Ableism: Discrimination Against Disabled People by The Wheelchair Teen

The act of writing forces us to contemplate things more deeply, to question what we believe. Bloggers, novelists, all writers lay ourselves bare when we publish. When we communicate our passions, readers are challenged to think — and they challenge us!

Thank goodness for the world of blogging, a Utopian alternate universe where anyone with access to a smartphone or computer, along with the internet, can send their unfiltered voices all over the world.

Without blog-topia, I would never have stumbled across Simone’s The Wheelchair Teen blog. There she lets us into her often fun, sometimes heartbreaking life. With good humor and patience, she teaches everyone to live with joy and compassion…

The Wheelchair Teen in her wheelchair.
The Wheelchair Teen in her wheelchair.

Ableism: Discrimination Against Disabled People by The Wheelchair Teen

Hello, everyone! I’m The Wheelchair Teen and I write about my life as a black, disabled teenager. I’ve been disabled ever since I was born and a permanent wheelchair-user since the age of thirteen. I’m British but currently residing in the Netherlands with my parents and sister. Thank you so much to da-AL for allowing me the chance to write a guest post for her incredible blog to help me spread my message of equality for all disabled people. If you want to see more of me you can find me at my blog called, The Wheelchair Teen – My life as a black, disabled teenager.

Ableism is the term for discrimination against disabled people, but unlike other forms of discrimination, it isn’t viewed as negatively. Most people don’t get educated about disabilities and remain ignorant. It’s therefore harder to get angry at people when they act ableist towards me — they honestly don’t know any better. So, when I encounter ableism, I sort of just have to deal with it and let it slide  and it’s exhausting, alienating, and something I shouldn’t have to face. Ableism is everywhere, and until people start to educate themselves more about disabilities, it’s something I’ll have to continue to deal with in almost every aspect of my life. Here are the five main ways that I feel othered in society as well as things that you can do to educate yourself and help to end ableism:

  1. People treat me differently

Sometimes adults talk slowly to me or avoid addressing me by talking to whoever’s next to me when discussing me. People pick up my limbs and move them for me without my permission or make offensive assumptions. At school, I was often alone because students were unsure how to treat someone like me and would therefore ignore me altogether. People stare, point, or talk loudly and rudely about my body in front of me and assume that I can’t understand. Little children occasionally even run screaming from me when I’m in my electric wheelchair. All of this makes me feel extremely isolated, alienated, alone, and othered  and that’s not even mentioning the different ways buildings and companies discriminate against me when I leave the house or go on trips. I’ve been turned away from places that claim to be wheelchair-accessible and discriminated against by employees.

Photo of The Wheelchair Teen's electric wheelchair.
My electric wheelchair.

I talk a lot on my blog about inspiration porn which is the objectification of disabled people as two-dimensional objects of inspiration. People treat us like we only exist to inspire people. I’ve had absolute strangers pass me on the street and tell me that I’m their hero. In fact, most people either assume that my life is awful and therefore treat me with pity or treat me like I’m a superwoman simply for waking up every morning like everyone else. In reality, my life is pretty sweet. The most difficult part about my life is actually how I’m treated in society  not my actual disability. I know this isn’t the case for everyone but you shouldn’t instantly assume it’s not. I’ve been disabled for as long as I can remember  I can handle it, it’s ableism that’s the major issue for me.

  1. They don’t teach about us in school

More education about disabilities is key in our fight to help combat ignorance. I’m certain that if my classmates had known how to treat someone like me, they wouldn’t have been so hesitant to approach me. Also, if children knew more about disabilities there’d be less pointing and staring as if they’ve never seen someone like me before, not to mention the children that ran from me terrified. Libraries should include picture books about disabilities and we should be mentioned in every diversity class along with other minorities.

Photo of The Wheelchair Teen giving a presentation about disabilities to children at a primary school.
Me giving a presentation about disabilities to children at a primary school.

Ignorance can be deadly: it is estimated that between 33-50% of police violence happens against people with a disability (although it’s hard to tell because it’s rarely recorded for statistics). I cried while reading through all of the cases of police shooting disabled people that they had been called to help in the first place. It’s a serious problem that not enough people are talking about. The police force needs to be better educated when it comes to handling disabled people – whether it’s shooting a deaf person because they couldn’t hear the police telling them to stop, or firing at someone with a condition that makes it incapable for them to stand still and raise their hands. They must be held accountable and taught that their behaviour is unacceptable. And these cases need to be reported and receive the same attention as any other police brutality case.

