Count me in....and once again I say...."Where two or more are gathered together ".... That's where the KT power comes from... My prayers have been sent.... patti

Well,I just talked to DS .DDIL was at work when he was talking to my DH earlier.She is a nurse.She wasn't feeling well so she went to the ER,they checked her over and her blood pressure was high.She told them that she was worried about the baby and why,and they did another ultrasound.Everything was fine! What the other one was showing was baby girl Jillian's foot! Now how in the world could they think that had anything to do with loss of amniotic fluid? The two technicians that did the first ultrasound were very unprofessional in the first place.After they spotted the "problem" they started whispering to one another and wouldn't tell DS and DIL what was going on,just that they needed to go to her regular OB on Tuesday.I understand that they were not qualified to make a diagnosis but they shouldn't have been whispering and acting suspicious.Anyway,she is on her way home now and feeling much better and I thank you gwanny23 and anyone else who said a prayer.

My experience is that in most states you have to be seizure free for a certain amount of time before you can drive, but that is usually with epilepsy...I'm not sure if the same rule applies if the seizure has other causes (like a TBI). People who have seizures due to TBI, like those who have epilepsy, cannot drive until they are seizure free for a certain period of time. Cardamom, I wouldn't worry about that right now if I were you. Many, many people are able to take seizure medication and drive. Right now you don't know if he will continue to have seizures or not. And if he does have seizures, you don't know if they can be effectively prevented by medication. Try not to worry about that part of it right now. I know very well how frightened you must be. Take care of yourself as best you can. Remember that you will have a lot to do as he recovers, so take care of yourself while he's in the hospital. And remember that whatever happens, you will be fine and you will be able to do what you need to do. You will get a lot of advice from different people, and you will have to sift through it and find what works for you and your family. My advice would be different from marie-ndcal's. I did ask a lot of questions about things pertaining to rehab, etc. But I didn't ask a lot of questions from everyone I dealt with. For me, I found it was best to narrow my information pipeline. I got so much conflicting information from people, including health care professionals, that after awhile it was more practical to streamline the information flow. And also (and this is different for each individual), there were certain details about his injuries that I just couldn't handle. I could only cope with so much at a time. I never asked about his Glasgow Scale score at all, and I thank God I didn't know or find out until way later down the road. I would have crumpled to the floor like a little baby. Fortunately, my husband's parents are very intelligent and capable health care professionals and looked over his meds, statistics, etc. I noticed that they didn't ask a lot of questions, either, about his medications, etc. That's probably because they knew what should be done and knew he was getting the right care for the situation. If, like marie-ndcal's daughter, you want to or need to ask a lot of questions, don't hesitate to do it. I will say that from the time my husband entered neuro intensive care onward, the doctors, nurses, therapists and social workers were very good about keeping me informed about everything I needed to know. If you feel that you aren't being given enough information, don't hesitate to ask. You will need to be your husband's best advocate, so be as informed as you need to be. Although I didn't ask a lot of questions about my husband's meds, etc., I was very proactive with anything to do with rehab, including making sure he got all of his testing lined up as quick as was reasonable, so that he could be transferred to a rehab hospital as soon as possible. I tried to observe as much as I could there and ask a lot of questions. We were able to support him and help him much better once he came home because of that. Ravencajun is right, every brain case is different. The doctors and nurses will tell you that. You will find what works best for your husband's situation. Take care of yourself and make sure you eat something every day. Whatever you do, remember that you will be fine, and that you will be able to do everything you need to do. My thoughts and prayers will be with you.

What a hugely hurtful thing it is to lose a precious child. I pray that you and your loved ones may share good memories of your son during these days which will help to carry you through. Sometimes I think that the boundaries between this life and the next are not as strong as we think ... sometimes it seems to me that we taste of the firstfruits of heaven while we journey through this life. I trust that he is finding a glorious new vista of life opening out before him, so that he can rejoice in not only his present but his future. May you who are left behind find comfort and peace during these coming difficult days. I pray that God may bless you and yours through it all. ole joyful