CAREGIVING: The following few weeks in June had their ups and downs but at least it wasn’t the roller coaster that it was when Kathy was in the hospital. There is a routine that we got into and although there are always changes and tweaks, a schedule helps a Huntington’s Disease patient. It is one less thing to get anxious about,… Read more →
Tag: PEG
First days home
CAREGIVING: The first few days home were generally pretty good. I guess anything was better than pneumonia in the hospital. But this is still Huntington’s and we are biding time. The first morning was my first poop clean up since the feeding tube started. Took some getting used to but it wasn’t bad. Some of the neighbors called to… Read more →
TGIF? Coming Home
HOME / June 6th: Friday morning was an anxious time. I wanted to be with Kathy, but had to be here to direct everything. A guy from Baystate Infusion called about delivering the suction machine and then someone called about the feeding pump and supplies and wanted to make sure some one was home. They called from the hospital and… Read more →
We’re sending Kathy home, today. Huh?
HOSPITAL / June 5th: In the morning, before I went to my doctor’s appointment, I got a call from the discharge case manager at Baystate. “We are trying to arrange to send Kathy home today, Thursday. ” I said,”Huh? What about the rehab place?” “No rehab. Dr. Kampe talked with Physical Therapy and they said she is good to go home.”… Read more →
Movement
HOSPITAL / June 4th & 5th: The next two days were consumed with getting the house ready and making sure Kathy was ready for her return trip home. Her feeding rate was gradually increased from 25 ml/hour to 35 ml/hr until she was doing fine with 55 ml/hr. At the same time the nurses were training me to administer her meds… Read more →
A Good Day
HOSPITAL / June 3rd: Tuesday morning Trisha and Mary stayed at the house to do some “rearranging.” They cleaned, folded and vacuumed and they had some ideas of where to put things so that my caregiving might be easier. They were worried that they were disrupting my method of doing things. Not to worry. I think almost everything is where they repositioned… Read more →
Feeding tube
HOSPITAL / June 2nd: I’m writing this from notes and memories. On Monday, they put the feeding tube in. I was actually driving to the hospital when the doctor called. He was trying to say he wanted her in for a follow-up visit in a week or two to take out some stitches. Thinking about the trauma of ambulances to and from… Read more →