Submitted on Sunday 29th January 2017
Published on Thursday 2nd February 2017
Current status: Closed
Closed: Tuesday 2nd May 2017
Signatures: 81
Make PIP more accessible to people with rare illnesses
I have suffered from Guillain Barre Syndrome for five years. I have pins and needles in my feet which make it very painful to walk, and muscle weakness and pains in my arms. I am currently waiting a decision from the Upper Tribunal. There are many other people out there in the same position.
There are approximately 1 in every 200,000 get GBS and 20% of these have some form of residual issues. I returned to work because I wanted to try and get back to normal. This hasn't happened and I had to became part-time. I only work two days at a time because I get too tired. I have to get taxi's when I go anywhere because I am unable to use public transport unless someone is with me. Nerve damage means I will not recover. Disabled people need your help.
You can't sign this petition because it is now closed. But you can still comment on it here at Repetition.me!
18.116.90.161 Thu, 21 Nov 2024 21:21:23 +0000