TBI – Survivors, Caregivers, Family, and Friends

Archive for the ‘Survivors SPEAK OUT!’ Category

Survivors SPEAK OUT! Jessica Taylor

Survivors SPEAK OUT! Jessica Taylor

presented

by

Donna O’Donnell Figurski

 

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Jessica Taylor – Brain Injury Survivor and Author

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

Jessica Elizabeth Taylor

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

Vancouver Island, British Columbia, Canada

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

Age 31

4. How did your brain injury occur?

A fall down a steep staircase head first into a steel-plated door

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

My husband knew I was sick, but he did not know I had a brain injury. (I was not told that I had brain injury until six years after the injury!) I didn’t know who I was, who my husband was, and who my children were. I became a child again. I had to relearn everything. My personality was greatly changed. My balance was off for some time. My left hand curled inwards, but I trained it to straighten. I also had contusion of the back, a hemorrhage behind my right eye, and scalp laceration.

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

Intensive care

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

I was in a semi-coma for several weeks.

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)?

I had rehab only in a psychiatric ward as a day patient for some months at a time in two different countries. I trained myself by learning again and also by becoming positive and never giving in to depression or my disabilities.

How long were you in rehab?

I had no proper rehab. I was just given many IQ tests and psychiatric care. This did not help matters!

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

Recent recall was and still is a problem. I cannot take on too may projects at a time. I have to avoid stress at all times.

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

My life has been enhanced through training my dormant brain neurons myself and by having spiritual knowledge. As a result, I am a happier person.

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Jessica Taylor – Brain Injury Survivor and Author

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

I do not look back.

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

I enjoy being who I am.

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

I don’t think about the past. I just put up with my disability as a part of my life.

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

No

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

I had distant relationships with my husband and my children, as well as with all who knew me.

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

My new and holistic view of life has changed all that I do and think.

17. Who is your main caregiver?

ME

Do you understand what it takes to be a caregiver?

I know what caregivers should be aware of with regards to brain injury.

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

I hope to keep sharing my knowledge through the publication of my books and by giving talks.

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?

11 Taylor, Jessica Book Cover copy

From Tragedy to Triumph: Journey Back From the Edge by Jessica Taylor

I only wish that I had been taught by specialists how to retrain my brain in the early years, as opposed to doing so later.

If so, please state what it is to potentially help other survivors with your specific kind of brain injury.

Know that we can train and activate dormant neurons through studying a subject that is of interest. This has to be done frequently.

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 to study spirituality and to read as much as possible about the subject. I do not mean in the religious sense – study people like Deepak Chopra and watch Super Soul Sunday on TV. Stay positive and learn not to give in to negative thoughts. Try hard to rise above fear, jealousy, hatred, greed, envy, etc., and your vibration will increase in frequency. All this happened to me through my self-rehab.

To learn more about Jessica Taylor, click on the following links.

Jessica Elizabeth Taylor website
Jessica E. Taylor Facebook
Jessica E. Taylor Twitter
Jessica Elizabeth Taylor Linked in

Jessica’s book

“From Tragedy to Triumph: Journey Back From the Edge”

 

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

 

As I say after each post:

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Survivors SPEAK OUT! Jeremy Dorr

 

Survivors SPEAK OUT! Jeremy Dorr

presented

by

Donna O’Donnell Figurski

 

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Jeremy Dorr – Brain Injury Survivor

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

Jeremy Dorr

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

Lynchburg, Virginia, USA

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

September 15, 2013. I was 25.

4. How did your brain injury occur?

Car accident

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

My brain injury was first noticed by the doctors at the hospital.

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

I had a tracheotomy.

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

I was in a medically induced coma for one and a half weeks.

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 outpatient rehab at the Sheppard Center for six weeks.

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

I have a problem with control of my emotions. Others say that I am slower than before.

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

I worked at UPS, and I drove a Bobcat. I lost both jobs as result of the traumatic brain injury (TBI).

