OB/GYN doctors get sued all the time when a baby isn’t “normal”, it may be a reaction to that.
The thing is that by aborting more downs babies there is less cause to find a cure or genetic therepy for children with Downs which if we could find a way to fix the issues with Downs we could solve a LOT more other genetic disorders that regular people are afflicted with.
Was this the first time they had ever met the doctor? Who were they going to for prenatal care?
Of course I have a bit of a reputation in my family for being a hard-ass when it comes to doctors. But honestly, if I don't like them, why should I ever go back? And there have been a few that have seen me walk out the door, occasionally with a one fingered salute for good measure!
Once in a while, I see a Down’s Syndrome parent shopping or doing something with their “child”, even though they usually look like adults, and, you know, I’ve never seen even a hint of a smile or a look of contentedness by any of these parents.
Ever!
I have a son with DS. He’s a little over 2 1/2 years old.
He’s an amazing blessing to our family and I honestly wouldn’t change a thing about him.
I would rather have him than a don who grows up to be a doctor who acts like one of the doctors mentioned above.
All kids bring challenges. Plus there’s no test for how much joy a child with DS will bring.
A liberal sees a DS child and sees a burden on society that could have been avoided. They don’t see that with any other type of child because.....disability.
Anyone remember the last time a DS child shot up a school?
I was alone when my doctor and the pediatrician broke the news to me that my son has Down Syndrome. Not the type of news you want to get when you are alone. I had many questions about what life would be like for my son who is now 20. Rather than trying to give me an answer since only time would tell what his development would be like, my doctor told me to take it one day at a time. It was the best advice I could have gotten. There are days when you truly have to just take it one day at a time.
http://www.mayoclinic.org/diseases-conditions/down-syndrome/basics/risk-factors/con-20020948
It has been screamed from the rooftops for 30 years to past-prime parents that they have a much higher risk of bearing children with severe genetic anomalies. Doctors will strongly advise in emphatic terms for testing of both parents for tell-tale genetic markers - both before and after conception - as this woman's doctor did.
The mother in this article was too lazy to test, too irresponsible and too selfish to involve her own husband in testing, and then gets offended that the medical staff is incredulous of her stupidity. I'm sure she'll be even more offended when hubby walks out the door.
There was no doubt that he was going to be loved but when you have a child that isn't perfect you have to come to terms with it and accept the gift you've been given. We spent the whole day coming to terms with it.
Almost 16 hours after he was born a doctor came in and checked him out and told us what we already knew, that he had Downs Syndrome. We all nod our heads and he just thinks we are in denial not that we have discussed it all day, not that we hadn't bawled our eyes out and then felt guilty. And I mean what are you going to do? Put him back in and start all over? The Dr. did tell us that he was healthy and didn't seem to have some of the health issues that other DS children had but then started telling us all the grave things that could happen. Like we didn't have a clue.
I'm happy to say that he's now 11. He has diabetes and Celiac’s but otherwise is healthy. He's pretty smart but nonverbal but he's learning sign language. Everybody loves him not just family. He is happy and loving and well-loved.
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I've experienced this kind of attitude from a doctor. It's ugly.
I have one natural grandson and one adopted granddaughter with Down Syndrome. Both are a delight.
A very good friend of mine has a downs syndrome daughter and she is married to a downs syndrome man. They are very happy and keep very busy. Through my friend I have met several downs syndrome children and adults, they are wonderful people.