Universal Credit Act 2025 - Latest Updates (05.03.26)

13

Comments

  • Danny123
    Danny123 Community Member Posts: 229 Empowering

    What if you voulterrilly moved over to UC from ESA support group in mid 2022 and was put in the lcwra group automatically because your ESA support group automatically qualifies you for lcwra group ..... What I mean is because technically I've never been assessed for UC lcwra does that mean I'm a new claiment or am I seen as an existing claiment

  • Danny123
    Danny123 Community Member Posts: 229 Empowering

    Yeah reading that I think I'll be alright

  • deelee
    deelee Scope Member Posts: 77 Empowering

    @MadMilan2019 your posts here are always very inspiring to say the least. Thank you for speaking from your heart and sharing valueable truth about disabled rights. Green Party are the only party which seem to give a hoot about the disabled which is why I will also be voting for them too. Hope you haveing a good afternoon and everyone else too :)

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    I am going to start a Parliamentary Petition which if it gets a 100,000 signatures has to be discussed in Parliament, and may change the law.

    Please Google ''Parliamentary Petitions U.K.'' to find out ,more how they work.

    For now I'm asking Campaigns Dept, all staff at Scope including this online discussion forum to respond by listing all the disabled and mental health and grey power. elderly/ pensioners groups with full addresses, postcode email and telephone numbers.

    Having a full list of such groups in the UK I will then draft a Parliamentary Petition, ask for amendments and improvements,

    then send it to the full list

    The petition's aim will be to reverse the £2.5bn cuts in disability welfare benefits, to stop the welfare suicides, brutal, inhuman and degrading, stigmatising treatment of disabled people

    and

    suggest the positive things we want, as policy to support disabled people now, and in the future.

    Please give your suggestions, ideas thoughts, and total positivity, please do not indulge in doubt, depression, anxiety and trauma, we need to do the very opposite no matter how bad we feel, or good, I am feeling S*** today had 2 spasms last night, only 3 hours sleep.

    Even some suicidal feelings, but hey, I do NOT want Scope staff to ring or email me, because I WONT DO IT and let myself and you all down.

    I have great compassion, joy compassion, spirit, will not take no for an answer, will try and try and try and fight and fight and fight again,.

    I am a politico-spiritual warrior for love, compassion, against stigma, for social justice.

    All demons are diamonds geddit?

    WE ARE ALL WORTH FIGHTING FOR

    AND GENUINE HELP TO WORK OR NOT, SUPPORT, MORE NOT LESS BENEFITS

    AAND THE EXTRA COSTS OF DISABIL;ITY, AND DISABILITY DEFINED HELP BY US NOT THE SOP CALLED LABOUR GOVT.

    Any one any idea of even a rough date of next general elections; we need to design strategy and tactics in the run up to next general election,

    I am standing in the local elections to

    • get gang crime down, youth counselling, safer streets and estates
    • - For more green gardens tree planting, too as therapy and joy for volunteers
    • - And to get council and housing associations to stop treating their tents as 2nd class citizens, as the Grenfell report said.

    Wish me luck, I wish you all joy the best of luck, lots of love, and courage freedom, and growing ever more everyday.

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    You are extremely kind inspiring and strong to say such deep compassion.

    Moved to tears, my friends are rallying round.

    Never ever give up folks talk to friends cultivate new reliable friends, meditate on line e.g. Tich Nath Hanh, Eckhart Tolle, Buddhist mediations, Google all of these latter.

    I promise you won't regret doing so.

    WR ARE DISABLED PEOPLE NOT PIECES OF S** WE ARE HUMAN BEINGS WHO DESERVE FAR BETTER FROM SOCIETY, WE HAVE BEEN THROUGH SO MUCH.

    FOR MANY OF USE TRAUMATISED OR NOT IT IS A GREAT ACHIEVEMENT THAT WE ARE STILL ALIVE.

    WE CAN CHANGE THINGS

    YES WE CAN

    LIFE UNFAIR WE DO NOT DESERVE THIS S** TREATMENT,

    BUT REALISTICALLY NO ONE IS GOING TO DO IT FOR US.

    WE HAVE TO ORGANISE AND TAKE POWER.

