Traumatic Brain Injury and the Identified Patient – Part 2
Posted by Second Chance to Live on November 17, 2007
In the event that you have not read Part 1 of this article, please do so at this time by clicking this link: Part 1.
Hi, and welcome back to Second Chance to Live. In the first part of this series I spoke about displaced sadness, shame and the identified patient as these topics relate to family systems theory. After reading the first part, you may find yourself scratching your head and asking yourself how does this apply to me. I will seek to clarify and tie together those questions today. My experience has taught me that assigned or assumed family roles — such as the scapegoat, hero, mascot or lost child — seek to control and constrain parts of the individual that displease or disrupt the family system. In the process the individual is covertly or overtly expected to discard parts of themselves to maintain the system and contain the conflict, secret or unresolved loss. The roles become substitutes and the actors become reactors. The individuals within the system adopt a false self. The false self evolves out of the individual’s drive to comply in order to avoid being criticized, shamed and / or threatened with emotional or physical abandonment.
When the individual seeks to maintain their role or identity to avoid losing love / approval or to prevent being shamed, blamed and criticized they become hyper vigilant. Like a cat on a hot tin roof they seek to avoid conflict in order to maintain the role. In the process of complying the individual’s creative energy is redirected to enforce the unspoken code of the family. The individual’s creative energy is used to validate their role and to maintain denial. Denial is used to dismiss any need to address or process the conflict, secret or loss. When an individual with in the family system has or acquires an invisible disability, denial is used to dismiss the need to address the disability. Consequently the individual with the invisible disability internalizes their struggles. Such internalization sets the individual up to be blamed, shamed and made to be the problem with in the family. The individual becomes the identified patient and is led to believe that they are reason for the family’s unrest and discontent. In these circumstances the individual then takes on the responsibility for what is out of their control – their invisible disability for which they may be unaware of themselves – the irritability, restlessness and discontent of the family system.
When the individual leaves the nuclear family system, they take their role with them. The role once again becomes the vehicle that drives them as they interact with other people – beyond the family system. Consequently, life for them becomes a gauntlet as they attempt to fix and compensate for the restlessness, irritability and discontentment found within their relationships. Their overdeveloped sense of responsibility is mirrored through and in other interpersonal relationships. The identified patient or scapegoat consequently becomes hyper vigilant in their relationships as they attempt to repair or fix the restless, irritability and discontent to avoid being criticized, blamed, shamed or abandoned. As mentioned in part 1 of this series, these individuals become human doings rather than human beings. In the process of doing their creative energy is exploited to manage the unmanageable. As with other roles with in the family system, the identified patient trades their creative energy for a crusade that can not be won. In the event that the identified patient continues in that crusade their essence will slowly be drained and distracted.
In my experience, I had to begin to accept myself as a person with an invisible disability before I could begin to break free from the role as an identified patient. I had to learn how to accept myself as a person who has an invisible disability, rather than a person who is disabled. I had to realize that although I have deficits and limitations, I am not those deficits and limitations. I had to stop living the lie that I am responsible for other people’s irritability, restlessness and discontentment. Through identifying and accepting my reality — rather than buying into anyone’s denial system for me — I have been able to use my creative energy and learn from my experiences rather than internalizing my deficits and limitations through the eyes of shame. I sincerely believe that I became an identified patient because of a lack of information. No one is to blame and pointing the finger in anyone’s direction is of little value. My motivation in sharing the above is not to complain, but to use my experience to illustrate a reality. People with invisible disabilities many times are criticized, belittled, ostracized and shamed for matters that are out of their control.
The sad reality is that as an individual with an invisible or visible disability, you may have people in your life that want to make you the problem — identified patient. I have good news for you. You are not the problem. The problem exists because of a lack of willingness to understand and empower. In the event that you have people in your life, who for whatever reasons want you to live through their denial, I want you to know, you have a choice. You no longer need to buy into their denial system my friend. You are the solution. You are not your disability, your deficits or your limitations. You no longer need to live in the shadows of shame and contempt. You are a beautiful person who has an invisible disability. You are remarkable and resilient. Through accepting yourself as a person with a disability you will find a new vitality. You will learn to embrace yourself and fly like a bird that is set free from the cage that once limited the bird’s flight. You will discover your creative energy and you will use your gifts, talents and abilities. You will move in the direction of your dreams and you will fulfill your destiny. Please read my post, Following your bliss…regardless. Be encouraged my friend. More will be revealed!
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This entry was posted on November 17, 2007 at 5:28 am and is filed under acquired brain injury and feeling alienated, adult children of alcoholics and traumatic brain injuries, Adult Children of Alcoholics living with traumatic / acquired brain injuries, Brain Injury Education, Caregivers for people with traumatic / acquired brain injuries, celebrities with brain injuries, characteristics of traumatic brain injury, combating brain injury isolation, Families impacted by brain injuries, Fulfilling your Destiny, Identified Patient, living with a brain injury, Living with a Disability, Living with a Invisible Disability and feeling shame, living with a traumatic / acquired brain injury, Living with a traumatic brain injury and feeling shame, Living with an Invisible Disability, living with meaning and purpose, messages of hope and inspiration, Military Personell impacted by Traumatic Brain Injuries, Military Traumatic Brain Injury Support Meetings, Overcome Being Bullied, Overcoming Societal Stigmatization, Parents of children with Acquired brain injuries, Personal empowerment, Post Traumatic Stress Disorder, Post Traumatic Syndrome and Suicide, PTSD, Revealing your Destiny, Soldiers and Marines who sustained traumatic brain injuries, spinal cord injury, stroke, Suicide and Hope, tbi adults, tbi children, tbi families, tbi veterans, Traumatic Brain and Comfort, Traumatic Brain Injury and being Bullied, Traumatic Brain Injury and Hope, Traumatic Brain Injury and Significance, Traumatic Brain Injury and What is my Destiny?, traumatic brain Injury in adults, Traumatic Brain Injury in children, traumatic brain injury in schools, Traumatic Brain Injury Self-Esteem and Self-Worth, Traumatic Brain Injury Support Groups / Meetings, traumatic brain injury treatment, Veterans Living with Brain Injuries, What is my Destiny?. Tagged: Adult Children Of Alcoholics living traumatic brain injuries. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.