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

I miss the friends and working. (My “hobby” was working.)

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

Helping others.

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

I dislike the loss of my prior life. I also dislike the effects that my TBI has had on my daughter.

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

I learned to look for the positive in all situations and to stay positive.

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

Dorr, Jeremy

Jeremy Dorr – Brain Injury Survivor

Yes. I pay attention to my family more. My brain injury has brought me closer to them.

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

Yes. I rarely hear from the friends I had before – if I hear from them at all.

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

I am my own caregiver. Yes, I do understand what it takes to be a caregiver.

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

My plan is to help TBI survivors after they come home and are getting their lives back together. I want them to know that they are not alone.

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.

Be positive, no matter what. Positive brings more positive. Remember, you’re still here, so you can help make the change also. Believe in yourself.

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

The outlook on life has changed, but with change, great things can come. Let go of the hatred of what happened and embrace the “new” you. You are awesome! Don’t respond to negativity. Believe in yourself.

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

 

As I say after each post:

Feel free to leave a comment by clicking the blue words “Leave a Comment” below this post.

Please follow my blog. Click on “Follow Me Via eMail” on the right sidebar of your screen.anim0014-1_e0-1

If you like my blog, click the “Like” button under this post.

If you REALLY like my blog, share it intact with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it intact with your enemies. That works for me too!

Survivors SPEAK OUT! Ann Boriskie

Survivors SPEAK OUT! Ann Boriskie

presented

by

Donna O’Donnell Figurski

 

Boriskie, Ann Survivor 011116

Ann Boriskie – Survivor: Brain Injury Peer Visitor Association Director

 

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

Ann Boriskie

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

Alpharetta, Georgia, USA (a suburb of Atlanta, Georgia) aboriskie@braininjurypeervisitor.org

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

November 12, 1998, at age 48

4. How did your brain injury occur?

My brain injury occurred in a car wreck less than five miles from home. I was headed to a regular dental checkup.

A woman was talking on her phone while driving, and she obviously missed her turn. She stopped suddenly, but I was able to stop my car and not hit her at all. She just sat there at the bottom of a hill on the two-lane road. She did not move. A young student (16 years old) came down the hill. He said he was messing with his radio and just did not see us. He hit my car going 50 mph and pushed my car into the woman’s car.

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

About 48 hours after my wreck, I started having concussion symptoms. I experienced dizziness and mental “fogginess.” I could not walk. There was bruising under my eyes. The toes on my right foot went numb. My left eye was out of focus.

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

None. I walked away from the wreck thinking I was just fine. After 48 hours, I went to a 24-hour clinic, but they just sent me home. They told me I had no real problems and I would be fine. I also went to an eye doctor right away, but again, I was told there that nothing was wrong physically with my eye. Several months after my wreck, one neurologist told me that I had “post-concussion syndrome” and to go home – that I would be just fine. No one else mentioned my having a brain injury for one year. Then a dental TMJ specialist told me that I had a brain injury. That was what was causing my mental symptoms. (TMJ = temporomandibular joint)Peer Visitation Banner

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

No

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?

My brain injury went undiagnosed for over a year. The physical therapy that I received was in relation to each of my physical injuries (see #9), especially to help after the surgeries that I had to have to repair the parts of my body that were injured.

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

a. My brain injury caused depression, anxiety, and anger (more so in the first several years). I had lots of memory issues. (I could not remember friends or faces. I got lost. I could not write. Then once I could write, I couldn’t write in cursive – I still can’t.) Some memory issues remain today. I permanently lost many of my past memories. (I can’t remember family events or experiences or places where we had lived. I lost memory of cities and our time there.) I lost a lot of my math skills (I was an A+ math student, and I was in advanced math classes), but I have regained many of these math skills.

b. My neck was injured. (The C4, C5, C6, and C7 vertebrae were knocked out of line.) I had to have neck surgery (for fusion and a metal plate holding these four levels together). My neck is in CONSTANT PAIN.

