Hi farm gal, my DH and I are in a very similar boat... he has myotonic muscular dystrophy (MD) and we have decided to go down the PGD route also as there is a 50% chance of passing it on and it magnifies with each generation
We've done heaps of research and counselling over the past couple of years about our options, however we now have to go to Sydney as no-one really has the technology here (Brisbane). We have a referral for someone at SIVF and I'll be ringing them next Tues (his office is closed until then) and i'm told that we should be able to start in July ()
Would love to exchange notes with you as it's difficult to find anyone who is going through exactly the same thing!
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