Another good day for Pops, praise God. He went from three hour breathing sessions yesterday to...five hours today! Unbelievable! They now only take him off the respirator twice daily, but for five hours each time. We couldn't ask for any better than that...a two hour jump in independent breathing is awesome. Although he is exhausted, dad seems to understand that this is good progress.
He also got a power wheelchair today, which means he can sit for longer periods and recline at regular intervals to prevent excessive pressure on his body. Tonight he would doze off for awhile, then wake up, look down at the wheelchair control at his right hand, and ask me "How do I run this thing?". I told him he would learn how, but he has to be disconnected from all tubes before he can go cruising around. He would give a smile as if to say, "yeah, I know", and then doze off. I think he's just happy to finally be around something with a motor in it. His quote of the day came when mom and I were with two of his nurses talking about his new power chair. He piped up and tried to ask what we thought was a serious question. After the third try, we finally got it. His serious question was, "Does this thing have blinkers?"
He was also able to talk a little more today when being taken off the respirator. You can tell it's a huge deal for him to talk. His voice comes out very raspy and, quite honestly, a little freaky. He was relieved to know it was only temporary, that when he's done with the trach his speech will be effortless and his voice back to normal. Until then, his odd voice, along with the fact that the breathing treatments cause a slight fog to come out of his mouth when he speaks, gives the eerie impression that dad is in fact a dragon. Probably not good for the grandkids to see him quite yet! But it's all great news, and so encouraging to see him happy with his own progress. He knows that he's slowly getting better...and that does wonders for his overall attitude.
So thanks be to God for a positive day. I can't help but smile as I am reminded of his funny comments and sweet expressions. All such tiny things that I took for granted a month ago. Thank you God for opening our eyes to the many reasons we love our dad.
Pray for more healing...more progress. Pray for changing hearts. Pray that dad doesn't figure out his power chair control in the middle of the night and pulls all his tubes out as he shoots across the room...
Wednesday, January 3, 2007
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4 comments:
http://www.mayyoubeblessedmovie.com/ go to this website for my wish for you. Carol Foss
Thank God for the wonderful progress today.
Also thank God for putting Pat together with a motor again. He out to love that.
Most of all we will keep praying for all of the Bohrmans.
well, stearns...i can sleep better tonite since we talked...and talked... and laughed and laughed. what a neat thing to have shared back then as well as now....guess who?? hint: the queen blogger
amy, your comments each day are excellent. such an honest, transparent and funny style. you capture our attention and hearts as you journal your days. what a special gift and delightful talent you have been blessed with. so many of us wait for the daily update and are so eager to lift up your family in prayer. i can see pat checking out the wheel chair and looking for the blinkers. he will probably end up inventing many things along this journey that will benefit others. that's your dad. always giving of himself with such a servant's heart. how awesome that you all love him just as he is and remember all of his unique expressions, comments and mannerisms. that is so special. humor goes with the bohrman family. i have spent many hours laughing with the bohrmans. joy defines your precious family. linda lentz
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