Survivors SPEAK OUT! . . . Abi
Survivors SPEAK OUT! Abi
presented
by
Donna O’Donnell Figurski

Abi – brain injury survivor
1. What is your name? (last name optional)
Abi
2. Where do you live? (city and/or state and/or country) Email (optional)
Columbia City, Indiana, USA
3. On what date did you have your brain injury? At what age?
I had my TBI (traumatic brain injury) at age 20.
4. How did your brain injury occur?
I was hit by a freight train in a suicide attempt.
5. When did you (or someone) first realize you had a problem?
I knew I had a problem when I started speaking, as my voice pitch changed quite a bit. Also, when I was asked to remember things from the day before, I had trouble doing so.
6. What kind of emergency treatment, if any, did you have?
I was taken to a hospital right away. In addition to the problems noted above, I also had a messed up back and an amputated right arm, so those were tended to right away. I was also immediately given stitches to close up a wound on my head.
7. Were you in a coma? If so, how long?
I don’t think I was in a coma, but I don’t recall very well the two days after my incident.
8. Did you do rehab? What kind of rehab (i.e., inpatient or outpatient and occupational and/or physical and/or speech and/or other)? How long were you in rehab?
I had occupational therapy, physical therapy, and speech therapy both as an inpatient and as an outpatient. I was in the rehab inpatient therapy for at least six weeks. I was in outpatient therapy even longer, but the outpatient therapy focused more on my missing arm. I also had in-home therapy.
9.What problems or disabilities, if any, resulted from your brain injury (e.g., balance, perception, personality, etc.)?
I have poor balance and slurred speech. I experience personality changes.
10. How has your life changed? Is it better? Is it worse?
I believe my life has changed for the better, as I’ve met so many who are worse off than me.
11. What do you miss the most from your pre-brain-injury life?
I miss nothing from my pre-brain-injury life, as my personality changed for the good. But I do miss people understanding me.
12. What do you enjoy most in your post-brain-injury life?

Abi – brain injury survivor
I like to meet others with a TBI and other disabilities.
13. What do you like least about your brain injury?
I dislike my slurred speech and sounding different than I used to.
14. Has anything helped you to accept your brain injury?
Yeah – meeting those worse off
15. Has your injury affected your home life and relationships and, if so, how?
I’m much better, as I’m more social.
16. Has your social life been altered or changed and, if so, how?
Yeah. I went from being deathly shy to a social butterfly.
17. Who is your main caregiver? Do you understand what it takes to be a caregiver?
My mother is my main caregiver. Yeah, I do understand what it takes. It’s hard work.
18. What are your plans? What do you expect/hope to be doing ten years from now?
I plan to have a family and to be a counselor helping suicidal people.
19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other survivors with your specific kind of brain injury.
Don’t give up.
20. What advice would you offer to other brain-injury survivors? Do you have any other comments that you would like to add?
My advice is Don’t give up, and be you.
(Disclaimer: The views or opinions in this post are solely that of the interviewee.)
If you would like to be a part of the SPEAK OUT! project, please go to TBI Survivor Interview Questionnaire for a copy of the questions and the release form.
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(Photos compliments of contributor.)
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I was diagnosed as being moody at nine years old. I still have that diagnosis to this very day: “mood disorder due to brain injury.” I also have anxiety and panic attacks. I still have today most of the same problems I had back then, just in an expanded manner.
I know my parents wondered why I acted out, and they took me to multiple specialists during my youth. I was diagnosed with optic nerve damage, but no other problems resulting from my head injury were identified. Each doctor gave my parents the same answer: “There is no logical explanation as to why she is doing this now when she did not do it before the head injury.

During my teenage years and into my 20s and even 30s, I had depression on and off. It got better after I had a hysterectomy. When my behaviors started to level out a lot, I was able to control myself better and move past other issues by actually learning not to do this or that.

SPEAK OUT! Itty-Bitty Giant Steps will provide a venue for brain-injury survivors and caregivers to shout out their accomplishments of the week.
I finally smiled again – I mean a real smile. It is the simple things, folks … the simple things.



I am new to this diagnosis of brain injury. For the last few years, I have had several unexplained symptoms – my life was spinning out of control. No one was listening to me. No one was asking the right questions. A few weeks ago, my father took me to the Emergency Room. He was desperately seeking help because I had no control of my emotions. I was placed in a locked-down psychiatric unit.

It can happen to anyone, anytime, . . . and anywhere.


I am writing my story, I drive, I went to college, I got two Associate degrees, and I worked for fifteen years. There is so much more, but anyone who reads this story should know that anything is possible. You may not accomplish as much as I did, or you may accomplish more. Just know that you should never give up on yourself. Feel proud of your body. If they had been in your shoes, they could never have done what you did, and that is to survive! Be proud!
I recently got out of hospital. I was in because of epilepsy from my acquired brain injury (ABI). My discharge was HUGE for me! I was finally put on the list for rehab for fine motor skills, speech,
walking, reading, and writing. I am able to start being me again. I’m super excited! My injury happened in February of 2015, and I have had no help. Now I am finally getting some. YAY!

The major challenge of brain-injury survivors is to eventually accept the “new” persons they have become. From the SPEAK OUT

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