I had to go to a tribunal because the ATOS assessor told lie after lie, I asked for the evidence they had with regards to the claims the assessor made about me, I got NOTHING, I ended up getting a 10 year award thanks to the tribunal
Having mobility allowance for over 41 years i got standard rate pip and im losing my mobility car on 22nd october and will be housebound as i cannot access buses, ive done a mandatory reconsideration which will take 15 weeks then i will appeal if unsuccessful. I broke my neck when i was 16 in a diving accident in 1984 which im slightly paralysed in my right hand side, with severe sleep apnea and type 2 diabetes with diabetic nerve pain in both legs and hands and i dont sleep well.
Heart failure comes on the list, but I tried from 2001 to 2020 to get dla as it was back then I had a double heart bypass in 2001 heart failure diagnosed in 2004 but DWP classed me fit for work failed 3 tribunals 2020 I got pip because I has cataract and have arthritis in both hips and have had meneries disease since 1981 which I don't I have much control over my balance from 2001 to 2020 I was putting sicknotes in every 13 weeks is the most a doc can be give u so lots of sicknotes over the yrs
I can not lie straight on my back or sit back because i Scream aloud in agony,i can not walk or even stand still for more than a few min without pain ,i get plantar facilitis in the foot a few times that latsed a nummber of years ,i have a bad shoulder for 40 years with a recent tare ,i get cronic fatigue from being on beta blockers to slow my fast heart of 200 beats resting ,i now get exhausted doing anything after a few min ,i am getting worsening memory and speech ,i get inner vibrations /dizziness /pins and needles /sitting in a car for last few years can be very bad ,i have had some very bad attacks of screaming and severe anger alomg with breathing like panic ,i wanted to be with Jesus in 2018 thought i was going to be raptured even went in middle of night 3 times back in 2018 ,i got that angry after my assesment the first time i stormed in their office so angry shouting at them they are liars as i got OOOOOOOO points ,i have gone through hardship not being able to work for around 18 years ,SO WHERES MY MONEY SICK WORLD .??????
My original application was rejected, the reasons given contradicted everything I had written in the form, I appealed and it was overturned, I believe they reject the vast percentage initially in the hope that they give up.....I have had surgery twice on my neck to remove discs that were pressing on nerves and squashing my spinal chord causing horrendous pain, and am left with extensive degeneration and arthritis, I have chronic back pain, sleep apnoea, fibromyalgia, shoulder and knee problems, bipolar disorder.....I can't stand or sit for more than a few mins and am totally reliant on the help of others, I'm confined to my bed for 90% of the time, the original rejection was ridiculous.
@@martinarscott3524 O SO SORRY you seem worse than me ,I THINK HOW BAD DO i NEED TO BE TO GET PIP ,who decides wether we are disabled ?is it the doctor or the benefit center ?
I've had .. family.doctors.solicitors even several people from dwp telling me im entitled to pip.so i gave in applied and got turned down . They said it was because I can plan a journey on my own.. i sufferd a brain ijunry and can't go out incase i get lost cuz of memory issues..
That’s dreadful! You clearly are genuine and in need of this support. My neighbour lied to get his PIP. Claims that his anxiety and mental health are too severe that he is unable to leave the house! He’s out all the time etc. Benefit fraudster!!
@@martinmuldoon603 There is some truth in what you say. Until very recent my cousin got the same PIP as I do because she is fat, and that apparently affects her mobility I had cancer that was in my spine causing ridiculous pain. The reason we got the same award was because I played down my pain and mobility problems and she played up her suffering. These decisions seem to be made on the basis of one phone call. Luckily, I appealed, so they had to consult my doctors. I am now on the highest level and am eligible for a car. The trouble with our society is that those that shout loudest often get their own way, whilst those that like a quiet life are often ignored.
