Stones

Mom has been drinking and sobbing beside you for hours now. When Dad left for 9 months, he took you aside and gave you two chores: keep the lawn mowed and don’t let your mother kill herself. You are almost certain this is the night she is going to die. For fourteen years this woman has been a mystery to you, a fact which proved no obstacle to her cementing herself in your heart. You have known your whole life that she was unhappy. You have known for five years that she drank more than was a good idea. But the weeks since your father gave you your orders have proved an education in exactly how great the obstacles are that she has to try to surmount.

 

Your mother’s mind is different from yours. It functions, as far as you can tell, much like almost everyone else’s. Yours — the one that makes sense — is a model that is unique in your lived experience. You have been dragging Mary MacCracken, Eleanor Craig, and, by the time you were eleven, Bruno Bettelheim home from the library just to make reflections, to create a sense that you are not alone in the world. All but one of your friends are imaginary. You have fantasized about the potential for community in segregated special ed, but your parents are adamant: you should just buck up and be normal.

 

So far you haven’t pulled it off. You have long ago realised you never will.

 

Mom cries.

 

You had not realised other people felt pain as deeply as you. They clearly do not feel the searing agony of light touch, the excruciating scrape of clothing, the burn of sunshine. And they seem incapable of understanding psychological pain. When you finally worked up the nerve to tell your mother of your own most recent suicide attempt, drunk on beer she had forced you to drink as a social lubricant, hoping against your knowledge that she would help, she said, “Ssshhhh, I’m watching M*A*S*H.” It was a commercial break halfway through a rerun. But here it is.

 

You have read in books about children who are loved and cherished. You have seen the way Mom is with your sister, the way Dad looks at your brother. You have fantasized about a life like that.

 

But you also know that people like you end up in institutions as adults. You cannot find a single representation of an adult who reminds you of yourself who lives free. And you have looked. There was one who got day passes…. You have been steeling yourself for the inevitable for half your life.

 

You think back to the first day at Red Hill Primary, your bladder straining, as you tried to determine what the other children were doing to attract Mrs. Sainsbury’s attention. She called on them and they asked to use the toilet. Why did she never call on you? What were they doing? As your socks became soggy, you had a sudden insight: this was it. This was why your parents looked at you like that. They wanted a child who just knew … the way everyone else’s child did.

 

Mom launches into another story. You concentrate, willing yourself to understand her, casting for details to help you help her.

 

You already knew your parents had met in the Dominican Republic, married in New York, conceived you on their wedding night and moved to Mexico City. You have already heard from Mom that she smoked and drank throughout the pregnancy to try to cope, that after your birth you were too demanding for her to get to the store for cigs, but that she had needed to drink more and more to cope with being the mother of a child who screamed when held, who refused to accept girlhood from the start, who was hospitalized until her milk dried up, who could not cope with a three-child playgroup, who broke bones and seemed not to be in pain but cried over nothing, who interpreted words oddly, who began running away as a pre-schooler, who seemed unafraid of abandonment at the library but refused to be left at the church creche.

 

Now you hear about the pregnancy. “There was another family with the name in the community,” Mom slurs. “They notified the wrong woman. I would have had an abortion … but everyone knew already.”

 

You pat her arm awkwardly, wondering whether this is true or just a backward projection of the intolerable pain of having a perfect blue-eyed, blonde-haired daughter, a handsome, charming brown-eyed, blond-haired son, and you. You do the inventory again: how young she was, how often she moved, losing her support system again and again, how early your father left for the office and how late he stayed, how you must be as alien to her as she is to you.

 

And yet you do not think that you are all that bad. You like the way you think, the way you solve problems, the way you carve up the world. At fourteen you have become involved in political organising, found a role you can play in a group. Unlike every other kid you know, you get no allowance; rather, you work for your pocket money — and at low wages, recognising that the families you work for are strapped. If you could grow up free, you think, you could be someone — even in this world of alien and hostile minds.

 

“It was the worst mistake of my life.”

 

She sobs.

