Timeline

MY TIMELINE: CLICK ON ICON BELOW TO OPEN (and close).

Showing posts with label Pain clinic. Show all posts
Showing posts with label Pain clinic. Show all posts

Tuesday, December 13, 2011

4 Pain Clinic.



I have now been at the pain clinic at the University Hospital.
They always talk big words, but i wonder if they will do anything.
They are more interested in being a good coworker than putting the patients first.
They said they now would like me to try cognitive therapy, and hypnosis, and would call my psychiatric nurse, but they haven't. I would be surprised if they had.
Second they said my family doctor should sent me on a second opinion to Haukeland hospital in Bergen.
But again, my family doctor hasn't gotten the summary, or gotten a hold of the doctor, so then she does nothing!
Third, my family doctor wants the pain clinic to assign every aspects of my treatment from them,But they don't see why they should, they think my doctor


Thursday, August 25, 2011

0 Esophagus spasms speaks Alex language

I have been to my doctor today (pain clinic), and I am confused... The last 4 months have been about me taking morphine based supplements, and nothing about my real problem.
We did write a angry but fair letter last week, were we stated what we think needs to be done. My last gastro doctor has written to things in my medical journal that he did not want to treat me and said that my treatment was completed.. I thought what the f&/%k??? How can they say that? my spasms are just as real now as they were 12 months ago, or 24 for that matter.


Tuesday, December 14, 2010

8 Painclinic and Doctors!


Now i have been to the pain-clinic, and he said that i am staying on the dosage that i am on. A huge relief to me. The doctor at my local hospital said that i didn't need the Durogesic patch, and that my pain couldn't be treated with opioid s. he couldn't be more wrong, and i must say, i do find some satisfaction in that. I am also going to use Lyrica, Catapresan and Sarotex.

I am going to use that until February, where we are going to look into different things if the pain isn't smaller. They are going to check my lung capacity, pain school, hypnosis, psychologist, and make sure that i don't develop a fair of eating.
 I am starting with the psychologist already i January because i have post traumatic stress disorder because of the local hospitals treatment of me.think that you can have nightmare because they were so mean to you?? we have mailed Vestre Viken HF about what is going on, and that it is irresponsible and unworthy. i hope they don't treat other people that have a unusual disease.
They didn't belive that i had pain, they belived it was just psychological, but as my doctor at the national hospital said is; it not psychological pain, but you can use you're psyche to better deal with the pain :) They will also look at the botox, because its not the best treatment longterm, because the effect will be smaller, the more you take this treatment.

We also talked about if botox is not a treatment for the future, the botox i get is experimental, because they inject it into my entire esophagus (you can get a sleeping medicine so you don't need to be awake during the procedure.)
Then they will try to find drugs or treatments in other countries that have more knowledge about this illness, and thats a big relief, but if what i have read on the internett is true, then there is not much different  drugs and treatments in other countries. Maybe we are to few with so severe pain that they don't use money on it.
But it could be that there is some doctor sitting in a small office in a basement, who are researching this topic.

Thats what really matter with the health care system, if the doctors or nurse don't belive you, its a terrifying situation to be in.
You can try a lot of different drugs and treatments if you're doctors belive you, because its the only thing you need to have: Trust

One thing i have though about is how the doctors talk to you. If they are arrogant,condescending,have made up there mind about you before they have meet you. Then you cant really work together, and the patient will get a worse treatment, and maybe be misdiagnose. Then you will not be getting the treatment that you should have.
We need not to be scared to tell our doctors what we feel. Doctors need to be able to get constructive criticism, and NOT want to help a person because they said you could think twice about you're languages, or why you don't help a person, when its obvious that the person is in big pains??
It still baffles me that some doctors, especially new ones who has chosen a specialty, and feels like they need to impress the more experienced doctors. They should try to impress the PATIENT not the doctors.
The one thing i have learned is that surgeons cant talk to the patients with dignity. They should all be locked up in the operating room, and never be in contact with a patient who is awake!


Tuesday, December 7, 2010

4 were are we going

Today i finally got an appointment to the Pain clinic on the 14 of December, and I am hoping with every bone in my body that they will find a way to make my pain less, so I can live a little more. I am starting to get tired of this couch. and I wanna decorate the house for Christmas, and eat without fear.

To have a disease that makes you scream by just swallowing food, liquids, and my own saliva. do I have to be scared to eat for the rest of my life? And I never know when the esophagus spasms are coming. sometimes I don't even have to eat anything.
what I would like is to talk to others that are in the same situation, and what has helped for them, or if they are in my position: maybe we could help each other. There has to be something out there that can help, but where? even if you don't have spasms but have found some coping techniques for living with chronic diseases?
Its not easy reading articles from different countries with Google translator... it's not always precise.