Categories: Deaf Stuff

Sherrie

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Community development has changed significantly in the last decade, and many community and activist organisations have changed to reflect this. However, it becomes a vague matter for marginalised groups where there are community organisations focused on the community development of these marginalised groups.

The Deaf community is a marginalised group, and there are many community organisations that provide services and advocacy for deaf community members. The question is: will they survive in the current context with the concepts of empowerment and participation?

There is a vast difference between various organisations within the Deaf community in how they approach community development, especially how they connect with the Deaf community.

There are two approaches in community development; top-down and bottom-up. Top-down approach is where decisions are made at the top and requires very little community participation. When decisions are made using this approach, the community is expected to implement it. If this approach is used in community development, the strengths, resources, skills and expertise of the community are usually ignored.

This can cause issues for the community, as they will feel ‘disconnected’ from their community organisation, which has been reflected with a couple of organisations and their relationship with the Deaf community. In the last few years, the Deaf community has begun feeling ‘disconnected’ from a number of organisations, thus they have lost trust in their preferred organisation; this was shown in declining membership numbers and lack of participation.

Power lies in the grassroots; however this has been forgotten as the top-down approach is constantly used in regards to making decisions for the community. Bottom-up approach is also known as grassroots development – we will use grassroots instead of bottom-up approach. A number of organisations effectively use this approach in order to work with the grassroots members within the Deaf community, and are committed to ensuring they have access to basic human rights, as this commitment is required to empower ordinary people so they can have real options for their future.

Deaf people are the ones who have experience living as a deaf person in the dominant society that consists of people who can hear. The grassroots development approach is also based on the argument that people who are affected by decisions about their future should be empowered to effectively control or influence decisions through collective action.

In 2012, Deaf Victoria submitted an inquiry into the provision of Auslan interpreters in Victorian public hospitals because they were receiving numerous complaints from deaf people across the state about public hospitals failing to provide Auslan interpreters when requested for their medical appointments. This is an excellent example of the grassroots development based on a group of people influencing decisions through collective action with the support of a community organisation.

Deaf people are often left powerless when it comes to decision-making, as they are often rendered marginal through their inability to hear. This is also considered audism, which is the belief that those with the ability to hear are superior or “normal” (Callis, 2015). Using the grassroots development approach is also an effective way to combat audism within the mainstream society.

Discrimination occurs when the needs of deaf people are ignored by others such as access to information in sign language and/or live captioning, provision of captions for films and television programs, access to education and other basic human rights. This happens often if the top-down approach is used in regards to making decisions for the deaf community. However, segregation also occurs within the deaf community where members are separated into two groups — ‘elites’ and ‘grassroots’.

Padden (2008) said that the difference between ‘elite’ and ‘grassroots’ varies in Deaf communities around the world. Based on discussions with fellow Deaf colleagues, the Australian deaf community sees ‘elites’ as these deaf people who are university educated; are members of a deaf family; hold professional jobs; and are leaders in the community, whereas ‘grassroot deaf’ are these who are deemed average people; do not hold a leadership role within the community; did not seek further education beyond high school, and are from hearing families. However, it is important to note that the deaf community in Australia is not too concerned about the segregation of ‘elites’ and ‘grassroots’ but there is the issue of the ‘tall poppy syndrome’.

Tall poppy syndrome is rife in the Australian culture, but even so in the Australian deaf community. Deaf people, who achieve something they have worked so hard for, or are well on their way to success, are often cut down by other deaf people in higher places. This kind of issue does not empower deaf people, especially these at grassroots level.

We often forget that we are humans who are productive, social and creative beings and we enter relationships with other humans in order to produce our world (Marx, 1977). Essentially, Deaf community organisations need to establish a strong rapport with the deaf community so they can support us to realise our fullest potential as equal citizens.

Empowerment is crucial for the deaf community because deaf people need to be empowered to be able to make decisions for themselves, as the concept of empowerment aims to increase the power of marginalised people. Community organisations have a social responsibility to empower their members, and we need to commit to the collective empowerment of ordinary people — that is grassroots — and to transform social structures, relations and processes. Essentially, Deaf community organisations need to give power to the deaf community so they can take matters into their own hands whilst being supported by these organisations.

