More work than if I could get to work!

I’ll start by putting it bluntly, I hate benefits!

The work you need to put in to apply, send proof, fill in questionnaires, call to check everything’s been received cos you haven’t been told it has, send more info, correct what they’ve mucked up and do all this with no money is insane as you do your best to budget the little money you have! And people prefer this over working for your money??!

I can honestly say I would never choose this! It’s out of my hands for now though, I have no choice! It’s just another way of making me feel lost. It just gets you down and even trying to manage your mood gets tiring. Spending my life walking round in circles at the moment, September just can’t come quick enough.

So to those who screw the system, you cannot seriously tell me this is easier than working for a living. Hopefully next months appeal will sort me out again. Allow me to take control of my money, my life and my freedom!

In case this post has gotten you down, just remember, when it comes to MS, it’s all in your head! 😀 (Hope you get this otherwise some people are gonna be mad!)


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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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