death becomes her....
Also - a link to Not Dead Yet a US organisation of disabled people opposed to euthanasia. Obviously a US specific site, but presents some interesting thoughts.
Thank you both for your considered responses. This is what I love about blogging - getting to discuss the big issues with fabulous people. And these are sad, difficult issues.
Rhea writes regarding some private people "Perhaps even the best quality of care would seem for some people like an unacceptable intrusion in their lives?"
I can imagine that this would be difficult, I really can. I definitely feel it an intrusion myself, and me, well I'm the kind of person who keeps a diary on the internet ;) But I find it really hard to understand how someone could hate it so much, that despite it enabling them to live full lives, to see their friends and families that they would rather be dead. The personal care side of things is a relatively small part of life, after all.
It is hard to make that adjustment though, and I can see that.
I'm worried (justifiably so, according to press reports) at someone deciding my life isn't worth living but also feel that another person with similar limitations deciding theirs isn't worth living somehow bothers me. This may say more about me than you really needed to know! But its also about wanting to share the knowledge I have about living independently, and that I reject the idea that by getting on with my really fairly ordinary life that I am doing anything unusual or special.
All comments welcome of course. If it wasn't for you lot, this'd be a lonely old place.....
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