Eloka On The Eclectic

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Eloka On The Eclectic The Eclectic is a podcast where we discuss a variety of issues, bordering on different aspects of life and its intricacies.

So join us as together, we embark on this journey towards making life-changing discoveries.

The Eclectic PodcastHosted By Eloka Oduah Storytelling, Inclusion, and the Future of African YouthBlessing MicahSign Lan...
10/11/2025

The Eclectic Podcast
Hosted By Eloka Oduah
Storytelling, Inclusion, and the Future of African Youth
Blessing Micah
Sign Language Interpreter
and Youth Advocate.
In this episode, we explored Blessing's journey, her passion for building inclusive narratives, and how digital spaces can become powerful tools for accessibility, and advocacy.
🎧 Listen now https://open.spotify.com/episode/6VIn5sHC8edkT84h6V7PqG?si=xSTsSGrkSbyoz0CCIB7RCA or read 📖 https://docs.google.com/document/d/1wKJZmrWhVVIsC9eOtNbBsyY4BlVcureZ/edit?usp=sharing&ouid=102186582647928362400&rtpof=true&sd=true
Image Description
The poster has a blue background. To the left center is a picture of a vibrant, sun-drenched scene that depicts a group of African youths gathered in a circle. A young woman animatedly tells a story using sign language, her hands forming expressive shapes. Several youths, some with visible disabilities such as hearing aids or using wheelchairs, attentively watch and engage with the storytelling.
At the bottom are the logos of The Eclectic Podcast and the Rotary Club of World Disability Advocacy

What does it mean to heal, advocate, and love fully and unapologetically?The Eclectic PodcastHosted By Eloka OduahThis w...
26/10/2025

What does it mean to heal, advocate, and love fully and unapologetically?
The Eclectic Podcast
Hosted By Eloka Oduah
This week of The Eclectic Podcast, I sit down with Tara Jo Kadlec, founder of Love Your Journey Inc. and host of The Love Your Journey Podcast. Tara Jo helps women reclaim their voices, reconnect with body wisdom, and create lives rooted in authenticity and joy.
Her story is also one of advocacy, inspired by her late brother Cory, who had Down syndrome. His legacy continues to fuel her mission to create inclusive spaces where every person feels seen and celebrated.
🎧 Listen now https://open.spotify.com/episode/4wOzDBhoBiTs9cprjsqxS4?si=bOfyy92XQ_iMKIP6Mq82Dg or read 📖 https://docs.google.com/document/d/14m-oyXEyIeBAxDaG1HEcuCxIi9GoY-w3/edit?usp=sharing&ouid=101962272319320992200&rtpof=true&sd=true
Image Description:
The poster has a black background. To the right centre, there is a linear perspective of a series of candles glowing in the dark. At the bottom are the logos of The Eclectic Podcast and the Rotary Club of World Disability Advocacy.

There was a time I hated my white cane. I may have been ashamed of it without realising. But I know that I wasn’t comfor...
15/10/2025

There was a time I hated my white cane. I may have been ashamed of it without realising. But I know that I wasn’t comfortable using it, and my dad would always ask why I was not with it.

The very first White Cane I had was gifted to me in 2005 by Prof. Rev. Sis. Theresa Abang, God rest her soul. As I have already admitted, I hated the Cane and had no intention of using it until something profound happened back in 2012. I don’t recall what happened, but whatever it was, it made my principal, God rest his soul, insist one assembly morning, that all visually impaired students were to henceforth, use their White Cane.

That pronouncement was like a prison sentence as I heard it. But Mr. Ojemere was not done with his seemingly life-imprisoning sentence. He went further to instruct our fellow students not to assist us. In fact, his exact words were, “Don’t help them”. I recall thinking, what sort of wickedness is this.

Though that may have seemed harsh of him at the time, I am, however, grateful for that decision. While I grudgingly used my Cane as I obviously had no choice following the decree, I eventually, over time, became comfortable using and identifying with the White Cane.

It later occurred to me that I may have subconsciously been shying away from the White Cane because of the negative perception society has about things like that. Too often, we don’t get to see enough of people with disabilities living a happy and fulfilled life. What we see more of is how life takes a somersault for all the wrong reasons once an impairment happens. I guess I did not want to be associated with the type of blind people we saw in Nollywood who were pitiful and had nothing to offer the society.

