The CARE SYLLABUS Advisory Collective Presents

I CAN’T:

FEELING THROUGH
BURDENS OF CARE

INTRODUCTION
INTERVIEW
ART
PRACTICE
FURTHER READING
KEYNOTE EVENT

To admit the “I can’t,” the theorist Jan Verwoert has suggested, may sometimes be “the only adequate way to show that you care — for the friends, family, children or lovers who require your presence, or for the continuation of a long-term creative practice that takes its time.” 

Which admissions of limitation, and which textures of refusal, are yielding new ways of navigating this current moment of personal and collective exhaustion?

How might the burdens of care (and the process of deciding how we distribute our care) reconfigure binary logics -- like I vs. you, giving vs. taking, publicity vs. privacy, strength vs. vulnerability -- that structure popular discourses of care? 

How is saying "I can't" a privilege? What happens when refusal is not an option, but rather -- because of ableism, ageism, racism, misogyny, classism, homophobia, and transphobia -- a boundary consistently undermined, or a reality regularly enforced?

INTRODUCTION

In a recent article surveying the precarious conditions of labor, Sarah Jaffe writes, 

“Burnout is not a problem we can individually solve. It is a symptom of a world set up to exhaust us to the point where we cannot resist […] It is the gap between promise and reality, the feeling that your feelings themselves have gone on strike.” 

At CARE SYLLABUS, we are questioning the conditions that produce ableist allegiance to unchecked labor; to the feeling that we are not doing enough, that we need to do more, faster and better at that. We are interrogating the ideologies of individualism which fuel cultures of supremacy — and in doing so, we meet the limits of our capacity over and over again. Part of this practice is feeling through burdens of care and routinely facing our constraints. To care is to embrace an inherent failure that is also a form of belonging together to the quandaries of being human.  

...We may fantasize about care as limitless,” Maggie Nelson, our keynote speaker for this module, writes in her recent book, On Freedom, yet  “...in our daily lives, most of us run up against the fact that care, too, is an economy, with limits and breaking points” (53). 

Even when our load is lightened by a division of labor and uniting of spirit, care often has us on edge: standing at the precipice of our depleted energies, calculating what more, if any, we have to give. 

In our fifth module, “I Can’t: Feeling Through Burdens of Care,” members of the CARE SYLLABUS advisory collective have assembled an array of contributions spanning multiple genres – essays, interviews, excerpts, photographs, film. Together, they touch upon various textures of refusal to illuminate tensions between care and constraint. If this abundance of offerings counters an admission of exhaustion, what we find in these pieces are the liberatory impulses of desire where sometimes saying “no” is a form of saying  “yes” to ourselves, to each other, and to the futures we dream of.  While the term “burnout”  evokes a sense of running too hot — desire may (or may not) have stroked an early flame – all too often, the untenable conditions of the present make little space for passion. We talk about “setting boundaries” as a method and means of self-preservation and collective care, but in practice, to say “I can’t” can be a dangerous or even impossible proclamation for people of color, femmes, poor, disabled, queer and trans folx. The world is not designed for most of us to stake claim to our desires and refusals alike, let alone for them to be heard, accepted, and honored. 

Guiding the contributions are considerations of art’s role in navigating our capacities and duties to care. As Nelson reminds us, “art has long served as a place for people to act out what they want and think about stuff they want to be thinking about” (62). In a moment when there is so much in need of repair – and to which most institutions have responded with renewed commitments to diversity, equity, accessibility, and inclusion – what responsibility, if any, does art and artistic engagement have to care? Care cannot merely be found in yet another program, project, or protocol governed by utilitarian logic, animated by virtue signaling and fueled by racial capitalism. Is art with its reserved space of experimentation, defiance, “freedom and fun,” to use Nelson’s terms, uniquely positioned to hold care in relation to repose and resistance? Perhaps it is not Art (with a capital A) but the art of the everyday – what artist and activist Tourmaline suggests, are “the small things, but really are the big things! The everyday acts of liberatory glamour, care, and openness that keep us alive”-- that contain the most fervent of freedom dreams. 

Throughout the pieces of the module, we see the contributors orienting care’s relation to refusal on a minor scale – these are forms of worldmaking negotiated moment by moment, breath by breath, no by no. In an interview for this module with Erica Wall, Director of Gallery51, artist Joshua AM Ross, locates the quotidian domain of care in the “willingness to understand the conditions that inform our lives in various ways, that have an effect on our ability to engage and be with one another.” Sussing out the module’s key term, “I can’t,” Ross quips, “you can’t not care.” Sometimes, however, it is the body that says no. When her deteriorating hips restricted physical movement, artist Melanie Mowinski found mobility in new forms of creative experience as shown in selections from her series, Long-Distance Drawing, a growth from her series, Wayfinding . Finding a way to move differently is less about pushing corporeal limits and more “about trusting the way and understanding that many paths get to the same destination, literally and figuratively.” Through his offering of a recipe for Cháo Trắng,  Tu Le – owner and operator of 328North, a sustainable and regenerative farm in the Berkshires – finds within ritualistic meal-making, and the memories and histories contained therein, sustenance for surviving intergenerational trauma. Writing of his Vietnamese-American-Queer identity, Le shares, “living in the Diaspora, straddling three cultures, can be a lot to carry and live up to.”

