Tuesday
After Mike and Scott returned from work, we headed to the hospital. No lengthy report today. Much the same as yesterday.
Sleeping off and on.
Only a few bites during meals.
Glucerna continues to be his main source of nutrition.
His voice is quite weak.
He seems to be gradually weakening in physical strength.
When awake, he is mentally alert.
He frequently stares off into a daze.
He still has diarrhea.
His hands showed some welling; perhaps his arms too.
The kidney doctor said that the catheter must remain.
Dr. B. (oncologist) is expected to pass by tomorrow. Chemo was halted upon his arrival at the hospital on Friday. I wonder what they’ll decide about that.
Wednesday
Due to the diarrhea becoming slightly worse, Dr. R. decided to change the meds for that. Blood pressure readings are about 160/80 and pulse about 115. Oncologist never came.
Thursday
To relieve some of the stresses on the digestive system, Dr. R. decided to remove the IV from his arm and insert a catheter type tube into the neck. This will allow him to receive nutrition while giving his belly and colon a break.
The oncologist finally came. Due to a glitch in communication somewhere, he was never told that Carl was awaiting his arrival at the hospital. He said that blood testing would be done daily. Depending on what the blood screening shows this day, chemo may begin again on Friday. He also explained that the rapid decline in health and physical strength is not due to the cancer, but caused by the bacterial infection.
After receiving the catheter to the neck and having x-rays to view that it was correctly in place, the boost of nutrients began. During the day, Carl had a whole cup of broth by mouth - more nutritional intake than in the last week.
In the evening hours on Thursday, we visited with Carl and Hilda. Though they had little sleep the night before or during this day, they both appeared to be doing rather well. Carl’s color seemed a bit improved, he was awake and even more alert, he showed no sign of the frown which we noticed in our last visit, but the diarrhea persists. He said that food had begun to have taste. Though his voice is still quite faint, he participated in more conversation and even laughed as Mike joked with he and Hilda.
When we left the hospital on this evening, we felt cautiously optimistic. Optimistic, but afraid that this would only be one good day preceding what we might face the next.
Friday
Due to low blood counts, Carl will be receiving two units of blood. As of 8pm last night, that process had not begun. The oncologist ordered that the chemo be held until the blood count was better. His bowel movements seemed to have become less frequent, but diarrhea persists. He drank all of the broth that was served to him today. It was reported that the pneumonia seems to be a little better. Hilda got a bit more sleep during Thursday night, but Carl didn’t. Ambien will be given on this night to assist with that.
During the 8pm call with Hilda, she told Mike that Carl had sat up 2x at the side of the bed and physical therapy assisted him into the chair for a short time during the day.
The nurse that tended to Carl in ICU during last Friday night and Saturday morning stopped in. She said that Carl looks a whoooole lot better than he did at that time.
One of nurses commented that since Carl’s stool has become “slimy”, that is a good indication that he may indeed be passing the bacteria and begun to beat it.
Two of the great-grandsons visited him yesterday. One of them approached Carl’s bed and said, “Read, Paw, READ!”
Your continued prayers are appreciated. It is by the grace of God that we still have Carl with us. In our prayers, we always trust that God’s will is better than our own, but hope that His will is that we have Carl for a long time coming.