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EDI Scholars-in-Residence: Disability Justice Book Club — Disability Allies Cohort with Dr. Jennifer Gagnon

EDI Scholars-in-Residence: Disabled and Proud Cohort — with Dr. Jennifer Gagnon

EDI Scholars-in-Residence: Disabled and Proud Cohort

EDI Scholars-in-Residence: Disability Allies Cohort

Disability Justice Book Club Discussion Questions: Month 3

Welcome to the Disability Justice Book Club Month 3

Leah Lakshmi Piepzna-Samarasinha’s Care Work: Dreaming Disability Justice

Led by Dr. Jennifer Gagnon (and her service dog Ziggy)

Supported by the EDI Scholars-in-Residence Program and the Peña Fund

Land Acknowledgment

We acknowledge that UBC’s two main campuses are situated within the ancestral and unceded territory of the xʷməθkʷəy̓əm (Musqueam) people and in the traditional, ancestral, unceded territory of the Syilx Okanagan Nation and their peoples

If this is your first time attending the book club

If you’re joining the Disability Justice Book Club for the first time this month – welcome! We are so excited to have you with us! Please review the Month 1 Discussion Guide which contains important information on the structure of the book club, the two different cohorts: 1) Disabled and Proud and 2) Disability Allies, and ways that we are incorporating Disability Justice into how the book club works. The Month 1 Discussion Guide is available online here.

Accessing the Text:

We will be reading Leah Lakshmi Piepzna-Samarasinha’s Care Work: Dreaming Disability Justice. The book is available freely and for purchase in a variety of formats. However, most free access is in ebook format through either UBC library or your public library, (the text is unfortunately no longer available in Open Access). If you are joining from beyond UBC, your institutional or public library are likely the simplest to access. As always, if you encounter any challenges accessing the text, or require a different format for accessibility, feel free to reach out directly to Allan Cho (allan.cho@ubc.ca) or Jennifer Gagnon (jennifer.gagnon@ubc.ca) for support.

E-book format

  • Available at UBC Libraries here
  • Available at Vancouver Public Library here

Paperback format

Audio format

  • Available at Vancouver Public Library here
  • Available from Audible here with a free trial
  • Available from Spotify here with a premium subscription

DAISY format

  • Available at Vancouver Public Library here

Confidentiality

A core practice of Disability Justice is confidentiality. Accessibility, safety, and inclusion all require that we are mindful to not disclose confidential information about the lived experiences of others. Many disabled folks have heightened concerns about confidentiality because of their experiences with ableism, discrimination, and marginalization. While some of us might feel comfortable sharing our experiences with disability and ableism, no one is required or expected to disclose. Folks may also not be “out” about their relationship to disability in all contexts and places at UBC and beyond. To further support control over disclosure of our identities and experiences with disability, we have created two cohorts for the Disability Justice book club 1) the Disabled and Proud cohort for folks who self-identify as disabled and who are interested in discussing Disability Justice with other self-identified disabled folks, and 2) the Disability Allies cohort for folks who do not presently identify as disabled or who would prefer not to disclose their relationship to disability. We always assume the presence of disability and access needs in all our meeting spaces. To support confidentiality and safety in these spaces, please treat the experiences of individuals as confidential and do not disclose anyone’s lived experiences without their enthusiastic consent. This Book Club is an opportunity to grow our knowledge and understanding of Disability Justice, and potentially “read yourself in” to Disabled community or explore how disability and ableism are already present in your experiences.


Discussion Guide

Page numbers refer to the ebook format available through VPL

  1. “I started writing from bed. I wrote in old sleep pants, lying on a heating pad, during the hours I spent in my big sick-and-disabled femme of color bed cave. I wasn’t alone in this. I did so alongside many other sick and disabled writers making culture.” “Preface” p. 11

“It [Disability Justice] means we are not left behind; we are beloved, kindred, needed.” “Preface,” p. 15

“Inclusion without power or leadership is tokenism.” “Ch. 7 Cripping the Apocalypse,” p. 82

  • What does writing/working from bed mean or look like to you? How are advocacy and activism often inaccessible?  How does Disability Justice shift activism away from the streets and into our beds?

