#ultra light wheelchairs

[forzamedi]

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[elvenmoans]

People act like people faking disabilities are such a common issue and require violence and threat of violence to fix.

But I am an ambulatory wheelchair user like 70% of wheelchair users. I have never met one of us who didn't fake not being able to move their legs to avoid actual literal violence

I once had my leg twitch on the train which happens in most spinal cord injuries even complete ones. And this guy screamed at me for several minutes threatening to kill me, and he only didn't beat me up because the entire fucking train cart had to stop him

Disability faking is such a strong paranoia on our society that ironically they create it by making disabled people fake more "acceptable" disabilities when alone in public for their physical safety

[five-thousand-loaves-of-bread]

not all wheelchair users use manual wheelchair

some wheelchair users use giant group 3 CRT power chair that weigh 300lb+ / 136kg+ n cannot collapse or folded must be transported by big vehicle with wheelchair lift or ramp. that wide & bulky n can’t squeeze through tight space.

but also. not all manual wheelchair user use custom ultra light active wheelchair with low backrests, that really light, that easily maneuverable, that narrow n easy fit through tight space with tight turning radius, that can be collapse n put into small car trunk easily conveniently

some wheelchair users use hospital or off-the-rack wheelchair that really hard to use

some wheelchair users fat n so their wheelchair need be wide

some manual wheelchair users use manual tilt in space wheelchair

some manual wheelchair users use custom wheelchair, often even with ultra light frame, but their seating positioning needs make custom wheelchair bulky & big & heavy. over 50 lb / 22kg. some even approach 100 lb / 45 kg (frame for manual tilt in space can be heavyyyyy). my wheelchair like this n it meet (some of) my needs but it inconvenient as hell n absolutely not light n airy. n wish people like. remember we exist

[urbancripple]

To able‐bodied people, wheelchair users have a certain mystique. They’re constantly asking us about how our bodies do or don’t work, whether we can have sex, why we haven't just killed ourselves yet. But despite their intrusive questioning, there is one area that ableds seem to be absolutely certain about: the existence of ultra‐convenient readily‐available accessibility modifications and mobility aids.

As wheelchair users, how many times have we been told to “put some chains on that thing!” As we struggle through the snow? How often is it suggested that we get a hand‐bike so that we can cycle to work like our coworkers? If I had a nickel for every time someone suggested I attach some tried‐and‐true motor to my chair, I’d have enough money to pay someone to invent it.

People are constantly sending me links to articles and videos to supposed life‐changing mobility aids that can climb stairs or move over rough terrain. They tell me that things can’t be that difficult with a constant stream of new, convenient doo‐dads being put out in the world. Hell, when discussing how difficult it is to find a single‐story home in Seattle (existing or custom), the suggestion was made that I simply build a multi‐story home but also put an elevator in.

Here’s the thing though: has anyone, wheelchair‐user or otherwise, actually seen any of these so‐called solutions in person? The stair‐climbing wheelchair? The magical snow tires? The super fast motor? I haven’t. As for the elevators and hand bikes, I can count the number I’ve seen on one hand and I’d need way more fingers and toes to show you the price tag.

Despite their near non‐existence or insurmountable financial cost, people keep telling me I just need to “get me one of those…” and continue to cast my existence and the problems that come with it in a mythical light.

An elevator for your house starts at around six‐thousand dollars. If you want one that doesn’t look like the rickety stair‐lift at your local Eagle’s Club, it’ll cost you upwards of sixty‐thousand.

The price of an average, entry‐level bike is four‐hundred bucks. If you want an accessible hand bike, you’re going to start around a grand.

Custom wheelchair tires can vary anywhere from two to five thousand, often times costing more than the chair they’re attached to.

That stair climbing chair? Eleven grand. Want something that’s a little more “every day”? That’ll cost you seventeen grand. Just need a motor for your day chair? Six grand and it weighs fifteen pounds.

Now, some folks might be thinking “sure, it’s expensive now, but the price will come down as technology improves and more people buy these devices��. But with an employment rate of roughly 7 percent (before COVID) and rules governing the amount of money disabled people on SSI can have in the bank (no more than two-thousand dollars), most wheelchair users can’t even save up to buy one of these devices. And no, insurance won’t cover any it.

