Saturday, July 31, 2010
My Stem Cells Are Back
The whole process took about two hours. The three bags of stem cells came inside a liquid nitrogen container. It looked very science fiction. Each bag was defrosted in a warm water bath and added to my drip line. At that point it looked like a regulare blood transfusion. There were assorted other drugs added to the drip to prevent vomiting and to prevent other side effects from the preservative they had added to the stem cells for freezing. That was all over bt 10:30 AM. Now the stem cells have to find their way into the bone marrow to replace the ones we killed two days ago.
Thursday, July 29, 2010
Chemo Is Done - Now the Fun Begins
The chemo drug (Melphalan) was put in through my port yesterday afternoon. I got 1000ml in one hour. To minimize the mouth sores that are coming, I had to make my mouth as cold as I could stand. I kept crushed ice in my mouth from 30 minutes before, to 30 minutes after the chemo infusion By the time I was done, it seems as if my speach was affected from my frozen mouth. Boy, did I pee for a while after all that ice! All of the potential side effects will take 3 to 12 days to show up. My hair loss will happen in abut 2 weeks. I do not have any side effects today. Today is a day of rest. My stem cell infusion will be tomorrow (Friday).
Wednesday, July 28, 2010
Checked Into Mayo Hospital Today
OK, it begins. We checked in today (7/28). The high-dose chemo will begin at 4PM and will take a couple of hours. The biggest concern for today is the potential mouth sores that 'may' develop from the chemo drug. To fight that, I have to suck on ice chips before, during and after the chemo treatment. They say that if I keep the skin in my mouth really cold, the mouth sores will be minimized. We will see....
The Bleeding Has Stopped
Good news! The bleeding has stopped and the nurse that did the last cleaning was gental and did not open the wound again. I hace two days off before we check in on Wednesday for the chemo and stem cell infusion.
Sunday, July 25, 2010
The Central Line continues to ooze.
Every time they clean the catheter, they distrub the stitches and it starts to bleed again. Then the dressing gets full of blood and it has to be changed. It stops bleeding over night. Then they clean it and it starts to bleed........... I have been to the Hospital to have the dressing changed three times since Tuesday and this is getting old! When I go in Sunday (7/25), I am going to suggest that they do not clean it. Just change the dressing and let me go until I check-in for the procedure on Wednesday, 7/28. Clean it then so that I don't have to drive again for a dressing change every day.
The Harvest is complete on 7/22.
Yea! Another 5 hour session, and there were enough stem cells harvested to stop. The goal was 8 million cells. We got 5.1 and 4.3 over the two sessions of 7/21 and 7/22. There were 4 sessions scheduled just in case I needed them.
The Harvest Started 7/21
They started to harvest Stem Cells Wednesday, 7/21. I was hooked up to an Apheresis machine for 5 hours! The whole process looked very similar to a Dyalisis process. My blood was sent thru the machine, the stem cells removed, and the blood was returned to me. Did I say that I sat there for 5 hours!
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