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December 23, 2025 24 mins

This week, Simon revisits the discussions he had earlier this year with Dr Rita Kleinfeld-Fowell, Deborah Kazich and Linni Oliver.

Legally Deaf and blind, Rita has faced - and overcome - immense challenges. Through resilience, strength and determination, she has transformed adversity into advocacy, using her lived experience to support and uplift others.

Now Head of Disability Law Practice at Sussex Street Community Legal Centre, Rita is passionate about empowering people with disability through knowledge, rights and representation.

For more information about Rita's work and the legal services available at Sussex Street Community Law Service, go to their website: sscls.asn.au

Deborah Kazich is a Deafblind advocate sharing her vibrant, active life, and Linni Oliver is a dedicated Communication Guide.

Deb has many interests including public speaking training with Toast Masters, and she never misses an opportunity to share her passion for her community and to help bring awareness of people living with Deafblindness.

    More information about Deafblind West Australians can be found on their website.

    Support Vision Australia Radio: https://www.visionaustralia.org/donate

    See omnystudio.com/listener for privacy information.

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    Transcript

    Episode Transcript

    Available transcripts are automatically generated. Complete accuracy is not guaranteed.
    S1 (00:17):
    Hello and welcome to In Plain Sight, a program where
    we highlight people who are making a positive impact in
    the community and disability sector.

    S2 (00:25):
    Shining a light on those who would be otherwise hidden
    in plain sight.

    S1 (00:29):
    And it's a pleasure to bring you these stories on
    a weekly basis with you here on Vision Australia Radio.
    In this holiday season, we're presenting a series of compilations
    of selected in Plain Sight programs from this year. Today
    we'll hear excerpts from the mid-June program celebrating Deaf Blindness
    Awareness Week.

    S2 (00:48):
    We are, and it's a pleasure to bring you this
    really interesting program today. And firstly, we're going to hear
    from Deborah Keswick. And Deborah is a delightful, passionate, interesting,
    fun person who is a really passionate deaf blind advocate
    and advocate for all people with a disability and a

    (01:09):
    strong representative of her community. It's really fun to hear
    from Deb, and we'll also learn a lot about what
    it is like to live with deaf blindness and how
    Deb then advocates for other people in her community.

    S1 (01:23):
    We'll also hear from Lenny Oliver, who's a communications guide,
    which is a very specialized area of of support work.
    After we hear from Deb and Lenny, we'll hear Simon's
    conversation with Doctor Rita Kleinfeld for who's the head of
    disability law practice at the Sussex Street Community Legal Centre
    in Perth.

    S2 (01:47):
    Introducing Deborah Kasich to the audience now. Hi, Deb. How
    are you going?

    S3 (01:52):
    Hi, Simon. Hi, everyone.

    S2 (01:54):
    Thanks for joining us, Deb. Now, Deb, I'll start with
    the bare basics. First. You're deaf.

    S3 (02:00):
    Blind, correct?

    S2 (02:01):
    Tell us about that. What is that condition caused by
    my conditions?

    S3 (02:05):
    I was born deaf blind with rubella syndrome because my
    mum was pregnant with me. Caught German measles. It is
    with syndrome because she you got German measles. My vision.
    I've got limited sight in my left eye. No sight
    in my right eye. My hearing is I can hear

    (02:28):
    the sound. And I wear hearing aids when I'm in
    a loud environment. I use my Roger Penn.

    S2 (02:37):
    And what's that?

    S3 (02:38):
    It's the microphone that connects to my hearing aids.

    S2 (02:41):
    Oh, yes.

    S3 (02:42):
    For those of you who doesn't know about the Roger pen,
    many people who are deafblind can use when they go
    to a large environment, like, for example, the Shakespeare run
    for reasons. Yes, the Roger pen really helps me to
    focus on my support worker or family member, whoever I

    (03:04):
    was with on that day.

    S2 (03:06):
    I follow you on social media, and you're very active
    member of the deafblind community and the very active person
    within our community in general. What do you do for work, Deb?

    S3 (03:17):
    I work at Sammy's in Canning Vale on Mondays. I
    work in the canteen on Wednesdays and Fridays. I work
    in the warehouse.

    S2 (03:28):
    What's the warehouse?

