She's already done one where she covers A LOT of relevant stuff. It's called something like "PIP claims for mental health". ADHD, depression and anxiety are explicitly addressed. Hope that helps! (Edited because: appalling spelling)
I've just sent my mandatory reconsideration, I'm Recovering from breast cancer and has been left with severe Anxiety, bone pain and Arthritis ,my quality of life is poor , I explained all of this ,can't believe I was 2 points away from receiving pip , so this time I got a letter from my oncologist and from my cancer counselling which I'm starting, my cancer was aggressive with a chance of secondary cancer ,this could end my life so how the hell I'm not titled just waiting again now ,don't no what I do if I'm turned down again all this has caused even more stress 😢
@@Debilee16 am in the same place as you . The problem being the real people are being turned down who needs the HELP to move forward and have some quality of life 💖. It's sad as am only 57 years old and had to retire from my NHS Job I loved for 8 years plus and my dream job I thought 🤔 for life or until my retirement age of 67 . My stress levels are through the roof we now my side effects from chemo and radiotherapy becoming more and more. Over last few years ,walking going up and down the stairs ,cooking meals ,preparing food ,dressing etc. My daughter and husband is my unpaid carers help in between they full time and husbands part time am / pm shifts ( Monday till Friday)around 24/7 at weekends etc..( NIL CARERS payment as over the 10p to get it !!! ) The system is 💔 Broken with DWP and also the NHS. Sorry to say as am NHS through and though with excellent treatments I had for my cancer and secondary cancer now. But here to tell my tale . I could write a book on it and would be a best seller !.
Another great vid Charlie! Wish I’d known this a few weeks ago when submitting my forms. I have my assessment call on Tuesday this week. Wish me luck. I’m blind btw.
Make sure if you can that you record the phone call and tell them that the phone call is being recorded so that you have it for your own record and personal use due to your disability
Hi Charlie, great information and vlog as always. Yes it all makes since to me. Keep up the good work up. Pip usually has all the previous medical documents from previous claim, and those don't needs the sufficient evidence to send in if you're circumstances hasn't changed. Everyone works differently...😊❤
Hi, from my own personal experience, never assume that the dwp still have all your previous evidence etc... I always resend all my evidence for reviews, as you are relying on them still having your info (& even being bothered to look)... Always resend with claims/reviews... I realise others may do things differently, but feel it gives you a better chance, as it's all attached to your form 🙂
In my experience i've noticed they definitely always look at my previous pip award/review ect, but I still always on a new review send the same evidence eg diagnosing illness ect as well as new evidence.
Charlie I've been receiving pip for a few years now. Last year, I was in hospital with pneumonia and found out I've have copd, I told Pip, and they cut my pip in half .
Photos are great. If you understand and know about MetaData and when, where and what phone that picture was taken on! If you know what that means then you don’t need help! Look it up!
My MS specialist consultant puts in my letters how many seconds it takes me to walk up the corridor! 😡 I’m glad that my next appt with him is by video call.
Just completed a review. My son has told them that I his parent does the necessity due to preexisting conditions and already receiving Pip . Daily reminders , prompting etc . Along with professional evidence. Just last week he was diagnosed with a form of leukaemia with ongoing tests etc. we are at the moment trying to process this devastating news whilst completing the review form.
Oh my gosh, I’m so sorry to read this. As a parent, I can only imagine the anguish and shock that you are going through. I’m pretty sure that when it comes to Cancer or Leukaemia, there’s either a charity (Marie Curie or McMillan) for example that will do the PIP forms for you. Depending on how old your son is, there may even be someone within the clinical department who can assist you with the forms and advise you on anything else you may be eligible for. Sending you lots of love from my home to yours. XxX
Oh gosh. I avoid clothes because of pain. Im just in Primark leggings and t shirt most of time! No buttons involved. I didnt think to mention on pip form. Thinking of the reading with adhd - the information processing. Its an issue. I cant comprehend complex overwhelming information. Ive just been told to withdraw from uni degree because of my difficulties. Im going to mention to the tribunal people.
