Pop up toilets with a hoist and changing bench – Part 1

Standard

This month we invited companies to tell us about their alternative solutions for venues who want to provide accessible toilet solutions for people who need a changing bench and/or hoist.

This week features MigLoo … and here is what they told us.


MigLoo

Summary

  • Mobile, set up/take down system as and when required.
  • Three types (MigLoo Freedom, MigLoo Festival and Naked MigLoo)
  • A gantry hoist system with a changing bed and camping technology for sink/toilet supply.
  • Cost: £6000 to purchase.
  • Hiring options.
  • Website: www.migloo.co.uk
  • Contact: Leave a message or telephone us on 07789 147663.

Where did the idea come from?

Director John Robinson’s concern at the difficulty people experience in finding suitable facilities. He started out by inventing a mobile Changing Place for Andy Loo’s in 2006. He got one of the very first Changing Places Awards during the launch of the Changing Places campaign at the Tate Modern, in 2006. John then realized there was a huge need for facilities that people could take with them. This gave him the idea of inventing an inexpensive yet completely versatile and fully mobile solution to these needs. This led to the three products we have today.

John was inspired by people with profound disabilities’ character and their neglected situation, which still continues today. He still feels that ‘we can do better than this!’

Why do these facilities make such a difference and what do customers and users think of them? 

Operation with MigLoo’s mean that facilities can be put where people need them, rather than having to seek them out. They also are low cost making it easy for people to make those ‘Reasonable Adjustments’ required under the Equality Act.

Users of the facilities (which means carers as well as wheelchair occupants) are delighted by the MigLoo’s and often moved emotionally that they can stay for a full event or that someone has bothered to provide what they need. We’re deeply moved by this and extremely motivated to develop MigLoo’s and the many other inventions in the pipeline.

How long have you been running and where are you based?

We started off in 2005 when John Robinson gave up his job running Pershore Day Care Centre to develop his inventions. Co-director John Morgan joined him in 2009 and the parent company, Protorus Solutions Ltd, was formed in 2014. However, the current MigLoo operation commenced in late 2017. The entire MigLoo manufacturing, production and operation is based in Pinvin, in darkest Worcestershire.

How many types of arrangement do you have and what areas do you cover?

We cover the whole of the UK with sales. We prefer businesses and organisations to buy MigLoo’s because of their very low cost. However, we also make some MigLoo Festivals available for hire when we have the capacity to do so.

There are 3 MigLoos

Migloo Freedom

The MigLoo Freedom (above) is 2m x 3m and has a changing bed, gantry with hoist and tent to cover. This means it is small and light and can be erected on fairly level sites by 2 people virtually anywhere.Migloo Festival

The MigLoo Festival is 4.5m x 3m and is an accredited Changing Place. It has everything that other Changing Places have, including a sink, water from a tap and a loo. It is self-sufficient, being independent of mains water or electricity, using camping technologies, which make it incredibly flexible and cost effective.Naked MigLoo

The Naked MigLoo is simply the MigLoo Festival without the tent structure. What we are doing here is providing pop-up Changing Place facilities that can be put into an empty suitable room ANYWHERE!

From businesses through shopping malls, supermarkets, museums, local authorities, empty shops on High Streets – essentially opening up huge amounts of otherwise redundant spaces into accredited Changing Places for profoundly disabled people to use.

We’re seeing this as a temporary solution to the lack of facilities; they are low cost making them a very reasonable adjustment and helping to prove the need for permanent facilities to be installed.

We also realize that MigLoo’s can also enable organizations to find the optimum site for a Changing Place, thus avoiding the embarrassing situation that some businesses/authorities have made in putting them in locations that few will use! Because of their extremely low cost, Naked MigLoo’s are also perfect “standby” Changing Places for when the permanent Changing Place breaks down.

  • A Naked MigLoo takes only 30 minutes to be erected and become fully operational.

Can they be installed/hired for a few days or nights?

Yes. We will hire them out for anything from 1 night to many, although installing at a great distance simply isn’t feasible or cost effective as it would be too expensive for a relatively short period.

Does anyone stay with the set up to help learn how to use that particular hoist/gantry or empty commodes etc?

