request it , but then suddenly its available weird lol!
@@DynamicDuoUK Why aye! Mind I did say you can record a call with an interviewer, but do it secretly, for later ;)
The snoring part is true. Some friend of my mum's seems to think she can apply for snoring . But this explains why so many of my service users fail. A GP and a Consultant Psychiatrist vouches for them as well as OTs and social workers and nurses but the DWP still want to fail them. If they can fail someone with severe mental illness, they will fail everyone .
It's so odd because the DWP themselves state you can apply for this benefit for sleep apnea and it's like okay snoring is a part of it, I snore myself a lot and I always wake up with a closed throat and struggling to swallow or breathe through it, I sit up and usually it's fine, if that's the case then myself I qualify according to their guidelines. But I wouldn't do it because at the end of the day I'm fat so its bound to happen and snoring etc. I certainly wouldnt be phoning them tomorrow saying I snore lol
@@DynamicDuoUK Yes, you can definitely apply for sleep apnea. But , on Tiktok, it says you can apply for simply snoring. By that token, I could apply, and I don't have sleep apnea, which is ridiculous. The system is completely flawed. It is indeed a scam. I have fought for people on more than one occasion. If you have a disability/ health problem, any disability/ health issue, you can apply for PIP. They are supposed to look at how that disability affects your day to day activities and quality of life. The problem is that they make people who deserve it think that they don't, even when they have a formidable person like me strongly advocating for them .
Over riding a qualifying GP and putting life’s under a none professional will lead to the DWP going court and forking out millions in damages.
GP`s are nothing compared to your consultant etc and they do cost the tax payer millions in tribunal costs.
But no-one will take them to court because it will cost a fortune in court costs and all public services have a policy of taking court cases right to the very end including as many appeals as they can get no matter what the cost. They will not award damages they would rather spend the money on court costs.
I took The Pensions Regulator to court and this was explained to me by the judge
I recently just had a pip assessment via phone call . I have had my large bowel removed due to ulcerative colitis and wear a ileostomy bag . I still bleed and get chronic flare ups still , in my lower part of my bowel which makes me anemic and constantly fatigued.
I’ve worked all my life as a flooring installer since I was 16 I’m now 45.
The woman who was the pip assessor was completely unemotional. Robotic script reader . Cut me off lots of times when I was trying to give details of my condition ( I thought they wanted as much info as possible! Not to cut you off half way through your sentence)
It just felt as if she wanted to get it over and done with with zero empathy or professionalism and get onto the next application as soon as possible .
Just wasn’t interested one iota . I have 6 weeks for the result but I know I will get knocked back .
There's always one good apple in the DWP barrel....dont give up.
@@shax3364definitely!
@@shax3364 yes this is very true . Thank you .
So absolutely despicable! The DWP management must be brought to task in the courts to determine who is responsible for such despicable 'guidelines' and face criminal prosecution!
I am going through this right now, diagnosed with bipolar and bps 15 years ago, have emphysema and coronary artery disease…I take meds etc like I have too! I have given the dwp all the evidence proof they have asked for and they have just failed me! I have been lied to by 1 assessor then guy on phone doing reconsideration and just failed that, been told the guy who just did the reconsideration also lied! Now I have to wait for a letter to go to a tribunal which will take months, I told them on the phone they have made me out to be a liar and suicidal..My doctor wrote a report and left out important info so I asked her why? She was adamant she did not write a report, I phoned dwp and they gave me the date she wrote a report, what she I feel purposely left out and was told her full name and they seemed to enjoy telling me she also got paid for it! Ok for her to get paid by dwp tho! I am hoping to speak to her tomorrow and see what lies she comes up with now, probably ban me from the practice as I am angry with bipolar!
You can see your medical records and will be able to find out when and what date and who wrote said report, it will be on your drs file at your surgery, how can a doctor say they didn’t write up a report? When there is always paper trial and backed up data!!
Also I would advise anyone to photocopy or screenshot ANY and ALL correspondence you get sent or send personally…..
When I got my assessment notes sent I read through and also noted points made which were totally false!! 😡 but as I had screenshot my forms I looked back and found where the lies were manipulated. I made a complaint against said person and was sent apologies and papers on was reprimanded and given a warning…should not be allowed to make up stories when people’s well being and emotional state are not taken into consideration….should be ashamed of themselves…
I hope all goes well with your tribunal…😁 Take Care 😁😁
@@marieparrott7944 Thank you....Spoke to my doctor the next day and says she did not write a report, so i asked her to write a letter to the dwp which she is doing and also giving me a letter too explaining details...i don't think she would do this if she was lying because it would back track on what they said she wrote and got paid for?
I was interviewed by ATOS and I recorded it. I then made a transcript that was accepted by the Appeals Tribunal (Scotland). Their was 14 factual 'inconsistencies' between what ATOS declared and what I submitted. The Tribunal saw right through it and awarded my appeal and increased it a bit.
