Oh I total agree with you in regards to the PGD. I to have been saying that it seems crazy not to cover PGD. In the long run surely it would be a cheaper option to cover this for famlies with known genetic conditions, then the medical bills for that child. The average life for CF'ers is around 36 years (and getting longer), you can't tell me that covering PGD would be more than the medical bills for 36 years.

Yeah your chances are the same as CF. We struggled for about a year over whether to try again naturally or do IVF. We felt the IVF was the better option for us. I just don't want another child to go through CF like Alana.

I to find it hard knowing that I am carrier too. I have done a lot of "Why me?".

The feasibility test is different to the genetic testing, its specific to doing IVF. Our genetic testing was also free.

Alana is doing really well. We have been very lucky that she has had no hospitalisations. They are doing heaps when it comes to research for CF. I just keep hoping that oneday I will get notified that they have found a cure. That will be the best day of my life!