Showing posts with label ableism. Show all posts
Showing posts with label ableism. Show all posts

Monday, May 25, 2020

It's Not Too Much To Ask You to Wear a F*^king Mask and Stay Home



I'm just going to repeat that:

It's not too much to ask you to wear a fucking mask and stay home.

The pandemic isn't "over," and life is not "going back to normal." What is "normal" is the craven irresponsibility of the privileged and even the not-so privileged. This is the high school that I graduated from back in the Stone Age. It was basically a one-room school-house then (hyperbole intentional since privilege was rarely recognized in the Stone Age) but is pretty much unrecognizable now. You can read the story here. 

My take on this shit-show?

(Anonymous commenter -- you'll have to forgive me my anger as I know it offends you, makes you "exhausted") This pandemic is demonstrating with crystal clarity that the lives at risk are expendable. That if you are a person of color, a disabled person, an old person, a person who takes care of another, an "essential worker," you are EXPENDABLE.

WE are expendable.

The rest of you are "free" to do -- in what seems to be the most grotesque interpretation of freedom I've ever understood -- whatever the hell you want.

All is transactional.

So, go on with your best self, as they say.

Have a party.
Travel!
Get your hair cut.
Go bowling.
Go to the beach.
Go to church.
God will take care of you. 
You've got to start somewhere.
Don't muzzle yourself. You're free.
Social distancing is a hoax.
Bill Gates is out to track all of us.
Get back to normal.
Make America great.


I'll say it again. America is terrible and exhausting.

Sometimes, it's not. Read this:
It Just Burns Me Up

Friday, August 9, 2019

Help



The title is not a cry for it.

Help!

On help

I learned recently that Sophie was eligible to receive a home health aide, but I felt dubious about the whole thing for reasons I won't spell out since you've heard them ad nauseum for as long as I've been tapping away here. When she received a very generous number of hours, thanks to the great State of California and the Regional Center, I told my father and he said, I find that hard to believe, and I said, I know. I told my therapist about it, and she said, Wonderful! and I said, What will I do with myself in the mornings? and she said, Rest! and I said, What do you mean? and she said, Lie on your bed and read or go into your room and write and I mused on that for a while, lying there on the couch in her office where I've spilled the darkest of my guts and wept and been guided and helped for years. Asking and receiving help is acknowledged by most caregivers I know as two of the most difficult things to do, and while a lot of that has to do with the actual busy brain and body work it takes in terms of time and arrangement (CEO of Sophie, Inc. reports), a lot, I think, has to do with this deep, psychic attachment we have to our unique children and young adults.  It's less about burden, more about acceptance  and everything about love. Throw in guilt and responsibility and the ridiculous and very much American ideals of individualism and pull yourself up by your bootstraps culture, coupled by an ableist society that looks on disability as something so hideous and burdensome that we hear things like would you have had an abortion if you knew? or I'd rather be dead than dependent on someone or I could never do what you do -- well, it's damn hard to ask for help and even harder to receive it.

I am receiving it, Reader.

Sophie's morning aide is a delightful young woman who comes to the house weekday mornings and gets Sophie up and dressed and groomed (see above). She makes her breakfast and feeds her, brushes her teeth, packs up her stuff that she needs for her adult day program and then drives her there in our accessible vehicle. She talks to Sophie and is incredibly gentle and meticulous about her hygiene, the style of clothes she will wear that day and can fix Sophie's outrageous hair into all manner of amazing styles. She gives her choices and treats her with dignity and respect and humor. It's unbelievable, actually. The only thing that she's not allowed to do is administer medication, so I do that. It took me some time to train her and even more time to will myself into letting go, but guess what?

Reader, I am resting.
























The universe is abundant.








Here's that Extreme Parent Video Project that I made years and years ago with the help of other caregivers, many of whom I had only met online. You'll see that asking for and receiving help was a common theme. Enjoy, share, ask for and receive with gratitude and grace.


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