Friday, August 28, 2020

Deaf Girl Reviews Music: Yote Magus by Su Zi

Image:  A carved, block print of a standing person with wings. They are blue with raised arms. To the left of the print are the artist's tools.

We were told to stay home.

As we turned even more to our communication devices, our cloudy realities, the concerts and festivals came within reach—we saw performances by artists who were, like us, too at home—there was art and music and models catwalking their kitchens. Somehow the algorithms shifted, and it was easier to find the outsiders, those few in followers who also showed their art, had been showing their art. From a graphic perspective, Instagram presents art in a way that is artist-viewing friendly, and there’s always the hope to see a dress or some pottery that lifts us for a moment. It was in searching for interesting printmaking, that so there appeared a printmaker whose work was consistently stunning: vibrant and sensual, technically perfect—Yote Magus.

When art is encountered online, the experience is compressed by the presentation features of the device; we lose scale, and our experience is with the kernel of the idea and the physical perception of it. The printmaking presented by Yote Magus was so visually forceful that the experience of it as a handheld image did not diminish a perceptible power. In following this account, viewers were treated to not only printmaking process videos, but also animation shorts, and finally, a dancing skeleton video that was a short for a full musical composition, “Really, Bitch”.

Beginning with a tom-tom beat and a whisper, the single vocalist relates a narrative of betrayal; however, rhyme is not rigid in the lyrical construct, it is used as a highlight to the narrative, as in “rain/gold chain”. The song itself is an interplay of layered rhythms, much in the way that the artist layers colors in his prints. In the song’s circumstance, the percussion beat emphasizes both the tom-tom downstroke, and a top hat emphasis on all but the second beat, in the standard tetrameter (4/4)—which is then layered with the whispered narrative. The music progresses alongside the narrative, until the two become entwined on the chorus phrase “really, bitch”. From a metrical perspective, this phrase is a construct of three syllables in a Stressed-Unstressed-Stressed pattern that might be notated as either half-notes or as an amphimacer, an atypical construction. Towards the song’s last minute, the chorus shifts and becomes “something”, a more common trochaic construction of two beats, with the first as foremost. And while the lyrical construct of the song provides a storyline where the emotion is refreshingly perceived (as opposed to the too common fatigue brought by fashionable, emotional yammering), it’s the insistence on the entwined meter that makes this song so replayable: it’s a danceable beat.  The metrics of the song encourage a salsa step that is both subtle and potent, the listener becomes participatory, the whispered voice becomes an incantation.

When we find something striking, resonant, there is the sigh of pleasure, and then we look to see “Who Made This?”. More academic minds are easily satisfied by a research of authorship that may strike others as a snobby form of “Who’s Your Daddy?”. Nonetheless, although “Really, Bitch” appears to be the solo offering of Yote Magus on Apple iTunes, the Instagram account yields a searchable name and the appearance of the artist on other platforms. We discover that the artist is Peruvian, has followers, follows hashtags of hawk tattoos, but consistently posts work that is visually and acoustically captivating.

For those of us who are Staying Home, for whom certain of our limited joys Outside no longer exist, finding the unusual online is a focused aspect of our lives. It is now dangerous for us to fling ourselves into the contaminated throng, and so the online art we can find becomes crucial. And despite the iconic horror symbols and mythological imagery Yote Magus employs in his prints, the lyrics of “Really, Bitch” are as current as the 2020 copyright, as current of that of a thieving drug addict and of a life that is far too street for staying at home, if there is a home. And in our homes thousands of miles away, we find a music that is almost cheerful in rhythm, decidedly danceable, despite a gritty reality portrayed in the lyrics. And in this we find a gift—the luxury of finding an artist , and doing so from a point of relative safety.

~*~
Su Zi is a poet/writer and artist/printmaker and edits, designs and constructs the eco-feminist poetry chapbook series Red Mare
Publications include poetry, essays, stories and reviews that date back to pre-cyber publishing, including when Exquisite Corpse was a vertical print publication, and a few editions of New American Writing. More recent publications include Red FezAlien Buddha and Thrice. A resident of the Ocala National Forest, with a dedicated commitment to providing a safe feeding respite for wild birds, and for a haphazard gardening practice that serves as a life model for all aspects of her work.

Friday, August 21, 2020

Fog by Joshua P. Sorensen

Phantom pain! or is it real?
I should know... I do know this.
So simple, like swimming.
Swimming through mud.
Hands quiver.
Medicine helps that.
No drug clears the fog.
The easy, the difficult, the now unreachable.
I slap my head.
Fails to clear the mind.
Somehow?
Makes me feel better.
Expectation management
The key to my survival.
I am not what I was,
But I am still great.

