The Thin Blue Line.

This past week has sped by so quickly for me–as is evident by the fact that I’m writing this on Monday rather than the usual Friday–so I only heard in passing about the incident between a police officer and a high school student in South Carolina, and I only managed to read anything about it yesterday. But I did hear a discussion about a related issue on the radio later in the week, and during this talk, the interviewee discussed the issue of police violence, in particular in relation to persons of colour. Racial prejudice in the police force was something which needed to be addressed, he said.

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The Week Links: in which our blogger does battle with ants.


I have managed to get rid of most of them but oh, how persistent they are. Now, I could understand their wanting to come into the kitchen, where all the food is, and they have indeed been in recently to get crumbs that our Offspring leave on and under the table, and then they leave when I clean up. But then the other night, the Handsome Sidekick and I were about to climb into bed when we discovered our bedroom — where no food is consumed! — was under attack. They had swarmed all over my bedside table and were even on the bed. After almost 45 minutes we got the last of them. Phew, it was a late night.

On that note, I’m off to double-check that all the surfaces in the kitchen are still clean and ant-free. Enjoy the links!

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His and Hers.

This post is late for a number of reasons. First and foremost, though: my laptop began to die on Friday. Of course, it’s 6 weeks out of warranty, which is annoying, but not unexpected. The fan had become so noisy that I couldn’t even work. But it’s a common problem with this kind of laptop, apparently, and the Handsome Sidekick was able to do some internet sleuthing and find a solution. Hooray! Only a couple of days later, I’m able to sit down and work again, albeit to the heady fumes of WD40 (never fear, I’m in a well-ventilated area).

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The Recurring Rove.

Sunday again, and wow, the last day of November. Christmas will be upon us before we know it. Thank goodness I found the advent calendars yesterday. I confess I didn’t win NaNoWriMo this year but I was still busy writing, so in that sense, it’s a win. The other win is some amazing gardening weather, so I’m heading out shortly to pick up some raspberry canes from an acquaintance. I’m so excited about growing my own raspberries!

Of course, the following links have nothing to do with raspberries, but I hope you enjoy them anyway.

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What Were You Expecting?

People often wonder how it was that, despite the fact that Hitler was very clear about his feelings of anti-Semitism in particular and xenophobia in general, he managed to quite legally (if very sneakily using rather questionable loopholes and mass intimidation) become dictator of Germany in the 1930s. We wonder, when we look back, how it was that people were convinced to let him even hold office, when only a few years earlier, he’d tried to overthrow the government.

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Bundles of Joy, With a Focus on the Joy.

Gut reactions are an interesting emotional experience. Sometimes, they’re totally on the mark, like when I hear about a terrible accident somewhere, or when someone has mistreated a child or an animal. But other times, it niggles. I feel a certain way, but then logic gets in the way. I find myself asking what it is that’s making me uncomfortable or angry; I often have to accept that my initial reaction is based on some kind of prejudice or assumption. Once I realise that, I usually feel a bit foolish and vow to be more open-minded, and I am, until the next time when I realise I’m not. I guess we’re all a work in progress.

My gut reaction to this blog post, by Veronica Foale, who has some ‘genetic quirks’ as she likes to put it, was probably one of judgement. Foale has Ehlers Danos Syndrome, which was diagnosed after she had already given birth to her first two children. It was recommended to her that if she were to have any more children, that she pursue the route of IVF so that the embryos could undergo preimplantation genetic diagnosis. Doctors could then determine whether the foetus would have the genetic blueprint for the disease.

Foale did become pregnant with her third baby, and elected not to have the genetic testing. As she points out, her ‘version of EDS doesn’t cause intellectual disability, nor does it decrease life expectancy, and as it is a spectrum disorder, I would have no way of knowing how severe my child’s issues would be (if any) until they were born.’ Foale writes that someone recently made the comment that she should not have had children because she is disabled.

And I suppose, my first thought to that was, ‘yeah, I suppose I agree.’ After all, if someone has a disability which is proven to be hereditary, then isn’t it irresponsible to pass those defective genes onto the next person?  Except… this seems rather draconian. And judgemental. And prejudiced. And makes assumptions on quality of life based on some arbitrary, subjective experience.

As Foale explains:

‘Eugenics is an insidious thing, because in theory, it seems almost sensible. Breeding in order to create desirable traits – surely there’s nothing bad in that?

Until you think about all the amazing flawed people you know, and imagine a world without them here.’


