TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Horse accident’

Survivors SPEAK OUT! . . . Barb George

Survivors SPEAK OUT!   Barb George

presented 

by

Donna O’Donnell Figurski

1 Barb George 1

Barb George – Brain Injury Survivor

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

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

Hoquiam, Washington, USA

3. On what date did you have your brain injury? At what age?

2004, and again in 2005     Age 45

4. How did your brain injury occur?

I was head-butted by my daughter’s horse. The second accident – we think I fainted. I was again in the hospital.

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

We don’t know how long I was “out,” as I was alone at the fence line. But, my husband realized there was a real problem when I did not recall all the work we had done on the property (fences built, pond in, etc.). He put me to bed, but I remained out of it, so he called an ambulance.

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

I had no surgery, but I was in the hospital for four days.

7. Were you in a coma? If so, how long?Image result for Cartoon Horse Head Clip Art

No

8. Did you do rehab?

I had nearly no professional rehab. We lived in a very rural location, and I was unable to get to things. (My husband was working out of country for much of the first three years.) So, I was on my own.

I did create some of my own rehab. With reading, I got help from computer-friends, who were willing to put things into LARGE, ALL CAP type. My farm chores helped with many balance and stability issues.

What kind of rehab (i.e., inpatient or outpatient and occupational and/or physical and/or speech and/or other)? I did have a small time of physical therapy. That helped with balance.

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

a.) My vision was reduced from perfect to nearly nothing. I could not read anything with lower case letters or anything with under a 16-20 pt font.

b.) My stability and balance were horrible. I used shovels to maintain my balance in the fields, and I used the walls and furniture in the house.Woma Head Pain

c.) Head-pain was tremendous.

d.) I experienced various moods.

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

I had just launched my company in a new location, but I had to close my business. My relationships suffered. It was rough.

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

Stamina. I live an “every other day” sort of life. I do not sleep well, so that is difficult.

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

I have had four more grandkids since my accident. (I had 2.) I have gained two sons-in law. I am grateful to be alive.

13. What do you like least about your brain injury?

I miss not having the ability to plan for anything. Life is a crap-shoot. I never know what will be possible.

14. Has anything helped you to accept your brain injury?

Organization. Honesty with self and others. Creating a support-group around myself. (I facilitate the only support-group on the Washington coastline from Canada to Oregon.) Learning!

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

My brain injury has strained many family dynamics. It is hard. My husband is not very available emotionally – that is just the way he is. One child sees me as a “whiner.” The other sees me as open and honest. Two kids have been pretty distant.

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

I was never a party person, but I did like to go out in the evening hours. Now I cannot. Well, rarely. I cannot cope with loud restaurants or movies.

2 Gray's Harbor Barb George

17. Who is your main caregiver?

I am very self-reliant. My husband would say he is my caregiver since he is the only other person here. He does the paperwork (for which I am grateful). Other than that, I am on my own.

Do you understand what it takes to be a caregiver?

Yes. I would give anything to share more of the responsibilities.

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

I would love to develop my skills enough to peer-mentor and advocate at a higher level. I would love to have an actual paying job at some point. I would like to continue to be self-sufficient as much as possible and to do some traveling. I plan to continue to be an involved grandmother and friend.

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.

The truth – that I really didn’t need to jump back in to life so quickly.

3 Barb George 3

Barb George – Brain Injury Survivor

I wish they would have sat my husband down and explained to him that this was a BIG deal. He didn’t get it.

The word “aphasia” was huge for me! No one could explain to me why my words were so garbled. When I learned that word, it was like “Well, it has a name, so it must be a thing.”

Communicating with other survivors helped me. I had a couple of HEROES in my corner. They gave me bits of wisdom and friendship that carry me through today – twelve years later. I am grateful to them.

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

Give yourself TIME. I see people every single day making comments such as “I am six months out. When will I be 100%?” or “When will my spouse be normal again – it has been four months?” Obviously, their doctors have neglected to tell them that TIME is a gift. That makes me angry. Yes, everyone is different, but no one, after an intense hit, is perfect in a couple of months (IMHO). By pushing (or being pushed by others), there are higher chances that other injuries will occur, and healing goes back to zero or further!

