of Downs Syndrome. That's the news I got today. Going into the MMS tests hubby and I knew there was a chance of a false positive. Wondering if anyone else has experienced this. We go Monday morning for an ultrasound. Right now I am very emotional and scared. Hubby is on his way home from MS and I can't wait for a hug!!! Lord knows I need it ![]()
Re: 1 in 232 chance
Ditto this.
But 1/232 is only something like 0.4% chance. That's seems really low to me. I hope everything turns out well for you.
Keep in mind that that is less than a half percent chance, so your odds of a perfectly healthy baby are over 99.5%. I'll be thinking of you and hoping you get reassuring news soon!
It always seems worse when you look at/hear the ration - percentage wise, that is .004% chance.... you can also think of it as 231 of 232 that your baby is perfectly fine
This. Mine did the blood work and u/s together.
This exactly. Sending a lot of positive thoughts your way!
Those tests are only screening tests and are not diagnostic...and therefore can cause a lot of false worry. The sonogram should hopefully give you more peace of mind. I'm sure your MD will discuss with you the option of the amnio, as you are at the minimum number of weeks that you can have it done. T&P to you.
We had a 1 in 249 chance after our MMS test. After 2 ultrasounds we have a healthy baby that shows no signs of Downs.
Edited: Oh and they have now drops our chances to 1 in 800.
Yes, you should find out the cutoff percentage for risk from your doctor. When my doctor told us about the tests he had mentioned a percentage but I forget. So if .004% is still below that cutoff, then that 1/232 should not worry you as much.
Also, how old are you? Since I'm 34 the doctor told me that I will most likely get a false positive for risk for DS because all kinds of factors like age and race are calculated in the statistical analyses to come up with that 1/232 figure. So the doctor suspected I would just be worrying myself if my fetus ended up at risk when it was just my age putting me into the risk category. He also said that if I refuse to do amniocentesis (which I do) and terminate, then what's the point of the bloodwork when I won't be able to definitively find anything out without the amnio?
I wanted the bloodwork just to prepare ahead of time and get services lined up if there was a problem. I work with kids with disabilities so DS is not the end of the world to me compared to the myriad of other things that can go wrong with a child. But my husband didn't want to know anything and worry for 9 months if we weren't going to do amnio or consider termination if DS was the result.
I was told 1 in 180...and I'm like, positive that everything is just fine.
So many things can alter the effectiveness of the blood screen. My U/S is on the 17th, so I am happy that I got to get my U/S moved up, but I did freak out once I first heard about it...
I know how you feel, but just think...over 99% of the time, there's nothing wrong! something like 1 in 20 women gets an "high risk" result and we all know that 1 in 20 is not the actual rate of Downs.
I am actually positive that my due date is a week off (since my cycles are long and they used LMP to determine my EDD), and that can mess up the results of the test.
Try not to stress
Your U/S is really soon, so that's good!
Your chances are extremely low.
Either way that baby will be wonderful, and loved. Babies no matter what are a blessing, and sent for a reason. I used to work with special needs children and honestly children with DS are the most loving people out there. They show a love like nothing else on this earth, and every day presents something new and wonderful for them.
I hope your child is perfect and doesn't have DS. Children don't need to face any more complications in this world.
GL hun, and I'll send you positive thoughts.
Make a pregnancy ticker
We were told the exact same thing and had to go in to see a genetics counselor, etc. the day before our wedding (they called with the odds 2 days before our wedding). We declined the amnio and have had 5 ultrasounds to take measurements, etc. and the doctors are quite confident that she does not have downs.
I didn't know anything about these tests when I initially had them done and since my "scare", a lot of people have told me about how doctors told them their baby DID have downs or a great chance of downs and their babies were perfectly healthy. I know until you hear a doctor tell you that you are in the clear you will worry (I know I did), but just take into account that these false positives happen a LOT. We will never be doing diagnostic testing again. Good luck-- I'll be thinking of you!