Tag Archives: local government

More recognition for the role of carers

Janet Down only realised she was a full-time carer for her disabled husband when she fell ill a few years ago and could not look after him. Suffering back pain from lifting and depression from coping unsupported, her inability to care for 65-year-old Dave exposed just how much she did for him. This prompted her to recognise her role, accept she needed help and find leaflets about caring at her library.

Carer aware, an innovative project that Down subsequently participated in and designed by Dudley borough council, is making it easier for carers like Down to get support. The online mini-training toolkit offers an explanation of carers’ rights, better access to support and reassurance that professionals are recognising carers’ issues. Down now champions the scheme as chair of Dudley Carers Forum. “Knowing how and what the carer is entitled to receive is empowering,” she says. Read the full piece here on the Guardian Social Care Network.

Decent homes for the homeless

“Homelessness doesn’t have a face,” says Janet Marsh, “it can happen to anyone, anywhere.” Marsh, 65, from east London, lost her privately rented home in her 50s after her marriage ended, then became ill with epilepsy and arthritis. “People think homelessness is something you’ve done to yourself, there’s stigma and misconception,” she says.

Though Marsh is now living in temporary accommodation in Newham, her housing situation could not contrast more with the popular image of a tenure defined by shoddy, unregulated properties and unscrupulous private landlords. Marsh is a tenant of Local Space, an innovative housing association that uses private finance to buy homes on the open market, refurbishes the properties and leases them back to the council as temporary accommodation. Read the rest of my piece on the Guardian’s housing network.

“I remember when she could make herself a cup of tea”

When I asked my kids to tell me how they felt about visiting their grandma, who has dementia, in her care home, they were honest. “It can be a bit spooky because there are a lot of people there who can’t remember things,” said my eight-year-old. “It’s sad sometimes when we see her, especially when she says she thinks you’re her sister. I don’t really like hearing that. I remember when she was in her own house and she could make herself a cup of tea.”

Hard as it was to hear those words, I can’t say I find my daughter’s reaction surprising. I often find a visit to my mum “spooky” too. Although her care home is very good, it’s not somewhere I’d ever wanted her to be. It’s tough seeing her now, so different from the active person she once was, and the behaviour of people with dementia can be disconcerting and at times downright distressing. I initially found the resident who repeatedly cries out: “I feel terrible” very upsetting – and I’m supposed to be the adult.

The children and I have talked about how my mother used to be, why she gets confused now and why it’s so important that we spend the time that we do with her. My five-year-old summed it up well: “If we didn’t go, she’d be upset and she’s your mum.” But although we have often talked about dementia, and how it makes them feel, I’ve sometimes felt I was struggling to explain what was going on.

That’s why I was so impressed to find The Milk’s In The Oven, a booklet published by the Mental Health Foundation, to help children understand a bit more about dementia. Simply written, with practical exercises to encourage children to think about what it might be like to lose their memory, it’s an effective tool both for the classroom and for families affected by dementia.

Toby Williamson, head of development and later life at the Mental Health Foundation, explains that the booklet, originally published more than a decade ago but updated this autumn, is designed to help address some of the stigma surrounding dementia. “What we are trying to do is help young people understand what dementia is and how it affects the person,” he says. “It addresses the fears children might experience and the feelings they might have of being embarrassed or angry. What it is saying is actually you might well have those feelings, it’s understandable and you can talk about it. We want to reduce the fear of going to visit people with dementia. Social relationships are incredibly important for people with dementia – even in the final stages, a bit of contact, just holding hands, can mean so much.”

As Williamson points out, most families in the UK will, at some stage, have a relative or friend with dementia. It’s important, he stresses, that people know more about the disease, both so that they can support the person affected and so that they can encourage relatives to get an early diagnosis, often so valuable in terms of treatment and preparing for what’s ahead. And even for those children who don’t know anyone with dementia, there’s huge value in learning more about it.

Schools are increasingly teaming up with health professionals to build the links which can foster greater understanding. One impressive project is in Doncaster, where pupils from three schools now visit day centres across the town, taking part in activities like baking, sewing, singing and playing dominoes with people with dementia.

