Tuesday, February 12, 2013

Hospital Timeline

We were admitted Monday night, unsure of our future but certain that Archer would have an MRI Tuesday morning. It was a restless night for all of us, but especially him.

Tuesday morning came early, 4:30 for Archer and I and brought a neuro surgery team. There were 4 or 5 of them. They addressed Chance and I, didn't introduce themselves to Archer, and told us surgery would be at 9 the next morning. He went down for his MRI soon after, and we waited for results all day. We didn't hear anything.

Tuesday night was sleepless for me, wondering and worrying. The MRI would determine if the spinal column was clear and it was frustrating to know that someone had the answer to that question and they weren't telling us.

Wednesday morning came early again, the 4 am vitals check woke him for the second day in a row. Around 8 the neuro team came in again, after my family arrived and showed us an MRI of a very large tumor above the left ear, spinal column was clear. My first little breath.

They took us back to holding before surgery soon and our little guy was too quickly being pried off of me and taken into surgery. The wait began. It was estimated at 6 hours.

We sat in the waiting room surrounded by family and close friends. It was an amazing feeling, knowing that so many people cared so much for us to sit vigil while we waited for news.

Less than 4 hours later the nurse called. Her voice was neutral when she said, "They're closing up, if you want to go to the third floor Dr Gross will be in to talk to you." My stomach dropped. It was too soon. She didn't say anything positive. She didn't say he was stable, she didn't say it went well.

Chance and I went down stairs to wait. It was the longest 30 minutes of my life. Then the doctor walks in with a smile and I breathed in for the first time in hours. The tumor was out, my baby was fine, she believes it's benign. Relief flooded through me and Chance says I exploded verbally. I felt it happening, but I couldn't stop. I didn't know what to ask, but I wanted to make sure she wasn't going to change her mind.

We were allowed to go into recovery one at a time. He was crying when I got in there, and that was a helpless feeling. He was so afraid and I just wanted to get in bed with him and hold him. I was scared too. He looked different and had this scary incision mark and I couldn't help.

I followed him up to the PICU and then we waited again. Waited for him to wake up and be well enough to move to a regular room.

He didn't really wake until late that night. He was in pain and he was upset. He was scared of the nurses and doctors. He flinched when they came in. We got no rest.

Thursday brought another MRI and a move back to a regular room. The second MRI was clear, the doctor had gotten the entire tumor out. I breathed again.

We had more visitors that night, and he seemed to be doing ok. Then Chance decided he was running a fever and he had to go home. Archer slept very little and jumped like he was falling every time he went to sleep. I slept at the foot of his bed because he needed me close and I was afraid of hurting him.

On Friday the swelling became worse. He withdrew, his speech was affected and he was scared to pee. His pain seemed low, and he was only taking Tylenol. He had lots of visitors, but he wasn't interactive. The physical therapist came and brought a wheel chair for him to tour around in She made him walk from his chair to me and sit in my lap out of bed. He still hadn't eaten and they wanted him to eat something. He decided he would rather climb out of the chair with me than eat. It made me giggle because he said "Go away." to his tray and pushed it. Then he started sliding out of my lap in an effort to get in bed. Then he told me to go away because he didn't want me telling him to eat. The speech path came by and checked his swallow, which seemed normal. He just needed to eat. Later that day he said he was hungry, he just couldn't find the words to tell me what he wanted. I made a picture album on his iPad so he could point to some food items, still nothing. Chance's cousin came by that night with his favorite kind of apple sauce. I had tried a similar one early in the day, but it wasn't our normal brand.

Saturday Chance came back, bringing more applesauce. We had tons of visitors bring every food imaginable, but all he wanted was the GoGo Squeeze applesauce. By 6pm he had eaten a small box of them and tried a few other things. My cousin went for more. That night he was still having a hard time expressing his needs and he was still in constant fear of moving his IV arm and the nurses.

Sunday morning was the best. He ate his breakfast, drank some milk, had a few bites of eggs and biscuit. And more applesauce. When the doctors came by they said they saw no reason why he couldn't go home. We were ecstatic. We got some lunch and waited for my family to bring Foster and help us load everything we had accumulated. His speech was slowly improving and he was getting up more.

It was the end of one journey and the beginning of another.

Stay tuned tomorrow for the emotional side of this timeline.


Tami Raines said...

Oh Sally.... You have all been thru so much in a very short period of time. Thank you for taking the time to share that journey with us. I can't imagine all the emotions but have realized quickly how amazing you and your family are and how very blessed you are to have one another.
<3 Tami

Related Posts Plugin for WordPress, Blogger...