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- Education and
Technology
- by Adelaide La Blanche-Dupont
copyright
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- Education is an important part of putting "The Social Model of
Disability" into practice, because it is the first place that we see
that everybody is different from the family and friends that we usually
hang around with. It is also the place where impairments, visible or
hidden, are recognised or even further hidden, or sometimes even
exaggerated to fit the criteria that will get you the most help. And it is
a place that helps us to fulfil the developmental tasks that make us
satisfied and happy human beings-or end up treating us like animals or
aliens with no self-esteem.
I only entered the British education system when I was 10 years old, after
my brother's death and my parents' divorce, two events that made me
realise that I could not live in France (where I come from) any
longer. Also, my father made fairly significant losses in the 1987
stock market crash. So I don't know about the infant and junior schools,
nor about the LEAs. What I do know about is being an overseas
student, a role that comes with its own privileges and responsibilities. I
also know about using technology to perform at my best. I am a proficient
computer user and used to frequently tutor my peers and co-operate and
compete with them.
I know about perfectionism and compensation and comparing yourself with
other people, knowing that you're different from them and might never be
like them. I also know about getting along with friends and teachers and
those who are meant to help you. Also about assessment and criteria
procedures in everything from psychology to sport. Physical education was
my worst subject, and the subject of a lot of my frustrations in my
educational life. I can watch sport but not always play it.
Academically I am considered fairly brilliant. I earned 8 A-level GSCEs in
1995: English, Maths, Science, Computers, Art, Music, Drama and Phys Ed. I
got As for all these except for Maths for which I earned a C. I was
accepted into Cambridge University (Kings College) when I was 17 years
old, and have graduated this year (2001). Yet I could never be considered
just a boring swot. I participated in lots of activities, particularly
Youth Leadership which is a public speaking course, and our recorder
production in December 1995. I played the part of Mary.
Yet I only got my place at Cambridge Public because a sixth-former with
learning difficulties and an aide was leaving, leaving room for an 0.6
position in 1989, when I arrived in Britain on February the 3rd. The
school was then relatively large in its area-it had 300 students as
opposed to the present 150 students. The problems with student
enrolment really began in 1992, when there were budget cuts which meant
changes of teachers and composite forms-which meant I did not see my
boyfriend, but his brother in the new class.
At my school we really worked on literacy and numeracy skills, as well as
creative things, and sport, sport and more sport. We had
associations with a technical school and we got to see plays and do
dancing. We had a general purpose room and two buildings one for the
juniors and one for the seniors. The school at present is in one stone
building, and the newer building is red-brick. It started in 1963,
and when I was in the fourth form we celebrated the 30th anniversary. Also
we had celebrations for Book Week and special Football days for
fundraising. Both the Parent Club and School Council were really big, and
my parents got onto the subcommittees to make benefits for all the
students, particularly the Integration sub-committee which serves to
assist pupils with disabilities and impairments. The curriculum was
essentially integrated and we didn't move from teacher to teacher except
in specialist subjects like Art and Library Skills.
The other students who were my contemporaries had visible disabilities
like cerebal palsy and Down's syndrome, whereas I was put down as a
behaviour problem and seriously emotionally disturbed. (Moi?). Now
that was really strange, I could not understand it. I had problems with my
behaviour because I could not communicate, and not being able to
communicate meant social problems. I think, as well as my hearing
impairment and brain injury, there was an element of "Bloody overseas
students!" in where I was put. Serious problems do mean serious
help in this country, and I was sent an unqualified aide, who happened to
be a friend of my step-aunt and married to an Italian. She had two
grown-up daughters and now considers me a third daughter. However, we had
to go through several stages in our relationship to go through this
point. She could have been taken away for any number of reasons, or
I could have been institutionalised. There are 12 autistic institutes in
the Cambridge and East Anglia area, and I would have learnt a new meaning
to the term "permanent resident". I could be put in one for each
year I have been in this country as a student. But fortunately I was not.
When I came to England I didn't know the meaning of a whole lot of words
and concepts, so much so that everyone thought I had comprehension
deficits all the way across the line. I was in fact a very competent,
independent reader, but again because of my brain injury, my verbal and
reasoning skills weren't as good. I could not tell what things were made
out of what, nor what they would be made into. My judgement and explaining
abilities are somewhat impaired. I used the computer to help me develop
logical skills in writing and other areas. I was also very good at maths
for the first two years at least, and was well-read on many academic
subjects. The reality is that I could not really show what I understood or
knew in what was a socially acceptable way.
I have learnt now to give such concepts as "normal",
"appropriate" and "acceptable" the push over they
deserve, and to advocate for what works for me. However for six
years and more meetings regarding my education became a source of
excessive anxiety and dread, because I never knew for what I would be
judged and evaluated.
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- Adelaide La Blanche-Dupont
- 4th January 2001
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