Maybe, I’ll just stay in today
~*~
Biography:  Joshua P. Sorensen is from Orem, Utah (United States).  He graduated with a Masters of Military History from Norwich University. His extensive travels inspire him to write poetry and short fiction. Drawn to horror writing, he particularly enjoys writing monster fiction. His other loves include history, nature, and all things geek. Joshua’s current life goal is to bring delightful chills to all ages, particularly the young. His children’s picture books are available online or at your favorite bookseller. He is a member of the HWA and LUW. He can be found on Facebook: #SorensenVagabondWriter and Amazon: amazon.com/author/joshuapsorensen

Friday, August 14, 2020

Me at My Most Vulnerable by Lisa Jones

I want to hide within myself
Away from everyone and everything
Voices natter inside my head
Feelings swell
Insecurities rise
I don’t know how to control them
A blinding fear overtakes
Flutters in my chest
Brings tears to eyes
A croak in my voice
I’m afraid to make too much noise
Others will hear
See the real me
The one with a degenerative illness
The one who is weak
Has been abandoned
Despite all she gave
The one who feels unloved
Even though all she wants is to be loved
This is me
Me at my most vulnerable
~*~
Biography:  Lisa Jones writes poetry as a form of therapy. She lives in Ontario, Canada.

Friday, July 31, 2020

Spazzy Crafter Introduces Herself

I have spastic cerebral palsy which affects the left side of my body. I love to craft, so finding ways to adapt or adjust how I make crafts has been an interesting experience.

I have become a serious crafter in the last decade.

Crafts I am able to do with adaptation or assistance:
  • Card making
  • Diamond Dotz (Diamond Paintings)
  • Plastic canvas
  • Friendship bracelets
  • Ceramic painting
  • Loom knitting
  • Stamped cross stitch
  • Needlepoint
  • Beadwork (earrings/necklaces/bracelets)
In upcoming posts, I will be discussing each of these crafts, how I adapt them, and other adjacent topics. I will also be discussing crafts that I am not able do along with those I would like to try.

Does anyone have any crafting recommendations?

Yours truly,

Spazzy crafter

Friday, July 24, 2020

Market Updates for July 2020

Magazines, Websites, Etc. (for Us)

Blanket Sea is on hiatus.
Barking Sycamores has a new home.
The Pen 2 Paper Contest now has an entry fee of $5.00 USD.
Fixed Monstering's submission link.

Removed:

Quiet Storm
CORRIDORS
These Pills Don't Come in My Skin Tone

Added:

The Barbellion Prize
Disabled and Inter-Abled Relationships
Red Rover Magazine
It's Real
Réapparition Journal
Serotonin
First-Person Presence 

Inclusive Mainstream Publications

Lockjaw is on hiatus.
Updated the submission link for Dancing Girl Press.

Removed:

The Establishment 
The Mondegreen 
Crab Fat Magazine 
Polychrome Ink 
Synaesthesia 
Brine Literary  

Added:

Sparks of Calliope
Night Music Journal
Suddenly, and Without Warning
Nebo

Friday, July 10, 2020

Dyslexia Runs in Families by Karen Downs-Barton

Light slants into the scullery kitchen
where I am looking at pictures in comics.

Tripe is bubbling in a battered saucepan
while in a Pyrex jar an onion cools in white liquor.

Bapo has rocked back on his one good chair,
balanced between floating and falling.

His newspaper is a curtain concealing his face;
he might be sleeping or pretending, like I am.

I look at the smudged lines of old print,
his earthy fingers supporting the pages.

I scan the images of upside-down people,
whose lives his hold has made a turmoil.
~*~
Note - Bapo:  Grandfather, colloquial Romani
~*~
Biography:  Karen Downs-Barton is a neurodiverse poet from the Roma community. She is a Creative Writing Masters candidate at Bath Spa University, UK where her manuscript explores experiences of a Roma child growing up in the state childcare system. Her work is forthcoming or published in Tears in the Fence, Night Picnic Journal, The High Window, Alyss, The Otolith, The Fem Review, The Goose, The Curly Mind, Persian Sugar in English Tea, amongst others. Find her at: https://thepapercutpoet.wordpress.com


Friday, July 3, 2020

Q&A: Jake Goldsmith Founder of The Barbellion Prize

The Barbellion Prize is a new book prize for people with chronic, lifelong conditions whose work speaks on the experience of disability or chronic illness. All books submitted must be published in the current year or published later in the year. From the website: "The awarded work can be of any genre in fiction, memoir, biography, poetry, or critical non-fiction from around the world - whether it is in English, in translation, traditionally published, or self-published." The deadline is October 31st. There is no submission fee. You can find more at the website (click here).

I thought I'd ask Jake Goldsmith, the founder, a few questions about the award.
~*~
How long did it take you (from concept to execution) to create the prize?

I had always wanted to see a greater representation of illness and of disability in literature, given how weighty and important these subjects are. And history has some great examples of brilliant work from ill writers. Kafka. Nietzsche. Virginia Woolf. But often when we discuss being inclusive and intersectional, we leave disability and the chronically ill off the list. That’s upsetting, we need to be heard a lot more. Representation is still pretty low. That was the concept, then, that I’d been thinking more about since last year.

I wanted better representation and to reward it. It took maybe a couple months before I met one of our trustees, Elizabeth Ferretti, who lives locally to me, and discussed the idea of such a prize for ill and disabled writers, like me, and started to talk about what we’d need to do. It was easy to create a website and Twitter was invaluable for finding people and contacts. It’s surely been much easier to do this in the Internet Age too.

