#Mobilityaids

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#Mobilityaids Reel by @thefibroguy (verified account) - If you are living with hypermobility, fibromyalgia, or chronic pain, and you keep wondering whether a mobility aid might help, then this video is for
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@thefibroguy
If you are living with hypermobility, fibromyalgia, or chronic pain, and you keep wondering whether a mobility aid might help, then this video is for you. Mobility aids are not giving up they are tools that can improve your quality of life and even support your rehab. Walking sticks, scooters, and wheelchairs can help you move with less pain more confidence and more freedom. 2026 is the year you stop worrying about other peoples opinions and start doing what actually helps you feel better. Your wellbeing matters and you deserve support that works for you. #chronicpain #hypermobility #fibromyalgia #mobilityaids #qualityoflife
#Mobilityaids Reel by @chronicallyjenni - Things Disabled People Are Expected To Do That Non-Disabled People Would Never Be Asked Here are things disabled people are expected to do that non-d
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@chronicallyjenni
Things Disabled People Are Expected To Do That Non-Disabled People Would Never Be Asked Here are things disabled people are expected to do that non-disabled people would never be asked. Once you notice them, you cannot unsee them. 1. Prove our disability on demand Non-disabled people are never asked to list symptoms, injuries, or diagnoses just to be believed. Yet disabled people get questioned about mobility aids, parking, time off, and adjustments as if our lives are court cases. 2. Be grateful for the bare minimum A lift that works, a ramp that is not blocked, a toilet you can actually get into. These are treated like luxuries, not access. No one else is expected to be grateful for simply being able to enter a building. 3. Plan everything around other people’s comfort We are expected to avoid being an inconvenience. To take the longer route, or the harder option, so no one has to move a chair or hold a door. Non-disabled people do not have to apologise for existing. 4. Justify needing rest or support Non-disabled people can say they are tired and nobody asks for evidence. Disabled people say they are tired and it becomes a debate, a judgement, or an accusation. 5. Accept reduced opportunities with a smile Jobs, events, education, social plans. Disabled people are expected to be understanding when something is not accessible or equitable. As if we should be grateful to be included at all. 6. Teach everyone else about disability for free We get asked to explain policy, access, language, and lived experience at any time, even by people who could easily look it up. Non-disabled people are never expected to be walking encyclopaedias of their identity. 7. Stay positive so other people do not feel awkward We are expected to soften the truth so it is easier for others to hear. Non-disabled people are allowed to have bad days without being inspirational or disappointing. What else would you add to this list from your disabled or chronically ill life? Your insights help people understand the reality behind the expectations.
#Mobilityaids Reel by @chronicallyjenni - Disability Myths vs Reality What disability myths do you still hear that need busting? Let me know in the comments! Today we are breaking down some
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@chronicallyjenni
Disability Myths vs Reality What disability myths do you still hear that need busting? Let me know in the comments! Today we are breaking down some of the most common misconceptions about disability and what the reality actually looks like. 1. “If you really need a mobility aid, you would use it all the time.” Reality: Disability is not consistent. Many disabled people use different aids on different days or for different situations. Someone might walk short distances, use a wheelchair outside, or need mobility aids only when symptoms flare. Using an aid sometimes does not make someone “less disabled.” No one used a wheelchair in bed! (do not try it at home!) 2. “It’s easy to get support if you’re disabled & people fake disability for benefits.” Reality: Accessing support is often long, confusing, and exhausting. Finding out what help exists, completing applications, attending assessments and chasing responses can take months or years. The admin alone can be a full-time job. Most support does not even cover the extra costs of being disabled, let alone provide comfort or ease. 3. “Disabled people are lazy or rely too much on others.” Reality: Many disabled people push themselves far beyond safe limits just to be taken seriously. We problem-solve constantly, adapt everything and often overwork ourselves to prove we are capable. Needing support is not the same as being lazy and independence does not mean doing everything alone. 4. “Being disabled means life is miserable or over.” Reality: Disability is often shown as the worst possible outcome in TV, films & workplace training. While being disabled can be incredibly hard, it is not the absence of joy. Many of us experience deep, meaningful, joyful lives. Life may not look how we once imagined, but that does not make it less valuable or less full. If this helped you understand disability a little better, please save this post so you can come back to it, and share it if someone in your life needs to read it. And if you are disabled and reading this: your experience is real, valid & not up for debate. #DisabilityEducation #DisabilityMths #DisabledVoices