 

2. “This is an essay about care –about the ways sick and disabled people attempt to get the care and support we need, on our own terms, with autonomy and dignity… It’s about our attempts to get what we need to love and live, interdependently, in the world and in our homes, without primarily relying on the state or, often, our biological families…. This is about some of the ways we are attempting to dream ways to access care deeply, in a way where we are in control, joyful, building community, loved, giving, and receiving, that doesn’t burn anyone out or abuse or underpay anyone in the process.” “Ch. 1 Care Webs, “ p. 29-30

“People’s fear of accessing care didn’t come out of nowhere. It came out of generations and centuries where needed care meant being locked up, losing your human and civil rights, and being subject to abuse.” “Ch. 1 Care Webs, “ p. 25

  • How does disability justice change and complicate our idea of care, and of giving, receiving, asking, managing, refusing, and challenging care relationships? What is at stake in seeing care as work, labour, and love?

 

  1. “The care webs I write about here break from the model of paid attendant care as the only way to access disability support. Resisting the model of charity and gratitude, they are controlled by the needs and desires of the disabled people running them. Some of them rely on a mix of abled and disabled people to help; some of them are experiments in ‘crip-made access’ – access made by and for disabled people only, turning on its head the model that disabled people can only passively receive care, not give it or determine what kind of care we want.” “Ch. 1 Care Webs: Experiments in Creating Collective Access,” p. 26
  • What is a care web? How would you map your own care web? What are some challenges that can arise in building a care web?

 

  1. “Many of us who are disabled are not particularly likable or popular in general or amid the abled. Ableism means that we — with our panic attacks, our trauma, our triggers, our nagging need for fat seating or wheelchair access, our crankiness at inaccessibility, again, our staying home — are seen as pains in the ass, not particularly cool or sexy or interesting…

And: I am still arguing for the radical notion that we deserve to be loved. As we are. As is.” “Ch. 3 Making Space Accessible Is an Act of Love for Our Communities,” p. 49

“Love as an action verb. Love in full inclusion, in centrality, in not being forgotten. Being loved for our disabilities, our weirdness, not despite them.” “Ch. 3 Making Space Accessible Is an Act of Love for Our Communities,” p. 49

  • How can love promote inclusion not only for those that ableism deems “likeable” but also for those who ableism perceives as “unlikeable” or “difficult to love?”

 

  1. “There are official statistics now that show that at least half of the racialized people murdered by law enforcement are also physically or mentally disabled, Deaf, and/or autistic.

There are both protests where we name racism and ableism, and protests where the role ableism plays in our people’s deaths gets forgotten. At this moment in time, I remember that we are the first to remember theses connections, know why our people were murdered, and fight like hell to end this world that wants us dead.” “Ch. 4 Toronto Crip City,” p. 56

  • How do we stop ableism from killing, especially those at the intersections of other forms of oppression? How can we de-centre whiteness, sexism, settler colonialism, heterosexuality, and other forms of oppression and privilege by rethinking our relationships to and with care?

 

  1. “It’s not about self-care—it’s about collective care.” “Ch. 5 Sick and Crazy Healer” p. 69

“Too often self-care in our organizational cultures gets translated to our individual responsibility to leave work early, go home – alone – and go take a bath, go to the gym, eat some food and go to sleep. So we do all of that ‘self-care’ to return to organizational cultures where we reproduce the systems we are trying to break.” “Ch. 5 Sick and Crazy Healer” p. 69

“Most folks I know come to activist spaces longing to heal, but our movements are often filled with more ableism and burnout than they are with healing. We work and work and work from a place of crisis.” “Ch. 5 Sick and Crazy Healer” p. 62

  • Why are the narratives of “wellness” “self-care” and “cure” not disability justice? How does mutual care resist the narrative of self-care?  How do we resist without burning out ourselves and those struggling with us?

 

  1. “If care labour is, well, labour, and we participate in an emotional economy all the time, what would a just care labour economy look and feel like?” “Ch. 8 A Modest Proposal for a Fair Trade Emotional Labour Economy” p. 90
  • In her answer, Leah Lakshmi Piepzna-Samarsinha emphasizes consent, drawing on disabled knowledge, reciprocity, rejecting sexism, time off, and a culture of appreciation. How would you answer her question of what a just Fair trade Emotional Labour Economy would look like?

