Yeah, SA is definitely something else.
I have seen specials on television about that little girl. Born without a face is not the appropriate term here. I am also shocked that over $3 million has been spent by US taxpayers for the unholy twists of modern medicine that are necessary to keep this little girl alive. I remember poignantly her nurse describing what her life with the little girl is like. That's right, there's a registered nurse who is paid to sit with the little girl every night, all night, to make sure that her trach tube doesn't get knocked out or whatever so that she can continue to breathe. I wonder how much a nurse gets per 8 or 12 hour shift, for every single night that this little girl has slept. The nurse said that the little girl can cry, and does cry, but because of her trach tube and her facial deformities nobody can ever hear her cry. I thought that was awful for her to cry and yet nobody can hear her. I know that she has a family who loves her, but how far is love going to take her? What kind of life is she going to have? I hope that she will have a happy life because I wish that for everyone, but it just kills me to think about what her life is like, and what it is going to be like in the future.
Imagine all the horrible, painful surgeries that this child has endured. Her parents keep saying that it's only fair for God to decide who lives and who dies. I think that the medical community is playing God by all these ridiculous measures to keep her alive.
I do think that it's horribly cruel for the SA author to keep calling her a monster. She is a human being, like the rest of us. However, if it were my child I would not force her to go through all that. I would have just let God take her when he chose rather than spend millions of other people's dollars to keep cheating death.