I started this blog as a place to write my reflections on whatever subject came to mind. Since December 2013 I have been the primary caregiver for my mother. My world has changed since then and much of what I write has to do with this experience. I look forward to reading your comments.
Thursday, December 13, 2012
Chemo: Cycle 1, Day 4
It was also beauty appointment day. A wheelchair came in very handy. Later, we went to the Doctor's office. Oh my goodness, so many details! Getting Mother in and out of the car is a real treat. Oxygen bottle, tubes, wheelchair, lock the wheels, adjust the foot rests, back up, move forward. It gets to be funny some times like a Laurel and Hardy routine.
Next week is going to be busy. The lump in Mother's breast will be biopsied. Our heads are spinning with details about blood tests, biopsy, going to St. Pete's in Olympia on New Year's Eve day to have a "pick" inserted, and medication adjustments, and scheduling the next chemo dates.
Nevertheless, Mother is sitting up. She wants a hamburger for dinner. As they day goes on, she gets stronger. Thanks be to God!
O Lord, your compassion never fails and your mercies are new every morning: We give you thanks for giving our Mother both relief from weakness and renewed strength. Continue the good work you have begun; that she may increase in bodily strength; through Jesus Christ our Lord. Amen.
Wednesday, December 12, 2012
Chemo: Cycle 1, Day 3
Guilt and shame are really stupid companions during these times. I could have showered and tossed a load of clothes in the laundry before going. I realized this later in the day. I knew Mother was not in critical need, she was breathing and able to talk, She didn't complain of aches and pains or fever. The extra 15 minutes would have been better spent. But, this is 3 pm hindsight along with the realization that the caregiver's self-care includes showers and laundry.
When I do arrive it is clear that this definitely is the third day of treatment. She feels tired, hardly has any energy. No fever, but a little bit clammy. She can get up and walk to the bathroom, but needs to hold on to my arm as she returns to bed. Today, fluids and nutrition are the key. Actually, that's my goal. Mother's goal is to stay in bed and sleep as much as possible. Every now and then, she announces that she is getting better, especially if one of the family has called in. Then she announces loudly enough for the person on the other end of the phone to hear.
Her breathing is more labored when she sits up or walks. This is something to watch. She breathes easily when sleeping and her oxygen is on. I'm going to look for an oximeter later today.
Tuesday, December 11, 2012
Chemo: Cycle 1, Day 2
The day was planned so nicely - shot at 11:30, nice lunch somewhere and then return to Mother's apartment to finish the Christmas decorating. Well! Come 10:45 Mother gets a "where are you" call from the Imaging Center. Turns out she had a 10:30 mammogram appointment and nobody told us! Of course, it all got sorted out so Mother could have shot first and mammogram second. I suspect lunch at a restaurant is out of the question.
Mother's feeling a bit weak today. Her breathing is a little more labored today. It's hard to know if the fluid over her lung is building up again or if the side effects of chemo are kicking in. My guess is probably both.
Lord Jesus, you give us ears to hear and hearts to love, we pray for discernment to give her the proper care and loving words. Amen.
