— Rainycat (@rainycat) June 6, 2010
While on the mend, I finally wrote my first blog to the world via dictation to my family. I remember saying the words with tears in my eyes. Of course it had to be Hello World, as there was nothing more fitting. The joke about hospital food was my injection of humour, although I have to say the hospital kitchen/restaurant really looked after me while I was there. I was given quite plain food but they kept checking about my allergies all the time. Actually far more than the doctors (as you will see in the next week)
It was great being able to talk again although I still have the trach scar, which will never go away now. I couldn’t explain how much the cards and comments meant to me and my family. I was kind of overwhelmed to know I had touched so many peoples lives and they in turned felt it was worth reaching back.
I was looking forward to moving out of ICU because this about the time when I started really getting better really fast. It was like my body was just repairing its self at a rate the hospital had never seen before. Amazing when you consider the life expectancy of people who have bleed on the brain
If subarachnoid hemorrhage from aneurysm, about 50% die within the first few days in hospital. If intracranial bleed, with/without stroke, the death rate within year one approaches 60%. Figures have remained constant for years.
I am one of the very few lucky ones and believe me don’t I know it, and there is no way I will forget it
😀 @cubicgarden speaks: "hello world": http://ur1.ca/05mha
— Tim Dobson (@tdobson) June 6, 2010
[Message below was dictated by Ian this evening, no internet connection in hospital]
‘Hello world! Thank you very much for taking the time to find out how I am doing. I am doing okay. I am still in hospital, but making a positive recovery. Thank you to everybody who has written to me and my family and thanks for writing such amazing things.
The trach tube is out and I can speak again. The feeding tube is also out. I had solid food for the first time yesterday–it was horrible! Of course it was hospital food.
Thank you for all the messages to my family. I’m on the way to recovery.’
[Ian is due to be moved out of ICU and on to the ward as soon as a bed becomes available.]
Ian is continuing to do well and they are hoping to move him out of ICU and on to the ward soon (possibly this weekend). He was a bit tired today and slept more, but he did spend most of yesterday out of bed and sitting up.
Ian’s flatmate Tim brought his laptop in for him, but there is not a wireless connection to use so Ian will not be online yet.
Unfortunately Ian missed some visitors today because he was sleeping. For anyone else who is visiting, please be aware you might not get to see him if he is tired, but we do appreciate you coming to visit!
They hope to put some sort of valve into the trach tube that will make it possible for Ian to speak, but I am not sure when they’ll do this.
At the moment Ian is still in the ICU. They had thought they were going to move him to the H.D. unit, but there wasn’t a bed available, so for now the plan is for him to stay in ICU until he is ready to move to the ward.
Ian is ready to have visitors now, but in ICU this is limited to two people at a time. If you want to come visit, please leave a message in the guestbook letting us know what day and time you plan to come (and please leave a contact number in case we need to reach you). Visiting hours are from 1pm-9pm daily. They are quite strict about what can be brought into the ICU due to infection control.
Ian still cannot talk due to the trach tube so it can be difficult to communicate with him. He is finding it frustrating, but appreciates visitors coming as he is getting bored.