Now that I am more aware and understand the importance of self-acceptance, I join the rest of the millions of White Cane users all over the world to commemorate this very important day. I am no longer ashamed of who I am. I am a proud user of the White Cane. It is not just a tool for independence and mobility. It is a symbol of strength and resilience, and I say happy International White Cane day to all the unabashed proud White Cane users!
Eloka Oduah


How do we create a world where every child is celebrated for who they are, not forced to fit into narrow boxes?The Eclec...
12/10/2025

How do we create a world where every child is celebrated for who they are, not forced to fit into narrow boxes?
The Eclectic Podcast
Hosted By Rotarian Eloka Oduah
This week on The Eclectic Podcast, I sit down with Amy Bodkin, an Autistic adult, parent, and special needs Consultant serving families worldwide. With her Holistic Developmental Approach, and homeschooling of her two Autistic children, Amy is transforming the way we think about education, neurodiversity, and advocacy.
🎧 Listen now https://open.spotify.com/episode/2Jk9hRC7WGDi5uLgaPo7TQ?si=osPyR1glR6G-tkrplDWJLQ or read 📖 https://docs.google.com/document/d/1Ofb-4hGa2lNPGhl5f0rPsY2qfjHOvIhC/edit?usp=sharing&ouid=102186582647928362400&rtpof=true&sd=true
Image Description
The poster has a brown background . To the left center is a warm and inviting scene of a parent patiently teaching two young children at a cozy home study, with books neatly arranged on shelves and natural light streaming through a nearby window.
At the bottom are the logos of the Rotary Club of World Disability Advocacy and The Eclectic Podcast
# Neurodiversity

How do you turn stigma into strength?The Eclectic Podcast Hosted By Eloka Oduah.On The Eclectic Podcast this week, we sp...
28/09/2025

How do you turn stigma into strength?
The Eclectic Podcast Hosted By Eloka Oduah.
On The Eclectic Podcast this week, we speak with Grace Ochoche, a psychology graduate, model, disability advocate, and a person with albinism.
Grace shares her powerful journey of self-acceptance, breaking stereotypes, and finding confidence through modelling. Her story reminds us that being different is not a weakness, it’s a unique kind of strength. đŸ’ȘđŸŸâœš
🔊 Listen now https://open.spotify.com/episode/6FEq0Nt3sumcidLB2C2ESB?si=1jhAeU5pThCrKpFVSP_b1Q or read 📖 https://docs.google.com/document/d/1yvhHTd6bCA2KR7_S8vvdAPUoxjOKUviISu9D7b0ZoZU/edit?usp=drivesdk
Image Description
The poster has a blue background. To the left side is the close-up photo of the area of the face surrounding the eye of a person with albinism. At the bottom are the logos of The Rotary Club of World Disability Advocacy and The Eclectic Podcast

21/09/2025

“Never forget what you are, for surely the world will not. Make it your strength. Then it can never be your weakness. Armor yourself in it, and it will never be used to hurt you.” J. R. R. Martin.
In a world that often tries to define people with disabilities by limitations rather than possibilities, this quote offers both a challenge and an invitation. It reminds us that self-acceptance is not passive resignation but a deliberate act of empowerment. It is an act of empowerment because what self-acceptance does is that it allows you engage on your own terms, without unnecessary pressure.
I recall speaking during a panel session a few months back where I was asked how I have used humour as a tool in my journey, and the role it plays in how I relate to the world? This question I found very significant because as the moderator of the panel rightly pointed out, disability is often viewed through a lens of pity or sadness, and many people tend to get uncomfortable when discussing it or engaging with persons with disabilities. Yet, I navigate my disability with such a refreshing sense of humour.
The truth is that, for many persons with disabilities, society has already written a script, one that is clouded by stereotypes, ableist assumptions, and lowered expectations. To “never forget what you are” in this context means refusing to internalize those limiting narratives. Instead, it means embracing disability as part of one’s identity, not something to conceal or apologize for. I had to come to a point in my life when I realised that being visually impaired is part of who I have become and it is nothing to be ashamed of. Living in denial was doing me more harm and denying the obvious will not change the fact that I cannot see. The quote by J. R. R. Martin upon which I have based this piece is a very powerful quote, one that I believe everybody can relate with regardless of whether you are a person with disability or not, even though Tyrion, the fictitious character through whom the author made the statement, is a person with disability. Nevertheless, my focus in this entire piece, is on the power and importance of self-acceptance.
When disability is seen through the lens of strength, resilience, and lived expertise, it transforms. The very characteristics society might frame as a “weakness” can become the foundation for innovation, empathy, advocacy, and leadership. This is not about denying challenges, but about refusing to allow them to define worth.
Self-acceptance becomes an armour not a barrier that isolates, but a shield that deflects stigma. It is the inner resilience that allows individuals to walk into spaces where accessibility is lacking and still demand equity. It is the courage to speak up against exclusionary practices, knowing that authenticity itself is a form of resistance. So, when I’m asked how I can find humour in my disability, the answer is in the fact that I have accepted my reality and that self-acceptance has become my shield, the reason I can navigate my disability with a sense of humour.
But inclusion requires more than personal armour; it demands a collective shift. Organizations, communities, and institutions must recognize that true inclusion is not about asking people with disabilities to “overcome” but about addressing the barriers that force them to fight in the first place. When spaces are designed inclusively, individuals no longer have to carry the full weight of defending their identity.
Disability is not a weakness to be hidden. It is an identity, an experience, and a perspective that enriches society. As Martin’s words suggest, when embraced and wielded as strength, it cannot be weaponized against us. Self-acceptance, then, is not only personal liberation, it is the foundation of a more inclusive world.