 

You hold your body as tight as you can, trying not to let her see your reaction. You are not entirely sure she could, even if you began to scream, but you don’t want to take the chance.

 

The thing is, she’s right. Your relationship is not good, and even in 1981, in your parents’ community, you are tied to her like a weight.

 

You cannot be the kind of person she wants, and you know she cannot imagine a good life for herself if you are anyone else.

 

Can you fix it? If you tried again, and this time finished the job? You are not good at suicide. You first tried ten years earlier, after the second move, the second obliteration of your entire world. Your family is not a haven for you, and so every move — by now there have been nine — requires you to construct a universe from scratch. What if you ran again, and this time you never came back? Would that give her a good life?

 

But, no: it wouldn’t. She cares too much what the neighbors think. The people at her job, at her church, on her block, at the endless round of cocktail and dinner parties your father’s job require her to go to. For the rest of her life she would be That Woman Whose Kid Ran Away, even if no-one else so much as thought it, and it would be intolerable for her.

 

There is no way out for either of you. You cannot get away from your future; she cannot get away from your past.

 

She is still sobbing.

 

And in that moment, you see it: she should have killed her kid. At birth, in the first month, when you were still small enough for a pillow to do no bruising, and the neighbors would have thought it was a tragedy. You would have missed out — on so, so much — but it would have been the best thing for her. She should have killed her kid.

 

You are almost a decade from learning that, in her own inept way, she tried.

 

***

 

The next year, “St. Elsewhere” runs an episode that hits much too close to home. A family learns they are about to have a longed-for boy. He is going to have Down Syndrome. The doctor talks about the prenatal test as if it’s certain, which you know it isn’t, and then begins to make horrible predictions. The future of a child abandoned at birth and growing up in an institution like Willowbrook, Pennhurst or Beatrice is described as though it were the future of a child raised in a loving home, given a free and appropriate public education. The mother wants to raise the boy; the father suggests they get a pet instead. They choose abortion.

 

The show is defended on the grounds that, while it is inaccurate, it is at least compelling television. You know better. It’s pity porn playing to prejudice and contempt … which all those people with the wrong kind of brains spin as compassion.

 

Meanwhile, the self-advocacy movement, with its roots in Sweden in the sixties, is building. People once crowded in filth, decay, neglect, abuse and exploitation are planning conferences, talking to the media, and convincing elected officials to support smaller more integrated institutional settings like group homes.

 

Jason Kingsley and Mitchell Levitz are boys with Down Syndrome growing up in the free world. As young men, they will write “Count Us In,” a book that changes everything for so many. Their lives look nothing like the one described on “St. Elsewhere.”

 

By 2017, you will sit and watch Charlotte Fien, a poised young woman with Down Syndrome, address the United Nations. And yet the moment will be bittersweet: her topic will be the use of new technology to eradicate people with Down Syndrome through targeted abortion. “I have an extra chromosome,” she will say and so what?

 

People very similar to yourself are coming together, too, outside institutions, building community, seeing themselves reflected in one another, reveling in it. You begin to see children whose parents can name what is different about them, support and celebrate them. You begin to hear jokes you understand.

 

People are mastering communication systems, getting jobs, getting advanced degrees, raising families and documenting it all. If you were fourteen today it would be easy to imagine alternatives to the institutions you spent years in. The failure of imagination that led you to discount the value of your life is washed away.

 

But your Mom’s culture of devaluation and death continues.

 

Abortion isn’t an option for kids like you. People don’t know in advance. So they turn to murder.

 

For you the tipping point comes when six-year-old Charles-Antoine Blais is drowned in a bathtub and parents come together to support his murderer, his mother. She is offered a job at a charity supposedly supporting kids like him. When Michelle Dawson calls to ask what that is about, she is told children like Charles-Antoine ruin their parents’ lives.

 

A major disability charity releases a video normalizing disability filicide, and you are furious. Alex Spourdalakis is fourteen when his mother and grandmother murder him. Issy Stapleton is fourteen when her mother tries to murder her. It hits home.

