The excitement of taking rubbish out to the bin….

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.

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Victory, at what cost?

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…

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Why should I have to use my DLA to pay for my care and support?

Steve

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.

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Radio for deaf people?

by Liz Ball

Liz BallRadio’s inaccessibility to deaf people is perhaps one of those facts of life most of us simply accept. But could that be about to change?

I had good hearing until my mid twenties. I used to enjoy listening to the radio, especially dramas, documentaries and current affairs programmes. Since becoming deaf, radio has been inaccessible to me and, although it has never been a big issue for me, I have sometimes missed it.

So I was very interested to read about a project in the United States to make radio accessible for deaf and deafblind people through live text captions. And I was pleased to have the opportunity to put some questions about it to one of the project team on BBC Radio 4’s In Touch programme.

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A punishment for claiming benefits?

Pyrrhus

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 .

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Proper educational support for deafblind children

Molly Kearney

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.

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Social Care: a cost or a saving?

Katie Vecina

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.

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Much more is needed to address the crisis in social care

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.

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Mobility is more than waving a cane

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.

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