I really enjoyed that this reading focused on a new genre
that has arrived recently in our culture. I had never heard of pathographies
before (and even Microsoft Word doesn’t recognize it as an actual word) but I
really like that it’s transformed into a form of writing where people who
suffer from illnesses can write about the experience in a narrative way. I
thought it was interesting when she talked about how it’s come to be. The fact
that it used to be done privately in journals or diaries but has now made its
way into the public is pretty fascinating. It’s a topic we’ve grown comfortable
with in talking about and reading, and so people are commonly writing about it,
deserving of its own genre.
The way we used to view illness to the way we see it now is also
something worth noting. Because medicine wasn’t as advanced back then as it is
now, people viewed illness as a natural part of life, but because of modern
medicine nowadays, we view it as isolated from the person, something to be
corrected. To use the battle metaphor she so often discusses, a foreign enemy
come to attack the person’s body. “But the person with the disease needs
attention.” (223). Doctors tend to focus on attacking the ailment, curing the
ailment, and forget that there’s a person underneath. “Disease can be treated
and in some cases even cured; people, though, require healing.” (223). And
that’s the fascinating thing that pathographies do, they place the person at
the center of the discussion. The person writes their interpretation of the
experience rather than just simply recording it. They see their self as a
capacity for change (not just in how the illness is affecting them and altering
them) but in how they respond to it. This transformative self, or the
self-in-process as Rogers stated form the other reading, helps in that healing,
as does the whole genre of pathographies.
Hawkins’s essay mainly focuses on physical illnesses, but I
think it’s important to look at mental ones as well, especially when thinking
about healing. I think it’s kind of scary the statistics of college students
that will suffer from/already live with a mental illness, and it’s not
something widely discussed throughout our campus. In fact, it’s not really
talked about at all, and it still receives a negative stigma (take last year’s
fight that CAPS had in trying to get another counselor for the department, it
had to take so much energy and pleading). The influx of students CAPS was
getting also says something: we all are going to struggle with this at some
point or another. Last year was one of the worst semesters I have ever had, and
I was way deep in depression and anxiety, still am too at times. Writing about
it for other classes was extremely helpful for me in remembering that there’s
still a person underneath it. I’m still me underneath it all. Illnesses in
general really do place the focus on the disease, seeing it as not a part of
the person. And that’s part of the stigma, we see it as something that needs to
be fixed for the person to go back to “normal.” We don’t see it as something
that we may now have to live with, something that is now and may be forever a
part of us. We see it as a stranger, I know I did. I was not familiar with it
at all, and it felt so strange for me to experience it then. But I think the
significant thing to note is that, even if it’s something you develop, even if
this illness comes into your life, you’re still the same person underneath, the
only difference is that the illness has coincided with yourself, but it doesn’t
have to define you.
No comments:
Post a Comment