    WE HAVE TO CAMPAIGN

    OR ALL FORMS OF DISABLISM IN INCLUDING BENEFIT WITHDRAWAL SUICIDES WILL GO ON AND ON.

    HOW MANY 1OS OF 1000S OF DISABLED PEOPLE HAVE SUCIDED IN THE LAST B30 YEARS DUE TO BENFIYT CUYTS, HAS ANY ONE A RELIABLE FIGURE, DOES ANYONE KNOW AN ACADEMIC WITH A RELIABLE FIGURE? CAN SOMEONE PLEASE FIND OUT.

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    Thank you Catherine21.

    I DO Care deeply.

    You cared enough to respond kindly.

    Let me start my list of disability physical charities and advocacy groups UK, to build a cross group and cross party alliance to reverse the £2.5bn cuts:

    It Can be done: 13m disabled people, 8 million pensioners or v.v.? memory problems =s 21m voters.

    There 67m people in the UK. That is enough if

    - disability, mental health, and pensioners charities pull together in a n alliance.

    Its not lack of voter numbers who are adversely affected but lack of confidence, self-esteem, internalised oppression, and at present the lack of 3 social movements pulling together to make our case, reasonable rational and realistic - and unstoppable

    Mental charities advocacy groups:

    Mind

    Physical charities advocacy groups:

    Disability Rights UK

    Scope

    Pensioners advocacy charity groups/ Grey Power

    Please everyone I we need you, add to the list above.

    I will redraft and amend by saving the proposed strategy to reverse the 2.5bn cuts and republish on Scope forum, consulting this forum many times.

    Date of next general election anyone

    propsed writing to MPs, and lobies of Prilsament, peaceful deomos too

    Sharing startegy on social medias

    List of all social media need:

    Facebook

    LinkedN

    X

    Reddit

    Threads etc. .

  • deelee
    deelee Scope Member Posts: 77 Empowering

    @MadMilan2019 Thank you for these words. It is very inspiring and very true - we all make up a huge number of voters and can do this. We should never give up hope because together we can be a powerful voice.

  • deelee
    deelee Scope Member Posts: 77 Empowering

    @Catherine21 wow that is really good to read - thank you for sharing that

  • sarah_lea12
    sarah_lea12 Community Member Posts: 442 Empowering

    If I get reassessed for LCWRA I now live in an adapted social housing bungalow and waiting for a level access (wet room) to be installed ,my conditions are certainly not going to change . I am hoping PIP will give me an ongoing award next year too, the stress of the assessments and reviews cause my mental health to get worse . I would also add to the LCWRA assessment that i have profound hearing loss wear hearing aids and still miss words that people speak to me 🤣

  • luvpink
    luvpink Community Member Posts: 4,901 Championing

    @sarah_lea12

    I had a pip reassessment last year.

    I used to get three year awards each time but this time I wrote on my form requesting a longer award, and to my amazement I had a paper based assessment, kept high rate on both elements, and I was given an 'ongoing ten year' award.

    I wish you the best outcome when you have your assessment.

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    Dear Delee,

    Thank you for your deeply compassionate words of strength power and encouragement.

    I will keep going, on with redrafting a proposed strategy to get back the £2.5bn disability welfare benefit cuts.

    Life is very tough at the mo.

    A new 9th MSK diagnosis: Herberden's Nodule, my last joint on my left little finger is swollen and painful sometimes, a form of osteoarthritis, net keeps cutting out and my mobile too so its difficult and time consuming to make phone calls and emails.

    I DO need help to find an academic to get the accurate figures of 13m disabled people, number of pensioners 8m, and and to help with other requests.

    Much info can be Googled.

    I need more than moral support, I need volunteers re any tasks to create an Effective Proposed Strategy to get back the £2.5bn Disability cuts via an Alliance odf Disability, Mental health, and Pensioners Groups.

    United we stand divided we fall.

    Tasks

    Please do them with joy, if you can. with a fighting spirit of resistance knowing we are creating compassion for all.

    An academic in statistics to get accurate figures see above please

    Can someone email Jeremy Corbynn and ask will he support the reversal of the 2.5bn cuts, Google Your Party please.

