unwellsnail

He was a pain in the butt, I loved him!

Oh wow how neat, I had a red & white husky named Kiba when I was younger! What a handsome fella.

‘Do the best you can until you know better. Then when you know better, do better.’ - Maya Angelou

Thank you for saying this!

Also, if positive for covid seek a paxlovid prescription if available. It’s an effective treatment that can reduce illness time and severity but has to be taken early in your illness. Same with a flu test and Tamiflu if positive (though less likely to be flu right now depending on where you live).

My GSD used to hang out in the tub while I was in the bathroom getting ready. It started when I told her there was no room for both of us in there so she found a space for herself, then she just did that from then on.

Hello, just wanted to give a friendly suggestion to use terms like “wheelchair user” or “person who uses a wheelchair” instead of “wheelchair bound” or “confined to a wheelchair”. There are many articles explaining why in more detail for those wanting to know.

Toe tufts! They can sometimes get matted or the cat could become obsessive about cleaning them but if those things aren’t an issue there’s no real reason to trim them. There’s no harm in trimming them if wanted but also not necessary.

Instead of different bean recipes I like to make a variety of beans. There’s a great website called Rancho Gordo with a lot of different heirloom beans that are phenomenal, I love trying new beans. I usually cook each new type the same with simple spices to experience the base bean flavor before using them in more complicated dishes.

More absolutely predictable than ironic, it will not impact him and he has no love for the disability community. I imagine he has a ton of internalized ableism and believes himself as different from other disabled people. He has a long history of doing things like this, look up his tort reform work. As a wheelchair user I really hate that one of the most prominent wheelchair users in politics is this fuck.

Yea unfortunately that’s the disability tax, most things designed for disability are expensive. That’s a cool design, I hadn’t seen it before. Maybe in another decade the tech will be replicated in mobility aids.

Another reason besides price for why the 2 wheel balancing chairs aren’t used more is just functionality. Many people who use power chairs aren’t able to balance well, my own is pretty poor, so there’s an even more limited market and unfortunately we live in capitalism.

There are some! Unfortunately they haven’t really caught on well, not easily available unless purchasing outright and they’re usually 10s of thousands (most power chairs are) and not covered by insurance. I really want to try one, this is one I’m really interested in that can climb stairs.

Seat elevator on power wheelchair. I got a chair with a seat elevator in my late teens and it was a total game changer for me. I was suddenly able to access so much more of the world and operate more independently, and eventually live alone on my own. I was barely able to get it and had to fight insurance as it was very costly at the time. Now in the USA, they just became standard through CMS (Medicare/Medicaid) which typically becomes standard industry wide, meaning seat elevators in power wheelchairs are now available to everyone with insurance. That’s pretty amazing to me that this type of technology will be the default now.