I provided a 30 page psychiatric report and still only got standard. Amazed how many are saying they are emotional cripples and yet they are chugging pints down the local and playing pool. I hope Labour weeds them out 😠
Is there anyone on this channel with genuine physical disabilities due to accident or serious illness. I was paralysed by a virus but all i see nowadays are people claiming for autism or ADHD or agoraphobia or depression. Anyone can claim these things knowing it is difficult to disprove. This is why genuine cases are now at risk of losing their benefit because of unscrupulous fraudsters who should be working.
I know! This woman claims for “brain fog” and has an inability to “understand directions” so she claims the highest rate in mobility benefits. She claims she is so disabled. She can’t cook for herself. Heaven forbid chopping vegetables is too difficult for her and she needs to claim for that. Carrying things too and from the microwave are way beyond her abilities so she needs to claim for that too. In each video I’ve noticed her nose get longer and longer… 🤥🤥🤥🤥🤥
Yes I’m totally genuine, I was healthy, working , living life until about 10yrs ago, I claimed PIP due to a doctor telling me I needed to. Unfortunately there are people who will lie to get extra, and yes, I believe the genuine ones suffer for it
@@kellie8291 Yes. I accept you are genuine. And there are many who are who should not have to suffer the degradation of constant interviews and tests. Unfortunately people have jumped on the bandwagon knowing they can lie and get money for nothing.
@ Kevinkenny6975. I am genuine , I suffer from Osteoarthritis in most of my joints now , I also have lumbar and cervical stenosis , am in varying levels of pain 24/7. They also suspect I have fibromyalgia now as my pain levels have become so much worse . I have had 3 major surgeries on my cervical spine and still the pain persists . I need a 10 hour plus surgery on my lower back which I have been advised against as there is a chance of paralysis and I will still be in pain after the surgery . I also suffer from severe depression and anxiety and have done since childhood . I rarely go out , can’t mix with people because of the crippling anxiety and quite frankly I exist as opposed to live . I too hope the fraudsters can be caught , it’s SO bloody unfair that the rest of us are tarred with their brush ‼️. Best wishes .
Send in pictures of your kitchen and it proves you are capable of methodically planning and organising your day. The best method is to get someone to take the pictures of you in a state of distress looking like Anne of Little Britain 😅
I recently bought the kettle!!!! I struggle with the weight of a kettle (arthritis/joint replacements/weak grip); and, I have parental responsibility for 2 very young grandchildren, so nervous about dropping it. The kettle is a godsend! *It ONLY heats 1 measured cup at a time so no worries if a child were to.pull it down after you just made a cuppa. The rest of the water is still at room temp *FAST! Literally flick a switch and you have a cup ready poured in 30 seconds!!!!! * It is a measured cup so theres a good inch clear which helps avoid spills *temp (for me) is a less hot than I like, but its drummed home im not doing myself any favours making my drinks too hot. Def safer if you spill, less chance of bad burns. * great looking - visitors thought it was a coffee maker. * can add water using a small jug rather than taking kettle to tap. * £40 is good value. Im really loving this. Has lowered my stress levels about burn risks - and theres no waiting for the darn kettle to boil❤ Thank you❤❤❤❤❤❤
Yes yes yes!!!! Driving a car vs chopping food. Ohhhhh the stories i could tell from my interview on this one Re Dr letters I am extremely fortunate. My GP offered to write a letter to send with my app. When i appealed he came with me to my interview. He was very firm about 'how my conditions affected me'.... The result of his support... I was asked if we had a personal relationship. She changed the question at my look of horror and said she had meant were we related. I was mortified. I have a GP who always gives me a long appt, goes above and beyond to ensure im getting the best care and he was slapped in the face😢
@@leighstevens1075 shocking behaviour from a personal person but are they professional people doing this job 😞 am on the fence on it all !!. As so wrong the treatment and way you were treated .
