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do you ever miss your normal life

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    #31
    NOTE: This reply is far too long (800 or so words). If long replies are anathema to the "normal" protocols of this forum, please feel free to move on to the next reply.

    I have been a severe chronic pain patient for nearly a quarter of my relatively young life. Do I miss leading a normal life? The question is so tantalizing that it encouraged my first reply to a thread in a forum I have long followed but have just registered with moments ago.

    Normal is such a subjective word. I have "met" so many normal people in these forums over the years just as I have read the stories of exceedingly above normal people in the very same forums. Sadly, I have come across too many who appear to be under the care of a unqualified and/or narcissistic team of medical practitioners that seem to care little of "quality of life" issues and provide treatments that are just as debilitating as the conditions they are supposed to treat. And sadder yet, albeit rarely, I come accross forum members who are clearly depressed, despite a doctor's misdiagnosis or their own misdiagnosis.

    I admit, it can be too easy to look at a person who doesn't suffer my maladies and appears "normal" based on my momentary misunderstanding of the definition, and feel a bit envious. It doesn't accomplish anything; nearly every human engages in this behavior far more often than they admit, and I would be dishonest to my new friends if I were to say there isn't a feeling as if I am missing out when I see a dad tossing a baseball to his teenage son. That does not take away any of the skills that I may pass on to my children; and of course there is the distinct possibility that the dad tossing the ball to his teenage son wishes he had the normal relationship that I share with my kids.

    Despite a laundry list of major malfunctions among some of the 7-trillion trillion atoms that make up the individual I refer to as me, I feel normal. Like most, I yearn for the days I could climb trees and my only bills were the money I saved up for frozen treats purchased from the ice cream man on a hot summer day. I think it's normal to remember those halcyon days of summer, just as long as I understand that, thanks to Einstein, I am pretty sure I will never be in "that place" again.

    When I could play basketball fairly well at a towering five-foot nine, I think it was normal to wish I was just over seven feet tall. I am sure I would have been in the NBA and debating which house I would spend the off-season in.

    I have been known to wander back in time and regret some of the decisions I made, either out of ignorance or stupidity; wondering if my life would have been more "normal" had I not made those decisions.

    I have a minor in psychology and have spent many years in the medical field. Half the time as a caretaker; the other half as a patient. Sometimes I wonder if we create an impossible definition for normal that goes along the lines of, Normal: what I am not and everybody who is not like me, is. When an elderly man or woman in the golden years of their lives occasionally pines for the days when they cradled their now grown sons and daughters in their loving arms rocking them gently to sleep, isn't that normal? They will never have the opportunity to do it again, will they? Oh, they may try, but I imagine that would surely be looked upon as embarrassing to say the least!

    We are all normal in the fact that we are each human, we each have our respective burdens to carry, we all have plenty to offer each other, we all make mistakes, we all feel good when we can put a smile on someone's face, and we all remember times we could do what it is we cannot do now.

    We are all human, and last I checked, there are books and materials on how to be rich, how to win friends and influence people, how to split atoms, and how to whip up a tasty chicken Marsala, and even textbooks, such as the DSM-IV which discusses true abnormal symptoms. But even during my scholastic career, I never came across any definitive book on how to be normal. Maybe it is because to be normal is to be human.

    I apologize for the inordinate length of my initial response and promise that future replies will be much more succinct. I have spent years following this forum and so many of you have helped me in ways that you should be proud of.
    Last edited by MacDelta; 07-22-2012, 12:25 AM.

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      #32
      MacDelta

      Welcome to becoming a member of BT hope you enjoy and get as much out of it as many of us have over the years .

      Having said that you have followed BT for some time then you are most likely aware it is not as busy as it once was, that said there is still some very caring knowledgeable people here that continue to post and are very helpful to the ones coming to seek advice or comfort. I am ashamed to say I'm not one of them as I don't get here very often any longer.. I am sure after reading your post you have much to offer the ones that are seeking help also.

      I hope you enjoy your time with BT more now that you have joined.

      Linda

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        #33
        MacDelta, thanks for your reply and I agree with what you have to say. I have worked hard to not let my pain and disability hurt my relationship with my kids or my wife but the reality is my limitations are severe enough that they have major impacts on all our lives. I don't like to use the word normal but in this post I used it so each person could relate it to their own perception of how they would like to live. I never saw myself as normal nor did I want to be normal as I wanted to excel in all I did.

        The biggest disruption in my life is the sleep disruptions and the amount of each day I have to be asleep or limited to my chair to keep the pain under control. I could handle my disability much easier if I could regulate my sleep schedule but even sleeping pills haven't worked especially since I take enough sedating medications without them. It is my wish that each of us could be out of pain but a more realistic wish is that we could have days like most people in our society. Days were we do the best we can and nights that we are able to sleep waking up in the morning with the same routine our families have.

        I am very thankful for my wife and kids as they haven't given up on me despite turning their lives upside down. There is a reason so many people that become disabled end up divorced as 80% of spouses can't deal with the disruption in our lives. I really feel for people that have lost their spouses because they didn't ask for this change in their life but I know that our spouses can have regular lives by leaving us. I don't often feel bad about my disability but now and then it really hits that I can't do what I see regular people doing knowing my family and I enjoyed those things in the past and would still enjoy them now.
        1979 spinal issues, 1993 lumbar microdisectomy L3-4, 1996 360 3 level lumbar fusion L2-5, 1999 open thoractomy fusion T8-9,
        2002 C3-7 herniations and T4-7 herniations, 2004 total disability, a new limited life

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          #34
          Thank you

          Thanks, Mark N., suede, I appreciate your kind words. I confess that there have been periods in which I taken somewhat of a hiatus from following the forums. Life's responsibilities offer no respite for the disabled. Perhaps it is good that they don't. I do often wonder what has happened to the many familiar names, some going back as far as HarleyGuy, Jenn123 and so many of the somewhat more recent contributors to the group. Wherever they are, I am sure they have not been forgotten. I hope that both of you check in from time to time, and I have the opportunity to converse with you and so many of the other contributors who have had the courage to share their stories –and the compassion to lend a hand when needed. I am sure we will always have much to talk about.

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            #35
            MacDelta, I will hang on here as long as there are others helping and needing help from me. It is important to have a site like this or another one that gives us a chance to talk to people that understand what we are going through without always loading more on our families. It is good to see you posting again and I too wonder about the posters of the past and what they are doing. We and our families have hard lives with many days just getting through the day. It puts stress on our families at times and this site helps to keep some of the stress off of them.
            1979 spinal issues, 1993 lumbar microdisectomy L3-4, 1996 360 3 level lumbar fusion L2-5, 1999 open thoractomy fusion T8-9,
            2002 C3-7 herniations and T4-7 herniations, 2004 total disability, a new limited life

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