Friday, July 26, 2013
The visit to the cardiologist went well today. His heart and lungs look good. We are going to try and wean some of his medications, because his heart is doing good. Hopefully he will not be so sick to his stomach, once we wean the meds. Thanks for checking in and have a great day.
Thursday, July 25, 2013
Things are going well. I seem like I am more busy now that I am home. I have so many things to catch up on. Here is picture of Ben giving the camera cheese! The tests seemed to have gone well on Tuesday. Tomorrow we have a cardiologist visit. I am keeping my fingers crossed that he is looking good and recovering well. My only concern is how much nausea Ben has and his eating has not picked up yet. His incision looks great, and I am getting in the grove on the medications. Keep praying.
Saturday, July 20, 2013
Well today's x-ray looked perfect! They are planning to discharge us today. We are waiting on another prescription. Although there is a risk that his effusion could come back. So on Tuesday we will be at Helen Devos in Grand Rapids having some tests done to make sure everything looks good. Then on Friday we will meet with the cardiologist. Thanks for all your support and prayers.
On Monday we will hit the 3 week mark. Things are going good. We've been close to getting discharged all week. Sometimes I wish they would not even tell us tomorrow because we get our hopes up. Dan really is getting antsy. I am doing ok, I just miss home. Ally is her happy self. She really looks forward to the sibling group every day. Our doctor estimated Mon for discharge, but I am not getting my hopes up like before. Ben has been asking to go on walks a lot. We have been talking with another boy named Colton parents. He was here the same time as we were the first time. Colton has HLHS and cerebral palsey. Just trying to hang in there. I may get away from the hospital today with Ally.
Friday, July 19, 2013
Everything has looked great to go home until Ben's x-ray this morning. The effusion is still bad enough that we cannot come home. We were starting to pack up and are bummed. Although once again I would rather stay here than need to come back right away. We may be here for a few more days. Thanks for checking in.
Thursday, July 18, 2013
Today Ben has been fussy, but doing fine. His effusion is looking better again. They still are talking Fri-Sat for discharge. Although we will need to follow up with Dr Lacina right away to make sure things are on track. We are all doing ok and I am getting nervous about going home, just because he will be on 7 medications. Of which 3 are critical to him staying on track and need to be given in a very timely fashion 3-4 times a day. Today I plan to take Ally to the gym to get some of her energy burnt off. Have a great day.
Wednesday, July 17, 2013
Today Ben's chest x-ray looks better today. The drugs seem to be working for Ben. We will need to continue to monitor this situation. If it stays on the right track we will be heading home on Friday or Saturday. We are completely off oxygen and just doing spot checks. He has lost the ng tube as well. He seems to do worse with it in than without it. Hopefully he will eat good again today so they don't us make us put it back in.
There is 13 year old boy here with HLHS that is waiting for a new heart. His name is Devon and has been here since Dec when his heart started failing. He has befriended Ben and brought him a stuffed doggie. We have been visiting him. Ally made him some art for his room. He is such a strong and beautiful person. Please keep him in your prayers as well. Devon is from the Rockford area. Thanks and have a good day.
Tuesday, July 16, 2013
Just got news the chest x-ray was not good to go home. We will not be coming home tomorrow. There is fluid around his right lung called a effusion. We need to try and get it out with drugs. Worse case scenario we will need to put a chest tube back in. Kinda bummed, but glad they caught it before we got into trouble. Ben is starting to eat much much better at least. Hopefully we will lose the ng tube soon. Gotta run.
Benjamin is great, they just feel it would be good to observe him a little longer. He has been off oxygen since 7:30 this morning. The hope is he will not need it again. Yesterday I learned how to place the ng. Dan is going to do it today. I did a CPR refresher today, and Dan will this afternoon. We watched all the discharge videos and he had a chest x-ray. All of his tests have looked good. We just are working on the eating. I think we will be heading home tomorrow. Probably with a ng tube for awhile. They are settling up all his orders for therapy, medications, and the at home plan. Here is a picture of the little man.
Monday, July 15, 2013
This morning at rounds they decided the chest tubes are coming out at about 11:00am. Then he is going to have a Eco and EKG to check everything over really good. We have been testing room air for longer periods of time and he seems to do ok. We still cannot get him to eat really well. He may need the ng tube at home. So I am going to re-learn all of that. They did say there is a possibility he will get to go home tomorrow. Which is awesome and scary at the same time. I hope he is doing well enough so we do not need to return. He will also be on many more medications that I am going to need to learn the ins and outs of. We will have a ton of apts and things to handle when we get back to GR. Thanks for your thoughts and prayers.