Of course, we don’t think of this kind of attitude as eugenics, or we don’t like to. But it is. We wouldn’t deny an able-bodied woman the choice to pursue a pregnancy, or even the choice to give birth to a baby who was disabled. However, we consider that because a person is disabled, s/he will be unable to parent a child, at least, not without financial or physical help from others. 

This train of thought carries with it a lot of broad assumptions about other people’s lives, and other people’s bodies: that disabled people might require assistance in some aspects of their lives, therefore they should not have autonomy in other parts of their lives; that disabled people are a burden on society because they need financial or physical help; that those in society who aren’t disabled would naturally make better parents.

One of the interesting things about discussing disability is that it can quickly become a focus on what others can’t do, as opposed to what they can. It’s very easy to judge people for not being able to do something we can do, and to make leaps of logic as to what kind of an impact that must make on their lives. But in reality, we can’t imagine what someone else’s life is like, regardless of how able-bodied the other person is. Deciding how well someone might cope really isn’t possible, because while we can make broad assumptions based on basic human needs, each person’s perception and experience of life is unique. We can’t get inside someone else’s head. We can’t imagine how difficult or easy life is for anyone, besides ourselves.

When it comes to children, of course we want the best for them. We want to protect them from harm, from pain. We want to make their lives easier than those of the previous generation. We try to create environments where children will be protected, and so we place emphasis on parents being mentally and physically healthy, and if they don’t measure up to this fairly narrow definition of ‘a good parent’, we can be pretty scathing in our judgement of their perceived failings. We rigorously screen adoptive and foster-parents to attempt to ensure that children who might have had a rough beginning have a better future. But the problem with all this is twofold. First, we can’t control everything. Even if we wanted to, we can’t make life soft and problem-free. We love our children, but sometimes, life is hard for them, and that is the case, whatever their abilities. And second, we can’t plan for every eventuality on a personal level. Two friends of mine were in very successful careers, doing jobs at which they were highly competent. When they got pregnant, both of them suffered from ante-natal depression, and one of them was so depressed after the baby was born, that she needed help everyday. Without it, she told me, she wouldn’t have been able to even get out of bed. And yet, before she had a child, nobody would have doubted her capability to cope.

We make decisions about who should and shouldn’t have children based on what we think we know, or what we think we can predict. But if we start judging who can and can’t reproduce based on the quality of one’s genes, where does it end? Take my own situation: both the Handsome Sidekick and I need to wear glasses (due to an inherited condition). He is colour-blind. My father has a hearing difficulty which developed as a child and which may be hereditary. My paternal grandfather died of heart failure, my paternal grandmother died following a stroke, my maternal grandfather died from complications with Parkinson’s disease. There are other mental and physical health issues in both our family trees. And yet, we have four children, who may have inherited any number of these diseases. I didn’t think twice about these conditions when we decided to plan a family, and nobody has ever asked me whether I’m concerned about my children developing these problems when they’re older.

I understand that this is a very emotive topic.  There is no one-size-fits-all approach.  What’s more, the concept of what is disabled and what is not is in constant flux.  Even ten years ago, we knew far less about conditions such as autism or Alzheimer’s disease than we do now.  Research and advances in medicines and treatments have changed how we engage with these conditions, and our society has had to alter its perceptions, as well.  This is not to say that science is going to attempt to mould us into some kind of bland copy of the person who came before us, but it does mean that we need to become more accepting of the diversity which exists in our community, rather than trying to deny it’s there, or prevent it from coming into being.

I understand that people, when deciding that a disabled person should not become a parent, are really making that decision on what they think it would be like to be disabled and a parent, or what it would be like to parent a child with a disability, or what it would be like to be a child with a disability. I know this last is where my thoughts were, in my first reaction to Foale’s discussion of her third pregnancy. But as I realised, and argued above, each person’s experience is different–that’s what makes us all so interesting! And we are more than just our genes. We are people with personalities, which encompass strengths and weaknesses, and qualities both irresistible and undesirable, and the perception of which are which is highly subjective.

Deciding whether or not to have a child is not a rational, straightforward decision. It’s fraught with emotion and expectations, and the resulting offspring often inspires more of the same. But telling someone that she cannot have a child because you’ve decided she won’t be able to manage, or she will do a poor job as a parent, or she simply isn’t physically up to the task, is not only condescending, it’s mean. Rather than judging, wouldn’t it just be better if we went out of our way to help out parents, regardless of their abilities, because no matter where you’re coming from, it’s hard work. And every parent I know could use a little less ideological postulation, and a little more solidarity. Count me in.