  1. There’s no one like me on screen

Disabled people are the biggest minority in the world with around one billion people around the planet being disabled. Despite this, we have one of the lowest amounts of representation in films and TV. Only 2.3% of speaking characters in films are disabled. Growing up, I used to think I was strange because I hardly ever saw anyone like me on TV – and I wasn’t the only one. We’re talking about representation in media as low as 1% for a minority that is around 20% of the world. 

Photo of The Wheelchair Teen with her hand over her mouth and the words: “Stop stifling disabled voices in media” on them.
Me with my hand over my mouth and the words: “Stop stifling disabled voices in media” on them.

95% of disabled roles are played by non-disabled actors, which is unacceptable! Able-bodied actors are critically acclaimed and win numerous awards for pretending to play a disabled person – but a lot of their performances (from the perspective of a disabled person) border on imitation and mockery. By not getting actual disabled actors to play these roles, you alienate disabled people by making them seem like mystical beings that cannot appear on screen, that can only be mimicked and impersonated. I’m not a ‘challenging acting feat’ – I’m a real person.

Meanwhile, real disabled actors struggle to get hired because people would rather see famous actors curl their fingers, twist their legs, tilt their heads, and pretend to be us for another guaranteed Oscar-nominee feel-good film. Filmmakers don’t want the real thing – they just want their own version of it, which audiences will then mistakenly believe is reality. I dream of a future where able-bodied actors playing disabled roles is seen just as negatively as actors playing other minorities when they don’t share their experiences.

  1. No one celebrates disability day

While throngs of people and numerous corporations celebrate International Woman’s Day, Pride Day, and Black History Month, the International Day of Disabled Persons goes under a lot of people’s radar. There is honestly so much beauty in being disabled, there’s so much to celebrate, and so many rights that still need fighting for. Help to raise awareness about disabilities by educating yourself and spreading the love this third of December. 

The Disabled Teen having fun in front of a carnival wall.
The Disabled Teen having fun in front of a carnival wall.

Like other minorities, multiple people throughout history have fought for the rights of disabled people. One day I was sitting in a history class at school when I realised that I knew about the suffragettes who had fought for my right to vote as a woman and the incredible civil rights activists who fought for my equality as a black person, but I knew nothing about the people who had fought for my rights as a disabled person. I did some research about disability history and I was so proud to see all of the people who had stood up for people like me. Their stories deserve to be taught in schools and history classes too. They deserve to be remembered.

  1. Disabled representation is awful

We’ve all seen disabilities used as plot devices: like the disabled or scarred villain who has a disability to show their dark, twisted mind or past on their bodies in a physical way; the action character with a child who has asthma so that tension can be built in the film when the main character has to rush to get the inhaler at a critical moment; the protagonist who ends up in a wheelchair in their weakest moment but manages to walk again once they continue to believe in themselves. And we’re all sick of it.

A disabled character created by The Wheelchair Teen for a comic.
A disabled character I created for a comic.

A few weeks ago, I burst out crying after watching a show with a character in a wheelchair that wanted to end their own life. It had been the THIRD show/film I’d seen in a row with a character in a wheelchair that wanted to do this. How can this be a theme in so many films with disabled representation? What kind of message does this send to people like me? If this is the only kind of thing a disabled person sees – what do you think they would start to believe? It made me angry. It made me feel like society thought that I’d be better off dead. Disabled people go through enough without having to put up with these types of horrible representations. (In most of them, disability was not the main focus of the show – it was just a side storyline. One was a comedy series, one was an anime, the other a romance film). I can’t believe that we’re still at this point when it comes to representation.

I’d love to see more casual disabled representation where character’s disabilities aren’t the focus of their entire existence – where they’re treated like normal characters that don’t even need to be the main focus of the story, representation where they aren’t healed at the end so people don’t think you can’t have a ‘happily ever after’ with a disability, intersectional representation where disabled characters can also be black or be members of other minorities, representation where their disability isn’t due to an accident – they’re merely born that way, etc. I’m currently working on creating a comic book about a team of disabled superheroes. It’s set in a sci-fi, Afrofuturistic world so there’s plenty of intersectional representation in it.  