Sunday, July 14, 2013
Hello! The x-ray showed that there is just air in the bump above Ben's chest tube. They are just going to watch it and hopefully it absorbs into the body. We have been taking him for stroller rides and he has been sitting up in a chair. Tomorrow we may be able to take his chest tubes out. He is eating a little bit better. He just not eating enough by mouth yet. He still has the ng tube in and is on .75 liters of oxygen. Things are improving. My parents have been here this weekend and our going back today. Ally and I played hide and seek in the court yard yesterday. She was thrilled. Today she will go to the child life group. Have a great weekend. I think we may hear the H word this week. HOME!
Saturday, July 13, 2013
Ben is getting up and riding round in a stroller. He is still draining pretty good. His stomach has been upset and he has vomited a few times. The plan is to wean the ng feeds during the day to get him to eat by mouth. He is only on 1 liter of oxygen right now and we plan to wean as we can. Things are improving. They have been watching a bump above his incision. It is pretty raised and feels like there is fluid in it. They are going a x-ray to check it out today. Have a great weekend.
Friday, July 12, 2013
Ben was moved yesterday at about 4pm. The new rooms are wonderful and I slept very well in his room. We are in 53. He did drink some apple juice and eat 5 noodles by mouth yesterday. Most of his calories are through the ng tube. He is still draining from his 2 chest tubes. He is also on regular oxygen. The plan is to wean him of the oxygen to room air. The occupational therapist worked with applesauce. He ate a little of it. His stomach has been upset.He is happiest watching tv or playing with people he knows. Dan went home to get a few things done and is planning on coming back soon. Talk to you later.
Thursday, July 11, 2013
Hello! Benjamin is doing well. He just got off the high flow and is on the regular oxygen. Last night he had some vomiting and desats. He also vomited this morning. He really just need to poop and was better after he did. They adding prune juice to his diet to help with this. They pulled nj tube and put in ng tube. This goes to his stomach. He sat for 40 min in a chair. Physical therapy came and we worked with him on a floor mat. Occupational therapy came and made him left arm splint to wear at night to help with his hand. She will be back this afternoon to work on starting to eat by mouth. The plan is to get things back to normal. We may move to the floor today when there is room. There is a ton more things to do on the floor to keep the kids entertained. Thanks.
Wednesday, July 10, 2013
Last night Ben did well with the high flow. They want to aggressively wean it today, so we can move to the floor tomorrow. Ben puked last night. They think the meds make him do this. He seems to be much happier and has been watching tv. The real concern is his central line. They are going to pull it today, because it looks pretty bad and they do not want infection. We are going to hold him today and get him up. Thing are looking good. Slow but sure. Yesterday Ally got to see Monsters University again. The cartoonist were here signing there sketches and showing the movie. Benjamin got physically therapy and tomorrow they plan to do occupational therapy. Since he is here we do not want to get behind with his therapy. It will also help gain his strength back after surgery and get back to where he was before surgery. Things are looking good.
Tuesday, July 9, 2013
I got up to the hospital just before rounds. Dan and Ben are still sleeping. Ben is making progress. His heart and chest x-ray looked good. He just has to overcome the lung hypertension. The doctors think that today we will try to wean the c-pap. If he does well with it we will get to move up to the floor tomorrow. One step closer to home. Ben has been asking for juice. Which is a good sign. He also told me that he all done, and he wants to go home. Last night when Ally left for the night he cried. He calmed down when we told him dad with staying with him. We are starting to miss home. There is going to be a ton to catch up on. Our friend Chuck says the pets are great. Other than the cat dislikes him. She had growled at him. This does not surprise me as she is protective. Thanks for checking in, I will post a picture later.
Monday, July 8, 2013
This morning things are going fine. Ben pooped last night! Yippee - the pain in his side is not as bad. Today they plan to take out his middle chest tube. He is off the bi-pap and nitric and down to straight c-pap. Hopefully we don't need to go back. They may take out the tube by his lung as well. We are still sucking out thick junk from him. We think he may have had a small cold before surgery. I stayed the night with Ben and got plenty of sleep. I am a heavy sleeper unlike Dan. Melba, Steve, Kate, and Elizabeth visited yesterday. The McCarthy's are back up and Ally stayed with them last night. I think Ben's lungs just need to recover from the cold and change in pressure. Thanks for all the support.
