Need Advice My father died from ALS two years ago. It was a horrific experience for him. He had an intermediate number of repeats (30) for ATXN2. Since then, I was tested and also have 30 repeats. My husband and I went through the long, emotional, and expensive journey of IVF to do pregenetic implantation testing for the gene. We transferred one of our “healthy” genes embryos in February and I am now 13 weeks. We did the CVS test to confirm whether the fetus is all good to go and I just got the results. Repeat lengths of 22-29. Which leads me to believe my 30 repeat gene has morphed into a 29 repeat gene. Which means that she doesn’t have a risk of ataxia but does have a risk for ALS. No one warned me that this could happen with a gene that passed the PGT testing. My husband and I did all of this to avoid passing on the gene and now here I am, faced with either terminating or potentially passing along an ALS risk. The only upside is that she won’t have ataxia.…