Coffee? Tea? Serenity?

A Mix of Updated Info

In His Steps — Posted by cndgsnr @ July 28, 2008 16:58
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Here is an update of info and events of the recent days. Please be patient with the lack of correct order of events. I am composing this while running like a thirsty chicken amid my own house trying to catch up on tasks which need doing, but wanting to share info with all of you.  I can multitask!  (More)

Our Parents

In His Steps — Posted by cndgsnr @ July 25, 2008 06:24
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Our families could use all the prayer time that you can spare.  (More)

Saturday through Tuesday (7/22)

Mr. Carl & Myeloma — Posted by cndgsnr @ July 23, 2008 11:38
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Saturday and Sunday, Carl’s condition remained pretty much the same. If any changes were noticed, they did seem to be slightly improved, though the diarrhea continued to be persistent.

Monday

I had a follow up appt. at 9am on Monday in Lafayette. Mike took the day off to be able to attend with me. All is good for me in boobie land. In six months we begin the mammogram and ultrasound process again. Both the radiologist and doctor have said that there is nothing to be concerned about UNLESS changes take place in the fibroid-whatever thingy, then I must call for immediate appts.

When we left the appt, the first thing that I did was check my cell phone. I saw that I had a missed call. The missed call was from Hilda. I phoned her immediately. She said that Dr. R. had decided that because the diarrhea was still present, he felt it best that Carl be transferred to Lafayette. By ambulance, they rode to Lafayette. We met them there. By 4pm, all was done and they were settled.

During that settling in, Dr. B (oncologist) came by for a brief visit. He encouraged Carl by saying, “Your job is to work with physical therapy and to EAT. Gotta eat to fight the battle which is right now with the bacteria.”

Hilda said he ate well during the Monday supper.

Tuesday

Though the diarrhea still persists, the bowel movements seem to have decreased in frequency.

Stool specimens are telling us that the bacteria is no longer present.

Gastro doctors visited and said that they may want to check to see why Carl has the sensation of the food not wanting to go down.

Carl ate well from his breakfast tray. He is being given meds and vitamins to help with appetite and nutrients.

Dr. B said that chemo would resume tonight.

Carl’s lunch tray had gumbo. He really likes gumbo. He ate nearly the entire bowl.

Keep those prayers going. Prayers are so very powerful in all of our trials.


Tuesday through Friday

Mr. Carl & Myeloma — Posted by cndgsnr @ July 19, 2008 08:20
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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.


Monday Visit

Mr. Carl & Myeloma — Posted by cndgsnr @ July 15, 2008 07:41
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I arrived at the hospital during mid afternoon to learn that the good news that we’d been hearing had now turned into not-so-good news. (More)

Discharged and Readmitted

Mr. Carl & Myeloma — Posted by cndgsnr @ July 14, 2008 10:16
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On Thursday, July 10, Mr. Carl was released from the hospital after receiving two units of blood and eating what he could from his breakfast tray. They returned home during mid morning. His stay at home did not last long. (More)

Carl was Admitted

Mr. Carl & Myeloma — Posted by cndgsnr @ July 10, 2008 06:16
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Carl went to see his oncologist yesterday, July 9. After one look at him, Dr. B. said, “You don’t look good!”  (More)

Ecouragement Received

Mr. Carl & Myeloma — Posted by cndgsnr @ July 07, 2008 15:48
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 (More)

ATTN: Cancer Patients, Cancer Survivors, and their Families

Mr. Carl & Myeloma — Posted by cndgsnr @ July 06, 2008 17:00
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ATTN: Cancer Patients, Cancer Survivors, and their Families:  God has placed it upon my heart to call upon you to come to my aid.  (More)

Oncologist on 7/2/08

Mr. Carl & Myeloma — Posted by cndgsnr @ July 06, 2008 07:16
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Concerns that we had going into the visit were:  (More)

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