#Mobilityaids Reel by @graceisnotinvisible - my very first folding cane that i got almost exactly six years ago when i was first getting diagnosed with hypermobile ehlers-danlos syndrome as a you
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@graceisnotinvisible
my very first folding cane that i got almost exactly six years ago when i was first getting diagnosed with hypermobile ehlers-danlos syndrome as a young teenager 💔 all the old mobility aids i have in my house really do form a drag path. it's the journey to be where i am now :( - #disabledlife #dragpath #chronicillnesswarrior
#Mobilityaids Reel by @bren_hucks (verified account) - This encounter got me thinking about how I used to feel the urge to police handicap spots, and how much my perspective has shifted since then. 1. You
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@bren_hucks
This encounter got me thinking about how I used to feel the urge to police handicap spots, and how much my perspective has shifted since then. 1. You can’t judge someone’s health by looking at them. Invisible disabilities exist, and many people who rely on accessible parking don’t look disabled. It’s not our job to decide whether someone “looks sick enough” to park there. Ideally, that’s handled by whoever monitors the lot, and if there’s clear abuse, it should be reported through the proper channels: not through side-eye or confrontation. Though this is exception and not rule because sometimes it’s CLEAR and maybe they need a gentle reminder to have empathy for the disabled. 2. Lack of education around accessibility is a real issue. Since becoming disabled, I’ve learned that for some people, no accessible spot = no entry. They physically can’t get out of their car without that space, especially if they need room for mobility aids. That’s why I only park in those spots when I need to, and I never park in the yellow lines. They aren’t just decorative or “extra room” - they’re essential for access. We need way more education around this. Not just on social media, but in schools, workplaces, and public spaces. 3. Not all accessible tags hang from a mirror. Some are on license plates. So before you glare at someone for “not having a tag,” maybe give it a beat. Mine’s on my plates, and I’m tired of the stank looks. Accessibility isn’t always obvious. And disability doesn’t always look like what you expect. Let’s lead with curiosity and compassion. 🫶🏼 Also I will match energy so careful how you confront 😂
#Mobilityaids Reel by @josephakibler (verified account) - Ambulatory Wheelchair User. Full text below: Anytime I talk about walking or standing while I'm seen in my wheelchair people get so confused. A lot
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@josephakibler
Ambulatory Wheelchair User. Full text below: Anytime I talk about walking or standing while I’m seen in my wheelchair people get so confused. A lot of people with disabilities who are in wheelchairs can still walk or stand in some way or for short distances. (Or even longer distances). Disabilities can be variable and the type of mobility aid we use can change depending on the day or even just the activity. Over the course of my life I went from being in a wheelchair to a walker, crutches to a cane and then back to crutches and now back to my wheelchair. If I’m around my house I will often just use my cane or if I’m only going one location straight from a car and I don’t need to do a lot of walking. A lot of people who are like me are referred to as Ambulatory Wheelchair Users. We are kinda like action figures… accessories included… depending on insurance. It’s important to remember not to put mobility aids in a hierarchy and not to praise someone for using a cane over a wheelchair. Disabled people should feel comfortable to use the mobility aid they need in the moment they need it. And if you are sitting here right now, watching this video and you’re wondering if you need a mobility aid… The fact that you’re wondering is probably a good indicator of needing one. It DOES NOT make you LESS than to use a mobility aid. It just gives you MORE options for a better quality of life. #ambulatorywheelchairuser #ambulatorywheelchairusersexist #disabled #disability #disabilityawareness #wheelchair #wheelchairlife #mobilityaid
#Mobilityaids Reel by @katestanforth (verified account) - Learning / Falling 🎥 Just Capturing some real life action for you and showing you that it's not all graceful 😆 This year has been a lot of learnin
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@katestanforth
Learning / Falling 🎥 Just Capturing some real life action for you and showing you that it’s not all graceful 😆 This year has been a lot of learning about myself and my mobility aids with a few bruised knees in the process 😆 Advocacy Kate needs to tell you that even a basic wheelchair is not often provided on the NHS, nevermind anything you can dance in. My Omeo, as you probably know, is on a loan and has truly changed my life thanks to @myadaptability. We crowdfunded/paid for two of my past wheelchairs and grant funded my other two. (Over the span of 15 years!) If you’re looking for support @accessyourlifeltd is the place to go! And if you’re learning any wheelchair skills, let me know, because 17 years later I’m still learning every day 🫶🏻 #DisabledDancer #Wheelchair #WheelchairSkills #ChronicIllness #FrankSinatra #BabeWithAMobilityAid #Dancer #Comedy #WheelchairBallerina
