Ask your MP to act!

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Comments

  • Amaya_Ringo
    Amaya_Ringo Online Community Member Posts: 228 Empowering

    I would love to support this, but I've had several conversations with my MP about disability rights before, with mixed results. The last time he refused to oppose the snooping on benefit claimants proposals, which we're now facing again. I don't think emailing him will help in the least, this time :/

  • Nashota
    Nashota Online Community Member Posts: 453 Empowering

    I think I already sent the useless local MP an email through a different charity but I was totally ignored.

  • egister
    egister Posts: 559 Empowering

    https://disabilitylabour.org.uk/blogposts/how-charging-policies-are-are-affecting-disabled-people/
    In 2019 SCOPE the National Charity did a report on the extra cost of being a disabled person. The findings of this report calculated this to be £583 per month. I am only using this report to try to illustrate that PIP was never meant to pay for care. It is also important to say PIP has never kept up with inflation.

    for memory…

  • Loulou82xx
    Loulou82xx Online Community Member Posts: 1 Listener

    Hi everybody this is my first ever comment so I apologise in advance if I make any mistakes.

    My situation is I am disabled and have been since 2006 my husband is my fulltime carer and in 2022 my daughter was diagnosed with acute lymphoblastic leukaemia at the age of 24 we have been caring for her ever since that time as she has no immune system and the treatment is brutal so she needs support. She receives PIP and also ESA but nothing else as she was saving for a deposit for a house so has more in savings than is allowed. She worked for the NHS in the ICU and worked so hard during Covid including so much overtime to enable her to save money.

    Anyhow we don't receive any extra benefits to care for her or any allowance made due to her living with us, we have to keep the temp high due to her not having any immunity and any temp above 38 means she has to go to hospital straight away for IV antibiotics to try and keep sepsis at bay. She has already had sepsis twice and we thought we were going to lose her.

    The cost to keep the heating on 22 degrees is huge for us to bear on Universal credit we have just migrated over and I have to keep providing FIT notes whilst waiting for them to process my UC50 form we have to buy the best possible food we can afford to give her system the nutrients so lots of fresh fruit and vegetables and lean meat including red meat for her iron levels so our food bills are huge and we are already under so much stress due to the fear and grief we are going through at the possibility of losing our precious daughter.

    I have emailed my MP explaining our situation but have not heard anything back. We are fortunate to have had help from Leukaemia care and Macmillin who have given us small grants which helped pay for a new bed for her and I am forever grateful to the NHS for all they do for her but her PIP only covers so much we have transport costs daily which eats into her PIP and so many extra expenses for medical supplies such as dressings. She is so much pain after chemo that she cannot bear to sit and wait for hospital transport which sometimes takes four hours and she feels so sick so we end up getting a taxi home which is £30 per day so the PIP soon goes.

    I really think there should be some help available for people in similar situations and hope that MP's listen and stop making life so hard for people in genuine need.

    Sorry for such a long message but the above is basically what I have sent to my MP.

    Thanks for your time in reading.

  • WhatThe
    WhatThe Online Community Member, Scope Member Posts: 2,614 Championing

    Loulou, welcome to Scope 💜 thanks so much for your time in writing. You have explained beautifully. I hope there is financial support for you to access through members' knowledge and that your UC migration goes smoothly. From UK Parliament -

    What should I do if my MP hasn’t answered my email/letter?

    MPs receive a large amount of correspondence, so cannot always reply immediately. If you haven’t heard back from them after about two weeks, you should follow up your email or letter with a phone call, or make an appointment to go and see them at their local surgery.

    💜

  • chiarieds
    chiarieds Online Community Member Posts: 16,671 Championing
    edited October 23

    Hi @Loulou82xx - & welcome to the forum. I'm sorry to read how much you as a family are going through, & every respect to your daughter having worked in ICU during Covid. It must be devastating to see her so ill now.

    Do get your husband to say he's a carer for your daughter, if you haven't already done so, as, with your own health issues, should you be awarded Limited Capability for Work & work-related activity (LCWRA) with UC, then you can't also receive the Carer's element, rather LCWRA, as this higher amount would apply instead, but your husband can get the Carer's element.

    Do also please keep on providing fit notes yourself until a decision is made following your Work Capability Assessment (WCA). Gaps in your fit notes can affect when money is paid from/due.

    Possibly Scope can also advise with your energy costs:

    https://www.scope.org.uk/community-disability-energy-advice

    As a family, & as parents looking after your young daughter, you deserve all the help that can be found.

    I have had a reply from my MP, but unfortunately it really didn't say too much.

  • Nashota
    Nashota Online Community Member Posts: 453 Empowering

    I received a response from the local MP about the following, I don't know if it's the right place to post it, if not, please feel free to put it in the correct place admins :)

  • Nightcity
    Nightcity Online Community Member, Scope Member Posts: 2,670 Championing
  • Albus_Scope
    Albus_Scope Posts: 8,327 Scope Online Community Coordinator

    That's great, thank you for sharing @Nashota

  • Nashota
    Nashota Online Community Member Posts: 453 Empowering

    No problem @Albus_Scope :)

  • Amaya_Ringo
    Amaya_Ringo Online Community Member Posts: 228 Empowering
    edited October 29

    Is it my imagination, or did some copying and pasting happen in the text of that letter? :) She mentions putting disabled people at the heart of things twice.

  • charlie72
    charlie72 Online Community Member Posts: 32 Contributor

    Iv'e emailed my MP numerous times and never get a response from him, I appreciate he's probably very busy but I just feel ignored, especially when its about benefits changes. They just don't seem to care at all about letting us know what's actually happening, keeping us in the dark like mushrooms. They won't clarify anything, conflicting answers from different mp's about W.C.A, it's all very annoying, frustrating, and highly stressful, especially when alot of people suffer from mental health issues, made worse by this useless government and rubbish PR team.

  • Nashota
    Nashota Online Community Member Posts: 453 Empowering

    I received the following today: -

    Dear Lilian,

    Thank you for your letter of 29 October to the Secretary of State on behalf of Ms (I obviously removed my details here), about reform of the Work Capability Assessment (WCA). I am replying as the Minister of State for Social Security and Disability.

    The WCA is simply not working and needs to be reformed or replaced. This needs to come alongside a proper plan to genuinely support disabled people to work and, in turn, bring down the benefits bill and we will continue to deliver the savings set out by the previous Government.

    We know that change is desperately needed but, equally, these sorts of changes should not be made in haste. We are taking the time to review this in the round before setting out next steps on our approach in the coming months.

    We know that disabled people face various and complex barriers to work and things like the WCA and disability benefits more broadly should not be used as a blunt tool to address the issue. We will bring forward our own plans to support disabled people back into work, bring the benefits bill down, and deliver the long overdue reforms our welfare system needs.

    This Government is committed to championing the rights of disabled people and to the principle of working with them, so that their views and voices will be at the heart of all that we do. So, as we consider our next steps, we will continue to engage with stakeholders to keep the views of disabled people and people with health conditions at the forefront of our decision-making.

    The new Government is very concerned at the undermining of the social security safety net, which has occurred over the past fourteen years. Our aim is to make the system fit for purpose in the course of the decade of national renewal, which the Prime Minister has committed to.

    With all best wishes,

    Rt Hon Sir Stephen Timms MP

    Minister of State for Social Security and Disability.