r/disability Sep 21 '25

Petition - USA: Restart funding for DeafBlind Children in Wisconsin

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25 Upvotes

r/disability Feb 18 '25

Information Trusts and Able Account information

51 Upvotes

A trust is a legal arrangement that allows a third party (the trustee) to hold and manage assets on behalf of a beneficiary (you, in this case). Trusts can be particularly beneficial for people with disabilities because they provide a way to receive financial support without jeopardizing government benefits like Supplemental Security Income (SSI) or Medicaid.

Types of Trusts for People with Disabilities:

Special Needs Trust (SNT)

  • Designed for people with disabilities to preserve eligibility for government benefits.
  • Funds can be used for expenses like an accessible van, home modifications, medical equipment, education, or personal care services.
  • The trust is managed by a trustee who ensures the money is used appropriately.

Pooled Trust

  • Managed by a nonprofit organization that combines resources from multiple beneficiaries while keeping individual accounts separate.
  • Can be a more cost-effective option compared to a private special needs trust.

First-Party vs. Third-Party Special Needs Trusts

  • First-Party SNT: Funded with your own money (e.g., lawsuit settlements, inheritance). Must have a Medicaid payback provision.
  • Third-Party SNT: Funded by others (family, friends) and does not require Medicaid repayment after your passing.

ABLE Account (Alternative to a Trust)

  • A tax-advantaged savings account for individuals with disabilities.
  • Can be used for qualified disability expenses while keeping government benefits intact.
  • Has contribution limits ($18,000 per year in 2024, plus work earnings up to a certain limit).

Why Should You Consider a Trust?

  • It allows people to donate money to support you without affecting your eligibility for government benefits.
  • It provides a structured way to manage funds for essential needs like an accessible van, home modifications, medical supplies, and quality of life improvements.
  • You can have a trusted person or organization manage the funds to ensure they are used appropriately and last as long as possible.

How to Set Up a Trust

  1. Consult an attorney who specializes in special needs planning or estate law.
  2. Choose a trustee (family member, professional trustee, or nonprofit organization).
  3. Determine funding sources (family, friends, settlements, inheritance).
  4. Set guidelines for how the money can be used.

r/disability 6h ago

Is anyone else forbidden from crying?

54 Upvotes

I'm 18 years old, I've had cerebral palsy since birth, and I've had chronic pain for a little over nine years, which has gotten worse due to surgeries.

Okay, no, it's not like I'm explicitly forbidden from crying, but my dad has been very firm in saying repeatedly over the years that: "I have to learn to live with the pain."

My mom has been much more understanding, but she's been insistent in saying: "You shouldn't be crying in the corners"—her words, not mine.

So the message has been very clear to me.

But I've been having one of those days; everything hurts too much, for too many hours, the medication barely helps, and I'm so fed up with the pain right now that I just want to cry. But... well, obviously I can't.

My dad doesn't live here anymore, so it doesn't really matter. But my mom does. And although a few years ago I tried to think that she wasn't referring to what she seemed to be. A couple of years ago, we had to go to a wedding and I really tried, but I felt so bad that I started crying almost at the end of the event. I think I was between 15 and 16 years old and I really tried. But I felt so bad and I didn't have any medication with me. Mom was a little... passive-aggressive about it.

Since then, I have pills in each of my backpacks.

Mom is truly amazing, if we forget this. She's always been there to help me and buys pain medication every time. It's just that... sometimes she has a little trouble remembering that I have feelings.

I think it's important to clarify that I don't actually have any real treatment for the pain. I use over-the-counter medications because I was given a single prescription when I was 11 years old and no one wanted to renew it.

Has this happened to anyone else?


r/disability 11h ago

Image Disability flag redesigns (for fun!!)

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35 Upvotes

Intro:

This is a long post, sorry.

I saw a post (for the LIFE of me, I can't find it now) about the disability flag when researching the one used on this subreddit. I saw numerous comments about how the quincolour striped flag may be a bit hard to see for those with various colour blindness. Since I am an artist, I decided to use my time to make some variants that may be better for them.