Mary Beardsley, the team manager for the local NHS trust’s Doncaster Community Memory Therapy Service says, the youngsters involved, who are aged between nine and 11, usually don’t have any personal experience of dementia. But thanks to the project they have built strong relationships with the service users, gaining a real respect for them as individuals. For the older people too, it’s been an overwhelmingly positive experience.

“Our patients gain so much confidence – it puts them in a position of power being able to teach the children something,” says Beardsley. “When you get dementia, you lose your confidence and you don’t think you are good enough. Seeing the interaction between children and patients is fantastic. The children grow to love them and the patients can’t wait for them to come.”

That recipe for a better understanding of dementia through building new relationships is one I can see developing in my own children. As they talk with some of the residents at my mum’s home, I hope they are seeing that older people with dementia need our support and respect. It’s a lesson that, as the numbers with dementia rise, more of the younger generation will need to learn.

Public health: councils have the will, if not the way

“Smokers Wanted”, announced the sign above an information stall at a sixth-form college in Swindon. The quirky take on the usual stop-smoking message drew students’ attention to the public health campaign by multi-agency group the Swindon Tobacco Control Partnership. Read the rest of my piece on the Guardian Local Government Network today.

The vital role of creative thinking in care

Supporting people to make the most of their community, pic: CareTech

Seven years ago, no one could have imagined Martin* living anywhere but in residential care. The then 24-year-old, who is autistic and has a moderate learning disability, was exploited by ‘friends’ who dealt drugs from his housing association flat in London, leading him to lose his tenancy. Head to the Guardian Social Care Network for the rest of my piece on the importance of transition services when supporting the vulnerable to move from residential care towards more independent living.

I was in care, now I’m working to improve the system for looked-after children

Guest post by teenager Matt Langsford

Matt Langsford, improving care for looked-after children
I’m Matt Langsford, I’m 19, I was in care for nine years, I lived in over 15 different care placements and I was homeless twice.

I was in care due to my mother’s mental health problems – she is agoraphobic, has bipolar disorder and suffers from alcoholism. I’m back in contact with my twin sister but no one else in my family.

My care experience was poor. I was told by my care workers that I’ve had “bad luck” with carers as two of them were de-registered and a couple resigned with immediate effect. When I was homeless I slept under a bridge, in a shed and in a garage.

My experience at first made me not trust any authority figures and made me lose my confidence, but I’m putting that to good use to help improve services for looked-after children and young people. I work with the LILAC (Leading Improvements for Looked-After Children) project. I understand better what happened with my care, and I want to improve the care system.

LILAC is project funded by the Big Lottery Fund and hosted by the charity A National Voice (ANV) which ensures looked-after children and young people are involved in decisions about their care and in the practices of the services that look after them. I assess how well services involve their looked after young people, deliver participation and LILAC standards of care. I think the standards are important as they are key areas of involvement for young people and children. They help gauge how an organisation involves and includes their young people. I am one of 60 young care experienced people recruited as LILAC assessors and so far we have assessed 18 different care settings from fostering agencies to local authority care homes.

I heard about LILAC in January this year from a role I had with ANV as the West Midlands regional development coordinator. I did some research and applied for the post after thinking what a great opportunity to build on many of my skills and get employment and to meet some like-minded young people. I was then interviewed and selected to become an assessor. Getting to the training course was a race against time for me; I travelled throughout the night on a 12 hour journey to get to the course (half a day late!). The training course took place in Manchester and I was living in Aberdeen at the time.

I think that the hardest part of the course was the role-plays because I’m rubbish at acting. The most rewarding part was gaining my qualification, meeting new young people and meeting the great staff at the project.

I think what we do at LILAC is important because we are going in helping organizations and local authorities improve the services they provide to their looked after children and young people. An example of how important LILAC assessment is that Wigan were assessed at the start of the project and only achieved some of the standards, after the LILAC team fed back their recommendations, Wigan started to implement them. A year on Wigan invited LILAC back to re assess them and they have achieved all of the standards.

My first assessment was in Birmingham – a private fostering agency – I had a briefing meeting before the assessment and it all went great.

