lynniecat, thanks a lot for all the information and the link too. You know a lot about this. You would make a brilliant IVF consultant

It must be really exciting working in a lab and knowing about all this stuff.
I've been reading about CGH or as they also call it Staggered IVF (St-IVF) and it's amazing how much it improves the birth rate per embryo transferred! It says it can be used to identify chromosomally normal embryos/blastocysts but nothing was mentioned about whether it can be used to identify single gene disorders.
To be honest, I don't know much about PGD as this is going to be our first attempt. I remember they mentioned in the first appointment that they were going to test the embryos for the gene change or mutations running in the family and then use DNA linked markers
Anyway, it's definitely worth investigating about CGH and see if it can be used in our case because it would be brilliant to check for all chromosome problems at the same time. We are still waiting for our probes to get ready and then we'll have an appointment with a consultant, which hopefully should be in June or July.
So you are expecting a girl

....Congratulations on being pregnant. I should've known from your signature!!! When's she due?
In our case, if the embryos tested were carriers of my trait or my DH's, they will still be transferred because there's no problems with that. It's just that the two traits together will cause a serious disease!
Thanks again for your help.
Bighope x