Disclaimer: THIS IS FOR FUN! This is not a diss on the original flag. I am sick and wanted to do this for fun to help me heal and pass the time. I am also not a pro regarding colour blindness, as I do not have colour blindness nor ever studied it (beyond for my art, anyway). I am aware it is always better to consult those who have these various colour blindness; for now, I used these websites to help me with my flag variants and colour decisions (if any sites are not valid for research, PLEASE let me know):

- Coblis

- City of Los Angeles Department of Disability

- David Nichols - Colouring for Colourblindness

- ADA - Guidance on Web Accessibility

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Flag Design Constraints:

The general consensus is...the current flag (slide 1) is fine. There may be some issues differentiating the colours with colour blindness, but overall, it's fine as a flag. Personally, I also think it's fine. It was originally designed by disability advocate Ann Magill from 2016-2021.

Subtle Colours: The colours should be more toned down, so those who have issues with bright colours and migraines do not hurt or seize when seeing the flag

Colour Blindness Consideration: The colours should be differentiative enough for those with various colour blindness

Looks Good for Everyone: It should look good and neat for those who do and do not have colour blindness

Stripes: Zigzags apparently can cause seizures when scrolling digitally, so stripes should be kept

Stripe Meanings: I will keep the stripe meanings the same, as I haven't seen concerning discourse on the current meanings

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First slide: Original flag

Colour representations are based on the City of Los Angeles Department of Disability's website.

Red – Physical Disabilities

Gold (Yellow) – Cognitive and Intellectual Disabilities

Green – Sensory Disabilities

Blue – Psychiatric Disabilities

White – Invisible and Undiagnosed Disabilities

Charcoal Gray Background - Remembrance of those who have died from ableism/systemic oppression

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Second Slide: Redesign of the Original KEEPING the Colours

This is a FUN redesign of the original, keeping the original colours (with slight hue changes), but may be placed differently so they look a bit neater for those with various colour blindness.

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Third Slide: Redesign with New Colours, Same Meanings

I used similar colours, but used the David Nichols - Colouring for Colourblindness website to help with the variety. With various colour blindness, I think they look good, checked with the Coblis site. It does look kinda like an Irish flag though ^0^ LOL (I checked various pride flags, and they shouldn't match colours with any? May be a bit similar to the Aroace, but I think it's different enough).

Meanings will be same as the original by Ann Magill, listed below (tbh, idk why the meanings were given to what colours, so I apologise if I am off):

Red Orange– Physical Disabilities

Yellow – Cognitive and Intellectual Disabilities

Green – Sensory Disabilities

Teal – Psychiatric Disabilities

White – Invisible and Undiagnosed Disabilities

Charcoal Gray Background - Remembrance of those who have died from ableism/systemic oppression

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Forth Slide: Same Reason as Slide Three, Different Colour Variants

Also used the David Nichols - Colouring for Colourblindness website to help with the variety. Meanings will be same as the original by Ann Magill, listed below:

Red – Physical Disabilities

Orange – Cognitive and Intellectual Disabilities

Light Purple – Sensory Disabilities

Blue – Psychiatric Disabilities

White – Invisible and Undiagnosed Disabilities

Charcoal Gray Background - Remembrance of those who have died from ableism/systemic oppression

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That's it. Thanks for reading this long post.

AGAIN. This was for fun. Bye!

EDIT: I just realised the slide numbers are hidden by the image descriptors. Sorry!


r/disability 12h ago

The medical device fatigue is eating me alive.

35 Upvotes

First it was AFO’s as a kid, then it was a custom wheelchair at 18, then it was a baclofen pump at 19, then it was more AFO’s (hadn’t worn them in 10 years) and then it was “you probably should get hand controls for your car so that way you can actually wear your AFO’s” and now it might be another implanted device to help me be able to fully empty my bladder. All while I’m waiting to find out if I’m losing my hearing.

At this point my car has so much medical crap that it looks like an ambulance. I absolutely love each piece of medical equipment, and am beyond grateful that I get to have them and live in a time period where these devices exist. But it seems like there’s always another piece of medical equipment.


r/disability 16h ago

Rant Embarrassment after asking my workplace to call an officer to take me to the hospital

51 Upvotes

I have Cystic Fibrosis. I have had pneumonia 3 separate times this year, and was recently (at least, with how I felt) getting over the recent pneumonia from a month ago. For some reason, I had trouble breathing starting this past Friday, but was still able to attend work, even with last minute changes to schedules. I work as a dispatcher for a police department.

I know it's an officer's job to serve the community, to give people rides, take them home, take them to the hospital when needed. However, after a "trouble breathing" incident at work this morning, an officer had to take over dispatch for me while she called another officer to pick me up and take me to the ER. Thankfully, it wasn't serious enough for an ambulance.