c. I had an injury to the L5 and S1 levels of my spine. (The last two vertebrae are not attached now to my spinal cord). Surgery was recommended, but my neck did not fuse properly, so I decided not to have back surgery. I am in CONSTANT PAIN in my lower back. The pain often radiates to my hips and legs.

d. I popped a tendon from its bone in my right elbow. (I braced my body on the steering wheel in the wreck.) It required surgery. The doctor said it was one of the worst tears he had ever seen.

e. Permanent nerve damage was created in various body areas.

f. The left part of my jaw was knocked out of line. It literally took years of appliance therapy to get the bone back into its correct place.

g. A valve was torn on the left side of my heart. This caused irregular heartbeats for a while. It repaired itself.

h. My left side remains weaker than my right side.

i. Numbness remains in my hands (which makes it harder to use my hands). I also have numbness in my feet, down my arms, and down my legs.

j. Sometimes my left eye will not focus or work well with my right eye.

k. I have a shorter attention span.

l. All of these physical injuries caused me to have fibromyalgia and constant body pains.

Boriskie, Ann Podium

Ann Boriskie – Survivor

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

In the long run, I have to say my life is truly better. All three of our children are in the medical field. (My husband and I have raised one daughter, now a neonatologist who takes care of premature babies and helps the moms; raised a son, now a doctor of internal medicine who works as a hospitalist; and raised another daughter, now a Registered Nurse in a mental-illness hospital unit.)

My priorities changed in my life. I went from being a “work-oholic” and a person who was very competitive to a person who lives to help other people, including my family and friends.

I slowed down my life’s pace. I had to learn that I could no longer work at a full-time outside-the-home job. (For years, I could not work at all.) I also had to learn to take care of myself – due to all of the physical and mental problems that the wreck created.

I was at home, and thus I was “there” more for my children and husband. I was able to give them more help and more attention.

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

I miss my higher energy level. I miss many of my memories. I miss all of the physical sports and activities that I can no longer do (water skiing, snow skiing, kayaking, swimming, playing golf, etc.).

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

I enjoy running the Brain Injury Peer Visitor Association and being able to help thousands of brain-injury and stroke survivors throughout the United States and the world. I’ve done this each year since 2006.

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

I dislike being in constant pain (which also affects my brain). I also dislike having to push myself more and having to work much harder to accomplish my goals and to do my work than I did prior to my wreck.

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

  1. Helping other people helps me also.
  2. Sharing my experiences with others and listening to each brain-injury survivor’s problems (This helps me to better understand my own brain injury.)
  3. Attending support-groups (and being very open to sharing my own problems, experiences, successes, and methodologies)
  4. In the past, gaining the help of neuropsychologists
  5. Going to medical doctors who treat brain injury (e.g., a psychiatrist)

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

Yes. I am much more dedicated to my husband and three children. I treasure our relationships. I also treasure my friendships more. You really better understand that life is way too short and can change in a second.

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

Yes. I no longer like to be in big crowds or in a noisy environment. Going to a party is now a struggle and sometimes a chore. I just avoid noisy places and huge crowds. This requirement definitely limits the activities in which I can participate.

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

My wonderful husband is my main caregiver. I am blessed that he “stuck it out” with me and helped me go through all of my physical and mental recoveries. He is also one of my biggest supporters – even financially supporting my association and approving of all of the volunteer hours that I dedicate to the Brain Injury Peer Visitor Association.

Boriskie, Ann Training in Florida Survivor 011116

Annn Boriskie – Survivor

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

I plan to continue running the Brain Injury Peer Visitor Association as long as I possibly can. My dream is to continue to grow the association throughout the United States and even internationally.

I also plan to continue to enjoy and spend time with my immediate family and their families.

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.

