PIP assessment nightmare.: I have been diagnosed... - LUPUS UK

LUPUS UK

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PIP assessment nightmare.

SprockerMe profile image
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I have been diagnosed with Systemic Lupus, Auto Immune Hepatitis and Osteoporosis since July 2000. I was given indefinite full motability and low care package. This summer I had two TIA’s that involved double vision only for about a minute with no other symptoms. The stroke consultant diagnosed that it was a low probability being TIA and more like a reaction from the Lupus. I contacted DLA under the impression that my medical condition had deteriorated, and they arranged for a PIP assessment. Big mistake!!!! In their opinion, I am now so well, I can care for myself and walk everywhere and use public transport, even though my hospital appointments can involve a 114 mile round trip to arrive at 9am. The whole situation has been a nightmare, which is not helping, as you can imagine. I am appealing, and I can keep you all up to date with my progress if you wish. I am asking Lupus UK to help me, and possible represent me at the appeal meeting. I am so scared. I live on my own, in the country, miles away from nearest bus transport. My life, and my health would be destroyed. Any help or advice anyone can give me, I would be very grateful.

So sorry for the long post. Can anyone help me? Thank you.

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SprockerMe profile image
SprockerMe
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2 Replies

I cannot help love but it might comfort you to know they have done this to me too. Had a lifetime award. Car and money now gone

Appeals are taking a year in my area. X

Chanpreet_Walia profile image
Chanpreet_WaliaLUPUS UK

Hi SprockerMe, I have sent you a private message regarding this post :)

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