No, not really. The equipment is easy to use and we make sure hirers are trained, thus having someone who can advise on hand when folk use it. We sort the waste out.

Can any disabled person or carer use your facilities or are they only for hoist/bench users (and their carers/assistants)?

This is really for the event organizers. The Elsan loo we have has armrests and a backrest and is designed for those who need support, but there are not the grab rails you would find in an ordinary wheelchair loo. The organisers may well feel that users with profound disabilities should have priority and should not have to wait for someone in a wheelchair, who has an alternative loo.

For people who might use them, would they be allowed to leave their sling with you in a locker or do they need to carry it around the venue?

They would need to take the sling around with them, as we have no locker, but it is something we could consider. By the way, it is looped slings that fit our hoists. This is because most people use this type. We could cater for clipped systems, but this would need advance notice and be a little more expensive (as they are not used very much).

What types of venues have you been to and how do people know if you are attending?

Here’s a list of what we’ve done so far; Fun Days in a football club, Fetes, Disability Awareness Days, Children’s Play Schemes, College Events, Exhibitions, School Events, International Theatre, Conferences, 7 day Festivals….. We put the events on our website and social media and make sure the organisers advertise that a Changing Place will be available; after all; ‘If you billed it they will come’ – but not if they don’t know about it!

If I wanted one for a day at my event/venue, what space would I need and where is the best place to have one e.g. inside the event, in the car park etc.

The MigLoo Freedom is 2m x 3m, the MigLoo Festival 3m x 4.5m but some space is needed around the structure for guide ropes if it is windy. It is best to put the facility as near to where it is needed where people are, rather than making them have to go some distance away (it’s often hard work wheel chairing!).

Do I need a permit or special insurance to have one near/in my event?

No, though we would ask that you insure the facility, just to cover any damage. Our parent company, Protorus Solutions Ltd carries £10m in public liability insurance.

How can people find out the cost of hiring a Migloo arrangement and attendant?

Just go on our website www.migloo.co.uk and leave a message or telephone us on 07789 147663. We don’t provide an attendant as this will push the costs way up and normally the event puts someone in charge. Carer’s also know what they need to do when they see the very familiar set up inside the MigLoo. We could consider this, however, and supply an attendant if necessary.

What do you hope for the future of Migloo?

Simply to support as many people that need it as quickly as possible. There is a desperate need in the UK for these facilities as we have all seen in recent national TV and other media coverage. Our MigLoo family offer real “reasonable adjustment” and the Naked MigLoo is potentially a game changer, changing many many lives for the better, once it has become more recognized. We would also like the low cost MigLoo concept to be taken on by the “event loo” industry in the UK and make it available to other countries. As MigLoo grows, we will employ staff to run the operation.

Can people find you on social media?

Yes, on

Twitter @MigLoo4U #GotaRoom4CP

Facebook : MigLoo4u LinkedIn :      www.linkedin.com/company/migloo

Child Protection: Campaigning with dignity

Standard

This article is about safeguarding and contains information that every parent campaigner should know. Warning, may involve triggers related to sexual abuse.


When it comes to campaigning for Changing Places or Space to change toilets, a large number of campaigners are parents of disabled adults and children. Children and adults vary in age range and mental capacity, some having severe learning difficulties.

In this article we refer to disabled children but equally this applies to disabled adults with reduced mental capacity regarding consent to the use of their image.

Important information can be found on:

NSPCC image use in child protection

Images in campaigning

Parents will generally want to share images of their disabled children (or send them to other parents or organisations ) so that they can be used on posters, in booklets, attached to Tweets, made public on Facebook or printed in letters / e-mails for example.

Many images involve a child laying on a toilet floor, others show a child in distress or semi clothed/wearing only incontinence pads from the waist down.

Losing control over images of disabled adults and children.

Every potential campaigner, organisation or business who provides or collects an image of a child/adult, needs to be aware of how to protect their dignity and privacy and safeguard them from abuse.

The potential for misuse of images can be reduced if organisations are aware of the potential risks and dangers and put appropriate measures in place. [NSPCC:2018]

This is particularly important when each campaigner is acting as an individual (there is no ‘single campaign’, rather a shared desire to raise awareness and encourage the provision of more accessible toilets).