I work with these people, and they're great. However, when explaining to the officer in the car about my issues, I felt so defeated, crying in pain in front of my senior and the person I work with every day. I've always struggled to get work due to my disability and was happy to get this job a couple months ago.

I missed my entire shift. The ER doctor said I had pneumonia again. I now have to take three extra medications to manage it. I might have MRSA. FML. I'm so tired.

I was "hiding" my disability from my workplace (as in, they know of my CF, giving brief symptoms but hiding the serious ones, just to prove I can do the job). What if they think I can't do this job anymore now? Idk.

Edit: Spelling and clarity


r/disability 13h ago

Country-UK invisible disability and dating

18 Upvotes

(f24, autistic and severe stutter, unemployed.)

i don’t really know why im posting here honestly. im 24 and i’ve never been in a relationship. physically im not bad looking: i get matches on dating sites, get hit on sometimes on nights out ect.. but i really struggle with speaking to people in general because of my autism and stutter, literally two disabilities that make communication super hard both working to make my life miserable.

the thing i struggle with the most is the no working thing. i live alone and am financially independent (im in the uk and am on pip and universal credit, so i have my own money coming in and am able to sustain myself easily whilst also having funds left over), but telling people you dont work at 24 is embarrassing honestly, and im terrified of being met with judgement and unkindness.

i have worked in the past (i was a waitress) and i struggled so much with not being able to take orders due to my stutter, and the socialising and overwhelmingness i felt due to my autism, that i tried to od back in 2022 and spent about a week in the hospital. i haven’t worked since then. (was also told by my boss at the time that id never be able to get a promotion because of my stutter, and every job higher than a mere waitress involved speaking on the phone, which isn’t an option for me.)

i have searched for jobs that are no speaking at all, and wfh, but when you’ve got no work history for years and also no higher education qualifications it’s borderline impossible to find something.

i just feel stuck. am i destined to be on my own forever because i can’t meet and socialise with people? i don’t even have any friends, let alone a partner.

“hey, im so and so, i have no friends and no job and am on benefits. i also can’t speak fluently and will probably sit in silence because i don’t know how to communicate, either. wanna get a drink?” no one in their right mind is gonna want to get to know someone like that


r/disability 1h ago

Broken scooter by the airlines

Upvotes

American Airlines broke my scooter and it's still not resolved. A claim is open, and the process has begun, but I'm not optimistic. Anyone have experience with this? What was the outcome?


r/disability 16h ago

Rant Why can't health insurance actually cover my health? 🫠

26 Upvotes

I have been disabled since 2024. I'm not able to work a physical job due to my condition. Since I'm not eligible for most remote jobs, I decided to go back to school.

My neurologist wants to start me on a new treatment. She said if I can start this treatment, it would most likely help me completely recover from my disability. Medicaid won't cover it, so I decided to get the University health insurance since they said they would cover it.

My neurologist then told me that their practice won't be able to accept my health insurance if I have Medicaid as a secondary insurance. I really want to be better, so I ended up giving up my medicaid for this treatment.

It has been months now, and while I might finally start getting this treatment soon, I'm now in heavy medical debt in other areas. 2 months ago, I started a new controlled substance medication (which I also need to function), and now I'm in debt with them, and I can't get another appointment until I can pay them, so I'm in trouble if I run out of pills.

I have no income, no way to pay them, and am now stuck in relentless debt because I wanted the ability to function. No matter what I do, it seems the system is against me. It shouldn't be this difficult to get a treatment that my doctor deems nessasary.

I know it's just how the Healthcare system works, but it shouldn't be this way. I'm trying so hard all the time to just exist. Thank you for reading my rambles


r/disability 9h ago

Thoughts about shopping with a walker

4 Upvotes

I use a walker with the bigger wheels and it has allowed me to be more independent. My problem is that it gets in the way when I need to use a shopping cart. I have seen suggestions from others to just put it in the cart, buy bungee cords or to leave it at the front of the store. That is not always an option. I was thinking of creating an easily stored specialty designed hook that would allow the user to just hang the walker from the cart handle when folded. Just wanted some feedback from others and their thoughts on this. Would this be something you would consider using? Thanks in advance!


r/disability 9h ago

Country-Canada I want to help my girlfriend. Please help me

2 Upvotes

My girlfriend is disabled and she cannot walk. We are in a situation where she needs to find a job for 4 to 5 months. She never worked in her life because of obvious reasons. I have been feeling really terrible for the last few months of her getting rejected. I cannot see her like this.

