Many of us who have this condition have been born with it and therefore don’t have any idea what it’s like to live without it. Also, you can’t miss something you never knew. I posted this on Valentine’s Day and have had a few people ask: “What’s it like to live life without Hydrocephalus?” The short answer is; Anything you know right now, the opposite of that. (Hydrocephalus-related, of course) A definite case of; “You don’t know what you’ve got until it’s gone…” A conversati