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Second Chance to Live

Empowering the Individual, Not the Brain Injury

Traumatic Brain Injury and News Networks

November 11, 2007 By Second Chance to Live

Hi, and welcome back to Second Chance to Live. While listening to the news recently I heard several reporters comment on the topic of head and brain trauma. In the first incident the reporter mentioned that although a man had died and was without brain activity, he was revived and then remained in a 3 week long coma. The reporter went on to say that the man woke from the 3 week long coma and although he is having difficulty speaking he is OK. In the second incident, the reporter told of a woman who accidentally accelerated her SUV as she was pulling out of her driveway. As a result, her SUV went off of a 200-foot cliff and then rolled several times. The reporter went on to say that fire fighters were able to pull her out of her SUV. The reporter went on to say that the woman sustained some head injuries, however those injuries did not appear to be life threatening.

Both of these reporters illustrate a common misconception. In the process they minimize and marginalize the significance of brain injuries. I have heard other reporter’s state, she/he was in an accident, but she/he is OK; she/he just had a head injury. I do not know if these statements are made out of ignorance or a lack of awareness. The brain in each person is a massive computer that regulates every function that the body executes which in turn enables the individual to perform activities of daily living. When a person’s brain is damaged – for whatever reason – their lives are forever changed. So when you in the media and news outlets report on a soldier or someone else who has sustained a traumatic brain injury please do not exhibit a cavalier attitude toward their traumatic brain injuries. Brain injuries are forever. I can speak from personal experience.

My traumatic brain injury occurred in 1967 as a result of a motor vehicle accident and I remained in a coma for 3 weeks. Please read My Journey thus Far to gain further insight. My point is that I have experienced many subsequent events related to having an invisible disability. For sake of providing practical insight I will include a list of what I now know. Today I now know that I am an empowered being who is learning to live life on life’s terms because I know that my circumstances are not meant to keep me down, but they are meant to build me up!

I know that I was in a car accident.
I know that I fractured my left femur
I know that I fractured my skull
I know that I was in a coma for 3 weeks
I know that I had right frontal lobe damage
I know that I had a severe brain contusion
I know that my brain stem was impacted
I know that I was in traction for 5-6 weeks
I know that I was in a Spica or full body cast for 4-5 months
I know that I was not supposed to live the night of the accident
I know that I had brain and skull surgery
I know that I had follow-up testing after I underwent brain and skull surgery when I was 10 years old –EEG’s and other cognitive / psyche /social testing
I know that I was not supposed to succeed beyond high school academically
I know that I taught myself how to walk, talk, read, write and speak in complete sentences because of the injury to my brain
I know that I obtained both my undergraduate and graduate degrees
I know that I had ongoing difficulties interacting with people because of my traumatic brain injury
I know that I have difficulties learning sequences of information
I know that I get overwhelmed by too much information / external stimuli
I know that I have a hard time connecting the dots in complex situations
I know that I have an invisible disability
I know that I have been misunderstood too many time to count
I know that I need more time to learn and synthesize information
I know that I had many times in my life when to give up would have been much easier
I know that I am a not a victim
I know that my tenacity and persistence has benefited my ability to overcome barriers and obstacles
I know that I have come along ways in my recovery path from codependency, shame, people pleasing, approval seeking and feeling responsible for other people and their choices
I know that I had many jobs that ended — due to being let go, given the option to leave or terminated because I was told that the job and I did not fit
I know that I went for many years believing that I was bad, wrong or some how defective because I did not know I had difficulties reading subtleties and social nuances because of the damage to my executive center
I know that I was told that if I just keep my mouth shut, I would not have difficulties with people
I know that I have difficulties following instructions that involved sequences of information
I know that I have difficulties adjusting when the rules would change and I would be expected to adapt immediately
I know that I learn best through repetition when I can set at my own pace
I know that in my experience I had to learn what my role was in the family system so that I could break free of that role
I know that I had to begin to accept that I was a traumatic brain injury survivor before I could begin to heal I know that my circumstances and experiences are pointing me in the direction of my destiny
I know that I can not see my reality through the eyes of another person
I know that I can not convince anyone of anything when they do not have eyes to see or ears to hear
I know that I have been minimized and marginalized through out my lifetime because of ignorance
I know that I was criticized for not being more when I was doing my very best
I know that I lived in a world of debilitating shame and debilitating guilt for too many years
I know that in many instances I was expected to carry people’s shame for what they did not understand
I know that when people do not carry their own shame, they will seek to have other people carry their shame for them
I know that I am not responsible for how people chose to react. Reacting is a very personal choice
I know that hurt people hurt people
I know that I can not afford to live in another person’s denial system for me
I know that I have specific talents, gifts and abilities that are not subservient to my disability, deficits or limitations.
I know that I am not my traumatic brain injury, my deficits or limitations
I know that I am meant to succeed in life because of my disabilities, deficits and limitations.
I know that I needed to make peace with myself before I could be able to discover and celebrate my worth and value as a person who has been impacted by a brain injury.
I know that I had to embrace and love the child within me who grew up with an invisible disability without knowing the impact

