So, I’ve slowly been withering away to a skeleton while on hold for days/weeks/months to the DLA helpline (now, that’s a euphemism if ever there was one). It struck me that the experts here would probably know more. My six-million-dollar question is: does anyone get high rate mobility for their teens? My DD1(15) is registered blind and is diagnosed with autism and ADHD, among other developmental disabilities. I only started claiming DLA for her when she was 11.5, six months after she had lost her sight, suddenly and unexpectedly.
After a mandatory reconsideration, or whatever they’re called, DD was awarded higher rate care and low rate mobility. That was fine then when she was 11/12 and I took her everywhere, but now she is 15 and it has struck me that she has never been on a public bus or train solo. She travels to her mainstream school on a private coach and has a designated disability seat. She has to walk about 300m on a safe route from our home to the bus stop every morning and I met her from the bus for the whole of Y7 (further to walk and busy main road).
I would love to know if anyone else’s teen gets a higher rate of mobility allowance (DD will never be able to drive) and how you went about it.