    S3 (03:29):
    The warehouse is based in Canning Vale. We got a
    whole range of jobs in the warehouse. And we march house.
    I do the folding the clothes in the factory, and
    I make sure all my peers work colleagues are happy
    with their job.

    S2 (03:49):
    Okay. How long have you been working there?

    S3 (03:50):
    19.5 years. This Christmas. I'll be there for 20 years.

    S2 (03:56):
    Wow. 20 years. Sounds like you enjoy that job. And
    I know that you also do Toastmasters, where you're learning
    public speaking and you are a public speaker. Is that right?

    S3 (04:07):
    Correct.

    S2 (04:08):
    Tell me about that. What do you do there at Toastmasters?
    For those who don't know what Toastmasters is.

    S3 (04:13):
    For those of you who don't know about Toastmasters? Toastmasters
    is a group where we go and learn to do
    public speaking.

    S2 (04:21):
    Why do you want to be a public speaker, Deb?

    S3 (04:23):
    The reason why I want to Toastmasters to do public
    speaking is because I want to do presentations at census
    and the information Australia's present on technology and many other things.

    S2 (04:38):
    Because that's the main reason I want you in here,
    because you are a very proud, hard working representative of
    your deafblind community and you are a strong advocate for
    people who are deaf, blind and the disability sector in general.
    And I really find it fascinating and fabulous that you
    work so hard at what you do. Deb, what motivates

    (05:00):
    you to be an advocate for deafblind people?

    S3 (05:03):
    When I'm in my local community and I've seen some
    of the places not accessible, and I get out there
    and get strong advocate for the deafblind community and a
    lot my area to know, to understand many of our
    people who are deafblind.

    S2 (05:21):
    What are the main things you would like people to
    know about being deafblind?

    S3 (05:26):
    Well, the main thing is I would like to see
    the community to understand how to work with people who
    are deafblind, like the support workers and Kong guides and
    health professionals. They need to know how to understand with
    people who are deafblind.

    S2 (05:44):
    Yep. Being deaf blind. Are you able to use sign
    language or Auslan as it's known?

    S3 (05:51):
    I know a few basic listening. Just recently on Sunday,
    when we have our Metronet open line for the line,
    I demonstrates a few items with our Premier of Western Australia,
    Brian Cook. And he was so impressed with me, with
    the with my Auslan skills. And I told him I'm

    (06:12):
    coming on this show to thank you.

    S2 (06:15):
    Well done And so do you. Use the touch sign language?

    S3 (06:19):
    Yeah, yeah. Mainly use the general Auslan. And we do
    haptics as well. The VW connect hub.

    S2 (06:28):
    Now I might bring in Lindy Oliver now. Hi Linda.
    How are you?

    S4 (06:32):
    Hi, Simon. I'm good, thank you.

    S2 (06:34):
    Great that you could join us today on a really
    busy time for you guys.

    S4 (06:39):
    Yeah. Happy to be here. Thank you.

    S2 (06:40):
    Now I'll just start with the basics with you to
    Lindy that you're a communications guide. Is that right.

    S4 (06:45):
    A communication guide? Yes.

    S2 (06:47):
    Can you tell us what that is?

    S4 (06:48):
    A communication guide is like a support worker, but with
    specialised skills to work 1 to 1 with a person
    who is deafblind. So we've done some additional training to
    give us the skills to help people to safely navigate
    around their environments, the skills to be able to give
    them environmental information that they're missing out on, and communication

    (07:09):
    support as well.

    S2 (07:11):
    How long have you been doing that? Lynnie.

    S4 (07:12):
    Oh, I was involved in the initial pilot project that
    introduced communication guides to um, Australia. And that was 14.5
    years ago.

    S2 (07:23):
    Fabulous. And you're also involved with what I call Diwa,
    which is deaf blind Western Australia. Is that right?

    S4 (07:30):
    Yes. That's right. I am very much involved. Yes.

    S2 (07:34):
    And you participate in these hubs that was just talking about.

    S4 (07:37):
    Uh, yes I do. I help support the haptic, um,
    lessons that we do there and also support some of
    our deaf blind clients that come along to the hub.

    S2 (07:47):
    Now, Deb mentioned haptics a few times, and I've seen
    it happen. I don't fully understand it. Can you tell
    us what haptics are and how they work?