Remember victims, identify ur RECEIPTIONIST, covering for UR " doctor ", who's too busy working PRIVATELY to care about U, u can SUE THEM PERSONALLY AS WELL AS UR SAD EXCUSE FOR A DOCTOR AND THE SURGERY, WHICH WILL BE SHUT DOWN AND ALL SO- CALLED DOCTORS ON SITE WILL BE # STRUCK OFF # and jailed, report these cowards on U TUBE, tape them Always❤
I'm terrified, because of this ,i have stage 3 to 4 copd also M.hlth ie,cptsd agoraphobia eupd many more ,I Can't cope with the worry of being seen by average person, who could decide no, she's ok ,im not ok amd unaliving very soon iss my only option , ,Government literally jys6t killed aother one of us ,ohh well I guess statistics on unaliving not important. can not dooo this madness, its to much, im just going to unalive to solve the problem.,yes I attempted before but now knowww a definite way to unalive x god bles u all xx😢😢😢😢😢😢
Try to see that tie life is more than if you get pips, as the queen song goes, don't try suicide nobody's worth it, you are correct about any government you are just a statistic on their books. Look at the war at war in Ukraine for example, soldiers there are only a statistic, Russia is loosing an average of 1000 soldiers per day and Ukraine claim a third of that are lost every day, so winning is based on disposable lives each country can afford to loose, it's a sad reality we are only a number.
Having a named condition doesn't get you an award its how that condition affects your life and how it restricts / stops you from doing something which would be easy to do if you didn't have the symptoms of your medical condition which prevents you from doing it or taking part
Government are going stop pip and give us vouchers to live on when don't so will have no money to spend they want us to work I blame mp I want write a letter to mp and put my foot down tell him not fare and stopping our bus passes too I'm worried and angry and all people will quite upset about this things happen it will change our liveing and will stuck at home 🏡 be I will feel emotional get depression be we will lose our day to day liveing going out like shopping and getting around on the bus 🚌 and seeing our friends
I had to go to a tribunal because the ATOS assessor told lie after lie, I asked for the evidence they had with regards to the claims the assessor made about me, I got NOTHING, I ended up getting a 10 year award thanks to the tribunal
Me too😔
@@melluques8475 lets go SHOPPING 🤣🤣🤣🤣
Having mobility allowance for over 41 years i got standard rate pip and im losing my mobility car on 22nd october and will be housebound as i cannot access buses, ive done a mandatory reconsideration which will take 15 weeks then i will appeal if unsuccessful. I broke my neck when i was 16 in a diving accident in 1984 which im slightly paralysed in my right hand side, with severe sleep apnea and type 2 diabetes with diabetic nerve pain in both legs and hands and i dont sleep well.
@@scootdevon7102 this might be of some help at the tribunal
CPIP/665/2016 PIP Walking Distance Tribunal Decision
its not about what you can do its about what you can't do!
Excellent information
Heart failure comes on the list, but I tried from 2001 to 2020 to get dla as it was back then I had a double heart bypass in 2001 heart failure diagnosed in 2004 but DWP classed me fit for work failed 3 tribunals 2020 I got pip because I has cataract and have arthritis in both hips and have had meneries disease since 1981 which I don't I have much control over my balance from 2001 to 2020 I was putting sicknotes in every 13 weeks is the most a doc can be give u so lots of sicknotes over the yrs
I can not lie straight on my back or sit back because i Scream aloud in agony,i can not walk or even stand still for more than a few min without pain ,i get plantar facilitis in the foot a few times that latsed a nummber of years ,i have a bad shoulder for 40 years with a recent tare ,i get cronic fatigue from being on beta blockers to slow my fast heart of 200 beats resting ,i now get exhausted doing anything after a few min ,i am getting worsening memory and speech ,i get inner vibrations /dizziness /pins and needles /sitting in a car for last few years can be very bad ,i have had some very bad attacks of screaming and severe anger alomg with breathing like panic ,i wanted to be with Jesus in 2018 thought i was going to be raptured even went in middle of night 3 times back in 2018 ,i got that angry after my assesment the first time i stormed in their office so angry shouting at them they are liars as i got OOOOOOOO points ,i have gone through hardship not being able to work for around 18 years ,SO WHERES MY MONEY SICK WORLD .??????