Dr. Liisa Kauppinen (2015) stated that deaf people are a part of the human diversity and that we have a social responsibility to apply the CRPD to our everyday lives so we can live as equal citizens. This is where community organisations come in so they can advocate for our right to be included in the society as equal citizens. Diversity is an important part of community development as it takes place in a range of groups, and third sector organisations have a commitment to human rights and empowering marginalised people (Kenny, 2011).

Deaf community organisations have a social responsibility to strengthen the human diversity within the deaf community and in the dominant society. According to Kenny (2011), community development encourages a diversity of views, lifestyles and cultures. This is important because the deaf community is diverse, especially having Auslan recognised as the language of the Australian deaf community.

Holcomb (2013) said that the diversity of the Deaf community is so much more than just various racial, religious, ethnic, and economic backgrounds. Diversity in the Deaf community makes it possible for academicians and community development practitioners to approach the Deaf experience in terms of Deaf culture and sign language (Holcomb, 2013). Deaf community organisations need to embrace the diversity of the Deaf community and to welcome people who are hard of hearing, parents of deaf children, educators, and sign language interpreters.

Participation is vital in community development especially with marginalised communities. In the Deaf community, participation is essential especially using the bottom-up approach. However, this can become problematic when people are consulted or information about a decision but has little or no power to affect it (Ife, 2013).

A strong response from the community can be expected if they are not consulted about changes to their community organisation/s. It is essential to hold community consultations with the whole community, rather than just members, so they can make decisions based on a grassroots approach, rather than using the top-down approach.

Ife (2013) says that community organisations should seriously attempt to encourage and develop community participation to overcome skepticism. The majority of the deaf community is skeptical of a number of Deaf community organisations nowadays, so they need to look at ways to overcome this — perhaps start with using the grassroots approach and establishing a rapport with the entire deaf community, rather than taking all the power and making decisions for them. This will not be achieved overnight, as it will take time as Ife (2013) said it is a slow and developmental process and requires sustainability.

There is a number of fantastic Deaf community organisations and they have done so much for the Deaf community. However, they will not survive in today’s society if they use the top-down approach, especially if they fail to establish a good & strong rapport with the Deaf community.

The bottom-up, or rather, a grassroots approach would allow the Deaf community organisations to survive in the current society – especially whilst representing Deaf people on all levels (national, state and local). Listen to the Deaf community and find out what they want, and effectively use advocacy tools to ensure Deaf people have access to basic human rights so they can participate in the society as equal citizens. Empowerment and participation are essential for the survival of Deaf community organisations, especially so they can connect with the deaf community at grassroots level. After all, Deaf community organisations are the organisations of the Deaf community.

References

Callis, L. Deaf Discrimination: The Fight For Equality Continues. Published on 18th July 2015 in The Huffington Post. Retrieved on 23rd August 2015 from http://www.huffingtonpost.com/lydia-l-callis/deaf-discrimination-the-f_b_7790204.html?ir=Australia

Holcomb, T. 2013. Introduction to American Deaf Culture. New York: Oxford University Press.

Ife, J. 2013. Community Development in an Uncertain World. Melbourne: Cambridge University Press.

Kauppenin, L. 2015. Deaf People: An Important Part of Human Diversity. Presented at the XVII World Congress of the World Federation of the Deaf on 28th July 2915. Istanbul, Turkey.

Kenny, S. 2011. Developing Communities for the Future. 4th edition. Melbourne: Cengage Learning Australia.

Padden, C. 2008. The decline of deaf clubs in the United States: A treatise on the problem of place. In H-D. Bauman (Ed.), Open your eyes: Deaf studies talking (pp.169-176). Minneapolis: University of Minnesota Press.

Editor's Pick

    Today’s the third day of Lockdown 6.0 and I’m still processing how I feel about this. I haven’t written in a while, and I thought it was high time I got back into blogging and doing what I love, writing. There’s nothing more cathartic than writing.

