From the [Toronto, Canada] National Post:

Barbara Farlow and her husband Timothy are facing what is expected to be the end of their legal challenge to Toronto’s Hospital for Sick Children over the 2005 death of their daughter Annie, who had Trisomy 13. If a judge rules today that the case cannot be heard in small claims court, as expected, the Farlows have said they will withdraw their challenge for lack of funding.

Barbara Farlow has claimed that the hospital denied Annie proper treatment, issued a “do not resuscitate” order without her parents’ consent, and gave her a lethal dose of painkillers as part of  an unspoken policy to deny life-saving treatment in the case of infants with genetic disorders.

She says she wishes not to blame doctors but to provoke a broader discussion about the discriminatory policies used to treat children with disabilities.

[Barbara Farlow] said the trend in genetic screening for birth defects is “discriminatory,” in that people who choose to terminate genetically abnormal pregnancies are offered care and support, but those who choose not to are “on their own.” Once Annie was born, she alleges, she was falsely told doctors would provide life-saving care for her respiratory distress and other ailments related to Trisomy 13, when in fact, she alleges, they intended to let her die naturally.

Earlier posts here and here.

(Photo from the National Post)

This entry was posted on Monday, June 22nd, 2009 at 10:41 am and is filed under NOT2BEMISSED, discrimination, end of life, genetics, hospitals, human rights, intellectual/developmental disabilities, law, parents, patients. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.  Email This Post