    S4 (07:57):
    Absolutely. Haptics are touch messages that are given on neutral
    areas of the body that provide the person who is deaf, blind,
    or a person who is blind as well, to receive
    additional information that they're not receiving through their hearing loss
    and their vision loss. So what sighted people and hearing

    (08:17):
    people can see and hear. We provide that information through
    haptics to the deaf blind person so we can give
    information about, like when I arrived here today, she wanted
    to know what this room looked like. So I mapped
    that out on her back for her to let her
    know what the layout of the room was like, where
    she was sitting in the room, and where everyone else

    (08:37):
    was positioned in relation to where she is as well.
    So we can ask people if they want a cup
    of tea or coffee without having to, you know, communicate
    that verbally to them and you can just do seamless
    additional communication with the person through haptics, through the touch messages.

    S2 (08:55):
    So that's a separate thing to the fingerspelling for deaf
    blind and the physical Auslan that might also have to do.

    S4 (09:03):
    Absolutely. Yeah. Yeah. Haptics is not a language. It's a
    communication tool that provides additional information. So it's not like
    Auslan where it's a full language, but it does use
    some signs from Iceland for the touch messages.

    S2 (09:19):
    Just for those listening. A great example of this was
    just recently on the ABC TV program The Piano, where
    one of the people on that program who was playing
    the piano is a deaf blind woman by the name
    of Michelle Stevens. They showed how her assistance communicated with her.
    And what it also showed was that Michelle is a

    (09:41):
    wonderful piano player and that music can communicate with everybody,
    regardless of their ability or disability, and it was a
    fabulous representation of deaf blindness in action.

    S1 (09:57):
    On Vision Australia Radio, you're listening to a special compilation
    program of In Plain Sight. We've just heard from two
    passionate disability advocates, Deb Keswick and Lynnie Oliver. And next
    we'll hear from a program also from June where Simon
    spoke with Doctor Rita Kleinfeld Fowle, who is the head
    of disability law practice at the Sussex Street Community Legal

    (10:19):
    Centre here in Perth.

    S2 (10:21):
    And like Deborah, Rita is also deaf blind and we
    learn about how Rita deals with the difficulties of having
    a dual sensory loss as she was born with a
    syndrome called Usher's syndrome that affects both her hearing and
    her sight, and she has had these difficulties since she

    (10:43):
    was a young child, and we learn about how she
    overcame these difficulties not only with great success, but then
    moved into the world of being a successful lawyer. She
    moved into this area of work because she is very
    passionate to ensure that people with these types of disabilities
    are not left behind and are not neglected and are

    (11:07):
    treated with fairness, kindness and equality, which is very important
    to read and is the driving force with her personal
    life and her professional life. And it was a pleasure
    to hear from Rita. You're currently working as a disability
    discrimination lawyer at the Sussex Street Community Legal Service. Is

    (11:29):
    that right?

    S5 (11:30):
    Yeah. That's right. Yeah. I'm head of disability practice. We
    have a team of, um, advocate, and we have lawyers
    who do the legal side of it.

    S2 (11:41):
    Now we'll go back in time. You are legally blind
    and legally deaf. Is that right?

    S5 (11:46):
    Yeah.

    S2 (11:46):
    So what we terminology is deaf. Blind?

    S5 (11:50):
    Yep. The terminology is indeed deaf blind. Um, but I
    would diagnose, uh, when I was about three and four. Um,
    I was born in King Cross in Australia, but then
    went back to the UK, and it was only when
    I was in a day nursery that a social worker
    picked up on my behaviour. I was the nightmare child. Gosh. Um,

    (12:13):
    I was banned from nursery and then I went through
    a diagnosed assessment and that when they picked up on
    the deafness and blindness.

    S2 (12:22):
    So, Rita, what's the nature of your deaf blindness? What's
    it caused by, and what's the name of it? Well.

    S5 (12:29):
    Um, ironically, I've only just been diagnosed, um, by the
    Lyon Institute, um, eye clinic. Um.

    S2 (12:36):
    And hats off to syndrome.

    S5 (12:37):
    Yeah.

    S2 (12:38):
    Usher syndrome. Yeah. So that was at the Lyons Institute? Yes. Yeah.
    Here in Perth. Yeah. What a fabulous organisation.

    S5 (12:46):
    They do a lot of good work. Yeah.

