Following the surgery to remove the colon cancer I wasn't able to eat anything at first. Then I was allowed clear liquids. Then I was allowed some soft easy to digest food just before being transferred back to the rehab hospital. During that time I lost quite a bit of weight.
For the time being I'm on a diet of low fiber food to make it easier for my colon to heal. My abdomen is still bloated, but I'm eating as much as I can to regain weight.
I managed to get up into my wheelchair on Wednesday, Thursday and Friday to build up muscle strength. Lack of eating, and being bedridden has resulted in loss of of strength and I want to get built up again as quickly as possible so I can get home to be with DebbieLynne.
Unfortunately on Saturday I had a temperature of 102 degrees. Tests determined it was due to a urinary tract infection. So I didn't get out of bed on Saturday or Sunday. I'm now on antibiotics which should eliminate the infection.
I felt better on Monday (yesterday) and practiced getting from bed to chair and back a few times. We even raised the level of bed a level to make it more like the bed at home. I stayed up in my wheelchair between lunch and supper.
Today I've done two sessions of wheelchair to bed and back transfers. What used to be so easy is now hard work, but should get much easier as I regain strength. I got into the wheelchair after lunch and plan to remain in it until after supper.
I'm also using a device to strengthen the muscles used to inhale when breathing. The better I can breathe on my own and use my arms to do transfers, the better I will be able to do things for myself and DebbieLynne once I get home.
We're hoping I'll be back with DebbieLynne sometime next week. Please pray that will work out. Pray I will regain weight and strength with no more running of a fever. Also please pray for my abdominal bloating to subside.
Thank you for your praying. And thanks again for those who've been helping DebbieLynne while I've been hospitalized now for over two months.
Blog about the love story of a disabled man and woman who are now facing the new challenges brought on by his having been diagnosed with colon cancer,
Showing posts with label rehab. Show all posts
Showing posts with label rehab. Show all posts
Tuesday, June 5, 2012
Tuesday, May 29, 2012
On the Mend From My Colon Surgery
It had seemed like I was making little by little progress each day following the surgery to remove the colon cancer on May 15. But yesterday I was so bloated that it was hard to breathe even with my ventilator. I could barely talk on the phone with my wife.
Why was my condition so much worse yesterday than the previous day? Was the treatment I was getting here at the rehab hospital doing me more harm than good?
Well, I theorized that maybe I had the night time tidal volume on my ventilator set too high. Maybe it was causing air to go into my stomach as well as my lungs. So I lowered the tidal volume and then lowered it some more until it was as low as I could have it and still have acceptable oxygen levels reading on the monitor.
That change made a great difference. When I woke up early this morning I was no more bloated than the night before, and I felt rested and refreshed.
Yesterday I was so bloated they put me back on a clear liquid diet. Today, with the bloating significantly down I got to have a lunch of baked fish, mashed potatoes, well cooked cauliflower, and a small cup of canned fruit. It tasted sooo good!
After lunch the therapist helped me get my back brace on. Then she stood by while I with considerable effort transferred from the bed into my wheelchair. It was the first time I'd done that since the surgery two weeks ago today. Praise God.
Building up the strength in my arms to do transfers is important, so I'll continue to work on that for getting in and out of bed and on and off a commode.
I'll also be working to extend the amount of time I can be off the ventilator. For two months I've had to use it 24 hours a day. It will so good when I can be at home with DebbieLynne and not have to use the vent while having meals together. And in time we hope I'll be able to go venturing outside and even into Boston without the ventilator doing my breathing for me.
Thankfully the new ventilator can be strapped to the back of my wheelchair so I could use it when I'm out. But when it's back there I'm not able to turn it on or off. My respiratory therapist is trying to figure out a way it could be turned on or off without reaching the controls.
My physical problems yesterday were distressing. But today things are looking up again. I wanted to share that with you. That's why I'm making this post.
I abundantly thank you for your prayers and for your caring about DebbieLynne and me.
Why was my condition so much worse yesterday than the previous day? Was the treatment I was getting here at the rehab hospital doing me more harm than good?
Well, I theorized that maybe I had the night time tidal volume on my ventilator set too high. Maybe it was causing air to go into my stomach as well as my lungs. So I lowered the tidal volume and then lowered it some more until it was as low as I could have it and still have acceptable oxygen levels reading on the monitor.
That change made a great difference. When I woke up early this morning I was no more bloated than the night before, and I felt rested and refreshed.
Yesterday I was so bloated they put me back on a clear liquid diet. Today, with the bloating significantly down I got to have a lunch of baked fish, mashed potatoes, well cooked cauliflower, and a small cup of canned fruit. It tasted sooo good!
After lunch the therapist helped me get my back brace on. Then she stood by while I with considerable effort transferred from the bed into my wheelchair. It was the first time I'd done that since the surgery two weeks ago today. Praise God.
Building up the strength in my arms to do transfers is important, so I'll continue to work on that for getting in and out of bed and on and off a commode.
I'll also be working to extend the amount of time I can be off the ventilator. For two months I've had to use it 24 hours a day. It will so good when I can be at home with DebbieLynne and not have to use the vent while having meals together. And in time we hope I'll be able to go venturing outside and even into Boston without the ventilator doing my breathing for me.
Thankfully the new ventilator can be strapped to the back of my wheelchair so I could use it when I'm out. But when it's back there I'm not able to turn it on or off. My respiratory therapist is trying to figure out a way it could be turned on or off without reaching the controls.
My physical problems yesterday were distressing. But today things are looking up again. I wanted to share that with you. That's why I'm making this post.
I abundantly thank you for your prayers and for your caring about DebbieLynne and me.
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