there is no way to avoid losing your PIP payment when the system is loaded against the claimant ... it starts before you even get into the assessment room which they place 51 meters from the reception area chairs and then they watch you walk how ever much you struggle even on your hands and knees ... they are evil ... because the pass criteria for walking to the assessment room is 50 metres!
When I got into the room, the chair I was asked to sit in was about 6 foot away from her desk. I looked down at it,worked out I wouldn't be able to drag it closer so just sat down and said "can you still see me?". Testing you before even asking questions yet again.
What happens if like me who suffers from chronic fatigue syndrome and fibromyalga where it fluctuates...and it's a consequence of doing things that lay me up for days, the constant pain, and I mean pain, brain fog, and fatigue that's always there but can hit you like a train in flare ups, so yes I function, I can walk, although like I say in constant pain and then end up in bed never freeing myself from this malaise and overwhelming tiredness....🤷♂️
@@njkipBe sure to tell them how much physical distress the assessment is causing you and how much physical impact it will have on you. If they ask you about any kind of activity, always stress how much it will affect you afterwards, and also tell them if you can't do the activity safely, repeatedly and reliably at a reasonable pace and without undue pain or fatigue. The best way to deal with it is to request a home assessment because attending an assessment centre will have a negative impact on your condition and could put you at risk of a relapse. It is your legal right to not put your health at risk by pushing yourself beyond your limit. With luck, they will say you don't have to have an in person assessment and will just use the information provided on your application form 👍
When it's nearly impossible to be able to see an actual doctor and you get stuck with a practice nurse who then puts into your medical records that you have Asthma instead of Emphysema, it's guaranteed your PIP will be stopped. This is happening to me now, I have complained but it's still not changed. I was taken to hospital with the onset of Pneumonia at the start of this year, I was told I would be admitted but, 23 hours later, sent home with antibiotics. that visit is not in my medical records. I'm due for a review in 2 years time, just right before my retirement age (convenient much). Emphysema does not get better, only worse.
its easier to rob a bank than see a GP, i did everything i could n they still screwed me over so now they will meet my lawyer n this one is mean. i wonder if they can human rights breach
Hello can somebody please help me i have claimed for carar’s allowance on 8th april and still waiting didn’t receive any response from them:( When I phoned them they said your application receive decision maker what can i do
That's what I'm expecting myself ...up for assessment next year...bloody first time I've ever claimed anything in my life....worked 40 years after breaking my back in an accident, living off pain medication and developing chronic fatigue syndrome...30 years ago....my heads like mush don't know where I am or what I'm doing....very best of luck hope you wipe the floor with them....if your lawyers anywhere near Leeds....🤷♂️ I might need him...
@@Liya12334 I had carers allowance for my mam, I can honestly remember how long it took to come thro....you could try going on their website and I'm sure they'll be some Info on there....I'd be more inclined to ring up and chase it.....I know its a rat run on the phones but at least you'll get an answer...
@@njkip i wish you the very best of luck i advise that you dont be rude but certainly dont be nice its just hurts more when at a later date you discover the nice polite person lied to your face and changed your life im now house bound i'm not disabled enough to have motorbility assistance yea yea good one i cant bloody walk i need intend to leave a whole in there armour
I saw Dr Bacon as I had severe heart pain and couldn't walk I was told my heart was only working 30 percent he didn't do anything and I was so unwell four times I went to A and E I was given indigestion pills that made me feel worse
Double heart bypass in 2001 Heart failure 2004 28% ejection fraction, and I was classed as fit for work. I went through 4 tribunals and lost over a 21-year period until 2020. I got pip for severe arthritis in my hips
It would be of great help if the system and the people employed within in were not both inept and sociopathic towards the people that need it. That seems to be just how the government wants it. For those of us who have mental difficulties, with interrelative disorders, especially autistic, around face-to-face communication and C-PTSD, that sort of pressure can destabilize an already precarious mind state that has built up. Actually, it would be more accurate to say that, if you are autistic, the disablement often isn't the autism itself. The disablement stems from the people we have to face up to and their attitudes. The latter is what triggers the precarious mind state in the first place. This government and their aggression towards the disabled are part of the problem. Being the centre of their target is intrinsically unnerving.