 

In 2014, Julia Bascom, from the Autistic Self-Advocacy Network, reports that when reading a list of names of disabled people murdered by parents, she “could have sworn time stopped; we read down one poster, and then another, and every time I thought we were done, there were more names.” Many of the killers are praised to high heaven all over the place and given token punishments. After all, they have suffered so much already from their children’s existence.

 

***

 

Dahlia, the woman on the bed beside you has been restless and groaning in pain for hours now. She’s asleep or unconscious — you’re not sure which — but she is not at peace. She writhes slowly. Her breathing is uneven. Sometimes it stops for 45 seconds or more. Her catheter bag is empty: no urine has collected in about eight hours. You know this is the night Dahlia is going to die. The hospice nurse had snapped it at you when you called to ask if you could administer more morphine. “What did you expect?” she had asked. “Her kidneys are shutting down. It’s painful. This is how they die.”

 

You are the only one awake in the group home, where women with physical and intellectual disabilities live. Another staff person, this one making a little less than you, just under minimum wage, is sleeping in the back.

 

You are okay with Dahlia dying. She has been dying since you met her. You are not okay with it happening like this. Not suffering. But you don’t know what to do. You don’t want to touch her; you are afraid of inadvertently hurting her more. And your singing voice is no comfort to anyone. So you begin to speak. Whatever comes to mind, just so she knows she’s not alone.

 

You talk about how good it has been to get to know her. You talk about how glad you are that the staff at the home have come together to support her. Group homes are small institutions; they can be as soul-deadening as any other and because of small staffs and high turnover they can go from good to awful seemingly overnight. But you think this staff has done this one thing well.

 

You talk about what you know of Dahlia’s life, of her friends. As an overnight worker you never meet them but you see their names in the log. When was Dahlia placed in the state institution? You aren’t sure. Childhood, definitely: she has the taste for congregate living that comes from growing up in overcrowded cottages. She wouldn’t want to have her own apartment.

 

You tell Dahlia that it is okay to let go. A part of you hopes she does. All you can imagine in her future is pain. A part of you holds out for it not happening this way. But you cannot imagine a future for her other than suffering and death. Your mother’s voice scratches at your mind. Wouldn’t the kindest thing to do be to kill her?

 

Anne calls from down the hall. You tell Dahlia you will be back.

 

Generally you try to take your time with Anne. She is the sort of person you would enjoy being friends with, if you knew her on the outside. And she has been particularly badly served here: she grew up in a family and doesn’t have the automatic deference that even the good staff seem to expect — quite the opposite. When she got to her first, crisis placement group home, she could walk with a walker part-time, but the staff found her annoying and they took the walker as a surreptitious form of restraint. She atrophied. Now she can barely stand to transfer.

 

So usually the two of you go slowly and gently. But tonight you tell her Dahlia is having a hard time and together you hustle her into her wheelchair, onto the toilet and back to bed. Her eyes are teary. You know she is terrified of Dahlia’s coming death. You promise to do everything you can.

 

Back in Dahlia’s room, though, you don’t know what that might be. She seems worse, rolling back and forth on the bed, making sounds. And finally, in desperation, just to be doing something, you begin to take apart the catheter setup as if to empty the already-dry bag.

 

Then you see it.

 

Whoever did this chore last left a cap on a tube. That tube slides into the end of another one; the cap is invisible until the tubes are separated. But Dahlia has been making urine all evening and night, and has been unable to drain it from her bladder. That’s the pain.

 

You pull the cap and jam the tubes back together before too much liquid spills out, and you watch the collection bag begin to fill. You empty it; it fills again.

 

Slowly, as dawn comes, Dahlia drifts into peaceful sleep.

 

At a staff meeting, people question whether you should have left the cap on.  It wouldn’t have taken much longer.

 

When the end comes, weeks afterward, it is on someone else’s shift, a few minutes after Dahlia is told she is being sent back to the hospital, a place she does not want to go.  You understand that you made the right choice.

 

***

 

Years later, you read a column in the newspaper about a man who, faced with his beloved son’s short life, a life without the things the man seems to feel give his own life meaning, holds him while he dies, then struggles with the growing conviction that he should have killed his kid.

