" I disagree. She’s being honest. It’s a hard life. I have a friend who has a 23 yo D who just graduated Yale and is Miss Accomplishment – and a 20 yo S who is non-verbal, not toilet trained, cannot be left alone, and requires lifelong care. It’s a horrible life. People in those situations need to be able to say it’s horrible."
Mourning a living child as if they were dead is horrible. An autistic child is not horrible. She can be honest all she wants, and I can disagree with her mourning a living child who will likely live through the next day.
Life is not a contest. A non-verbal child who requires lifelong care isn’t a source of horror. Giving birth to an anencepahlic baby is much worse. To think that comparing a child with autism with “mourning” a child with zero future, like an anencephalic or other child would have, well, that shows a serious lack of education or lack of empathy. A future of having even one smile is different than death, or being bed-ridden and non-responsive.
Ever hear of the book “Wonder”? The kid has a facial defect and has had many surgeries, and has missed a lot of school. Well, look up the medical condition on the Internet, and see pictures of children with the real disorder, not the fictional cases. I am not listing the condition here because if anyone is truly interested, they can look it up and find out more. The photo of one of the children is unbelievable that they survived birth, and there was nothing to do but let the poor thing pass away. (and to the topic at hand, some of those cases are thought to be related to prescription or illegal drugs).
Your counselor, your religious leader, your psychiatrist, your best friend, whoever you go to for help with dealing with day to day tragedies is the one to hear that you mourn your children so you can work through those feelings. I really feel that the story was a car crash, and the comments of many in the same or worse situations bear out that no matter what one’s lot in life, if one has the grace of having living children who have even a small degree of autonomy, as she clearly lists her children have, they need to look on the positive side for their children.
She needs significant help. And it is being projected as normal, yet many many MANY of us know that if we feel what she does, essentially PTSD, we would need to seek professional help and not chalk up near psychosis to “valid feelings”. I am not judging her, I am saying that my feelings are that her feelings indicate a need for professional help, NOT for sympathy.
Back to the topic at hand: Life is a cost-benefit analysis. If maintaining the health of the mother outweighs a small risk of birth defects, then the health of the mother wins. If the mother dies, her pregnancy will end. There are prescription drugs on the market with known and clear birth defects associated, and people still take the risk to have a child that they won’t be “one of the few”.
http://www.webmd.com/epilepsy/news/20100609/birth-defects-linked-valproic-acid
Autism isn’t a death sentence, and certainly there are other forms of developmental let alone physical disabilities that can be much worse. My nephew will never live on his own, and there is a real danger he will hurt himself or others. My brother lives with that but he and his wife aren’t putting on sackclothes and ashes, they are making legal arrangements so he will be cared for after their passing, they are making sure he has money to live on but receives proper government benefits. They bring him to events and in their case, they are lucky that he responds well to bribery like a 5 year old would (he is 20).
And by the way, pot use by the father is linked to genetic defects in sperm which may lead to disability in the child:
http://www.upi.com/Health_News/2012/06/24/Sperm-of-smoking-dads-can-hurt-child-DNA/UPI-53121340570130/