Skip to main content

HAWMC Day 15: My Writing Style

Today, I'm talking about my writing process. How do my blog posts get from my head onto the internet? Well, most of the work comes before I actually sit down to write a post. I sometimes spend insane amounts of time thinking about a blog post before it actually ends up here for you all to read. The most recent example of this has been my Why I Named My Colon post. That one had been rolling around in my head since sometime in February. I'm not exactly sure why it took so long to actually write down. I think because it's such a funny thing to talk about, naming an organ, and yet it really had such a profound impact on my life. I wanted to make sure I was talking about it in a way that underscored the importance of this ultimately pretty silly thing that I did.

Other times, the reason it takes me so long is because I want to make absolutely sure I'm coming at the subject in the right way. This was the case with my post about pep talks. That post could have so easily been an accusation. "Why do you say these things?! I hate that! Stop it now!!" Not only is that completely off putting and unhelpful, it was not what I wanted to say at all. Part of talking about Crohn's is learning how to speak about the experience effectively, and I would never want to attack someone for trying to broach the subject. I may try to figure out a way to reframe some of their comments so that a more constructive conversation can take place, but no one wins if we just shut people down every time they say something we don't particularly care for.

After I've done the hard work of figuring out the topic and the language I want to use to speak about it, the actual writing is usually pretty smooth sailing. I mostly just write it, edit it, and post it. That seems a little anti-climactic, but the truth is that most of the really tough work takes place in my head before I even sit down at my computer. So when I do finally go to write a post, I just type it up. I mean, I'm not saying I don't edit. I absolutely edit. I love editing. But that's all relatively easy compared to the prep work.

As far as my actual writing style goes, I think that what I've said already pretty much covers it. I'm trying to find effective ways of talking about a really complicated subject. So, I try to make my writing as accessible and conversational as possible. I pretty much write the way I talk. Or, at least, the way I would talk if I could edit myself as a spoke. I'm just trying to have a conversation about something that doesn't normally get talked about, and I hope my writing reflects that.

Comments

Popular posts from this blog

Exciting News!!

Alright folks, something really and truly exciting is in the works over here. I've been asked to contribute to this really awesome new channel that will center solely around Crohn's Disease. WEGO Health  is this really amazing online community and they're currently launching a series of channels that deal with different diseases/illnesses/ect. For those of you who aren’t familiar with WEGO Health, they’re a different kind of social media company – with a mission to empower the top 10% of online health social media contributors to connect with one another and with healthcare companies. They call those folks Health Activists – but they’re people like me and you who are community leaders, bloggers, on Facebook, on Twitter, leading online forums, and usually “all of the above.” As part of their mission, WEGO Health has recently launched a new Health Activist video platform called WEGOHealth.tv where they are presenting the authentic voice of the online community in the form...

HAWMC Day 2: The Quote(s) That Changed My Life

I've been thinking about this a lot recently. How, in my life, there are a series of identifiable moments when someone said something and it opened up the world in an entirely new way. These are often called "aha moments" in the feminist community. I've had a lot of these moments. Not all of them have been these incredible moments of clarity that allow me to better identify and speak about the injustices of the world, many of them have been much more personal. Instead of these sweeping realizations, they are slight awakenings. This does not mean that they have had a smaller impact, however. In fact, I think these  moments, more than the grand moments, change the way I live my everyday life. I've had a few of these moments in relation to Crohn's, and I know I'm bending the prompt (to pick a quote and write about it) a little bit here, but I'm having a hard time choosing which of these moments was more important to developing my understanding of what...

I'm My Own Woman! But could I get a little help...

I went to this panel/performance at Access Living  last Friday. It was on the intersections between disability, race and community. Very interesting. There was one thing that the moderator said, though, that really struck me. It's something I've read and taken note of before, but for some reason hearing it in this context really drove the point home. He made the point that disability and disease challenge the idea of "the individual." In American society, we're pretty much taught to take care of ourselves. Individualism is extremely important to the way we conceptualize our bodies and our minds. The "I" is at the center of the American dream. If I work hard and educate myself, I can rise through the ranks of society. So, what happens to this concept when a body must depend on others to perform certain tasks, or even to make it through the day? This is more of an issue for some types of disability than others. With Crohn's, for instance, as long a...