I know that I am not a victim of my circumstances
I know that my reality can no longer be defined through the eyes of my parents, my peers, my teachers or my experiences.
I know that my worth is not based on how I perform, but who I am
I know that I am in peace with God.
I know that I can trust the process, a loving God and myself

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Filed Under: Brain Injury Recovery -- An Ongoing Process

Comments

  1. timethief says

    November 11, 2007 at 5:13 am

    This part especially rings true for me:

    “I know that I am not responsible for how people chose to react. Reacting is a very personal choice
    I know that hurt people hurt people
    I know that I can not afford to live in another person’s denial system for me
    I know that I have specific talents, gifts and abilities that are not subservient to my disability, deficits or limitations.
    I know that I am not my traumatic brain injury survivor, my deficits or limitations
    I know that I am meant to succeed in life because of my disabilities, deficits and limitations.”

    Reply
  2. secondchancetolive says

    November 11, 2007 at 5:07 pm

    Hi timethief,
    Thank you for the comment. The power of identification is phenomenal!

    Have a simply amazing day my friend.

    Craig

    Reply
  3. Carol says

    November 15, 2007 at 12:45 am

    Wow, what a timely blog. We are just learning that some of my husband’s mental health issues may actually be due to a TBI when he was younger. I have only read a few of your posts so far, as I’m kind of short on time, but we are told he has damage to his left frontal lobe. He went to see a neuropsychologist today and said the person administering the tests was rather surprised that my husband could not complete some of the requested tasks. This gives us a lot to think about, until we learn the results “officially” in a couple of weeks. In the meantime, I went looking for information and found your blog. Thank you so much!!!

    Oh…and I think you are absolutely correct in pointing out how the media addresses brain injury, I have noticed that myself. Just the other night the news was doing a story on a man who “was severely injured in Iraq, but survived.” They made it sound so great that he survived, then when they interviewed him, it turns out that he has a “new” vocabulary of about 20 words (he had lost all other language skills), can’t read or write, can’t be left unattended, and his speech was unintelligible to all except his wife. It was stated that “although he will never be independent again, he is happy to be home.” So it wasn’t nearly as “great” as the news made it sound.

    Thanks again, and I am bookmarking your blog so I can learn more from someone who’s “been there, done that”.

    Carol
    http://bipolarhubby.blogspot.com

    Reply
  4. secondchancetolive says

    November 15, 2007 at 2:57 am

    Hi Carol,
    Thank you so very much for taking the time to leave a comment. If I can be of assistance, please let me know. As you read through Second Chance to Live and you have the time leave a comment and I will respond to your comment and / or question. You are a blessing to me. Please say hello to your husband for me. Thank you.

    Please read my 4 part series https://secondchancetolive.org/2007/08/14/my-struggle-living-with-an-invisible-disability/ and my 2 part series, and my 2 part series, https://secondchancetolive.org/2007/08/21/having-an-invisible-disability-%e2%80%93-the-consequence-of-denying-my-reality%e2%80%94part-1/ . Both of these posts will give you further insights in to the matter of living with an invisible disability.

    Thank you again for taking the time to leave a comment. I look forward to hearing from you again.

    Have a pleasant day!

    Craig

    Reply
  5. cavmom says

    November 28, 2007 at 1:25 pm

    “I know” that you are a very special person and your shared experiences are helping many.

    Thank you, I am looking forward to reading more of your posts!

    Reply
  6. secondchancetolive says

    November 28, 2007 at 1:42 pm

    Hi Mom,
    Thank you for your kind words.

    Have a simply amazing day!

    Craig

    Reply

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