life talking through a communication aid.
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Transcript life talking through a communication aid.
LIFE TALKING
THROUGH A
COMMUNICATION
AID.
A personal story of how I
communicate using AAC.
By Scott Stack
Communication Matters Trustee
AIMS AND OBJECTIVES:
AIM:
To tell you about how my communication
aid helps me to talk, live and work.
OBJECTIVES:
How I raise awareness of AAC.
Give a description of how I personally communicate.
How my communication aid has changed my life.
Pros and cons of my particular device.
Plans for the future.
Questions at the end please.
A BRIEF INSIGHT TO MY LIFE:
I live at Cornerways Residential Home, in Tavistock.
I share my home with another 2 friends.
We have carers 24 hours a day.
We make the decisions on how we live.
It is important I can tell them what I want, by using my
communication aid.
ECO 2:
I use an Eco 2 to talk.
I use it everyday, for talking, over 15 hours a day, 7 days a
week.
If I can’t use it, I will eye point, use gestures, hand signals or
body language.
But my favourite way to communicate is my Eco 2.
COMMUNICATING:
I was 17 years old when I got my first communication device.
I am a single switch user, and I operate it with my head.
The communication aid will scan through the icons, and I press
the switch, that is in my headrest, when the light is over the icon I
want to select.
This is time consuming, and also takes a lot of concentration and
energy from me.
IMPORTANCE OF USING A
COMMUNICATION AID:
I need to communicate as much as possible
It’s the best way to understand me, and what I
want on a daily basis.
And to get to know me – my daily routine, my likes
and dislikes and my opinions.
LONGSEDALE SCHOOL:
When I was at Longsdale school, I started to communicate with Bliss
Symbols.
This was by eye pointing at various symbols around the room.
My body language was misunderstood, so I think the teachers were
telling my parents that I was progressing better than I actually was.
I fooled people into believing that we were having a conversation,
whereas they were actually having a conversation on their own and I
was just helping them with it.
LEARNING TO READ:
Taking away my Bliss Board and replacing it with a board I had to
read from, was a very difficult time for me.
Eventually I was given a picture book, with 20 photographs of my
family and teachers, and 30 symbols, expressing my basic needs
and feelings.
I did not learn to read letters or words.
But I learned to read people.
And to listen to their voice. And to read their face.
GETTING MY PATHFINDER AT DAME
HANNAH RODGERS:
Being given the Pathfinder gave me more opportunity to take more control
of my life.
It was re programmed with a new language that I had to learn –
MINISPEAK.
I started with 24 pictures with single messages., which I had to learn.
It let me express myself, for the first time in years.
I could finally talk about everything, that I had been accumulating for years.
TODAY’S LANGUAGE:
I now use,144 pictures and a 3 layer sequence.
It is the same programme, that over the years I have expanded.
It took a long time to go from expressing myself with behaviours as a
way to communicate, to being actually able to say so.
But I got there.
It feels good to be able to explain to people why I behaved badly.
SEPARATION:
When I was at school, my parents split up.
I did not deal with the situation very well.
I refused food and drinks as well as showers.
I used to lash out at my carers.
I used to throw myself out of my bed.
I screamed nearly all night. I also used to self harm myself.
This was my way of dealing with what was going on at home with my
parents, especially because I was away at boarding school.
LIFE WITHOUT MY COMMUNICATION
AID:
I can not imagine not having my communication aid.
I often think of my eco 2 as a part of my body!!
And when it goes wrong or breaks I feel ill.
FRUSTRATIONS:
If my device stops working, I stop talking.
When I am outside I struggle to use it:
When it is sunny I cannot see the screen.
When it rains I cannot use it at all!
It constantly needs charging. So I have to rely on my carers
to remember spare batteries and to charge it every night.
ROLE MODEL:
A friend of mine inspired me.
Best of all, he helped me to dream. He helped me to wish and he
showed me it was possible.
The best advice he gave me was::
Work hard, talk, practice.
The best thing he did was that he showed me to always aim at what I
want and reach for it.
I liked being able to help others like he helped me.
COMMISSIONERS MUST KNOW THAT:
If I did not have my communication device, I would not be able to live my
life the way I want.
Because I cannot talk with my mouth. My machine is a necessity to me like
your voice is a necessity to you.
Training for me and my carers, from suppliers on how my device works is
important.
Without my device, I could not have the jobs and opportunities that I have
now.
My disability needs to be thoroughly understood, so the right device is
given to me.
OVERALL:
I can keep in contact with my friends and family.
It has also given me huge opportunities to do more than just
sitting at home everyday.
I can talk to people, so my carers do not have to talk for me.
And most importantly having a device to talk makes me feel
more equal to all of you.
THANK YOU.
My communication aid is like a part of my body.
I would be lost without it.
Thanks for listening to me.
And if you have any questions, I will do my very best to answer.
You have been great to talk to.