PIP, DLA and AA
If this is your first visit, check out the community guide. You will have to Join us or Sign in before you can post.

pip mobility MND and pension

WILLMASONWILLMASON Member Posts: 1 Listener
edited November 2018 in PIP, DLA and AA
my wife has suffered mobility problems since breaking her ankle 4 years ago.in april she applied for pip and was awarded standed rate pip on living allowance and mobility allowance she was aged 64.  in july she was eventually diagnosed with MND and fast tracked onto higher rate living allowance but because she had turned 65 years old in may,the law says your not allowed to get the higher rate.this does not seem right is there anyone in a similar position ?

Replies

  • Pippa_AlumniPippa_Alumni Scope alumni Posts: 5,851 Disability Gamechanger
    Hi @WILLMASON, and a warm welcome to the community.

    Thanks for sharing this with us. I'm not sure of the answer to this myself, but hopefully some of our knowledgeable community members will be able to advise. @poppy123456, can you help? 
  • Anderson66Anderson66 Member Posts: 3 Listener
    PIP is a nightmare to get hold of
  • Anderson66Anderson66 Member Posts: 3 Listener
    I been waiting 44wks to hear if my tribunal has been won
  • MatildaMatilda Member Posts: 2,616 Disability Gamechanger
    @WILLMASON

    Once someone passes 65 the rate of mobility they are on cannot be increased - unless they are appealing a lower award when a tribunal might increase the mobility rate.

    There's an explanation on the gov.uk website.
  • poppy123456poppy123456 Member Posts: 22,218 Disability Gamechanger
    Hi,

    What do you mean fast tracked onto Enhanced daily living? A diagnosis wouldn't fast track you a higher award, unless the it's a terminal cancer diagnosis (less than 6 months) and a DS1500 form is used.

    Did you request a Mandatory Reconsideration and the decision was changed? Or was a change of circumstances reported?


    Proud winner of the 2019 empowering others award. This award was given for supporting disabled people and their families for the benefit advice I have given to members here on the community.
  • Milly123Milly123 Member Posts: 34 Connected
    Hi Willmason,
    First of all may I say how sorry I am that your wife has been diagnosed with mnd. I know first hand just how devastating this must be for both of you. I lost my husband to mnd in 2005, he was just 53yrs old. He passed away just three years after he was diagnosed. For the three years that we had left together, I was his sole carer. In the last year of his life, he could no longer do anything for himself at all. It was very hard for me to cope but I would not, nor could not, put him into a hospice. I wanted to spend as much time as I could with him as there was no knowing how long we had left together. I married him in sickness and in health and I meant every word, I loved the very bones of him and it half killed me inside to see him like this. He was so active before mnd. He got to the point where he didn't want to be here anymore. As you know, the mind is still alert, its just their body that lets them down. He wasnt scared for himself, he was only scared of leaving me on my own. He was taken into hospital on Christmas eve as he couldn't breath properly, he had a chest infection that turned into pneumonia and he was put on a breathing machine until he passed away in early January. He wouldn't let go until I told him it was ok to let go and that I would be fine. A couple of hours after, I was holding him in my arms when he took his last breath. Im only sorry that I was unable to let him have his last wish....to die at home. I know I did my best for him. I tried all along to give him hope by saying there could be a cure just around the corner. I tried not to break down in front of him. We had a long garden with a railway line at the back. Sometimes when I felt I couldn't cope or I was just hurting so much from all the lifting I had to do, I just went down the bottom of the garden and when a train went by, I just used to scream my head off. It seemed to help a bit that I was able to let out all my frustration, anger and hurt. I still miss him dreadfully, he was a lovely man, my best friend and sole mate. He was also the bravest person I've ever known for putting up with this awful illness the way he did. It must have been so frustrating and humiliating for him to go through. He did it all with dignity. I'm so proud of the way he coped with it all.
    I hope your wife doesn't suffer too much. My heart goes out to you both. Stay strong for each other and try to enjoy the time you've got left with each other.
    I hope they do carry on paying you pip, you both deserve to get it. You have enough going through all this without all this stupid pip/dwp rubbish. You could do without that added stress. Take care both.
Sign in or join us to comment.