    Given we only exited Lockdown 5.0 just over a week ago, it feels as if we haven’t been given an opportunity to fully enjoy life post-lockdown before being ushered back into lockdown. How do we process our feelings and thoughts post-lockdown? We’ve barely had the time to process the last lockdown and its impact on us as individuals.

    When the announcement came on Thursday morning stating that Victoria would be going back into lockdown as of 8PM, I felt numb. I didn’t have any words to describe how I felt at the time. I thought I was okay about it, but if I have to be brutally honest, I’m not okay about it. Like everyone else, I barely had two days to get used to life post-lockdown after Lockdown 5.0 was lifted. Did I get used to post-lockdown life this time around? Probably not.

    Lockdown 6.0 is due to be lifted on Thursday night, but I’m not holding my breath. Delta, a variant of COVID-19, is a sneaky fucker. The transmission rate is higher compared to other COVID-19 variants. If the Victorian Government sees the need to extend this lockdown to get the pandemic under control, then so be it. NSW is seeing case numbers in the high 200s every day, and there’s no way Victoria wants to repeat what we went through last year.

    The real question remains: how do I feel about this?

    Defeated. It feels like this virus is determined to keep us at home, apart from our loved ones. I’ve been living on my own for 6 months and whilst I love it, I miss being around people. Fuck, I miss hugs. Human touch. Connection.

    Speaking of connection, I miss being with my fellow Deaf people. I miss getting my Deaf fix. Catching up with friends on FaceTime or Zoom is wonderful, but it doesn’t replace the feeling of being able to sign with your Deaf peers in person.

    Being able to see your language in its wondrous 3D form, like it’s supposed to be.

    That feeling you get when you laugh merrily with your friends. Laughing so much until you cry.

    Being present with your Deaf self whilst being with others.

    I’ve seen many older Deaf people reminiscence on the golden days of Deaf Clubs, and how they wish for Deaf Clubs once again. Having been through five (soon to be six because this one isn’t done) lockdowns, I can empathise with them on the loss of Deaf Clubs. Opportunities for us to get our Deaf fix are now rare.

    It’s funny how you don’t realise you miss something until it’s gone…and you realise you’ve taken it for granted.

    I wanted to be able to celebrate my birthday(s) with my loved ones, but I hesitated on making plans because of the uncertainty. I do still want to be able to let my hair down and hit the town at some point, to celebrate me with my loved ones.

    Goddamn it, I fucking miss being with people.

    As a Deaf person and professional, I also miss face-to-face appointments with Auslan interpreters. For more than 18 months, like many Deaf people who use Auslan interpreters, I’ve utilised video remote interpreting for personal or professional appointments. Whilst VRI is fantastic and has grown so much the last two years ago, I miss being able to engage with my interpreters in person. The opportunity to debrief and/or chat with the interpreter(s) afterwards is rare as hen’s teeth nowadays. These 10 minutes you get to connect with your interpreters – oh how that feels rather sentimental.

    Zoom closes. Interpreter moves onto their next job. I (or other Deaf person) move onto the next task or meeting.

    I do love being able to stay in touch with family and friends through social media, text messaging and video calls. It does get tiring at times – so I need to keep reminding myself that other people are doing their best to stay in touch too.

    It’s also hard to stay motivated during this time, too. I’ve had to put my platform – I Sign. I Wander., and Deaf Stories on hiatus – simply because I don’t have the motivation. I also have a few personal projects planned, but I haven’t been able to find the motivation to get started.

    I’ve been trying to stay kind to myself, but when things become repetitive, it gets to the point where I say “fuck this, I’m just doing the bare minimum“.

    I shower, I feed myself, I go to work (at home), and I make sure I am warm and healthy. I have things I can do around the house. I have books. I have Netflix.

    Until this outbreak eases, there’s not much I can do but to keep doing what I’ve been doing and to remain connected with my loved ones in ways that works the best for us.

    So, to say… I still don’t know how I feel. I’m getting there though. Maybe next time I write, I’ll have a better idea. But until then, I’ll continue processing this.