 

  1. “For years awaiting this apocalypse, I have worried that as sick and disabled people, we will be the ones abandoned when our cities flood. But I am dreaming the biggest disabled dream of my life—dreaming not just of a revolutionary movement in which we are not abandoned but of a movement in which we lead the way. With all of our crazy, adaptive-deviced, loving kinship and commitment to each other, we will leave no one behind as we roll, limp, stim, sign, and move in a million ways towards cocreating the decolonial living future. I am dreaming like my life depends on it. Because it does.” “Ch. 7 Cripping the Apocalypse” p. 87
  • How do we continue to do (and receive) care work in dark times? How do we continue to dream Disability Justice into being?

 

  1. “Stacey Millbern: “How have you found crip ancestors? ….

Leah Lakshmi Piepzna-Saarsinha: I stumbled upon them. I dug them up. I fought to find them. I dreamed them. Others shared them. I remembered them.”  “Ch. 19: Crip Lineages, Crip Futures” p. 161

  • Who are your crip ancestors? How does finding and honoring your Crip ancestors support you in dreaming crip futures?

 

 Thank you for gathering with us today to discuss Leah Lakshmi Piepzna-Samarasinha’s Care Work: Dreaming Disability Justice

November 20th is Transgender Day of Remembrance

History of Transgender Day of Remembrance

Transgender Day of Remembrance was co-founded by Gwendolyn Ann Smith, Nancy Nangeroni, and Jahaira DeAlto and first observed on November 20, 1999. The group created this day to memorialize the murders of transgender people as a result of transphobia and was first inspired by the deaths of Rita Hester and Chanelle Pickett, both trans women of color.

Violence against transgender people is intertwined with racism, classism, the housing crisis, colonialism, sexism, and homophobia. Because of this, transgender communities, especially indigenous, black, and racialized gender diverse people, are disproportionately impacted by violent crime and mental health issues compared to other communities. 70% of trans youth in Canada experience sexual harassment or violence of some kind and trans and non-binary youth are twice as likely to have thought of self-harm in their lifetime compared to cisgender youth.

On this day each year, we should reflect on the lives lost and the hardships faced by the transgender community as a result of systemic transphobia. However, the day also serves as a call to action to combat this discrimination and provide support and resources for individuals as well as advocating for systemic changes. Consider showing your support this year at one of the community events listed below.

Events at UBC

Remembrance & Resistance: A Teach-In for the Transgender Day of Remembrance on Thursday, November 20, 2025 from 12:30 – 2pm in Farris Hall, Rm 106

The transgender flag will be flown in place of the UBC flag from November 13-20 in observance of Transgender Awareness Week from November 13-19 and Transgender Day of Remembrance on November 20 at UBC’s Vancouver and Okanagan campuses. Additionally, the flags will be lowered on Wednesday, November 20.

Events in Vancouver

A Trans Day of Remembrance Gathering and drop-in will be held at the Birdhouse (44 W 4th Ave, Vancouver BC) on Thursday, November 20, 2025 from 5pm – 7pm to hold space and gather, reflect, and support one another. There will be live music, letter writing, drag performances, and healing moments.

The Simon Fraser Student Society is hosting an annual Trans Day of Remembrance Vigil on campus and over zoom on Thursday, November 20, 2025 from 5:30 – 7:30pm to remember the trans siblings lost to transphobic violence.

A Trans Day of Remembrance Gathering hosted by the Crescent Justice Collective, the Society for Gender-Affirming Healthcare, and the “Vancouver” Trans March will be held on Thursday, November 20th from 7pm-9pm at MacLean Park to come together in mourning and memory. This is an outdoor event with food, beverages, and performers.

UBC Resources

The Pride Collective at UBC is a safe, supportive, and empowering home for 2SLGBTQIA+ community at UBC. It is a student-led resource group that offers educational and social services dealing with sexual and gender diversity to the UBC community.

The Pride Collective also runs a Trans Mentorship Program each year, beginning in the fall. While applications are now closed, keep an eye on their Instagram for the next round and future events!

The UBC Trans Coalition is another group to keep an eye on for resources and events at UBC.

A team of trans and non-binary students at UBC created the UBC Trans & Non-Binary Student Guide to help trans and non-binary students access resources and support on campus. It is honest, open, and collaborative.