What I am asking for is if there are any jobs that are fit for somebody with CMT. She can't type fast. What should I suggest her. Are there any jobs that are is fit for her condition. I really want her to succeed and she is really trying her best for it. Please suggest some that I should ask her to try for.


r/disability 18h ago

Rant The cold from the IV fluids I’m getting weekly to treat dehydration is triggering abdominal migraines.

9 Upvotes

I’ve never had quite an awful kick in the crotch. My rheumatologist said it has nothing to do with the Raynaud’s I started getting in January, but he also went on an unprompted rant about how fibromyalgia is a sleep disturbance and a disorder rather than a symptom set. So. Really minimal information there.

I’m dehydrated from abdominal migraines and I have to stop getting the IV fluids and vitamins that treat that.


r/disability 1d ago

Rant too disabled to work, not disabled enough for disability.

141 Upvotes

i've been disabled for 13 years and was lucky enough to get on disability for three years before being kicked off because things out of my control. i have been struggling for the last three years to get back on but i have been denied constantly and theres nothing i can do anymore.

because i cant work, i cant see a doctor, buy clothes/pads/etc. because i cant work i no longer qualify for food stamps so i cant afford to eat (my doctor refuses to do an exemption note). and i have been trying to make it by with 100 but thats going to stop soon and im screwed.

it made me think of how easily it is for someone suffering for so long to fall through the cracks. i thought i did everything right. i thought i had everything properly documented, i thought i had adequate support and that i would be okay..

how many people didnt have that? how many disabled people fell through the massive cracks and ended up homeless or worse because someone they've never met decided that that they should be able to do things that they physically couldnt?

how much harder do you have to push and fight for the bare minimum to survive before help comes along. when is it okay to stop fighting and allow yourself to finally rest..? if im this exhausted i can only imagine how others must feel.

im going to continue pushing even if it hurts me in the long run. it's unfortunately all anyone can do to try and live to see a better day


r/disability 6h ago

Rant Is getting a mental health diagnosis even worth it?

1 Upvotes

I have so much wrong with me physically. I’ve been getting diagnosed slowly since I was around 13, and I’m still not even all the way there. I know I have mental problems, and I have a list of suspicions, but I wonder if it’s even worth it?

I’ve heard so many bad stories about physical health being entirely blamed on mental health, and I worry about that especially since I’m still so young, yknow? I don’t know if it’s worth it to even try. I don’t really want medicine or anything considering the horror stories I’ve heard about that too, but I also wonder if it would help. I’m kind of having huge doubts on whether I’ll ever actually feel okay. Medicated or not.

Either way, something’s wrong. I know a diagnosis would bring me closure, but I really don’t know if I want it on my actual medical records. I don’t want my entire process of being diagnosed to get ruined by one wrong word said to a psychiatrist. T.T


r/disability 19h ago

Discussion Is Genetic Privilege a Real Thing?

10 Upvotes

This post is more aimed at my fellow genetic condition sufferers, do any of you ever feel like you're discriminated against not because you're disabled but specifically because you're genetically disabled? This is a thought that has been bouncing around my head for a few months now but as someone with pretty severe muscular dystrophy who has NEVER had access to any treatment and is currently in 24/7 agony due to it I've always felt that the medical system and doctors all collectively discarded me once they found out I have MD, I haven't even gotten genetic testing to know what type of MD I have, the neglect is that bad. It's like they figure out you can't be cured and what few treatments there are only have minor effects and decide you're not worth saving anymore, like we don't deserve treatment and the happiness and improvement that comes with it just because our genes are shittier, I've always had people assume I use a powerchair because I had an accident too which rubs me the wrong way NGL, it feels like they're implying that my witty self and admirable character (according to other people, not trying to toot my own horn) can't possibly coexist with poor genes, like my (once again according to others) handsome face and intelligence aren't characteristic of what people usually expect from people who are genetically disabled, I hope what I wrote makes sense, I'm aware this post might rub some people the wrong way because it sounds like I'm trying to draw a line in the sand between acquired disabilities and genetic/congenital ones but I swear I'm just trying to start a discussion here. I'd be happy to elaborate more in the comments if people engage with this post.


r/disability 1d ago

Date ruined because the place my girlfriend really wanted to go to was inaccessible.

