This blog will be on hiatus from today (December 16th) until Friday, January 6th. I'm a spoonie and, with the holidays, I'm finding it severely difficult to keep all cylinders firing. (I will still be on Twitter.) I love this blog, but it's mostly a solo operation.
Before break begins, I want to leave you with a resource page from my personal blog. It lists helpful writing newsletters, free classes, free (legit) ebook sites, and more. I hope you find something of value. CLICK HERE.
Also: The Perch Magazine (an online journal about mental health) will be added to the "Links of Interest" page.
Lastly: Thank all of you for reading/listening. I hope this blog continues to have value for you all.
Have bright holidays, my lovelies.
Friday, December 16, 2016
Friday, December 9, 2016
Interview: Sami Jankins of Tiny Tim Literary Review
Sami Jankins: Editor of the Tiny Tim Literary Review. |
Why did you start Tiny
Tim Literary Review?
I spend a lot of my
time looking for what isn't out there. After college I created a non-profit
that encouraged access to arts programs for teens and young adults with chronic
health problems. Now that I've graduated from graduate school, I
feel like Tiny Tim isn't quite going back to that idea, but instead retooling...and redefining the purpose of how I can
accomplish the encouraging of the arts for people with chronic illness or
disabilities. While the arts is a great means of expression for the disabled
populace, it's not always an entirely welcoming place. I guess I've always
tried to be a bit defiant to naysayers to show that disabled doesn't mean that
we can't create and do awesome things, but we're doing awesome things
regardless - it's not that "it's awesome because someone disabled created
this." This is why I decided to name it Tiny Tim. It's tongue-in-cheek
about the inspirational disabled trope. I want this review to be authentic and
that includes the full spectrum of the human experience. It doesn't just have to
focus on disability narratives, it can be an ancillary aspect to a piece. The
arts are often the only place people are exposed to people not like themselves
and I wanted to provide more visibility for medical and disability narratives.
The more, the better.
How does your
publication differ from other literary magazines focused on disability?
I know some focus on
specific disabilities whereas we are kind of welcoming to anyone. I can speak
about the difference between other health magazines. I've been fortunate to be
published numerous places, but the pieces that were always easiest to place
were on dating or being a twentysomething. A lot of general health-based online
magazines want pieces on how people are overcoming the odds, what they do to
make their disability easier (vitamins, yoga, etc), and there are definitely a
lot of parent narratives about their children who have disabilities. It's easy
to place those types of work. When it comes to a critique on the medical system
or the rawness of how not pretty disability can be, it can be more challenging
to place. What's great is I notice there are other lit magazines popping up
trying reach these groups that don't fall within mainstream neutralized
disability stories, and that's awesome! I've seen great work get rejected
because an editor couldn't understand the structure of a piece from someone who
is neurodivergent. Those aren't the kinds of things that should be altered. I
think those are the works that are the most exciting. Why are we trying to fit
everyone into the same literary box just because it's different? I think other
places are catching on, but mostly when I started this I noticed a lot of
people asking questions of where to place work that I wanted to see read by as
many people as possible.
Medical professionals
will also have a place within your publication. What factors were behind
that decision?
Yes! I'm very excited
about this. I wanted to create a duality in the spectrum of health, disability,
and overall medical narratives. I was always very interested in books by Atul
Gawande or Oliver Sacks. It was unique for me as a patient to read the flipside
of the experience. Since a patient journey can be frustrating, it can be easy
to assume that doctors are either these gifts or roadblocks in our lives. It's
easy to forget they are fallible humans too who have a great deal of
responsibility upon them. I researched a lot of film and TV portrayals of
doctors in graduate school that really illuminated the aspect that medical
professionals as a whole are also so often reduced in public portrayal. Again,
if people assume all medical professionals are like what they see in movies,
it's rather reductive. Reading Paul Kalanithi's memoir at the end of my MFA
program solidified for me that there is a great need for the full medical
experience to be included in the entire range
of the health narrative spectrum.
I hope poetry from a patient perspective juxtaposed to a nonfiction piece by a
nurse will help destigmatize the disability aspect while humanizing the
sometimes sterile view of those practicing medicine.
What does your ideal
submission look like and do submissions have to have a disability-related
element?
The submission does
need to have some tie to disability, health, medicine, mortality, etc. Again,
the health aspect doesn't need to be the main element. There isn't really a
specific ideal submission. I hope to include pieces that may have unique
structure to them. Above and beyond it just needs to be solid work. I'm looking
for work that people put their hearts into. By no means do the stories have to
have a specific message to convey or somehow be wrapped up in a bow. There
doesn't need to be a moral to the story because sometimes those moments just
don't work out that way in real life. Authenticity and heart are the two big important
factors. While we do light editing, we want pieces that are generally complete
without much need for further input. We're looking for writers who have an
opinion and something to say. Passion tends to shine through.