A lack of accessibility is not something we can just “tech” our way out of and disabled people should not expected to purchase access to a world that everyone else gets for free. Talking about mobility aids you’ve never used or seen when someone is trying to explain to you the barriers they face in their day to day life due to a lack of accessibility isn’t helpful, it’s dismissive. Quit doing it.

[the-indigo-symphony]

Y'know, one of the common fakeclaiming accusations is that a system or person is just "roleplaying DID" (which is kind of a ridiculous thing to jump to when most of the folks receiving these accusations make no claim of having DID, but I digress), but honestly? I don't think I'd give a shit even if someone was roleplaying my disorder

Like, what's the worst that can happen? Oh no, they're educating themselves on what DID is like! Oh fuck, they're unlearning their biases against dissociative disorders! However shall the DID community recover from some random person deciding to portray DID in what's essentially a form of interactive improv, thus introducing it to more people in a neutral to positive light instead of the negative rep they probably would've come across?

This isn't "let's stick a class of students in a wheelchair for an hour so they end up thinking they perfectly understand all disabled experiences". These are casual actors who tend to put in more work to accurately portray something they don't personally experience than most professional actors I've seen. I don't give a shit if someone roleplays DID unless they're promoting the old serial killer stereotype or acting as if they're the ultimate authority on it. Hell, ask me questions about specific parts of it if you want tips on how to write it! Whatever! I don't care!

It's just. I get why it's seen as a negative thing. But I'd rather have people make some mistakes when roleplaying and cause some minor misinfo that I can work on combatting... than have more people out there whose only understanding of DID is as "the super ultra rare disorder that basically guarantees you're gonna suddenly turn evil one day".

It's free representation. Might as well help make sure it's as good as it can be.

[doctor-who-binge]

Disability Representation Win!!!

RTD went fearlessly with represention so far, he clearly has no fear of backlash. And the disability representation as a wheelchair user I was fucking ecstatic. Even more so than my excitement because I'm an enby, trans representation is amazing especially being Donna's daughter and a trans actor. But a wheelchair user character? We are always forgotten about. Also she's played by an actor who is a wheelchair user!!! I'm so happy. And they didn't shy away from making her an authority figure who should not be pitied.

Because fucking Chibnall's wheelchair representation was Yazmin's grandma feeling sorry for herself because "I was the first woman married in Pakistan , now look at me, in a wheelchair with shop bought cake" and it really fucking hurt. I remember how much that line in that episode hurt.

Credit where credit is due Chibnall did have disability representation. However, I feel like Ryan's dyspraxia was kind of shoe horned in as "see representation!" but it felt like he had dyspraxia when it was convenient to mention it and didn't have it in many other instances AND importantly the actor himself did not have dyspraxia, which cheapens it a little in my eyes. I also enjoyed that Diane not having an arm wasn't a huge plot point at all, she just doesn't have a lower arm, no biggie and it was a reflection of the actor who does not have a lower arm. Representation using actual members of the minority group ftw.

I don't remember if Moffat had any, he probably did? But not memorable I suppose.

I'll admit Shirley Anne Bingham having darts and explosives on her wheelchair was cool as fuck and makes sense since she works for a military-intelligence agency. The fact that it was a custom ultra light weight wheelchair not some annoying hospital one was also amazing, showing actual life of us wheelchair users (which make sense since the actor is one!)

[neon-kazoo]

Former Hero Gets a Wheelchair

Today was the day.

After months of hardly getting out of bed, months of fighting the agency’s insurance plan, months of insisting that the hero’s condition was, in fact, service related, they were finally getting a custom wheelchair delivered.

Today, they got their independence back.

The doorbell rang and Hero had never moved faster on their cane, rubber tip taps and accompanying footsteps echoing through their entryway as they reached the door. Opening it, they were greeted with a beautiful sight. A smiling worker stood behind their brand new chair.

The rigid frame was coated in a metallic blue, with shining push rims to match. Black metal completed the footrest and backrest support, blending into the black wheels and side guards. It looked sleek; It looked perfect.