-Acceptance

10/09/2025

As promised, I am back to talk about the one stereotype or myth about men with disabilities that makes me laugh. So, the first time I heard someone say, (if you say he is blind, how was he able to make love to his wife” was so many years ago. At the time, I thought it was a comment made in gest. Several years have past since I first heard that comment, and several more times have I heard that question asked. Honestly, I don’t know if the people asking that question are truly ignorant or that they are being intentionally cheeky. Nevertheless, I thought it necessary to give my thoughts on the erroneous notion that finds it strange that a blind man can perform his conjugal duties to his wife.
The first thing I would usually say is that when sighted people want to do the same thing they wonder how a blind man is going to do, they sometimes turn off the light. So, my question is, how can they see what they are doing in the dead of night in the dark? At that point, how different is the sighted man from the blind man. They both cannot see what they are doing. They are guided by the sense of touch rather than the sense of sight. Yet, the sighted man wonders how the blind man can find his way around there. Funny right?
The truth is that these things are not rocket science. They are just simple logic. The problem is that most people tend to overthink things and so, something as simple and as natural as a blind person feeding themselves, becomes a mystery to a sighted person. I recall being asked a few times how I am able to find my mouth since I cannot see? My usual response to this question is, you who can see, do you sit in front of a mirror when you want to eat? If your answer is no, then how do you find your mouth? Because if you are not feeding yourself in front of a mirror, you are no different from me in that we both cannot see our mouths when we are eating. So, my dear readers, please help solve the mystery and provide an answer to the question 😀.
Please don’t get me wrong, I am an advocate for asking questions. It is my belief that you cannot go wrong by asking questions, and no question is silly. The point I am trying to make in this post is that while we as persons with disabilities sometimes do things differently, we are not different from you as a person without disability. So, the simple things you do may not always have to be different for us. Just keep an open mind and yes, don’t stop asking questions!
Eloka Oduah


07/09/2025

A few weeks ago, a friend, whom I would like to call a comrade in the advocacy for disability inclusion, reached out and asked if I would be interested in taking part in the project that she is working on. The project is called “The Body as Canvas”. She asked me to record a 1–2 min video, answering a few questions which I did. The best part of her requirements was that I should just be me and that was wonderful! No pressure of trying to impress and make a perfect video. For those of you who make videos, kudos to you guys! I hope to get there someday in the nearest future 😀.
Meanwhile, I’ll drop the link to the video in the comment section, please watch it and show some love. In the video, I talked among other things, about my audio editing skills, and that’s what has inspired this post. In a separate post, I will write about what I said in the video concerning one stereotype or myth about men with disabilities that makes me laugh. But that is a story for another day 😂. For now, let’s focus on the current story.
During my youth service, I struggled to make the kind of impact I would have liked to make. Serving at FRCN in Abuja was a mixture of varying emotions. Listening to my fellow corpers and other interns take on various audio editing tasks, left me feeling frustrated because I couldn’t do what they were doing. I couldn’t do what they were doing not because the technology was not available, but because the knowledge was lacking. I did not know at the time, that there were other audio editing softwares I could have used, and used perfectly.
I recall trying all I could to be able to use Adobe Audition, which was the audio editing software that everyone in the office used. Unfortunately, I could not use it because it was not accessible to my screen reader or because I did not know better. That was how I spent an entire year of my service, not being able to edit a single audio while I made myself useful in other areas.
Less than ten months later, during the Covid lockdown, I discovered the joys of Audacity and GoldWave, two other audio editing softwares that were perfect for my screen reader. It was a bittersweet feeling because I found myself thinking, if only I knew then what I know now, I would have done a lot more at FRCN than I did. While it is true that sometimes, certain things are actually not accessible for a screen reader user, I have since learnt the importance of seeking alternatives before concluding that something cannot be done just in case, because truly, if I knew then what I know now about audio editing, I would have enjoyed my time at FRCN much more better than I did.
Thank you Eva for letting me take part in your project and inspiring me to write this. I hope I am able to write a lot more often 🙏.
Eloka Oduah