Most importantly, I hope that disabled people are consulted while creating such a work. People praise films like Me Before You or Music until they hear from the actual disabled people that the film is representing and realise that they’re outraged at the bad representation. You can’t ignore the community when you make or watch films like this. Nothing for us without us. 

What can you do to help end ableism?

  1. Educate yourself and others

I recently started working on a story with disabled characters and I had to do a lot of research for it. I learnt so many new things like: the correct way to refer to certain disabilities, terms that are actually found offensive within the community, ways to make yourself easier to lip-read when talking to a deaf person, wheelchair etiquette, things that are okay to ask and things that may be rude, basic phrases in sign language, not to interact with guide dogs when a blind person is using them, etc. Education is key, I teach people about disability and even I still have a lot to learn.   

  1. Watch and read more disabled representation

There needs to be more outrage about films and books that go out of their way to discriminate against the disabled community and more attention for the ones that don’t. Read more books written by disabled authors and watch more films and tv-shows with us in them. Listen to our stories, we’ll show you that we’re much more than 2d objects of inspiration or pity.

  1. Support disabled content creators 

Apps like Tik Tok were found deliberately preventing videos with disabled people in them from going viral. More attention for disabled content creators means more normalisation of disabilities for their followers. I’m not the only one out there sharing about life with a disability. Also, add subtitles to your videos and captions to your pictures to make your posts more accessible for disabled followers.

Research citation: https://www.forbes.com/sites/joewalsh/2021/05/18/new-york-ags-investigation-into-trumps-business-turns-criminal/?sh=7ed291937332 

What do you think about media depictions of disabled people?

When Life Gives You Oranges: chat+video w artist Uzo Njoku by da-AL

Books + Art = Happiness

Dear readers, that’s why, when I learned of Uzo Njoku through Bust Magazine (a lifestyle/feminist publication started in 1993), I thought of you. Many of you are novelists like me, most of you writers and creatives, and lovers of books.

"When Things Fall Apart," by Uzo Njoku: "My favorite book by Chinua Achebe."
“When Things Fall Apart,” by Uzo Njoku: “My favorite book by Chinua Achebe.”

Her self-published coloring book, “The Bluestocking Society,” launched the statistics-turned-art-major a couple of years ago when she was a 22-year-old college student. It’s filled with images and facts about all sorts of wonderful women throughout history. She also offers free printable coloring pages.

Uzo moved from Lagos, Nigeria, to the United States as a child. Here’s a writeup about her by the University of Virginia, and here’s another by their news magazine.

"When Life Gives You Oranges" by Uzo Njoku: "I created this when dancing the idea of me being an orange farmer if I was not an artist."
“When Life Gives You Oranges” by Uzo Njoku: “I created this when dancing the idea of me being an orange farmer if I was not an artist.”

Along with Uzo’s comments on these paintings, what follows are the answers she kindly emailed back to me…

Question: How does being bi-cultural play out in your day-to-day life and influence your art? And in terms of how you regard your own loveliness and potential?

Answer: Being in the middle of two worlds gives me more content to work with. My work addresses important issues such as identity, duality and spirituality, yet is approached with a particular openness snd beauty. The themes addressed in my work stem directly from my life experience as a female artist living and working between cultures, and yet the aim is to show how a single person’s ‘double vision’ can produce images that possess much wider social effects by collapsing racial and cultural borders.

"Stretch," by Uzo Njoku: "Exploring the limitations of the body with a simple leg stretch image against the stark contrast of a flower pattern."
“Stretch,” by Uzo Njoku: “Exploring the limitations of the body with a simple leg stretch image against the stark contrast of a flower pattern.”

Question: Many of my readers (myself included) are struggling creatives. How do you juggle making art, marketing, fulfilling orders, and attending university? How did you initially let people know about your amazing coloring book? How do you continue to expose people to your art?

Answer: Everything I have done starts from my friends supporting me. Constantly telling others about my work and word-of-mouth helping to spread the news. A lot of artists don’t have a business mindset, and I believe that is how a lot of them do get exploited initially. I took an arts administration class in college, and that really opened my eyes to what goes on behind the scenes. This helped me understand more what it takes for shows to happen and the right people to reach out to.

I studied Statistics in college before switching over to art, so by nature, I am a very technical person. I see numbers alongside art a lot and understood when it was time to pay a marketing personnel to run ads when I released a new product on my website. I don’t really know exactly what to advise people because everyone is different, but I learned everything from Google and YouTube videos. So a lot of research.