Waved in by the former hero, the worker lifted the caster wheels over the door frame, pushing the chair up and inside before locking the small silver brakes.

“You ready to take her for a spin?” They asked, and the hero grinned from ear to ear. They took a seat, sliding back till their hips were settled. The worker pointed out the buckle and Hero clicked it shut.

“Safety first,” they nodded and the worker chuckled in response.

Brakes unlocked, they pushed, and they glided like they were on a cloud.

They sighed at the ease of movement, moving down the hallway with little pain. It had been so long since they could just move. They missed moving just for the fun of it, for the rush of wind in their hair and adrenaline coursing through their veins. They missed jumping across rooftops, turning their feet on a dime, climbing walls, and starting fights that they could actually win.

Overwhelmed with the return of that feeling, they found themselves increasing their speed more than what may have been advisable around the house. Consequently, when they tried to turn around, they clipped the doorframe, leaving a scuff mark on the plaster and a slight damper on their confidence.

“Takes a little getting used to,” the worker assured.

Hero continued, slightly abashed at their excitement. The worker watched, then suggested they raise the footplate a little to accommodate Hero’s thin soled shoes. After a moment with an Allen wrench, Hero was properly fitted into their new wheelchair.

Now, it just needed a name.

In their time as a Hero, they had practiced restraint when fighting countless villains. They never aimed to maim or hurt more than necessary, even if the villains pointedly did not return the favor. Ever since being forced to retire, Hero carried that sentiment into their civilian life too. However, there were times when they wished to be a little petty. Sometimes, when people blocked ramps or stared at them a little too judgingly, they wished warm pillows and bad hair days upon them. Their prayers for minor inconveniences rose especially when they saw news of a certain villain, who Hero suspected to have a set of very crushable toes.

Maybe, Hero would have to pay them a little visit, with the help of the brand new Metatarsal Muncher.

They couldn’t wait to get out of the house, to be able to function on a daily basis. They were going to get groceries, get out to retirement-events, go outside with a sense of focus not being spent on trying to stay upright, shop without a mind clouded with pain.

If only it hadn’t taken them this long to accept what they needed.

The worker showed them how to disassemble the chair. The ultra-light wheels came off with a button press in the middle, the cushion was removed so the back could fold down. Hero got to assemble it back themselves and, satisfied, the worker bid them goodbye with some maintenance and care instructions.

Far too excited to wait, the former Hero loaded their chair into the car and headed for the park, thrilled to go watch the robins and blue jays hop between the trees. Once, the former hero had envied their freedom, the ease with which they traveled and lived their lives. They had wished they could soar above the sky and dive down back to the ground. Now, as they followed the smooth concrete path through the oaks and the birches, they made peace with their own kind of freedom.

It may not look the same as it once did, but life moved on.

If they had earned nothing else in their time as a hero, it was the right to live their life in the least amount of pain possible. Despite any reservations, they would use this tool to help them, and if anyone had a problem with that, they would meet the wrath of the Metatarsal Muncher.

[kurtvrich]

Tumblr Hunk…

Handsome young para shows descending a long staircase with his ultra light wheelchair isn’t a problem. I’m now waiting for the sequel where he and his chair effortlessly ascend the steps. Part One.

[nonspeakingkiku]

Being deafblind is hard 😵‍💫

Yesterday Kiku found some audio books Kiku could understand and were stories Kiku wanted to hear (audio books are hard because APD and hearing loss, and weren't really accessable before Kiku got noise canceling earbuds) and Kiku ended up listening for 6 hours, with no breaks, and got a migraine 😵‍💫😵‍💫😵‍💫 apparently, just like with reading print, it's still a migraine. (ultimately the solution is likely braille, but Kiku is stuck with braille and not entirely sure why. (part of the problem is likely that the books Kiku has been able to get are not UEB (united english braille) so they are slightly different than the materials Kiku is using to learn)). Hearing and visual fatigue suck so much.

