What tashy said is true they might not be able to test for some things here i know part of my test was from England.

And tashy is correct in saying make sure they get everything organised at the same time so there is no going back and forth then less waiting.
We were told of a few possibilities before we lost Abbi and then when the autopsy was done it was narrowed down to 2 possiblities (one genetic and the other a freak one off mistake )based on all her abnormalities so i guess we were lucky they that knew where to start looking they knew which genes are involved so it ended up being smith lemli opitz syndrome.
We had Abbi in march and didnt get the final results until the 1st of june (i will always remember that day) then we had to wait for a test to be developed to be able to find it in our embryos and that wasnt ready until the october we had all our bloodwork done the day we got the autopsy result (1st of june) and it was sent to be matched to Abbi's liver sample in SA and looked at to find the mutations in DH and myself which they were found so we new we were both carriers and the reason our daughter was affected so we had our answer.
As SLO is rare in australia we didnt have to pay a cent for any testing or even all the testing with ella's pregnancy.

All i will say is i rang constantly and was on their case all the time pushing and pushing to get answers as quick as possible as age was against me also i was 35 at the time and they dont rush so make sure you badger them to get what you want otherwise they take their time.

Tash-did you have your scan today hun any news