rightsinreality

Thoughts on the crossroads of law, politics and society – for when a tweet isn't enough. This blog contains general information and commentary on legal matters. It is not intended to provide legal advice. This blog discusses the law in England, unless otherwise stated.

It’s not funny, to cut SEND money

I have shamelessly stolen the title for this blog post from Milo, a young man involved in the successful campaigning on SEN cuts in Hackney. Milo chose a donation from me to the fund to help save the Kids playground in Hackney as the price of this theft. Milo explained why as follows: ‘I am choosing the Kids adventure playground because I like it and it’s really cool to play in because disabled children can play there with their brothers and sisters.’ Please support the playground if you can.

So local authorities across England have now set their budgets for 2018-19 or will do so in the coming weeks. Some have taken every possible step to protect the services that matter to disabled children, young people and their families. Others, not so much. This blog post highlights some points of interest for all concerned with saving these vital services and challenging cuts.

First, I’m taking part in a webinar with Contact and Alex Rook from  Irwin Mitchell solicitors on ‘Using the law to challenge cuts’. The webinar is now fully subscribed but will be available to view through Contact online after the event – details tbc. If you can’t attend the webinar but have questions for us please either leave comments here or tweet me (@stevebroach). There is also very helpful advance reading in a guest blog from Alex’s colleague Mathieu Culverhouse dealing with the practicalities of using the law to challenge cuts.

Alex was the solicitor for the amazing families in #NascotLawnJR. In the unlikely event that there is anyone reading this blog who doesn’t already know, this case involved a number of families whose children have complex health needs who came together and fought the decision by their Clinical Commissioning Group (the local NHS) to pull funding for an overnight short break centre. The CCG’s funding decision has now been held unlawful and quashed by the court not once, but twice.

The outcome of Nascot Lawn is powerful evidence that judicial review can achieve real benefits for disabled children, young people and families – ensuring cuts cannot be made unless and until a lawful process has been adopted. It is important to emphasise that even ‘process’ challenges – for example concerning a failure to consult lawfully or to discharge the ‘public sector equality duty’ – can have real and lasting benefits. Where a cut is quashed because it was adopted following an unlawful process it routinely happens that the public body do not remake the decision but instead find the necessary savings another way. This is supported by excellent research from the Public Law Project which found that ‘Claimants for JR gained a wide range of tangible benefits: the most common of which were conferment or retention of a service by a public body…’.

However in relation to the coming round of cuts it may well be possible to go beyond the typical ‘process’ challenges in judicial review. In fact Nascot Lawn itself was more than a ‘process’ challenge – the CCG’s funding decision was held to be unlawful in substance as the CCG had failed to appreciate that Nascot Lawn was a ‘health service’ under the NHS Act. As this blog post explains, services for disabled children, young people and families are supported by a range of ‘specific’, ‘sufficiency; and ‘due regard’ duties. It may well be that some of the proposed cuts are unlawful in substance because they will result in the local authority (or CCG) breaching one or more of these duties. This will not then just be a question of the decision being quashed and the local authority or CCG being required to think again – if any of these kinds of challenges succeed then the cut would not be able to be made at , or at least not in the form held to be unlawful by the court.

Of course local challenges will only be able to do so much in the current context. Local authorities cannot magic up sufficient money to replace the central government funds they have lost. This is why campaigning efforts towards central government such as this petition by the Disabled Children’s Partnership are so important. It is only through work like this that we can move away from making sure that cuts are lawful to a focus on the kind of investment and expansion in services and support that families really need to see.

A final point – I wanted to emphasise that cuts are a human rights issue. The ‘socio-economic’ rights under the UN Conventions on children’s rights and disabled people’s rights all require ‘progressive realisation’ – as the Disability Convention states (Article 4(2)), the government has undertaken to ‘take measures to the maximum of its available resources…with a view to achieving progressively the full realization of these rights’. In simple terms that there should be ongoing progress towards achieving the rights to education, health, independent living and so on for disabled children and young people. This is why the UN Committee, in its General Comment on the right to education, states that ‘any deliberately retrogressive measures’ on education funding ‘must not disproportionately target learners with disabilities at any level of education’. In my view the same must hold true for health, social care and all other areas of public life which matter to disabled children and young people (i.e. everything).