Do submitters have to
disclose disability/neurodivergence status in the cover letter or
biography? Why or why not?
No. Again, we're also
including medical professionals who may not have any kind of disability. Who am
I to ask what someone's disability is? I've had people ask along with their
submissions if they are disabled enough to be included. This generally makes me
sad. I wonder who made them question that in the first place, and I'm not sure
how I became the authority on disabled enough. We accept submissions that will
get published under anonymous as well as a pseudonym. These are topics that can
be challenging to write about, in order for it to see
daylight, there needs to be
anonymity to go with it, that's perfectly alright. Just frankly it's not my
business what their health status is beyond what they wish to disclose. I want
people to feel safe to submit great work. This isn't like applying for a job
where the options are yes (you're disabled), no (you're not disabled or you're
just saying you're not), or prefer not to disclose (maybe disabled?). It's not
a trap. These are sensitive topics and we appreciate that.
Who are writers
(disabled/neurodivergent and not) you admire?
I guess this is my mix
of writers who have inspired me disabled or not. When I was in my senior year
of college, I saw Spalding Gray:Stories Left to Tell. It changed
everything for me. I never wrote actively before seeing that. I didn't realize
that I could write in a way that could be so conversational. It spoke to me.
Before starting graduate school I read a lot of Jonathan Ames. I'm also a huge
fan of his screenwriting. Screenwriting is what I went to graduate school for
and found Stephen Falk's attention to getting the details of mental health
issues right more important than whether the viewer would continue to
categorize his show You're the Worst as "funny
enough" a bold thing to do.
Emily Rapp Black was
my professor for non-fiction throughout graduate school and has taught me a
great deal about essay writing. Her essays are also some of the best I've read.
Instead of just looking as an essay as something flat, I began to see the
intricate weaving between dialogue, imported knowledge, description, and
exposition that needs to take place. Writing started to feel almost like
painting to me after a while, a delicate balance of many things. I hope to be
as good of a writer as her someday. Karrie Higgins is one of the most
outstanding and outspoken disability advocates that I feel more people should
be paying attention to. Her writing is arranged in non-typical formats because
that's just how her brain works, and it's an amazing brain at that. Her photos
are equally effective and moving. I find Jillian Lauren's writing to be
exceptionally raw and candid. I know that's not an easy thing to do, and
reading her work and hearing her speak has pushed me to write outside of my
comfort zone. Lastly Jennifer Pastiloff and her entire Manifest-Station, Girl
Power You Are Enough, and other movements have been hugely influential to
me.
Where do you see Tiny
Tim Literary Review five years down the road?
I'd like to gradually
expand beyond the the online presence and be more interactive with writers and
the health community. I would like to hold workshops for medical professionals
and disabled individuals to attend to work on finding their voice. Everyone has
a story, it's just a matter of finding it and feeling like you have the right
to own it and tell it. I also want to find a way to get audiobooks and books
available for patients in the hospital. I know that stories were everything for
me during my lengthy hospital stays whether in book or other creative format.
However, unless a patient brings something with them they may not have access
to that escape of sorts. I know some hospitals have general libraries for
medical literature, but I think there is something worthwhile to having patient
libraries, even if they are small. Long-term patients especially would benefit
a great deal from it, and I'd like to help make that happen however possible
with whatever medical facilities are interested. Provide access to stories,
encourage the realization and power behind their own story, and hopefully have
more people wanting to share their work.
What advice can you
give to someone hoping to get accepted into your magazine?
I know how frustrating
the process can be. Truthfully, we were only able to accept about 10% of the
submissions we received. I encourage people to keep writing. Even if a specific
piece didn't work for us, it might be placed elsewhere. Also, always submit for
the future. I never want someone to feel defeated by a rejection. You don't
have to be at a certain level to submit and get accepted. We have everyone from
college students to professors to beekeepers. Write what speaks true to you.
That's probably the best advice I can give.
Is there anything else
you want people to know about you or Tiny Tim Literary Review?
I wanted Tiny Tim
Literary Review to fill a void that I saw within the writing community. There's
been a longstanding failure of including the disabled community or caring if
disabled characters were even accurately portrayed. I hope this review acts as
a branch of sorts. Who better to address how disabled individuals or health
professionals are portrayed than the people themselves? As for me, I've spent a
lot of time doing patient advocacy and being involved in a variety of patient
communities. I'm also disabled. I've been told in my life that the arts aren't
possible for people with disabilities. Idina Menzel was my "kid's
wish" almost a decade ago. She told me if you can't find a niche for
yourself within the arts, make one. It's something I've continued to try to do.
While I do love publishing work of my own, I also like having outlets that work
to encourage other people to share their stories as well. I hope that any
accolades or praise that may come as a result of Tiny Tim is for the incredible
writers whose work is being made available. I'm happy to take a backseat and
let them shine.