There is a good reason why they say that you are not allowed to record interviews...they lie so much and ignore information to suit their purposes and then say you have no proof. Fortunately for me I have memory issues so they had to let me record.
a physiotherapist is NOT a doctor!
I'm a physio and trust me I'm better than most doctors. I've caught cancers etc when gp's have referred them to me for treatment.
Had a re-assessment when went from life time award from,DLA to Pips ..dunno why they bothered coming to my house , had a bad chest infection, she took lots of notes, and basically said I lied about everything had all the relevant paperwork for her , but she didn’t wanna take it , when I appealed got a very shirty if not rude response from them , but she still lied ..she told me nothing wrong with my hands, yet have had a op on each hand , and that don’t suffer from depression despite showing all the paperwork to the contrary …she doesn’t know me , but decided was lying about everything…as a result lost my car …karma awaits those that are not nice people ..tribunal time was 6 months wait , and was so distressed , my two sons dissuaded me from appealing as was falling off my perch at the time . There was a lot of bad stuff going on in my life .
I failed PIP twice i have a spinal disorder and can hardly move, i got disability through UC but still failed PIP until it changed to ADP and passed with no assessments and got full mobility and medium care within 5 weeks! When i applied for PIP it was all lies produced by the assessors and people really struggle because of these liars and causes hellish mental health problems!
You have highlighted fraud on the part of the DWP, under instruction from H M Government. Individual civil servants need to go to their trade unions and take a collective stand against the Government. All employees have the right to refuse to comply with any instruction from an employer which they know or reasonably believe is unlawful or illegal. And DWP managers need to realise that if they continue to push the fraud, there is only one place they will be going. The Civil Service unions have got to take a stand on this and put the Government in its place.
What is ADP
@@christinenewcombe5450 I wad about to ask that
Adult disability allowance
In Scotland
i am a bit confused because any information or letters i recieve from the dwp are always from belfast and im in the north of England
I used to receive dla at higher rate but since pip replaced it i have had nothing but trouble with them and had to fight my corner, i have daily epileptic seizures with no warnings and have received many head, facial and body injuries which have left me with arthritis, i am also partially sighted yet my award is basic, they even said i could work in a factory where there is machinary, been there done it many years ago in my 20s and near broke my spine having a seizure.
from what i have learned over the years, they the dwp and pip hate anyone with epilepsy.
When he said snoring...does he mean from sleep apnea? Because that can cause such fatigue and can kill you while you sleep...
He didn't specify he just refers to it as snoring, because there's a lot of advertising in Google etc and news saying you can claim up to £790 a month for snoring or the following conditions etc.
Snoring can be a part of sleep apnea , I snore badly doctor says it's weight related I do wake up struggling to breathe or swallow through the mouth the nose is okay but it clears once I've awoken so could be something similar, no point in me telling my GP he doesn't give a dam none of them do anymore now
@@DynamicDuoUK I got "possible" narcolepsy and sleep apnea. You wake up with the most horrific headaches.
You don't need to be overweight or snore for sleep apnea. I don't snore. I snort myself awake and I gasp 😂 I laugh because I'm a female who's 5ft 2.
Stress can bring sleep apnea on. You'd be suprised how many people with ptsd have severe sleep apnea.
It worries me that these assesors are looking at these applications and thinking xyz condition isn't as bad as they think..
Sleep apnea and kill you while you sleep.
Have you had a sleep study? What was it like?
Mines not for another year. The hospital they'd send me too has a really long waiting list.
@@HillbillyYEEHAA Cara firstly shouted Your a girl ?!??? I thought it was a man !! 🤣🤣 So apologies for that she was like shocked 😧 lol.
She's also five foot nothing ❤️❤️🤣
I had a sleep trial thing done about 2 years ago from castle hill hospital in Hull. I took the machinery home for the night and returned it and never heard anything back. Never contacted me. Never got in touch with my GP. Nothing so to this day I still don't know what the hell happened.
I do wake up with severe headaches sometimes and I am awake several times during the night needing a toilet etc as well.
Stress does certainly bring it on more that's true!
Getting my doctor to listen to any concerns I have is difficult all I get is "it's mental health"
@@DynamicDuoUK 😆 🤣 😂 don't worry, not offended lol
I'm like a chihuahua who bites likes a staffy lol
Those drs suck. I'm making it a point to ask the dr or nurse, what thier differential diagnosis is when they blame mental health on everything.
And magically ,ill get somewhefs. I had to beg for bloods .
If you go again to the Dr about sleep apnea, make sure to tell them if you have super vivid dreams, any sleep paralysis ect
I get sleep paralysis nearly every night . My dreams feel real. I can't distinguish them from real life.
I fell asleep riding my bike once lol
I'll never get better having cptsd with narcolepsy and sleep apnea. They play into each other.
You'd think drs would want everyone to be healthy by referring them what they need.
@@HillbillyYEEHAA hahaha small and mighty!
My doctor's just use Google for everything it's legit unreal.