EQuality Training

Equality and awareness

Showing posts with label inclusive practice. Show all posts
Showing posts with label inclusive practice. Show all posts

10/3/24

Unveiling Ableism: Silenced Narratives in Academia

This post is a summary of the "Notes for Academics chapter of the memoir, where i seek to explain the methodological choices I made: 

Unveiling Ableism: Silenced Narratives in Academia

 

In academia, certain voices have long been sidelined, particularly those of disabled individuals. Ableist narratives have overshadowed their experiences, insights, and knowledge. This post aims to shed light on this, exploring the challenges of researching the cultural and linguistic oppression faced by disabled people.

 

Understanding Reality and Knowledge

Before I could begin writing with authenticity, I had to delve deeply into the voices and experiences that shape our understanding of disability. Traditional academic approaches often fail to capture the nuanced realities of disabled people, focusing on experimentation rather than lived experience. These methods tend to ignore systemic barriers and oppression. 

 

Instead, I adopted an approach rooted in activism, culture, and society, drawing on traditions from queer theory, feminism, and post-colonialism. This anti-ableist stance helped me challenge widely held assumptions and amplify marginalised voices. Language, in particular, plays a critical role—both as a tool of empowerment and as a mechanism of oppression. I wanted to challenge harmful stereotypes and hold myself accountable to the disabled population in the way I used language.

 

A Missing Reference Section

A decade ago, a colleague pointed out that the book I was reading lacked half its reference section. This omission denied recognition to many of the scholars cited. It stuck with me, especially in professional settings where terminology like "anti-ableism" was lacking, unlike the clear terms used for other forms of advocacy. As an MA supervisor, I would gauge my students' engagement with authoritative voices through their references. This led me to question why disabled people aren’t acknowledged as a collective, and why their allies aren't seen as activists, much like feminists or anti-racists.

 

Disabled People as Knowers: Testimonial Injustice

 

Ableism keeps disabled people from sharing their knowledge, treating them as lesser and excluding them from academic discourse. This injustice seeps into research, creating ethical concerns about the way knowledge is produced and shared. Our words shape reality, and they can either harm or empower. Careful storytelling is essential in preventing the reinforcement of harmful stereotypes.

 

The Power of Storytelling

 

Storytelling can either amplify silenced voices or further silence them. While it holds the potential to empower marginalised communities, it can also perpetuate oppressive narratives. Storytelling must be seen as a tool for justice, ensuring that it uplifts everyone, particularly those who have been historically marginalised.

 

Language Matters: Speaking Up Against Injustice

 

The language used by the disability rights movement is critical in reflecting the societal treatment of disabled people. Terms like "ableism" shine a spotlight on societal injustices. Disabled People's Organisations use language deliberately to challenge unfair narratives and shift societal perspectives.

 

Fighting for Fair Representation

 

In research, it’s crucial to ensure that disabled voices are heard and that the methods used are inclusive. Disability studies provide valuable insight into the societal issues faced by disabled individuals. Listening to their voices can create stronger, more inclusive stories and discussions.

 

My Testimony: A Journey Through Inequality

 

In the first seven chapters of the book, I reflect on shared human resilience. Childhood activities like riding a bike or playing with friends often contribute more to development than clinical interventions. However, clinical approaches can isolate disabled people, undermining their sense of belonging and making them vulnerable to abuse.

 

Chapters 9 to 19 address the long-term impact of being treated differently. While friendships helped buffer some of the discrimination I faced, the weight of inequality remained heavy. Without language to define ableism in institutions and society, it’s neither acknowledged nor measured. 

 

Chapters 20 to 27 highlight the success achieved when individuals facing sexism, ableism, and xenophobia recognise their own power in the face of oppression. Acknowledging the challenge is the first step towards empowerment.

 

Towards Empowerment and Justice

 

Storytelling plays a pivotal role in dismantling ableism and amplifying disabled voices. It’s our collective responsibility to challenge dominant narratives, break down oppressive structures, and create a more just future. By centring disabled people’s experiences and expertise, we work towards a world where all voices are heard and valued.