UBC also has a list of book recommendations for Trans Day of Remembrance as well as a Transgender Reading List

UBC Library Materials:

 

Bey, M. (2021). Black trans feminism. Duke University Press. https://doi.org/10.1215/9781478022428 [Available at UBC Library]

Nicolazzo, Z., & EBSCOhost. (2017;2023;2016;). In Nicolazzo Z. (Ed.), Trans in college: Transgender students’ strategies for navigating campus life and the institutional politics of inclusion (First;1; ed.). Stylus Publishing, LLC. https://doi.org/10.4324/9781003448259 [Available at UBC Library]

Shraya, V. (2018). I’m afraid of men. Penguin, an imprint of Penguin Canada. [Available at UBC Library]

Snorton, C. R., & JSTOR (Organization). (2017). Black on both sides: A racial history of trans identity (1st ed.). University of Minnesota Press. https://doi.org/10.5749/j.ctt1pwt7dz [Available at UBC Library]

Thom, K. C., & EBSCOhost. (2019). I hope we choose love: A trans girl’s notes from the end of the world (1st ed.). Arsenal Pulp Press. [Available at UBC Library]

Web sources consulted:

Khan, A. (2023, November 17). Transgender Day of Remembrance. MOSAIC. https://mosaicbc.org/news/transgender-day-of-remembrance-2/

Peter A. Allard School of Law. (n.d.). Remembrance & Resistance: A Teach-In for the Transgender Day of Remembrance. University of British Columbia. Retrieved November 6, 2025, from https://allard.ubc.ca/about-us/events-calendar/remembrance-resistance-teach-transgender-day-remembrance

Trans Care BC. (2023, November 20). Transgender Day of Remembrance. Trans Care BC. https://www.transcarebc.ca/about/news-events/transgender-day-remembrance

Women and Gender Equality Canada. (2023, November 20). Statement by Minister Marci Ien on Transgender Day of Remembrance [Statements]. Government of Canada.

Disability Justice Book Club Discussion Questions: Month 2

Welcome to the Disability Justice Book Club Month 2

Margaret Price’s Crip Spacetime: Access, Failure, and Accountability in Academic Life  

Led by Dr. Jennifer Gagnon (and her service dog Ziggy)

Supported by the EDI Scholars-in-Residence Program and the Peña Fund  

Land Acknowledgment

We acknowledge that UBC’s two main campuses are situated within the ancestral and unceded territory of the xʷməθkʷəy̓əm (Musqueam) people and in the traditional, ancestral, unceded territory of the Syilx Okanagan Nation and their peoples

If this is your first time attending the book club

If you’re joining the Disability Justice Book Club for the first time this month – welcome! We are so excited to have you with us! Please review the Month 1 Discussion Guide which contains important information on the structure of the book club, the two different cohorts: 1) Disabled and Proud and 2) Disability Allies, and ways that we are incorporating Disability Justice into how the book club works. The Month 1 Discussion Guide is available online here.

Accessing the Text:

We will be reading Margaret Price’s book Crip Spacetime. The book is available freely and for purchase in a variety of formats. If you are joining from beyond UBC, open access or your institutional library are likely the simplest to access. As always, if you encounter any challenges accessing the text, or require a different format for accessibility, feel free to reach out directly to Allan Cho (allan.cho@ubc.ca) or Jennifer Gagnon (jennifer.gagnon@ubc.ca) for support.

E-book format (free)

  • Available through Open Access as a viewable or downloadable pdf here
  • Available at UBC Libraries here

Audio Book

  • Available through Audible currently for free here

Paperback format (purchase)

    • Available from the publisher here for $26.95

Confidentiality

A core practice of Disability Justice is confidentiality. Accessibility, safety, and inclusion all require that we are mindful to not disclose confidential information about the lived experiences of others. Many disabled folks have heightened concerns about confidentiality because of their experiences with ableism, discrimination, and marginalization. While some of us might feel comfortable sharing our experiences with disability and ableism, no one is required or expected to disclose. Folks may also not be “out” about their relationship to disability in all contexts and places at UBC and beyond. To further support control over disclosure of our identities and experiences with disability, we have created two cohorts for the Disability Justice book club 1) the Disabled and Proud cohort for folks who self-identify as disabled and who are interested in discussing Disability Justice with other self-identified disabled folks, and 2) the Disability Allies cohort for folks who do not presently identify as disabled or who would prefer not to disclose their relationship to disability. We always assume the presence of disability and access needs in all our meeting spaces. To support confidentiality and safety in these spaces, please treat the experiences of individuals as confidential and do not disclose anyone’s lived experiences without their enthusiastic consent. This Book Club is an opportunity to grow our knowledge and understanding of Disability Justice, and potentially “read yourself in” to Disabled community or explore how disability and ableism are already present in your experiences.