    See you on the flipside,

    S xx

     

    Deaf Stories was originally established with a vision of deaf people sharing their experiences as business owners. With Janelle Whalan as my filming assistant, we interviewed four deaf people – Neil Wood, Bobbie Blackson, and Ivan Callaghan & Nicole Cooke about their businesses. The first round of Deaf Stories was funded by Deaf Services’ Life Enrichment Grant which helped us to cover expenses such as travel, software, equipment and other costs associated with Deaf Stories. 

    After filming, editing and releasing each interview, the engagement from the deaf community I envisioned wasn’t happening. Something was missing.

    I saw there was a dire need for deaf people to share their stories on a public platform. With deaf clubs disappearing from our very own eyes, where were opportunities for deaf people to share their stories in a casual and relaxing environment? 

    One of my favourite memories from my childhood was when deaf children from various schools across Southeast Queensland would get together for a day to celebrate Deafness Awareness Week at New Farm Park in Brisbane. Every year I wound find myself sitting with my fellow deaf peers watching Julie Lyons tell stories through Auslan and visual vernacular. The feeling of being captivated and being taken into another world through a deaf person’s storytelling skills – that was something I carried with me for so many years. I still carry this feeling with me today.

    Deaf people are notorious for being excellent storytellers. This is because storytelling is a fundamental part of the deaf community. Ledwith (2011) stated that stories act as social-cultural glue, which means they define societies, cultures, and communities. Like sign language, storytelling acts as glue to bring the deaf community together.

    For the second round of Deaf Stories, I was planning on reframing it to include stories from various deaf people around the country. My original plans were thrown out of the window when Australia was hit by the COVID-19 pandemic. With travel restrictions in place, this meant I was now unable to travel around the country collecting stories from deaf and hard of hearing Australians.

    The first couple of weeks in lockdown, I watched numerous creators change their plans and projects. I also saw a number of friends in the arts make changes to their projects. Everything had to be moved online. That gave me the idea: why not make Deaf Stories an online platform for the deaf community watch interviews happen in real time? Give the deaf community a sense of belonging, similar to being at a deaf club. Hence the decision to reframe it as Deaf Stories LIVE.

    The first Deaf Stories LIVE interview with Andrew Wiltshire was a huge success. I saw the engagement I had longed to achieve. I saw deaf, hard of hearing and hearing people respond to the interview. 

    Through the first interview, Andrew displayed his skills as a brilliant storyteller. According to Davis Haggerty (2007), being a skilled storyteller becomes an influential trait in the deaf community. Andrew is considered a role model to many deaf people. 

    Role models like Andrew are essential in the deaf community, particularly for young deaf people who are still figuring out their identities. Young deaf people should have access to role models within the deaf community, as Sutton-Spence (2010) believes it helps young deaf people to develop their personal, linguistic, and social identities.

    Nović (2016) says deaf culture is founded on storytelling; it’s a culture obsessed with its own language.  With the use of sign language such as Auslan, we work on the art of storytelling in various forms such as poetry, visual vernacular, sign singing, etc. It’s not something that is perfected overnight; it takes a lot of practice and consultation by our fellow deaf peers to ensure the stories are easy to understand through Deaf eyes.

    Deaf people often learn best through storytelling. We are encouraged to participate through participation and understanding; belonging and confidence grows as we are listened to, valued and taken seriously (Ledwith, 2011). Without storytelling, how can change occur within the deaf community? How can we learn about the world around us? How can we connect with the deaf community using the Deaf experience?

    “We tell our stories to transform ourselves; to learn about our history and tell our experiences to transcend them; to use our stories to make a difference in our world; to broaden our perspective to see further than normal; to act beyond a story that may have imprisoned or enslaved us; to live more of our spiritual and earthly potential.” ~ Rachel Freed (2011)

    Storytelling empowers deaf and hard of hearing people to share their experiences; to start discussion; and to create change within the community and in the mainstream. Change doesn’t occur without sharing personal stories. Stories also encourages us to connect with and understand each other better. 

    I strongly believe in the power of storytelling and it’s why I chose to frame Deaf Stories around the notion of storytelling we have come to know and enjoy for many years within the deaf community.

    In my next blog/vlog, I will be talking about vulnerability and why it’s an important element in storytelling.

    Big love, 
    S x

    References:
    Davis Haggerty, L. (2007). Storytelling and leadership in the Deaf community. Rochester Institute of Technology, USA.