Accept your limitations, but continue to “push yourself” to improve. Realize that, even though you are different from the pre-TBI you, you are still a valuable person in the world. Let your “old self” go. Realize that person won’t be back. Embrace the “new you,” and learn to love yourself for who you now are. Remember that YOU CAN. Don’t defeat yourself by focusing on all of the things you can no longer do.

2011 Community Service Awards from WXIA 11

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

Help others. Get involved. Volunteer. By helping others with a brain injury, you truly help yourself in so many ways. You will help yourself get better, and you will gain confidence.

 

You can hear Ann Boriskie on my radio show, “Another Fork in the Road” at 5:30pm PT (6:30MT, 7:30CT, 8:30ET) on Sunday, January 17th on the Brain Injury Radio Network (BIRN)

Click here on Sunday 5:30pm Pacific Time. Another Fork in the Road: Ann Boriskie – Director of Brain Injury Peer Visitor 

You can call in to listen to the show or talk to the host by dialing this number. 424-243-9540

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it intact with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it intact with your enemies. I don’t care!

Feel free to “Like” my post.

 

Survivors SPEAK OUT! Jenn Von Hatten

Survivors SPEAK OUT! Jenn Von Hatten

presented

by

Donna O’Donnell Figurski

 

Von Hatten, Jenn Survivor & Hanna 121315

Jenn Von Hatten – survivor and daughter, Hanna

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

Jenn Von Hatten

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

Trenton, Nova Scotia, Canada     jlvonhatten@gmail.com

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

My brain injury happened on Valentine’s Day 2011. I was 35 years old.

4. How did your brain injury occur?

My brain injury resulted from a motor vehicle accident caused by freezing rain.

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

The paramedics found me clinically dead at the scene. The doctors wanted to airlift me to the Queen Elizabeth II (QEII) Health Sciences Centre in Halifax, which is the biggest hospital in Nova Scotia. But the freezing rain affected the rotors on the helicopter, so I had to be taken by road ambulance.

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

The pressure in my brain needed to be monitored to see if I needed surgery. I also lacerated my liver. Fortunately, I did not need surgery for either. I also fractured a rib and three vertebrae.

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

I was in a coma for seven weeks. First, I was in a coma from the accident. Then I was in a medically induced coma because of my fractured rib and vertebrae. I managed to develop pneumonia, and I had a tracheotomy.

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 was transferred to the Rehab Centre in Halifax around Easter 2011, and I was discharged in July 2011. Besides being a patient at the Rehab Centre, I’ve had to go to physiotherapy and occupational therapy. My spastic muscles affected my speech, so I also went to speech therapy.

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

Von Hatten, Jenn survivor Son Liam 121315

Jenn Von Hatten – survivor and son, Liam

My balance has been severely affected. I used to be in a wheelchair, due to fractured vertebrae. I’ve since “graduated” to a walker, a quad cane, and a mini-quad cane. I’m a Fall Risk, and I get the Disability Pension.

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

I have joint custody of my seven-year-old daughter, Hanna. I am no longer able to work as a nurse. My life has definitely changed, but I can’t say if it is better or worse. All I can say with certainty is that my life is DIFFERENT.

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

I miss being able to work as a nurse the most. As much as I would like to a work as a nurse, I know I would NOT be safe – mentally, in terms of remembering if I gave a client medication or treatments, or physically.

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

I enjoy my time with Hanna. It is her time, as I don’t work anymore. I now have a cat, Spunkster, which I got from the local SPCA. When Hanna’s not with me, I hang out with Spunkster.

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

I had graduated as a nurse only seven months before my traumatic brain injury (TBI). I had wanted to be a nurse for over fifteen years. At least I can say I turned that dream into reality! I sometimes miss being able to drive. My rehabilitation doctor says I still cannot drive, as my reflexes are not up to snuff. However, I can say that my driver’s license has NOT been revoked!

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

Becoming a nurse was my dream. I finally realized that, just because I am no longer able to work as a nurse, I STILL AM A NURSE! Being a nurse is STILL a part of me.

