Twelve years ago, when I was 12 years old, my best friend Cara and I created a column in which we pretended to be “superheroes,” Spaz
Girl and Stumblina. We would crack ourselves up writing stories about our
adventures and make jokes about how we would definitely trip over our capes and
fail miserably at saving cats from trees. I remember laughing together that
with our motor skills, a cat would probably save us. Flash forward and we are
24 and 25, working together to save something for real. It may not be a cat,
but it sure is important. We are working together to save Medicaid, the
government healthcare program at risk for serious cuts under recent government proposals.
Cara now works for the National Council on Independent Living in Washington D.C
(NCIL) and I couldn’t be prouder. She and
her colleagues have participated in multiple actions with national ADAPT,
storming the Capitol to tell our legislators why Medicaid matters. I’m in New
York for the summer, doing the best I can to share accurate information about
Medicaid and how it serves as a lifeline for people with disabilities. I am
also in graduate school at the University of Illinois, studying to be a social
worker. Working together with my friends is always a blast. But for once, we’re
not trying to photoshop crutches onto a poptart for a disability awareness
breakfast. We’ve dusted off our capes to save Medicaid and we need your help!
Why, you may be wondering, have we sprung into action? What’s
up with Medicaid and how does it affect us? Medicaid, created in 1965, is a
government program providing health coverage for low-income seniors, children,
pregnant women, and people with disabilities. With the Medicaid expansion, some
non-disabled adults who are low income are also covered. Medicaid helps so many
Americans in so many ways. Medicaid covers 49% of all births, 33% of all
children, and 64% of all nursing home care (Champaign County Healthcare
Consumers, 2017). Medicaid helps fund the special
education system, providing nearly 4 billion dollars in reimbursements. Medicaid
supports Americans in ways that so many don’t even realize.
I could go on about the many populations Medicaid serves,
but as a disabled woman who needs Medicaid to survive, I am going to focus on
how Medicaid is essential for people with disabilities in your community. I was
born with cerebral palsy and my brain was injured before birth. My disability
affects my coordination, balance, and motor skills. I use a wheelchair to get
around and I need help with activities of daily living from bathing to getting
out of bed. Medicaid covers personal care assistance so I can hire caregivers
to help me with those tasks, an expense not covered by private insurance. I am
fortunate to have a family that will help with my care, but Medicaid-funded
caregivers give me independence from my family and will help me remain in the
community when my parents cannot care for me. Without Medicaid, I would be in a
nursing home instead of out in the world with my friends and family. I will
work as a social worker when I graduate. But the fact is, no salary or private
insurance plan for my parents or for me could possibly cover all of my medical
expenses. Ironically, unless one is extremely wealthy and can pay out of
pocket, Medicaid pays for nursing homes too. So, any threat to Medicaid
basically tells sick and disabled folks they shouldn’t exist.
A low-ball estimate for personal care services is $32,000.
My wheelchair costs $30,000. The Botox treatments I receive to prevent further costlier surgeries are roughly $25,000. Private insurance either covers
these costs partially or not at all. Wheelchair: depends on their mood. Botox:
partially. Personal assistance: Nope. Paying out of pocket would bankrupt most
working folks, and definitely me. Medicaid comes in where private insurance and
work earnings can’t. The ignorant people who think it’s as simple as “get a job”
ought to know that without Medicaid, I couldn’t afford the help I need to go to
the job. Medicaid is a lifeline, plain and simple.
In the days since I appeared in a video by Mic News speaking
out against proposed
healthcare “reforms” that threaten Medicaid, I have encountered heinous
ableist comments. I have been sharing them widely in case anyone ever tries to
claim ableism isn’t real. In the course of arguing with me, my very right to
exist has been challenged. People have tried to pit me against other Medicaid
recipients who “don’t work” or aren’t disabled and thus, don’t “deserve” the
coverage that I do. The fact is, some Medicaid-eligible people can work and
others cannot. Many recipients, disabled and able-bodied, work hard every day
and still can’t afford other health insurance. Think of those who work in
service industries to help us, but only make $12 an hour. Those who “don’t work” may be
unable to due to their own illness or because they are caring for a sick or
disabled family member. My own mother, the most selfless, hard-working woman on
the face of the Earth, gave up her own work life to care for me and make sure I
was properly supported in mainstream school. There is no room for horizontal
oppression in this fight. Human beings should not have to prove their worth to stay
alive. Yes. Stay alive, because without healthcare, people die.
The proposed healthcare bill includes deep cuts to the
Medicaid program. Under the new bill, Medicaid would switch to a block
grant model, reducing the federal commitment to the program. States would
be responsible to cover the costs not funded by the federal government, and if
they come up short, they will have to choose between fewer services covered by
Medicaid or fewer people covered by Medicaid
(caps). If this is the case, people with so many different needs will suffer.
