>The news that I had not been turned on was a schock as well as a relief. Five miutes later I was a functioning human bbeeing again, not only a shadow of what may have been.
Now I had some great weeks and months ahead. I even went on holiday to Milan together with my 13 year old daughter, which was great, even though we never got our luggage (before the morning we were going home!) and it was rather hot all the time.
During summer, my status as a patient was also moved from Rikshospitalet to Haukeland.
Mr Parkinson, I presume
Notes on mr P and his whereabouts
Why this blog?
It is a substantial decision I take when I start this blog, making my own situation a public matter. But I believe to be frank and open-minded as superior to the opposite. Of course I hope to aquire certain advantages from this blog mysef, why would I care to invent it if not!?
First and foremost my ambition is that this will be a place to share thoughts, despair, frustration, yes; anything u or I find of relevance to include. To reach as many as possible I find it necessary to edit this part in English.
Also I do not deny that I would like to produce some fiction where a character suffering from Parkinson will be central, and I will as time goes by probably share thoughts on this baby to be, as well as try out passages on you. This part will have to be in Norwegian as I do not master English well enough to write stories.
mandag 6. juli 2015
søndag 14. juni 2015
After 14 months I start to feel like a human being again...
Its been a long time without me posting anything on this blog.. but now I will try to get across a rather short summary about what has taken place since I indeed went through the deep brain surgery on April 2 2014.
The operation itself was a success, at least thats what was said afterwards and what I must believe of course. Exhausting it was; probably the fact that it takes about 8 hours will see to that in itself. I had a bad experience at the post operation unit, but I do not believe I can say much about it as I was heavily drugged at the time.
After approximately 1 week I was feeling fit enough to go home. And coming home was probably so welcoming in itself that I felt much better than I really was. Anyway one of the first days after coming home I crashed my car. You may find it strange that I was driving at all at the time, but I as I felt great compared to some weeks earlier and NOBODY had said a word about avoiding it , I did not regard it as a problem. Luckily, I only drove my car into another car waiting for a green light and at such low speed that it only resulted in minor damages on the cars.
Then the true problems occured. Day by day I felt weaker and generally out of shape and having some bad dreams at night; being convinced that the house I stayed in was about to burn down.. This led to at least one new stay at my local hospital (Haukeland). Several doctors checked me but nobody found anything to be wrong. After some more time without any improvement, my regular doctor managed to get me back at Rikshospitalet where I of course was operated. The day after my return there they told me that apparently the power regulating the sensors in my brain had not been turned on after the operation, so that the good feeling I had in the beginning was a sort of placebo effect and at the same time making it very understandable why I had not been functioning well after some weeks (This took place approximately four weeks after the operation).
(To be continued)
The operation itself was a success, at least thats what was said afterwards and what I must believe of course. Exhausting it was; probably the fact that it takes about 8 hours will see to that in itself. I had a bad experience at the post operation unit, but I do not believe I can say much about it as I was heavily drugged at the time.
After approximately 1 week I was feeling fit enough to go home. And coming home was probably so welcoming in itself that I felt much better than I really was. Anyway one of the first days after coming home I crashed my car. You may find it strange that I was driving at all at the time, but I as I felt great compared to some weeks earlier and NOBODY had said a word about avoiding it , I did not regard it as a problem. Luckily, I only drove my car into another car waiting for a green light and at such low speed that it only resulted in minor damages on the cars.
Then the true problems occured. Day by day I felt weaker and generally out of shape and having some bad dreams at night; being convinced that the house I stayed in was about to burn down.. This led to at least one new stay at my local hospital (Haukeland). Several doctors checked me but nobody found anything to be wrong. After some more time without any improvement, my regular doctor managed to get me back at Rikshospitalet where I of course was operated. The day after my return there they told me that apparently the power regulating the sensors in my brain had not been turned on after the operation, so that the good feeling I had in the beginning was a sort of placebo effect and at the same time making it very understandable why I had not been functioning well after some weeks (This took place approximately four weeks after the operation).
(To be continued)
onsdag 5. mars 2014
Four weeks!!