    This is the start of a cross partly non-party political campaign, NB. Because Scope is a charity and cannot support any one political party, charity law.

    Need people to give details of all disability, mental health and pensioner/ grey power national groups charity. advocacy groups in the UK,

    Just post the Googled results to me c/o this forum.

    There are great physical pains, backache, joint and muscle pains triggered traumas, but recovery nis quick insomnia etc, you know 34 diagnoses to cope with and process to freedom and compassion, day and night.

    Tears and joy, joy and tears.

    No different from what the world changers of this world, heroes and heroines in every social movement for social and compassionate justice and equality experienced.

    Never give up, ever see the best in you, because of pains, disability, see the best in friends, allies, even enemies.

    Reduce bitterness, turn it into love via the fire of clear thinking and or meditation,

    Sayings of The Buddha - please Google latter, it will inspire you: -

    ''In thew crucible of determination the Master finds true freedom.''

    ALL demons are diamonds,

    with courage and the right insights for the individual.

    Turn hurt stigma in to a fire of love and win our human right dignity and well being back.

    WE ARE NOT PIRECES OF S*** UNDER SOMEONE'S SHOES, BUT WE HAVE FELT LIKE THAT.

    WE ARE HUIMAN BEINGS WHO DESERVE LOVE, JUSTICE AND RECOGNITION AND POWER.

    AND WE WILL NOT TAKE NO FOR AN ANSWER.

    WE WILL SHOW THE GOVT OF THE DAY WE WON PARTLY the govt wanted 5bn cuts, got 2.5bn

    AND CAN WIN FULLY OUR BENEFITS BACK, TO BE TREATED WITH REPECT, HUMAN DIGNITY NOT CRUELTY AND COMPASSION AND EQUALLY.

  • deelee
    deelee Scope Member Posts: 77 Empowering
  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    Life continues to be tough but I I am not a masochist and recognise there are many good and sweet things in life like the sunshine, the darling buds of March?! in my large wildlife gardens, the kids playing in the street, their joy and spomtaneity, kidstuff, good freinds who rally round, most of whom who have trauma.

    Can anyone please help with the tsks need to complete a Strategy to get out 2.5bn£ cuts back outlined in the my last few posts.

    W have to work for our freedom and this, if we sit and wait for others to do it well it will never happen:

    the realism of courage and recognising reality.

    Life and this 'Labour' govt is SO unfair, we need to organise and act and work together with love and support, and even joy - you might even enjoy the struggle,

  • ColonelBlink
    ColonelBlink Community Member Posts: 907 Pioneering

    My struggle is transferring onto the toilet, so no barricades for me 🚽 - Libres et sans culottes!

  • SwiftFox
    SwiftFox Community Member Posts: 1,169 Championing
    edited March 31
  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    I do not understand the comment above re barricades? Please enlighten me.

    This is from the free paper on the bus in Leeds:

    Metro.co.uk Thursday June 26th 2025

    Letters

    [ ] Can we ever imagine a time when the British government of the day wont seek to make the sick and disabled pay for its spending choices in other areas?

    Philip Duval, Manchester.

    [ ] Sir Keir Starmer is buying 12 F-35A US jets to expand our 'nuclear deterrence'.

    We have been aware of the threat from Russia for many years, even before Vladmir Putin invaded Ukraine in 2022 (or 2014 if we are counting Crimea) yet we have been happy to let Ukraine fight this wart on behalf of the rest of Europe instead of giving them what they need to actually push Russia back, which you would think would be the most effective way of protecting the UK from Russian aggression.

    This newfound appetite for defence spending is clearly being driven by Donald Trump's threat of withdrawing from NATO unless European states spend more, which effectively highlights who it is that determines UK defence policy.

    Is this really the best way to protect the UK in modern warfare, which is highly digitised and much more reliant on new technology such as drones.

    In particular, is it really the case having 10 times as many nuclear weapons equates to 10 times as much nuclear deterrence, given a single nuclear strike would have such huge consequences?

    Sir Keir Starmer has chosen to prioritise an arms race over welfare, climate change, international collaboration and human rights.

    What a difference a year in power make

    Federico Moscogluri, Hertford.

