Carol and her mother Mildred came to visit mom and cut her hair. That just seemed to perk her up and she seems to be doing better and not in so much pain. I don't know how she does it! Just when you think it's about the end, she perks up! Never as good as before. I notice a real difference in her voice. She is taking several different medications so is often a little "hi", but her appetite is back and she is awake probably 5 or 6 hrs a day. She does go to bed at 6 and sleeps till about 8 or 8:30. I think many of us are envious of that. I do have a monitor in her room now so in case she has problems she can call me or I can hear if anything is out of the ordinary.
Sunday, January 18, 2009
Tuesday, January 13, 2009
Choices!
Hospice asked mom if she wanted quality of life and still a little pain, or no pain. She chose no pain.
They have her on several medications including steroids and morphine, but nothing totally gets rid of the pain. She's feeling a little better though. Her bath aid came today and she survived it. Lately she has only been awake maybe 1 1/2 hrs. a day, for meals. Today she has been up a few hrs total. She eats mostly carnation instant breakfast, soups and cottage cheese and pineapple which she craves. She can't be left alone any more so I'm mostly home. Les has been good trading off while I go to the gym. I gave up working at the temple which was really sad, but he is still going. Since she still has quite a good appetite even though not much solids, I think she will be here for awhile. Her attitude is good and she's nice most of the time, just a little demanding. I need to decide what she can do for herself, so that I'm not just the maid. Gee I thought I was done with that when the teen agers moved out.
Anyway hospice has found a volunteer to come in a couple of hours a week, so I can get out a little, and our friends the Overman's have also been good to help. That will be nice.
They have her on several medications including steroids and morphine, but nothing totally gets rid of the pain. She's feeling a little better though. Her bath aid came today and she survived it. Lately she has only been awake maybe 1 1/2 hrs. a day, for meals. Today she has been up a few hrs total. She eats mostly carnation instant breakfast, soups and cottage cheese and pineapple which she craves. She can't be left alone any more so I'm mostly home. Les has been good trading off while I go to the gym. I gave up working at the temple which was really sad, but he is still going. Since she still has quite a good appetite even though not much solids, I think she will be here for awhile. Her attitude is good and she's nice most of the time, just a little demanding. I need to decide what she can do for herself, so that I'm not just the maid. Gee I thought I was done with that when the teen agers moved out.
Anyway hospice has found a volunteer to come in a couple of hours a week, so I can get out a little, and our friends the Overman's have also been good to help. That will be nice.
Friday, January 9, 2009
Getting Worse
They started mom on morphine about 2 weeks ago, since then they have trippled the dose trying to get the pain down. At first that caused vomiting, but I think we have that under control . And of course she's on depends now. We finally talked her into a hospital bed, which took awhile. Her worse pain is in the back, neck and back of the head, so getting up from a regular bed hurts terribly. With the hospital bed we can get her to sitting position before she gets up. Hopefully that will be better. I think the bed comes tomorrow. I have really been feeling burnout and that I am a shut-in, which is really what I am now. I called the social worker today and he is going to get me someone to come in a few hours a week, just so we can get out of the house. Right now, Les and I can't go anywhere the same time, not even church. He starts back at the tax commission for a few months, so I wouldn't even have that. So hopefully between the hospital bed, more morphine and a little help, things will be better. Who knows how long this will go on.
Wednesday, January 7, 2009
More Pain
They doubled her morphine dose and hope that will counteract the pain. She went from 15ml to 30 ml a day and doubled the amount of liquid morphine she could take in between, and she can take that every two hrs as needed. I only hope that helps. It's so hard to see her in pain. Surprisingly though, I was told her appetite would decrease, but so far that isn't happening. She is now eating soup, or cottage cheese and fruit, and other mini meals in between pizza and what ever else she craves. The bath aid is working out well. She even let me curl her hair with a curling iron yesterday. She didn't feel I could do it, but I did and it turned out fine.
Saturday, January 3, 2009
Better for awhile, but going down again
Mom was in excrutiating pain last Sunday, so Monday they put her on morphine. Hospice also started her with a bath aid, because mom just didn't feel she could shower anymore. The hospice nurse found several new lumps. She was still not well for a couple of days, but then seemed pretty much back to her old self. She did fine after the first couple of days with the morphine. Today, Saturday, she is nausious and not feeling well. and pretty awnrey. We will just see what tomorrow will bring.
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