Saturday, October 25, 2008

Beginnings and endings

Today, the weather turned very nice in the afternoon, and, looking out the front window, I was struck by the intensity of the cherry tree fall colours on our street. I recalled the nice spring colours and thought I'd post a couple of pictures. For good measure, the rainbow which appeared late in the day a few days ago is also shown. Nature's way of displaying the constant beginning and the ending of life.



April's finery














October's dress















Can you see the rainbow's reflection on the raindrops?

A little outing

Yesterday evening, we invited Derek, Airdrie, Marina, and Lauren to dinner, keeping in mind that Derek has to watch what he eats. He decided that Earl's would be a good place; so we all went there. Derek enjoyed his "Alfredo" noodles, and each one of us had our own individual food choice; all chosen menu items were very well prepared. It's good to see that Derek is on the way to eating more normal food.

After dinner Derek and family went to see the "High School Musical III" movie, which Marina and Lauren were anxious to see. I'm sure they all had a good "quality time", something that Derek has had to largely forego while fighting his cancer. He's in the middle of making some very important decisions regarding what treatment direction to take. You may want to read about this on his blog at http://www.penmachine.com/2008/10/to-fight-or-to-live. As Derek's parents, we are very much concerned, of course; while we can, and have, provided family help, it hurts to be unable to directly contribute to his fight and to his hoped-for recovery. His cancer is always on our minds. We'll support him in whatever decisions he makes.

Thursday, October 16, 2008

Resting

Derek's resting today, and will post only a little. He is feeling somewhat tired, and will likely spend the next few days mostly sleeping, I would think.

It's great having him back home. We're all relieved that the surgery has not resulted in some complications, and we hope that will continue.

Wednesday, October 15, 2008

Taking a rest

Derek is home now. Things have improved sufficiently for him to continue his recovery away from the hospital.

He was going to continue resting, but I think he'll be posting something on his blog in short order.

We're all glad to have him back among the family.

Tuesday, October 14, 2008

Coming home.

Derek had some more substantial food today - some pasta noodles and another one of his favorite scones from the hospital cafeteria. His pain is much diminished, and he's handling it with regular Tylenol. He's also managing his diabetes himself again - the nurses agree that he knows better than anyone regarding the timing and amount he needs.

His bowel movements are still minimal. With the more solid food today the expectation is that he'll be more active "down below". If all works out, he'll continue his convalescence at home, starting tomorrow. It'll probably take about 6 weeks before he'll be back on his regular diet. In the meantime he'll be on the same kind of diet as the one he was on when he got his ileostomy bag attached. Now that it's been removed, he's looking forward to a more normal life, without the restrictions that the bag imposed.

I expect he'll be posting soon.

Monday, October 13, 2008

It's a gas

For those who've read this post before: check the update below.

Derek phoned, asking us to bring him some of his favorite broth from a delicatessen located on our way to the hospital. Apparently, the doctors have decided that some more substantial, though still liquid food is indicated. And the indication is? Well, there has been some activity at Derek's "lower end" - he's passed some gas. Who would have thought that "breaking wind" would ever be cause for celebration? In any case, we're happy to fulfill Derek's wish.

Mothers, being mothers, will always think of their children in need of motherly help, regardless of how old their children are. Our mothers were the same - I remember it with great fondness and a sense of nostalgia and a little sadness. That is why, in addition the requested broth, my wife is also preparing some clear beef broth and some clear chicken noodle broth here at home to take to Derek in thermos bottles. There is a chance that the delicatessen is closed today (Thanksgiving) - and she wants to cover all bases. Derek can always rewarm the broth in the microwave oven located in the "patient room" on his ward.

More later.

Update at 15:20 (3:20pm): We've just returned from our visit with Derek. He consumed, with obvious relish, the chicken soup broth we had picked up from the delicatessen. He also had the cream of potato soup which came with his dinner tray, along with some ice cream, and asked us to get him one of his favorite scones available in the hospital cafeteria (he's been in that hospital often enough to know what's available there). Liquid food is still the order of the day, but that scone apparently "melts in his mouth" (he really likes them). It's great to see him having a good appetite.

I expect that some more substantial motion will come soon "down below". His surgeon came by to check on him, as he has done every day (he has the best specialist gastro-intestinal surgeon - every doctor we talk to tells us so). The surgeon said: "you poop, you go...", meaning that Derek'll be discharged from hospital when things get to that stage. Derek thinks that it won't happen until Wednesday, and he won't leave prematurely, because when he did that before, he was back in the hospital a couple of days later .

Airdrie and the girls are going to visit Derek this evening. I think that it's possible that Derek might feel well enough to get the hospital's computer room; in which case he'll likely post a bit himself.

More tomorrow.

Sunday, October 12, 2008

More today

Derek is making good progress. He's off the intravenous line and has had some vegetable broth. His portacath has been reactivated, in case he needs some intravenous treatment. No motion yet below; it usually takes a few days for any activity, after operations like this.

We had (decaf) coffee together this afternoon, and took a walk around his ward floor. He's doing this several times a day now, it's considered to be good physiotherapy. Any pain is now controlled by Tylenol three alone.

It is a measure of his good spirits that we discussed the various political parties competing in our elections on Tuesday. If he were in pain, he'd not be interested. He was also happy to receive copies of the latest news magazines (MacLeans)- we subscribe to it. He also keeps up with current events by watching television.

We hope his recovery continues on like this. More news tomorrow.