I can't do this. I have copd state 3 to 4 ,..m.hlth eupd agraphobia cptsd ,.im only able to have tv on hour ish a day 24 hrss as triggered by diulds amd noises ...Seeing this ,It is to much,..Now im going to b Just another unalived person/number,.statistic ....this to much I can't cope no more 💔 god bless every soul on here I hope u all stronger than me x
I hear you, and can relate somewhat. It’s exhausting suffering with mental illness for years, on top of other health conditions... and constant triggers 😔. I’m alone apart from my pets, it’s them I think about... cos no one would discover me for few days if I did something. I love my pets more than myself. At those times, I try to get through half an hour at a time, then an hour at a time, using as many distractions as I can... like writing, drawing, RU-vid. Night times are worst for me, there’s no one to phone... and I don’t use social media. Just watch YT occasionally. Hang in there ❤️✌🏻
@vickyhone1834 - Hi Vicky, I just wanted to reach out to you as I want you to know that your comment made me cry as I know how desolate you feel and want you to know that even though I feel like you and don't want to wake up to reality each day that there are people that truly do care for you even though I don't know you. I must care because I've tried writing this comment 3 times but for some reason as soon as an advert comes on my comment disappears before I can finish 😊 so I keep plugging away and that tells me you're worth more than you realise and I was meant to write this to you as I don't believe in coincidences. I dread even using the phone so I truly do understand, can you do me a favour and just try to phone the Adult Care Team in your town and ask if they can help you as you can't get out to the Citizens Advice Bureau for help, and they will come to your home, tell them how you feel, just be honest and speak from your heart. You see departments like Pip etc won't tell you this so I am, the helplessness, the loneliness, feeling powerless because getting through each day is a marathon. All we have sometimes is hope and I want you to have that. ♥️
I have a wet room which has a seat there for my also have 2 rails where the shower is. I have a loo frame. I have a kettle rocker to help me make a hot drink plus a perching stool . I need other things to help me in the kitchen. My daughter helps me put the bottom half of my clothes, including socks and shoes
I did keep everything such as old forms e.t.c. but my carer left and i have no idea where they are, or if they've been deliberately thrown away. My condition is deteriorating and i now live alone, i am honestly dreading my next assessment.
Hi Charlie, I am on Universal Credit and suffer clinical depression and anxiety. I have recently received PIP due to my circumstances and mental health. I am trying to get myself back into work so I have enrolled in various different work courses. I recently passed my PTS Railway course, my Telehandler Course all of which I have done myself, universal credit have done nothing to help me, only try and prevent me from getting a job. I have travelled at my own expense 800 miles, I have submitted my fuel receipts and they keep messing me around saying they I have to go into the Job centre, then 1 day before my appointment they change it for a later date, and then refuse to do anything else about my fuel receipts. I was wondering if I can go over there heads and get someone who is in a position of authority to sort things.. As you can imagine it is having a massive effect on my mental health and and physical. I have made loads of complaints but nobody is bothered. Regards Peter
Unless the DWP sent you to do those courses they are not going to help you with travel expenses. I have asked before doing the course and was told no. Don't waste your energy you are not going to get any money unfortunately.
I use a caravan step to aid me getting in the bath and have grab handles to get up and out of the bath. I did use the sink but had a fall after the sink came off the wall.
I have virtually no evidence, I take daily pain meds, have fit notes so can't work too many hours, have disabled bus pass but no actual diagnosis... yet. I use aids which I can show evidence kn, but not much else.
Waiting on my MR after a assessment and decision. We definitely shouldn't have to do all this just to get what we are entitled too. Thank you for all your videos Charlie
I was awarded LCWRA thanks to watching your videos and arming myself with the knowledge of what to write and the language and terminologies to use. Thank you, it has made a significant difference to my life.