"Strangers," by Uzo Njoku: "I had a conversation at a bar with a man who essentially told me everything going on in my life, and then I went about my normal life the next day because we were still just strangers even though he told me everything."
“Strangers,” by Uzo Njoku: “I had a conversation at a bar with a man who essentially told me everything going on in my life, and then I went about my normal life the next day because we were still just strangers even though he told me everything.”

Question: How has the horrific politics of late as well as the pandemic affected you and your work?

Answer: I am not a social artist, so I do not create art based on political events. But in regards to Oluwatoyin passing away, I feel it was my duty to beautify her image because I know a lot of media outlets would try to show her in a negative light. A good amount of the sales during this period I have been able to donate out to small BLM groups and artists struggling during this pandemic.

Artist Uzo Njoku in her studio.
Uzo Njoku in her art studio.

Question: How do you find and choose your marketing personnel?

Answer: My marketing personnel reached out to me. He had been following me for years and felt that he could reach new customers for me. Basically, anyone who understands how to market on Social Media is an asset.

Question: What are one or more mistakes you see artists making business-wise most often?

Answer: I would say the biggest mistake is forgetting to follow up on business taxes when tax season comes by. It can bite you if you’re not careful. Also, you need to get into the habit of having a second pair of eyes look at contracts with you, whether they are those of a family member, a friend, or a professional.

Dear reader, if you didn’t do what you do now, what would farm oranges…or what?…

Guest Post: Alone on Valentine’s Day: I Promise, It’s OK by R.K.B.

Blogger/poet/writer/daydreamer R.K.B.

Is there a certain day that you least enjoy spending alone? Valentine’s Day is meant to be about love — let’s start with ourselves! It’s only a day — only one day — as are all days — wise reminders from guest blogger/ poet/ daydreamer/ writer R.K.B. …

Take a Shot -Facing Bipolar, Depression, Anxiety and Suicide

Lonely-WomanYou won’t die. It’s not the end of the world, but I know it feels like it.

I get it. This day might even cause you to become depressed every year.

This year, let’s change that.

You are still worthy. 

You are not worthless. 

You have love, because you love yourself.

I know, it sucks because you might want to know what it feels like to be spoiled on this day. Or maybe, you just would like to know what it feels like to be acknowledged and told that you are beautiful. Sure, you can take yourself on a date and get all dressed up, but you’d want to know the feeling of having someone else to appreciate it and share it with.

I get that, too.

This isn’t your typical, feel-good post about how “loving yourself will cure all wounds,” because even though that is true, nobody really wants…

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Guest Blog Post: Lynn Love’s Lessons in Novel Writing Rejection

How do you deal with rejection? Whether you’re a fellow novelist — or you adore reading fiction as much as I do — or simply you too are human — at some point we all experience disappointment and frustration.

Here, while I take time off to complete my upcoming novel, “Flamenco & the Sitting Cat,” Lynn Love opens her heart to us. This is how she keeps rejection from getting the better of her novel writing…

Word Shamble

Image: Pixabay

Writing novels is a strange way to spend your life.

You take months (in my case, years) working alone on a project then there comes a point – if you want your baby to develop, to grow and not remain swaddled to your over-protective breast forever – when you must push what you’ve made into the world and watch from a safe distance to see if it will fall on its face or walk, perhaps even run.

But what if it manages to both face plant and saunter cockily round the block on the same day?

A few weeks ago, I learned I’d come second in a Writing Magazine competition (more on that nearer publication day). My prize was either a modest amount of cash or a critique of 9,000 words.

Now, as I’m a writer with heaps of artistic integrity and a yearning to polish my craft…

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Does Your Light Frighten You? by da-AL

“Our deepest fear is not that we are inadequate. Our deepest fear is that we are powerful beyond measure.

It is our light, not our darkness that most frightens us. We ask ourselves, Who am I to be brilliant, gorgeous, talented, fabulous? Actually, who are you not to be? You are a child of God.

Your playing small does not serve the world. There is nothing enlightened about shrinking so that other people won’t feel insecure around you.

We are all meant to shine, as children do. We were born to make manifest the glory of God that is within us. It’s not just in some of us; it’s in everyone. And as we let our own light shine, we unconsciously give other people permission to do the same.