Yeah had a problem with the job centre as they asked me for a fit note but I had trouble with the GP as I told my GP that I needed a fit note but it wasn't until some 3 weeks later that I made an appointment to see my GP and when I did finally get to see my GP I had to remind my GP to give me a fit note to hand in it to the job centre and while I was there I told my GP that another problem had arsen with me as I had a throat infection and my GP went through the procedure to check my throat out and she said there's nothing there and yet I had the coughing sessions for a whole month until I eventually went and got some throat spray and the spray is curing the throat but even now 2 months have gone by and it's slowly going but it's gonna take time for my throat to get better and that could be another month or two to clear and my voice is still etchy because of this infection that's happened.😊
It took me 2 years to get diagnosed with COPD and enphysema, my doctor kept sending me for xrays and I think that he was hoping that I would get fed up with it all and not bother applying, he then told me to see the nurse, and when I tried to get an appointment with her, the receptionist said that she was booked up for 9 months, so I waited 9 months, tried to get an appointment to see her again, and the receptionist said that she was on some course for about 3 months. After 3 months I tried again and was given another excuse. So after a while I tried again, and got hold of the nurse, when I told her what I'd been told, she said that she had no idea what the receptionist was talking about, and she had been here all the time, and dosent know why she said that she wasn't here. So I'd been lied to, and it wasn't the first time, I've been lied to on a number of occasions by the receptionist, and my doctor, I think that they are told to make it as difficult as possible for people who are trying to apply for pip, it's not on, your doctor should help you with things like that, it's not like I've got a minor illness and am trying it on, I have osteo arthritis, a torn knee cartilage, copd, enphysema, a nodule in my lungs, I suffer from depression since I became a full time carer for my elderly mother, it's very difficult looking after someone, and my health has really deteriorated since I started doing it, I have no family to help me, so it's just me. I also have a build up of cholesterol in the arteries around my heart, and I had to fight just to get the low rate pip, they wouldn't give me the higher rate they said I didn't have enough points, I know exactly what they are like during the interview because I told them about my health issues, and I got refused pip on 3 occasions I think, and I had to appeal, and then I only just got it. It's absolutely ridiculous, they ask you questions about your health and take no notice of them, if I hadn't gave up work to look after my mother, who knows, my health might be better, and I might of still been working. They treat you like a lier or a criminal, it's not fair at all.
U can't avoid losing it. i know i claimed DLA back in 2007 and 12 months down the line, it stopped. There was no given reason there wasnt a phone call nothing
Just had review, about 30 mins on phone and a lovely lady on the other end. I was told it would be 2 weeks before a decision is made. My letter arrived this morning. I refused to empty my mailbox until 1600 this afternoon. I was awarded the higher rate which I was overjoyed with, next review 10 years time, there is a god after all and my prayers were answered. ❤
Hello can somebody please help me i have claimed for carar’s allowance on 8th april and still waiting didn’t receive any response from them:( When I phoned them they said your application receive decision maker what can i do
It doesnt matter what you tell them during your assessments. There going to fail you. Even if you've been totaly honest with them. They get paid to fail you. no assessor will turn down the £80 for each person they fail.
The system pays the assessors £80 per claim rejected so they set you up to fail,even if you appeal! Disgusting
And £1000 for every one they removed from PIP🥺
They definitely have targets for each week.
Probably do 5 assessments per day and only pass 2. It's a nice bonus
Bastards
BS!
Thank you very much for giving such good advice.
there is no way to avoid losing your PIP payment when the system is loaded against the claimant ... it starts before you even get into the assessment room which they place 51 meters from the reception area chairs and then they watch you walk how ever much you struggle even on your hands and knees ... they are evil ... because the pass criteria for walking to the assessment room is 50 metres!