    S2 (12:48):
    One of the most renowned, leading research institutions, not only
    in this country but around the world.

    S5 (12:55):
    Mhm. Yeah. I mean I've lived in the UK for
    a long, long time and they didn't really pick pick
    up on it. It was the Lion Institute in Western
    Australia that diagnosed me.

    S2 (13:06):
    The little I know about Usher's it's for people who
    are deaf blind. It's one of the more common diagnoses
    isn't it. Yeah.

    S5 (13:15):
    Correct. Yeah, yeah.

    S2 (13:17):
    You mentioned you're from the UK. Whereabouts from the UK from?

    S5 (13:20):
    Yeah, I'm from the north west. Um, in a little
    seaside resort called Southport. I do have a Liverpudlian accent,
    so the twang did come out when I go back
    over there.

    S2 (13:33):
    I always find it fascinating. Um, that's part of the
    nature of this programme. What motivates people to move into
    the space of. Okay, I've faced something myself and I
    want to get over that hurdle. But not only do
    I want to get over that hurdle and be a

    (13:54):
    stronger person in myself, but I want to be a
    role model and help other people. What? What do you think?
    What do you think initiated that within you, Rita?

    S5 (14:03):
    I think because I went through that personal experience of
    facing barriers and could they around me that people with
    disabilities were facing similar issues? Um, I decided to go
    into law and try and make a change. So I

    (14:23):
    qualified as a solicitor in the UK and then became
    a High Court solicitor doing judicial review. So that basically,
    were you challenging the government for failure to carry out
    their community care assessment, which is the equivalent of the
    NDIS here? So some really high profile cases, um, you know,

    (14:46):
    often I'd be travelling down to London on, on a
    weekly basis, you know, and that's like a four hour
    journey on the train. It was. Yeah. Nightmare. But I
    made a different I made a different. Yeah. And then
    I took a life change balance. I wanted to go
    back to Australia. I really, really wanted to go back
    to my home country.

    S2 (15:06):
    You are working as a lawyer. We'll get into the
    specifics of the kind of work that you're doing at
    Sussex Street shortly. But, um, I know I've known a
    number of blind people who are lawyers and solicitors and
    barristers even. What sort of assistance and and help do
    you need? Being blind within that kind of role?

    S5 (15:29):
    I have like, um, a video reader. Mhm. Um.

    S2 (15:34):
    For those who don't know, can you tell us the
    basics of what a video reader.

    S5 (15:37):
    Though a video reader is a bit like the old
    CCTV camera where you sort of enlarged the a written document. Yes. Um,
    but but the though now that they're quite portable and
    they can, you know, they can be carried into court. Um,
    I also put the court on notice, you know, the magistrate,
    the judge or the tribunal, you know, let the court know.

    (16:02):
    And they are very, very accommodating. Um, they also have
    those special, um, heads there that are, um, looped into
    the microphone. So, you know, just just be mindful if
    you ever caught yourself asked for the special microphone and headset.
    If you've got a hearing impairment but a really, really good.

    S2 (16:24):
    We'll move into what you actually are doing within Sussex
    Street Community Legal Service now in the area of disability discrimination,
    because that is one of the main important areas, not
    only for what you're doing currently, but our audience are
    very interested in. And that's one of the themes of
    our show. Can you tell us some of the main

    (16:46):
    things that you're doing?

    S5 (16:48):
    Yeah. Of course. So I, I thought of, um, uh,
    started with 18 months ago. Um, they sort of created
    a new role ahead of disability practice. And I think
    because on the back of the disability royal Commission, there
    was an increase in demand for people with disabilities seeking

    (17:11):
    advocacy and legal services. Um, but like 18 months now
    on um, what I've I've done I we do do
    disability discrimination. Uh, we only have funding for one lawyer. Um,
    but the demand is absolutely huge. We're trying to get
    funding in from the government. The Labour government. Hopefully that

    (17:35):
    will happen. Um, but what I've, what I'm doing at
    the moment is trying to provide a wraparound service because
    there's nothing worse when a person with disability who's been
    traumatised in the past is having to be bounced from
    pillar to post. So, you know, a person with a
    disability might come to us and say, hey, I'm facing

    (17:57):
    discrimination in employment or my child is not getting the
    education that he or she needs because the reasonable adjustments
    are not put in place. So we provide a wraparound
    therapy with the legal services, and we provide them an
    advocate to, you know, to support mum or the person

    (18:18):
    facing employment barriers. But we also do civil law. We
    do race. Um, sex. Um, we do guardianship. So as
    long as you've got a disability.

