Dad now has some pnumonia beginning in his lungs. His blood pressure is very difficult to keep up. They have an IV medication to increase his blood pressure so they can use the epidural for pain relief, as well as the narcotics, etc. I count 10 different IV lines.
He still sort of wakes up occasionally and tries to move his leg. We know those bruises on his hips are hurting him. The nurses turn him every two hours.
Mom and Cindy have gone to the Cancer Society house tonight to sleep.
Dad needs those prayers, a lot.
This is a blog to keep everyone informed on Dad's Deep Brain Stimulation Surgery in August 2011, and also dealing with malignant stomach endocarcinoma treatment diagnosed November 2011. Brain Surgery Stage 1, 2a, 2b, 3, & 4. Soon the stimulator will be programmed (increased) every three days again with a hand held device. ( Most recent post is on top) Double click on the picture below to go to the picasa picture site. Please click on the archive dates to see previous postings.
Thursday, March 8, 2012
Setback :(
They tried to remove the ventilator this morning but had to put it back in. The epidural has been stopped to help his breathing. Otherwise he is doing ok according to the drs. He can't communicate much at all and mostly sleeps due to strong medications. Mom and Cindy and I are making sure someone is always with him. The staff here at Vanderbilt is great. ( Mindy is working on this floor and she is here today) Drs have been by multiple times. He is getting his Parkinson's meds through the j tube so at least that helps too. Tomorrow he will begin a small bit of nutrition in his j tube. I really really hope Dad will not remember this part. It has been very hard.
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- Posted using BlogPress from my iPhone
Location:Capers Ave,Nashville,United States
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