  • ColonelBlink
    ColonelBlink Community Member Posts: 907 Pioneering

    My attempt at humour is all, we need humour in our lives.

    All this politics and campaigning is a waste of time, the public aren't interested in benefit claimants.

  • SheffieldMan1976
    SheffieldMan1976 Posts: 2,211 Connected

    Actually, the public loves to complain about benefit claimants and tar us all with the "workshy slave to the benefit system" brush, even though it's a known fact there's a myriad of disabled people out there for whom it would be mentally and/or physically impossible for them to go out and work.

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    New PIP Claimants after UC PIP Bill 2025:

    - do they have the same criteria for getting PIP as before the Bill, or different?

    • Are there more frequent and stricter tests to be able to claim PIP?

    Please advise Scope benefit advisors, or anyone else qualified to answer?

    The public at least 20 million of them out of UK population of 67 million claim some kinmd of disability welfare benefit, or could do., so we are the public, and have friends and allies, who care for us.

    So, if we galvanise our disability, mental health and elderly/ grey power groups we can reverse the OPIP changes.

    Also, I am still continuing to ask charity lawyers, including Mind Legal Unit, poro bono solicitors if there is any legal challenge at all, as the PIP changes, and ESA changes too have been described as unfair yes, but also illegal.

    IU have been asking for 1 year now, and may actually take the govt to court, have set 3 legal precedents in my life. One was to overturn the decision of the DSS who refused me Income Support, a measly £16 odd, back in 1981, because I was not 18 years old, or estranged from my parents.

    I told the DSS manager via complaint from a solicitor, at Chapeltown and Herehills Law Centre, Leeds 7, that I saw on the 10 O'[ Clock News, both BBC and ITN, that it said if someone is a citizen of the UK and destitute through no fault of their own, they are entitled to welfare benefits.

    I said further, that the DSS is there to support people and after 5 months of no income, leaving home after 11 years of domestic violence by 5 members of my family, I would rather starve to death than go 'home.'

    And that I was trying to improve my life by doing A Levels and they should support me.

    I did not have a diagnosis of depression, anxiety, and PTSD, or mood disorder, all these came at least 20 years later, so I missed out on disability benefits, and appropriate healthcare from the NHS making my physical and mental health worse. So costing the DDSS more and the NHS because of lack of early diagnosis.

    I gained a small amount of compensation for severe hardship, after writing to my MP, Dennis Healey at the time.

    Also I publicised my story in local and national newspapers, and said the DSS should be totally ashamed of themselves for causing me intense worry, stress, increasing anxiety and depression, .

    I did get an apology from the DSS District Manager.

    It was a horrible traumatising experience.

    And then 10 years later I became a disability and mental health advocate.

  • MadMilan2019
    MadMilan2019 Community Member Posts: 190 Empowering

    Dear Catherine21

    I am sorry you too had similar and different struggles re your mental health.

    The fact that you became a support worker was a great achievement, even if were not able to sustain this valuable role. You were are an expert by excperience.

    And should be PROUD of gaining paid emnployment, giving support care and compassion, as well as apt challenges to other disabloed and distressed foilk.

    You work was invaluable.

    We are so stigmatised Catherine, and everyone, we devalue our achievements, against trhe odds because of the cruel anmd hatefrul stigma.

    This is interenaliused disablism, and we can recgnise it as such for what it is, baggae from oppression, a hateful society, at least in part; of course there are those whjo care aboyut uas deelpy too. Other disable people anmd mental health survivors.

    There are allies whjo belive we are worth supporting, as capable as intelligent as any no disabled persons.

    We need to STOP devaluing ourselves.

    We are human beings who deserve far better; we do not need to sie from suicide - because that is the indicator of just how badly we are treated - viciouysly in fact. We are worth huiman dignity life and love and support anbd recognitioin,. We are NOT pieces of **** uindrer someones shoe, althougfh we have felt l;ike that, because of constant messages thjat we are not quite equal, or not wrth listening to, not worth our benfits, that we are scroungers. All of thois is disablism and it saps the life, and fight the life foirce from us.