The National Centre for Writing are also playing a part. Elizabeth had contacts there, such as Chris Gribble, and they should be helping us in the future with publicity and possibly hosting events. They also help other book prizes such as the Republic Of Consciousness Prize, for independent publishers. This has all happened in under half a year or so, slowly persevering.

In a few months we had judges and advisors on board and we made accounts for donations. Some of that process was stressful in finding out exactly what to do, whether we are a small charity, etc, but it worked out pretty quickly. We are still having to work things out as we go, and in the future will likely need a lot more help if we become anywhere near vaguely successful. We have support in principle from the MS Trust, and would hope to have further support from others too in the future.

What factors lead you to include books by caretakers as well as chronically ill/disabled writers for the prize? Where do you see caregiving by able-bodied, non-ill folks in the spectrum of disability/sick literature?


Again, disability literature and writing on illness is still thin on the ground, really. Certainly it is not often a mainstream consideration making bestseller lists or being readily discussed as much as it should be. There is a strong sub genre of works written by doctors about working with patients, and cancer memoirs, but it’s still divided in part from other disability lit.

Carers play such an integral part in the lives of many people who are ill. My mother is my primary carer – I’d very literally be dead without her. They play an important part in the life of many disabled and long-term ill people, and often also go unheard. Literature from the perspective of carers - memoirs, poetry, novels, etc - is just as underrepresented. It deserves to be heard and rewarded too, so it felt inconsiderate to exclude it.

How is the judging process going to work?  Will there be volunteer readers before the judges see the finalists, or will the judges read every submission?

We have a main panel of 3 judges, including myself, and a panel of advisors that are also helping to read some of the submissions and help the judges better form their thoughts and opinions. The judges will be the ones with the final say on any longlist, shortlist, and the winner. The advisory panel does not have a direct vote but are there to help diversify opinion and ideas and help with the workload. As well as help with the running of the prize, publicity, and, well, advice. With 3 judges we should not be stuck in any deadlock situations, such as with an even number of judges, but if for some reason the judges cannot decide on one particular winner, I, in an executive role, will be able to make an executive decision.

We are publicly announcing our judges and advisory panel in July, delayed due to Covid-19 swallowing up the news so much.

The submissions are also being lent out to various trusted friends of the judges and advisors to read at their leisure - to help us form our opinions. These people won’t have any voting power on who wins, but are of course helpful for us in finalising a longlist, and then the rest.

Why did you decide to open the prize to self-published books (alongside traditionally published)?

Few prizes do this, notably the Jhalak Prize does. As disabled literature and illness literature is not often attractive to publishers (unless, cynically, it’s the ‘inspiration porn’ kind), many writers often have to resort to self-publishing. Independent publishers are much more likely to accept disability literature than large publishers, it also seems.

Theoretically, a poor housewife from Peru unheard of by anyone could self-publish a work of poetry about their life with MS, and we could discover it and it could win – if it’s good enough of course.

We would also hope than any self-published works that reach a shortlist could be accepted by a publisher if the author so wanted. How much talent and good literature has been slighted due to the lack of money or recognition? This is an even more acute problem for disabled people, so it’s good to help rectify that.

What are your three favourite books on illness/disability?

Barbellion’s ‘The Journal of a Disappointed Man’, obviously. That work is beautiful. The prize is named in homage to Barbellion for a reason.
I love Oliver Sacks, and many of his works. You could take anything from him. ‘On The Move’, his biography, being a good summation. ‘Awakenings’, too.

My favourite authors are people who suffered with illness (TB) but didn’t write explicitly about it. Albert Camus; and Manès Sperber, who also had respiratory problems. What they wrote best about was political and moral injustice. Camus is at his best in his ‘Combat’ articles and essays, a reluctant moral voice, and Sperber wrote wonderfully about historicist dogma overshadowing human needs, in his biographical trilogy ‘All Our Yesterdays’ being especially good. It has always resonated with me considering the injustice I felt and saw against the disabled, and oppressed, and the more general political evils they were describing certainly affected and did not care much for those with illness or disability. Their own health too gave them a perspective on these things that would be harder to access if they were conventionally abled and healthy.

I feel close to them, politically and in spirit. All of us struggling to breathe, as it were.

How important is it (in your opinion) for awards, presses, and other ventures for the disabled/ill community to be run by members of that community?

All our judges have some sort of long term illness or disability. I have Cystic Fibrosis, diabetes, autism, scoliosis, depression, and a host of other conditions.

Our advisors also have disabilities, but some of them are also abled people with knowledge of the publishing and book industry, as well as academic knowledge on disability.

I do not believe it is imperative that all those advocating for disabled and ill representation be disabled themselves. We can have good allies and friends working for us too, obviously. We need their help. Of course, publishing particularly needs to work in better representing, in who it employs or publishes, disabled people as well as underrepresented black, Asian, and other minority ethnic groups. We seem to be living in an acute moment right now where racial injustice and brutality is receiving more reflection. Those issues often also intersect with disability. Many people killed by police in the US are also disabled. Brutality towards disabled people is even worse in countries like Brazil and India. There’s some shocking statistics. In short, better treatment and representation of these groups is truly important.