We have a safeguarding policy for project participants and a code of conduct which you can view here.

What every parent needs to consider.

  • First and foremost the privacy and dignity of every child should come before any campaign gains.

Every disabled adult and child, as a human person, has a right to dignity and privacy.  Whilst it can be argued that laying on a toilet floor is undignified, this doesn’t mean the person should be open to further enduring indignity (and loss of privacy) through having their photograph made public on the Internet for example.

If your child is too old to be placed on a baby changing unit, they are probably to old to be shown in a photo wearing a nappy/pad/pull ups.

  • If your child had full awareness / understanding about the Internet and who would see their image (friends, teachers, families, random members of the public, paedophiles etc) would they agree to you posting that particular picture?

An image example that was shared across the world via social media involved a 14 year old girl with severe learning difficulties, laying on a public toilet floor in her incontinence pads. There are probably no 14 year olds without an impairment who would consent to such images going public – so consider age appropriateness when thinking about dignity, privacy and consent.

  • Question who is asking for this photo – how well do you know them?

Just because a person says ‘please share your image for the campaign’ doesn’t mean they are genuine. Anyone can create a Facebook or Twitter profile and appear to be an understanding parent in the same position.

  • Who is using the image of your child?

Remember, once you share a photo with any individual campaigner (privately or via social media), you have no control over what this person will do with it – or what the next recipient it is passed on to will do with it.

Did you know, we are often sent images of disabled children, not from their parents but from other campaigners and told to ‘use the images as we see fit’. You probably don’t know I have them nor what I intend to do with them. *Note we immediately delete these images.

  • Never share your child’s image with a business, charity or organisation unless you see a copy of their child protection and safeguarding policy.

Use of your child’s image in sexual ways or to locate them in person

You have no control over how the photo you provide to people will be used (it might even be used for a different disability campaign, in any country). You have no control over who will store the photo, if the image will be altered, in what format it will be kept, how secure it is, and how long it will stay there.

It could turn up in the hands of a paedophile or be shared amongst a secret Facebook group of people who will find them sexually stimulating. No parent wants their child’s image to be used in this way?

By posting your photo, where your child may have their face showing, and saying ‘please have a picture of [x]’ you have given your name and that of your child.

A sexual offender or ‘admirer’ [someone who has a sexual preference for a person with specific impairment or medical issue such as being a continence pad user] now knows enough to start following links to seek more information or imagery.

They can visit your profile and see anything you have made public, find out where you might live, perhaps match up your children’s image with anything from a local newspaper/charity/school or blog. Very soon they could pinpoint you to an actual school, know your routines, start befriending you, maybe meeting in person several months down the line as a ‘similar parent’.  They have your whole profile and possibly that of your family and friends (whom they can also contact and befriend).

Gradually they get ever closer to their prize – your child. Then one day you meet up, they offer to sit with your child whilst you pop to the loo. Very slowly your have, unknowingly, compromised the safety of your child … all because of a photo you shared a few years ago on the Internet.

Does this really happen – yes it does. A man contacted me and several other disabled men and women. First the conversation was about what type of mobility equipment/wheelchairs, medical equipment did they use – as if asking for peer advice. A few conversations later the topic turns to asking about the best incontinence pads to use … then asking for pictures of people in their wheelchairs, asking to be friends, liking photos and asking to meet in person. The person found that seeing a particular type of impaired person, in a wheelchair, knowing they were incontinent was sexually stimulating … and they quickly deleted their profile and resurfaced under another name when the disabled community felt that something wasn’t quite right. They wanted images and a visual viagra. They would start to bully and harass people if they did not get their fix. This happens. Be aware and be safe.

  • Once an image is ‘loose’ on the Internet, you will have no control over where it goes or who keeps it or for how long – and will not be able to ‘get it back or delete it permanently.
  • Schools, local authority staff, local authority foster carers, care workers have to work within strict policies about photographing children for posting on the Internet or elsewhere. Images of children have to be ‘appropriately clothed’ and pictures of children in a toilet would be a safeguarding concern and investigated.  As a parent, you will know that you have to consent in writing for every photo a school uses and be informed where it will be shared and how it will be stored. A school has to classify it as personal data under the Data Protection Act 1998.

