Four months ago, I blogged about a Montana couple who had filed a lawsuit because their daughter was born with cystic fibrosis. They contend that the doctor, hospital, and childrens’ hospitals should have tested them so they could have aborted her and saved themselves emotional and financial stress. A judge ruled a week or two ago no the case (no link to the article because the Great Falls Tribune now requires a paid subscription) and said that the lawsuit could go forward.
W.T.F.??????????
Do they hate their child that much?!?!?!?!?!? I mean, it sucks to be them or the parent of any child with special needs but guess what… YOU DON’T GET TO PICK YOUR F-ING DESIGNER BABIES!!!!!!!!! Yes, their life sucks and yes, it is stressful to have a kid that sick; but their daughter will eventually grow up and learn to read and she’s going to discover that her parents would have aborted her if they’d had the chance. How exactly are they going to explain THAT?
As the mom of a son with autism and developmental delays, I can tell you that it is a really hard life and there are a lot of days when it is an absolute struggle to drag myself out of bed because I feel overwhelmed. It’s why I’ve built up a support system around me where I can call someone and say, “I really need prayer today” or “I really need to vent about how frustrated I am.” I’m far from perfect, I throw the best pity parties around, but I can’t imagine my life without Daniel. Almost losing him last March almost killed me and I still tear up and cry a year later at the memory of that night. My life is so much immeasurably better with him in it and his laugh makes up for all the stress of the emergency c-section, my pregnancy from hell, the NICU stay, the PICU stays last year, and the struggles to get him where he is now. IT. IS. ALL. WORTH. IT.
I just want to ask people to pray for this couple that they get out of their selfish mindset. Right now, it’s a struggle for me not to curse about them any more than I have.
Wow, that’s so crazy. They really do need prayer, and their daughter too. I totally agree with everything you said.
Dude, I thought the EXACT SAME THING when I saw that on the news, “Now everyone in the country knows that her parents wish she were dead.”
God protect us from ourselves.
Well. Since when are CF carriers routinely tested? I could imagine a scenario like in Israel,w here pretty much everyone knows their Tay Sachs carrier status, or if they don’t, the matchmaker does, and makes sure carriers don’t marry. But with this arguement all the parents should request testing for every genetic disease known to mankind…
Ugh. They disgust me on more than one level.