Lachlan was born in 2010. During our pregnancy we were given a 1:2 risk of trisomy 21 ( Down's Syndrome) or trisomy 18 ( Edward's Syndrome). We never confirmed this risk and it was only after birth we found out that Lachlan had trisomy 18. Lachlan continues to defy the odds. This is his journey
Lachlan has exactly two weeks to go until two years old. He goes once a month to see a physiotherapist at disability services. Julie normally works him pretty hard. even doing simple things like standing and sitting with support take a huge effort on Lachlan's part. He usually is not very impressed with the effort he has to make over the hour. Today he was on a fit ball and they have just installed a mirror. He liked being on the ball.