Submission Medium: written

Children’s art as visual narrative

This article about visual narrative highlights the effectiveness of non-verbal expressive arts like drawing, painting, and constructing as therapeutic and restorative experiences. Trauma survivors, including children, may find it challenging to articulate their experiences verbally, as trauma can impact the brain’s language centers. The article contrasts previous approaches that encouraged forgetting traumatic events with the current understanding of the importance of acknowledging, validating, and providing mental health intervention for survivors, allowing them to tell their stories through creative acts. The article references the project “Forced to Flee: Visual Stories of Refugee Youth from Burma,” which compiles a book of art expressions by young refugees (a page for the kickstarter campaign for the project was available as of 12/20/23 at this link). The project showcases how visual narratives, conveyed through art, can tell powerful stories, open hearts, and build bridges of understanding. By honoring the visual narratives of youth, the project not only raises awareness about human rights issues but also offers a glimpse into possibilities for reparation and redemption for young survivors.

Neurodiversity Poems

This anthology houses a multitude of poems related to neurodivergence. The authors all have different backgrounds as this is an open site where anyone can publish their work. The site is searchable and poems are tagged. Some examples include a poem about masking, the perception of “normal,” and “praying for a neurotypical brain.” One poem details an individual’s experience with growing up and feeling like they constantly are on the outside looking in and having to hide aspects of themselves to fit in. This site could be utilized as a resource for creative writing in terms of neurodivergence. As poems from personal, first hand experiences of neurodivergence, they provide insight as to the nuances to individual experiences that caution us against generalizations and stereotypes.

Neurodivergent Narratives

Sandra Coral is a student, teacher, writer, podcaster, and learner all about neurodivergence. They have multiple social media sites (instagram, twitter, Facebook) that are publically accessible and focus on promoting education and awareness about neurodivergence. She is autistic and has ADHD and shares her own experiences via through written posts, videos, and podcasts on topics such as sensory processing, fitting in, masking, and burnout. Sandras’s sites could be utilized in a classroom setting as narratives from someone who is neurodivergent told in their own voice. The link below is to the Facebook page, where the About profile provides links to other platforms. Her social media posts are useful not only for discussing neurodivergent narratives, but also for reflecting on what constitutes a narrative (small individual posts retelling everyday life? the accumulation of posts over time?). In contrast, her Substack includes longer posts that more clearly resemble stories.

Mental health Poems for Teens

The Poets.Org website of the Academy of American Poets has curated this collection of 14 poems related to mental health that were selected for teen readers (part of a series of “Poetry for Teens” on various topics). Some themes throughout the poetry are depression, anxiety, as well as hope and resilience. Each poem includes a description of some of the themes within it as well as details about the author. The pieces span a range of time periods and a variety of authors with different backgrounds including, for example, Emily Dickinson and Sylvia Plath, as well as Naomi Shihab Nye and Ada Limón.

Personal Stories of Mental Health

Black Dog Institute is a nonprofit organization dedicated to medical research related to mental health. This online collection houses 18 different stories related to mental health (including bipolar disorder, PTSD, anxiety, depression), each representing the lived experiences of those who wrote them. Each story has a short description. A majority of the stories are from patient perspectives while some of them are based around a provider narrative. Since the themes throughout the stories vary so much, this site could be utilized in any syllabus focused on mental health. Such stories show the personalizing of diagnoses as well as show variability in how they are experienced, which can help to expand the general notions and stereotypes that are held around mental health

A Body, Undone: Living on After Great Pain

“A Body, Undone” is a memoir by Christina Crosby, an English professor chronicling her life after a paralyzing cycling accident in 2003. A respected English professor at Wesleyan University, Crosby explores the physical and emotional pain of her disability through a critical feminist and queer thinking lens. She puts into words the experience of life in a broken body that seems beyond the reach of language and understanding, discussing how we construct a livable life in the midst of unimaginable pain. She situates her personal narrative within the broader social critiques of care labor and the financial burden of disability and injury within the current economic systems and structures in the US. The novel would be relevant to disability studies and feminist theory, but its prose that is rooted in humanity and the events of daily life function to make it accessible to a general audience . This book is a patient narrative that challenges the dominant discourse of disability, and could be relevant to discussions about disability, pain, and care and its intersections with gender, sexuality, and class.

Aliceheimer’s: Alzheimer’s Through the Looking Glass

This graphic memoir captures the author’s journey with her mother, Alice, who is diagnosed with dementia. Through a creative blend of writing, visual art, and comics, Walrath weaves elements from Lewis Carroll’s Alice’s Adventures in Wonderland throughout the text to explore the transformative power of storytelling in navigating the challenges of mental illness, loss, and social stigma. The memoir offers a unique perspective on aging and caregiving, emphasizing the healing potential of graphic narratives by speaking to how visual mediums can communicate more than, or differently from, written text. Collaged illustrations, made in part from Carroll’s text itself, are accompanied by a textual vignette. The combination of text and art results in a cohesive narrative that would lack the same depth and detail if considered in isolation. Graphic medicine, Walrath writes, “lets us better understand those who are hurting, feel their stories, and redraw and renegotiate those social boundaries.” Aliceheimer’s provides a way to introduce and educate people about Alzheimer’s as a medical condition, while highlighting the humanity involved in dealing with it as a family.

This novel could be used in classes regarding narrative medicine, graphic medicine, and/or caregiving experiences. It invites discussions on the role of storytelling in reshaping medical narratives, the impact of stigma on health, and the potential for creative expression in coping with complex health challenges. With Walrath’s background in Medical Anthropology, this book could also be used to ask how researchers personally connect to their work.

Caring for a Parent in my Home

This article describes Beth’s caregiving story as she cares for her elderly mother post-stroke. Beth’s journey captures the complexities, sacrifices, and resilience inherent in caregiving roles. The narrative explores familial dynamics, emotional strains, and the importance of planning and seeking external support. Beth’s evolving experience offers valuable lessons for educators seeking to illustrate the intersection of health, family dynamics, and personal well-being in caregiving narratives. Caregiver.com aims to provide community and support for nontraditional caregivers, such as children caring for their aging parents. As such, the story emphasizes the significance of communication, planning, and self-care.

Living with HIV: Six Very Different Stories

This article from The Guardian features six diverse narratives of individuals living with HIV, highlighting the evolution of the HIV/AIDS experience over the past 30 years in Britain. For example, Jonathan, diagnosed during the early epidemic in the 1980s, reflects on living with HIV for over half of his life, explaining how he managed without medication until 1996 and has come to embrace life with HIV through activism. Another example is Jo, diagnosed at 60, who discusses how she navigated the shock of her diagnosis and the perceptions associated with being an older woman with HIV. She’s open about her diagnosis because she wants to change perceptions about people living with HIV.

This article offers students an opportunity to reflect on diverse experiences with the same illness, and brings up topics such as stigma, activism, and media representation of illness and how these change through time.

Taking Turns

Taking Turns is a graphic novel that explores HIV/AIDS Care Unit 371 at the Illinois Masonic Medical Center in Chicago during the peak of the AIDS epidemic. Through archival records, oral histories, and MK Czerwiec’s first-hand experiences as a nurse on the ward, the novel sheds light on the challenges and resilience of the community during this critical period. With simple illustrations and a practical four-panel format, “Taking Turns” delivers a direct and accessible narrative, offering readers an opportunity to not only absorb the history easily, but prompting empathetic reflection for each member of the community – patients, families, and medical staff. This novel could provoke discussions about caregiver narratives, and the efficacy of graphic novels in communicating narrative.