    Freed, R. (2011). The Importance of Telling Our Stories.

    Ledwith, M. (2011). Chapter Three: Doing Community Development in Community Development – A Critical Approach.

    Nović, S. (2016). At Home in Deaf Culture: Storytelling in an Un-Writable Language.

    Sutton-Spence, R. (2010). The Role of Sign Language Narratives in Developing Identity for Deaf Children. Journal of Folklore Research.


Leave A Comment

  1. Karen Lloyd November 18, 2015 at 5:16 pm - Reply

    Excellent post, Sherrie. Couple of points:
    1. I think that tall poppies are cut down not just by people in positions above them but even more so by grassroots people.

    2. When people talk about member based organisations they often seem to talk about them as if they are somehow separate from the members, as if the office, staff, board are the organisation. But it is the members who are the organisation – without members there is no organisation. By not becoming members and being actively involved in the organisation’s activities, deaf people give up their power – no one takes it away from them, they give it up. If people want an organisation to speak for them they need to be involved and mould the organisation to be and do what they want. There is a lot of agreement on many issues within the community and the grassroots but there is not agreement on everything and there is often not agreement on how to deal with issues, ie on what an organisation should do. So member based organisations must rely on members involvement and votes to make decisions, they can’t just make decisions willy nilly to suit ‘the community’ or ‘the grassroots’ if the community and the grassroots aren’t participating and voting.

    if people don’t join and get involved with their organisations and exercise their power and have their say and their vote on what they want, then what happens? The organisations slowly die. Then the community has to set up new organisations from scratch with everyone volunteering and do it all over again. And the same thing will eventually happen again when people start seeing the organisation as the office, staff, board and are less involved.

    I absolutely agree that there needs to be a lot more community empowerment but this isn’t something that organisations can do separately from the community – for it to happen, the community, the grassroots, need to exercise their power and get involved.

  2. Robyn Whitney November 18, 2015 at 8:30 pm - Reply

    Interesting read, especially with the elites and grassroots. I have observed from personal experience, that deaf community organisations start off as grassroots organisations and over time, change to top-down approaches and thus become disconnected from the people they originally ‘listened’ to and supported. Then new deaf community organisations emerge, adapting to the needs of society at the time and the cycle begins all over again.

    I wonder what criteria will define the elites and grassroots now that more deaf people are completing university and holding professional jobs? I suspect the definition will change as the deaf community develops and grows over time.

  3. Lorraine November 19, 2015 at 4:40 am - Reply

    Your getting there Sherrie keep it up. It’s sad to see the mantras of the previous Deaf generation still being repeated in the contemporary deaf speakers, bloggers, writers. I wish times would change but sadly it hasn’t. Keep speaking out even when you feel silenced by either elitist or grassroots!! Your voice is loud clear and strong well done!!

  4. tumsifu frank January 22, 2016 at 7:50 pm - Reply

    interesting read
    its real happening especially in 3 world countries.
    i work in the organization dedicating to help elders and volnerable children to get their rights and access to health and education.
    and now we are looking for the organization that we can partner to implements the projects to help these deaf community
    thanks

    summer.tumsifu@gmail .com

    contacts me if you know any charity that can help with projects implementation
    we are in TANZANIA east africa

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Related Posts

    Today’s the third day of Lockdown 6.0 and I’m still processing how I feel about this. I haven’t written in a while, and I thought it was high time I got back into blogging and doing what I love, writing. There’s nothing more cathartic than writing.

    Given we only exited Lockdown 5.0 just over a week ago, it feels as if we haven’t been given an opportunity to fully enjoy life post-lockdown before being ushered back into lockdown. How do we process our feelings and thoughts post-lockdown? We’ve barely had the time to process the last lockdown and its impact on us as individuals.

    When the announcement came on Thursday morning stating that Victoria would be going back into lockdown as of 8PM, I felt numb. I didn’t have any words to describe how I felt at the time. I thought I was okay about it, but if I have to be brutally honest, I’m not okay about it. Like everyone else, I barely had two days to get used to life post-lockdown after Lockdown 5.0 was lifted. Did I get used to post-lockdown life this time around? Probably not.