    S2 (18:31):
    You'll qualify in a legal sense. How do we define
    disability discrimination.

    S5 (18:38):
    So disability discrimination can be direct. So direct as blatantly
    saying you're not allowed into the restaurant with your guide dog.
    Or it can be indirect where a policy may say,
    for example, have a policy for apprenticeships, but the stipulation

    (19:02):
    is that the person, the young person had to have
    a Tod. Now, this would put the disability community at
    um at a disadvantage, because we know that people with
    intellectual disability will not gain that level of high school education.

    (19:25):
    So that indirect discrimination that a typical example.

    S2 (19:29):
    Another common one in regards to employment or seeking employment
    that the blind community notice quite frequently is that in
    every job ad it says must have a driver's license. Oh,
    and even when we explain, hang on, I'm going to
    go to the office and then be in that office.
    I don't I'm not driving anyone anywhere. Why do I

    (19:52):
    need a driver's license? And there are other ways of
    going around it.

    S5 (19:57):
    So I've had a few cases like that where, you know,
    people have been legally blind and have had real social
    workers or teachers. In theory, if they put in a
    recruitment advertisement, you need a driving license. It indirect discrimination.
    And that's where they're putting a condition on somebody with

    (20:17):
    a disability.

    S2 (20:18):
    Yes. doing this highly stressful work. Being a disability lawyer,
    you must have life balance. So what do you do
    for your life balance? Reader, in regards to recreation and leisure?

    S5 (20:30):
    Look, I, I go to the gym. I love my, um,
    bodypump class.

    S2 (20:38):
    Bodypump.

    S5 (20:39):
    Yeah. And body comeback, which is like a martial art. Um,
    but my passion is ballroom dancing. I've only been doing
    it for about two years. Um, and I thought I
    came across it on Facebook. Um, Darryl Davenport. Yes. He
    he sort of owned the dance school. He's done amazing

    (21:00):
    things for people with visual impairment. Uh, and I love dancing. Um,
    I love going into competitions. It's really good for mental health.

    S1 (21:15):
    It was great to revisit those conversations from earlier this year.
    And as we heard from Deb and Rita, their working
    lives are in very specialized areas, but they're both passionate
    ballroom dancers.

    S2 (21:27):
    Yes, they both do enjoy ballroom dancing, and I like
    to acknowledge the organization where they do their ballroom dancing,
    which is ballroom fit, which is run and organized by
    the wonderful, lovely Darryl Davenport. And I'd like to say
    hello to Darryl. And, um, in both cases, they both
    find ballroom dancing a great community participation event, as well

    (21:50):
    as being a wonderful way of relieving stress from their
    daily lives, and a great way of participating with others
    with similar interests and similar passions. It was also really
    fabulous to hear from both Deb and Rita, to learn
    about what it is like living with these impacting disabilities.

    (22:15):
    One can only imagine what it would be like to
    live with severe sight loss and hearing loss in one package.
    I don't know about you, but I would find that
    really challenging. These two individuals have demonstrated how they've moved
    beyond those personal challenges, learnt from that, and also now

    (22:40):
    want to help others who are living with similar challenges
    and advocate to assist other people with other disabilities to
    help forge a more equal and humane society. And I
    really take my hat off to these wonderful people, and
    this is the joy and the beauty of creating a
    program like this, where we bring people together. We are

    (23:03):
    creating a virtual community here on the radio and podcast,
    and I really like to thank my participants and in
    this case, Deb, Lynn and Rita for participating and helping,
    demonstrating to others what it means to be firstly an
    active member of a community and secondly a person who

    (23:24):
    dedicates their time and energy in their passions to helping
    others and ensuring that people are treated with dignity, respect
    and equality. And I thank them for that and I
    thank you for listening. Bye for now.

    S1 (23:50):
    That concludes in Plain Sight for this week. Join us
    at the same time next week on Vision Australia Radio,
    VA radio, digital and online at VA Radio.com. You can
    also listen on demand by searching for In Plain Sight
    by Vision Australia Radio. Wherever you get your podcasts, or
    ask your smart device to play in Plain Sight by

    (24:12):
    Vision Australia Radio. Thanks for listening.