 

It does not persuade you.

 

There is more to life than breathing easily.  There is also being held by a father who loves you enough to be there with you in your pain, even as his own is unbearable.

 

Too often, you have learned that your beliefs about what makes a life worth living are not trustworthy. Sometimes they are right, and you never get what you need. Sometimes they are wrong, and you learn new ways to live.

 

 

You realise for the first time that your Mom, all those years ago, was wrong. Even if you leave aside your own experience, your own hunger for a life, and even if you accept that you represent the greatest mistake of her life, you realise, you realise that her mistake consisted not in failing to embrace your death, but in failing to free you from her insistence that life has to follow a specific path to be worth living and set you free to explore the possibility of your life.

 

She couldn’t have given you everything you needed or much of what you wanted. She didn’t have it to give. But the insistence that if your life didn’t fit a certain pattern it was not worth enduring … she could have chosen not to give you that.

 

Just because you cannot imagine how a particular life can be good doesn’t mean there isn’t a way.

 

It might still have been bad. Life often is. And you would certainly have suffered from the strain of being isolated among people whose minds are alien to you. But it wouldn’t have been worse to have a parent who was open to possibility; and as you think back to the recent wedding photos of two people whom Mom would have equally hated being saddled with, the beaming guests, the wedding party at a ball pit, you think to yourself, it might have been amazing.

Mike Pence

I can see gods today.

Not in gilded dining rooms
and marble corridors.

But in the parks,
sweat-drenched and open-faced, arguing;
and in the streets,
harrying daughters past the leers;
and in the schools,
tearful, under a teacher’s body,
mouthing, “Let me go.”

I can see the god of hands:
flapping in joy,
dancing full of language,
poring over six-dot cells of knowledge,
easing joysticks across broken sidewalks,
torn between frustrated teeth,
cracked and callused and sore,
dowsing for love on screens,
flipping tables, throwing chairs,
juddering to a rhythm of the nerves,
loose and still,
knotted,
contracted,
balled into fists,
wrapped around guns
that turn out to be trinkets,
bruised,
bloodied,
wet with tears.

I can see holiness
in the rising,
in the sharing,
in the reaching out to one another
against rejection,
in the demand
for freedom, food and futures,
even as your forces array against it.

I can see your god crucified:
barbs cascading over them,
as they stand clutching beltless pants,
vacant eyelets in their shoes,
greasy and swaying;
mascara on her cheeks,
arms held outstretched by leather cuffs,
she labours to breathe,
to stay awake
as the shot closes in on her brain;
scars upon scars,
darkened gauze over his side,
a shackled wrist,
his sulphured clothes in evidence bags,
a guard outside the door.
Can you not see your god?

I can see your god in anguished triumph,
resurrecting from the bed each evening,
tracks and all,
and going out to try one more time
to make a life
before dying.

But not in gilded dining rooms
or marble corridors;
not in perfumed, manicured bodies
honed in home gyms;
not in silk ties and tailored suits
or moisturized hands
gripping pens,
signing away millions’ freedom
with a swathe of ink.
I cannot see your god
in boasts of power and piety.
I see only you.

Give me instead the bodies bouncing off floors,
the half tooth in the quiet room drain,
the wail of a figure holding a limp child
outside the locked emergency room.
I would rather look away.
Still,
give me not people trumpeting their godliness,
but give me people inhabited by gods.

Because Medicaid is Investment in Freedom

People are asking why disabled people are suddenly protesting. It’s not new. The disability rights movement grew out of other movements of people labelled “unable” so it’s hard to date its beginning, but it was well underway at least by the Congress of Milan nearly 140 years ago, when hearing people decided that to be equal you needed to speak and to understand speech and set about stamping out Deaf language and culture.  Although a great many Deaf people reject the label “disabled” that many other groups accept and even take pride in, their critique of “ability” is echoed by every other strand of the movement.

But I’ll tell you why disabled people are protesting right now.  It’s because Medicaid is an investment in freedom.

