Nerve demage: kiss, eat, make love.

I'll go with the personal questions. I apologize for my poor English from the start.

Many people here have already had the surgery and have gone through life after recovery. I'd like to ask you, what is it like to perform common situations after surgery? Do you feel the same as you did before surgery when you kiss? When you eat? And sorry for the inappropriate and intimate question, but do you have trouble performing oral on your partners?

Oh, and for women who are thinking of getting pregnant, I read in a Facebook group that a woman was told to book an appointment if she was thinking of getting pregnant because the hormones could change your bones. Terrifying.

I'm still refusing to have the surgery. I'm a skeletal class 2 and I have severe retrognathism, asymmetry, and long face syndrome.

EDIT: Thanks to everyone for responding!

I think I'll try to avoid surgery for a while, maybe try TADs but I'll still go to the maxillofacial surgeon.

All the doctors say that the risk of nerve demage is not that common but I read more and more comments about it happening to them😔

It's amazing that it's so normal, in a bad way. I'd even say that it's more normal for it to happen to you than not. I'm mad ...