Hi, my names Hannah and I’m 20. I was diagnosed with an autoimmune disease September 2021 after months of being unwell. I’ve had the symptoms since I was about 4 but nobody ever knew what it was.
I have a lot of symptoms including many from arthritis and lupus. I use crutches to walk as well as insoles in my shoes to align my legs. I also have anxiety and depression as well as asthma and I’m waiting for an autism assessment date.
I applied for pip at the start of July and had my assessment (phone) in the middle of September. It lasted over an hour. She seemed nice. We spoke a lot about the daily living parts which I can’t really do much of (thankfully my mum is amazing) but she never really said anything about mobility. Mobility is really hard for me currently and I’m in extreme pain after even 4 steps. Is it normal to not be asked about one area? Should I worry?
I’m going to try and get a copy of the assessment sent tomorrow but they didn’t have it the last time I called and I’ve been in hospital since then. I now have had the text. For some reason capita took 2 weeks to send the write up through.
I’ll appreciate any advice, words of encouragement, anything honestly. I’m kind of terrified, especially after being off work again and getting sick pay.