I’ve decided to split up my posts about my life into sections, so my posts are shorter and a bit easier to read and digest.
So as the title states this one is about PIP and ESA…Oh the joys!
Well after having to go to a tribunal, the DWP decided they might appeal the court’s decision. I am currently still waiting to hear from them.
I did get the statement that the tribunal sent to DWP but that’s all. I am really hoping I hear this week, as the wait is killing me! I just want it over with and I just want it sorted. It physically hurts, the wait is just agonising and just unreal.
The sad thing is I know I’m not the only one going through this and its heart breaking to think about all the pain and suffering that has been caused by this benefit change-up.
I feel like as a person with disabilities, I am being picked on and treated like a criminal. Even though my issues are legitimate and real, whether you can see them or not. My disabilities are there and they affect me every day.
The system certainly doesn’t cater for people with physical and mental health issues. For example, I would love to be able to work on the days I felt well enough and then on the days I need to rest then I could take off. But I just doesn’t work like that, jobs aren’t that flexible. Most jobs these days are zero contract hours, so I wouldn’t be entitled to statutory sick pay and benefits takes months or in my case over a year to sort out. Or similarly people with mental health issues, could be well for say 3 months at a time. So they could work that 3 months and then take time off to rest or if they become unwell then to get better again. But as I said it just doesn’t work like that and to me it doesn’t make much sense and I feel that it should be working this way, so then at least people who are unable to work all the time are at least paying taxes, even if it’s for a short while, not to mention the fact that it will give people with long-term health issues purpose, self-esteem and pride in themselves. I despise not being a productive member of society but we have a system in place that’s all or nothing. You are either able to work or you’re not, which is silly to me.
Well that’s my personal opinion and views on where the system is going wrong.
I am also still without my bus pass, which is making me feel trapped because I’m unable to pay for the bus with the little money I do get. I’ve emailed my OT again to get her to chase it up, as it was meant to have been processed last Monday and I should have got it last week, so I don’t know what’s going on with that. It’s so frustrating having to always chase things up. I just wish things would start running a bit more smoothly so it’s not so bloody stressful.
Anyway that’s all for now, I will post more when I know more.
Category: anger, benefits, chronic fatigue, chronic illness, chronic pain, D.L.A, E.S.A, fed up, granulomatosis with polyangiitis, my life, P.I.PTags: benefits, bipolar, bus pass, disability benefits, ESA, frustrating, granulomatosis with polyangiitis, hyper mobility, mental health issues, physical health, PIP, the system, trapped