Find unique ways to simplify your life. And change it up. We gave up our mountain-dream-home-in-the-country for a smaller space in a small town. But, it is close to everything. I have less than half the home to care for. If I am unable to drive, I can catch a bus. I can walk to many things. People thought we were crazy – but being rural is a lot of work. Life was never perfect before the accident. It isn’t perfect now. But, life is worthwhile.

 

If you would like to be a part of the SPEAK OUT! project, please go to TBI SPEAK OUT! Survivors Interview Questionnaire for a copy of the questions and the release form.

(Clip Art compliments of Bing.)

As I say after each post: Please leave a comment by clicking the blue words “Leave a Commentanim0014-1_e0-1 below this post.

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Survivors SPEAK OUT! Lee Staniland

Survivors SPEAK OUT!  . . . . . Lee Staniland

by

Donna O’Donnell Figurski

Lee Staniland -  TBI Survivor

Lee Staniland –
TBI Survivor

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

Lee (Liana) Staniland

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

Oxnard, California, USA     leechar101@gmail.com

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

Age 25

4. How did your TBI occur?

A horse took me under a tree.

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

My husband came home and found me unconscious under the tree in our pasture.

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

My husband took me to the Emergency Room. They sent me to another hospital.

7. Were you in a coma?

Yes

If so, how long?

I was in a coma six weeks.

8. Did you do rehab?

Yes. I did rehab for a while.

What kind of rehab (i.e., inpatient or outpatient and occupational and/or physical and/or speech and/or other)?

I did rehab both as an inpatient and an outpatient.

How long were you in rehab?

I had rehab for a month. Then I got impatient with the drive to get there, so I quit and did my own rehab.

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

I have issues with balance and memory.

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

I think my life mostly changed for the better. I’m a better and nicer person.

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

Nothing

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

I got back most of my old self, so I can do most everything.

13. What do you like least about your TBI?

The fatigue

14. Has anything helped you to accept your TBI?

I was blessed that my mind just let me accept the new me.

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

I don’t let people push me around. I divorced my husband whom I was married to when the accident happened, and I married a more accepting man.

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

I am a morning person, so when it starts getting dark, I fade.

17. Who is your main caregiver?

I am my own caregiver.

Do you understand what it takes to be a caregiver?

Yes

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

I’m 62 now, and I am just going to take life easy.

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.

NEVER, NEVER GIVE UP!

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

I’m adding my story to this so that you can understand better. Over 20 years ago, six other couples started the Brain Injury Support Group. It is now a non-profit organization called The Brain Injury Center of Ventura County. I was even the president for a while. I drew our logo, and I have taken many photos for them. My message is to get involved. Thanks!

You can learn more about Lee in her Guest Blog article called, “What I Remember” on my blog, Surviving Traumatic Brain Injury.

 

Thank you, Lee, for taking part in this interview. I hope that your experience will offer some

Lee Staniland  TBI Survivor

Lee Staniland
TBI Survivor

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 Lee.)

 

SPEAK OUT! . . . . . . . . . . . . . . . . . . Guest Blogger: Lee Staniland . . . . What I Can Remember

SPEAK OUT! Guest Blogger: Lee Staniland

What I Can Remember

Girl Blogger cartoon_picture_of_girl_writingIt was June 11, 1978, in Somis, California, so I’ve been told. Because, you see, I have no memory of what happened that day.

I know that I had just gotten back from Arizona, where I became the godparent to my young nephew. I had brought my mother back with me, and for Mother’s Day, I had taken her to Solvang for the day. I also remember taking her to the Burbank Airport for her to go home. I remember all that very clearly, but the actual day of the accident, I remember nothing.

I have been told things so many times that they now have become my memories. I was told that I had been outside washing windows when my husband left to go somewhere. I was probably upset about something or someone because that is the only time I would wash windows.

I put my dogs up in their kennel like I always did when I rode my horse. My husband came home and could not find me anywhere, until he looked out in the pasture, which was in the front of our house. He noticed my horse with her bareback blanket on and a hackamore hanging from her neck.

