I am sorry beyond words. As Nikki said, the experience of your husbands disease with the accompanying FTD does not mean you will follow the same path.
It is so unfair, and so incredibly rare, that you both contracted what is already a rare disease. Rare doesn’t even do it justice, as the number of documented and researched cases is less than 100 worldwide over the past fifty years. Little consolation, though, because it happened to your family. I just can’t express enough my sorrow and empathy for what you went through with your husband, only to be facing the same disease. If you don’t mind me asking, when was your husband diagnosed?
We are here to offer support and advice in any way we can. You are not alone. Kevin