[Note: this is an old reflective journal entry, but I'm not able to find a Blogger option to backdate it - still, it makes for interesting reading now more than two years on from the start of this whole odyssey, and especially with my last post in mind... - CL]
Wed 12 Mar 2014
So this is the first entry in what I hope will be a
regularly kept, private journal of my thoughts, experiences, epiphanies,
regrets, and joys relating to my postgraduate research. I’m aware I was about
to write ‘my PhD research’ there, but as confident as I have been in recent
months about where this is all going, the sheer volume of work and the
complexity of some of the issues I’ll have to untangle make me think…. Nope,
let’s wait a second before I unthinkingly say to myself. ‘A PhD is what I’m
getting out of this’.
So. My research.
I guess in a way it really all started in earnest yesterday,
after meeting the Director of TEaching and Learning to discuss some very brief technicalities. Upon
hearing I would be expected to put in a LOT of hours a week of work, I
had a little panic attack – fearing overspill of it all into work, affecting
income, and personal life, affecting relationship and physical well being – and
it wasn’t until I’d timetabled it all out for myself that I calmed down. Yeah,
it was possible. I almost didn’t to think about giving up any work at all! Mind
you, it also meant one weekend day gone, sacrifices to study. Plus, nearly
every weekday evening holed up in the study (now finally becoming a ‘study’).
But, it was feasible. And it wouldn’t bankrupt me, plus, my partner has been
amazingly supportive.
So after that little kick, and the realization that almost
every spare second I would need to be doing something, I popped into TCD
library and took out six books, most relating to disability research and how to
‘do’ it. A lot of Mike Oliver, Barnes and Campbell. And I was dreading it, in a
way, because I envisaged a lot of blank staring at pages as concepts failed to
deliver themselves to my easily distracted brain.
Instead, I was on fire! I’d decided to look specifically at
issues relating to reflexivity and research production; I decided if I was
going to tout myself as carrying out ‘emancipatory research’ then I might as
well know what the hell it meant. And in my readings I realized there was so,
so much to draw on here, so much
relevance to myself. (I haven’t quite worked out the thorny relationship
between disability research and Deaf historical research – indeed, the whole
social science–history overlap or opposition – but this stuff jumped out at me.)
Power, power, power. I’m so much more comfortable with that
term than privilege, though of course they no doubt refer to vastly different
concepts. But It was very enlightening to think, really think hard, and
critically, about not just how I intend to proceed with this, but what I have
done so far. I’ve tended to see the last few years as beginning with a lot of
reflection and consultation followed by progress and success. But. To what
extent did I consult? Or think?
There are numerous traps to be fallen into, and just because
I haven’t been caught in a pit by any hunters, doesn’t mean I haven’t fallen
prey. Yes, I have avoided – have gone to lengths to avoid – secrecy or hoarding
of sources, I’ve tried to avoid definitive interpretations in how I present
material… but don’t I still fall into the Saviour trap? ‘Hey, I’ve found out
all this info that you didn’t know – now let me tell you about it all!’ There’s
real power in that.
I’ve thought a good bit about ‘native’ Irish Deaf
historians, their profile and the ways in which they disseminate findings, and
realized that young, tech-savvy and adaptive as I am, I have huge advantages in
getting my message out to the Deaf community … over Deaf
historians.
And I’m an interpreter. Not just a hearing person
good at sign. I’ve been privy to, and privileged to be at, countless intimate
discussions, major meetings of decision makers, and occasions where Deaf people
recount their memories, their experiences, their cultural selves. Nine years of
that incidental but nonetheless intensive information-gathering has resulted in
what I see now as being in the nature of a huge cultural resource. I know
Deaf people have gone through this stuff. I know how it manifested itself, I
know about the atmosphere in the schools and how it can be remembered fondly
and with horror. I’ve seen stories about
what it was like to be a boarder, or to arrive as a small child in the pre-oral
days to be confronted by tall, strange, intimidating black-clad figures moving
their hands. I’ve seen those stories, but I’ve also seen more of them by
virtue of my occupation, and not only that – I’ve become those stories,
empathized with them simply through voicing them. I come away from those nine
years and yes, it’s contributed to a pretty good level of ISL in terms of
storytelling and community networks, but it is nonetheless something I have
gained through working in the Deaf community. It is a benefit that I’ve got
from my job, that I cannot but utilize and exploit in my research.
Again, I have that power. I have the use of resources here that other hearing
researchers do not. So while few enough people would quibble with using this as
a research resource in this field, the responsibility is huge. This is what I
have been given, this is what I have.
Again, Oliver’s point about emancipatory research is worth
bearing in mind. I cannot emancipate Deaf people. Deaf people must, by Oliver’s
definition, emancipate themselves. The very best I can do is assist that
process.
But, really and truly, HONESTLY – how will this thesis, this
process, really help to do that?
Thankfully. Trickles of answers have begun to come from
discussion with Deaf colleagues, who really need to be where I get a lot of my
inspiration. My colleague Teresa Lynch’s notion, which I’ve already considered, of this research
creating the potential for new cultural resources. If new narratives are
uncovered, then the Deaf community can utilize them in any fashion they can –
drama, poetry, writing…
I guess in a way it boils down to ‘how this will benefit the
Deaf community’. What I really need to be doing is thinking, what benefits can
I bring that change things so that the next big shift in Irish Deaf
historiography doesn’t come from another hearing person… How can I change the
system?
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