If a school teacher, care worker, foster carer can’t share images of children who are not appropriately clothed (i.e. in knickers/pants/pads) then you might want to think twice about sharing and the implications this can have.

  • If you are invited to make a photo as ‘shocking as possible’, consider that ‘shocking’ is likely to impact the dignity and privacy of your child.

Be aware, be safe, protect your child’s image.

All change for changing places

Standard

News from The Changing Places campaign:

We wanted to share the news that Muscular Dystrophy UK is taking over from Mencap to lead campaigning activity across England, Wales and Northern Ireland, and will co-chair the Consortium alongside PAMIS.

More about this news can be found at:

http://www.changing-places.org/news/changes_to_the_consortium.aspx

Aveso say:

Tell it as it is – for world toilet day.

Standard

19th November is World Toilet Day , a global opportunity to explain how lack of toilets impacts many aspects of life.

Join our Tell It As It Is event to share your story about the lack of usable and accessible toilets in the UK.

Starting on the 18th of November, we will be putting up a Facebook post on our page – inviting you to tell it as it is.

How does the lack of usable / accessible toilets impact your life?

Whether it’s just a sentence or a short story or photo – please do drop by and share your story by replying to that post on the 18th or 19th.

You can also join our Twitter hashtag #tellItAsItIs and also use the main tag #WorldToiletDay

*All replies will be moderated and those advertising a product or not meeting our adult and child protection policy will not be displayed.

Helpful or not – petitions

Standard

There are over 80 petitions on Change.org calling for signatures to back calls to governments and businesses for accessible toilets. Most are by individuals calling particularly for Changing Places toilets.

Are petitions helpful?

Psychologically petitions and demonstrations by disabled people and carers are useful – providing the 'I feel I am doing something rather than nothing'. People who sign genuinely want to say 'this needs to change'. However, the reality is that petitions rarely achieve results.

No amount of signatures is going to change the law or monitor adherence to building regulations. In the UK, the government have heard, via parliamentary debates, how we need accessible toilets. They end with empty promises.

As we speak the draft of revised access standards has been drawn up – setting British standards for what could be used in buildings which last over 50 years. They don't include any change to toilet provision. They are based on the dimensions of wheelchairs, for example, from 20 years ago. Petitions won't impact these.

Dilution of support

Petitions aim for x number of signatures …. people might sign one or two but 80? If campaigns were centralised into one petition there could be thousands of supporters rather than a few hundred.

Change in strategy

The movement to ensure toilets for all is disjointed. Often it's based on promoting the needs of children rather than the needs of disabled people of all ages. People with obesity, dementia and autism are often totally ignored. Many campaigns are based on the need for hoists and changing benches – yet we still have toilets being built that are supposed to follow strict building regulations, but don't for 'independent' disabled people. There are failings at every level. Equality laws do nothing to persuade businesses that disabled people need accessible toilets.

What can we do to actually make a difference?

  • Share a petition rather than recreate one for yourself
  • Look out for opportunities to comment on building regulation guidance, local access consultations, health consultations etc.
  • At every opportunity provide feedback about toilet access. Use social media, review websites, council feedback forms, patient feedback cards at hospitals etc.
  • Use formal complaints procedures.
  • Write to your MP
  • Provide witness statements for parliamentary debates

Sounds like a lot of effort? That's why it's easier to sign a petition and have our social guilt relieved – we've done all we can, right? Now everything will be ok?

No it won't – but deep down you know that.

Draft of BS 8300 -2 available for comment

Standard

British standards are helping businesses thrive. Some of them define access for disabled people outside and inside public buildings.

What is a British Standard?

Standards define best practice in many different areas. They’re put together by groups of experts and come in a number of different kinds, from a set of definitions to a series of strict rules. 

… Standards are not the same thing as government regulations, but they’re often used in legislation to provide the technical detail.

(BSI, 2017)

Standard BS 8300 defines access requirements from ‘set down points’ in car parks to the distance to the toilet or width of lifts. There is a section about toilet access, dimensions, fixtures, fittings etc which is best practice. 
A new draft for BS 8300 is available to read and comment on. There are two parts – the toilet section is on 8300-2.

Link to draft BS 8300-1 and BS 8300-2 (enter 8300 in the search).