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

My youngest daughter’s father threw me out, as he said he was not happy. I remind myself that not many relationships survive a TBI.

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

I don’t really have a social life, except maybe for going grocery shopping. I go by cab, so I interact with the cab divers, who are husband and wife. They own the cab company, and they are now good friends of mine. I prefer to interact with people in small groups.

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

Von Hatten, Jenn survivor daughters Emma and Hanna 121315

Jenn Von Hatten – survivor and daughters Emma and Hanna

I am my own caregiver now. Yes, I do understand what it takes to be a caregiver, as I used to be one. When I was in school to become a nurse, I worked as a CCA (Certified Care Assistant). A CCA can also be called PCA (Personal Care Assistant) or PCW (Personal Care Worker).

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

My plan is to be helping others who are TBI survivors or caregivers. I can provide info and support.

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.

Understand that a person does not need to be working (and therefore getting paid) to be fulfilling whatever he or she was meant to be. Find other ways – perhaps volunteering.

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

Figure out what you like doing and makes you happy. If you can’t remember, that’s OK – find out. (It’s what I wish I knew back in the beginning when I was first dealing with this.) Find out what you like and makes you happy RIGHT NOW! Everybody, brain injury or not, is constantly evolving.

 

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it intact with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it intact with your enemies. I don’t care!

Feel free to “Like” my post.

 

Survivors SPEAK OUT! Jennifer Stokley

Survivors SPEAK OUT! Jennifer Stokley

presented

by

Donna O’Donnell Figurski

 

Jennifer Stokely Survivor 0526151. What is your name? (last name optional)

Jennifer Stokley

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

Kutztown, Pennsylvania, USA

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

May 10, 2007, was the day of my traumatic brain injury (TBI). I was 42.

4. How did your brain injury occur?

I fell out of a second story window of my home to the sidewalk below. I did what I now call my “Amazing, Exotic Jeni Bounce.” I was home alone. Please don’t ask me how the fall occurred. I have no clue, other than I know that back then I was a hard-core alcoholic. My TBI cured me of that completely! No withdrawal. I just never desired alcohol again. Odd, but wonderful!

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

My ex found me on the sidewalk. He thought I had fallen outside (no external injuries, strange). I used to have a seizure disorder back then, so my ex and some friends carried me inside, up the stairs, and put me on the bed. Then I started to have trouble breathing. My ex immediately called 9-1-1. The paramedics arrived, took me back downstairs, across the street at night, and worked on me under a streetlight in a public park. They understood something was terribly wrong then.

The thing I find funny about the whole thing, though, is that the emergency folks cut my clothes off right then and there – for the whole city block to see me naked – under lights! I showed my butt to the city! (LOL) Thank goodness I don’t live there anymore.

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

I had two cardiac arrests during the life-flight to the hospital. I had ruptured my bladder (which they had to stitch back together like a patchwork blanket). I punctured my lung, due to one of my five broken ribs. I had broken my pelvis in three places. I also had broken my neck.

The only things I remember for sure are a breathing tube down my throat, the surgery on my belly to put my bladder back together, and the two times they restarted my heart. The rest is unknown to me. I haven’t asked; they haven’t told. That is my past. I survived. I do not wish to relive the past while I’m so busy living my present and focusing on my future.

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

I was in a full coma for three weeks. My coma was a 3 on the Glasgow Scale. It’s the lowest score before death. (A score of 3 indicates a severe brain injury.) After all my surgeries and the use of all the professional skills to save my life, the surgeon actually came out to my Momma and said, “We’ve done all that we can. Now it’s in God’s hands.” It literally was. One day prior to their disconnecting my life-support, I took my first breath on my own! They were able to take me off of life-support, knowing I was going to survive. To what extent, they still had no clue, but at least I was no longer in a coma on life-support.

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)?