Omg, citizens advice helped me with my forms. I have photos and she said it’s a pity you can’t send them photos for evidence. So I didn’t send any. Also when I said about the aids I used I was told that makes no difference.
Hi Charlie. Couple of questions for you. I can't take medication as I'm intolerant of anything that works on the brain (opiods, antidepressants, anti seizure) which seems to be common with fibromyalgia. Only thing I can use is water, heat and naproxen which isn't good on muscular pain. How do i put that over so they understand that not taking pills doesn't mean I'm not in pain? My partner is going through testing for narcolepsy type 1. They said that they're ignoring all evidence of fatigue as it's not diagnosed, but that's a lot of their struggles. They sleep half the day, if they do anything they start to fatigue, they can't walk far without falling asleep (often still standing). How do we get them to accept it or do we have to wait until diagnosis?
I couldn't afford lots of aids so to get my trousers I used two fabric belts one either side through the belt loops to pull them up whilst sat on the bed, once they're over the knees you can pull the legs up until your feet are through, my other half came up with that idea unusual for him lol I can't bend over due to severe lung disorder
I'm a bit confused, and with my level of brain fog, that's not difficult, lol. I live in Northern Ireland, and I never get results from MRIs or CT scans. I never see them on a screen or even see the consultant afterward. My GP just told me that I have problems in my neck area and middle back. That was it. I'm having excruciating pain in my tailbone, which showed nothing. I never get copies of blood tests, x-rays, or from consultant appointments. When I did my PIPs, I had no doctor's evidence because I never get any in my hand. The only thing I have is appointment letters. I do have aids that were given to me, but I could do with more now, but I don't know who to contact. I wonder if things are done differently in the UK, as my friend over there can see things online and order scripts, whereas we have nothing online at all.
Hi Pauline, you should be able to access your medical records from your GP.. So all your treatments, scans etc, there should be a record of your medical history... This may help - www.nidirect.gov.uk/articles/accessing-medical-or-health-and-social-care-records (there may be a charge, depending on your surgery) 🙂
You need to fill a form. Under freedom of information act hospitals are required under the law to send you all the records. You can phone the hospital or the form is available on each hospital website.
Excellent advise Charlie but my review form was submitted last November 2023 and my get face to face after june2025 at the earliest😢. Photos I have on my phone already will I show them it ???. No benefits only husband works 22 hrs per week and me on pip till june2025 review 😢........ How would I get it on this information if vouchers etc. X😮❤
I've tried sending a email asking for Good evidence template but it keeps coming back saying Email couldn't be found, I've even copied & pasted the email as well as typing it in & it still came back saying email address doesn't exist, is this a scam or is there a problem with your email 😔
hi duck got telephone apt with pip tuesday next week i,ve chronic lymphodema bad panic attacks when on phone i tend to waffle on, struggled with drugs but 8 years clean would you mention being clean etc or concentrate on my illness so i,m being tested for ADHD its on my record as a kid but hopefully get support for this. got osteoarthritis on hips , etc got abit of a list but the odema is the worsed one it effects everything many thanksx
I have never cooked a meal in my life, ever. Do I write that? My Mum used to cook, now my wife. I cannot abide dealing with food, it''s a problem related to my Autism.
You can always state due to sensory issues related to your autism that you are unable to prepare food yourself and need assistance in doing so with you explaining that meals need to be made for you. Hope this helps 😊
Hi, I had to have my bath removed as social care provided a bath lift but i couldnt lift my legs over the side of the bath and they were not allowed to do that for me. I had a shower tray the same size as the bath and i use a plastic wheeled seat with a rail on the back which i bought on eBay so i can be wheeled up to the shower.
I’m a little confused because I was under the impression that if you did use aids and that those aids enabled you to do the task for instance cut up food or get in and out of bath that you were then treated as ‘can do ‘ the task and scored no points. Is that correct? Thanks
I'v remove all my LED lights as they flash so fast you can not see it unless you record them with a smart phone and slow the recording down and you will see the flashing .
