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Unveiling the Reality: The Truth Behind PIP Assessments 

Laura Irons talks MS
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Personal Independence Payment is a welfare benefit in the United Kingdom that is intended to help working age adults with the extra costs of living with a health condition or a disability.
You can get Personal Independence Payment ( PIP ) if all of the following apply to you: you're 16 or over. you have a long-term physical or mental health condition or disability. you have difficulty doing certain everyday tasks or getting around.
I was advised by my GP to apply for PIP 12 years ago when I was going through a severe relapse and was incapable of looking after myself. The whole process from beginning to end was extremely stressful and no-one explains just how stressful this is! The citizens advice are extremely helpful, however it does not always guarantee the outcome that you might expect.
Here is my truthful experience about the PIP process that I went through.
#benefits #msawareness #pip #disability

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7 авг 2022

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Комментарии : 47   
@Christine-eb7fn
@Christine-eb7fn Месяц назад
Diagnosis should be enough for them. I can't stand having to do this each year. It's like they want you to fake it or lay it on thick in front of them so they can deliberately catch you out if you do. It's a ridiculous and draconian method. My condition worsens year after year. I still only get the basic even though I haven't been able to work since 1999 and have recognised mobility issues by my council and GP , I have never been awarded anything for my mobility from PIP. When I was on mobility with DLA previously for years. I'm suprised that they haven't asked for the money back if PIP claim I have no mobility issues. It's unbearable the stress of being unfortunate enough to have a progressive disabled that you are pressured to prove it when your diagnosis already proves it for you. I have more than 10 major disabilities. I get lowest standard rate on PIP. On DLA Before half my disabilities I received Higher rate care and I think it was mid rate mobility. Before I was diagnosed with 5 physical disabilities on pip . Bog standard for getting progressively worse.
@lauraironstalksms
@lauraironstalksms Год назад
This is my own personal experience of trying to get support 12 years ago when I had a relapse which left me physically very dis-abled. I wonder if this process has changed since that time or if anyone else has experienced something similar?
@Salvatore-1980
@Salvatore-1980 Год назад
Hello Beautiful!!! I can definitely understand your frustration. Unfortunately sometimes when we ask for a little bit of help it tends to be more stress than what it's worth. I don't ask for help very much nor do I seek anybody's pity. It's like for some people to understand that I have issues (and alot of them) I must be in a wheelchair and bleeding from my DAMN EYEBALLS.😡 Anyway...I guess it just another shitty thing we have to deal with. The good thing is that I'm fortunate enough also to have people understand my situation and are always willing to help me out without me having to ask. I tend to surround myself with people who see me as totally normal and have at least a small amount of understanding. I do think everyone sould be like that with or without MS. Anyways..... Good luck at your next time dealing with the PIP people. Don't let it stress you out!!! 🙏😘😏
@lauraironstalksms
@lauraironstalksms Год назад
Good morning 😊 Hope you are OK. You are right, it definitely turns out to be more stress than its worth. I always say to my Mum that you need to at least grow another head to even be considered for any help.. It is another shitty thing to consider and I have plenty more where they came from 😂 they always seem to be external problems too. I have such a supportive family and a very small but close circle of friends who, as you said understand my MS but also treat me normally but I think that's so important. Although these days I am beginning to spend more and more time with my own company, at least I'm getting to know myself.. Thank you, take care and good to hear from you.
@mla7071
@mla7071 5 месяцев назад
I received a 2 year suspended sentence back in 2006 because of a PIP claimant i was at my local pub when i overheard a girl explaining how much money she was getting because of her bi-poler (firstly i would like to add i don't believe in such conditions such as bi-poler, adhd, autism for example because i believe these are words used by work shy people to get 'free money' on the backs of hard working people) but i digress after overhearing this woman's conversation i asked her 'as i (a hardworking tax payer) didn't cause your alleged illness or the fact i didn't bring you into the world why am i responsible to keep you feed, housed etc why should i pay for your car, tyres, tax, insurance etc to which she had the cheek to take offence at a question asked by someone who works hard to pay her way in life she got very aggressive (not the type of behaviour you would expect from someone claiming to be 'very sick') so in self defence i smashed her in the face with a coca cola bottle absolutely disgusting that i an honest hard working family man now has a criminal conviction because of a workshy layabout
@adamjones7276
@adamjones7276 Месяц назад
Some valid points there
@Living__wild
@Living__wild Год назад
Hello laura. I was assessed by pip back in 2016 when my mum drove me and aided me into the building and stayed with me the entire time. The assessor reported that I attended the meeting alone and did not need aid. I also didn't bother to appeal as the stress was not worth the symptoms. Its 7 years on now and I'm also going to try to battle with them and have to proof how unwell i am and how the whole process will probably bring on more fatigue, pain and brainfog. We are entitled to full PIP lets fight for it because nobody else will do it for us!