First, I went to inpatient therapy from the Intensive Care Unit for two and a half months. I was taken to a rehab room (by wheelchair with my “fun-catheter” along for the ride) to exercise a bit and then attempt to stand. (They said my standing would never really happen because of my broken neck, but I showed them. I stand just fine now, and when I leave the house, I walk with only a cane.) Later, when I was discharged, I was in outpatient therapy for … I don’t know how long. There, I did physical therapy, speech therapy, and cognitive therapy. (Speech therapy was a hoot. The therapist would hand me things to read out loud. The problem was I couldn’t see! I’m legally blind now. “Come on. Read the medical records already.” LOL Cognitive therapy was just as much fun – pegs in holes I was unable to see. LOL That didn’t last too long.)

How long were you in rehab?

Inpatient, two and a half months; outpatient, more than six months, I think

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

I have a severe anxiety disorder, cerebellar ataxia, aphasia (not much now, but it used to be severe), bladder/bowel control issues, and taste bud issues. I’m legally blind. Memory issues are HUGE. My ability to smell has been affected. I have issues with concentration and making decisions. My personality did a 180 on me, and for that, I am actually grateful. I was not a very nice person prior to my TBI.

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

My life is harder than it was prior, but it is also so much better than it’s ever been. I will gladly take the difficulties to have such a wonderful life. I had no difficulties prior, and I had such a horrible life. Go figure. I gladly take the trade I’ve been handed.

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

I miss the memories. I lost 42 years of my life. All my memories are gone – my childhood, my college, my graduation, everything – poof, gone in a second. When I woke from my coma, I was a stranger even to myself. I was literally reborn. I was no longer “Jennifer.” I was “Jeni,” a child. I didn’t know anyone or anything. I had to be taught how to eat, how to walk, how to talk – like an infant. I was told things about Jennifer, but they were all foreign to me – even to this day. (But I sure don’t miss memories of three ex-hubbies, so I guess it’s cool with me anyway! LOL)

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

I enjoy that I am building my life from scratch. I am building it in a way that brings me joy and peace. I have reconnected with my family, which never would have happened if not for my TBI. That I guess is the best part of this all! I have my Momma and my big sister in my life now, and they never were before. Now they love me, look out for me, and help me just because they want to. I love them with all my heart!

13. What do you like least about your brain injury?Stokley, Jennifer Survivor 112815

I dislike my loss of independence and being legally blind. I will never be able to drive again, and, with my anxiety disorder, I can’t go anywhere without my family’s support anyway. So I can’t just get up and go, even if I feel like it. I have accepted it. But it doesn’t mean I always have to like it.

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

Time and God have helped. Please let me explain a bit. It took me nearly five years to find my way through my “brain fog” to the light of awareness, where I could even look around and understand what the heck is even going on. When I mention “God,” please know I am not a believer of any formal religion of any kind. I sure wouldn’t understand any of it anyway. Sorry. I am fully a spiritual gal. I know God saved my life. I speak and pray directly to him privately. I believe in angels. I also feel that I am a part of all things of this earth, sky, and everything in-between. I do not, have never, and never will step inside any church. That is not something that my heart desires. My connection is full and complete. I need nothing more and nothing less.

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

I had a “love of my life” prior to my TBI. He tried – truly he did – post TBI. He stuck it out for three years, but I myself never emotionally reconnected with him. I do know he loved me. He used to come home from the hospital, walk half way up the stairs, and collapse in tears. He became my full-time caregiver and friend, but emotionally I was unable to love him back. So I personally set him free to find love again, and he has – with a baby on the way. YAY!

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

My social life changed big time, but it improved big time. My social life had been with drunk folks at the bar and such. I never drink at all post TBI. I never miss drinking for some strange reason. So that circle of folks is no longer in my life. At first, my social life consisted of “my dad,” a neighbor who just cared so much that he would spend about an hour every day with me. Sometimes he would take me places. He always made sure I was safe. My social life now consists of wonderful, caring neighbors who accept me knowing my limitations. They help when needed and spend time with me “just because.” My biggest social life consists of my family, who, for 30+ years, really weren’t much of a part of my life at all.

