Good evening to all
How are you all? Hope all is well, here it is very cold, -23C. Andrea had a so so day, the Maxeran anti nausea seems to help, although she cannot handle the smell of food. Yesterday the doctors told her she might need an NG, or naso gastric tube put in to be able to get nutrition into her stomach as she is not eating at all. Since last Wednesday she has been getting all her nutrition by IV, but they don't like to do that long term because it is hard on the liver. So today they told her that today sometime they would like to put one in. She plead and begged them to wait till tomorrow as she was really dreading it, but the tube went in. It is quite uncomfortable and unsightly, it bothers her talking and swallowing some too. I told her that she had endured much bigger and scarier things before and that she would get used to it eventually. After they got it in she slept for 3 hours and was asleep again at 9;00pm. Now it is time to shut down here so good night to all.
thanks, Maynard
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"We Love Andrea" was created to update Andrea's friends as she went through a difficult journey. After her second heart transplant when her pulse began to speed up she was given a pacemaker, then a Heart Mate II or LVAD. She was in the Stollery Children's Hospital, then the Mazankowski heart unit in Edmonton, Alberta for 7 months. However, she peacefully died on May 11, 2011 when the rest of her heart and other organs could handle the strain no longer. If you come to this blog, pray for her family and friends, remember to tell your friends you love them, then sign your organ donor card.
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