@lauraironstalksms
@lauraironstalksms Год назад
Hi Charlie, sorry to hear that you had a bad time with it. Not sure if you watched my recent video, but I feel as though things have changed since when you and I both went and I would absolutely recommend you to go ahead and try again. I didn't appeal as like you the stress was too much, but you're right PIP is there for those that need it. Good luck 🤞🍀
@mla7071
@mla7071 5 месяцев назад
I received a 2 year suspended sentence back in 2006 because of a PIP claimant i was at my local pub when i overheard a girl explaining how much money she was getting because of her bi-poler (firstly i would like to add i don't believe in such conditions such as bi-poler, adhd, autism for example because i believe these are words used by work shy people to get 'free money' on the backs of hard working people) but i digress after overhearing this woman's conversation i asked her 'as i (a hardworking tax payer) didn't cause your alleged illness or the fact i didn't bring you into the world why am i responsible to keep you feed, housed etc why should i pay for your car, tyres, tax, insurance etc to which she had the cheek to take offence at a question asked by someone who works hard to pay her way in life she got very aggressive (not the type of behaviour you would expect from someone claiming to be 'very sick') so in self defence i smashed her in the face with a coca cola bottle absolutely disgusting that i an honest hard working family man now has a criminal conviction because of a workshy layabout
@ellie698
@ellie698 Год назад
They have always rejected every single claim I've ever made first time. Then they reject the appeal, then they accept my claim when I go to tribunal. Every. Single. Time.
@goddess.110
@goddess.110 Год назад
Best not even try for this then for MS 🙄😔
@ellie698
@ellie698 Год назад
@@goddess.110 Like I say I have to go as far as tribunal every single time. MS is incurable, how do they expect me to be any different. They must believe in miracles. I wish they'd send me one!
@goddess.110
@goddess.110 Год назад
@@ellie698 it's so bad the whole way its done. I can't imagine your stress.
@simonk1025
@simonk1025 4 месяца назад
One year on and nothings changed, I am among the 5% of Long Covid patients who aren’t recovering (pre-existing conditions made far worse, brain function, fatigue ) I am engaging a lawyer to represent me on a no win no fee basis.
@Zedmelia
@Zedmelia Год назад
You made me chuckle when you said - I mean why is it on a points system? I don’t know how I’m going to feel from one day to the next it’s just how MS is! Funny not funny really but the truth!
@lauraironstalksms
@lauraironstalksms Год назад
Well I mean!! It's the truth though isn't it 🙂 gotta say what I think.. Glad I made you chuckle though 🤗
@goddess.110
@goddess.110 Год назад
This is the biggest problem. People think you are fine. But theres no excuse for the ignorance when you can search online for anything. I get that comment all the time. 'Theres nothing wrong with you, your fine'. You should appeal and also take it to the end. But I can understand your stress
@lauraironstalksms
@lauraironstalksms Год назад
I just think that they should take on board what you are telling them instead of having to constantly justify why you feel the way you feel. You have MS which can give you so many dibilatating problems! Not sure what else they need to understand. Yep, the you look fine is just standard 🙄. Hope you are keeping well x
@PALWE
@PALWE 4 месяца назад
I hope you are ok. ❤ b
@johna9543
@johna9543 Год назад
I got assessed about 20 years back in the old system. Legacy award of DLA. Similar circumstances as yourself. Citizens advice helped me big time back then. After a recent relapse, I had to be assessed for sickness benefits which was exactly like you said. I was urged to apply for pip because it worked better for them. But I would have to basically give up a legacy award. Still not transferred old disability awards. Scotland is taking benefits & pensions over in 2023, so probably be around then when things change in these parts. Actually look to be better/fairer on assessment side of things with the small press releases on occasion I was told I would possibly be entitled to more. But going through assessments in recent times I can’t go through that demoralising process again. My only advice is - use a sort of no comment stance & tell them to speak to your neurologist because I can’t explain my condition very well (to a dummy - optional lol) My neurologist sent me a very condescending letter fao of them & now I get no hassles. Attend a jobcentre about 4 times a year & keep them up to date whilst I’m doing physio. Tell them the same - request access to my medical records - contact the neurologist. Trouble is after so many years of awareness & funding, people still have a biased opinion of how a disabled should look physically. I forgive the general public, professional medical assessors should know better
@lauraironstalksms
@lauraironstalksms Год назад
Hi John, hope you are recovering from your recent relapse. Yes I agree medical assessors should know better! That's very interesting about the no comment bit and thanks for sharing, I think that's a really good idea. So you won't go through the process again as you too felt it demoralising, I honestly think that's the case for most people. Surely it shouldn't be made to feel like this for people and it should be a supportive process?