#Mobilityaids Reel by @wheelsnoheels_ (verified account) - A little look into my everyday - with the tech and tools that help me move through life on my terms. From lap stacking to audiobooks, robot vacs to wh
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@wheelsnoheels_
A little look into my everyday — with the tech and tools that help me move through life on my terms. From lap stacking to audiobooks, robot vacs to wheelchair power add-ons… this is about making life mine. 💪 No shame in asking for help. 🛠️ No weakness in using what supports you. ♿ Mobility aids are empowerment. Audio book: The Ablest manifesto - @imtiffanyyu Bosse QC head phones Lapstacker: @adaptdefy code gem for free delivery Samsung jet bot Nespresso coffee machine Motability car Steering ball & push pull accelerator Bacet mini 2 @cyclonemobility @batecmobility #AccessibilityIsFreedom #DisabilityPride #MobilityAids #AssistiveTech #DisabledAndProud #DayInTheLife #SpinalCordInjury #Wheelchair #BabeWithMobilityaid
#Mobilityaids Reel by @mightymadilynn - Most people see her mobility aids first. So we thought we'd let her introduce herself instead 💕 This is Madilynn. She has a rare genetic condition t
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@mightymadilynn
Most people see her mobility aids first. So we thought we’d let her introduce herself instead 💕 This is Madilynn. She has a rare genetic condition that affects her balance and coordination. But that’s only one part of who she is. She has favorite things. Big opinions. A sense of humor. And apparently… her own perfume line (it’s water 😆). If you’re new here, this page is about progress, parenting, rare disease life, and celebrating “inchstones” aka the small wins that mean everything to families like ours. We’re really glad you found us 💕 #sca5 #disabilitypride #spinocerebellarataxia #ataxiaawareness
#Mobilityaids Reel by @andraealavant (verified account) - My chair survived this time, but @emilyladau's did not. Will we EVER be able to count on safe travel, @delta?! COME ON! Video description: Text on s
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@andraealavant
My chair survived this time, but @emilyladau’s did not. Will we EVER be able to count on safe travel, @delta?! COME ON! Video description: Text on screen: Warming up for another trip where I have to explain to airlines how ✨NOT✨ to break my wheelchair 🫠 Visual: Andraéa is a Black, disabled woman sitting in her #4Front2 power wheelchair at the airport. She has had her wheelchair broken on several occasions, as have most disabled folks with mobility aids. Andraéa is holding the leash for her service dog, Goji. Goji is a yellow Labrador retriever wearing a blue Canine Companions service dog vest. Andraéa is taking deep breaths in and slowly breathing out with her eyes closed. She stretches her neck side to side, then hangs her head low while exhaling out. Andraéa is wearing a comfortable, black, maxi dress with a denim jacket. She is wearing a black face mask, gold glasses, a black turban, and silver sneakers. She has a small, tan, crossbody purse across her chest. She is in front of the Delta Airlines check-in kiosks. Audio: TikTok mashup of “Teach Me How to Dougie” by Cali Swag District and a football game’s commentary. #DisabledLife #WheelchairTravel #DisabledTravel #RightsOnFlights
#Mobilityaids Reel by @the.annegirl - I have Functional Neurological Disorder. I'm an ambulatory wheelchair user. I'm a disabled parent. I'm a young person who uses mobility aids. When I
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@the.annegirl
I have Functional Neurological Disorder. I’m an ambulatory wheelchair user. I’m a disabled parent. I’m a young person who uses mobility aids. When I first got sick, I didn’t know people like me existed. I wish I had been able o see more people like me, especially to know that it would be possible to be a mom one day. But also to know I could be confident, beautiful, happy again. If you want to see content about parenting with a disability, using aids, and being confident from a wheelchair, with a cane, and battling the disability stigma then give me a follow. I know we’ll be friends. See you soon 🤍
#Mobilityaids Reel by @coolcrutches (verified account) - Ever thought having a mobility at your wedding was your worst nightmare?? THINK AGAIN! Whether it's a walking stick, crutches or any other mobility
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@coolcrutches
Ever thought having a mobility at your wedding was your worst nightmare?? THINK AGAIN! Whether it’s a walking stick, crutches or any other mobility aid it’s part of your day, your life and YOU 🤩 Just look at some of our incredible community on their wedding day - SIMPLY GORGEOUS 🩷 Share this post and let’s rewrite the narrative around mobility aids once and for all 🌈 #CoolCrutches

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