Filmmaker and activist Dominick Evans said this morning, “I am terrified of the health care bill…. I don’t want to die. I don’t want to end up in a nursing home.”  And he’s right. That’s exactly what he’s facing if it goes through.

~~~

Ironically, the season when we celebrate freedom is upon us. Two weeks ago we celebrated the notification to the last officially sanctioned slaves in the Union that slavery had been abolished.  In three weeks we will celebrate President Bush’s affirmation that disabled Americans have a rightful place in society. There is red, white and blue everywhere; there are picnics and parades and rainbow flags and everywhere we are saying: freedom! freedom! freedom! And yet our Republican national “leaders” are in the middle of a devastating attack on freedom and opportunity.  If they succeed, Americans will lose their health and their savings and their lives; parents will lose their children and children their futures; young people will lose their educations and their mentors; adults will lose their jobs and their homes and their peace of mind; that cherished dream of life, liberty and the pursuit of happiness will be snatched away from millions. Democratically elected legislators demanded that their constituents be represented, and Mitch McConnell and his gang said no.

Americans demanded a voice, clogged the switchboards and filled the voicemails insisting on being heard, wrote letters, signed petitions, marched, prayed, told their stories, and were sneered at by Kellyanne Conway and her crowd.  The Republicans campaigned on the need for more jobs; now they say there are so many jobs with great pay and awesome benefits that everyone can have one. They campaigned on cutting insurance premiums; now they are telling us their plan is to raise premiums on those who can least afford it and cut benefits for everyone.   And they are going after Medicaid, one of the greatest investments in freedom and opportunity this country has ever known.

~~~

In America today, some babies are born to parents who can afford to pay for their routine medical care so they can grow up healthy — and there is Medicaid to give other babies a chance.  Some children grow up in families that can care for them — and foster kids get Medicaid.  Some kids go to schools where the school boards can afford to meet their education-related needs — and some get help from Medicaid.  Some people have access to bathrooms and bedrooms and kitchens they can use without help — and some use Medicaid so they can hold down jobs, pay taxes, raise families and live good lives.  Some people can afford preventive health care so they don’t land in the emergency department with outrageously expensive emergency needs (that we all end up paying for) — and some use Medicaid.  Some people have good insurance or huge bank accounts when cancer or stroke or a car crash hits their family — and some turn to Medicaid.   People in America work hard. They deserve freedom and opportunity — all of them, not just a lucky few.  Some combine their hard work with luck, and some combine it with Medicaid.

~~~

So when the Republican leadership introduce the AHCA and the BCRA, they are trying to cut investments in freedom and opportunity.   For many Americans, it’s a numbers game. The destruction of a life, a family, imprisonment in an institution, the death of a child, it could happen to anyone.  It’s not very likely if you were born to privilege, but remember that President Roosevelt was born wealthy.  It’s a good deal more likely to happen if you’re an average college-educated working person with a full-time salaried position, more likely yet if you work two or three low-wage jobs.  But for disabled people this is more personal than it is for many others, because so many of us can name friends and loved ones who are likely to lose their jobs, their homes, their kids, their freedom and their lives.

That’s why there were protestors dragged out of Senator Mitch McConnell’s DC office, why an ambulance took a leader away from Senator Todd Young’s Indianapolis office, why a woman at Senator Cory Gardner’s Denver office did not resist as police experimented with her ventilator tubes, why people showed up at Senator Ted Cruz’s Houston office furious that he refused to even listen to them.  Because in this time to celebrate freedom, freedom is under attack, and Americans with and without disabilities are fighting back and calling on elected officials to do the same.  We asked nicely.  Asking didn’t work. We explained.  Explaining didn’t work.  Freedom is important: it’s time to insist.