If this post leads you to want to consider challenging cuts in your area, you may want to contact a specialist solicitor – and you will need to move quickly, as if funding is to be restored a judicial review would need to be heard within a matter of weeks if at all possible.

Easier read – what ‘we’ means

Thanks again to Anne at Barod CIC for these easier words.

When I blog, I keep saying “we”.

So who is “we”?

“We” means:

  • anyone who wants to change the law so disabled people have a right to live in the community and
  • people who are part of Justice for LB

 

What is Justice for LB?

Justice for LB is not an organization.

Justice for LB is a social movement.

A social movement means:

  • a lot of people believe the same thing
  • those people start to talk to each other
  • they try to change something

A social movement does not have a list of members.

You do not have to be invited. Anyone can choose to be part of the movement.

You are part of Justice for LB if:

  • you believe what happened to Connor was wrong
  • you talk to other people who think it was wrong
  • you want to stop it happening to other people

 

What is #LBBill?

#LBBill is not a project. No-one is the boss. No-one is getting paid.

#LBBill is a way for Justice for LB to try to change the law.

Anyone can be part of #LBBill. You do not have to be invited.  You are part of #LBBill if:

  • you tell people what you think about the Bill
  • you help other people to say what they think

You can do that by:

You could ask friends, family members or independent advocates to help you do any of these things.

Changing the law will not be easy.

I hope disabled people will want to work together to make the ideas for #LBBill into a law.

Easier read – #LBBill – how to make it happen

This is the easier read version of my post #LBBill – thoughts on process and timeline. Thanks so much again to Anne Collis at Barod CIC for these words.

 

Anyone can be part of writing #LBBill.

Here  is some information to help you get involved.

 

The Private Members Bills will be chosen in June 2015.

By then we must:

  • write the Bill
  • get lots of MPs to sign up to support the Bill

 

Writing the Bill

 

When we write the Bill, we must:

  • make sure everyone can have a say
  • make sure the Bill is what disabled people want

 

No-one can just sit down and write #LBBill.

#LBBill belongs to all of us, so we all need a say.

 

I think we can all have a say if we do this:

  • Write down our first ideas for a new law. We need to do this by September.
  • Send our ideas to lots of people
  • Lots of people tell us what they think
  • Have a go at writing #LBBill
  • Send #LBBill to lots of people
  • Lots of people tell us what they think
  • Have another go at writing #LBBill. We need to finish this by Christmas.

 

We do not have any money for the work on #LBBill.

This means we can’t pay for meetings or videos or Easy Read.

 

Some people are already helping for free.

Can you help for free?

Or maybe you have good ideas about how everyone can have a say?

 

If you can help other people to have their say, please:

You might want to ask a friend, family member or independent advocate to help you do these things.

 

Getting MPs to support the Bill

 

It is OK to start talking to your MP now. You can:

  • tell them about the problem
  • tell them we want a new law

 

By January 2015, we will have written #LBBill.

Then we can start asking MPs to sign up to support #LBBill.

 

We need as many MPs as possible to sign up because:

  • only 20 MPs get chosen for a Private Members Bill.

We must make sure some of the 20 MPs support our Bill.

  • for a Bill to become law, most MPs must support it.

It helps if the Government supports it too.

 

We will need to talk to:

  • all the political parties
  • civil servants who work for the Government

 

But for now it is more important to talk to the MPs.

If lots of MPs support #LBBill it is more likely that the government will support it.

 

Here are some free ways to get MPs to support #LBBill.

  • We can send emails
  • We can write letters
  • Local groups can ask to meet their MP.

 

If we can find some money, we can hold an event at the House of Commons.

 

We must make a lot of noise. We want to show MPs that people’s lives are important.

 

The May election

 

There is an election in May 2015.

We choose our MPs at the election.

The party with the most MPs gets to be the new Government.