    WE DONT NEED TO BUY THE DISABLIST PROPAGANDA, WE HAVE A CHOICE, HOWEER SMALL AT FIRST TO RECOGNISE OUR HUMANITY THE VALIDITY OF OUR THOUGHTS FEELINGS AND ACTIONS.

    There are 2 different things going on here:

    1

    Yes we have intenalised baggae stigma, from the stigmas of disanblism and mentalism, these bogus cruel oppressioons.

    Some of us on top oif that have sexism and racism internalised, yet we can recognise and feel that the opprerssors stuff and bigfotry are THEIRS NOT OURS. We can live again. The very fact we are live, that I am alive is a miuracle.

    2

    We have tr

    o deal with the harsh reality of Disablism in all its forms, just to survive, to build self esteem, to live and love, to feel joy, that we have a right to9 exist, because there are many Fascists and Nazis who want us dead.

    In other words, we have to know what the problem is.

    It is oppression in a word, we are victims or have been and do not need to be miserable depressed, anxious traumatised victims.

    We can live life to the full with friends allies and love, the strength of disabled comrades, whether they are socialists, like me, like you? or not.

    We need DISABILTY PRIDE.

    I am proud to be a disabled person, I am proud to be a mental health survivor and thriver, recognised by an outstanding achievement award in community work, and other forms of recognition. People say I'm a great chair of meetings, have a GSOH so wacky and Monty Python (great fantastic message their Life of Brian: #Lifes a piece of S*** when you look at it but … always look on the bright side of life.. a Buddhist mantra of course like, glass half full.) Bonkers humour. I am a true individual Bonkers Buddhist. I am madcap, Zany, and a crazy spontaneous and joyful dancer. Courageous.

    We need more meetings in the disability pride movement just to focus opn deconstructing the cruel oppression of disablism, and to construct to create a higher self-esteem.

    Your sentences are rather long, and sometimes it is difficult to understand what you are saying Catherine, I recognise this trait. The need to be heard to be recognised and valued, and the anxiety that accompanies speech.

    If you are saying its your brain that causes your disabilities, perhaps not, or only partly. There is the rough harsh reality of social oppression: bullying at home school, the workplace, and harassment, shunning of disabled people in public places such as pubs and restaurants.

    There is a capitalist investment in saying the cause are in our brains, genes, or some other 'constitutional factors, but not the psychosocial structural aspect.

    Hence the psychosocial model of disability not the biomedical model.

    It is definite psychol;gical and social oppression this disablist mentalist stigma. Also many oif us are poor always have ben, we are working class, or from families, like mine that are half unemployed with all the oppression of stigma of not working.

    It is also the vicious class system.

    Its it only our brains then medication is the answer, and not better opportunities for supported work, or being left alone on benefits, or openness and welcoming wherever we go in society.

    And the answer if it our brain chemistry is provided by multinational pharmaceuticals, and medication isn't perfect, there are '[side' effects, even adverse effects - Prozac nearly killed me via 3 weeks of insomnia - and then as suicide attempt back in summer of 1993.

    Fortunately, I survived anfd knew from that crisis on I had either to slowly but defginitely, gradually, rebuild my sel;f esteem, self compassion. Because real change is slow not manic . That I did and I am so glad I did that hard work of cultivating insight through therapy, setting up support groups, meeting new friends, survivors and thrivers i disability pride and mental health pride.

    All is not lost

    we can reverse the changes, the cuts of benefits, but it will require ,ore responsiveness, not indulging in despair, creating courage and getting the practical task done, people volunteering for the tsks to make a strategy outlined in previous recent posts.

    If we don't believe we can do this and go along with disablism, and not organise unite and fight back not with bitterness, but sweet reasoning, and lovemaking a case.

    No one is going to liberate us, do it for us.

    We have to do it ourselves, united proud and strong, alive, really alive, instead of the misery, the AGONY of suicidal feelings - which we definitely DO NOT deserve.

    And WE CAN DO IT

    rebuild our human dignity, self worth, our self-esteem, self compassion and the best in our disability pride humanity

    AND

    Get the £2.5bn cuts reversed, if we organise together.

    ''Because you are worth it!'' Think Loreal advert for skin cream; told you I was wacky, bonkers madcap Milan Ghooooossshhhh!!!