PIP, DLA and AA
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Hi, new and need help with PIP please?

jennyt3jennyt3 Member Posts: 3 Listener
edited February 2018 in PIP, DLA and AA
Hi all,

Long story short: 
I am 27 years old and have scoliosis, developmental dysplasia of the spine, ehlers danlos syndrome, and (supposedly) fibromyalgia. I cannot stand up straight for the first couple of hours of the day, I experience frequent subluxes of various joints, including my jaw, knees, toes, and fingers. I struggle to walk around a small shop without sitting down. Since 2016 my partner has not worked, as I am unable to do basic things for myself, and do not leave the house alone for fear of subluxing something and having a fall (which was the ultimate reason for him eventually giving up his job in 2016 as he was working 3 hours away when I had a fall outside out daughters nursery). 
I work as an Independent Research Consultant, and have slowly increased my hours since my OH gave up work to try to support us, until I am now working over 100 hours per week. This is all getting too much for me, so I was recently persuaded to apply for PIP. 
Went for PIP assessment, told her my main issues were not leaving the house without another person, needing help washing my hair (or anything with arms above head), needing supervision whilst eating (subluxing jaw every five seconds whilst chewing is an obvious choking hazard), to name a few.  
Two weeks later I have had my decision back - 0 points. 

The reasons given are that I am able to work (note it does not state 'from home', which is an important point since my job does not require me to go anywhere!) so therefore do not struggle with disability, and that I do not take pain medication, so therefore cannot be in pain (even though my conditions are chronic so I have voiced my reluctance to begin pain medication at the ripe old age of 27, and also pain medication would prevent me from feeling the warning signs that usually let me know I am about to sublux something, like those I have. Even experiencing in my hips recently which require me to lie on the floor to prevent them coming out of their sockets). 

Surely under the Disability Act and Equality Act they are required to support my ability to work? I have had no other choice!

The letter basically suggests that if I gave up work and started taking pain medication I would be eligible. 


Am I wrong in thinking I should appeal this?
I am at the point where I need to decide whether to start using a wheelchair so I don't have to miss out on my little girls' activities, days out, etc. And this has totally invalidated how much pain I put up with and how much I struggle everyday .

Replies

  • wilkowilko Member Posts: 2,325 Disability Gamechanger
    @jennyt3, hello and Welcome, I personally recommend you ask for a MR and appeal further if you need to. The scope site has a lot of resources, also the site benefits and work has members only help,pages and lots of information on appeals ect, you have to join £20 to gain acess the member only information but is well worth the exspence. Best wishes.
  • lillybellelillybelle Member Posts: 458 Pioneering
    Definately contest it, even to court if need be.
    Dont give in and good luck you deserve it
  • jennyt3jennyt3 Member Posts: 3 Listener
    Thank you to both of you. I think I will have a long hard think about how to fill in the Reconsideration request.
  • SimonHSimonH Member Posts: 7 Listener
    It is better to get CAB or similar organisation to do it for you 
    There is a general rule that its more about why you are unable to do something I.e  I cannot do X because of X
    and not about trying to explain your condition,  its easy to get it wrong

    I am not an expert this is based on my experience  and thru reading  a lot of info  provided by professionals

    I'm new here just fumbling my way thru there appears to be a huge amount of support.  Maybe best to ask an Advisor on this site
    After Mandatory Reconsideration  I got High rate Care  , The ATOS Report gave me 0 Points

    Best Wishes Kindest Regards
    Simon 
  • jennyt3jennyt3 Member Posts: 3 Listener
    Thank you Simon, and thank you for sharing your ultimately positive experience of MR, it is obviously worthwhile in the long run. 
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