MANDATORY RECONSIDERATION

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So i have asked for my MR today. After thinking about it for a few weeks and also going through the report with a fine tooth comb i thought that there were so many things that were incorrect i felt i had no choice. The case manager who i spoke to gave me the usual lecture that the whole award will be looked at again and they will let me know as soon as they can. I also told her i have sent in all my medical evidence and that on my letter from my doctor it stated that due to my condition and my meds this causes me to have low moods. On my report she stated i am not on any meds for my low mood. I spoke to my doctor today who informed me that this is not the case. One of my meds is amitriptyline which is a trycilic drug. This acts as a pain killer and a anti depressant and because this is the case instead of having more meds on top of the 30 a day i have to take that these would have a dual use. Also the assesor had said that i seemed lucid and coherant with no signs of confusion. This also was untrue as i did get confused on neumorous occasions. So much so she suggested that she wrote a note for my carer as to the documents which had to be posted. Off her own back may i add so this in itself should add more points. Also she has stated that i do not need help to take meds ect. I told her that on the rare occassions when my carer is not here i need my tabs in a box marked with days of the week. This is because i have previously taken to many tablets as i have not remembered i have taken them due to being out of it on meds. So that should have been points as well. Also i told her although my bills get paid by DD this was set up because i got myself in to debt because of my poor memory if i forget to pay them and i need ongoing help with budgeting. Yet again 0 points. She scored me 9 points in total where the citizens advice did a self assesment and scored 69 HELL OF A DIFFERENCE ! So i will keep you all updated

0 likes, 8 replies

8 Replies

  • Posted

    Hi Michelle

    I received my MR results last week and they again used the info given by the assessor. Which was all wrong. They said they bad used info from my consultant and GP. But they obviously haven't. I have MS which has now spread to my spinal cord as will as the the left side of my brain. Which effects the cerebellar and ataxia.

    I have sent in the appeal with all medical documents and letters from my nurse specialist. So it seems mist MR decisions come back unchanged. So hopefully you'll have better luck.

    Can anyone tell me how the mailing system works. I see t it to the courts in Bradford to be signed for on arrival. But it is a P.O. Box number. Will it still be signed for.

    Thanks Stevie

    • Posted

      Sorry about spelling I'm not to good today.

    • Posted

      Hi stevie im not sure ho the mailing system works. Good luck with your appeal keep us posted
    • Posted

      Most MR decisions remain the same but 65% of Tribunals are successful but only if you appear in court. Paper based decisions at Tribunals are much less successful. I have no idea about the mail going to any courts i'm afraid. If you sent it to be signed for then it'll have to be signed by someone. Good luck.

    • Posted

      Thank you Denise.

      I will be attending as mum and dad will support me by driving me there. My mum is my representative.

      I'll keep you all Informed

      Stevie.

  • Posted

    So guys after much thought i have decided to withdraw my request for a MR. As i have been awarded standard care and hugh mobility for 5 yrs i think even though it is a difference of over £100 a month short of what i was getting on dla i neither have the strength and cannot be bothered with the stress of having to wait to see what will happen. Also reading some horror stories i am extremley lucky as most people even more disabled than myself seem to be getting their claims rejected. So i am not going to rock the boat even though i disagree with the desicion

    • Posted

      I'm sorry to hear you've decided to do that Michelle. Sometimes though it's better to just let it go. I thought exactly the same thing when i first applied for PIP. Didn't want or need the extra stress so just let it go. Decided that something was better than nothing. xx

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