Your money is being given to the asylum seekers that come over and stay in the five star hotels with new mobile phones bikes close money, cigarettes
@@Gangstergranny1950blatant racism
My original application was rejected, the reasons given contradicted everything I had written in the form, I appealed and it was overturned, I believe they reject the vast percentage initially in the hope that they give up.....I have had surgery twice on my neck to remove discs that were pressing on nerves and squashing my spinal chord causing horrendous pain, and am left with extensive degeneration and arthritis, I have chronic back pain, sleep apnoea, fibromyalgia, shoulder and knee problems, bipolar disorder.....I can't stand or sit for more than a few mins and am totally reliant on the help of others, I'm confined to my bed for 90% of the time, the original rejection was ridiculous.
@@martinarscott3524 O SO SORRY you seem worse than me ,I THINK HOW BAD DO i NEED TO BE TO GET PIP ,who decides wether we are disabled ?is it the doctor or the benefit center ?
I've had .. family.doctors.solicitors even several people from dwp telling me im entitled to pip.so i gave in applied and got turned down . They said it was because I can plan a journey on my own.. i sufferd a brain ijunry and can't go out incase i get lost cuz of memory issues..
That’s dreadful! You clearly are genuine and in need of this support. My neighbour lied to get his PIP. Claims that his anxiety and mental health are too severe that he is unable to leave the house! He’s out all the time etc. Benefit fraudster!!
@@NicolaRankine-jm7oeit's appears you have to lie to get pips.
@@martinmuldoon603 There is some truth in what you say. Until very recent my cousin got the same PIP as I do because she is fat, and that apparently affects her mobility I had cancer that was in my spine causing ridiculous pain. The reason we got the same award was because I played down my pain and mobility problems and she played up her suffering. These decisions seem to be made on the basis of one phone call. Luckily, I appealed, so they had to consult my doctors. I am now on the highest level and am eligible for a car. The trouble with our society is that those that shout loudest often get their own way, whilst those that like a quiet life are often ignored.
Very good right to the point spot on
Remember victims, identify ur RECEIPTIONIST, covering for UR " doctor ", who's too busy working PRIVATELY to care about U, u can SUE THEM PERSONALLY AS WELL AS UR SAD EXCUSE FOR A DOCTOR AND THE SURGERY, WHICH WILL BE SHUT DOWN AND ALL SO- CALLED DOCTORS ON SITE WILL BE # STRUCK OFF # and jailed, report these cowards on U TUBE, tape them Always❤
I'm terrified, because of this ,i have stage 3 to 4 copd also
M.hlth ie,cptsd agoraphobia eupd many more ,I Can't cope with the worry of being seen by average person, who could decide no, she's ok ,im not ok amd unaliving very soon iss my only option , ,Government literally jys6t killed aother one of us ,ohh well I guess statistics on unaliving not important. can not dooo this madness, its to much, im just going to unalive to solve the problem.,yes I attempted before but now knowww a definite way to unalive x god bles u all xx😢😢😢😢😢😢
Try to see that tie life is more than if you get pips, as the queen song goes, don't try suicide nobody's worth it, you are correct about any government you are just a statistic on their books. Look at the war at war in Ukraine for example, soldiers there are only a statistic, Russia is loosing an average of 1000 soldiers per day and Ukraine claim a third of that are lost every day, so winning is based on disposable lives each country can afford to loose, it's a sad reality we are only a number.
Having a named condition doesn't get you an award its how that condition affects your life and how it restricts / stops you from doing something which would be easy to do if you didn't have the symptoms of your medical condition which prevents you from doing it or taking part
Government are going stop pip and give us vouchers to live on when don't so will have no money to spend they want us to work I blame mp I want write a letter to mp and put my foot down tell him not fare and stopping our bus passes too I'm worried and angry and all people will quite upset about this things happen it will change our liveing and will stuck at home 🏡 be I will feel emotional get depression be we will lose our day to day liveing going out like shopping and getting around on the bus 🚌 and seeing our friends
you need to get your facts right. receiving PIP does not ever entitle you to anything else.