And going out is fun because recently Kiku has been in a lot more pain, and trying to aknowledge that walking hurts Kiku and Kiku needs to use mobility aids more, but Kiku's crutches are slightly too tall where the cuffs sit and it's difficult to use crutches and white cane at the same time (working on it but it's very tedious). Kiku needs a wheelchair but Kiku needs an ultra light chair and they are so expensive 😵‍💫 and Kiku can't use Kiku's cane and walker together at all. So it's just a lot.

Oops, this wasn't entirely meant to be a vent but Kiku guesses it's a vent now.

Also if anyone has suggestions for crutches that would be cool, but the problem is Kiku is short and the cuffs of Kiku's current crutches sit way too close to Kiku's elbow, but they don't adjust any lower.

Kiku wants to get a nimbo posterior walker eventually (because it's behind Kiku hopes will be able to use Kiku's white cane with it, without running into the problem Kiku has with the crutches).

Kiku doesn't like having to choose between using Kiku's white cane and not running into and tripping over things and using one of Kiku's other mobility aids and having reduced pain.

Kiku has also been trying to research Cerebral Palsy more, because Kiku really suspects that might be what is going on with Kiku, but it's really hard to find resources on it that aren't medical based and cognitively inaccessible. And Kiku keeps getting told to talk to doctors, which isn't helpful, because that's just not possible right now. Kiku is going to talk to a doctor whenever that becomes possibly, but until then Kiku still has to deal with what is possibly CP and it's very frustrating.

Kiku has began to identify what Kiku believes are spasticity flares, and triggers for them, and has determined if that is what is going on, this has happened as long as Kiku can remember, Kiku just didn't realise it wasn't normal.

Kiku is processing the things that have happened in the last few weeks-months so might be more posts that are ramblely like this.

[feverflushed]

i would like to know more about the mobility aid whump !

Alright!

Disclaimer: Please notice that I'm going to talk only from personal experience, so what I'm saying might not apply to everyone!

(For context! My condition is characterised by extremely frequent and painful dislocations, so my aids aim mostly to avoid that or to give me the time and stability needed to recover from bad dislocations! Aside from wearing braces daily, and from these acute episode recovery times, I live a very active life, so the issues I've encountered are radically different from someone with a SCI, for example.)

Now, let's get straight into the whump (on top of the whump your poor fave is already experiencing):

-Braces: Fantastic, fantastic invention. They make everything easier, but can be awful if they're not used carefully. Personally, I wear AFOS, (they basically keep your ankles in place and prevent things like foot drop, therefore reducing the likelyhood of tripping on your own feet). Now, here's the issue. Shorts are a terrible idea. When it's really hot and you want to wear shorts and you're planning to go for a walk, the only way to prevent chafing your shins to the point of bleeding is wearing knee high socks. 🥲

Same thing goes for all rigid braces that come in contact directly with the skin, like knee braces and rigid corsets.

And while braces can help a lot with stability, if used improperly they can lead to issues like atrophy.

Also, not whump, but honorable mention for finger splints. The metal ones are sooo comfy and make your character look extra badass. Just saying.

-Canes/crutches: Blisters, blisters, blisters. Blisters and tendinitis to no end. When canes are used only for balance, it's not a huge issue, but if you have to put pressure on them (this applies more to crutches than canes tbh), you tend to get blisters all over your hands and tendinitis in your wrists. Especially with crappy hospital crutches. That's why most long term users tend to have their own customized aids. It's a game changer, honestly.

Also consider. A character who faints often using canes to give themselves enough stability to safely get to the ground instead of faceplanting.

Last thing: perpetually cold fingers during the winter.

-Wheelchairs: This only applies to manual wheelchairs. I know nothing about electric ones.

Hospital wheelchairs, once again, are terrible. They will most definitely give you terrible sores on your palms from propelling yourself. The pushrims BURN your skin if you only think of doing sudden movements. They're heavy, bulky, get stuck everywhere, and there's an extra chance of ruining your furniture. 😮‍💨

Active/custom wheelchairs, on the other hand are a whole other universe. They're tailored to the user's needs, they are ultra light and compact, and super easy to maneuver, and you can actually do wheelies in them to roll over obstacles or difficult terrains (unlike hospital chairs). However, this makes them less stable and a higher fall risk.

