pip mandatory reconsideration
Posted , 8 users are following.
I know the success rate of pip mandatory reconsideration is only 20% get their decision changed at this stage as this is what the government have told to do , but it still means one in five will get there decision overturned has anyone on here had a successful pip mandatory reconsideration?
0 likes, 9 replies
Bobbybo1 paul_34196
Posted
Hi Paul
Even with all the evidence my MS would only get worse. It effects my memory balance plus many other things. The MR came back the same. I took it to tribunal and was awarded high rare care and mobility. All back dated. Awarded for 10 years.
if you've put in an MR good luck but be prepared to take it to tribunal.
denise15811 paul_34196
Posted
There's only 1 person that i know of on here. It's extremely rare to have it changed at MR stage. You maybe 1 of those rare ones but as Bobby says, be prepared to take it to Tribunal.
paul_34196 denise15811
Posted
You see this is what I don't understand if they say the success rate of an overturned decision is 20% that's one in five I would not say that extremely rare . I'm guessing those figures are actually wrong and maybe it's only 1 %
mary86724 paul_34196
Posted
Bobbybo1 mary86724
Posted
So pleased this happened for you. But when I was diagnosed with MS Ali g with the disabilities I already had. The assessor lied. And I was put in standard rate care + lost my mobility.
But due to having a loving mum. We took it to tribunal and and I said to Paul. Was awarded high rate care + mobility. Stressful yes. But worth doing. XxX
lors23 paul_34196
Posted
I think l am the 1 person that had my desition changed at MR. And the only reason they did it was because l got a letter from my MP to send to them and to complain to the lady that done my f2f. Otherwise l would have been at a tribuneral. The full thing is a joke.
Good luck
Laura
Bobbybo1 lors23
Posted
lors23 Bobbybo1
Posted
Good Luck Bobbybo1
Bobbybo1 lors23
Posted
Hi Lors23.
I actually won my appeal at tribunal. I was awarded high rare care + mobility. Indefinitely. Which means 10 years.
But if it wasn't for my mum fighting for me. Neither myself or partner would have known what to do. XxX