 

Txtual Worlds: The Absence of Disabled Voices in Research

 

When diving into research papers, I frequently encountered a lack of references, particularly on global disability issues. Despite the rise of Disability Studies in the '80s, key authors were often absent from mainstream narratives. This led me to question why disabled people aren't trusted as storytellers.

 

Ableist Storytelling

 

Ableism in storytelling manifests in several ways:

1.  Lack of representation:  Disabled characters are often underrepresented or misrepresented.

2.  Stereotyping and tropes:  Harmful stereotypes oversimplify disabled experiences.

3.  Exclusion and invisibility:  Disabled perspectives are frequently ignored.

4.  Limited perspectives:  Able-bodied viewpoints dominate, restricting narrative diversity.

5.  Inaccessible narratives:  Storytelling mediums are often not accessible to disabled audiences.

6.  Reinforcement of ableist norms:  Stories can perpetuate harmful ideologies.

7.  Missed opportunities for inclusion:  Unique perspectives are often overlooked.

 

Challenging Ableism in Storytelling

 

We must strive for authentic representation of disabled people, diversify narratives, and challenge ableist stereotypes. This blog aims to offer an accessible testimony of the experience of ableism, sharing insights through personal narrative.

 

Conclusion: Towards Ethical Storytelling

 

Understanding the impact of ableism is crucial for ethical research. By embracing intersectionality and honouring the unique experiences of disabled individuals, we can ensure that their voices are heard, respected, and valued. Storytelling must not only be inclusive but also challenge the status quo, paving the way for a fairer, more just world.

5/25/24

C-Change- Realigning the stars


At C-Change, our colleagues are committed to embracing diversity, challenging conventional practices, offering choices, inspiring hope, and fostering inclusive environments. We are on a collective journey to explore the history of C-Change, adopt an allied stance, understand the principles of inclusive practice, and discuss ways to promote equality and diversity. This is not my story; it is an organisational account framed through an equality lens.


Exploring the 5 Ps: Integrating Key Principles into Organisational Life


[Description: C-Change constellation: five stars labelled People, Public, Privilege, and Political]



People make C-Change

It’s Personal: If You're Affected, You're Involved


It was a delight to begin by listening to a colleague who shared how things started for the organisation. With the closure of Lennox Hospital, several ‘patients’ with complex requirements were left in need of homes within communities. From the start, C-Change was innovative in finding ways to support the well-being of those previously locked in institutions. With the support of colleagues and the direction of families, people were not only supported better but also more cost-effectively, as intervention costs often dropped over time. I pointed out how the ‘cheaper’ aspect has become important again, sadly, under austerity. Fundamentally, at C-Change, human rights come first, not ‘care’ or ‘aid’ because it's all about prioritising well-being and rights. The conversation continued with longer-serving colleagues explaining to newer members the importance of enabling people to enjoy family homes within their localities. 

I'm always struck that the roots of the organisation mirror the emergence of the Disabled People's Movement and its fight for deinstitutionalisation. I was working for a DPO at the time but was too young and inexperienced to grasp the significance of the Movement. Only later did I connect the dots, and realise the meaning, the coalescence of smaller groups of d/Disabled individuals seeking to leave hospitals so their well-being needs were addressed as well as their medical needs. Hence, the Medical Model/Social Model distinction, while criticised today, made much more sense in this historical context and the nature of the fight.


I always enjoy C-Change's culture of ‘Radical Hospitality’ because it is about empathy and interaction, not just an initial greeting. It’s about fostering a sense of belonging and anticipating changes, understanding that while needs may be universal, individual wishes and preferences matter immensely. I don't need to declare, identify or fill in a form to ask for help. Plus, because I know the answer will be ‘yes,’ I'm never afraid to ask. It’s the intentionality behind my colleagues' interactions that fosters well-being, far more than rigid lists of do’s and don’ts, which can often be limiting.

Question: Well-being?

