SUSIE MALLETT

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Showing posts with label Clothing. Show all posts
Showing posts with label Clothing. Show all posts

Tuesday, 8 January 2013

Buttons




Buttons

A supplement to something that I wrote last year about the joy of success –


Learning and development

How pedagogic specifics bear upon upbringing developments

Spreading joy

In that earlier posting I wrote about the joy of a little girl learning to do up the button at the top of her trousers. This joy spread throughout the group, at home and over many days. This success had a domino effect and started a renewed spiralling in all our lives.

Later I thought about that child’s future and about what changes that resolved problem will make to how she lives her life. Having a button to do up without turned to the trusty Velcro, and therefore having learnt to do it up by herself, means that as an adult she will be able to choose freely what trousers, skirts shirts and jackets she can buy. She will not always have to pay someone to alter her clothes. Hopefully she will never have to change buttons to Velcro and rarely have to compromise on her choice because of a lack of motor skills.

We could have asked her mother to use Velcro or to buy her trousers with an elastic waistband but we did not. Many of the non-disabled children in the Kindergarten have buttons and they all run and ask us at some time during the day for help to undo them or do them up, until they solve the problem with our help.

I have often considered things that have occurred to me since that previous posting. One question that I have asked is why alter her trousers now when she is only five-years old and learning fast? Why lay down a need to alter them in the future when we can encourage her to learn something now, something that she can achieve, and in the process of learning this develop so much more? Why should we miss out of this valuable step in a wider learning equation?

This is not specifically a question of a button on the trousers but of something more general and more important, the personal change in this child, her motivation to learn, the relationship that she is building up with me and other conductors as she blossoms, and about all the other new things that she can now do in her joy of learning and achieving.

I have considered all the skills that have that have developed since, that need her to concentrate and to look. Because she has now learned this very difficult task of buttoning her trousers, she looks more often at her hands, she uses her left hand more and she is so happy because she has learnt something that she wanted to do it. She continues to learn things through life and play each and every day, affording her more independence and bringing her such joy. Far, far more than doing up a button, this little girl is blossoming, and this is in itself also a part of huge developments at this stage in her upbringing. She listens and talks and helps others and smiles a lot.

That is the biggest behavioural change: she now smiles a lot.

A paragraph from a life

There may be good reasons why a child is not given alternative means, not given an easier option, like an elastic waistband instead for example. If we as conductors thought that she could not achieve, or it was psychologically harmful for her to try, then we would not try to teach her.

This little girl is very young, she will be going out into the world disability one less signal disability. In the future she will not need to have her clothes altered because we did not teach her to do up a button. That button is just a paragraph, not the whole story.

Other children

How important it is for this little girl to be like the other children in the Kindergarten and have a button on her trousers, and be able to do it up. Of course, if she were fifteen and could still not do it up, that would perhaps be different, and need to be rethought and approached differently. Now at five, though, she does not feel any different in her group, there are non-disabled four- and five-year olds who still ask for help with their clothes. Now through her success she feels very special, just as her peers do in their turn.

The whole group has celebrated with her. This gives her far more than taking half a year longer to do up a button takes away from her. It also gives her the opportunity to do so many other things now that she has learnt it, all with the knock-on effect of more praise from us and more acknowledgement from the disabled and the non-disabled children that she is doing so well.

She really is a very happy little girl at the moment. Giving her an elastic waist or Velcro fastenings on her trousers would have removed many of the moments that are making her happy, because there would be many things that she still could not do.
 
Since learning this skill she is much more conscious of her hands, she has to look at her hands to achieve this success. Learning to direct her eyes on something means that she is now able to look at us when she speaks to us and at her friends and at their toys while they play.
 
Has there been a 'price' for of not being able to do up a button till now? She is still just five. There are four- year-olds in the Kindergarten have had elastic trousers until recently who also ask for help with the button. They are not hemiplegic and have no motor disorder, they just have not been taught. Nobody comments that they take long or wonder why they cannot use scissors or a knife and fork. They will learn when they are taught. Do we ask what price they pay for having to ask us to do up the button? I always consider the gain for these littlies from the contact and the learning experience in those few seconds it takes to help, not of any price paid.

And by the way, using Velcro can be difficult too in my experience and does not always encourage hand-eye coordination and two-handed movements. Elastic-waist trousers present more difficulty when tucking in vests and shirts. All these are skills to learn, all appropriate clothes and fastenings in their place but not as a replacement for learning to do up a button when that skill is learnable.

