I have lupus nephritis and claim DLA , in December I had to renew my claim. I got a letter to say if I don't hear anything after 8 weeks to contact the DWP/DLA office to find out what was happening (letter dated 20-12-10).
I telephoned the office and asked what was happening on 3-3-11 only to be told they had decided to ask my GP for a medical report.
I'm not worried by this but I did question why they waited until 16-2-11 to ask for the report seeing as they have had nearly 2 months to get any information they needed.
I wasn't given a reason at first but after a few more phone calls I was asking again why wait so long when the woman on the the phone said it was because; while looking at my claim they realised I was claiming carers allowance for ds ( ADHD/ASD ).
She went on to say that because I am a single parent they found it hard to believe that I cared for my son and claimed CA for him if I was claiming DLA for my self as I wouldn't be capable of looking after him if I had a disability or serious illness! ( if I was in a relationship and myself and my partner claimed DLA with middle/high rate care we could claim CA for each other with no questions asked.)
I was told to claim CA by the DWP even though I told them my 2dd's were in fact looking after my needs and ds needs.
AIBU to think it was out of order to say that.
I was upset after the phone call and even started to question if I should be a mum. 