1. What is important for me?

2. What is important to me?


 Allied Position and Unearned Privilege

While many individuals will experience things differently, it is crucial for us, as colleagues, to acknowledge and address the disadvantages many face without reinforcing the common stereotypes imposed on them. C-Change has a long-standing tradition of viewing each person as unique; they are team leaders, responsible for the decisions made about their support (or helped to do so). Our colleagues amplify diverse voices, ensuring that each individual's needs, wants, dreams and unique identities are fully acknowledged and respected.


The feedback to the questions I raised, was intended to raise the matter of practice based on medical ‘musts’ rather than human needs, wants, and wishes. I shared with colleagues that I've often forgone things that may appear essential to others (e.g., parking) in favour of things that bring me huge joy (e.g. fires). Very quickly, colleagues understood how personal choice is, and that with limited time, energy, and money, the freedom to choose was important in order not to simply focus on need but the wider range of things we each require for our well-being. If we reduce access to essential needs, most will struggle or suffer. Furthermore, if we only apply well-being to health matters it's too late.


Public Matter - Professionals Natter

We then began a conversation about Personalisation, Standards, and Citizenship. I offered that during my time at C-Change, I'd observed that the organisation had a counter-narrative. One that moved in the opposite direction to many service providers within the care sector. I felt that working in different ways, with alternative wording, and an aim to uphold human rights, produced a culture that was often (positively) at odds with institutional and public assumptions.

A huge amount of great practice was shared, with colleagues keen to explore how and why things go wrong at times.


Jo’s Narrative: Not a Service User but a Person We Work For

Jo is not a client but a brother, neighbour, student, voter, train enthusiast, and teammate. The narrative of Jo’s life challenges conventional labels, highlighting his full humanity.


A Privilege: Adopting an Allied Position


Mea culpa, I did shoehorn my willingness to share ideas of critical theory behind the word ‘privilege.’ For colleagues, privilege is a delighted pride they have in their roles, a tangible feeling of honoring the lives of those they support. The energy in the room rose as everyone shared their stories. “My colleague said they got more from the person they support than the person got from them!” was shared with huge joy - I teared up. Imagine if such feelings were shared across the entire social care sector. A stark contradiction, I felt, to the daily barrage of negative press many are subjected to. The flaying by paper-cut of thoughtless comments, reiterated niceties no doubt well-intentioned, but oppressive, dehumanising, and disempowering over time. Yet you can't say, “I've lost it,” because people judge, as they can't see you've been kicked repeatedly in the same spot over years.

From a critical perspective, privilege means being able to live without the disadvantage of a specific and characteristic discrimination. For example, my privilege is living free of classism, homophobia, and racism… no one other than me knows exactly how far or narrow the extent of my overall unearned dis/advantage spreads. What I can say is that from this intersectional position, facing ableism is a disadvantage (not my lack of ability). If my advantage is not facing racism, then the privilege of many is not facing ableism. In domestic violence organisations, the political alignment is to feminism. Therefore, I’m gappy to say that reference to disability equality is instinctive C-Change because of the population within the org. My colleagues are anti-ableists almost intuitively, but I’d guess it is because there has been much work/learning in the past and along the way.


“Non-disabled privilege is unearned advantage, the absence of the prejudice, discrimination, and injustice weighing on the disabled population. A position often left unarticulated and unchallenged.”


We talked a great deal about how privilege relates to politics, policy, and practice. Many voiced their intent to learn more.


Human Rights and Panel Principles: Participation, Accountability, Non-discrimination, Empowerment, Legality.


Political: Control - Fundamental to Well-being

Choice and control are not just important; they are essential to well-being because of their profound impact on health. At C-Change, discussions about finances are clearly defined by people's ownership of their money, empowering individuals to make decisions based on personal desires rather than imposed ideas about needs. This way, C-Change can offer choice and control, not just a few options, fostering resilience. Furthermore, the ongoing relationship with people ensures that preferences are understood and expected to change. Personal networks—family, friends, and neighbours—also play a significant role in daily choices, ensuring present happiness and long-term well-being.


Principles of Inclusive Practice - Choice: Ensuring respect in service provision without imposing restrictive norms of working practice.