 


Discussion Guide

Our discussion will centre Margaret Price’s core argument that the model of individual accommodations used by universities to implement access is not only deeply problematic but also a barrier to accessibility in post-secondary contexts. As a collective, we completely understand that reading a whole book prior to our meeting just might not be realistic. With that in mind, as a facilitator I will focus our discussion on core themes from the “Introduction” and “Time Harms” chapter, and the key quotes from throughout the book shared below. If there’s something not captured here that you really want us to take up together in discussion, please feel free to share with Jennifer either before or at our book club meeting. Page numbers given correspond to the print edition of the book, and the citation also gives the relevant chapter.

Discussion Questions and Quotes

  1. “Disabled academics know.

We know where the accessible entrance is (not in front). We know if there are cracks or gaps in the sidewalk leading to that entrance. We know if there’s no sidewalk at all, but only a lumpy dirt footpath. We know what to do if the door is locked, with a sign on it saying ‘Handicap assistance call 555-STFU,’ and we know what to do if that number leads to voicemail. We know what kind of handle the door has. If the door is unlocked, we know how heavy it will be. We know what the room we’re going to looks like, and we know how to ask – with charm and deference – if we need the furniture rearranged, the fluorescent lights turned off, the microphone turned on. We know how much pain it will cost to remain sitting upright for the allotted time. We know how to keep track of the growing pain, or fatigue, or need to urinate (there’s no accessible bathroom), and plan our exit with something resembling dignity. We know that no else will ever know.”  (Price, “Introduction”  p. 1)

    • What are your thoughts on this hidden knowledge of what Disabled people know? Does it resonate with you and your experiences with accessibility (or the lack thereof)? Are you surprised by how differently Disabled folks may experience the act of arriving in an academic space?
    • Spoon Theory discusses how Disabled folks need to carefully manage and allocate the limited spoons that they have throughout the day. How does Price’s statement that “Disabled academics know” connect to spoon theory?

 

  1. “We all seemed stuck on that word. Bafflement. We are baffling. We are tired of baffling. We are tired of being baffles. We are tired, period….This project is not about disability alone. It is about all experiences of being baffling— and baffled—in academic life. And therefore it’s also about the meaning and future of academic life. In a sense, the question of inclusion is the question of why an educational institution exists in the first place. If you believe the work of education is (at least sometimes) for the good, then we must find better understandings of what that work is. And we must find better ways of working together.” (Price, “Introduction” 40)
    • What are your thoughts on bafflement, accessibility, inclusion, and disability experience in academic life?

 

  1. “Crip spacetime is a material-discursive reality experienced by disabled people.” (Price, “Introduction” 7)

“Crip spacetime is precarious not only because it’s difficult and often risky to inhabit it, but because it is obscure.” (Price, “Introduction” 13)

“Crip spacetime as a reality is rarely perceptible to those not experiencing it.” (Price, “Time Harms” 74)

    • What is crip spacetime? How do you (or do you?) experience crip spacetime?

 

  1. “As the saying goes, ‘time heals.’ But time also harms.” (Price, “Time Harms” 73)

“Requests for accommodation tend to turn on precise measurements of chronological time, but most disabilities don’t run on chronological time. They run on crip time.” (Price, “Time Harms” 92)

    • How is crip spacetime more than just slowing down? How is it also an acceleration of time, or a falling out of time and space? In other words, how does crip spacetime both reflect time as it is for disabled folks and also distort or change how time and space are perceived?

 

  1. “Many academics know that disability accommodations can be difficult to put in place. But the extreme delays, and the systemic cruelty, built into the accommodations loop might not be as familiar. The loop is arduous to traverse; must be traversed over and over again; and extracts time, money, effort, and emotional cost….The loop is almost always invisible to those not traversing it.” (Price, “Time Harms” 100)
    • How do you react to this statement? What are your thoughts on the accommodations loop?