Older…

An older client of mine has tried Velcro but he does not want his lovely trendy jeans messed about with, he does not wish to be different. He wants to do up his buttons so we continue learning it. He is twenty-two years old now and sometimes he manages it and is as thrilled with this as the five-year-old is. (When he cannot manage it he discretely asks someone to do it for him. He has a belt that he can always do up himself so he is secure in the knowledge that his trousers will not fall down if the button is left open.)

Where there is a will there is a way. These happy souls continue learning.

...and younger

My own little niece is nearly three. She cannot do up a button on her trousers yet. She will be able to before school I expect, because she will want to do so, so she does not have to ask someone, just like our little girl wanted to learn so she no longer needed to ask and it was important to give her that opportunity.

What a happy little button-girl we have in our group, it is no wonder with so many hugs and so much praise.

I myself was already at school when had to find out the hard way. I remember it well. I had to go to the toilet, in the cold outside (the last time, I think, that I ever went to the toilet at school), I was about four or so. The teacher said she would come and help me but she did not come, I expect she forgot. I remember wandering around in the half-covered area in the dreary autumn cold, lost. When the teacher eventually arrived I had by then done my clothes up myself. No praise received for that success, just a telling-off because I was lost. I probably did not even say anything at home about that huge step in my upbringing. I would have been too afraid to but it would have been noticed, I am sure.
 
I am sure that we do better than that.

Tuesday, 28 February 2012

Clothes for people with disability… …and some new reading material too










Something to read on a Monday morning

Something nice turned up in my in-tray last night. Luckily I read it there and then as most of my day today has been spent seeing the world as if through the windows of a bus dirtied by a spray of brown slushy snow!

Yes, we do get buses like that here in Germany but not on too many occasions this year because the weather has been too cold or not snowy enough!

At eight-fifteen this morning I was at the Augenartz, eye doctor, getting the small blisters of detached retina checked for deterioration. Thankfully there was none, only the strength of the reading bit in my vario-focals needs increasing.

A combination of eye-drops and the gunge that was put directly on my eye made seeing anything rather difficult after the two hour stint at the doctor’s. Even the hundred yard walk home was pretty hair-raising.

Luckily I had read the article in my in-tray before the brown-slushy-window symptoms occurred. It is not a nice feeling not being able to read properly all day. Of course I spent quite some time counting my blessings, knowing that the window would soon clear and that I could afford to invest in a new pair of glasses. Knowing that this would make drawing, following a road map, and reading a train time-table easier again, made the symptoms a lot less frustrating and scary.

I had written a few notes between the eye-drops and tests in preparation for writing a posting but it was several hours later before I could read my own notes! This evening when I got home from work, after ordering the new glasses at a shop that is also just a hundred yards away from home, I promptly fell asleep.

 I am determined however to get something recorded about today before I collapse into bed.
The first thing that I shall do is to remind myself that it is better to make these doctors’ appointments after work and not first thing in the morning. The effects can then be slept off at night. It is a very, very tiring ordeal not being able to see properly all day and trying to do everything just the same. I shall certainly have something to share with the stroke client in my group tomorrow who has suffered from double vision since he suffered a stroke eight years ago.

Days like today are certainly sent so that I can continue on my path through life learning as I go!

Clothes show, a lot

It was only this weekend as I was reading the latest information bulletin from the association that I do a lot of work for, that I was thinking about the clothes that people with disability wear. There was a photograph in the brochure of a group of wheelchair-users on holiday in Italy. They did not look like there were very well dressed. I do not mean that they did not have good clothes on. It was just that the clothes did not fit while sitting in a wheelchair. Their image gave the impression of discomfort, not a relaxed holiday feeling.

Last Tuesday two clients turned up in my evening workers ‘group who were both wearing winter trousers bought from a local company that supplies clothes for wheelchair-users. They both looked smart and comfortable. There were no cold, bare backs and crumples of material that make sitting uncomfortable. The trousers fitted them. Not only are these trousers cut higher at the back they also have strategically placed darts to prevent all the bagginess at the front, and the legs have extra length to cover the shoes when sitting.

These two clients are lucky that they have families who help them financially so they can afford the luxury of these relatively expensive clothes. The jackets from the same company are also very well cut.

Lovely

Now take a look at the gorgeous clothes in these articles that I read last night:



I do not think that my clients will have the money to spend on dresses like these, or even many occasions to wear them but reading about this and seeing the lovely clothes reminded me that a friend and I have been making plans for a long time to offer our time on a Saturday afternoon to encourage our wheelchair-using clients to make the most of their clothes at only a little extra expense. We would like to have some fun hours with them learning together how to add a pretty accessory here, to make a few snips and changes there, and show them how to recycle outfits by adding a bit of flare.