Positive: Cultivating Hope

I felt it was ironic that we got to the exuberant and high-energy part just as I was physically fit to drop. As I set the groups up to work, I reflected on how much easier it was to work with three impairments, not five! And that when people observe you doing a job well, they’re largely unaware of the effort required. It used to be far easier to spend most energy on the job than now having to spend it on personal movement - both physical and mental. I often watch my colleagues work effortlessly with others, taking a minute to appreciate how much intentionality goes into making this possible!


Anticipation allows us to envision a hopeful future, creating a proactive rather than reactive environment. At C-Change, discussions about the future are filled with optimism, encouraging actions that turn aspirations into reality.


Questions:

1. What are six things that I value and take for granted in my life?

2. Can the people we work for do the same?



The conversation moved into party politics, unsurprisingly given recent events in the UK.


Web of Accountabilities

Closing the gap [legitimacy] between professional accounts and the voice of the people we work for demands that we add more to strategic conversations than financial consideration. At C-Change, when teams talk about the rights, they intentionally realign the conversation to the 5 Ps. This means that well-being is considered and human rights are honoured. As the (bad) graph below shows, when more time is given to what is possible, political, and a privilege rights are denied less often - colleagues don't stop at the individual (people).





Turning to the keywords in our discussions—hospitality, citizenship, choice, control, anticipation—these elements interconnect like a web, creating a space that could help sense, if not measure, accountability. At C-Change, I plotted a culture of proximity and trust, essential for recognising and responding to others' needs and feelings. Rather than stop at people, the organisational conversations I’ve been part of extend far further to encompass their strategic objectives.


Final Thoughts


engaging with C-Change's narrative provides many insights, but certainly articulates and reinforces the transformative power of accountability in whose voice and storytelling underpin change.


Note: I have purposefully omitted the more personal stuff we shared because, while illustrative, there is a difference between sharing personal experience and organisational know-how in public.


1/20/24

Progress and Leadership

 


Disability Equality gives us a way of articulating the voice of disabled people, but equality and accountability are part of an organisation's long-term vision. 

Therefore leadership teams need to ensure organisations develop alternative working practice that challenge the legitimacy gap.


 

While the recruitment of people who are visibly different is good, those who acquire impairments at work are estimated at 86% of the disabled workforce. If 400, 000 professionals leave employment every year, that is a huge cost to business. 

 

As John West-Burnham wrote: “Our judgements about almost all social interactions, organisations and communities depend upon our perceptions of the relationships involved’ and ‘If the prevailing orthodoxy is [discriminatory] …  on an equitable basis then the role of leadership has to be to question and challenge that orthodoxy. The more deeply embedded the orthodoxy the greater the need for transformational leaders”.  (West-Burnham, 2009, p. 12)

 

We cannot say whether discrimination or impairment is a causal factor, but we can state that the barriers facing professionals at interviews probably persist throughout their career, and therefore impact those who become disabled mid- or late-career. Therefore, institutional discrimination almost certainly plays a large part in the absence of disabled professionals at senior and board levels. Viewed thus, matters of diversity and adjustments are also important in the progression of skilled, talented and experienced individuals. 


A disabled professional’s CV will possibly show shorter than average spans in multiple roles within different organisations. This eclectic mix of knowledge and skills has become the norm. The disabled professional will also have gained rich experience within and beyond employment that needs to be recognised as strategic, extensive and maybe overachieving. This makes their suitability for promotion obvious, yet they rarely achieve it, preferring to leave instead. As we saw in the discussion about trust, assumptions about the lack of excellence within the disabled population need to be challenged and extended to the diversity of roles available across the board. 

 


 The power of representation

•       As the Disability Power 100 list shows, increasing the representation of disabled people as achievers is ever more important to counter misrepresentation and replace outdated ideas with the real experience of positive relationships. 

•       It is therefore critical to “recognise, celebrate and promote” the contribution of disabled individuals as equally capable, creative and productive workers in their field who bring knowledge, expertise and craftsmanship to their workplace. While helping to shift attitudes and expectations, visibility challenges culture. 

 


    the end of a tale but the beginning of a journey 

 

Together, the four posts sections spell out an alternative understanding of working with disabled professionals. Starting with language, workplace culture can change, and the transformation depends on us, as employers, to follow the lead of the disabled community*  those who have actively challenged the attack on their human rights. 

