Intro
Hi there! I’m Madison, and I just recently joined the PD Narrative gang. I'm a junior English major here at Ohio University, and I’ve been watching thousands
of YouTube videos this month so you don’t have to. Video seems to be the
favorite form of communication these days, and people with Parkinson’s are no
exception.
1. “Hi, my name is”
These videos are made by regular people, who begin with the dreaded diagnosis story, then move to
“where I am now”--how they came to terms with the disease and learned to
persevere.
Here’s two of the most
popular vlogs. “Popular” usually means a couple hundred views accumulated
over time, but these have significantly more than that.
Which one do you like
more?
2. Promos
These are produced by
prominent research foundations, and usually include basic facts about
Parkinson’s, ending with an appeal for donations.
These videos have titles
like “Face of Parkinson’s” or “____’s Story about Parkinson’s,” which assumes
that people won’t care about Parkinson’s until they can link it to somebody.
The following is a good example of a “collage” video (notice the
juxtaposition of Parkinson’s people with medical experts (in white coats, no
less!)):
The black and white
images and neutral backgrounds, combined with the dramatic music and the
relentlessly inspirational phrases was just too much for me. However, I
understand their intentions: to evoke an emotional response, to get the viewer
to reconsider perceptions of people with Parkinson’s and to create support for
their research.
Here’s an example of a
really interesting and creative promo from the Shake It Up Foundation in
Australia:
3. Celebrity Videos
These are pretty self
explanatory, right? Parkinson's people find it helpful to see hyper-visible celebrities talking about the disease, especially when they have it.
These celebrities include Ben Petrick, Freddie Roach, Jane Asher, Katie Couric, and of course, the ever-present Michael J. Fox. (Because they're celebrities, we figured you could find them on your own.)
Does it make a
difference to you if the celebrity has Parkinson’s or not? Does the video
lose credibility if the celebrity is just a spokesperson for PD?
4. Q&A
Here, doctors talk
straight into the camera--think a video version of WebMD. There’s a wide
range of videos, each focusing on a single issue, so it’s easy to search for an
answer to whatever question you may have.
Which example do you
like best?
5. Creative
As the apprentice video
producer here at the PD Narrative Project, this is my favorite category.
There’s dance, poetry, acting, all kinds of different ways to share their
stories. Instead of just a diagnosis story and a catalogue of symptoms,
these videos tell stories about living with Parkinson’s.
Here a woman with young
onset PD describes how PD changed her daily life and how music keeps her going
when her symptoms get rough:
Here a man uses poetry
and video to tell a story of how his PD symptoms made walking home difficult:
Of course, my ABSOLUTE
FAVORITE videos are our own! (And not just because I helped shoot one!)
We’re going into this project with an awareness of what’s out there:
we’ve spent a lot of time looking at other PD blogs and videos, and we’re figuring
out our place in this digital space. We want to share unheard stories,
and we want to help others tell their stories in imaginative ways.
Final Thoughts
Who knew that
Parkinson’s would be such a popular topic on YouTube! You’d be surprised
at what you can find. At this point I’ve only scraped the surface, and I’m sure
there's more to discover. Let me know in the comments if you’ve
found anything you’d like to share!
Thanks for reading, and
see you on YouTube!
You guys may or may have not come across this blog: http://youngandshaky.com/
ReplyDeleteI thought I'd share in any case: there's an interesting video in there on PD symptoms before-after DBS