Not to mention the perpetually frozen fingers during the winter months (hello frostbite!).

Due to inactivity, a whumpee in a wheelchair is more likely to feel cold, and to develope atrophy and muscular issues. Not to mention, wearing and tearing of arm/shoulder joints and contracture of the shoulders and back from the constant self propelling.

Not to mention, pressure sores! That's pure hell to put your whumpee through, and potentially dangerous!

[forzamedi]

Revolutionizing Mobility: Your Guide to Ultra Light and Portable Wheelchairs in India

The Ultimate Guide to Ultra Light Wheelchairs: Revolutionizing Mobility in India

In recent years, the demand for ultra light wheelchairs has seen a remarkable surge, particularly among those seeking greater convenience, portability, and independence. As mobility aids continue to evolve, these innovative wheelchairs are transforming the lives of countless individuals. Whether you're exploring portable wheelchairs in India, aiming to buy a wheelchair online in India, or searching for the best wheelchair in India, this guide is here to help you make an informed decision.

What Are Ultra Light Wheelchairs?

Ultra light wheelchairs are designed to provide maximum mobility and convenience. Made from advanced materials like aluminum or carbon fiber, these wheelchairs are significantly lighter than traditional models. Their lightweight design makes them easy to maneuver, transport, and store—ideal for active users and frequent travelers.

Key Benefits:

Portability: Ultra light wheelchairs are foldable and compact, making them easy to carry and store in small spaces.

Ease of Use: Lightweight frames reduce the effort required to push or self-propel.

Durability: Despite being lightweight, these wheelchairs are robust and long-lasting.

Comfort: Ergonomically designed seating ensures maximum comfort during prolonged use.

Why Choose Portable Wheelchairs in India?

India’s diverse landscape demands mobility solutions that are adaptable to various terrains and lifestyles. Portable wheelchairs are perfect for navigating busy cities, rural areas, or even traveling abroad. They cater to users who value independence and freedom of movement, without compromising on comfort or style.

Popular Features of Portable Wheelchairs:

Foldable frames for easy storage.

Adjustable components like armrests and footrests.

Compact and lightweight design for hassle-free transport.

High-quality materials that withstand Indian weather conditions.

Tips for Buying Wheelchairs Online in India

With the rise of e-commerce platforms, buying a wheelchair online in India has become easier than ever. Here’s how to ensure you’re making the right purchase:

Research Trusted Brands: Opt for brands known for their quality and reliability.

Check Specifications: Look for details like weight capacity, dimensions, and special features.

Read Reviews: Customer reviews provide valuable insights into real-world performance.

Compare Prices: Online platforms often offer competitive pricing and discounts.

Look for After-Sales Support: Ensure the seller provides warranties and customer service.

Finding the Best Wheelchair in India

The “best” wheelchair is one that meets your unique needs. Whether you prioritize weight, portability, or advanced features, here are some factors to consider:

Purpose: Are you looking for a wheelchair for daily use, travel, or specific activities?

Weight Capacity: Ensure the wheelchair can comfortably support the user’s weight.

Adjustability: Features like reclining backrests and customizable footrests enhance comfort.

Budget: Determine your budget and look for models that offer the best value for money.

Where to Buy?

Forza Medi is your one-stop destination for ultra light wheelchairs, portable wheelchairs in India, and a range of mobility aids. With an extensive collection of top-quality products, you can easily find the best wheelchair in India that suits your lifestyle. Visit Forza Medi today and explore a world of mobility solutions designed to empower and uplift.

Conclusion

Ultra light and portable wheelchairs are revolutionizing the way people experience mobility. With the right wheelchair, users can enjoy greater independence, comfort, and confidence in their daily lives. Whether you’re buying a wheelchair online in India or searching for the best wheelchair in India, Forza Medi offers trusted solutions tailored to your needs.

Take the first step toward enhanced mobility and freedom—explore ultra light wheelchairs at Forza Medi today!

[instantartific]

Anodyne's "Shadow:" a Would-Be Rockstar.