 

This makes it harder for us.

We will need to talk to the MPs who are MPs now.

But we will need to talk to anyone who might get elected in May as well.

 

What do you think?

 

These are my ideas about what we need to do.

 

What do you think?

Please let us know!

#LBBill – thoughts on process and timeline

I’m keen to write about all the excellent ideas that have been blogged, tweeted and Facebooked about the content of #LBBill, but I thought the priority was to say something more about the process and timeline as this has generated lots of questions.

Bearing in mind the anger and disappointment about the exclusion of disabled people and families from the Bubb group my hope is that we can make the often murky process of working on a Parliamentary Bill as transparent as possible. This post is intended both to provide information and stimulate debate about whether we are going about things the right way.

The deadline we are all working towards is June 2015, when the ballot for Private Members Bills takes place (I wrote a little about this in my first post). We don’t know the date yet so let’s assume it is 1 June.

By that date there are two key objectives that we need to have achieved as I see it:

1. Have a Bill which has the widest possible support from the disability community, with everyone concerned having had a proper opportunity to have their say about what it should contain.

2. Get as many MPs as possible signed up to support the Bill – in particular those who will be entering the ballot to have the chance to introduce their own Private Members Bill.

It seems to me that it is sensible to try to achieve these objectives in stages. We are much more likely to get MP support for a Bill which is ‘ready’ or close to ready than if we approach MPs with a less clear set of ideas. However there is nothing to stop anyone alerting their MPs now if the chance arises – as some supporters of #JusticeforLB are already doing. If you get any feedback from MPs please let us know.

So, the first job is to work on making sure everyone has the chance to have their say on the Bill. I am very grateful to all the wonderful people who have volunteered to work on easy read materials – and to Anne at Barod CIC for producing the easier read versions of my posts which are already online. Mark Neary is doing amazing work with the Facebook group and we will I’m sure all keep tweeting about #LBBill til the cows come home.

We have no budget for work on the Bill, so are relying on everyone concerned with it to make the process as inclusive as possible. If you have any ideas for events or communications in relation to the Bill please contact me through the comments here, by email sbroach@monckton.com or on Twitter @stevebroach – or contact the main Justice for LB account.

This phase of the process I think will last until roughly the end of October. Hopefully in September there will be a very rough draft of a Bill for people to discuss as it seems to me that this would provide a helpful focus.

Then around end October we will need a better draft of the Bill. After this is produced those interested in the detail can then work together on the drafting and there will need to be properly inclusive consultation as the text gets closer to being finalised.

I would like to see a final draft of the Bill which as many people as possible feel able to sign up to by Christmas. It still won’t be set in stone then, indeed whichever MP adopts it may wish to change it, but it will be clear set of ideas we can all advocate for.

Then in January we move on to objective 2, getting MP sign up. There will be lots of ways to do this – we can have an email campaign, template letters, constituency meetings for local groups, a Parliamentary event if we can scrape together the cash. In my view we want to generate as much noise as possible – one reason MPs say there is not enough focus on disability issues in Parliament is because people care more about the roads, the animals and the trees. Let’s prove them wrong.

Our work is complicated by the rather significant point that there is a general election in May. As we are not a charity I don’t think we will be prevented in any way from campaigning about the Bill in the run up to the election. However we will need to collect pledges from all candidates to support the Bill, not just the sitting MP for each seat, which increases the workload. Also, current Ministers may well find themselves as backbench MPs after the election, so there is no-one who should be ‘off limits’ in terms of supporting the Bill.

During this phase we will also need to have conversations with the political parties and officials at the relevant government departments, particularly the Department of Health. It is not realistic to think that we could get the Bill through into law without the formal support of at least one major party and we would most likely need some degree of government backing. However I think the first priority is to get as many individual MPs (or in our case candidates) signed up to support the Bill as we can.

So that’s my initial thoughts on the process and timeline for #LBBill – as ever all comments welcome. Next post should be thoughts on what might happen after the ballot next June before some further thoughts on content.

#JusticeforLB

#Justiceforallthedudes