~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*
Sami Jankins, Editor-in-chief and Founder of
Tiny Tim Literary Review says: “We can
be found at https://www.facebook.com/tinyt imliteraryreview/ and come
mid-December our website will launch with the first on-line issue at www.tinytimliteraryreview.com. Submissions reopen on December 5th and close February 19th for our mid-March issue”.
~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*
In the first issue they have:
*Multiple Pushcart prize nominees, Fulbright
scholars, Yaddo fellows, and individuals that if you like their work enough you
can buy their already published books.
*Appeared in The Bellevue Review, The Boston Review, Jezebel, Broadly, The Fem,
Wordgathering, and Deaf Poets Society (along with so many other places).
*College students, MFA candidates, college professors, editors for other reviews, doctors, and beekeepers who manage one of the oldest rare/used bookstores in DC.
*College students, MFA candidates, college professors, editors for other reviews, doctors, and beekeepers who manage one of the oldest rare/used bookstores in DC.
Friday, December 2, 2016
How We Write About Ourselves
I've gotten flack for referring to myself as a cripple. I don't understand disabled people who prefer the term "differently abled", but wouldn't want them to stop using what terms they identify with. "Disabled" is a decent standby word.
No one should force anyone else to use a specific term for themselves. If you fall under a certain umbrella of words/terms/phrases, you should be able to use any that apply. It means not taking crap over whatever people think is best. You know what you like.
People who aren't disabled can't generally use the words you choose. The umbrella of a minority group offers the protection to claim the words those outside will never have, even as an ally. A stranger shouting "cripple" at me on the sidewalk is a jerk, no matter how many times I've said it of myself.
~*~*~*~*~*~*~*~*~*~
Disabled/neurodivergent writers are often policed for how we write about ourselves. Not for just how we identify, but the topics we do (or don't) cover and what the slant is.
The surprising thing I'm seeing, is a fair amount of people criticising disabled/neurodivergent writers, are other disabled/neurodivergent people. They aren't taking writers to task about inaccuracy or cardboard portrayals. They aren't boycotting a disabled Jojo Moyes. They are tearing down phrasing that isn't problematic, criticising how authors (legally, without spam) market their books, what topics are covered... because of what an able-bodied/neurotypical audience is going to think.
While a few rare instances might have a bit of merit (like leveraging disability the wrong way for sales) most do not. We have become scared to let them (the majority) see inside the iron box of our lives and truths, the secret spots where it is vulnerable... or the fierce, barbed pieces. We want our tales to garner attention (only a specific kind) then have them stroll away, satisfied by what they glimpsed.
I understand writers pandering to a market and watering down the hard parts. I understand problematic portrayals giving people the wrong notion, and the disabled readers who won't put up with shoddy literature... from any writer. I don't understand the need to hide when it isn't your story, to bash what is thoughtful and complex, honest and raw.
Fight when you need to, but figure out why you're fighting. The opponent might not be who (or what) you're expecting.
Write (and read) on, my lovelies!
No one should force anyone else to use a specific term for themselves. If you fall under a certain umbrella of words/terms/phrases, you should be able to use any that apply. It means not taking crap over whatever people think is best. You know what you like.
People who aren't disabled can't generally use the words you choose. The umbrella of a minority group offers the protection to claim the words those outside will never have, even as an ally. A stranger shouting "cripple" at me on the sidewalk is a jerk, no matter how many times I've said it of myself.
~*~*~*~*~*~*~*~*~*~
Disabled/neurodivergent writers are often policed for how we write about ourselves. Not for just how we identify, but the topics we do (or don't) cover and what the slant is.
The surprising thing I'm seeing, is a fair amount of people criticising disabled/neurodivergent writers, are other disabled/neurodivergent people. They aren't taking writers to task about inaccuracy or cardboard portrayals. They aren't boycotting a disabled Jojo Moyes. They are tearing down phrasing that isn't problematic, criticising how authors (legally, without spam) market their books, what topics are covered... because of what an able-bodied/neurotypical audience is going to think.
While a few rare instances might have a bit of merit (like leveraging disability the wrong way for sales) most do not. We have become scared to let them (the majority) see inside the iron box of our lives and truths, the secret spots where it is vulnerable... or the fierce, barbed pieces. We want our tales to garner attention (only a specific kind) then have them stroll away, satisfied by what they glimpsed.
I understand writers pandering to a market and watering down the hard parts. I understand problematic portrayals giving people the wrong notion, and the disabled readers who won't put up with shoddy literature... from any writer. I don't understand the need to hide when it isn't your story, to bash what is thoughtful and complex, honest and raw.
Fight when you need to, but figure out why you're fighting. The opponent might not be who (or what) you're expecting.
Write (and read) on, my lovelies!