The beginning

February 12, 2011:  2 home pregnancy tests yielded positive results. 

February 14, 2011:  MD appt confirmed we were pregnant with our third child.  This pregnancy was quickly reminiscent of the first two (both boys) - no cravings, no morning sickness, etc. 

We had our routine 12-week ultrasound and were told that there were certain "markers" indicative of Down Syndrome.  Specifically - there was an unusual thickness in the baby's neck & a hole in his heart (VSD).  Shortly thereafter, we completed the two routine blood tests; the risks increased.  We were told "It is more likely than not, that your baby has Down Syndrome." 

May 16, 2011:  At the 18-week ultrasound, we learned we were having a boy (whom we would name Josiah).  We also learned that there were additional markers (shorter arm/leg bones, smaller nose, etc).  Carl & I decided to have an amnio to confirm the suspicion.  The amnio was completed immediately.

May 18, 2011:  Our OB called.  The preliminary results were in.....it clearly showed the triple 21 chromosome.  It was official.  Josiah has Down Syndrome (Trisomy 21).