LILAC has helped me on personal level as the team has gone out of its way to support me, with advice on attending college and also they have helped me develop my skills. I wouldn’t be where I am today without the hard work and dedication from the LILAC team. It has made me more confident and helped me to trust people again; I can talk to the team whenever I need a chat to keep me sane.

My plans for the future are to finish my level two and three health and social care BTEC and go onto university next September to get my social care degree. I am continuing my voluntary work with the local Children in Care Council which is something I have done for the past three years now, I’ve been the chairperson and co-chair here and I do things from outreach work to managing our team and budget.

For me the general public see looked-after children as trouble-makers or problem children, this is wrong as most of us in care are in care as our parents can’t look after us. The media unfortunately plays a mostly negative role in portraying us, as they only show bad things and don’t promote any good stories of looked-after children and young people; I am trying to change this.

Is Paddington the “big society” in action?

Big society in action is how civil society minister Nick Hurd described the award-winning Paddington Development Trust (PDT) which he chose for his first ministerial visit in May 2010. “Residents have real sense of ownership and power,” he enthused on Twitter about the west London regeneration organisation that supports residents to volunteer a total of 5,000 hours through 350 different volunteering opportunities.

But shortly after Hurd’s praise, the organisation was among the first victims of public spending cuts when £350,000 was axed as the government scrapped its neighbourhood programmes. The trust’s chief executive, Neil Johnston, has spent the last year figuring out how to continue its groundbreaking work. Read the rest of my piece for the Guardian’s Society pages here.

How the housing safety net is shrinking further

As councils tighten eligibility criteria for housing at the same time as benefit cuts hit, charities warn of an increase in homelessness. With the trend growing for councils to overhaul their allocation policies, there are fresh concerns about people being forced into the unaffordable private rented sector or pushed out into cheaper suburbs. Read my Guardian piece here.

No voice for the vulnerable

Can you imagine being so desperate for affordable legal advice that you go on an eight-hour, 300-mile bus trip just to get help? I came across such a case seven years ago; a Welsh man facing eviction from his council-owned cottage when the area was being redeveloped found that the only housing legal aid lawyer willing to take on his case was in West London. So desperate was the man to stay in the cottage he had been born in and so great was his fear of homelessness, he made the trip.

Although this tale is from 2004, it highlights the vital safety net legal aid (when the state pays all or part of the legal costs for those who cannot afford them) provides to society’s most vulnerable. The number of solicitors who carry out legal aid work have been falling in recent years (hence the Welsh man’s 300-mile journey) thanks to uncompetitive pay rates, hours of unpaid work and red tape. But now, under government plans to cut the legal aid budget by £350m, the situation could get worse for those wanting to access affordable legal help. It is estimated that around 500,000 people could lose out on legal advice amid the planned cuts as the government wants to remove clinical negligence, family law, education, non-asylum immigration and housing cases from legal aid’s scope.

Today is Justice for All day, with marches and petitions planned by a coalition of 3,000 charities campaigning against the cuts and you can also oppose the cuts at social action campaign site 38 Degrees.

The Law Society, which represents solicitors in England and Wales, has also launched Sound Off For Justice, a campaign for alternative reforms that it says will save more than the government’s own proposals and protect legal aid funding. The campaign encourages the public to demand the government reconsider its plans and look at the alternative measures which it says would save £384m in the next 12 months. You can record a voicemail for Justice Secretary Ken Clarke against the cuts here. The campaign is supported by, amongst others, housing charity Shelter, the Refugee Council, lone parent charity Gingerbread and housing association Eaves.

Here’s the campaign’s latest video:

There’s something rotten going on when an endless glut of super-injunctions protect the privacy, reputations and careers of the super-rich but a lone parent, for example, is denied basic access to his children because he simply can’t get the afford the advice.

“The kid who talked of burning down the place is now volunteering to paint it…”

Hutton Hall Community Centre - Community Asset Transfer
Hutton Hall community centre, photos by Podnosh

A year ago it would have been pointless painting a mural on the wall of Hutton Hall; it would have been covered in grafitti within a day. But after the building was transferred to community group Comm:pact by Birmingham city council in April, youngsters treat it – and its new exterior artwork – with pride. Read about how to make community asset transfer work in my Guardian piece today.