As we are liberated from our own fear, our presence automatically liberates others.”

Marianne Williamson, activist/author of, “A Return to Love: Reflections on the Principles of A COURSE IN MIRACLES,”

Marianne Williamson, activist/author of “A Return to Love: Reflections on the Principles of A COURSE IN MIRACLES”– Photo by Supearnesh – Own work, CC BY-SA 4.0

This famous quote — which surely Williamson is proud of however zillion times it’s attributed to Nelson Mandela — reminds me of how sneaky my fear of success can be. As a kid, I worried that setting myself apart would invite criticism, jealousy, and ostracism. My ultimate goal, I was firmly instructed when my imagination soared, was predetermined. Girls must be cute and sweet so they’d be attractive to boys. Women, I was told, were born to be wives and mothers.

Fears continue to gnaw at me. Now they’re sophisticated, requiring constant vigilance to upend them. Art begs an audience. When art is personal, it’s difficult to not give a damn what others might think, not to mention how wicked my own self-doubt can be. An hour after I was awarded an Emmy, a stranger asked me how the honor felt. My reply was blather. He reminded me that I had indeed won it…

Williamson is correct to point that that being our best benefits everyone. When I’m upset about my goals, I remind myself of her wise words.

Do you ever hold yourself back?

Video: Strength and Compassion in the Worst of Times by da-AL

In the worst situations, strength and compassion shine brightest. Terrible times strip away everything but what’s essential, leaving bare the best in us and those we encounter during our trials. 

The first time I learned the depth of this truth was when I co-produced a video for the Leukemia Society of America (nowadays Leukemia and Lymphoma Society). They’d hired my business partner, David Hunt (who has written for HBT here and here), and me (our non-profit company was called, Vista Educational Media) to encourage therapists, as well as people struggling with leukemia to get involved in the agency’s support groups. Executive Producer was Maureen Nunn. We videotaped at Wellness Community South Bay Cities, which is now Cancer Support Community Redondo Beach. The Los Angeles Times wrote of participant Roger Kahl’s valiant life here.

The way David and I worked was always to let subjects speak their truths, then we’d do our best to edit and narrate accurately. For each project, David and I would alternate who would be in charge and who would assist.

Thank goodness for this one David conducted the interviews, wrote, edited, and narrated. It took all I had not to sob while I stood to videotape behind the tripod. Reviewing it all these many years later, I still cry at the incredible bravery of the interviewees and David’s outstanding storytelling.

On David’s site, he details his experience with this project. Here’s his preliminary description for my site here…

“By the 1990s health educators understood that video-assisted storytelling was an effective way to engage patients and get them involved in their own health care. But many of the nation’s top health organizations, including the Leukemia Society, used actors as stand-ins for actual patients in their health education videos. In 1992 I was part of a documentary team that convinced the organization to trust people with leukemia to share their own stories.”

Guest Post: 7 Signs of a Toxic Relationship by Looking for the Light

Looking for the Light blog avatar logo
Looking for the Light blog avatar/logo.

Even in the best of times, relationships can be complicated. Sometimes we know something is wrong, but we’re not sure whether we should keep trying to make it work and whether the problem lies within our own actions or those of the other person. On her Looking for the Light blog, Melinda Sandor of Texas offers a link to a list of insights on how to ‘Keep Moving Forward’ in the worst of times…

Guest Blog Post: “Focus on what you can do, not what you can’t” by Caz

My inner cynic can loom monstrous enough to be laughable. When it skulks, it can be harder to address. Caz, who lives in England, understands that emotions are part of being human. Without being syrupy, without promoting denial, she offers practical help. Her Invisibly Me site deals with living with invisible chronic pain, including living with an ileostomy (not to be confused with a colostomy). Here’s a sample of her best advice…

Graphic: Focus On What You Can Do. Not What You Can't.

Photo of blogger Caz of InvisiblyMe.com
Caz made her first website when she was 13!

I wrote this with chronic illness in mind, but it also applies to other spheres of life, from living arrangements to your financial situation. 

Focussing on what you can’t do. It can become a vicious cycle, leaving us exhausted and disheartened before we even begin. It can happen for various reasons. Looking at how things used to be in the past, such as before chronic illness took hold. It may be from social pressures concerning what we ‘should’ be doing at this point in our lives. It may be from comparing your life to how you thought it would look, or comparing your situation to that of your peers.