And to show what a difference it makes to the appearance when there is no bare flesh when working out, when trousers reach to the tops of shoes and hang properly, and when jackets are shortened to waste length.

I have had a lot of practice at dress-making for a wheelchair-user. It is time to start sharing the experience with others!

This is definitely time to begin this next project now that the most recent one is completed:

My most recent project is something to read at your leisure

We have collected the books!

I shall give details of how to order the books below, but first I have to report today’s most important event, the little launch party for our new book.

I name this ship!

It was not quite a naming ceremony but I can now quite understand why such things are called a “book launch”.

I would love to organize something a bit bigger for Waltraud, maybe with the local press present, and I will be approaching our media manager at work soon, but today’s little gathering was enough excitement for the beginning.

Anticipation

The author and her husband were ready and waiting for me at our designer’s office this afternoon.

Both designers were waiting at the door to welcome us, and I was so glad to see that my sort-of-step-son, who is also part of the media company that has been helping us, was also there to join the party.

There was no champagne but there were flowers and chocolates for our wonderful graphic designers. They have spent so much time on this publication and have given much of it for free. They were so impressed by Waltraud’s energy and determination that they just wanted to help her, and help her they have.

They spent almost an hour this afternoon showing her the huge double computer screens on which they had worked, moving ideas to and fro. They took time to explain how they had worked on the layout of the double pages and on cutting the photographs.

Waltraud uses a computer at home and was quite able to follow their clear explanations and as her confidence grew she was able to ask questions.

Before we left Waltraud took out a pen and signed half a dozen copies of her book to leave for the designers Uli and Tine. Waltraud looked as though she had been book-signing for years!

As I have written in the book, it has been her party, and it was a pleasure to take a step back and observe how yet again my client was able to take yet another stride forwards life with her husband at her side. I realised again today how important this project has been for Waltraud’s husband too and today he really enjoyed the attention and the excitement of the moment.

Get your copy NOW

You can read about their joint journey on their path to life, in German and in English, in:

CONDUCTIVE LIFESTYLES

BOOK ONE

Er kam wie ein Blitz aus heiterem Himmel”

It came like a bolt out of the blue”

EINE GESCHICKTE NACH EINEM SCHLAGANFALL IN WORT UND BILD

A POST STROKE STORY IN WORDS AND PICTURES

Waltraud Heußinger

Bearbeitet and vorgestellt von/ edited and introduced by
Susie Mallett

Fotografie/photographs 
Werner Heußinger

I will be distributing this book at the Annual National German congress on 8-9 March but it is available from me from today at:
 
PS

I have offered to be the distributer of the book so, you can order as many copies as you wish from me. They will cost ten Euros a piece, plus packaging and postage. So write and tell me how many you need and where you are and I will tell you how much to pay.

I will get some copies over to the UK as soon as I can, to make distribution there cheaper and quicker. Gill Maguire will be doing the distributing for us there. Order from me and I will pass the mailing info on to Gill.

Thank you to Gill! She is yet another link in the chain that has worked together to make Waltraud’s dream of writing a book come true.

I have been keeping a list and there are about twenty names on it now.

Sunday, 20 June 2010

They are still talking about it

"Shoes on sale"
England, May 2010



What we wear on our feet


I have just discovered that over a year later people are still coming back to something that I wrote on the Conductive Community Forum, and on my blog, about what we wear on our feet!


I am still interested in what we conductors wear on our feet, and why,we choose what we wear. So if there is still anyone out there with something to say on the subject please do so, either here or on the Conductive Community Forum.


I am still sticking to my trusty lace-ups that give me a firm footing and also keep my feet warm. I am about to have some new inner-soles made by our shoe maker and I am hoping that these will make my shoes even more comfortable.


I have noticed that my colleague has made some changes recently in her work-footwear. She works in the integrated Kindergarten most of the time and I think that she has realised that she has different footwear needs for different activities. There are now three different pairs of work-shoes lined up in the changing room. One for summertime-outdoors, one for tougher work indoors and one for more for gentle work indoors like the singing, reading and playing at the table that happens during and after the midday rest period.


She is very consequent and changes her shoes regularly, she is hoping this will do her feet and legs good. Like the rest of us she is standing up and walking around all day long and feels the symptoms of this at the end of the day.


I think I may take a tip out of her book and invest in a second pair, lace ups again of course.


Read more at:


http://www.conductive-community.com/node/34

http://www.susie-mallett.org/2009/02/back-to-feet.html

http://www.susie-mallett.org/2009/02/what-do-conductors-wear-on-their-feet.html