Sunday, July 7, 2013
Ben is doing well. This morning he changed rooms back to the PCTU, because they had more room. Last night they put another drainage tube in near the left lung where Ben had the air pockets. He has a little fluid to drain. He has no no's on his arms to prevent him from pulling off his mask which he has done a few times. He has some pain on his right side of his stomach. We think it is because he needs to poop. He is tolerating the food through his nj tube well. I have nothing huge to report. He is not off the bi-pap yet. There is higher pressure in his lungs and his body is trying to adjust. We are hanging tight. Thanks for thinking of us.
Saturday, July 6, 2013
Ben is going good. He has not completely weaned off the bi-pap. Although he is getting pedisure through the nj tube. His lung is not collapsed anymore, we just don't want it to happen again. He wanted Ally yesterday, and she held his hand for a good half hour. We made the right call keeping her with us in Ann Arbor. She is more mature, and is happier with us. She really has not been trouble at all and she is enjoying all the activities at the hospital. Since today is my b-day I may take Ally to the movies to get away for a little while while Dan stays with Ben. I will try to update again when I know more. Thanks for thinking of us.
Friday, July 5, 2013
Benjamin is so strong. He is still on the bi-pap. He dislikes it on his face. He told us last night that he wanted to go home, which breaks our hearts. The plan for today is to get his lung back in shape, wean the bi-pap, wean the morphine, and put a nj tube in so he possibly can start eating. The nj tube is different than the ng tube. We cannot put food in his stomach, so it will go to his bowels. Last night Dan stayed with Ben. Ally and I took a break at Ronald McDonald together. We did laundry, took showers, and relaxed. I plan to stay tonight with Ben. Have a good one.
Thursday, July 4, 2013
Last night went much better. Benjamin had a good night and I got some sleep. I was at rounds this morning and they are planning on doing a Eco today. He still is having trouble keeping his sats high enough when they reduce the high flow oxygen. They think he is just needs more time or there may be an issue with his heart. Although the cardiologist thinks the chances are slim. They just want to double check. Dan's parents the leaving today and my parents are coming up. Have a great 4th of July. I am going to take Ally to a party at the hospital.
Wednesday, July 3, 2013
Benjamin is doing much better than this morning. They got the air pocket out from his lung so he can breath better. He has been resting since they want him to have some time to recover. This sats are much better in the 80's. Since surgery he has a couple of things removed. Two IVs in left arm, one IV in right arm, one central line, and the ventilator. They hope he will continue to improve. If not they will do a Eco. He is still getting some more air in the pocket in the lung and we need to figure out why that is happening. Ben feet look very pink, not more blue!
Benjamin is doing ok. Dan stayed overnight and he had about the same night as I had. Ben secretions had to be sucked out so he could breath good. This morning when I arrived Ben is in pain. He keeps desating and he has a air pocket around the left lung. They are going to try and get the air out and they plan to help him with pain meds. The plan for today is to stay in the picu and to try to wean the high flow, although we need to get through this lung issue first. His heart look good.
Tuesday, July 2, 2013
Ben is doing ok. His chest x-ray looked perfect, although he is still having breathing issues. Today the are very slowing going to wean him off the high flow. He is more aware of who is there. We will make sure someone is always with him. Tomorrow he will be moved to the floor if he does well with the breathing. I am going to take Ally down to the Child Life Butterfly exhibit today. Talk to you soon.
Monday, July 1, 2013
I stayed at the hospital in Ben's room. He is not having a easy night. He is having fluid secretions build up in the lungs after being taken off the ventilator last night. It is very thick and they need to suck it out every hour. That is why I am up at 2:30 in the morning. He is not liking it at all and screams out. Although when they ask him to cough he does, so I know he is the same little boy that try's to please. He is now on the high flow oxygen to help while he gets through this phase. It is just part of the process because this can happen when you were on the lung bypass machine. Keep him in your thoughts.
Hello! Ben is doing pretty good. They even working on getting him off the ventilator tonight. He is a fighter and has a temper even though he is not awake yet. They plan to try to take the vent off when he is more awake. Allison came up to the hospital, but we have not let her see Ben yet. It is a little scary. I will post a picture later. Dan is getting our key to Ronald McDonald House right now. So I am canceling our backup hotel. Thanks for all the support.
The the surgery Is finished already. Ben got on and off the lung bypass machine just fine. The surgeon has not came up yet, but after she does we may get to see him in two hours. I was getting so upset that I did not have a update, but what I got was wonderful news. The surgeon just came up, and was very pleased. Gotta run, but I post again tonight. Thanks for all the prayers.