Some will argue that Medicaid has been around since 1965… you’re disabled, so
why are you freaking? You’ll be covered! Think again. Slashed funding affects
all recipients. Caps affect all recipients. The bill proposes fundamental
changes to Medicaid. Furthermore, even if I were personally unaffected, this is
not just about me. It is about millions of Americans with genuine needs. In the
coming days, the character and compassion of our society will be tested.
An individual I will politely call a troll commented on my
video yesterday with the following. Ironically, she seems to be acknowledging
the role of Medicaid while implying that my life as a disabled person is worth
less than hers. The comment reads:
“This is no way to live. I would want them to just give me a
lethal injection if I was wheelchair bound. This Medicaid bullshit sucks. Can't
we just leave well enough alone. If my child didn't have Medicaid coverage we
both would not have a home or any money.”
This is ableism, people. It’s alive and
well. The comment was followed up by this remark, directed at a person who
tried to defend the value of my
existence.
"In
what way is she useful? Not being ugly just genuinely curious. She said so
herself she has to have physical help multiple times a day just to do basic
stuff."
Kind
person: What a nasty comment. There are more ways to be useful than being able
to toilet yourself.
Troll:
"Give me an example? Unless you're Stephen Hawking, I'm just not seeing
it. I think you guys are triggered happy and looking for something to get
butthurt about. Does it make you feel good?”
The reality of being disabled is that on a daily basis,
we still have to prove our right to be alive.
Apparently, based on this woman’s rant, we earn our existence by proving our “usefulness.”
I had no idea that transferring yourself, feeding yourself, and showering
without help made a worthy life. Stephen Hawking has accomplished incredible
things in a disabled body. But his scientific accomplishments are not the
reason he deserves life. All disabled folks have the right to “be,” whether we’re
researching black holes or going to the beach with our friends. We don’t have
to justify the space we take up and the things we need to survive. But, when
programs like Medicaid are at stake, and speaking out to save our own lives
generates hate speech toward us, it sure feels that way.
When I was 12-years-old, my best friend and I pretended
to be superheroes. I never imagined we’d actually need to be. But the time has
come. When there’s something worth saving, we don our capes and kick ass.
(PS: If you do, in fact, have a cat stuck in a tree, named "Medicaid" or anything else, Spaz Girl and Stumblina have not given up on past superhero goals. We'll do our best.)
Below is the video from Mic News, made by my new friend Sarah Singer.
References
Champaign County Healthcare Consumers (2017). The Better Healthcare Reconciliation Act. Retrieved on June 30, 2017 from http://healthcareconsumers.org/files/2017-06-26_BCRA_Presentation.pdf
Call your Senators NOW and tell them that the Better Healthcare Reconciliation Act is a threat to Medicaid and to millions of lives. This is not a partisan issue. It is a human rights issue, and as a person who needs Medicaid to live, I ask for your help from the bottom of my heart. Call your Senator.
Content warning for images below: ableism, eugenics, bullying
Image: Facebook comment says- This is no way to live. I would want them to just give me a lethal injection if I was wheelchair bound. This Medicaid bullshit sucks. Can't we just leave well enough alone. If my child didn't have Medicaid coverage we both would not have a home or any money.
Image: Troll says in reply to an attempt to state that the better dead than disabled thought is crap....
"In what way is she useful? Not being ugly just genuinely curious. She said so herself she has to have physical help multiple times a day just to do basic stuff."
Kind person: What s nasty comment. There are more ways to be useful than being able to toilet yourself.
Troll: "Give me an example? Unless you're Stephen Hawking, I'm just not seeing it. I think you guys are triggered happy and looking for something to get butthurt about. Does it make you feel good?
Me being a "superhero!"
Image: My chair affixed with a blue chuck sheet cape that says "Palsy Power!"
Cara being a superhero. A blue chuck sheet cape reads: Spaztastic Justice League, Spaz Girl
Image: A troll says... "This girl in a wheelchair should just stay in bed at home and shouldn't expect to enter society asking for handouts like 'medical care' and 'dignity.' When are people with incurable disabilities of no fault of their own going to pick themselves up by their bootstraps and pay the thousands and thousands of dollars of necessary medical expenses on their own? And they call us deplorable."
To make a point for this vapid human skidmark, I tried to pull myself up by my bootstraps. I only have brace straps. Despite my best efforts, I'm still in bed. #savemedicaid
Image: Me lying in bed trying fruitlessly to "pull myself up by my boot (brace) straps." I'm lying on my back reaching down toward my leg braces and not doing very well.
Don't let the trolls get to you. Their problems are always worse than your own.
ReplyDeleteLove your blog and the way you write. A friend once recommended "Me Before You" to me to read because she "absolutely loved it". I explained to her why there was no way in hell I was going to read it. It led to a larger discussion about the right to die and why a story about a recently disabled man choosing to die rather than live in his disabled body is not powerful. I've bookmarked your blog. I've recently begun blogging again (disabilityrants.blogspot.com) after a 10 year hiatus, if you'd like to check it out.
ReplyDelete