Individuals with Down syndrome can also give a presentation!
Erik de Graaf and Marian de Graaf
Erik and Marian de Graaf describe how they worked with their son David to help him develop his public speaking skills in Dutch and in English
de Graaf EAB, de Graaf M. Individuals with Down syndrome can also give a presentation!. Down Syndrome News and Update. 2003;3(2);46-48.
doi:10.3104/dsupdate.225
I am David de Graaf (Aj em Deevid de Graaf)
It all started with the question: 'What does one do if
one does not speak very well, one's speech is quite unintelligible and one is asked
to give a talk in school?' When our son David (born in 1984) was ordered (rather
than asked) to do so many years ago, we did our utmost to invent a way to keep it
from being a flop and just another failure experience. Realising that he could read
much better than he could talk, and that his reading was also far more intelligible
than his spontaneous speech, we came up with the idea of an oral presentation with
subtitling. We produced a series of cardboard 'screens' for David to hold up in
front of the class. On the front there was a picture and a very short statement
in catch words printed so large that it could be read from all corners of the class
room. On the back, facing towards David, there was a full sentence relating to the
picture on the front that David could read relatively easily. The class, then, at
least had the catch words, while David could read the extra information aloud. That
worked quite well. A few years later we realised that from there it was, in fact,
just a short step towards a PowerPoint-like presentation. Hopefully our experiences,
described below, will stimulate other people to do something similar.
We began by making a simple presentation on a laptop using
the programme Presentations (by Corel, long ago the precursor of Microsoft's PowerPoint).
Therein we had David 'tell', so to speak, about his own life with Down syndrome,
as he was living it. By showing photographs he explained what he did in life, what
he liked and what he didn't like, what he found easy and what difficult. Of course,
all this could only be done in close co-operation with David himself. It was our
intention that, while presenting, he would read the short texts on the successive
screens aloud. In that way, his audience could at least read along with him where
they could not understand his speech. In doing so, David would be understood quite
well, we hoped. But, apart from that, we thought that the simple fact that a boy
with Down syndrome in front of a group, with quite some flair and a mouse in his
hand, operating his own laptop, proved to be able to read aloud reasonably well
should make a very positive impression. Towards the end of 2001, we put the concept
to the test on a stand at a symposium of obstetric and gynaecology nurses. That
afternoon, David, standing beside the laptop, did his presentation almost a dozen
times with much flair and dedication, albeit only before a very small group of listeners
each time. But he enjoyed it very much, getting all that attention and telling his
own story.
A few weeks later, we threw him in at the deep end by letting
him give that same presentation in front of an audience of about 80 baby clinic
professionals, physicians and related personnel at the Leyden Academic Medical Centre.
There, for the first time in his life, he sat in front of his audience, facing it
and reading from his own laptop screen into a microphone, while his 'slides' were
projected in a huge size on the wall behind him. And it went all right! So, all
in all, this concept proved to be a powerful method of having more information given
by somebody with Down syndrome himself, particularly promising for the less (and
possibly far less!) able speakers.
Another 'exercise' opportunity presented itself during
an 'open day' at Parc Spelderholt, a venue for the education of individuals with
a disability towards a more inclusive life. Presenting from a stand behind his laptop
was by then a mere routine.
David at Parc Spelderholt
Is there a doctor in the house?
In the fall of 2002 was the celebration of the 15th birthday
of the Dutch Down Syndrome Foundation (SDS for short) in the Amsterdam Medical Centre
(AMC). At the very start of it, on the Friday afternoon, primarily meant for professionals,
David would be the first to speak. For months, the three of us fiddled with his
presentation. And at the supreme moment it went all right again. Spread out sitting
behind the computer, in front of the fairly well filled lecture theatre, we wanted
him to have some interaction with his audience right from the start of his presentation,
more or less in a comedian's type of way. (David loves cabaret!) We anticipated
what would happen via the dialogue below. With this type of text we wanted to express
that he was not pitiful and that it was all right to laugh at his presentation.
And, judging from the reaction of the audience, it worked:
- D.: Good afternoon!! I am David. Do you have Down syndrome
as well???
- Audience: much buzzing
- D.: No ??? I was afraid of that!!!
- Audience: laughter
- D.: Is there nobody else with Down syndrome in the audience?
- Audience: yes, here (from the public and set up beforehand!)
- D.: Oh, good!! I thought I was out here totally on my
own. Now, is there a doctor in the audience???
- Audience: cheering
- D.: That's a safe feeling!!
David making his presentation standing up
We then had him draw a parallel between physicians on the
one hand and individuals with Down syndrome on the other. Aren't there many incorrect
stereotypes upheld about both groups? Yes, there are. After making that point, David
asked the professionals present to avoid stereotyping individuals with Down syndrome
any longer. So he proceeded screen by screen with:
'You and I have very much in common! 46 chromosomes!!
I only have one more – that's all. All persons with Down syndrome have one extra
number 21: The smallest chromosome of them all. It's influence can only be very
small!! Therefore it is not people WITH and people WITHOUT Down syndrome. So, it
is not: 'you' as opposed to 'us'. Because there is NO clear boundary between what
they want / like / are able to achieve. They are much more equal than different!!'