 

Together they provide an extended terminology that will help employers to talk with more certainty about:

•       the disabled worker  the person, their skills, experience, qualifications and particular knowledge

•       disablism   the barriers, negative attitudes and working practices faced by disabled people but not by their non-disabled colleagues within organisations, sectors or professions (eg fear, lack of awareness, avoidance, micro-aggression, stairs, complex or incomplete policies)

•       ableism – the misrepresentation or silencing in the documents, communications and wider storytelling of organisations 

•       impairment, condition, difference or functioning – private information, the disclosure of which is a disabled individual’s choice to disclose: the same is true for their identity as a disabled person

•       inclusive practice an ongoing process of adjusting equitably to diversity.

 

It is all very good news, as addressing the prejudice, discrimination and inequality disabled workers face 

 


11/22/23

Account-ability: human rights in disability conversation

In the professional realm, the articulation of accountability within the framework of Equality & Diversity is pivotal. This approach also provides a lens through which to examine and address disablism and ableism in everyday practices. 

This post touches on:

- The Voices of Disabled People and THEIR Civil Rights Movement

Recognition of disabled individuals as the primary authors of their narrative, but foremost for business the role of D/deaf and Disabled People’s Organisations in articulating a collective story of shared interests
- Trust as a Foundation for Inclusive Practice 
 Accountability is viewed as a journey where positive exchanges contribute to a bank of trust, which serves as a buffer against lapses in practice, fostering a workplace environment guided by respect.
- Beyond Financial Considerations:
Accountability can be measured as the amount of time given in conversation to the interests of the disabled population [as defined by the Sustainable Development Goals].
- Account-Ability and the Social Model
The Social Model is used as a way of offering an alternative to the legitimacy gap as defined in the previous post.

This post addresses the Sustainable Development Goals, particularly 11, 12, 13, 16 and 17, which deal with inequality, sustainable institutions, governance, and peace & justice.


Sustainable Development Goals


Expressing Interests Equitably:

Disabled individuals are the primary authors of their narratives. The story they tell is a manifestation of their interests and experiences. Recognising and valuing their self-expression, professional knowledge, and group voice is fundamental in fostering an inclusive environment.

 

The Role of Civil Rights Organisations:

 

In the tapestry of disabled people's voices, civil rights movements play a crucial role. D/deaf and Disabled People’s Organisations serve as storytellers, articulating a narrative of shared interests. Their legitimacy is derived from being accountable to the disabled population, providing a genuine reflection of the challenges and interests within and across communities of disabled people.

 

Trust as a Currency

 

Accountability can be viewed as a journey where positive exchanges contribute to a bank of trust. When leaders appreciate the contributions of disabled individuals, acknowledging and adding to the metaphorical pot, the trust they demonstrate can help build a culture of mutual respect. Trust becomes a buffer, positive feeling in cases of inadvertent lapses in appropriate language, for example, fostering a workplace where communication is guided by respect.

 

Response Ability and the Social Model:

 

The Social Model, a cornerstone of critical disability theory, offers an alternative perspective to the prevalent Medical Model [see Figure 2]. It represents a recognizable voice guiding organizational conversations away from individualized or medicalized problem-solving. Instead, it promotes shared responsibility, recognizing Disabled people as a civil rights group with a legitimate voice for human rights accountability. The daily disadvantages faced by Disabled individuals are not solely physical; the model also highlights the societal fear and lack of understanding perpetuating discrimination.  In essence, accountability transcends mere policies; it is a collective journey undertaken by all workers. Shifting organisational storytelling to be able to count disabled people 'in' requires a holistic and inclusive approach. Each member of the workforce plays a crucial role in creating an environment free from discrimination, and fostering a workplace culture guided by respect, trust, and shared responsibility. By embracing these principles, organisations can truly become equitable by laying the groundwork for workplaces that are not only inclusive but also empowering for all.

