Normally, I don’t get my hopes up about what medicine will ever be able to do for my son’s future. I just focus on education, therapies, and looooooove. But every so often, I read something like this, and I have to admit, I get my hopes up a little. (NB: Fragile X is not my son’s syndrome.)
Researchers, thanks for what you’ve done so far. Now, to work with you!