The Worse Climate Disaster Gets, The More You’ll See Closet Eugenicists Start To Advocate For Letting

This is probably still good OpSec, but mostly I need to reblog this to cite it for a paper.

A disabled woman fell on the bus I'm on and I'm literally the only one who listened to her and didn't try and pull her up when she said she wanted to sit for a second, or crowd her saying what she should do next.

Can we actually listen to disabled people maybe? This is exhausting.

I think the reason a lot of leftists struggle with disability justice is that they haven't moved past the concept that discrimination isn't bad because it's objectively "wrong." yes, sexists are objectively wrong when they try to claim women are dumber than men. yes, antisemites are objectively wrong that jewish people are inherently greedy and run the state. yes, racists are wrong when they try to claim that white people are the superior race. and so on.

but then with disabled people, there are a lot of objective truths to the discrimination we face. people with IDs/LDs do fall behind and struggle with certain concepts. physically disabled people are often weaker and less capable of performing demanding tasks than able bodied people. many of us with mental illnesses are more reckless and less responsible. a lot of us are dependent on others and do not contribute much "worth".

and guess what? disabled people still deserve a place in the world. disabled people still deserve the supports they need. because they are people, and that should be enough to support them and believe they deserve a place at the table.

if your only rebuttal against discrimination is its objective inaccuracies, you are meeting bigots where they are at. you are validating the very concept that if and when people are truly incapable of being equal to the majority, that means they are worth less. this causes some leftists to then try to deny the objective realities of disabled people and/or become ableist themselves.

your rallying behind marginalized groups should start and end with the fact that people are completely worthy of life and equity, because they are fellow human beings and that should, frankly, be enough.

post by @ lucyedwardsofficial on instagram showing how the paralympics includes blind/visually impaired viewers of goalball!

My husband and I became catechumens in the EOC for which we are incredibly grateful. Here’s my dilemma though.

I can’t attend Divine Liturgy because of my chronic illness. The priest is very understanding of this and is genuinely trying to accommodate us the best anyone can.

He wants us to get plugged into the community despite my limitations and is thinking of safe ways for us to do so, since I am immunocompromised and my husband (who has lupus) is also facing potential new health concerns. Though we want community as well, I am having debilitating anxiety around it.

My illness is so unpredictable. I have good days and bad days. Some days, I need my wheelchair or another mobility aid (which I don’t like using because I don’t like being vulnerable but I NEED to use them for safety and/or energy preservation). But other days, I do not need anything. Chronic illness has SO MANY facets and triggers and layers of unpredictability! In the past, many people (mostly people from our old church) have accused me of faking my disability when they’ve seen me on a good day, or when they’ve seen me without a mobility aid after needing one a previous day. They’ve told me I’m making excuses, that I’m faking for attention, etc.

No one but my husband ever sees the “details” of my chronic illness, after all. They don’t see me when I’m curled up all night on the bathroom floor bc of gastroparesis agonizing and crying for it all to end, or being SO extremely fatigued due to POTS that I can’t move a limb out of bed. They didn’t see me when I fell that morning which warranted me using my rollator for the rest of the day to prevent another concussion. They don’t see the painful internal struggle of trying to walk in the summer heat without support. Anyone with a chronic illness can relate!

People from my last church (not an OC) said hurtful things and more and told me I’m going to hell for a number of reasons- because I don’t have kids, because I don’t go to church on Sundays etc. i had poured my soul into that parish. Then, everyone left. We felt abandoned.

This served as the catalyst to question our faith -tradition, theology, and everything- and ultimately, everything came together to lead us to Orthodoxy which is a HUGE blessing! But I’m just SO EMOTIONAL because though I’m more than ready to embrace the fullness of faith and the Sacraments when the time comes, I don’t think I can ever be a part of a community.

It’s exhausting to have to try to explain the ins- and- outs of my illness to new people, many of whom wouldn’t even believe me. And I just don’t want to get hurt again. I know it’s wrong of me to assume that every new person I meet will eventually judge me and leave, but that’s just what we’ve consistently experienced. That’s all we know. I have a small circle of friends, and I’ve known all of them for many years - those friendships have stood the test of time and I’m grateful for them.