 

Beyond Financial Considerations:

 

Accountability to the disabled population, 10% of any group, must not be compartmentalised into single policies or departments. The notion that 'disability' can be confined to a stand-alone file contradicts the idea that every worker may identify, and can willingly and effectively respond to prevent discrimination or speak out against injustice. Accountability can be measured as the amount of time devoted to talking about the disabled population's interests - not any one individual's preferences. In my work, I plotted these along five axes representing a human rights discourse: political, public, innovative, financial; and civic.

 


Shared Responsibility for Inclusive Environments:

 

The Social Model, like the Medical Model, is a shorthand for critical disability theory - as put forward by Disabled people.  A recognisable voice which represents an alternative perspective. The concept of response-ability, can be strengthened by the Social Model [Disability Studies], and urges organisations to embrace a shared responsibility. Through its lens Disabled people are not viewed merely as individuals with specific needs, but as a civil rights group advocating for human rights. The Social Model shines a light on the societal factors contributing to discrimination, emphasising the need to address fear, lack of understanding, and inequality alongside physical barriers.



The task of altering environments to eliminate disadvantages for disabled workers should not be the responsibility of a select few. Instead, it necessitates a collective effort from all workers. Shifting organizational storytelling to be accountable to disabled people requires a comprehensive and inclusive approach, where each member of the workforce actively contributes to creating an environment free from discrimination.





Conclusion 

In this exploration of accountability, it is evident that the power of disabled people's voices and civil rights movements is paramount. Recognising disabled individuals as the authors of their narrative and acknowledging the role of D/deaf and Disabled People’s Organisations in articulating shared experiences creates a foundation of authenticity and understanding.

 


11/13/23

Empowering Inclusion: The Power of Respectful Language in Conversation

Introduction:

In the realm of disability discourse, the choice of words becomes a potent tool to articulate barriers, disadvantages, and discrimination. This blog delves into the nuances of language policy, advocating for a mindful consideration of the words we choose and the profound impact they carry. By challenging negative narratives and stereotypes, we can cultivate a culture of inclusivity and understanding within organizations.


Respectful Language

Current terminology surrounding disability often carries negative and medical connotations, perpetuating myths prevalent in everyday conversations. Words like 'disability' attempt to encapsulate 'personal difference,' 'labelled group,' and 'inequality.' However, the focus should shift towards promoting respectful language that prompts individuals to contemplate the meaning and context of their choices, especially in public documents where terminology plays a crucial role in defining organisational culture.

The Workplace as a Potential Source of Barriers:

The workplace, often unintentionally, presents barriers through organisational and institutional practices that may contribute to disabling people. It is crucial for professionals to feel empowered to participate fully, irrespective of whether they have impairments themselves.


Words to Use with Care in the UK:

1. Ableism: A societal oppression embedded in workplace language, comparable to other forms of systemic discrimination such as homophobia, racism, sexism, classism, ageism, or religious intolerance.

 2.D/deaf and Disabled People’s Organisations: Organisations and groups run by Disabled people, including those who identify as Deaf and/or have their own language, such as British Sign Language in the UK.

3. Institutional Discrimination: Organisational oppression directly affecting disabled people, unchallenged within the workplace and across institutional boundaries.

4. Disabled People: The capital 'D' is used by those aligning with the Disabled People’s Movement, reflecting a political choice rooted in Disability Studies. In the UK, 'disabled people / dp' is preferred over 'people with disabilities.'

5. The Disabled Population: Acknowledging the large number of individuals experiencing ableism, 'population' denotes a statistical group. Not all disabled people identify with being Disabled, or join the Disabled People’s Movement, and some may not even like the term 'disabled.'

6.The D/deaf and Disabled People’s Civil Rights Movement: A network of disabled individuals, some supported by allies, viewed as a civil rights group, comparable to feminist or anti-racist movements.


Myths and Assumptions:


1. Scale: Challenge the myth that disabled people are a small, separate group by describing them as the 'world majority'—1 to 2 in 10 people could identify as disabled.

2. Fitting In: Avoid polarising disabled people as a separate subgroup. Instead, recognise them as part of a population facing common disadvantages.

