This week I am not going to talk about myself but about my
friends Sue and Paul and their daughter Eliza (obviously, not their real
names). And for once I'm going to post
this simultaneously on both my blogs because I know different people read them.
Eliza, a couple of years younger than my daughter Julie, has her
father's height and her mother's dark good looks, likes films and train rides,
and is also nonverbal and severely autistic.
In parenting terms, this means that Sue and Paul have been dealt quite a
difficult hand, but they have accepted this challenge and developed their own
ways of managing her condition. And the
remarkable thing is, that though their life is necessarily different because of
Eliza's autism, Sue and Paul don't let this define them. They are a joy to visit, very attentive to
guests, funny, observant and generous.
Paul still manages to work outside the home, they live in a wonderful
(if anarchic) old farmhouse, and they still make time for Eliza's younger
brother. And they have often been
extremely kind to my daughter Julie, going out of their way to help her see
that there is a good life to be had out there beyond her own immediate troubles.
Julie and Eliza were thrown together at school. Our local authority, lacking any specialist
provision for autistic children, arranged for Eliza to attend mainstream
school, where an entire team of adults was employed solely to supervise
her. In practice Eliza, like Julie, was
mostly unable to attend mainstream classes, and so was largely confined to The
Centre, a tiny (and cramped) in-school unit, catering for all ages and
disabilities. Some of Julie's friends
were registered blind, some were in wheelchairs, one had cancer, some had
learning disabilities, and Eliza had autism.
Eliza might not speak very much, but the girls struck up a quirky
sort of friendship. After so much adult
supervision, Eliza clearly preferred the company of someone her own age, and
revealed an unexpected sense of humour.
It was a natural step for us to start visiting her at home, where I
would enjoy a cup of tea with Sue while the girls bounced on the trampoline
together, Eliza shrieking with pleasure.
The story of how Eliza came to leave school and end up out of
education altogether is a story in itself, but all I will say here is that Eliza developed epilepsy,
and didn't tolerate the drugs given to control her seizures very well. It was too much for the school: she was sent home. Sue and Paul coped, and educated
Eliza as best they could themselves - because after all what else could they do?
But the physical illnesses meant regular trips to hospitals, and
trips to hospitals with autistic children often entail some friction. Sue phoned me out of the
blue last week, desperate: Eliza had been taken ill, they were at the local
hospital, but Eliza, distressed by the wait, the lights, the noises and her
assessment, was trying to leave, and the staff wanted to have her sectioned. This is the English term for being detained
under the Mental Health Act. She phoned
me because she guessed (rightly) that I had some acquaintance with this
process. A psychiatric assessment team
had been called, and they would have the power to detain Eliza, probably in a
mental hospital, and give her treatment against her will (one could guess this
would involve sedation).
I have some acquaintance with the Mental Health Act, but not much
that was relevant to Sue. For someone
like Julie it is better to avoid sectioning if you can: once you have been
detained involuntarily, you can then be legally discriminated against for the
rest of your life. We have always
avoided the curse of sectioning so far by simply consenting to treatment. When Julie was Eliza's age (underage) we
consented for her. You can do this with a clear conscience of course if you
already think this treatment is in the best interests of your child.
It was only when I hastily looked up the Mental Health Act for
Sue following her phone call that I even realised that it applied to people
like Eliza. Eliza is not mentally ill
(as far as I know), but she could be categorised as having a mental
disorder. If you have a learning
disability, you can be sectioned if your disability is "associated with abnormally aggressive or
seriously irresponsible conduct".
I feel ashamed not to have realised this, despite following Sara Ryan's blog, which last year described her son going through exactly this process. This puts Sue in a very different situation
from the one that I faced with Julie. My
daughter was distressed and heading for mental hospital anyway: I could
consent. But Sue's daughter is autistic,
she does not belong in a mental hospital.
It is not in her best interests to be separated from her family. And I did not dare tell Sue that once in
mental hospital, Eliza's sedation and restraint would be almost
inevitable. After our experience of
local mental hospitals, I cannot see what alternatives they would have, when
faced with the arrival of a traumatised and highly distressed Eliza on a Friday
night.
Now this story does have a happy ending. To our great relief,
common sense did prevail for Eliza.
Although the regular hospital staff clearly felt out of their depth in
dealing with her, once the psychiatric assessment team finally arrived (many
excruciating hours later), they quickly recognised Eliza's condition and
rejected their request to have her sectioned.
Their job was then to persuade the regular staff to attempt to treat her
again, making allowances for her autism, and her high stress levels. How they managed to persuade them to do this
must be one of their professional mysteries.
It is a nonsense and an abuse for us to threaten autistic people
like Eliza and their families with sectioning because she does not conform to our
rules of behaviour. We are not Victorians, and detention of autistic people is
barbaric. We know a good deal now about
how autistic people experience the world, the difficulties they have in
adapting to it, and why they might behave in ways that we find inconvenient as
a result. Tearing Eliza from her close
and supportive family, and moving her to a new place with unfamiliar people
would have been the worst of all possible decisions.
Thank goodness the psychiatric team agreed. But they should not have been faced with the
decision. The Mental Health Act should not be available
for use in these circumstances.

I totally agree and my heart goes out to Eliza and her family.
ReplyDeleteThanks for sharing.
J xxx
Thanks Joy, I'm just so glad the story had a happy ending. I was really upset at the thought of Eliza being shut up.
DeleteVery well said, and what an horrendous experience for Eliza and her family xx
ReplyDeleteIt was truly horrible - just when they were already trying to cope with her illness. Really hit me how vulnerable they were to an abuse of authority.
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