It used to be 50 metered it's now 30 metres fact
When I got into the room, the chair I was asked to sit in was about 6 foot away from her desk. I looked down at it,worked out I wouldn't be able to drag it closer so just sat down and said "can you still see me?". Testing you before even asking questions yet again.
What happens if like me who suffers from chronic fatigue syndrome and fibromyalga where it fluctuates...and it's a consequence of doing things that lay me up for days, the constant pain, and I mean pain, brain fog, and fatigue that's always there but can hit you like a train in flare ups, so yes I function, I can walk, although like I say in constant pain and then end up in bed never freeing myself from this malaise and overwhelming tiredness....🤷♂️
Hello how much time does take get carar’s allowance approval letter
@@njkipBe sure to tell them how much physical distress the assessment is causing you and how much physical impact it will have on you. If they ask you about any kind of activity, always stress how much it will affect you afterwards, and also tell them if you can't do the activity safely, repeatedly and reliably at a reasonable pace and without undue pain or fatigue. The best way to deal with it is to request a home assessment because attending an assessment centre will have a negative impact on your condition and could put you at risk of a relapse. It is your legal right to not put your health at risk by pushing yourself beyond your limit. With luck, they will say you don't have to have an in person assessment and will just use the information provided on your application form 👍
When it's nearly impossible to be able to see an actual doctor and you get stuck with a practice nurse who then puts into your medical records that you have Asthma instead of Emphysema, it's guaranteed your PIP will be stopped. This is happening to me now, I have complained but it's still not changed. I was taken to hospital with the onset of Pneumonia at the start of this year, I was told I would be admitted but, 23 hours later, sent home with antibiotics. that visit is not in my medical records. I'm due for a review in 2 years time, just right before my retirement age (convenient much). Emphysema does not get better, only worse.
its easier to rob a bank than see a GP, i did everything i could n they still screwed me over so now they will meet my lawyer n this one is mean. i wonder if they can human rights breach
Hello can somebody please help me i have claimed for carar’s allowance on 8th april and still waiting didn’t receive any response from them:(
When I phoned them they said your application receive decision maker what can i do
That's what I'm expecting myself ...up for assessment next year...bloody first time I've ever claimed anything in my life....worked 40 years after breaking my back in an accident, living off pain medication and developing chronic fatigue syndrome...30 years ago....my heads like mush don't know where I am or what I'm doing....very best of luck hope you wipe the floor with them....if your lawyers anywhere near Leeds....🤷♂️ I might need him...
@@njkip hello how much time does Carer’s allowance approval letter take
@@Liya12334 I had carers allowance for my mam, I can honestly remember how long it took to come thro....you could try going on their website and I'm sure they'll be some Info on there....I'd be more inclined to ring up and chase it.....I know its a rat run on the phones but at least you'll get an answer...
@@njkip i wish you the very best of luck i advise that you dont be rude but certainly dont be nice its just hurts more when at a later date you discover the nice polite person lied to your face and changed your life im now house bound i'm not disabled enough to have motorbility assistance yea yea good one i cant bloody walk
i need intend to leave a whole in there armour
I saw Dr Bacon as I had severe heart pain and couldn't walk
I was told my heart was only working 30 percent he didn't do anything and I was so unwell four times I went to A and E I was given indigestion pills that made me feel worse
Double heart bypass in 2001 Heart failure 2004 28% ejection fraction, and I was classed as fit for work. I went through 4 tribunals and lost over a 21-year period until 2020. I got pip for severe arthritis in my hips
Have you had you’re working assessment yet? They might suggest work as a postman or scaffolder 🤷🏻♂️
It would be of great help if the system and the people employed within in were not both inept and sociopathic towards the people that need it. That seems to be just how the government wants it. For those of us who have mental difficulties, with interrelative disorders, especially autistic, around face-to-face communication and C-PTSD, that sort of pressure can destabilize an already precarious mind state that has built up. Actually, it would be more accurate to say that, if you are autistic, the disablement often isn't the autism itself. The disablement stems from the people we have to face up to and their attitudes. The latter is what triggers the precarious mind state in the first place. This government and their aggression towards the disabled are part of the problem. Being the centre of their target is intrinsically unnerving.
