Crip the Lit launches "little book with big ideas"

Crip the Lit launches “little book with big ideas”

A new book, Here we are, read us: Women, disability and writing, creatively explores the sometimes complicated and often neglected relationship between writing and disability.

This little book with big ideas features eight diverse, well-known and emerging women writers. They are: Tusiata Avia, Steff Green, Helen Vivienne Fletcher, Charlotte Simmonds, Michele Leggott, Trish Harris, Te Awhina Arahanga and Robin Hyde (the only non-living writer).

They are novelists, poets, essayists, playwrights, memoirists and bloggers. The important thing they have in common is that they all share the lived experience of disability.

In Here we are, read us, they talk frankly about the intersection of disability and writing, sharing the insights and experience that enrich their work.

“Poetry is a language to hang on to when other languages start to disappear. I want to join those who travel light and lift darkness,” writes Michele Leggott.

In the book’s introduction, it says: “When the voice of disabled writers is strong, their words, our words, can transform worlds.”

Trish Harris, co-founder of Crip the Lit, which published the book, says: “Disabled writers producing quality writing can make an important contribution to the writing world, amplifying the disability voice as part of the human experience.”

Robyn Hunt, co- founder of Crip the Lit, says that disabled people have been a neglected audience. “Many of us have grown up without seeing ourselves and our lives realistically reflected in the books and media surrounding us. But we have lots to say, and we know there are voices to be heard and people who want to hear them. We want young disabled people to hear and be those voices.”

Robyn and Trish call on festival and event organisers to be more inclusive.

Here we are, read us was published by Crip the Lit with funding from Creative New Zealand,  It was supported by Arts Access Aotearoa.

It will be available at no cost in a variety of accessible formats: in hard copy including large print; and online as an audio book, an e-book with accessible downloadable files, and in braille from the Blind Foundation. It will be launched in Wellington on Sunday 24 March.


About Crip the Lit

Crip the Lit was formed in 2016 by Trish Harris and Robyn Hunt as a way for Deaf and disabled writers to have their unique voices, perspectives and stories included and valued in mainstream writing in New Zealand. We want to tell our stories our way.

Crip the Lit is here to challenge stereotyped and inaccurate portrayals of disabled characters in books, movies and on television. It’s critical that disability is represented and celebrated as part of the richness and diversity of humanity in all genres of literature, and in visual media.

Disabled writers also need a platform and community, whatever genre they’re writing in.

Crip the Lit has successfully presented at Lit Crawl each year since 2016 and at Disability Pride Week events.


For more information:

Trish Harris  027 279 3698

Robyn Hunt: 0274 493019



Prev   Next 

Latest Updates

  • Covid 19 and Epilepsy Update 26 March 2020
    26 March 2020

    Epilepsy New Zealand has been receiving regular information from the Ministry of Health and other agencies, often more than once a day, showing just how quickly the situation is evolving. No doubt there will be many people, including those with epilepsy, who have questions around their risk and what to do in these uncertain times. Hopefully the information below may help reassure you and where necessary, prompt you to contact your trusted health professional.

  • BPAC issues new guidelines for Lamotrigine
    26 September 2019

    BPAC issues new guidelines for Lamotrigine.

  • Petition against Pharmac's drug changes
    29 August 2019

    A petition is underway calling on Pharmac to reverse its decision on Lamotrigine.

  • Epilepsy NZ Position Statement - Lamotrigine
    28 August 2019

    We opposed this change from Lamictal to Logem from the start, and staff have advocated on behalf of people with epilepsy in discussions with Pharmac.

  • Don't Give Up by Adele Hauwai
    4 December 2017

    Adele Hauwai has shared her Living With Epilepsy story as part of the Epilepsy NZ Tell Us About It Competition. People were asked to send in their stories about epilepsy, the challenges they faced and the lessons they have learned that they would like to share with the world.

  • New ILAE Seizure Classification
    10 March 2017

    The ILAE announces the publication in Epilepsia of two new landmark classification documents, one of seizure types and one of the epilepsies.

Show Your Support

Shop Online

Epilepsy NZ has an online shop!


Donate Today