What is the Right Fit for Persons with Disabilities?The Distribution of WheelchairsIn the opinion of this episode's gues...
20/07/2025

What is the Right Fit for Persons with Disabilities?
The Distribution of Wheelchairs
In the opinion of this episode's guest, when a wheelchair doesn’t fit, it can harm more than help
In this eye-opening episode, hosted by Rotarian Eloka Oduah, we speak with Alex Kamadu, Executive Director International Society of Wheelchair Professionals. He shares with us his opinion about the real cost of mismatched chairs and why every person deserves the right fit
🎧 Listen in https://open.spotify.com/episode/5dqwVyQmgMfr9cP66L2cXI?si=W6GRe25mSEW4ygnkma_qWw or read 📖 https://docs.google.com/document/d/1li2YBs-8hgvId4MMkOtyC4KMSyDVZQuv/edit?usp=sharing&ouid=102186582647928362400&rtpof=true&sd=true to rethink what meaningful support for persons with disabilities should look like.
Whether you are a policymaker, donor, NGO worker, or ally, this episode challenges you to rethink what true inclusion really looks like and calls on all of us to ensure that assistive devices empower.
The Rotary Club of World Disability Advocacy
Image Description:
The poster has a background with dark blue to blue shading. A diverse crowd of a larger number of people of various ages and ethnicities, each expertly manoeuvring their wheelchairs along a sun-drenched city street. The scene is vibrant, full of life and movement, captured in a photorealistic style with a wide-angle lens, showcasing the individual expressions and personalities of the wheelchair users. The street is bustling yet clean, with diverse architectural styles visible in the background. The overall colour palette is warm and inviting, with bright sunlight highlighting the scene. At the bottom are the logos of The Eclectic Podcast and The Rotary Club of World Disabilities Advocacy

where are we now? 35 years ago, the Americans with Disabilities Act (ADA) broke ground for disability rights.In this spe...
06/07/2025

where are we now? 35 years ago, the Americans with Disabilities Act (ADA) broke ground for disability rights.
In this special episode of The Eclectic Podcast, hosted by Rotarian Eloka Oduah, we sit down with Angie Fuoco, a Rotarian, seasoned ADA Coordinator, DEI educator, and anti-ableism trainer to explore the wins, the gaps, and the future of inclusive design.
🔊 Listen in https://open.spotify.com/episode/35t3ayRnrlolSyJCPLYhmw?si=7qiAciXUTnW3abRrO1nkBQ or read 📖 https://docs.google.com/document/d/1lsp71cK1DUQnmGAqBWHPsodXFCi9bn0g/edit?usp=sharing&ouid=102186582647928362400&rtpof=true&sd=true as we unpack the legacy of the ADA and why true accessibility means more than just ramps and signs.
đŸ’„ Whether you're a changemaker, ally, or advocate; this is a conversation you don’t want to miss.
The Rotary Club of World Disability Advocacy
Image Description:
The poster features a blue background. To the left middle is a vibrant, photorealistic image depicting a diverse group of people of all ages and abilities passionately advocating for the Americans with Disability Act. They hold signs with slogans such as "Accessibility for All" and "Equal Rights," and their expressions convey determination and hope.
At the bottom of the poster are the logos of The Eclectic Podcast and The Rotary Club of World Disability Advocacy

We have the right to choose. To parent. Or not. To be seen as full people.This week on The Eclectic Podcast, we explore ...
22/06/2025

We have the right to choose. To parent. Or not. To be seen as full people.
This week on The Eclectic Podcast, we explore Reproductive Rights and Freedoms of People with Disabilities with Winnie Njeri Muthoni, a gender and disability mainstreaming officer.
🎧 Listen https://open.spotify.com/episode/2zz3CMk237XVLkkJD4J86t?si=leqiBVCaSL2KY7Va5f_MxQ now on Spotify, Apple, or wherever you get your podcasts.
💡 It's time to talk about bodily autonomy, accessibility, and justice—for everyone.



#

08/06/2025

How do you reclaim your voice in a world that often speaks over you? In Episode 7 of The Eclectic, we meet Laraba Barnabas, a Deaf young woman who is a communications specialist and fierce advocate. From living with a cochlear implant to speaking for women’s and disability rights, her story is bold, honest, and beautifully unmuted.
🔊 Click the link https://open.spotify.com/episode/1ycjLCzaZS0jwJhbQEs5tc for a powerful conversation on accessibility, identity, and what it means to truly be heard.



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