Aka, who Ano calls Moya!

✧

Several of AACE IDOL's fans have gathered small clips and glimpses of a figure standing at the base of Ano's stage when he performs, and even in the dark backgrounds of his promotional work outside of performances, yet none have ever captured this figure directly...

Until this strange figure reveals himself during the vs. B2J battle!

'Moya' acts as the creator, manager, "best friend," and functional Charter of Anodyne and the VA-Ultra District, though highly prefers to stay in the shadows where he's far more comfortable. Even the other Charters are unaware of his identity as Ano acts as a placeholder for him in their meetings.

Parts of his body are semi-bioluminescent, though the markings only appear under the blacklights of Ano's stage, or if he's under enough emotional strain for the colors to flare on their own. They weren't always like this, however; when he was younger, he used to be far brighter and glowed under far less conditions. Maybe it was all that stress made him grow darker over time...

✧

Few other things under the cut:

Moya's chronically disabled! In a sense, his legs are weak and he's unable to stand for very long without support! It often causes him pain to put full weight on his legs. The crutches are partial-weight bearing for this reason.

He does have a wheelchair for very low spoon days but tries to use it marginally.

Usually very low energy! The most active he is is when he's doing repairs on Ano, 'spotting' him during performances to make sure he doesn't get hurt, or doing Charter activities from the sidelines.

He is physically equivalent to a solidified shadow and can "melt" or "fade" apart under too much stress. He can also melt and fade through existing shadows and seemingly warp light. This is how he primarily attacks during the vs. B2J battle: he'll fall or jump into a shadow, vanish, and reform somewhere else to sling himself forward to suddenly appear out of nowhere.

He initially designed Ano after himself, though Ano ended up being somewhat smaller than he is due to mis-measurements. If asked, he insists that it was intentional. It was not. He was just incredibly convinced with the measurements on paper.

Moya designed Ano to be a simple AI companion when he was younger, since he was a fairly lonely teenager that couldn't keep up with his peers.

He initially wanted nothing to do with NSR or performing, but since Ano loves it, allowed him to continue to perform after his (incredibly spontaneous) Lights Up Audition (that Moya knew nothing about and only discovered due to them being broadcasted on live television.)

Moya's able to communicate with Ano remotely through an app on his phone! On Moya's end, it's essentially texting. On Ano's, it's internal messages that show up on his hud. Moya can type absurdly fast from that alone and Ano joking about how slow his typing is compared to the instantaneous 'thoughts' Ano sends.

[five-thousand-loaves-of-bread]

sometimes feel like ultra light manual wheelchair users who need high back rests (and like. headrests & co) are like unfavored step child of evil step parent (ultra light manual wheelchair manufactures & companies)

what do you mean my friend’s low backrest lighter than my AAC but my higher backrest heavier than my aluminum frame

[rainbowxocs]

Name: Hana Seta (花 瀬田)

Special Titles: Kōgō Hana, Princess Consort of Hell. (皇后花、地獄の王妃), Her Highness.

Username: @waitforit

Age: 20

Pronouns: They/She (In English.)

I Pronoun: Ware (吾) (A very formal almost literary form of I.)

Sexuality: Asexual, Lily (Yuri, 百合, Lesbian.)

Gender: X-Gender (Ryosei) (Xジェンダ,共生).

Species: Human Born Demon (Sloth). (Yurei) (Witch)

Disorders: Autism, ADHD, CPTSD, Bipolar 1, Somniphobia, Arfid, Anorexia, Perfection OCD.

Physical Conditions: Chronic Pain, Ambulatory Wheelchair User, Feeding Tube User, Hard of hearing.

Active Addictions: Hoarding, Self Harm.

Religion: Satanism, Paganism.

Job: Playwright.

Lives in: Okutama, Tokyo, Japan, 2024. (Also, Hell.)

Languages: Japanese, English, Demonic, JSL.

Height: 5'3”

Race: Asian.

Ethnicity: Japanese.

Accent: Shitamachi.

Vehicle: Purple and Black Rollerskates w Bat Wings.

Spirit Form: Just her, very calm, a little floaty.

