It's Labor Day weekend. It has been a relaxing weekend so far. We went over to our friends house for a bar-b-que. It was really nice. Devin had a great time swimming. He is so sweet. We have been monitoring Caleb's oxygen with a pulse ox that Hospice brought over. We need to make sure that the blow by we are giving him is adequate enough to keep his sat levels up. During the day when he is awake his sat levels are great. But when he is sleeping they dip down way too low. We will keep monitoring him for a couple more nights.
Sunday, September 6, 2009
A Father's Love
I put this video together for Steven. So many times we forget that our husbands are hurting just like we are. I see how much Steven loves his children. Caleb has really stole his heart. He walks by him and says he is the most precious baby I've ever seen. They spend time just staring at each other sharing a special moment of love. After showing Steven the video, he asked to add something at the end. He is a wonderful father. I just wanted him to know how much he is loved.
Wednesday, September 2, 2009
September 2, 2009
Caleb woke up this morning like usual at about 6:30 am. He is like clockwork. He starts flailing around because he wants out of his bassinet and wants to lay in our bed. Tell me he's not like any other baby :) Daddy & I layed there with him. It was a nice morning. Then he wanted to be held. This is something new. He usually wants to be left alone. Now he cries because he wants to be held. And don't you dare try to lay him down when he finally falls asleep...he knows...then he's REALLY mad. I love watching him sleep in my arms. His eyes roll to the back of his head, he gets this silly Mr. McGoo grin and sometimes I get a little laugh. What must he be dreaming about? Must be the angels playing with him.
Had his GI appt. Caleb is 10lbs 4 oz and is 22 1/2 inches long. Way to go son! Daddy & I love you so much. You continue to amaze us.
Had his GI appt. Caleb is 10lbs 4 oz and is 22 1/2 inches long. Way to go son! Daddy & I love you so much. You continue to amaze us.
Tuesday, September 1, 2009
September 1, 2009
I am finally getting Caleb's blog set up. It has only taken me 5 months to do! It was a pretty quiet day other than the arguing with different agencies trying to get respite care. It looks like it just isn't going to happen. It is hard when you don't have any help or just relief sometimes. But then I look at my little mouse's face and it all seems better. Caleb loves to get kissed on the forhead. He just laughs. I sat here thinking about all the things I'd love for Caleb to experience. Will he ever get to see a sunset, play in the sand, get to see Shamu or be able to hold his head up so he can rest on my shoulder. I would love for him to wrap his arms around me and I'd hold him so tight. I love him so much that whatever he does is such a miracle...I'll take it and cherish each and every moment.
Thursday, August 20, 2009
Brotherly Love
Devin loves his little brother. He is always wanting to do something for him. He was so excited to sing for him....he got his room ready with all the animals. They are such a blessing.
Wednesday, August 5, 2009
Seizures
Caleb didn't do well under sedation and after the MRI he was sent up to PICU to recover. He just wouldn't come out of it. At about midnight he started to go down hill quickly. I watched the monitors and his respirations went flatline then his sats dropped. He would gasp when he came out of what we think were seizures and apnea. It was horrible. I could tell when he was going to crash. It got more and more frequent. I just layed there on him and cried. The nurses & dr's worked so hard to try and stabilize him. They asked me what our wishes were. My stomach just sank...my heart hurt so bad. I didn't know what was best...no I did know I just didn't want to think about it. I prayed that God would guide me in these hard choices. I called Steven about 2 am and told him that I thought it was time and for him to come to the hospital quickly. Extra caffeine didn't work. They put him on a cpap. He finally was able to stay stable and rest. Caleb was also put into isolation because he had a fever and they weren't sure what all was going on. The next day he had an EEG done. Both the MRI and the EEG showed that he was having seizures. He was also diagnosed with Dandy Walker Malformation. Caleb hadn't cooed or smiled or acknowledged us for days. I was so sad. I kept thinking what did I do?? I was so afraid I wouldn't get my little mouse back. But we did. After we got home he really started to get back to his old self. Thank you Lord for continuing to keep Caleb safely in Your arms. You are our strength...You are with us always....
Wednesday, July 8, 2009
Unexplained Blood Infection
When we got to the ER we were met by Peds Surgery. The mic-key had come out again...bulb and all. They popped another one in and said for us to try a feed to make sure everything is working right. Caleb only took about 35 cc's and vomitted. They said he probably has a bit of a bug and to watch him. While they were getting all the paperwork filled out we waited in the room and watched "In the Heat of the Night". :) Steven was holding him and I decided to go over an touch Caleb's forhead. He felt a little warm. I asked the nurse if we could take his temp. It was about 100.4. I think 100.3 is their cut off. So they said they wanted to keep him over night for observation. While they were trying to get us a room, I noticed the moniter that took his vitals climbing. His blood pressure went up to 228 and now he was burning up. So once again I went to the nurse & said something is wrong his bp is getting too high. She thought it was the monitor reading wrong & I told her that I knew how to read a monitor that somethings wrong. She went & checked it out. I could see the concern in her eyes. His temp was now over 103. All of a sudden a team of dr's & nurses flooded the room. They said he is going into respitory failure and was septic...they needed to intubate him. My heart sank. I thought this is it. Steven went with Caleb to the other room where they intubated him. I couldn't watch. I sat there & cried in an empty space. They took my son. God what was happening?? Several nurses and staff came and knelt down beside me. I could tell they were holding back their tears. I asked if my son was going to die. They just looked at me & said it wasn't good. I called my mom who was at our house with our son Devin. I told her that Caleb crashed & she needed to get there quickly. I needed her there too. That was one of the hardest calls I've had to make. A little later we were sent to PICU. He had all kinds of tubes connected to him. It was horrible. They had a line in his collar bone area for access. They told us he had some sort of infection and started him on major antibiotics. They took blood for cultures to see what we were dealing with. Turned out to be Streptococcus Veridans. They couldn't understand how he could've gotten it. It is rare for a child his age to get it. He wa
s fighting so hard. Later they came in and said they needed to do a blood transfusion. What?? I was terrified. But he wouldn't have made it if we didn't. They had to also tie his hands up because he kept trying to get the tubes. He is a fiesty one. We ended up having to stay for 10 days in the hospital because he needed that long of antibiotic treatment. The sepsis did a number on his little body. But if it weren't for what we believed were the hands of God pulling Caleb's mic-key out that night, he would have died. It happened so fast. A wonderful part of this event was that we could say that God put Caleb right where he needed to be. No dr or nurse could explain what happened. I don't know how many times someone came in asking for us to explain what happened again. They had to hear it for themselves. And I was happy to keep telling them the story.
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