    S6 (24:14):
    Thank you.
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    The Burden

    The Burden

    The Burden is a documentary series that takes listeners into the hidden places where justice is done (and undone). It dives deep into the lives of heroes and villains. And it focuses a spotlight on those who triumph even when the odds are against them. Season 5 - The Burden: Death & Deceit in Alliance On April Fools Day 1999, 26-year-old Yvonne Layne was found murdered in her Alliance, Ohio home. David Thorne, her ex-boyfriend and father of one of her children, was instantly a suspect. Another young man admitted to the murder, and David breathed a sigh of relief, until the confessed murderer fingered David; “He paid me to do it.” David was sentenced to life without parole. Two decades later, Pulitzer winner and podcast host, Maggie Freleng (Bone Valley Season 3: Graves County, Wrongful Conviction, Suave) launched a “live” investigation into David's conviction alongside Jason Baldwin (himself wrongfully convicted as a member of the West Memphis Three). Maggie had come to believe that the entire investigation of David was botched by the tiny local police department, or worse, covered up the real killer. Was Maggie correct? Was David’s claim of innocence credible? In Death and Deceit in Alliance, Maggie recounts the case that launched her career, and ultimately, “broke” her.” The results will shock the listener and reduce Maggie to tears and self-doubt. This is not your typical wrongful conviction story. In fact, it turns the genre on its head. It asks the question: What if our champions are foolish? Season 4 - The Burden: Get the Money and Run “Trying to murder my father, this was the thing that put me on the path.” That’s Joe Loya and that path was bank robbery. Bank, bank, bank, bank, bank. In season 4 of The Burden: Get the Money and Run, we hear from Joe who was once the most prolific bank robber in Southern California, and beyond. He used disguises, body doubles, proxies. He leaped over counters, grabbed the money and ran. Even as the FBI was closing in. It was a showdown between a daring bank robber, and a patient FBI agent. Joe was no ordinary bank robber. He was bright, articulate, charismatic, and driven by a dark rage that he summoned up at will. In seven episodes, Joe tells all: the what, the how… and the why. Including why he tried to murder his father. Season 3 - The Burden: Avenger Miriam Lewin is one of Argentina’s leading journalists today. At 19 years old, she was kidnapped off the streets of Buenos Aires for her political activism and thrown into a concentration camp. Thousands of her fellow inmates were executed, tossed alive from a cargo plane into the ocean. Miriam, along with a handful of others, will survive the camp. Then as a journalist, she will wage a decades long campaign to bring her tormentors to justice. Avenger is about one woman’s triumphant battle against unbelievable odds to survive torture, claim justice for the crimes done against her and others like her, and change the future of her country. Season 2 - The Burden: Empire on Blood Empire on Blood is set in the Bronx, NY, in the early 90s, when two young drug dealers ruled an intersection known as “The Corner on Blood.” The boss, Calvin Buari, lived large. He and a protege swore they would build an empire on blood. Then the relationship frayed and the protege accused Calvin of a double homicide which he claimed he didn’t do. But did he? Award-winning journalist Steve Fishman spent seven years to answer that question. This is the story of one man’s last chance to overturn his life sentence. He may prevail, but someone’s gotta pay. The Burden: Empire on Blood is the director’s cut of the true crime classic which reached #1 on the charts when it was first released half a dozen years ago. Season 1 - The Burden In the 1990s, Detective Louis N. Scarcella was legendary. In a city overrun by violent crime, he cracked the toughest cases and put away the worst criminals. “The Hulk” was his nickname. Then the story changed. Scarcella ran into a group of convicted murderers who all say they are innocent. They turned themselves into jailhouse-lawyers and in prison founded a lway firm. When they realized Scarcella helped put many of them away, they set their sights on taking him down. And with the help of a NY Times reporter they have a chance. For years, Scarcella insisted he did nothing wrong. But that’s all he’d say. Until we tracked Scarcella to a sauna in a Russian bathhouse, where he started to talk..and talk and talk. “The guilty have gone free,” he whispered. And then agreed to take us into the belly of the beast. Welcome to The Burden.

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