Spirit Level: Acceptance.

Voice Claim: Madoka from Madoka Magica (JP Dub)

Powers: Divination, Immortality, Regeneration, Ceremonial Magic, Shapeshifting, Can use sigils to summon certain things, Can manipulate Technology.

Weaknesses: Basic Demon Weaknesses, Basic Undead Weaknesses. No known special weaknesses.

Weapon: Butterfly Knife, Sacrificial Knives.

Wand: Writes her spells and such on Tanzaku.

Alignment: Chaotic Good.

Text Color: Purple.

Main Hobbies: Writing, Singing, Sewing, Prop Making, Plays almost every instrument you can think of.

Favorite Drinks: Peach Ramune, Ultra Violet Monster Energy, Hot Chocolate, Green Mountain Dew, Red Mountain Dew, Grape Slushies.

Favorite Fruit: Pomegranate, Raspberries, Apples.

Favorite Meal: Miso Soup.

Favorite Snacks: Jiffy Pop, Corn Nuts.

Favorite Dessert: Strawberry Lemonade Italian Ice, Cherry Pie.

Favorite Flower: Wisteria.

Scent: Ink, Alcohol Markers, Paint.

Handedness: Right Handed.

Blood Color: Black.

Soul Form: Purple Flame.

Awareness: Aware (Effect: Positive.)

Birthday: June 13th 2003 (Gemini, Sheep, B.)

Theme:

Playlist:

Fun Facts: Was the leader of her Occult Club at school, but switched to the drama club after yknow, literally summoning the Princess of hell.

Has a whole room full of stuffed animals that she is put in to calm down.

Special Interests: America, Musical Theatre.

Stims: Dancing, Lots of Vocal Stims, Rocking, Balancing, Has one of those fidget pens, and uses her knife to stim, Stuffed Animals and Soft Things.

Stimboard: LINK

Moodboard: LINK

Fashionboard: LINK

Family:

Iwata Seta, Oka Seta. (Parents.)

Takano Seta (Sister.)

Lucifer Morningstar, Lilith Morningstar + The Morningstar Family. (In-Laws.)

Friends: Kagayaki, Keh, Atsu, Joji.

Romance: Lucy Ferr (Wife, Bonded)

Enemies: Hwan.

Pet: Spot (スポット) (Cereberus Puppy.)

Brief Personality: Hana is very excitable, she loves to talk people’s ear off about musical theaters and whether or not trees have feelings. She tends to march to the beat of her own drum, even if that means forgetting to do things like, eat, or take care of herself. She’s genuinely trying her best despite being a little bit of a klutz.

Brief Backstory: Hana was the second born to her family. Her family were small town religious folk and Her sister had a childhood illness that left her bedridden, so her parents often wrapped Hana in bubble wrap. Hana was homeschooled and wasn’t really allowed to go outside and make friends. Her sister eventually passed away, and her parents control got tighter. Hana often felt suffocated in her own home. Constantly being watched and constantly being supervised. Most of her education was just learning religious passages and Hana was bored out of her mind. She often dreamed about the outside world.

She finally convinced her parents to let her go to high school. And they reluctantly agreed. And oh my god Hana was so happy. She read every single book in the library, She made friends with everyone in school. And then she found out about MUSICAL THEATRE. The shows the lights the drama of it all! She was mesmerized.

She watched from afar, all the drama club kids and their pretty costumes. Hana however was committed to the occult club. A club she chose mostly to piss her parents off. She didn’t take it that seriously, a little candle here, a sacrificial knife here, some chanting ya da ya-

Wait a minute Hana just summoned a demon… a real demon.. she didn’t realize she could do that. Um this is awkward..

The demon was beautiful. And she took a liking to Hana. So Hana attached herself to the demon and hung out with her all the time. Little did she know that would be her future wife.

Hana eventually ran away from home and moved in with her demon friend. Living half in hell and half in okutama. And she couldn’t ask for a better life.

