I have my Personal Independence Payment appointment next week Thursday. I received a booklet of what to expect during the appointment.
I want to apply for Employment and Support Allowance (ESA) as I feel I may not receive Personal Independence Payment. Lupus is a very unpredictable disease sometimes, I feel good and sometimes I feel extremely weak and tired. The fatigue and overall pain are the worst.
What are some of our experiences with Personal Independence Payment and Employment and Support Allowance? And how do DWP see Lupus disease?
Written by
SLE-Warrior
To view profiles and participate in discussions please or .
My PIP assessment was good. Both of the interviewers were medical in background. One a physio and one a nurse. The questions allowed a story to be to,d rather than direct answers so I could explain the range of answers to a question. They understood Lupus and is variants. I felt very understood and a recognition that there was no single answer. I await my result but did not feel that there was a lack of understanding there.
Thank you for your relpy. I am hoping the interviewers are fully aware of what Lupus is and how unpreditable it is. I am trying to fully prepared as possible. No one will be able to come to my appointment with me. My mum is not talking to me and my older sister will be going to work. My back has been hurting for the last couple of days. I asked my sister for a back massage she said no.
Did you end up getting PIP claim? If not why did they not give it to you?
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.