Tuesday, August 19, 2008
Look What You Can Buy in Santa Cruz
I am a reader and often the only thing in the suitcase coming back from Canada is a load of books. Imagine my delight when I walked into the local grocery store and found a new selection of English books -- Vinyl Cafe Diaries by Stuart McLean, a Sunday at the pool in Kinglali. Yes, there would be a market for those and a variety of other English books. But Wayside Flowers of Alberta and Animal Tracks of Alberta? If anyone wants a copy for just under five dollars (I didn't say they were cheap), I will get you one.
Saturday, August 16, 2008
The Last Chapter
Monday, August 11, 2008
Isolation
Jhonny has two serious infections -- chicken pox and a severe urinary infection. The chicken pox is running its course and they are treating the urinary infection. Aside from that he is suffering from seizures related to the operations. These seizures are happening every five minutes and cause severe body contortions that also affect his breathing. When the seizure subsides Jhonny needs to be lifted back into a laying position. Because his mom is short she has difficulty doing this.
We talked to the specialist today and he is hoping that within a week or two Jhonny will be able to be transferred to the hospital in Yapacani and then to our house. He will need at least three months to rebuild his energy before they will consider radiation.
The lack of knowledge about brain surgery is quite evident. Only the specialist really knows what is going on and the rest of the doctors are on the same learning curve as we are. Thanks to the internet I have been able to research what is happening. Although it seems like ages to us it has only been six weeks -- not an unreasonable amount of time for brain surgery.
Thursday, August 07, 2008
Same stuff -- different day
Today Jhonny was moved to another part of the hospital -- into isolation. He has pimple-like spots on his body and they are not sure what is causing them. His room is very nice but he isn't enjoying it. He still is not responding except to noise and touch.
Because he has been in bed and inactive for so long his limbs are atrophying. It is very hard to move his legs at the knees although moving them does bring about a negative reaction. His hands are clenched, rigid, and bent backwards. When he lays his body is arched and his head lays at a peculiar angle. No matter how many times we straighten out his body it returns to that angle. His teeth are clenched and he often is grinding them.
It is hard to go every day and see no change. It is hard not to be discouraged. This is also affecting Erselia and she was very eager to go home for a day this week. It is the first time she was willing to leave the hospital for any length of time. We left Tuesday night and came back Thursday morning. Erselia was able to spend a day with the rest of her family and enjoy the Independence Day celebration in the community.
When we came back today Erselia and I talked about the future and she said she did not want Jhonny to continue to suffer. They want to know what his quality of life will be before they continue with more treatments, especially radiation. Our new challenge will be to get an answer to that question.