I woke up at four last night thinking I would rather sleep but in the same moment realising I could not because my attention was immediately drawn to this fact: Four weeks to go! (Should I set up a will?) If I do not get something to sleep on at the hospital I will surely not sleep much and after all I am supposed to stay awake during the operation! What seemed so simple on paper is really beginning to grow into something I am afraid I can not handle, especially because I feel very much alone. A grown up man is not supposed to be asking desperately for some sympathy, but I can not hold it back: I thought this blog would help, but it does not because nobody gives any response even if I only ask for some simple advice. Being neglected when begging for attention is sad.
Still, perhaps this is only Mr Destiny poking his nose at me, after all its only a few days gone since I turned down an offer from some of my best friends to help me out in some troublesome money matters which also occured because of MrP. So who am I to expect anything?
Luckily, as I woke up last night, I did not dream what I have been dreaming over and over during the last weeks, a nightmare surely. I dream that I wake up in a strange house which I anyway know where is. I feel trapped and I can not or -rather- am not able to find a way out in the unfamiliar surroundings.I have this strong notion that I must leave in a hurry or something terrible will happen. Some mornings I awake trying to find my way through the wall...
Still, perhaps this is only Mr Destiny poking his nose at me, after all its only a few days gone since I turned down an offer from some of my best friends to help me out in some troublesome money matters which also occured because of MrP. So who am I to expect anything?
Luckily, as I woke up last night, I did not dream what I have been dreaming over and over during the last weeks, a nightmare surely. I dream that I wake up in a strange house which I anyway know where is. I feel trapped and I can not or -rather- am not able to find a way out in the unfamiliar surroundings.I have this strong notion that I must leave in a hurry or something terrible will happen. Some mornings I awake trying to find my way through the wall...
søndag 2. mars 2014
The fear that I will not be fit for the operation
Today it is March 2nd. In exactly one month I will be on the operation table. Will I be cool enough to try to crack some jokes like Michael does in the film? I doubt it. Anyway, my main concern now is to get my body up on that table on schedule. I was reminded that this isn't happening if I am not fit when I woke up yesterday with a clear understanding that I do have a back.. Tha last time I felt more or less the same way was two years ago, and I had to undergo several treatments by the local chiropractor to be on my feet again without mobilizing everything to keep up the pain. So what am I to do now? Hopefully it will disappear (the distinct feeling that I do have a back) in a few days, but if not I suppose I must see the expert? Or should I see him anyway? What will yor advise me to do?
tirsdag 25. februar 2014
Some thoughts after lunch today
Today has been busy and I might fall asleep writing this at 21.30, be warned!! But I would like to say a few words about some hours spent together with a small group from the Parkinson family, who came together at a cafe in Bergen, having lunch together.
We shared views on different topics of course, and as always it is particularly interesting to hear what experiences and thoughts people in more or less the same situation as yourself have. Talking about the operation I face, it seemed that the persons in this group had very similar experiences in our meetings with the Norwegian Health system. There were many episodes mentioned to underline an obvious weak part; the way the system is organized. From my own list I will mention that I posted a letter to Rikshospitalet in December last year, which they still have not answered, sort of. I did get an answer because I asked the ombudsmann for patients to look into this on my behalf. It is sad that we have to find a whip to get a response..
On the other hand, when we meet persons working in the system, we all feel that we are seen as individuals and treated with respect and understanding. We know that this is just as important and we are very grateful to be able to meet up for something and expect that it will be a new good experience. This is building confidence, which can not be measured in money when it comes to the health deparment!
We shared views on different topics of course, and as always it is particularly interesting to hear what experiences and thoughts people in more or less the same situation as yourself have. Talking about the operation I face, it seemed that the persons in this group had very similar experiences in our meetings with the Norwegian Health system. There were many episodes mentioned to underline an obvious weak part; the way the system is organized. From my own list I will mention that I posted a letter to Rikshospitalet in December last year, which they still have not answered, sort of. I did get an answer because I asked the ombudsmann for patients to look into this on my behalf. It is sad that we have to find a whip to get a response..
