Oh yes, it is after three in the morning. I lay down in bed and try to sleep but it is not going to work. I had to take my hydos (a couple of them actually) to get out of the really bad pain earlier and I fell asleep for a few hours. So now I sit here hearing and feeling the snaps and pops as I move a hand or a foot. I have to say that they feel better now, somewhat anyway, as much as can be expected anyway. I just hate not being in control of a routine for sleep.
This pain is crazy. It amazes me how I have dealt with it this long. Seems like yesterday that it started but it really is all just a blur of when since it so gradually esclated to this point. I try search my memory for first clues of what forcasted this disease process. I try to figure out the different pains that I feel and label them accordingly while asking myself, "Is that the rheumatoid arthritis or the degenerative disc disease". Of course, I spend time wondering if my Bipolar disorder plays a role in the pain or of my feelings about the pain. I am just totally consumed by this process. Yeah, that's what I will call it, "This process".
So why do I spend my time consumed with trying to figure out pain and label the pain. Why does it matter that it has a label? I guess to make the doctors happy or to suffice my family with a title to what is wrong and why I have applied for social security disability benefits and why we lost our house when I could no longer work. A title to please the DEA when my doctor continues to prescribe me Hydrocodone 10/500 four times a day. Something to satisfy my own mind that I need for sanity maybe.
I've spent the past three days reading the boards on a website about chronic pain and the suffering of people all over the world. I thought it would help me some to know that I was not alone. I mean, I knew that I was not the only person suffering but it helped me put some of my thoughts and feelings into perspective and at least move out of my world for moments of time. I guess the surprising realization that I had was that there are people being stigmatized everywhere for being a person with chronic pain. I was amazed by the magnitude of this epidemic. The stories that I read over and over again pointed to thousands of people that could not get medical professionals to treat their pain appropriately. All of these poor souls left to be under treated, or untreated, and suffer in agony.
As a medical professional myself, I remember the patients that would want every pill coming to them. I heard the other nurses label patients 'med seekers' or 'drug addicts'. I actually remember thinking those labels towards patients that were mine periodically (and feeling horribly torn about it). I remember feeling frustration about a person's pain that seemed to be difficult to treat but I never withheld or refused to call a doctor and I always made sure that I remembered what I learned in nursing school, "Pain is what the patient says it is".
I know that there are so many people abusing drugs in our society but something has to be done to assure that our doctors are not afraid to treat pain. We cannot stigmatize people with chronic pain and realize that we may not actually ever see on a test result scientifically of why that person feels that pain. I find myself in fear of this new chronic pain patient role. I know the obstacles that face me. I am scared of them. I pray my surgical scars on my back suffice.
Wednesday, November 11, 2009
Tuesday, November 10, 2009
Painville

This page is black because this is what I feel today. It is raining outside. Ouch is all I can say. My feelings of frustration about my inability to control my chronic pain overwhelm me. For three years now I have fought this fight. I am now totally consumed by pain. I do feel a lot of support from my son and husband today. They don't seem to just blow off my complaints today. I thank God for that because this is a lonely fight. My daughter on the other hand seems to understand, or says that she does, but I am not really sure. It is difficult for others to understand. I am sure that it is just as frustrating to them to have a wife and a mother that is not able to do all that she did before. I mean, wow, I did it all! I was the main bread winner, the house cleaner, the person that everyone could count on the make sure it was all taken care of. Now I don't leave my house. Sometimes I remain in the quiet of my bedroom for hours with darkness surrounding my spirit because that is all I can take. I begin this blog in hopes that I can work through this and rise above somehow. I have to do something. Maybe this will help someone else that suffers. Maybe this will help someone else understand another person that suffers. Maybe it will help me to understand why.
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