TBI – Survivors, Caregivers, Family, and Friends

Survivors SPEAK OUT! . . . . . Doris


Donna O’Donnell Figurski

Doris 1 year after TBI 2007

Doris 1 year after TBI 2007

1. What is your name? (last name optional)

Doris F.

2. Where do you live? (city and/or state and/or country) Email (optional)

Tampa, Florida, USA

3. When did you have your TBI? At what age?

October 31, 2006     Age 46

4. How did your TBI occur?

I was parking my vehicle in the post office parking lot, and I passed out.

5. When did you (or someone) first realize you had a problem?

Post office employees found me unconscious behind the steering wheel.

6. What kind of emergency treatment, if any, did you have?

Doris - 1 day after the craniotomy - 2006

Doris – 1 day after the craniotomy – 2006

Craniotomy; clipping and coiling of a ruptured brain aneurysm

7. Were you in a coma? If so, how long?

Yes. 5 days

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 did not do rehab, but I saw a neuropsychologist after a few months of recovery.

9. What problems or disabilities, if any, resulted from your TBI
(e.g., balance, perception, personality, etc.)?

I am afflicted with anxiety, a severely bad memory, dizziness, and headaches, but I mostly have psychological problems
(e.g., balance, perception, personality, etc.).

10. How has your life changed? Is it better? Is it worse?

It’s worse. I lost my job as a veterinary manager; I lost my home; I lost my husband of 26 years (he wanted a divorce); and I lost many friends. My daughter has turned her back on me and does not associate with me – because, according to her, I am “weird” and “boring.”

11. What do you miss the most from your pre-TBI life?

I miss the ability to be productive and to socialize. I miss feeling healthy and strong.

12. What do you enjoy most in your post-TBI life?

I enjoy my pets – it seems like they understand. I feel close to them. I’ve also learned to play the guitar and sing. It brings me great pleasure and a feeling of accomplishment, especially when I practice a new song and it sounds good. (At least my animals think so! LOL.)

13. What do you like least about your TBI?

I hate what my brain injury has done to my life.

14. Has anything helped you to accept your TBI?

My friend, a neuropsychologist, has helped a great deal. He talked to me twice a week for almost a year. I am also grateful to my two long-time girlfriends. They were there through it all and still love me today.

15. Has your injury affected your home life and relationships and, if so, how?

Basically I lost all the people I thought were closest to me.

16. Has your social life been altered or changed and, if so, how?

I don’t really feel comfortable socializing. I feel like most people are fake.

17. Who is your main caregiver? Do you understand what it takes to be a caregiver?

I’m my own caregiver. Being a caregiver takes a lot of effort and discipline.

18. What are your future plans? What do you expect/hope to be doing ten years from now?

I would like to be married again. I miss a man in my life. I’ve always enjoyed taking care of him, keeping a lovely home, cooking, and having a close relationship.

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 TBI survivors with your specific kind of TBI.

I wish it would not have taken years for me to accept my TBI and my altered abilities. I wasted a lot of time being angry and depressed.

20. What advice would you offer to other TBI survivors? Do you have any other comments that you would like to add?

My advice to other survivors follows. 1. Take it easy – one step at a time. 2. Don’t disconnect from the world – you are not alone. Find a support group. 3. Do something that you feel passionate about (e.g., helping others, animal activism, crafting, volunteering, performing or visual arts, etc.). 4. Find a fun activity that requires repetition (e.g., learning to play an instrument, knitting, gardening, etc.). This will help in the recovery process and will improve the brain. 5. Be kind to yourself, and be a little selfish. You have survived a major trauma. There is a reason you are still here on this earth. God bless you all!Hope

Thank you, Doris, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

(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.

(Photos compliments of Doris.)

(Clip Art compliments of Bing.)

Comments on: "Survivors SPEAK OUT! . . . Doris" (2)

  1. I am entering this comment on behalf of Catherine (Cat) Brubaker. 011115

    Wow this really touched me. I think we isolated too after my tbi. I’m wondering why we didn’t reach out more for help and I see other people isolate too now that you are sharing your experience and wondered if it is shame or forgetting to reach out for not knowing to reach out or people are just unaware of how to help? It just speaks volumes to me on how much work there is to do on raising awareness about brain injury and the struggles we have so that others can be more prepared and help other survivors too.


    • This is my response to Catherine (Cat) Brubaker 111115

      Catherine Brubaker, I think you hit on many topics of why survivors isolate. I think many survivors had the rug pulled out from under them. They don’t know what to do. Their family and friends don’t either. They can understand the flu, a broken bone, MS, Cancer or any number of afflictions, but a brain injury is a totally different beast. Often a person is changed completely from the person they once were – maybe by appearance, maybe by personality, maybe they are a completely different person. How does one wake up in a new body or mind and make sense of it??? That is a rhetorical question. I don’t think any of us have an answer for. But this is why you in your way, and me through my blog, my radio show, and my speaking engagements will help to educate the world to better understand brain injury. Phhhewww, it’s a BIG job.

      Donna O’Donnell Figurski


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