On the other hand, when we meet persons working in the system, we all feel that we are seen as individuals and treated with respect and understanding. We know that this is just as important and we are very grateful to be able to meet up for something and expect that it will be a new good experience. This is building confidence, which can not be measured in money when it comes to the health deparment!
mandag 24. februar 2014
Motivated for the operation?
As we see in the film about Michael, he is highly motivated to go through this operation, in his own opinion as well as others, among them the surgeon Brian Koppel. I believe I am more or less at the same motivation level as Michael because I recognise his strong will to function better in everyday life.
Many tell me that they think I appear almost as I am not sick. Yes, thanks to all the pills I swallow every day thats true. But I already suffer considerably from side effects and I fear there will be an increasingly higher cost using extreme doses of medicines.
I am highly motivated because I know that the operation will remove a large amount of the medicines I am addicted to today. (I use 'addicted' in order to stress that to me there is no third option from my point of view; Its to use heavy doses of medicines as I do today or having the operation. The reason for this is that I by now without medicines function so inadequately that I would soon have to be nursed if I experimented with alternative medicine.)
I also know that after the operation I do not have to wait for the medicines to work every morning ( it takes at least 1 hour, on average 1 1/2 hours). This time is more or less wasted today. In fact I may have the electrodes on all the time if I like, the only drawback being that I will have to get new batteries in the pacemaker more often than if I save some by turning it off at night.
I think/hope/believe that I will function on a higher level than today, most of all because I will probably have more staying power than today, which, believe me, is not much. To not get very tired from doing very simple things like writing these lines, would be nice! This will also effect my ability to have a small position at work, which is important for many reasons.
I also hope I will sleep better, as Michael says in the film you get wired from the medicines, and on average I only sleep 3-4 hours a night.
A substantial drawback connected to the medicines opposed to the results of the operation, is that the effect of the one medicine (Stalevo) ends very abrubtly, meaning that if I forget to take a new pill in the interval, I experience a flashback with very demanding fluctuations. The opposite will surely awaken some of my old self, being able to handle more situations in a good manner.
I must admit that it is a sort of relief to hear the surgeon that operated Michael, pointing out the scariness we all will feel facing an operation in the brain. Yes, I am scared, and I will certainly be even more so in the weeks to come, but I am also confident that it will be a success!
Many tell me that they think I appear almost as I am not sick. Yes, thanks to all the pills I swallow every day thats true. But I already suffer considerably from side effects and I fear there will be an increasingly higher cost using extreme doses of medicines.
I am highly motivated because I know that the operation will remove a large amount of the medicines I am addicted to today. (I use 'addicted' in order to stress that to me there is no third option from my point of view; Its to use heavy doses of medicines as I do today or having the operation. The reason for this is that I by now without medicines function so inadequately that I would soon have to be nursed if I experimented with alternative medicine.)
I also know that after the operation I do not have to wait for the medicines to work every morning ( it takes at least 1 hour, on average 1 1/2 hours). This time is more or less wasted today. In fact I may have the electrodes on all the time if I like, the only drawback being that I will have to get new batteries in the pacemaker more often than if I save some by turning it off at night.
I think/hope/believe that I will function on a higher level than today, most of all because I will probably have more staying power than today, which, believe me, is not much. To not get very tired from doing very simple things like writing these lines, would be nice! This will also effect my ability to have a small position at work, which is important for many reasons.
I also hope I will sleep better, as Michael says in the film you get wired from the medicines, and on average I only sleep 3-4 hours a night.
A substantial drawback connected to the medicines opposed to the results of the operation, is that the effect of the one medicine (Stalevo) ends very abrubtly, meaning that if I forget to take a new pill in the interval, I experience a flashback with very demanding fluctuations. The opposite will surely awaken some of my old self, being able to handle more situations in a good manner.
I must admit that it is a sort of relief to hear the surgeon that operated Michael, pointing out the scariness we all will feel facing an operation in the brain. Yes, I am scared, and I will certainly be even more so in the weeks to come, but I am also confident that it will be a success!
fredag 21. februar 2014
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