~~~

This is a struggle for freedom.  Nothing less. Disabled people — like everyone else — have a right to life, liberty and the pursuit of happiness.  We are a movement with many strands, but we are all saying some of the same things:

 

  1. We all have things we can and cannot do — like everyone else — but we are all able to be valuable members of society. First and foremost we are people — like everyone else – and any inabilities we may have do not detract from our humanity – just like everyone else. Many of us reject the idea that they are any more unable than anyone else “Deaf people can do anything hearing people can do, except hear,” I. King Jordan said; Jacobus TenBroek reported, “Every time I think I have hit on some job that a blind man couldn’t conceivably hold, I find a blind man holding it.”   Others accept that there is a range of ability and place themselves toward the end of the spectrum. Personally, I look at 41-time Paralympics gold medallist swimmer Trischa Zorn, 23-time Olympics gold medallist swimmer Michael Phelps, and my neighbour Fred who likes to hang out down by the lake in his swim trunks.  I have a hard time seeing Zorn as the least able of the three just because she is blind.

 

We have the right to life:

 

  1. We have the right to survive. In a society with the knowledge and resources to provide health care to everyone, we have a right to life-preserving and independence-enabling health care. “The lives of disabled people are already devalued,” says Anita Cameron, but they can be good lives and we deserve a chance to live them.  Amy Schnelle, a former factory worker, died because she couldn’t afford the meds that stopped her seizures.  Mother Esmin Green died in a hospital waiting room from blood clots more than 24 hours after she was admitted, waiting  Medicaid provides that access to health care that is required for life to many people; Medicaid is freedom to live.

 

  1. We have the right to define ourselves, to have and express our own ideas and values. This is in the First Amendment to the Constitution. We have a right not to be forced to behave as if we were nondisabled, as Deaf people have been pressured to function as if they were hearing and autistic people have been pressure to behave as if they had typical neurologies. We have a right neither to be herded together in segregation nor to be dispersed into isolation within the larger community. We have a right to self-determination, to choose the course of our own lives, where we will live, how we will spend our time, and in whose company, to the same extent as others. Medicaid allows many disabled and chronically ill and severely ill people the chance to move beyond worrying about merely waking up the next morning and to worry about what kind of people to be; Medicaid is freedom of thought.

 

We have the right to liberty:

 

  1. We have a right to freedom from institutions. We have the right to avoid being outright coerced by courts and laws, as some people with psychiatric labels are, and we have the right to avoid being trapped because services we need are only available to us in institutions. People with intellectual and developmental disabilities have been forced into places like Willowbrook and Pennhurst and into group homes, people with psych labels have been forced into state hospitals, and people with physical disabilities and chronic illnesses have been forced into nursing homes.  “Are you in charge or is the staff in charge?” asked Roland Johnson, a Pennhurst survivor, calling for services that enable people to choose how they want to live — just like everyone else. Retiree and homeowner Chris Meadows is facing institutionalization for exactly this reason. Medicaid waivers help many people at risk of institutionalization stay out, or at least stay in more geographically integrated, smaller, more “home-like” facilities — but the waiting lists are enormous; Medicaid is freedom from unjust imprisonment.

 

  1. We have the right to access society, to things like being in spaces we can enter and having information in accessible formats and having housing and education and employment. These things allow us to be fully functioning members of society. They enable us to go to the supermarket and the movies. President Bush signed legislation that provided an enormous step forward.  But to do use it we often need specialized equipment like wheelchairs and communication devices. Harvard students are trying to get James Lappin, a man in their community, an electric wheelchair he needs, but many people don’t know anyone with the resources to help. Medicaid helps with that; Medicaid is freedom of opportunity.

 

We have the right to the pursuit of happiness:

 

  1. We have the right to supports. Americans believe in rugged individualism, but it’s a myth. To get dressed this morning I depended on other people to grow and harvest cotton, process it into thread, and dye and weave it. I depended on others to design and manufacture garments and to build ships and roads and trucks and an internet so I could get the clothes. I depended on an enormous number of people to help me get dressed, and so did everyone else — but we treat all this as invisible. If a person needs one more bit of help slipping a shirt over their head, that is considered dependence. It is no more dependence than anyone else — but for many people, that one need is enough to result in a loss of freedom; for communities, it can result in the loss of a valued member. Medicaid pays for assistance in dressing and eating; Medicaid is supports for freedom. 