And after that very important statement he continued by
explaining how he could do some things less well, and that that aspect was called
'handicap'. Successively he showed how many things he could do well and, consequently,
where he clearly had no handicap at all, e.g. swimming below the surface. Furthermore,
he outlined what had become very normal in 2002 for individuals with Down syndrome,
like good medical care for everybody, a better upbringing at home, more and more
children getting their education in mainstream schools. He came to a close with
the question:
'No more babies with Down syndrome? Yet, our government
wants fewer babies with Down syndrome. Baby in the belly ...... and away with it....
Still a 'you' (pointing towards the audience) as opposed to 'us'? (pointing towards
himself)? I hope that I have made you think .....'
For us as parents it proved extremely thrilling to watch
David in action – loosely making jokes between his 'fixed' (and extensively rehearsed!)
texts, initially clearly a bit nervous – and not being able to intervene. (If we
had done so, in front of the large audience, it would certainly have been to his
disadvantage!) But he did a wonderful job and certainly made people think.
A few weeks later David was invited to give a 'keynote
presentation' at the Dutch Fifth Day of the Child with a Chronic Illness,
and that would be even more thrilling, because an audience elsewhere was expecting
to hear both Marian and myself on that same day. Therefore, David, accompanied by
the present SDS director, Mrs. Jeannet Scholten, travelled to the lecture theatre
near the centre of the country, without either of his parents near at hand. And
as we were told by others, from the organisation as well as from the audience, it
went OK again. A new development was that we had taught David to stand up in front
of the audience instead of remaining seated, as he had done so far.
The Secretary of State
Around that same time our Secretary of State for Welfare,
Mrs. Clemence Ross, announced that she was planning a working visit to be informed
about Down syndrome. She wanted to talk with SDS officials and, much more importantly,
with individuals with Down syndrome themselves. Because she liked the idea of officially
opening the new SDS office outside our own house, where it had been for the first
fifteen years of its existence, 'using' David was obvious again. As his parents,
we knew very well that a spontaneous ad-hoc discussion with him would have a large
(much too large) 'soap' content (he simply digs TV soaps!). So, what better than
asking him to give a presentation about his own life once more? This time a presentation
with far less SDS political content, as had been the case so far. And so it happened.
And it worked again. David liberally varied his text projected in large scale on
the wall and, while doing so, could show very well how his life was organised by
the three of us together and enjoyed by him. He explained the importance of being
able to catch an accurate, local weather forecast in order to determine whether
he could travel to his internship by bike, how he went to school for one day a week
and what kind of difficult language concepts he had to master there to become a
'care assistant', what his hobbies were, etc. While doing so, we were able to illustrate
a fair number of the screens with digital photographs that David had taken himself.
David making his presentation to the Secretary
of State for Welfare
No longer in his native language
All in all, at that stage we had already concluded that
the development from an 'oral presentation with subtitling' towards a computer-presentation
for David had been a very good one. So much so, that we were not afraid of trying
the next step: a presentation like he had given for the Secretary of State, but
this time not in his own native language.
However
Houwewur
I did not write this speech myself.
Aj did not rajt dis spietsj majself
But
But
Many VIP's have their speeches written for them
.....
Mennie Vie Aj Pie's hèf dèr spietsjes rittun for dem ....
And still they know very well what they are talking
about.
En still dee noo verrie wel wot dee aar tokking ehbout.
And so do I!
End so doe ay!
Because of all his (forced) rambling around the Dutch school
system and the loss of time in a very unwilling secondary education scene, David
has had hardly any kind of structured education in a foreign language. However,
he has a keen interest in that, so we attempted to add more or less phonetically
written cues in smaller print underneath the lines of his actual presentation in
English or German. And in the course of time, David learned to read below his original
lines, while we gradually learned how to write these phonetics-adapted-for-David.
That is to say, we had to devise English sentences that were first and foremost
pronounceable for David rather than being 'optimum' English. In addition, using
real phonics would have required David learning quite a number of extra graphemes.
Much too time consuming!
And then the first test happened, notably a presentation
in English at a symposium in Luxembourg. Upon arriving at the theatre he had to
adapt to the fact that his computer was, totally unexpectedly, standing somewhere
amidst his audience and not in front of it and, in addition, he had to hold the
microphone in his own left hand (to be able to operate the mouse with his right
one) instead of having it fixed in front of him. Notwithstanding that, he did it
again and enjoyed very, very much to be able to do so.
Also:
Olso:
I do not speak English.
Aj doe not spiek Inglisj
But:
But:
Many singers sing in English but are unable to speak it!
Menni singers sing in Inglisj but aar uneebul to spiek it!
Modesty
During the development of the English version of the presentation
we deliberately took the time to add two screens to put the entire presentation
as well as David's capabilities in clear perspective (see boxes):
In the meantime, an official invitation for David to present
an updated version of it all at the next World Congress on Down Syndrome in Singapore
has already arrived. This time we're really getting somewhat nervous.