Our pasture has walnut trees in it, and he found me unconscious under one of the trees. He told everybody that he had always told me not to ride when I was alone.

He gathered me up and took me to Camarillo’s Emergency Room. They sent me to Ventura’s Community Hospital, where I stayed in a coma for six weeks.

I have been told stories of things that happened there, like the time they left me in front of an open window one day. I caught pneumonia as a result. Another time, they kept giving me Dilantin to control seizures, and I was allergic to it. Because of that, I was scratching myself so badly that they tied my hands to the bed so that I could not reach any part of my body.

I guess they must have done most things right, though, because I’m here today to tell you about it.

I came out of the coma six weeks later, and I was sent up to Santa Barbara Rehab, where I spent another 2 or 3 months.

That was where I got my first memory that stuck. I was in a room all by myself, and I could hear people out in the hall. I had no idea where I was or why I was there.

I have memories of little fragments of that time – like being with my family, my sister’s wheeling me around their hotel pool, another sister’s taking me for a car ride around Santa Barbara, and lunch at Micky D’s (MacDonald’s). Funny the things that you remember.

My husband took me out of the hospital to spend the day in Solvang for our first anniversary. That was a super memory. I got to be out of the hospital for a WHOLE day. Wow!

Other memories:

Trying to walk down the hall with a walker, and not doing so well.

The day my brother hid the belt that the nurses had tied around me so that I didn’t fall out of the wheelchair every time I thought that I could stand up on my own.

A great young gal who was supposed to be with me while I cooked a meal that I had chosen.  [There was no way that I could do that yet, so she and her boyfriend cooked and ate a steak dinner (or whatever it was that I had picked out to try to cook). It was so much fun just watching them enjoy it. It still puts a smile on my face whenever I think of it.]

Then there is the memory of crying and pleading with my family to take me home.  They all felt so bad and wanted to do it, but they knew I wasn’t ready, so they would leave and I would just fade out. That is the good thing about not having a good memory. You forget most things that upset you. I remember things a lot better today, but there are times, especially when I am tired, that the old memory just doesn’t work the way it used too.

Well, I finally got to go home. I was so happy.

My parents had moved down from Sacramento to help take care of me. I had to relearn to walk, talk, dress, and feed myself. My old self was a very headstrong person, but I just let everyone help me with life. It’s amazing how your mind protects you from yourself.

After awhile, it was time for my parents to leave. I love them so much, but my parents were smothering me, and I wanted MY house back.

I know my mom was so afraid to leave me to handle things on my own, but it was the best thing for me.

I want to tell all you caregivers a secret. I know that it is a lot easier if you just do everything for us, but please don’t. I believe that is how I got to be as good as I am. After my parents left, I had to do everything myself – from taking care of a big house to caring for cows, chickens, dogs, and cats and helping to run a carpet-supply warehouse. I sold my horse because I could not ride her then. Oh yeah, I just remembered that my rooster would chase me whenever I would go out to collect eggs. They always go after the weakest thing, and that was me.

I forgot to mention that we were also still in the process of finishing the house we were building and living in. Talk about crazy!

I am so thankful that the part of my brain that reasons things out was not damaged completely. Don’t get me wrong. I know that there are times when I get a little crazy about things. Maybe other people who do not have a brain injury would handle the situation a lot differently, but I do the best that I can.

I am now remarried to a man who does pretty well for someone who was not with me from the beginning. I think he has learned a lot from me. I have learned a lot from him.

When someone says to me, “Oh your head injury must not have been very serious,” I would like to shake him or her. I had to work very hard to get where I am. I had Someone looking over me, and He decided that my time was not up yet and that I have something that I’m still supposed to do. I believe my purpose in life is to be with my fellow brain injured and to give them and their families hope.

I am very satisfied with my life right now, and maybe that is because I have been given back most of my old self. And then Staniland, Lee-1maybe it is because I have some of the best people around me. So here is a big Thank You to all those wonderful people who have stuck by me through thick and thin.

I love you!

 

Thank you, Lee Staniland.

Disclaimer:
Any views and opinions of the Guest Blogger are purely his/her own.

(Clip Art compliments of Bing.)

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