[reverent-sacrifice]

In my version of Heaven for Blackberry Ambrosia, nearly all of my main characters are disabled. Their grace *can* heal many of the ailments they have, but they don't see the need to be rid of them. And in Michael's case, as the blind angel of Justice, his disability serves his role well. Wheelchairs and the like exist and can be made into ultra-light gliders for those who can still fly, and three of my main character's children have prosthetic limbs fueled by their grace/magical.

Its not hard to include people

Whgskl. Okay.

PSA to all you fantasy writers because I have just had a truly frustrating twenty minutes talking to someone about this: it’s okay to put mobility aids in your novel and have them just be ordinary.

Like. Super okay.

I don’t give a shit if it’s high fantasy, low fantasy or somewhere between the lovechild of Tolkein meets My Immortal. It’s okay to use mobility devices in your narrative. It’s okay to use the word “wheelchair”. You don’t have to remake the fucking wheel. It’s already been done for you.

And no, it doesn’t detract from the “realism” of your fictional universe in which you get to set the standard for realism. Please don’t try to use that as a reason for not using these things.

There is no reason to lock the disabled people in your narrative into towers because “that’s the way it was”, least of all in your novel about dragons and mermaids and other made up creatures. There is no historical realism here. You are in charge. You get to decide what that means.

Also:

“Depiction of Chinese philosopher Confucius in a wheelchair, dating to ca. 1680. The artist may have been thinking of methods of transport common in his own day.”

“The earliest records of wheeled furniture are an inscription found on a stone slate in China and a child’s bed depicted in a frieze on a Greek vase, both dating between the 6th and 5th century BCE.[2][3][4][5]The first records of wheeled seats being used for transporting disabled people date to three centuries later in China; the Chinese used early wheelbarrows to move people as well as heavy objects. A distinction between the two functions was not made for another several hundred years, around 525 CE, when images of wheeled chairs made specifically to carry people begin to occur in Chinese art.[5]”

“In 1655, Stephan Farffler, a 22 year old paraplegic watchmaker, built the world’s first self-propelling chair on a three-wheel chassis using a system of cranks and cogwheels.[6][3] However, the device had an appearance of a hand bike more than a wheelchair since the design included hand cranks mounted at the front wheel.[2]

The invalid carriage or Bath chair brought the technology into more common use from around 1760.[7]

In 1887, wheelchairs (“rolling chairs”) were introduced to Atlantic City so invalid tourists could rent them to enjoy the Boardwalk. Soon, many healthy tourists also rented the decorated “rolling chairs” and servants to push them as a show of decadence and treatment they could never experience at home.[8]

In 1933 Harry C. Jennings, Sr. and his disabled friend Herbert Everest, both mechanical engineers, invented the first lightweight, steel, folding, portable wheelchair.[9] Everest had previously broken his back in a mining accident. Everest and Jennings saw the business potential of the invention and went on to become the first mass-market manufacturers of wheelchairs. Their “X-brace” design is still in common use, albeit with updated materials and other improvements. The X-brace idea came to Harry from the men’s folding “camp chairs / stools”, rotated 90 degrees, that Harry and Herbert used in the outdoors and at the mines.[citation needed]

“But Joy, how do I describe this contraption in a fantasy setting that wont make it seem out of place?”

“It was a chair on wheels, which Prince FancyPants McElferson propelled forwards using his arms to direct the motion of the chair.”

“It was a chair on wheels, which Prince EvenFancierPants McElferson used to get about, pushed along by one of his companions or one of his many attending servants.”

“But it’s a high realm magical fantas—”

“It was a floating chair, the hum of magical energy keeping it off the ground casting a faint glow against the cobblestones as {CHARACTER} guided it round with expert ease, gliding back and forth.”

“But it’s a stempunk nov—”

“Unlike other wheelchairs he’d seen before, this one appeared to be self propelling, powered by the gasket of steam at the back, and directed by the use of a rudder like toggle in the front.”

Give. Disabled. Characters. In. Fantasy. Novels. Mobility. Aids.

If you can spend 60 pages telling me the history of your world in innate detail down to the formation of how magical rocks were formed, you can god damn write three lines in passing about a wheelchair.

Signed, your editor who doesn’t have time for this ableist fantasy realm shit.

[atplblog]

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