My Struggle living with an Invisible Disability Revisited– Part 5
Posted by Second Chance to Live on March 23, 2009
For context please read:
In August 2007 I wrote this 4 part series. In lieu of what transpired with Natasha Richardson and the subject matter of traumatic brain injury being discussed as an invisible disability — on ABC Radio San Francisco KGO AM 810 March 18, 2009 — I decided to reprint this 4 part series in its entirety.
My Struggle Living with an Invisible Disability
My interest is to empower individuals who are also living with an invisible disability — due to a brain injury or due any other type of organic, medical, psychological or mental health condition. May you find the hope and courage — by reading through this 4 Part series — to both love and accept your reality and yourself.
The perspective that I share with in this series is from what I have experienced while living with an invisible disability for close to 42 years. My goal is not to affix blame on anyone — as that does no one any good — but to share what has helped me in my process.
In my experience, denial kept me isolated and alienated from myself and other people — for many years — until I was able to begin to accept myself and my reality.
And now for the conclusion — Part 5
In these various scenario’s I seek to be kind and considerate, however I have learned that I need to limit the amount of time that I spend with such individuals.
My desire to bring about win-win outcomes teaches me to honor my limitations. When I honor my limitations I honor my relationships. Consequently, I have come to respect my limitations and value the abilities I possess. Because I have experienced the consequences of not respecting my limitations I made the decision to not place myself in a situation that would invariably produce a lose-lose outcome. In my attempt to provide a win-win outcome I decided to spend 2-3 weeks at the second location.
Through making the decision to spend my time at the second location, I was told that I never wanted to help the parties move in the first place. In reality, because I needed to respect my limitations, and because of previous information I received from the parties who will be moving, I made the decision to spend my time at the second location. The second location quickly became my priority because of love.
My prayer is that the matter I have shared throughout this 5 part series will be resolved in peace. Your prayers would also be highly valued. My struggle living with an invisible disability certainly has and continues to be a tool for instruction. I am grateful for the opportunities that my unique set of circumstances provides, because I know that my circumstances are not meant to keep me down but they are provided to build me up and point me in the direction of my destiny.
As an empowered individual, I can live life on life’s terms because I know that more will be revealed.
Update: I have since visited and learned a needed lesson. I need to limit the duration of my visits to 3-5 days. No one is to blame as it is as it is. By accepting this reality, I can practice live and let live.
I have also learned that when I do not respect my limitations — regardless of whether other people do — I set myself up for a lose-lose scenario.
Receive more articles like this one simply by clicking on Subscribe to Second Chance to Live by email.
All material presented on Second Chance to Live is copyright and cannot be copied, reproduced, or distributed in any way without the express, written consent of Craig J. Phillips, MRC, BA
This entry was posted on March 23, 2009 at 6:25 pm and is filed under abuse and neglect, Acquired Brain Injury, Bob Woodruff, brain injured soldiers, Brain Injury, Brain Injury Associations, Caregivers, celebrities with brain injuries, cerebral vascular accident, characteristics of traumatic brain injury, Children of Trauma, Closed Head Injury, Codependency, deficits, Department of Defence, Department of Veteran Affairs, Desert Storm Veterans, Destiny, empowerment, Empowerment and Inspirational Speaker, family, fear of failure, finding your bliss, flash explosion leading to brain Injury, Friends, goal setting, head injury, Healthy Self-Care, Identified Patient, Invisible Disability, Iraq veterans, Iraq War Veterans, Learning, learning disabilities, Life, life challenging experiences, Limitations, living life on life's terms, living my destiny, Living with a Disability, living with a traumatic / acquired brain injury, Living with an Invisible Disability, living with meaning and purpose, Major Media Outlooks, Major News Networks, Meaning and Purpose, messages of hope, messages of hope and inspiration, Mild Traumatic Brain Injury, Motivaional Speaker, Motivational / Inspirational Speaker, Ophra Winfrey, Parents of children with Acquired brain injuries, Personal, Practical Faith, PTSD, relationships, self-esteem, Self-Respect, spinal cord injury, Subdural Hematoma, The Grieving Process, traumatic / acquired brain injury, Traumatic / Acquired Brain Injury and Anger, Traumatic Brain and Comfort, Traumatic Brain Injury, Traumatic Brain Injury and You, Traumatic Brain Injury in children, traumatic brain injury in schools, traumatic brain injury Iraq, Traumatic Brain Injury Support Groups / Meetings, traumatic brain injury treatment, Veterans of the Iraq War, Vietnam Veterans, Virginia Tech Shootings. Tagged: respecting my limitations. 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.