In an excerpt from her book, Spain (2018) – an experimental travelogue detailing a writer’s residency – author Caren Beilin is fed up with patriarchy’s drain on her creative energies. Talking with CARE SYLLABUS about the book, Beilin pointedly reflects on the nourishing potential of saying ‘no,’ what she finds in “the little gestures of refusal, or the little moments of repair that can happen on a daily level, that maybe will fortify me for some of the bigger refusals that I might need in the future…” In the performative, multimedia piece, “I Caint,” Lisa Arrastia attends to the everyday terror of whiteness as found in a seemingly mundane yet insidiously unrelenting force of the neoliberal institution: the email. With her declaration, Arrastia further sensitizes us to the way inclusive gestures are deeply linked to these institutions’ exclusionary mechanics. Finally, with a nod to Yvonne Rainer’s “No Manifesto” (1965), the CARE SYLLABUS co-directors offer a work-in-progress that experiments in drawing lines within current interpretive paradigms.

In their aesthetic range and conceptual depth, political strategies and survival tactics, the collected contents of this module foreground the radical art of refusal  and the often messy, deeply felt exclamations of “I Can’t” that accompany it. Listen closely. 

-Victoria Papa, on behalf of the CARE SYLLABUS team

January 2022


Collective Member Erica Wall, Executive Director of MCLA Arts and Culture (MAC), spoke with artist-in-residence Joshua AM Ross on the occassion of his new exhibition at MCLA’s Gallery 51.

In their conversation, they touch upon: creative journeys, non-negotiables, the “choice” to care, the artist’s responsibility to their collaborators and viewers, and the process of finding and nurturing artistic community.

ART

Excerpts from Spain
Caren Beilin

2018, Rescue Press

Caren Beilin, collective member and Assistant Professor of English & Communications at MCLA, shares excerpts and connections from her experimental travelogue, Spain.

2016- Present

Melanie Mowinski, collective member and Professor of Fine and Performing Arts at MCLA, reflects on navigating new bodily realities, presenting galleries of work from two recent series of visual art.

March 2022


Meditations on grief, exile, and healing with family from farmer, chef, and collective member Tu Le



A ‘No Manifesto’ for Cultural Interpretation with Care

March 2022

The CARE SYLLABUS co-directors suggest some don’ts for your museum’s interpretation program.

I Caint
Lisa Arrastia


March 2022

A multimedia reflection by collective member Lisa Arrastia, Assistant Professor of Education at MCLA, about navigating whiteness in neoliberal institutions.

FURTHER READING

Below are links to articles that capture key aspects of collective exhaustion — including education, parenting, grieving, healthcare, and labor in academia and well beyond — over the months of the coronavirus pandemic. In their different approaches, these journalists and scholars honor the seriousness of burnout by studying the structural conditions that create and exacerbate it. Together, these writings develop a corrolarry proposition of this module: What happens when we accept an admission of the “I Can’t” as fundamentally political, because (and not in spite of) the ways that it is so deeply personal?

Sarah Jaffe, Dissent Magazine, Winter 2021

Parental Burnout Around the Globe: a 42-Country Study

Isabelle Roskam et. al, journal of the Society for Affective Science, March 2021

Ed Yong, The Atlantic, November 2021


Lisa Arrastia, Common Dreams, August 2020


Jacob Rosenberg, Mother Jones, January-Feburary 2022


A roundtable with the co-founders of CARE SYLLABUS and Insurrect!, ASAP Journal , March 2021

KEYNOTE EVENT

Radical Particularities of Care:
Maggie Nelson in conversation
with Marc Swanson

To celebrate the launch of the CARE SYLLABUS module,“I Can’t: Feeling Through Burdens of Care,” Maggie Nelson and the artist Marc Swanson came together on March 21st, 2022, for a night of conversation on the occasion of Nelson’s recently published book, On Freedom: Four Songs of Care and Constraint (Graywolf Press, 2021) and Swanson’s new MASS MoCA exhibition, A Memorial to Ice at the Dead Deer Disco.

With anecdotes from art and life, this conversation drew attention to the particularities of care as they arise in nuanced relation to the labors and limits of artistic creation and interpretation. When the rally cry of care sounds far and wide, where do we focus our energies? What role, if any, might art -- and artistic engagement -- play in navigating our capacities to give and receive care? In their discussion, Nelson and Swanson touched upon shared investments evident in their recent works, which explore connections between queer experience, alternative understandings of time, and climate crisis.