Reflection on the
Deaf-World
Oliver’s
article on the definition of disability was interesting. He wrote that one of the reasons why
definitions are important is because of the need to identify and classify
people. He said if a disability is see
as a tragedy, then disabled people were be treated as if they are the victims
of some tragic happening or circumstance (pg. 167). The other very interesting thing that I found
in this reading is Oliver said that poverty is a major cause of disability
(170).
Understanding
the politics of the definition of disability was important for me moving
forward in reading Liza Mundy’ article “A World of Their Own”. In this article she writes about two women (Sharon
and Candy) who are deaf. They also have
a deaf daughter. They sought out a sperm
donor that was deaf, so they would have a better chance of having another deaf
child. I found it interesting that
regular sperm banks did not allow deaf people to donate their sperm. The women had to ask a deaf friend to be the
donor.
Throughout
the pregnancy the women worried whether their child would be born deaf or
not. They were hoping for a deaf
child. Although they said they would
love the child either way, they really wanted it to be deaf. Three months after the child was born it was
given a hearing test. The test showed
the child was deaf in one ear, and severely deaf in the other. The child could have been provided with an
aided device that may have helped him hear something. Sandy and Candy decided not to have the
hearing aid. In a world where most
parents would have done anything to help their child hear, these parents
decided to wait until the child could make the decision. It seemed like in the article that by
waiting, the child would have lost his chance of hearing.
This raises
two questions. What are people’s thoughts on Sharon and Candy seeking out a
deaf donor to increase their odds of having a deaf child? What are people thoughts on Sharon and Candy
not providing the hearing aid to their child?
At first I
could not understand why they would have chosen either road. Then I read the article by Lane on Ethnicity,
Ethics, and the Deaf- World. I also read
the person essay. This shed a new light
on my feelings. The personal essay by
Heather Shaw was very moving. The most
powerful statement and reflection on myself I got from that essay was her words
“I am not disabled, until someone sees me as disabled”. This goes along with what Oliver state in his article about definitions, if it is seen as a tragedy, it will be treated as one. These articles, along with Lane’s article changed my
thinking about Sharon and Candy. Sharon
and Candy are part of a Deaf-World, to them this is their ethnicity, their identify.
The Deaf-World sees itself as an ethnic
minority group. They do not see
themselves as disabled, others see them as disabled. So in a world where woman are having test to
determine the sex of babies, spinal bifida, cystic fibrosis, Downs Syndrome,
and another of diseases, then making the decision to terminate their pregnancy,
then I cannot be angry with Sharon and Candy for choosing the child that they
wanted.
I felt bad
at first, then I thought who is to say that being able to hear is not a
disability. Who I am to tell a deaf
person that they have a disability? These articles have given me a new perspective on the Deaf-World.
Reading 18: Oliver, Michael – Disability
Definitions: The Politics of Meaning
Reading 19: Mundy, Liza – A World of Their
Own
Reading 20: Lane, Harlan – Ethnicity,
Ethics, and the Deaf – World
Personal Essay – Invisibly Disabled
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