£26 billion a year unclaimed benefits is the true number
Good advice
Yeah had a problem with the job centre as they asked me for a fit note but I had trouble with the GP as I told my GP that I needed a fit note but it wasn't until some 3 weeks later that I made an appointment to see my GP and when I did finally get to see my GP I had to remind my GP to give me a fit note to hand in it to the job centre and while I was there I told my GP that another problem had arsen with me as I had a throat infection and my GP went through the procedure to check my throat out and she said there's nothing there and yet I had the coughing sessions for a whole month until I eventually went and got some throat spray and the spray is curing the throat but even now 2 months have gone by and it's slowly going but it's gonna take time for my throat to get better and that could be another month or two to clear and my voice is still etchy because of this infection that's happened.😊
It took me 2 years to get diagnosed with COPD and enphysema, my doctor kept sending me for xrays and I think that he was hoping that I would get fed up with it all and not bother applying, he then told me to see the nurse, and when I tried to get an appointment with her, the receptionist said that she was booked up for 9 months, so I waited 9 months, tried to get an appointment to see her again, and the receptionist said that she was on some course for about 3 months. After 3 months I tried again and was given another excuse. So after a while I tried again, and got hold of the nurse, when I told her what I'd been told, she said that she had no idea what the receptionist was talking about, and she had been here all the time, and dosent know why she said that she wasn't here. So I'd been lied to, and it wasn't the first time, I've been lied to on a number of occasions by the receptionist, and my doctor, I think that they are told to make it as difficult as possible for people who are trying to apply for pip, it's not on, your doctor should help you with things like that, it's not like I've got a minor illness and am trying it on, I have osteo arthritis, a torn knee cartilage, copd, enphysema, a nodule in my lungs, I suffer from depression since I became a full time carer for my elderly mother, it's very difficult looking after someone, and my health has really deteriorated since I started doing it, I have no family to help me, so it's just me. I also have a build up of cholesterol in the arteries around my heart, and I had to fight just to get the low rate pip, they wouldn't give me the higher rate they said I didn't have enough points, I know exactly what they are like during the interview because I told them about my health issues, and I got refused pip on 3 occasions I think, and I had to appeal, and then I only just got it. It's absolutely ridiculous, they ask you questions about your health and take no notice of them, if I hadn't gave up work to look after my mother, who knows, my health might be better, and I might of still been working.
They treat you like a lier or a criminal, it's not fair at all.
well the new green paper on pip are talking about a voucher system and no payments given
idea is not to vote tory so it doesnt get made law
They love to torture the sick and disabled. They aim to mimic the cruel way that the Americans treat the sick and disabled. They have no shame.
U can't avoid losing it. i know i claimed DLA back in 2007 and 12 months down the line, it stopped. There was no given reason there wasnt a phone call nothing
They assess now over the phone🥺🕊🙏🏻
Just had review, about 30 mins on phone and a lovely lady on the other end. I was told it would be 2 weeks before a decision is made. My letter arrived this morning. I refused to empty my mailbox until 1600 this afternoon. I was awarded the higher rate which I was overjoyed with, next review 10 years time, there is a god after all and my prayers were answered. ❤
No need for all the background music - too much noise
Hello can somebody please help me i have claimed for carar’s allowance on 8th april and still waiting didn’t receive any response from them:(
When I phoned them they said your application receive decision maker what can i do
My daughter hasn't had carers since December. Her's with a decision maker they make you sick
@@lindalewis5787 did your daughter apply for carars allowance on December
Did your daughter apply for carars allowance in December
@@Liya12334 no before she had two m9nths payments and they just stopped
@Liya12334 no she had for a few months before it just stopped and they wanted more information she still wauting for payment
It doesnt matter what you tell them during your assessments. There going to fail you. Even if you've been totaly honest with them. They get paid to fail you. no assessor will turn down the £80 for each person they fail.