It’s nice to see genuine “useful” information on this channel that people who need it can use. There’s a channel on RU-vid that I stopped watching a while ago because it was so negative and basically a joke. Provoking people to react then crying because of the negative comments. And yet bring it on themselves. It became apparent to me that it’s was all done on purpose to create (what they think) is content because they don’t have anything constructive to say. Who constantly slander Charlie’s name and slag this channel off because Charlie p***ed on their parade of charging for services similar to Charlie’s channel. There’s no comparison but she knocked them back because she could see right through them. And it eats away at them which is why they’re obsessed with and police this channel. So sad. Anyway thank you Charlie for more great information.
DDUK will tell you to stop being a DCK in all honesty as that's what you are, their channel is about fun but also providing information as i didn't know if you knew this... HE WORKS FOR THE DWP U FOOL! Unlike this woman who basically charges £650 to lie to receive benefits, this is why the government want to change it so people like her don't have to make a profit in lies and deceipt. She can clearly work and do a normal job and she's clearly faking all of her illness but you see her as an angel .. as for charlie p*ssed on their parade at least they have a job and don't scrounge off the system like this woman does. So take your mates with the 4 ish likes and stop moaning like a little b*tch.
@@jillmaltby this is what i said jill, unfortunetly charlie and her beloved scamming angels reported and removed my comment. the sooner she's shut down the better the con artist.
I used ChatGPT (as last resort-as there is _de facto_ no legal aid for UC claimants) and it uses all the correct legal terminology and quotes UK Employment and Welfare Law as well as ECHR and UDHR articles-It knows all about DWP and Universal Credit because it has read everything on Earth (including stuff they don't want you to know about)
My daughter has had xrays she is waiting to see the consultant next week,she has back and pelvic arthritis, its been 2 years waiting as her DR sent referral from but then cancelled it. If she gets PIP can they back date it to then she is in terrible pain all the time. Thanks
Do you think its fair to charge people 650 pounds to fill inPIP form to vulnerable people?? I got help from citizens advice and they helped me complete my firm for free
She never responds to anyone unless she pays them either, i genuinely feel sorry for people commenting asking for help and she simply ignores it until your lining her pockets, its disgusting and wrong.
You can get all your hospital records including x-rays and other digital scans via Freedom of information act. You will find a form on your hospital website. They will send it to you within a month. I have done it. I got everything including all x-rays and CT scans.
if you only eat sandwiches and shakes because you dont prepare meals then there wont be mess visible will there..? and what happens if you dont bath or shower and use wet wipes only.? my next pip in 2028..i will be 62..
Same-no shower or bath for years-the WCA doctor took note of that (I had to correct 2 mistakes in that sentence-I notice I make lots more mistakes-not the mental energy I once had-I just take 3 hours to do things that took 5 minutes-and nobody is fair enough to pay for that) I'm no Scientologist but sandwiches and shakes sounds like extremely valuable evidence of a disability to prepare meals (and is likely viewed by any doctor as a hazard to health due to lack of dietary variety) Same-my brother buys me chips too often for convenience but saves the energy of cleaning (I never use a plate just fingers) At 60-after I was terminated for having pneumonia and after ICU-I find it hard to go to the bin every 5 minutes with a teabag (especially in winter) so they just pile up - apple cores banana skins egg shells (I've never liked flip top bins full of bean juice and now you have to separate everything) What looks like a bit of clutter to some people looks like a horror show to my mum; but it does not need to look like one of those hoarders with 9 pets Some people are slaving their life away keeping a cold kitchen clean (just for their landlord when they check the gas once a year) otherwise they would have more free time to rest and damn the _clutter_ that can be cleaned every month (as we old people don't consume much) with no money (the slugs come in clean or not)
Just tell pip people who looks at your claim to pull Thier finger out and complete evidence with doctor snd hospital end of iys not our fault they can't get anything RIGHT WITH ANY BENEFIT
I’ve been trying to find out if Labour are planning on changing legislation for any benefits, yet I’m unable to find any information. Do you happen to have a link regarding their manifesto for benefits, disability benefits in particular? Any information would be greatly appreciated. Take care. XxX
I do understand what you are saying with taking a picture of a disability aid in situ but, am sorry to tell you that this is not evidence at all. This shows a disability aid and there is no proof at all that it is ‘your’ aid nor your kitchen (or whatever room you use. Would you not advise your listeners that they are better to take a short video, and an still photo from that video could be submitted as evidence and then if the DWP say it’s not being considered, the claimant could send the video to the tribunal? I only say this as I have submitted photos to the DWP and it’s gone all the way to tribunal and they dismissed my evidence as there was no evidence of it being my injury! You need to evidence all you send them. Have your claim form on the side. Your face in the picture. It could be anyone’s home, you could have bought that stool to cheat the DWP!
