Upcoming changes to benefits

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Comments

  • secretsquirrel1
    secretsquirrel1 Online Community Member Posts: 2,052 Championing
  • tcellmutation
    tcellmutation Online Community Member Posts: 341 Empowering

    So it seems likely that these changes will take a while to implement and may not even go ahead but for those severely disabled, they probably won't have to have any other reassessments on the back of this, despite many changes not actually coming into effect

  • Wibbles
    Wibbles Online Community Member Posts: 3,040 Championing

    What's going to happen to the thousands of motabilty cars that people have on PIP ?

    If several 100 thousand get reduced PIP ?

  • Maggie37
    Maggie37 Online Community Member Posts: 79 Empowering

    Just watching the real architect of this( class traitor) Pat McFadden walking into Parliament. No empathy, reptile like intent. Paisley poor boy, Irish Heritage before being born in Scotland. **** Cummings in a tartan scarf. He must be self- loathing or something. I hope he comes a cropper like Cummings did. This is all an experiment for them though.. they’ve all( especially Reeves)got their off ramps worked out in consultancies to Europe and America. Starmer taking a backseat.. just in case he’s dirtied by any backlash. What a bunch of wrong’uns!

  • luvpink
    luvpink Online Community Member Posts: 3,214 Championing
  • Maggie37
    Maggie37 Online Community Member Posts: 79 Empowering

    God look at this and try not to shred your curtains! They’ve been spending OUR cash. https://www.bbc.co.uk/news/articles/cvgp3ge97glo

  • Mysteriouskitten
    Mysteriouskitten Online Community Member Posts: 40 Empowering

    They Are the biggest scroungers in this country. Disgusting

  • Catherine21
    Catherine21 Posts: 8,623 Championing

    Just horrid can't enjoy anything hope it's not as bad as we think

  • Catherine21
    Catherine21 Posts: 8,623 Championing

    We got this we are together let's hope it's better than we think remember this is thier wish list it's not written in stone breath in and out its scary but we will know and everyone will be on them thier waiting big big big hugs we will be ok no one is going to accept this

  • Catherine21
    Catherine21 Posts: 8,623 Championing

    Xx

  • Maggie37
    Maggie37 Online Community Member Posts: 79 Empowering

    Same. I was paying NI from 16 and put myself thru Uni by working as a domestic at nights. ****. I was an academic lecturer/ researcher and funder for Scottish Enterprise for decades, cared for Ma and Pa before their deaths( no carers allowance claimed).. as I still did a bit of work. I’m done in now.. autoimmune, Lupus, mental health but still fighting. I mean.. How Dare They!

  • secretsquirrel1
    secretsquirrel1 Online Community Member Posts: 2,052 Championing

    I haven’t read anything about mobility award or motability . I’ve found that strange.

  • tcellmutation
    tcellmutation Online Community Member Posts: 341 Empowering

    It seems like the 90% of people in this thread are not physically disabled (deemed unfit from the new criteria) but suffer from things the government do not want to recognise anymore. Things like ME or mental health etc

  • secretsquirrel1
    secretsquirrel1 Online Community Member Posts: 2,052 Championing

    Thing is I’d consider myself severe but it’s all down to the assessors and that’s pot luck on who you get . Would they consider fibromyalgia and ME as severe ? To them possibly invisible so doesn’t exist.

  • tcellmutation
    tcellmutation Online Community Member Posts: 341 Empowering

    The government make a lot of money on this scheme. They won't want to abolish this

  • Santosha12
    Santosha12 Online Community Member Posts: 3,085 Championing

    Thank you so much, I'll be 62 tomorrow yeeks. Mum used to tell me i came at 445pm, just in time for tea. I used to always sit in the kitchen 20 mins before it would be ready sat with knife and fork in hands waiting. 🤣

  • Maggie37
    Maggie37 Online Community Member Posts: 79 Empowering
    edited March 28

    I’ve a good pal in New Zealand who has EDS( joint hyper mobility)plus severe mental health issues.. she has worked in her life. She struggles. There is no assessment as we recognise it for disability. A govt body contacts her doctor directly and she is left alone. It is not the done thing to demonise people who are disabled.

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