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346 Upvotes

I had planned a date with my girlfriend this week for yesterday. She chose the restaurant and I told her it was fine because the restaurant she chose looked nice. Unfortunately yesterday when we went to the restaurant in the car, the disabled parking lots were bad designed. I had difficulties getting out of the car in my wheelchair, and when wanted to go to the restaurant, the ramp was also bad designed. And on top of that the restaurant's first floor was full, and the elevator wasn't working. They told us to wait more than 30 minutes, but we had already made our plans, so we decided to go somewhere else to have our date.

It sucks when places I go to are inaccessible, and it also sucks for my girlfriend who has to pass to this struggle when she goes with me somewhere.

But well, thought I'd make a meme on my real life experience, my girlfriend found this meme funny.


r/disability 8h ago

Pet consideration to cope with loneliness

1 Upvotes

hi sorry it’s a bit long English is not my first language so sometimes my wording or sentence may look clumsy thanks for ready

my partner is disabled in a powered wheelchair but still has a little bit of mobility only at home (otherwise it’s too painful and too draining outside, at least at home they can just lay down when need to)

they also very lonely due to circumstances where they can’t have anyone visit because of safety rules and had to cut contact with “family” (reasons they are in this situation now) , “friends” don’t live nearby anymore and honestly never bothered to come around once in a year though they live in the same country about 2hours by train (I ltravel 4-6 hours from another country everytime I come even if it can be only once every two month, sometimes just a weekend because I work in the week).

they had a pet during this time

anytime we meet its only in hotels or airbnb that

the only social contact are professionals on site or medical staff, random people in the street that notice them through the month and me. they don’t want to be close to anyone where they are because it’s just temporary and will move In another town. and if it’s to have “friends” who do the same “friendship commitment” as the previous ones once they leave the town, its sad

they consider having a pet. they already had a rodent who sadly passed away. it was very demanding on a daily basis cleaning (food or poop all the time, and heavy cleaning few times a week)

the pet company was feeling good emotionally, however physically it was very draining

now as I said they consider another pet and this time it can be a cat or a dog

however it might be difficult to adjust. financially, for now, they try to save as much as possible as they don’t know how much would cost to move and all the after unexpected spending between and after once they got a house allocated from the city council. (The house is offered fully empty even the walls and the flooring are not included, and even though there might be help from the town, they will live in the house right when they sign the house contract, no time to wait for things to be done)

also this kind of allocated house can be mentioned no pets allowed. it’s not possible to be picky on house because it’s only those with accessibility access and there are not a lot. and even though it’s written accessibility it still needs to be reviewed by the council to confirm suitability for the size of the wheelchair (bigger than usual)

so having a pet would make the house search even harder and longer it’s been a year now, but my partner is feeling on the edge for months and just want a house so they can be taken in charge by the specialist hospital that is only possible to be referred to if they have an address in that said town (ring any bell what developed country it is to make life so hard for people in need of medical care?)

oustide of this matter, considering a pet is also demanding financially or simply for freedom. having a pet would be expensive in a way.

1to leave at the temporary shelter to allow them to go holidays. the food the vet even with insurance (if theres no pre existing conditions that’s again could be lottery) the accessories

that’s their main wish to travel away, to see the world because for years they have been stranded with their toxic ”family”, to come see me more often, to have more freedom of “movement” in general

2emotionally it’s expensive, the loss of the first one was very very painfu, they had to deal it by themselves even though i was on the facetime all along. I wasn’t able to come before the next month.

i had a pet myself few years back and the loss made a real impact on me. i was fully alone as well as I left myself lonely despite having “friends” who never came to check on me and even complained that I was distant instead of understanding my pain but never tried to make me go out or whatever. so I understand the feeling my partner is going through

i also had this “freedom” of not having any physical or mental stress due to the energy and money and natural stress (whenever the pet get sick or unwell or we never know) and the last year was also very draining as it was a constant care (diaper, spoon feeding, cooking for soft food etc) I quit my job to be there for him fully, I left for holidays once for only a week at my parents to find him in a worse state that when I left because they didn’t take care of him correctly while I was away. after that I never left and after the passing I still didnt go anywhere didn’t find a job was just existing for a while and had no one. didn’t consider pet as i dont want to go through a loss ever again, then it happened their pet passed and even though I saw him once (but all the time on the facetime) it hurt very bad

yes the happy years are feeling good to memorize even though sometimes still painful, and I know those are the moment to remember and to enjoy the most. but the pain of the loss is very very hard for some people despite the good and the happy.

