Saturday, August 28, 2010

Post op pathology

Wednesday was the day I returned to the doc’s office for removal of the catheter, and an update on the pathology on the materials removed during surgery.
Evidently the cancer was aggressive, and the concern now, is whether or not it has spread to regions outside the prostate; there might be a 50% chance that it has. He said the latest science would indicate the best course of action is to follow the surgery with a round of radiation in a few months.
I also scheduled my first post-op PSA test for September 30; It is the hope of every post op guy that their new PSA number will be close to zero; close monitoring of the PSA will continue for the next two years, I suspect.
There might be not much to report on this blog in the next couple of weeks, but if there is, this will be the place to read about it. Feel free to posts your own comments, and sign up for update notifications on the wiget in the right column.

Monday, August 23, 2010

What's next?

Ron is getting stronger by the day. He is feeling much better, sleeping better, and able to eat normal food.

We have an appointment with the docs on Wednesday (August 25th.) Ron will have a post-op check and they will remove the catheter. The pathology report should be back at that time as well. This will tell us what happens next. It is our hope and prayer that the cancer was fully contained inside the prostate gland so that radiation won't be necessary.

More later....

Saturday, August 21, 2010

First Full Day at Home after Surgery

The photo is one that I took at Mt Adams last week, it was from a series of shots early in the morning, and put together in Photoshop.
Last night was the first night at home post surgery. It was a difficult night, partly because I did not know what to expect from my body. But I am told that my experience is fairly typical. It is amazing how, for a normal person, the digestive system does "what it does" since birth, but in the traumatic changes brought about by surgery, some of these functions seem to be confused, and need to be retrained.
I have tried to talk to others that have been through the same procedure, to compare my experience so far with theirs, and to try to get a sense about what is ahead. I'm a little nervous, but given the fact that I am in God's hands, and I feel that I had the best care any person could have in the northwest, I am confident for an overall good outcome.

I would also encourage you to post responses to any of these notes, as you think of encouragements or personal experiences others can benefit from.

Friday, August 20, 2010

Home at last!

Ron was able to come home this morning. He is a bit exhausted from all the excitement that goes along with checking out of the hospital. He is eating regular food and we just took a short stroll in the sunshine. Now he is resting. You will hear from him soon!

Thursday, August 19, 2010

One more day....

The nurses are enjoying the Mahan sense of humor SO much they decided to keep Ron around for another day. Hopefully, he will be able to come home tomorrow. He is doing well considering they still won't let him eat anything other than funny looking soup, cream of wheat, oatmeal, jello and pudding. He was allowed juice and coffee! Yippee!!

He was up and around quite a bit today. In fact, another patient was quite impressed when Ron "lapped" her on the hospital race course.

That's today's news. Soon Ron will be able to give you his perspective of this adventure.

Wednesday, August 18, 2010

Surgery Day

Ron had surgery yesterday. (Tuesday, August 17th) According to the doc, all went well. He was able to use the robot for the entire surgery. The doc was able to remove the prostate gland while preserving the nerve bundles that surround the gland. His only concern was the left side of the prostate gland looked "a little ragged on the margins." The left side was the side that showed 70% cancer cells in the biopsy. We will wait for the pathology report to come back next week for the results.

Ron was up walking about the hospital last evening. No rest for the weary!! One of his complaints is he can't eat until noon today. And then he can only have yummy stuff like jello!

Our long-time friend Kathleen came to the hospital and waited with us for the better part of the day. Aly arrived yesterday around noon. Aaron is here... Drew was sent to Medford, Oregon on Monday to fight a fire in that region. It's great having at least 2 of the kids home.

Ron is scheduled to come home tomorrow. We appreciate your continued thoughts and prayers during the recovery phase of this adventure!