@johna9543
@johna9543 Год назад
@@lauraironstalksms honestly Laura, I think it’s all by design. Quite bloody nasty of the government. Someone told me the government do it on purpose & I’ve read a few things over the past few years that confirm that. I didn’t want to believe they could be like that but the evidence stacks. There’s some nice people at those places, but the general population doesn’t get a ‘peak behind the curtain’. Up in these parts people refer to them as the gestapo & the nickname makes some sense I’ve been in a few situations the past 20+ years where these assessor types have a kind of confusing look when I’ve taken time try explain my condition, can recognise that look pretty well now. I used to be in marketing & sales - one on one you can notice the opposite person basically ‘blag you’. Hard skill to lose as much as I would like to forget at times. I don’t think I could ever work in a public facing role ever again, 1 reason I quit my former career years back. Money ain’t everything in life. Last time I went as far as asking “what is your medical expertise?”, to be answered with deflection commentary, the people or persons are embarrassed to tell you their knowledge is limited so can try change the subject & keep it ‘relevant’. It’s an average person with a check list they employ. Let’s be truthful in modern day, if hospitals across the U.K. are struggling to find specific medical pros, what makes you think the dwp has any of them squirrelled away to use for their assessment purposes?? they don’t pay enough lol There’s ways to project one self without looking a-hole. Being complete no comment can look obstructive so don’t keep totally quiet, but don’t need to elaborate much with intention to explain better, the opposite person has limited knowledge of what your trying to explain & you don’t see what they are writing. A 3rd party uses the info they write for judgment. The assessor types desire is to be in control of the ‘interview’ & sadly many people won’t recognise that. Assessed persons desire should always try to make these situations more equal because it’s not a job interview, it’s a ‘medical’ assessment. The dwp are clearly trained the way they are because some nasty consortiums see it as a financial decision. Which is just wrong in my view. So play them at their own game, they aren’t your friends or colleagues, you don’t need to make any effort to ‘impress’ because you don’t choose the situation you can find yourself in. I find people like us can be nice pleasant folk & forget about their personal conduct during certain situations. Sorry long explanation lol
@johna9543
@johna9543 Год назад
@@lauraironstalksms things are going well health wise. I’m beginning to feel more of myself again with some blips where you are hard on yourself. No point dwelling on the past because it’s happened. Being able to see future self in a better light remains paramount. Just need to move on because it can eat away your well-being. Behind closed doors I can hide & be the depressed + tired etc. Close family & friends understand. Deep down their all that matters anyway
@lauraironstalksms
@lauraironstalksms Год назад
Absolutely true, my family and my very (very) close friends are the only people who really matter when it comes to understanding my MS. My dogs understand it and they don't even talk :-) but they are simply amazing. So glad things are getting better for you and your mindset is in a good place
@johna9543
@johna9543 Год назад
@@lauraironstalksms yourself & whoever else reads will get through it 👍 Hard part - keeping a positive mindset. Haven’t quite worked that 1 out yet. Seems with MS it becomes harder. Must be all those cloudy bits of the brain that cause those malfunctions. Well that’s what I tell myself lol
@Durace11Bunny
@Durace11Bunny Год назад
Yo! Makes you want to name and shame the place and assessor, so they can feel some pressure! Get them to feel like they need to defend themselves because that's the position they put ppl with MS in.
@lauraironstalksms
@lauraironstalksms Год назад
Yo Rich, hope you are good. Yep really feel for people who go through this process. I often wonder what they would be like on the opposite end of the situation.
@colincoburn7907
@colincoburn7907 Год назад
I think the problem is if you go in to the assessment and your honest about your symptoms they’re trying to find ways to weasel out of it. It’s almost like you have to lie to them or exaggerate Did you go through the appeal process - Ive had RR MS for 5 yrs, i work, never claimed benefits before and was recommended to apply for PIP but because I don’t have extreme symptoms (which obviously I’m lucky I don’t have) the process is putting me off which is probably what they want
@lauraironstalksms
@lauraironstalksms Год назад
Hi Colin, I didn't go through the appeal process no, but 12 years on I've just gone through the whole assessment process again (this time by phone) I was awarded PIP this time around. You don't need to have extreme symptoms of MS to get PIP support, you just need to be able to let them know how your symptoms affect your daily living and how long they affect you for. I.e 5 days out of evey week. Also is it causing you to take longer to do things than normal? I've never ever claimed anything, I too have worked all my life since I was 14, but now I'm at a stage with my MS where it does affect me and I do need that extra bit of support. If that's you, then I'd say that you should also apply, especially if you have been advised. It's highly admirable that you work, but a lot of people soldier on regardless and have trouble and just end up getting by.