I honestly don’t know why I’m making this dumb post. I’m not trying to throw myself a pity party, I just need a place to vent and let it all out. I’m also just in a totally bad headspace right now and my anxiety levels overall are insanely high with my husband preparing for a high stakes surgery in a few days and me having side effects from the rescue medication I had to take last night. But if you’re reading this and have any advice, please tell me. And please pray for us. Please pray for peace and healing in our lives, spiritually, physically, and emotionally. Please pray that i can stop myself from spiraling into depression - I can feel it happening. I feel like a burden to my husband and the few friends I have and the devil is probably angry that I made the decision to become a catechumen. Please pray that we can find joy this Pascha, even though we are separated from the Church, knowing that we rejoice in Jesus’s resurrection. The pain runs deep but His love runs deeper.

Thank you. 🤍

every time anyone talks about liberation for the intellectually disabled in any real material way (i.e. creating plain-language educational resources accessible to adults reading on a first-grade level, detangling literacy from basic requirements to participate in society, destigmatizing inability to benefit from pedagogy, criticizing the construct of financial literacy as a necessary skill, etc etc etc), some chud comes along calling it "anti-intellectualism" and blabbing about how you're a morally inferior person if you only read middle-grade novels for fun, i'm so tired and we are never making it out

Fuck this one hits home.

I found an extremely dope disability survival guide for those who are homebound, bedbound, in need of disability accommodations, or would otherwise like resources for how to manage your life as a disabled person. (Link is safe)

How to Get On

How to Get On

How to have a great, disabled life.

It has some great articles and resources and while written by people with ME/CFS, it keeps all disabilities in mind. A lot of it is specific to the USA but even if you're from somewhere else, there are many guides that can still help you. Some really good ones are:

How to live a great disabled life- A guide full of resources to make your life easier and probably the best place to start (including links to some of the below resources). Everything from applying for good quality affordable housing to getting free transportation, affordable medication, how to get enough food stamps, how to get a free phone that doesn't suck, how to find housemates and caregivers, how to be homebound, support groups and Facebook pages (including for specific illnesses), how to help with social change from home, and so many more.

Turning a "no" into a "yes"- A guide on what to say when denied for disability aid/accommodations of many types, particularly over the phone. "Never take no for an answer over the phone. If you have not been turned down in writing, you have not been turned down. Period."

How to be poor in America- A very expansive and helpful guide including things from a directory to find your nearest food bank to resources for getting free home modifications, how to get cheap or free eye and dental care, extremely cheap internet, and financial assistance with vet bills

How to be homebound- This is pretty helpful even if you're not homebound. It includes guides on how to save spoons, getting free and low cost transportation, disability resources in your area, home meals, how to have fun/keep busy while in bed, and a severe bedbound activity master list which includes a link to an audio version of the list on Soundcloud

Master List of Disability Accommodation Letters For Housing- Guides on how to request accommodations and housing as well as your rights, laws, and prewritten sample letters to help you get whatever you need. Includes information on how to request additional bedrooms, stop evictions, request meetings via phone, mail, and email if you can't in person, what you can do if a request is denied, and many other helpful guides

Special Laws to Help Domestic Violence Survivors (Vouchers & Low Income Housing)- Protections, laws, and housing rights for survivors of DV (any gender), and how to get support and protection under the VAWA laws to help you and/or loved ones receive housing and assistance

Dealing With Debt & Disability- Information to assist with debt including student loans, medical debt, how to deal with debt collectors as well as an article with a step by step guide that helped the author cut her overwhelming medical bills by 80%!

There are so many more articles, guides, and tools here that have helped a lot of people. And there are a lot of rights, resources, and protections that people don't know they have and guides that can help you manage your life as a disabled person regardless of income, energy levels, and other factors.

Please boost!

Things to research before getting your first custom manual wheelchair

one of the biggest things I can recommend to anyone getting a new custom chair (but especially a first custom chair) is to understand all of the parts of a wheelchair and what they do. I decided to make a guide with wheelchair parts to research and places to look for information to make this process a little bit easier. additional link suggestions are welcome.

