Posted By LAF Editor on May 28, 2015
Campaigns from California to New Zealand to legalise euthanasia in one form or another have focused on attractive young women with terminal cancer who want to avoid suffering pain or loss of mental function at the end of their lives. Their stories are powerful and persuasive.
But so are the stories that we hear less about, like that of California mother Stephanie Packer. The 32-year old wife and mother of four was diagnosed in 2012 with scleroderma, a chronic connective tissue disease which now makes it difficult for her to breathe and prevents her taking food except through a tube inserted in her arm.
And yet she is using the time she has left to advocate for other sclerodoma patients and the campaign against the state’s End of Life Option Act, modelled on Oregon’s assisted suicide law.
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