3. Societal Impact and External Cost: Present any cost of employing disabled individuals as a good investment to secure a more inclusive culture and a larger talent pool.

4. Illness and Institutional Practice: Differentiate between illness and disability to prevent viewing the disabled as having a problem to be cured.

5. Personal/Private Boundaries: give disability and illness separate definitions in workplace conversations /policy/guidelines in order to address the barriers, discrimination, and inequality the disabled population face with intent.


The Legitimacy Gap – The Medical Model:

An ethical articulation of accountability is one that qualifies equality and diversity, and helps all workers speak with confidence when addressing ableism in everyday practice.

A legitimacy gap arises when organisational storytelling fails to demonstrate accountability, and diverges significantly from a narrative that hours the interests of the disabled population. 

Acknowledging the character of this gap, for example, the significance of the Medical Model, allows business leaders to respond effectively in both personal and public conversations by addressing specific barriers, discrimination and injustice disabled people face in conversation.


the Medical Model



In Conclusion:

Understanding and embracing respectful language while dispelling myths in conversation about disability can help organisations create an inclusive and empowering environment for all. By fostering a culture of awareness and sensitivity, business leaders can contribute to breaking down barriers and promoting equality within our workplaces and beyond.

11/3/23

The Disability Employment Gap – A Closer Look

This blog sheds light on the gap in work opportunity for the disabled population. By exploring how:

- Workplaces often fall short in recruiting and promoting disabled workers, and

- They unwittingly contribute to the injustice imposed on the disabled population. 


EMPLOYMENT 

The low employment rate of disabled people is a human rights issue, which leads to a higher likelihood that disabled individuals struggle to secure employment and face extended periods of unemployment. The scope of the disabled population is larger than commonly thought. For instance, in a company of 1,000 employees, roughly one in ten, or 100 workers, may have impairments, whether they identify as disabled or not. This figure is significantly greater than the number of individuals parked in the few accessible bays outside the building. However, many people underestimate the size and diversity of the disabled population as a whole. Consequently, they tend to underestimate the extent of the problem and the cost of the disability employment gap to both the industry and society.

Clearly, the issue goes beyond the occasional lack of personal fit. Effective inclusive practices remain inconsistent, partly due to the diversity of impairments. While most differences have likely found accommodations in some form, overall inclusive practices are not yet a reality that disabled professionals can take for granted. Organisations and institutions often serve as sources of injustice, as disabled workers possess no less experience, skill, or wisdom than their non-disabled colleagues. However, they encounter far more barriers than most employers imagine. Many depend on organisations willing to take action to address the disadvantages they face. For business leaders, the challenge is to align organisational change to benefit both disabled individuals and the broader working community.

Culture Shock

  • The unemployment rate is 1 in 4, which drops substantially for people with learning disabilities, compared to 1 in 10 for others.
  • Fewer than 1 in 10 disabled individuals are currently employed, in contrast to 1 in 10 non-disabled people. This disparity has repercussions extending beyond finances, affecting well-being, self-esteem, relationships, and health.
  • An astonishing 86% of all disabled people in the UK acquire their disability during the course of their working lives.
  • The employment rate for disabled people stands at 45.4%, while non-disabled individuals have an employment rate of 81.2%, resulting in a substantial gap of 35.8 percentage points.
Why Being Seen at Work Matters

Efforts have frequently focused on accommodating impairments, with training solutions targeting frontline staff, while senior leadership teams have received less attention. Understandably, this has led to resistance from workers who felt overwhelmed by the amount they needed to learn. Moreover, without support from decision-makers, there has been minimal funding for strategy implementation. Additionally, it seems that disability training, when provided, often receives less time and attendance compared to other equality strands. This poses a challenge, as professionals realize the depth and breadth of knowledge required to address these issues. Many now recognize that without the backing of senior management, leadership teams, and boards, strategies often fail to align and achieve the necessary changes. Time-consuming and costly individual-level adjustments rarely result in significant departmental transformations within a company's purpose. Therefore, viewed in this way, few organizations do nothing, most take some action, and many could do more.

The net result is that few do nothing, most do something, and far more could make better use of what can and is being done together.


