People with dwarfism in the United States, like most other
people with dwarfism, face challenges directly related to dwarfism, and related
to how the world in which we live relates to dwarfism. These challenges may range from medical impairments
such as bowed legs and spinal stenosis, to difficulty accessing doctors with
expertise in dwarfism to acquiring physical accommodations in order to access
transportation and employment opportunities.
All of these things are legitimate barriers. Barriers that pose a serious threat to our
independence and well being f we are not able to accommodate them. Though they are all serious, a recent
newsletter from a group of little people in Uganda put some of those barriers in
perspective. The newsletter was produced
by Little People of Uganda, a group that was formed two years ago to provide
support for people with dwarfism in the country. One story in particular from the newsletter
stood out in my mind. It was a story
that we will hopefully never read within the pages of the LPA Today, the
quarterly magazine of Little People of America.
The story was from a young man with dwarfism whose baby girl had been
murdered by the mother of his girlfriend.
According to the writer, the baby had been murdered simply because her
father was a dwarf. It was not known
whether or not the baby girl was a dwarf.
It was devastating to read the story, and to come to grips with the fact
that the little girl was murdered because of her connection to dwarfism. While in the United States there is bias
against people with dwarfism, we have protections that will protect us from
what happened to the baby girl and her father.
In addition to the tragedy of the baby girl’s murder, it was difficult to read the story because it didn’t seem that the young man could do anything to hold the murderer accountable for what she did. There probably is more to the story than what I read, but it seemed as if no criminal charges would be brought against the woman who killed the baby girl. All the young man could do was seek support from other people with dwarfism in Uganda. In the Uganda newsletter, the young man wrote, "I felt relieved the first time I shared this story with the members of the Little People Uganda."
I am thankful there is a Little People of Uganda who could
give him support. And I am thankful
there is a Little People of America to give people with dwarfism in the United
States support. But in the future, I
hope more can be done. No matter the
bias toward dwarfism in the United States and around the world, what happened
to the baby girl in Uganda should not have happened to anyone. We do have resources to fight against such a
tragedy. While I don’t know the details
of the convention, the United Nations Convention on the Rights of People with
Disabilities is one tool was can use to stop this from happening again. Among other things, the Convention is intended to "guarantee that persons with disabilities enjoy their
inherent right to life on an equal basis with others (Article 10),
ensure the equal rights and advancement of women and girls with
disabilities (Article 6) and protect children with disabilities (Article
7)." Uganda has not signed the convention.
As LPA increases communications with
international groups, I am hoping we can utilize these types of resources to
bring international awareness to dwarfism and to strengthen our rights around the
world.
I would simply say to you all “awesome information”.
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