A Chilled Day….

Today has been quite a quiet day compared to others. Nice to have time to reflect on whats actually happening rather than being caught up in it.

I’m fairly sure THATS the last time i drive to pick up my prescription! Motability have done their best to keep extending when the car needs to go back , but now I’m entering the appeal process I don’t think I will get further extensions. Its good but at the same time it has thrown my previously well thought out plans out the window.

I see The Muscular Dystrophy UK charity has come out pointing out the ineffectivess of PIP on personal independence. I don’t know why the charities don’t all band together and protest and set up demonstrations against PIP? Its almost as though one makes their point and, by the time the next charity makes a similar point, the Tories have forgotten about it!

I am lucky in the sense that my loved ones, friends and people following my story are behind me all the way and all think a great injustice has been done to me. I hope its the same for the other people who PIP has ground their life plans down the sewer. Ok maybe not sewer but its sure as hell 6 feet down!

I’ve been on the computer all day listening to my itunes and the first song i wrote in regard to my MS popped up. Even 4 years ago I was asking questions quite fitting to what I have to do now with PIP and the DWP! Will it ever be enough?

Ever be Enough

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Fendercali

I was diagnosed with Relapsing/Remitting MS in 2004 when I was 20. I originally started this page document my progress using Oxygen Therapy but now the new PIP has started to replace DLA and I, like so many others, have been told i am no longer eligible to receive a Motability Car and so I am fighting against the DWP to explain exactly why they are wrong.

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