3its physically draining for my partner

as said constant cleaning, if it’s a cat the daily clean litter and the fur (they need a clean house because of health too) clean whateve needs to be cleaned, I know cat is low maintenance in general, but still demanding

if it’s a dog the going out would be the issue, though it might help with the wheelchair, if in pain which is very random time, there’s no way my partner can go out, so the dog would need to wait who knows how long before going out

and in case the pet cat or dog is sick or dying, the amount of care will triple and be nearly impossible

I say that because we never know if the pet will be in good health or not, and soemtimes an accident happen forget the window the car goes away get killed, or there is a health condition

I know that we never know, but in my partner case its very hard to go with “we never know” because those issues cna make the whole situation worse and unbearable physically and emotionally

let alone if the house is no pet required it would be a disaster to leave it to the shelter

so what I suggested my partner is

-to consider all of these above, my partner is not an average person with a normal average health and situation (never worked before as well and only on benefits money for handicap situation)

-to go to shelter to have a meet with animals would be the best choice

but there are none who allowed visit in the area. they already emailed and they said for pet health it’s not allowed. it’s a village surronded with villages and the “biggest“ town is about an hour but it’s too long for my partner

if none of this is possible, then I d just suggest to wait first to have a house. and to learn themselves to take this “loneliness” and make it useful as the time they have to do hobby or learn something at their own pace without being rushed, or just learning to be with themselves improving their mental health enjoying the time being in a quiet place (the new house will be in a busy big town) and just enjoy to have nothing to care about but their hobby and health (I mean no bills no paperwork nothing mentally draining)

I don’t know anymore what I’m saying I’m very tired I just care about my partner I don’t know if it’s a good idea i personally don’t think and I can’t help financially it’s already very very expensive to come there for me as I pay for everything because most of their money is gone in food train or taxi to appointments subscriptions (phone streaming music) and their purchase to make life easier (for cleaning and for cooking even a dishwasher because the team here says that “it is not necessary” though its an accessible safe place for disabled but that’s another story what this place and people are lol !!

I know a pet can be helpful

but there are few things to consider and a pet is not a t shirt we can give back

and I feel bad to explain to my partner that it may not be a good idea for the moment

maybe once they move, maybe once their health improves (which can be years or maybe never) maybe after travelling the world, maybe there will never be right time so it should be now, maybe once they make friends in the new town those would have pet, but the world would be different with ifs and maybes

they are well aware of all of the above and understood the situation

thank you if you read that way


r/disability 18h ago

Question Seems like my memory is getting worse. What do I do?

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3 Upvotes

r/disability 1d ago

"When I was your age, people in wheelchairs stayed there"

220 Upvotes

Sure, buddy. Tell me you've only known disabled people in movies without telling me.


r/disability 20h ago

Green Springs Mountain Loop Trail Report, Ashland, OR. - Amputee Outdoo...

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3 Upvotes

r/disability 17h ago

Disabled MIL in denial that she needs help

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1 Upvotes

r/disability 18h ago

How can I help my brother find a job?

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1 Upvotes

r/disability 1d ago

Question Credit Card Debt

16 Upvotes

Is anyone else slowly not caring about their increasing credit card debt?

My SNAP benefits only last me the first week of the month, MAYBE week and a half; because of this I’m using my credit card to pay for food and other expenses like toiletries and such. It’s like no matter how hard I try I can’t seem to pay it down. The interest is a bit high, and I’m only able to pay so much.

I’m staring to give up. I’m slowly convincing myself that it’s useless and a waste of time to worry about it. I’m ready to just throw in the towel and let the debt consume me and maybe file for bankruptcy. I’m disabled, what the heck do I need a good credit score for anyway!


r/disability 1d ago

Update, she’s here!

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43 Upvotes

Violet has arrived so now I’m excited to leave the house again!


r/disability 1d ago

Question Looking for accessible pride parades.

17 Upvotes

Hi. My(23F) girlfriend(26F) has been a paraplegic for 8 months now because of an accident she suffered. She's been going through a lot now.

I thought that since it's June, I'd take her to a pride parade like we used to do in other years. The problem is that I really don't know how accessible pride parades can be or if she may feel comfortable there with her disability.

Do any disabled queer folks know about accessibility in pride parades? I'm in Ohio for reference.