General resources:

Permobil - The Wheelchair Handbook

Motion Composites - Preparing for Your Wheelchair Evaluation: Before the Evaluation (Part 1)

Motion Composites - Preparing for Your Wheelchair Evaluation (Part 2)

1. Frame

Motion Composites - Folding vs Rigid Wheelchair Frames: How to Choose

Permobil - Manual wheelchairs: rigid and folding frames. How do you choose?

GTK - Oh what’s in a frame? Comparing Multiple Materials

Motion Composites - Wheelchairs: Carbon Fiber Versus Aluminum

2. Front frame angle

Motion Composites - Understanding the Impact of Rigid Wheelchair Front Frame Angle

Sunrise Medical - Rigid Frame Wheelchairs – Frame Angle and Inset

4. Seat dump

Permobil - Ergonomic Seating and Manual Wheelchairs

Spinlife - Wheelchair Back & Seat Angle

5. Caster size, style, and position

Motion Composites - Front Casters for Manual Wheelchairs Practical Guide

Sunrise Medical - Front Caster Position in Manual Wheelchairs

6. Caster forks

New Mobility - Caster Wheels and Forks

Sunrise Medical - Maneuverability in Manual Wheelchairs - What Fork to use?

New Mobility - Innovations: Emerging Trends in the Wheelchair Market (information about single sided forks)

7. Footplate

Motion Composites - Footrest Options to Support Function and Mobility

When Tania Talks - Active User Wheelchair Footplate Options

8. Calf strap

Spex Seating - Lower Leg Support Considerations in Wheelchair Seating

9. Seat pan

Permobil - Solid Seat Insert for Wheelchair: Taking a Closer Look at Cushion Components

10. Seat cushion

Permobil - What to Look for in Seating & Positioning Products

Permobil - How to Choose a Cushion in Long Term Care

Permobil - Cushion Geometry: Linear and Contoured

Freedom Mobility Center - Wheelchair Seat Cushions: 5 Tips for Choosing the Right One for You

Mobility Basics - Seat Cushion Rigidizer

Motion Composites - Selecting the Right Cushion for Your Wheelchair a Clinicians Guide

Motion Composites - Covering the Basics of Wheelchair and Back Support Covers

11. Seat belts

12. Clothing guards

Sherman Oaks Medical Equipment - Wheelchair Clothes Guards / Side Guards Guide

13. Arm rests

United Spinal Association - Wheelchair Armrests What Do They Really Do?

Spinlife - Wheelchair Arm Rest Choices

Motion Composites - Armrests: Getting the Support you Need

14. Back supports

Motion Composites - Solid vs Upholstery Backs

Mobility Management - How to Choose the Right Back Height for your Client

Freedom Mobility Center - Why a Solid Back is Preferred Over a Sling Back

Mobility Basics - Back Supports

Sunrise Medical - Tips for Selecting Prefabricated Wheelchair Backs

Motion Composites - Covering the Basics of Wheelchair and Back Support Covers

15. Head supports

16. Push handles

Motion Composites - Push Handles: Pushing Around

17. Wheels

Motion Composites - Rolling Along: The Importance of Rear Wheel Selection

Sunrise Medical - Comparing Wheelchair Wheel Spoke Options

Mobility Basics - Manual Wheelchair Wheels

18. Tires

New Mobility - Everything You Need to Know About Selecting the Right Wheelchair Tires

GTK - Solid versus Pneumatic Tyres

Mobility Basics - Manual Wheelchair Wheels

Motion Composites - Tire Selection: Balancing Performance and Maintenance

19. Brakes

Motion Composites - Wheel Locks: Unlocking Safety and Function

20. Push rims/Hand rims

Motion Composites - Getting a Grasp: Understanding the Impact of Hand Rims

DME Hub - Wheelchair Hand Rom Options and Factors to Consider

21. Anti-tip wheels

22. Camber

Motion Composites - Camber - Degrees of Performance

23. Center of Gravity

Motion Composites - Rear Wheel Position 101