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Archive for the ‘generalization of growth attenuation’ Category

I know Peter Singer’s assertion that children with profound mental disabilities are not entitled to “moral status”. I remember Dr. Diekema argued defending the Ashley case that Ashley is not entitled to the same dignity as others are because she is just like a baby. Now I’m shocked to read a paper written by a [...]

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 A law firm newsletter in Australia has done a detailed legal analysis on growth attenuation for disabled children because “there is anecdotal evidence that such requests by parents may be increasing.”
http://hwlebsworth.ensoconsultancy.com.au/health_sept09/growth-attenuation-therapy.html
They advise doctors to consider its ethical appropriateness cautiously and warn them not to agree to provide the therapy without the proper legal procedures to [...]

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 The University of Washington Disability Studies Program will present a public symposium, Eugenics and Disability: History and Legacy in Washington, on October 9th.
http://eugenics.washington.edu/index.htm
Browzing the sumposium site, I just find some things I’d like to point out here,  though I’m sure (and I also hope) they are totally unrelated to the discussion at the symposium.
First, the [...]

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According to this article of April 24, 2009 on the Medical News Today, the Seattle Children’s Hospital and the Gates foundation are hand in hand as “global health leaders” in an effort to eliminate prematurity and still births. The article is about a big international conference in Seattle, sponsored by the Global Alliance to Prevent [...]

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In their paper published in the June issue of the Pediatrics, the authors define profound cognitive disability “as including nonambulation and requiring assistance with nearly every aspect of daily living, remaining completely dependent on others for even basic care after careful attempts at training, and the inability to understand or express oneself in nuanced ways”. [...]

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I read the full text of the growth-attenuation paper written by Dr. Diekema and Dr. Fost with others in the June issue of the Pediatrics. So many questions and mysteries again. I will just point out some of them here for now. Some of the questions and mysteries will be reviewed more closely in my [...]

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The new January 2009 version of the Seattle Children’s Ashley story told by Dr. Wilfond at the beginning of the growth attenuation symposium goes like this; The public engagement. That’s what has been in our mind from the very beginning. That’s why the two doctors wrote the medical article. Ashley’s parents were kind enough to [...]

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I have been following the Ashley case for more than 2 years. I have been reading about other cases as well. Looking back on the Ashley case after so many cases of Emilio Gonzales, Ruben Navarro, Sam Golubchuk, Amber Hartland, Karen Weber, Lauren Richardson, Janet Rivera, David Coronado Jr., O.T. , Kaylee Wallace, Annie Farlow and [...]

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What follows is an excerpt from the WPAS investigative report on the Ashley case:
 
In order to ensure that a court order is obtained before a sterilization or growth-limiting medical intervention is preformed on an individual with a developmental disability, Children’s Hospital has entered into an agreement with WPAS to take the following steps:
 
A.     Implementation of [...]

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In the December 31, 2007 update of his blog, Ashley’s father revealed what he was considering to do to promote “the Ashley Treatment” for the quality of life of other Pillow Angels in the world.
 
・     He asks “pioneering parents” who want to do the same as they did to contact them through e-mail for information exchange. They are willing [...]

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