I’ve written and deleted this god knows how many times in the last few days. I don’t know why I’m writing. I guess just to see my own thoughts in front of me.
Here goes attempt number 12.
Our son, born in March 2012 had a severe congenital heart defect. After a very long and scary 5 months, he had life saving surgery and has made a wonderful recovery; confirmed when he was most recently checked in March. Nothing to worry about there… now.
We’re expecting our second son in October and last week had the 20 week congenital anomaly scan. We had been worried about another heart defect so as the sonographer was going through her checklist saying, “this is normal”, “that’s normal” we were having a wonderful time. It was then we got the kick in the guts that I’ll never forget. The nucheal fold at the back of the neck, a hard marker for Down Syndrome, is very thick. I can’t bring myself to look at the statistics, but the chances of our boy having Downs is high. The other markers such as lack of a nasal bone, spacing of fingers and the ovalness of the head were all missing / they were ‘normal’.
They took a sample of the amniotic fluid to do a 100% accurate test, but I can’t help but feel like I’m preparing for the bad news. The test will take 3-4 weeks, but right now, I don’t know how I can last that long. I always stayed, perhaps naively, positive with our first boy and it got me through. This time though, I feel I’m all out of positiveness and am just preparing for the worst. I’m so frightened that there’ll be other health problems. I’ve had dreams every night where we’re burying our boy.
I know my wife and I can cope. I’m frightened for our son. Everyone wants their child’s life to be easy; make friends, do well at school, get a good job, find a partner etc. I do know that having Downs and that list absolutely aren’t mutually exclusive, but it’s certainly not going to be easier for him.
I can’t bring myself to get any extra information about it all just yet. I want to wait to see if I need to when we find out for sure.
Has anyone else had a similar situation? Like I said, we haven’t been told our son has Downs, but we’re 4 days in to the longest, scariest and most difficult 4 weeks of our lives.
Mike