Dear Rachelle,
I recently read your article on the Huffington Post titled “Rachelle
Friedman, 'Paralyzed Bride,' Speaks Out: More Than Equality, We Want a Cure”. I applaud you for speaking out on what is undoubtedly
a difficult topic. However, your article
raised some trepidation for me that I would like to take this time to address.
As a disabled person myself who does not desire a cure, I am concerned that you profess to speak for "99 percent of us" (not sure if you meant strictly paralyzed people or people with disabilities in general; the latter would concern me even more). It is your choice to want a cure. However, please don't speak for the rest of us - you admit yourself that there are people out there who don't want a cure.
Additionally, I am concerned that you may be "throwing
the baby out with the bathwater", so to speak. Things like muscle spasms and skin breakdown
are only part of paralysis, though I don't mean to downplay the impact they
have on your life and the lives of many others (muscle spasms and chronic pain,
as someone with cerebral palsy, are something that I have to deal with as well). Those are parts of disability that have a
negative impact on our quality of life, and I would not hesitate to accept
treatment to mitigate or completely alleviate these symptoms. But desiring treatment for those parts of
disability that are painful or even dangerous is not the same thing as desiring
a cure. Just like wheelchairs and other
mobility aids, medication and other treatments are simply tools to help us get
along in the world – not cures that will eliminate disability entirely.
Lastly, the title of your piece makes me profoundly
uneasy. “More Than Equality, We Want A
Cure” implies that finding cures is more important than ensuring that people
with disabilities like you and me have equal opportunities and civil rights. And once again, it implies that all people
with disabilities (or at least all people with paralysis) agree with your point
of view – something that you, yourself, admit is misleading. As someone who has been a wheelchair user for
several years, I am sure that you have experienced the daily inequalities and
microaggressions that come with being disabled in public. From inaccessible buildings to preconceived
notions about our abilities, we face a myriad of obstacles just to get through
our days. None of these obstacles are
our fault. The social model of
disability says that our individual impairments (such as paralysis or cerebral
palsy) limit us, but it is societal attitudes and barriers that disable us and
prevent us from functioning. A truly
equal and accepting society would remove these barriers, so issues like health
care, funding for medical equipment and accessibility, issues that you cited in
your article, are all wrapped up in the fight for acceptance and equality. This is the reality of ableism, and a cure
won’t change that. Desire for a cure should not eclipse our desire to fight the very real injustices we face every day, and the two are not mutually exclusive.
Though cure research is important for those who desire a
cure, it is still simply research, research that will not affect us personally
until it transforms into something that will be available commercially, or at
the very least in clinical trials. What’s
important is concrete issues that affect us in the here and now – employment,
transportation, the marriage penalty for those on SSI or SSDI, the disturbing
trend of parents and caregivers murdering their disabled children...these are
all issues that we should prioritize over a cure. I will keep fighting for equality, acceptance,
and simple basic human decency until the day a cure for me is found, and
beyond. Because disability is so much
more than just a medical condition – it is a rich, nuanced culture intertwined
with complex sociological concepts that come together to create the reality of
disability today.
I hope you join the disability rights movement and fight
alongside us. Because at the end of the
day, cures mean nothing when there is still not justice for all.
2 comments :
"Desire for a cure should not eclipse our desire to fight the very real injustices we face every day, and the two are not mutually exclusive."
This line is fabulous and SO true.
Also, I loved your last full paragraph, about how research results are not yet tangible but equality can and should be there every day.
We are indeed a rich and complex culture, and equality needs to be a priority for all of us.
So I don't know what percentage of people with SCIs want cures, but I can cite a 1994 study that 86% of people surveyed rated their quality of life as average or better than average. That, and other factoids about people with SCI's self-descriptions here:
http://www.independentliving.org/docs3/gill99.html
--Nightengale
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