 

  1. “Accommodations, as currently practiced in academic workplaces, are predictive moves attached to an individual and designed to make that in­dividual’s disability disappear. Access, by contrast, is simply what you need in a particular situation as it becomes.” (Price, “Time Harms” 102)
    • Price argues that accommodations as practiced in academia not only do not work, but also serve as barriers to creating accessibility by defining the Disabled person as a problem to be “fixed” by accommodation. What do you see as the current challenges or problems with the accommodation model? How might a shift towards a system of collective accountability that centres collective access address these challenges?

 

  1. “Among the most striking elements of Mingus’ description [of access intimacy], to me, is that access intimacy can arise suddenly over time. Several interviewees in the Disabled Academics Study described moments when one of their colleagues abruptly seemed to ‘get’ the need for a quick access move…A defining characteristic of access intimacy is that it emerges through particular moments; it is not generalizable. Thus, one of many reasons that access intimacy is incompatible with academe – at least, academe in its oppressive and conservative forms – is that it resists being written into policy… Access Intimacy isn’t a best practice, and it can’t be an item on a checklist.” (Price, “Accompaniment” 159)
    • What do you think of Price’s take on Mia Mingus’ access intimacy? Where is access intimacy possible in academic spaces? Where is access intimacy impossible? Can the accommodations process support access intimacy or is it incompatible with access intimacy?

 

  1. “Gathering forces us to confront the dimensions of crip spacetime—space, time, cost, and accompaniment—and find a way to inhabit it to­gether. Often this cohabitation is painful and messy. But the gathering itself is a refusal to be separated and, thus, a commitment to collective ac­cess.” (Price, “Conclusion” 177–78)
    • What do you see as the power of gathering? Is gathering (and sharing experiences) a possible way to support true accessibility and inclusion?
    • How are we as a book club and a collective of people doing? Where have we been successful in navigating Crip spacetime? Where can we continue to work towards collective access and accountability?
  1. In contrast to the many failures of access that Price discusses, do you have any examples where access was done well?

 

  1. What do you hope others at the university takeaway from this book regarding how to support (and not support) Disabled colleagues and disability inclusion?

 

Thank you for gathering with us today to discuss Margaret Price’s Crip Spacetime 🙂

EDI Scholars-in-Residence Hosts the Disability Justice Book Club with Jennifer Gagnon

Video Recording of “The Life of a Writer” – A Conversation with UBC Library’s Writer-in-Residence Evelyn Lau


Description

On Thursday, October 16, 2025, Evelyn Lau joined us for an afternoon event as part of her programming as UBC Library’s Writer-in-Residence.  This is a special session featuring acclaimed poet and memoirist Evelyn Lau, in conversation with Bonnie Nish, Executive Director of Word Vancouver Festival. This engaging dialogue offers audiences a rare opportunity to hear directly from one of Canada’s most influential literary voices as she reflects on her decades-long writing journey—from her groundbreaking debut Runaway: Diary of a Street Kid to her most recent poetry collections.  This intimate conversation delved into Evelyn Lau’s creative process, her thoughts on the evolving literary landscape, and the personal themes that have shaped her body of work.

Speaker Bios

Evelyn Lau is a lifelong Vancouverite who has authored 15 books. Her memoir, Runaway, was made into a CBC movie starring Sandra Oh. Evelyn’s collections of poetry have received national awards, and her prose has been translated into a dozen languages. From 2011 to 2014, she served as Vancouver’s Poet Laureate.

Dr. Bonnie Nish is Executive Director of Word Vancouver and Pandora’s Collective Outreach Society. She holds a Master’s in Arts Education from Simon Fraser University and a PhD in Language and Literacy Education from the University of British Columbia, where she currently teaches. A certified Expressive Arts Therapist and faculty member at the Vancouver Expressive Arts Therapy School, Bonnie has led workshops across North America for over 20 years. She is the author of Love and Bones, co-editor of Concussion and Mild TBI: Not Just Another Headline, and co-author of Cantata in Two Voices with Jude Neale. Bonnie lives in Vancouver and is working on a new book.


More about the UBC Library Writer-in-Residence Program

The Writer-in-Residence program at UBC Library’s Irving K. Barber Learning Centre is an initiative designed to support and promote literary excellence within our academic community. This program provides a unique opportunity for a distinguished writer to engage with students, faculty, and the local community through various enriching activities and events. We aim to foster a vibrant literary culture, encourage creative expression, and offer valuable insights into the writing process.