    Lockdown 6.0 is due to be lifted on Thursday night, but I’m not holding my breath. Delta, a variant of COVID-19, is a sneaky fucker. The transmission rate is higher compared to other COVID-19 variants. If the Victorian Government sees the need to extend this lockdown to get the pandemic under control, then so be it. NSW is seeing case numbers in the high 200s every day, and there’s no way Victoria wants to repeat what we went through last year.

    The real question remains: how do I feel about this?

    Defeated. It feels like this virus is determined to keep us at home, apart from our loved ones. I’ve been living on my own for 6 months and whilst I love it, I miss being around people. Fuck, I miss hugs. Human touch. Connection.

    Speaking of connection, I miss being with my fellow Deaf people. I miss getting my Deaf fix. Catching up with friends on FaceTime or Zoom is wonderful, but it doesn’t replace the feeling of being able to sign with your Deaf peers in person.

    Being able to see your language in its wondrous 3D form, like it’s supposed to be.

    That feeling you get when you laugh merrily with your friends. Laughing so much until you cry.

    Being present with your Deaf self whilst being with others.

    I’ve seen many older Deaf people reminiscence on the golden days of Deaf Clubs, and how they wish for Deaf Clubs once again. Having been through five (soon to be six because this one isn’t done) lockdowns, I can empathise with them on the loss of Deaf Clubs. Opportunities for us to get our Deaf fix are now rare.

    It’s funny how you don’t realise you miss something until it’s gone…and you realise you’ve taken it for granted.

    I wanted to be able to celebrate my birthday(s) with my loved ones, but I hesitated on making plans because of the uncertainty. I do still want to be able to let my hair down and hit the town at some point, to celebrate me with my loved ones.

    Goddamn it, I fucking miss being with people.

    As a Deaf person and professional, I also miss face-to-face appointments with Auslan interpreters. For more than 18 months, like many Deaf people who use Auslan interpreters, I’ve utilised video remote interpreting for personal or professional appointments. Whilst VRI is fantastic and has grown so much the last two years ago, I miss being able to engage with my interpreters in person. The opportunity to debrief and/or chat with the interpreter(s) afterwards is rare as hen’s teeth nowadays. These 10 minutes you get to connect with your interpreters – oh how that feels rather sentimental.

    Zoom closes. Interpreter moves onto their next job. I (or other Deaf person) move onto the next task or meeting.

    I do love being able to stay in touch with family and friends through social media, text messaging and video calls. It does get tiring at times – so I need to keep reminding myself that other people are doing their best to stay in touch too.

    It’s also hard to stay motivated during this time, too. I’ve had to put my platform – I Sign. I Wander., and Deaf Stories on hiatus – simply because I don’t have the motivation. I also have a few personal projects planned, but I haven’t been able to find the motivation to get started.

    I’ve been trying to stay kind to myself, but when things become repetitive, it gets to the point where I say “fuck this, I’m just doing the bare minimum“.

    I shower, I feed myself, I go to work (at home), and I make sure I am warm and healthy. I have things I can do around the house. I have books. I have Netflix.

    Until this outbreak eases, there’s not much I can do but to keep doing what I’ve been doing and to remain connected with my loved ones in ways that works the best for us.

    So, to say… I still don’t know how I feel. I’m getting there though. Maybe next time I write, I’ll have a better idea. But until then, I’ll continue processing this.

    See you on the flipside,

    S xx

     

    Deaf Stories was originally established with a vision of deaf people sharing their experiences as business owners. With Janelle Whalan as my filming assistant, we interviewed four deaf people – Neil Wood, Bobbie Blackson, and Ivan Callaghan & Nicole Cooke about their businesses. The first round of Deaf Stories was funded by Deaf Services’ Life Enrichment Grant which helped us to cover expenses such as travel, software, equipment and other costs associated with Deaf Stories. 

    After filming, editing and releasing each interview, the engagement from the deaf community I envisioned wasn’t happening. Something was missing.

    I saw there was a dire need for deaf people to share their stories on a public platform. With deaf clubs disappearing from our very own eyes, where were opportunities for deaf people to share their stories in a casual and relaxing environment? 

