I have just found out that Alana has Triple X syndrome. Basically instead of having 2 X chromosomes, she has three. I have only found out a little amount of info at this stage, but from what I gather it can show no or few symptoms, to some having slight learning/developmental delays. So this could be the connection to Alana's delayed develpoment, like slow at walking and speech. We have an app with the Neuro dr at the end of this month, so hopefully he will shed some more light on this.

I have also found out that there is some abnormalities from an MRI that Alana had of her brain. Her CF paed didn't know much about it, but said that he will try to find more out and ring this afternoon. I am a little worried about this. I hope that there isn't anything serious She has enough already!