The importance of being visible at work lies in creating clear boundaries between private and public discourse, dispelling myths and uncertainties about disability, and fostering inclusivity. In the workplace, error is rarely as problematic as silence. People are generally flexible and understanding when they make an effort to use mindful language. However, in public documents and within organisations, terminology becomes far more critical, as it shapes the culture and values of an organization. Therefore, being seen at work and fostering open discussions about disability is pivotal in bridging the gap and promoting a culture of inclusivity.

9/26/23

Ableism - Lifting The Veil

Ableism: 

I will be posting a series of posts dealing with tackling ableism at work. The handbook capturing the series can be found here.

A Silhouette of Silence 

 

This piece outlines the challenges and limitations of addressing the aspects of culture and language that disadvantage disabled people. The first three sections specifically address ontological and epistemological issues that must be addressed before methodology or literature can be discussed.

 

I argue that experimental science is not an appropriate methodology for this type of research, as it is inherently oppressive to disabled people. Instead, I want to say that a caring methodology,  a feminist approach, for example, respects disabled people's experiences and perspectives. Research also needs to be emancipatory, meaning that it should seek to empower participants and challenge the systems that disadvantage them. Research, therefore, needs to be grounded in a social constructionist perspective of co-production, which means that it should be conducted in collaboration.

I  conclude by discussing the importance of language and culture in shaping the experiences and argue that ableism is often reinforced through language and culture unwittingly, therefore important to be mindful of this when conducting research.

Here are some key points:

·      Ableism is a form of oppression that disadvantages disabled people.

·      Traditional positivist experimental science is not an appropriate methodology for researching disability, as it is inherently oppressive.

·      Interpretivist-inductive methodology is a more respectful and emancipatory approach to researching disability.

·      Research on disability should be grounded in a social constructionist perspective of co-production, meaning that it should be conducted in collaboration with disabled people.

·      Language and culture play an important role in shaping the experiences of disabled people.

 

This blog critically examines the concept of ableism and its profound impact on d/Disabled individuals. I want to explore the social and systemic barriers faced by disabled individuals, emphasizing the urgent need for organisations and society to acknowledge and address these challenges. Accountability may be addressed by promoting the Sustainable Development Goals, particularly 11, 12, 13, 16 and 17, which deal with inequality,  institutions, governance, and peace & justice.

This piece encourages readers to reflect on their own biases, become advocates for disability rights, and actively contribute to positive change.

 

I. Introduction:

The issue of ableism has long been a subject of concern in contemporary society, I aim to provide a summary and analysis into the intricacies of this pervasive form of discrimination. By examining insights, we aim to shed light on the social and systemic barriers faced by disabled individuals.

 

II. Understanding Ableism:

Ableism refers to the prejudice and discrimination experienced by disabled individuals, stemming from societal attitudes and infrastructural barriers. This post emphasises an urgent need for society to recognise and address these challenges, as they significantly impact the human rights of disabled individuals.

 

III. Unveiling Social and Systemic Barriers:

I want to emphasise the importance of recognising and dismantling social and systemic barriers that perpetuate ableism. These barriers include inaccessible physical environments, limited educational opportunities, employment discrimination, and social stigmatization. Such barriers limit the full participation and inclusion of disabled individuals in various aspects of society.

 

IV. Promoting Equality and Opportunities:

In order to combat ableism, more needs to be done at strategic levels to address equality and opportunities for all individuals, regardless of their abilities. It highlights the significance of fostering understanding and empathy towards disabled people, I encourage readers to reflect on their own biases and assumptions.

 

V. Advocacy for Disability Rights:

The post serves as a call to action, urging readers to become advocates for disability rights. By raising awareness about the challenges faced by disabled individuals and engaging in open and respectful conversations, we can challenge ableism at both an individual and societal level.

 

VI. Conclusion:

In conclusion, the blogs that follow will provide a thought-provoking framework to explore the issue of ableism and its impact on disabled people. The crucial role of equality, understanding, and equal opportunities in fostering a more equitable society. By actively challenging ableism and advocating for disability rights, we can collectively work towards building a more inclusive and accepting world.