    One of my favourite memories from my childhood was when deaf children from various schools across Southeast Queensland would get together for a day to celebrate Deafness Awareness Week at New Farm Park in Brisbane. Every year I wound find myself sitting with my fellow deaf peers watching Julie Lyons tell stories through Auslan and visual vernacular. The feeling of being captivated and being taken into another world through a deaf person’s storytelling skills – that was something I carried with me for so many years. I still carry this feeling with me today.

    Deaf people are notorious for being excellent storytellers. This is because storytelling is a fundamental part of the deaf community. Ledwith (2011) stated that stories act as social-cultural glue, which means they define societies, cultures, and communities. Like sign language, storytelling acts as glue to bring the deaf community together.

    For the second round of Deaf Stories, I was planning on reframing it to include stories from various deaf people around the country. My original plans were thrown out of the window when Australia was hit by the COVID-19 pandemic. With travel restrictions in place, this meant I was now unable to travel around the country collecting stories from deaf and hard of hearing Australians.

    The first couple of weeks in lockdown, I watched numerous creators change their plans and projects. I also saw a number of friends in the arts make changes to their projects. Everything had to be moved online. That gave me the idea: why not make Deaf Stories an online platform for the deaf community watch interviews happen in real time? Give the deaf community a sense of belonging, similar to being at a deaf club. Hence the decision to reframe it as Deaf Stories LIVE.

    The first Deaf Stories LIVE interview with Andrew Wiltshire was a huge success. I saw the engagement I had longed to achieve. I saw deaf, hard of hearing and hearing people respond to the interview. 

    Through the first interview, Andrew displayed his skills as a brilliant storyteller. According to Davis Haggerty (2007), being a skilled storyteller becomes an influential trait in the deaf community. Andrew is considered a role model to many deaf people. 

    Role models like Andrew are essential in the deaf community, particularly for young deaf people who are still figuring out their identities. Young deaf people should have access to role models within the deaf community, as Sutton-Spence (2010) believes it helps young deaf people to develop their personal, linguistic, and social identities.

    Nović (2016) says deaf culture is founded on storytelling; it’s a culture obsessed with its own language.  With the use of sign language such as Auslan, we work on the art of storytelling in various forms such as poetry, visual vernacular, sign singing, etc. It’s not something that is perfected overnight; it takes a lot of practice and consultation by our fellow deaf peers to ensure the stories are easy to understand through Deaf eyes.

    Deaf people often learn best through storytelling. We are encouraged to participate through participation and understanding; belonging and confidence grows as we are listened to, valued and taken seriously (Ledwith, 2011). Without storytelling, how can change occur within the deaf community? How can we learn about the world around us? How can we connect with the deaf community using the Deaf experience?

    “We tell our stories to transform ourselves; to learn about our history and tell our experiences to transcend them; to use our stories to make a difference in our world; to broaden our perspective to see further than normal; to act beyond a story that may have imprisoned or enslaved us; to live more of our spiritual and earthly potential.” ~ Rachel Freed (2011)

    Storytelling empowers deaf and hard of hearing people to share their experiences; to start discussion; and to create change within the community and in the mainstream. Change doesn’t occur without sharing personal stories. Stories also encourages us to connect with and understand each other better. 

    I strongly believe in the power of storytelling and it’s why I chose to frame Deaf Stories around the notion of storytelling we have come to know and enjoy for many years within the deaf community.

    In my next blog/vlog, I will be talking about vulnerability and why it’s an important element in storytelling.

    Big love, 
    S x

    References:
    Davis Haggerty, L. (2007). Storytelling and leadership in the Deaf community. Rochester Institute of Technology, USA.

    Freed, R. (2011). The Importance of Telling Our Stories.

    Ledwith, M. (2011). Chapter Three: Doing Community Development in Community Development – A Critical Approach.

    Nović, S. (2016). At Home in Deaf Culture: Storytelling in an Un-Writable Language.

    Sutton-Spence, R. (2010). The Role of Sign Language Narratives in Developing Identity for Deaf Children. Journal of Folklore Research.