HI I recently went for my PIP assessment in August and now my PIP has stopped. I initially received DLA since 2011 for severe depression and anxiety. Since 2011 I have also developed Fibromygalia, a rare auto immune disease called Lichen Planus and have 2 discs and possible stensosis in my spine for which I'm due yet another MRI on the 20th this month. According to PIP I can manage my conditions despite being on several types of medication and occasionally using a walking stick...im 39. I had to give up work voluntarily 2 years ago as my body caved in. I suffer major panic attacks and get physically sick with anxiety. PIP also claimed I can manage finances which in I told them I didn't as my husband has deals with everything to do with house and car. PIP assessor also said I could sit and stand no bother and that i could touch below my knees which was a load of rubbish. I can't bend at all.
To make matters worse today I get a letter saying my ESA has now been reduced by£55 a week due to a change in income but yet no explanation. This has resulted in me vomiting twice since getting the letter. I do want to work but as I am social worker it entails long hours and stressful caseeloads and my conditions really flare up with it plus I can never tell when my back is going to go into spasm and I am unable to move for 2 to 3 days at a time. I explained all this and yet it seems to have fallen on deaf ears. I am extremely low at the minute and have been given yet more medication to manage my symptoms. I am now on 11 tablets a day. Would any of you say that is managing a condition. Never mind side affects.
I had to send a letter to PIP myself initially appealing as I ignored it for 3 weeks before opening it as I couldn't cope. I am in with a benefits advisor next week. Has anyone any advice on what I should do before then or get in place for him when I meet him