Kari Gerstheimer, Head of Legal Support Services
It has not been an easy year for disabled people. Local authorities are squeezing social care support to the bare bone, living costs are spiraling and many disabled people are worried about the changes in welfare benefit from Disability Living Allowance (DLA) to Personal Independence Payment (PIP).
The ‘bedroom tax’, a term routinely used to describe the governments ‘under occupancy charge’ or ‘spare room subsidy’, is a nationwide change in the way housing benefit entitlement is calculated. If tenants are assessed as having a ‘spare room’ they will see a reduction in their overall housing benefit of 14 per cent, or 25 per cent if the tenant has two ‘spare rooms’.
Continue reading “The impact of 'bedroom tax' on deafblind people”
One thing I am particularly pleased to see in the Care Bill is that local authorities will have to promote wellbeing in relation to a number of factors, including suitability of living accommodation. Having lived for several years in a flat that was inaccessible, I know what a difference suitable housing can make to wellbeing.
My old flat was almost perfect for me when I first moved there but, within a couple of years of moving in, I became a wheelchair user, making the flat totally unsuitable.
It was on the first floor. To get in or out, I had to drag myself up and down outdoor stairs on my bottom, in full view of several neighbours. Bye bye dignity.
Continue reading “The excitement of taking rubbish out to the bin….”
Pyrrhus, Sense Activist
Having ranted over the award of Employment Support Allowance (ESA) only being awarded for six months to ‘M’ on the Sense oldblog, for whom I am a benefits appointee, let me tell you the following tales of welfare reform concerning council tax benefit and housing benefit.
M’s local authority, which had previously not charged council tax, decided that with few exceptions, most people would pay a proportion. There was an “exemption from” category which M would be eligible for, but required a claim to be made…
Continue reading “Victory, at what cost?”
I am Steve, am 49 and have been totally blind and 80% deaf since 1980.
For the last ten years I’ve been a wheelchair user, having Alstrom syndrome which affects my heart, kidneys, liver and lungs. I also have problems with my back and neck as well as a form of osteoarthritis and nerve pain.
I need a lot of support with communication, having a social life and getting out of my flat.
Continue reading “Why should I have to use my DLA to pay for my care and support?”
I am the appointee for a young Deaf man, who I will refer to as ‘M’, who has autism and additional needs. In January I received his form to complete to claim Employment and Support Allowance (ESA).
Days and hours were spent filling it in, reading advice etc and obtaining supporting evidence to ensure a full picture was given of his needs and why he previously received Incapacity Benefit. Finally the day came when it was complete and I sent it by special delivery .
Continue reading “A punishment for claiming benefits?”
When I started at Sense less than a year ago I had very little idea how difficult families find it to get proper educational support for their disabled children. I quickly learned that it is a constant struggle for parents and carers, and for the deafblind children and young people who need this support to get on.
While many stories have been heartbreaking to hear, it’s also been incredibly inspiring to meet families who have fought so hard and won so much for their children.
Continue reading “Proper educational support for deafblind children”
Bureaucracy is the punishment for having the gumption to ask for support. Whether we need support from Access to Work, social security benefits, housing or social care, we must lay ourselves bare, on forests-worth of forms and in face-to-face assessments, revealing to a stranger everything about ourselves in the most intimate detail: our deepest, darkest secrets; our medical history; our finances; our relationships; and so on and so forth. We must justify, many times over, why we need the support we are asking for. It is a physically and mentally painful, exhausting, and demeaning process.
Why do we do it? Are disabled people all masochists, hell-bent on inflicting ever greater humiliation and distress upon ourselves? No. We do it, only, when going without the support is even more dehumanising.
Continue reading “Social Care: a cost or a saving?”
Last year, when the Dilnot commission made its recommendations on the funding of care and support, I cautiously welcomed some of those recommendations but expressed concern about what Government would actually do with them. Now that we know more about what the Government intends to do, I’m even more concerned.
The Government will set a cap of £75,000 on the amount any individual will have to pay towards their care and support costs. This cap will be lower for people under retirement age but the announcement on 11 February failed to specify how much lower, except to say it would be £0 for anyone with care and support needs before the age of 18.
Continue reading “Much more is needed to address the crisis in social care”
A report, Home Cure, published earlier this year by the think tank Demos, amongst other things, called for a more holistic and long-term approach to reablement services so that people are supported, not just to manage in their own homes, but also to engage with the community.
Engaging with the community – shopping, meeting with friends, using leisure facilities, taking part in activities, using public transport, simply getting out for a breath of fresh air – is one of the biggest challenges deafblind people face. Services that address that challenge are a must if deafblind people’s quality of life is to improve.
Continue reading “Mobility is more than waving a cane”