From time to time there is an obituary which triggers memories of the past. You never quite know who might in the lists and how far the reports will tell you about how and what they did or why. There are occasions when there is the "I was there" factor, especially in sports when in the crowd. Sometimes there is something more serious.
Mary Warnock
is a a person that I recall in relation to her major report on Special
Education for children in 1978. She also was involved in other reports, notably
on ethics, as well as having a heavy academic schedule. She could cut bad
argument to ribbons in the nicest possible way. The link is to The Guardian
obituary.
After the two
major reorganisations of the early 1970's, Local Government and Health, the new
authorities were faced with stringent central government financial restrictions
as well as having to deal with all the serious problems left behind by the
former ones. In many parts of the country for years small entities, often
inefficient and limited in vision.
In the past had
been that some local authorities and the local medical services saw themselves
almost on different planets with the others as intruding aliens. Across the
country there were local authorities and health authorities who failed to work
together in services for the handicapped and disabled.
But there was
one place, along with some others, which was taking effective action. It was
the Inner London Education Authority, the ILEA, which existed from 1965 to 1990.
The Warnock Report did not invent joint action and thinking, or for that matter
statements, some places already had them in one form or another.
See this
article from 2008 again in the Guardian giving a short summary of the work
it did. For special education it was allied to and worked with some regional
committees for this with an interchange of ideas and experience. It was needed,
because things were going to have to change, politics and admin' or no politics
and admin.
By the 1960's
research, developments in medical practice over a wide field had meant many
born with severe problems were now surviving, not for days or weeks, but for
years and decades. Also, the 1944 Education Act was quite clear. Any child over
five would be educated, how etc. was a matter for the local authorities.
For those with
problems this came to mean at first special schools to which the children would
be transported and serving a wide area. It was expensive but had to be done in
a world of large classes in ordinary schools, in old buildings and limited
facilities. But by the 1970's the drive to build new schools, expansion of
teacher training etc. had changed this.
At the same
time the rate of births dropped meaning many schools now having space to spare.
The parents of the handicapped had become more organised and had come to
dislike the long journeys, long hours etc. involved in special schools some of
which served very wide areas. Those who in effect lost their children to
residential schools would argue that the cost to the authority could be spent
in other ways.
If the local
school could be provided with the staff, teaching and non teaching facilities,
if only on a small scale the handicapped could be taught there and with
ordinary children. They in turn would become used to the handicapped who would
no longer live in another separate world.
Forty years on
from this we are again living in another world. Only we seem less likely to come up with answers.
"She could cut bad argument to ribbons in the nicest possible way."
ReplyDeleteWe still have such people here and there but they do not appear to have the status they should have and are too easily shouted down.
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