 

  1. Education is one of the most fundamental supports that every American child is owed, and Medicaid pays for many things disabled children need in order to benefit from the public education they are guaranteed, so they can live and work and participate as adults. The prospects for kids with Down Syndrome were lousy 35 years ago: lifelong institutionalization and early death were the norm. Today, simply because kids with Down Syndrome grow up in families, communities and schools, adults with Down Syndrome graduate from high school, get jobs and pay taxes. Some go to college. Charlotte Fien addressed the United Nations about human rights earlier this year. “I have a good life,” she said, describing a pretty typical young adult’s existence.  Without Medicaid, these costs would be the problem of individual school districts, many of which are already struggling to meet the needs of the children in their care today; Medicaid is freedom for today and tomorrow.

 

  1. We have the right to inclusion, to be considered part of society, to have out needs taken into account — just like everyone else. Most disabled Americans can and want to work, but we face discrimination in jobs. Many of us do have jobs, and many others contribute to their families and communities without getting paid, or get sub-minimum paycheques for pennies an hour. “Get a job!” they tell us.  Many of us have jobs, and many more are trying to get them, but we face employers wo mistakenly think of us as unable, just as many hardworking nondisabled people struggle to find work. Moreover, children too young to work, people who want to work and cannot find jobs, those who have worked their whole lives and have had to retire, and those who cannot work at all should not be excluded from the community. Medicaid is a safety net for desperate people, disabled and nondisabled, who cannot get paycheques for some reason. Medicaid is freedom to belong.  

 

These are the disability rights various groups disabled Americans and our families and allies have struggled for, fighting against oppression in the name of “ability.”  We have not come close to winning, but we have made real progress over the years.  (After her arrest, Denver protester Carrie Ann Lucas was transported by police on a lift-equipped bus, something that her group, Atlantis ADAPT, fought for and won decades ago.)  We are determined; and we are not prepared to allow Ryan and McConnell to roll back the clock and hurl us even further from the ideals Americans will celebrate this week.

If America is serious about the rights to life, liberty and the pursuit of happiness being at the very core of our humanity – as we will be hearing over the next few days – then that means disabled people and working people, too. If America isn’t serious — well, it should be.

And one of the fundamental ways that life, liberty and the pursuit of happiness are being provided to disabled and working Americans right now is Medicaid.

It doesn’t have to be that way. We could invest in freedom and opportunity some other way. Or we could make most of the costs of enabling disabled people invisible, as the costs of enabling people who were born to privilege are invisible, by addressing the problems in society that ensure that some of us have the tools to succeed and many others don’t. There are certainly other ways of doing things that we are open to looking at. But we will not abandon our demand for freedom.  And because right now, today, we live in a society that is set up to meet the needs of some people and not others, we need a system to invest in the freedom of those people whose needs are not met. For disabled people and the working poor and anyone who may become disabled, which is every single person, today the system that invests in freedom and opportunity is Medicaid.  That’s why disabled activists are in the news.

~~~

I’m not a Medicaid user now. I don’t need it right now. But if and when the day comes that I do, it should be there. It should be there for those who do need it.  I have been denied needed medical care. I have been brutalized in efforts to force me to act as if I were nondisabled. I have been institutionalized. I have been denied access to basic things. I have gone without needed supports. And I have been denied a meaningful place in society. It should not have happened to me. It should not happen to others. And the Republican leadership should not be preparing for another assault on freedom and opportunity when they return to Washington after the recess – but they are.

Happy Independence Day and thank you to everyone who has spoken up for disability rights and other civil and human rights since the introduction of the House and Senate anti-freedom bills.

YOU CAN MAKE A DIFFERENCE.  HERE’S HOW: 

  1. Sign up for and act on action alerts from Access Living or another group.
  2. Call your Senators to let them know you stand for no cuts, no caps on Medicaid and you expect them to support investing in freedom, too.
  3. If you have Republican Senators, call your Governor to demand that they support investing in freedom.
  4. Educate the people around you who don’t understand why it’s so important to keep Medicaid intact.
  5. Donate to or join ADAPT.