This Government and many previous Governments by their actions and even inactions, show that they do not care about disabled people, no matter what they say, as actions speak louder than words.
There are many problems which disabled people have to encounter and many are not covered by current legislation being the Equality Act 2010, https://www.facebook.com/southyorkshirepolice/photos/a.468321323096/10157791280883097/?__cft__%5B0%5D=AZUvaZGGRgKIYwsGr3ciNtRap9atuI4gfcbANohWzkgLCVYdeMbWNGtlCwTOzLhG5BPmNaVUlOVyeKqUfhjgzqDsMwQmwYxDBcVACqhJqYcrn9U-2yMIY2OQBH-r3EGA1udmoF1dh-P1Op_tb2jpGRDEBdt8Z71knJziqUooZmd70A&__tn__=EH-y-R.
It was not sufficient in 2010, but it was hoped it was a start, but now is even way more not sufficient.
Welfare benefits go some way to cover the costs to be equal and should not be judged as extra cash which is not used, as disability does increase the costs in endeavouring to live a reasonable life and certainly not a luxury life, which some people and organisation believe.
As when accessing social care persons are expected to contribute, but although there are Financial assessments these assessments don’t take into every account of costs involved in living a life. It is always you need to contribute, without any real investigation whether you can really afford to do so, as the system is there without any concpet of individual circumstances. There is much talk of ‘person-centred care, but in practice it is not really the centre, which it should be as the system is invariably the centre and systems don’t take individuals into account, just being a number in the system.
But, in effect this Government does not wish to recognise disablity let alone persons with disabilities. In fact, I tend to belo=ieve that this Government goes out of its way to ignore persons with disabilities to the extent that they would rather they not be there and then money will not need to be spent on them.
Sitting in her specially adapted bedroom, 15-year-old Ruby Walsh breathes slowly through a nebuliser, which covers her nose and mouth.
The teenager, who is deaf and blind, has cerebral palsy, and this is just one of the pieces of medical equipment needed to keep her alive.
But her need for a nebuliser, along with a ventilator and an oxygen concentrator, is pushing up her family’s energy bills at a time when money is already tight.
The cost of living squeeze means the family, who live in Basildon, Essex, have already seen their energy bills rise from £175 to £225 a month. They are reimbursed for the oxygen concentrator, but everything else comes out of the household budget.
Energy bills are set to rise even further after the energy cap rises on 1 April.
‘We just want a simple life’
Ruby is terminally ill and her mum, Charlotte Huzzey, wants…
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