@mandriod5255
@mandriod5255 3 месяца назад
They are on a bonus for each person they reject
@velociraptorwolf447
@velociraptorwolf447 Год назад
Hi Laura, I'm sorry I'm only watching this now. I used to work for PIP and I could have advised you how to answer the questions to ensure you get it. I get PIP, high rate mobility and standard living simply because I knew how to answer the questions properly. Please let me know if I can help.
@lauraironstalksms
@lauraironstalksms Год назад
Hi, thanks so much, I found a great website which I think has helped me loads. I had my telephone assessment a couple of weeks ago so just waiting to hear back. It seemed like a totally different assessment this time around and the woman was really understanding. Thanks again, will keep you posted. Hope you are well? I'm off to Ireland next week to see family. Looking forward to it 😊
@velociraptorwolf447
@velociraptorwolf447 Год назад
@@lauraironstalksms I'm doing a sponsored one mile walk for the MS Society here in Belfast on the 10th September. It takes me forever just to walk 20 feet, with the pain and dizziness kicking in immediately, so walking a mile is going to kick my arse. But I'm determined to do it though. My wife and family are going to be with me to support me. They're bringing a folding chair for me as well because I'm going to need it.
@lauraironstalksms
@lauraironstalksms Год назад
That is amazing! Well done you for participating in such a great cause.. I think it's the accomplishment that you'll feel when you've taken part. Go easy! I'm sure you'll smash it. I'll be leaving Belfast on the 10th but I'll be supporting you from the air :-) good luck 🍀
@Returned2Forever
@Returned2Forever Год назад
From your descriptions I am not sure you would have gotten it here in california either...Better luck next time I guess. Good luck.
@lauraironstalksms
@lauraironstalksms Год назад
Thank you, second process done now just waiting for the outcome..
@mohammedbaashar8238
@mohammedbaashar8238 Год назад
Hello Laura 👋 How are you? I think the employee you dealt with was the problem; she obviously doesn't understand M.S or extremely ignorant about the condition. Notice that some people will never think you have disability until you start tripping in front of them or sit in a wheelchair 😑 I hope your next process is better.
@lauraironstalksms
@lauraironstalksms Год назад
Hi Mohammed, hope you are well too. I think you are probably right. I think they are not medically trained in the conditions which they are presented with, and so just go by the information provided. It was 12 years ago so I'm hoping the process might have changed a bit, my next one is by telephone. If only people were more understanding of invisible illnesses. 🧡
@mohammedbaashar8238
@mohammedbaashar8238 Год назад
@@lauraironstalksms lol I can totally understand you, lots of people become more like robots due to routine, you must crawl in pain before they respond differently 😉. Take it as a good sign though: it means you "M.S didn't win over you yet 💪".
@mla7071
@mla7071 5 месяцев назад
I received a 2 year suspended sentence back in 2006 because of a PIP claimant i was at my local pub when i overheard a girl explaining how much money she was getting because of her bi-poler (firstly i would like to add i don't believe in such conditions such as bi-poler, adhd, autism for example because i believe these are words used by work shy people to get 'free money' on the backs of hard working people) but i digress after overhearing this woman's conversation i asked her 'as i (a hardworking tax payer) didn't cause your alleged illness or the fact i didn't bring you into the world why am i responsible to keep you feed, housed etc why should i pay for your car, tyres, tax, insurance etc to which she had the cheek to take offence at a question asked by someone who works hard to pay her way in life she got very aggressive (not the type of behaviour you would expect from someone claiming to be 'very sick') so in self defence i smashed her in the face with a coca cola bottle absolutely disgusting that i an honest hard working family man now has a criminal conviction because of a workshy layabout
@iryna_s
@iryna_s Год назад
Can you clarify what county you are in?
@lauraironstalksms
@lauraironstalksms Год назад
Hello, sorry. I'm in Wales (U.K)
@iryna_s
@iryna_s Год назад
@@lauraironstalksms Thank you for clarifying. These procedures are pretty bad in Ukraine too.
@Videostowatch24
@Videostowatch24 9 месяцев назад
My experience is too long to write but it was horrific. I didn’t get anything so i contacted my local MP who was amazing and now I have it. Did you get yours in the end?
@PALWE
@PALWE 4 месяца назад
Stunning hot 🤣
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