ignore the silly trolls, they are so far up her backside Rebecca they won't see the lies Infront of them, a woman who's been investigated by the dwp and hmrc on more than one occasion and they still buy into her bull, so sad.
@@CharlieSmithers-g1e I’m pretty sure you just had a melt about this word being used 😂😂😂, you’re one of those people that can say what they want but gets all judgmental about other people. Sweet dreams 👋
@@lisaroberts5889if she is so much pain why is she not groaning or writhing around. How can she just sit there casually chatting like she doesn’t have a care in the world. Maybe she has a bit of pain. Maybe she has arthritis. We all do as we get older. I have terrible RLS and sciatica. Don’t claim PIP for it, it’s just part of life and getting old. There are videos of her walking her dog. She looks perfectly healthy. Of course she will claim her pain comes on at night. There are videos of her and her mum going to car boot sales laughing and joking about what they’ve bought. They don’t look in pain then. But then she also claims she is in much pain she cannot butter a slice of bread to make a sandwich. It seems she has bought all of these aids to make her “look” ill. It seems she has Münchausen syndrome. She lives with her mum and her mum never seems to challenge her. I’m not saying she’s never ill or never experiences pain but it’s not on the level she claims e.g she claims highest level of mobility payments. She appears to be manipulating the system to get any payment she can. What irks me are there are thousands of people out there working 2 or 3 jobs to make ends meet. I’m not saying she isn’t entitled to some of it but it’s clear she has milked the system and is claiming well above what she is truly entitled too.
Unless you pay this women money she wont HELP you ..... 16 year's of claiming PIP and shes been rejected..... Speaks volumes .... Dont believe all of her crap .... if your a genuine person you will receive PIP
@@lisaroberts5889 Are you okay in the upstairs department? youtube works by paying people through clicks and adverts, if you see an advert it means the user is monetised which for every click they get paid based on number of views, so if she has 10k views lets say on a video and a long duration of watchers it could be anything from £60 to £200 a video, so yes she does get paid she just doesn't feel the need to tell you that because you all assume she's an angel for some reason.
@@CharlieSmithers-g1e no different to any other influencer you probably follow and line their pockets. If you have no use for PIP, I’m really pleased for you and you have no need to be here trolling along with others. So, she gets paid by RU-vid and if someone wishes to use her services they are made fully aware of the cost and what services they receive, what’s the problem?! And to answer your question no I’m not mentally stable, thanks for your concern:)
DWP spend 8 hours on a computer (in the warmest offices in the UK) they spent £2.9B finding 7 in 100 any type of task on Restart - The Work and Health Programme (Ofsted special measures) just abandoned people while they sat at a computer - They asked people "Do your teeth hurt" and did not even ask for their CV
This woman and terrible anyone can buy an aid or borrow one, doesnt prive anything. Hows about you just let them have access to your hospital records. This womans a con artists