For whatever reason, it’s good to work on acknowledging and accepting the situation and what you can’t necessarily change right now. Then, redefine what’s important to you, not what you feel you ‘should’ value or want. Write your own rules. Find new paths to explore and get creative to find ways to get there. Maybe you can’t do certain things, but there will always be options and alternatives. There are always small changes you can make and actions to take to improve your situation or live your best life. You may just have to look a little harder to find them.

It’s also about readjusting expectations and making them more realistic and manageable. Take note of the things you can be grateful for that often get lost in the midst of pain and illness, or stress and worry. It’s about looking at the things you’re good at and the positives you can eek out of your situation and experiences. You’ve become stronger and more resilient. Perhaps you’ve met new people in person or online, such as through blogging or support groups. Maybe you’re more compassionate, empathic, have found a new skill or have become more appreciative of the small joys in life.

When we focus on the negatives, the limitations or the things we can’t change, we give up our power. By honing in on those things you can’t do or have, or the ways in which you feel constrained, it limits your perspective and experiences even more so.

By focusing on the can’t-dos, you’re reducing yourself & your life. You are more than just the things you can’t do. 

Empower yourself by looking at what you can do, no matter how small. Look at the things you can change, the tasks you can accomplish, the things you can choose to do. 

Instead of ‘I can’t do…’, change it to ‘but I can do…’.

You’re doing the best you can, with the cards you’ve been dealt and the situation you find yourself in. A little jiggle of perspective can make a big difference. Don’t close yourself off from possibilities. Instead, think outside the box and take back some control over your life. You may just find that you’re capable of more than you imagined.

– Caz

Visit Caz at her blog and her facebook page and her Instagram.

Blogger Caz of InvisiblyMe.comInvisiblyMe.com logo graphic

How do you deal with invisible pain?…

 

Hope for Novelists and Other Writers by da-AL

Do you have an elevator speech? Book writers are told that they need an ‘elevator speech’ — a one-minute pitch for when they inadvertently meet their star-maker. It’s also useful for talking about one’s book with everyone else.

Theoretically, that is. My elevator speech rarely gets past the first floor.

Bunny rabbit outfitted person reads paper.
Ryan McGuire of Gratisography is a smart bunny.

But I love my books, which is why I keep at them. My two novels are in the final edit phase as I build an audience of followers (that means you, dear reader) who I hope will be interested in them when they’re self-published. They’re narrated by a 40-year-old woman, in the form of letters to a deceased grandmother.

“An epistolary novel: written in the form of a series of letters.” Merriam-Webster Dictionary

The Hope Part of this Post: This video reminds me of me pitching my book — and Maria Keogh Semple’s “Where’d You Go, Bernadette” did great!

Here’s part 2 of her pitching (this time to another very successful author), which is also shown comically yet realistically…

Semple’s book is so successful that Cate Blanchette is starring in a movie version of it!

What’s been people’s reaction when you tell them about your books?

Guest Blog Post: Antique and Vintage Photos by Val Erde

Val Erde’s sensitive and artful photo coloring truly brings history to life. Based in the U.K., she kindly contributes this for you to see…

Dog in garden before and after. Photo coloring by Val Erde

In my blog I show the colouring work I do on my collection of antique and vintage photos. I’ve been an artist all my life and have been doing these photos since I had my first pc and graphics program. I usually colour photos of people, though I have a few that include dogs and cats, but this is the first in a long while that I’ve done just of a dog. I hadn’t intended to colour it, but well… look at it. Wasn’t it barking calling out for colour? Or, more likely, food.

“Please give me a treat. Anything will do, really. Maybe something you’re eating? I like your food. I like everyone’s food.”

I haven’t a dog so have to rely on photos for colour references and as I don’t know what breed it is, I’m not sure I got this one right. I suspect it’s a bit of lots of different things. Well, doggy things, anyway.

So… any ideas what sort of dog it is? And – the dog aside, can you by any chance identify the flowers to the right? The ones on the left are roses, that I know, but the rest – what the heck are they? To me the blossoms look like Cosmos, but the leaves are wrong. Anyway, to be safe, I coloured the innards yellow and the outtards (yes, I know) varying shades of pink. But they could be anything really.

There’s more to do on this photo but I decided to call it a day. Well, actually, I’ve called it a dog.

My thanks to Da-AL for inviting me to guest blog!