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

I am and have been my main caregiver for six years now. I had no one after my ex-boyfriend/caregiver left. I was completely alone. I do, however, understand in many ways what it takes. Many of my dear friends who I know so well on the Internet are caregivers of survivors. They fill me in totally and honestly. I also help them to maybe know what their loved one is thinking when a reaction occurs, things that may stimulate the survivor, things that the survivor may enjoy, etc.

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

My life will be pretty much what I do now – “pay my life forward” to other survivors and caregivers by helping them – sometimes with info or sometimes with laughter, music, inspiration, joy, etc. I am permanently and totally disabled, so I truly believe that “work” is out of my future. That’s okay with me, truly. I love what I do now, and, as my father used to always say, “If it works, don’t fix it.”

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.

Realize it is what it is!

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

Please never rush it. You’ll get there when you’re ready to get there – not a second sooner. It may take years and years, but when YOU are ready, you’ll know it.

Tell folks to get over themselves and their ignorance if they ever say, “Just get over it.” It takes a lifetime!

If you’re unable to do something right now, always say, “I can’t do it AS OF YET!” It leaves room for possibility and hope for your future!

 

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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! Alisa Noah

 

Survivors SPEAK OUT! Alisa Ann Noah

presented

by

Donna O’Donnell Figurski

 

Noah, Alisa Ann L7l38moCWms-awgtIo9_70iApASPda_FVoPydfH1Eav5cCUnvpSudWfhdApNDrmPOqCkIcYbJLDfkrIxawI0Iu_D3IeGgzKZ1Whh7Lc2pmxdyJbB19_Vw114VdME3ant9vsNlq-qX9SNXn7SApjHhzoVZqU1ToqtwiFTpWcqKJ9lbUSBAV0pVh-fvnXN3tkGrsqt1hPzAODSjNBFrDOOjJ-u_iGQ547W

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

Alisa aka “El Dorado”

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

North Carolina, USA

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

February 2012

4. How did your brain injury occur?

My brain injury came from a motor vehicle accident. I wasn’t at fault. My truck was rear-ended at 50+ mph. Because my truck had no headrests, my head hit the back glass.

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

Immediately

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

I was first treated in the Emergency Room. Scans and X-rays were taken. Later I had a neck brace, cervical epidurals, other cervical injections, and physical therapy.

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

No

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)?

I did physical therapy.

How long were you in rehab?

Three months of 3 days a week

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

I have vision loss; migraines; balance issues; sleep problems; mood problems; memory loss; anxiety; and pain, pain, pain. Unexpected loud noises send me into a panic.

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

My life got worse for about three years. I have recently started to make progress with happiness and finding new ways to keep busy.

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

I miss my career as a horse trainer, and I miss college.

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

Retirement (LOL)

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

I dislike the pain and my physical limitations.

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

Friends and new hobbies have helped me accept my brain injury.

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

Yes. People don’t understand my thought process or mood swings.

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

Yes. I fear driving. I don’t engage in social activities much anymore.

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

My mother and my roommate are my main caregivers.

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

Hmmm, I’m not sure. I take things one day at a time. 🙂

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 let doctors just throw pills at you. After I had been told for almost three years that my condition is permanent, I recently learned that I can heal from it. Do your research. Some doctors are really no help.

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

NEVER let your “disabilities” define who you are as a person! You are and always will be just as valuable and important as anyone else. Never let anyone tell you otherwise. Stay strong!

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it with your enemies. I don’t care!

Feel free to “Like” my post.

 

Survivors SPEAK OUT! Sandra Williams

Survivors SPEAK OUT! Sandra Williams

presented

by

Donna O’Donnell Figurski

12200687_895719387130278_18176772_n1. What is your name? (last name optional)

Sandra Williams

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

Athol, Idaho, USA

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

My injury was on May 28th, 2012, at 10:00 am. I was 38.

4. How did your brain injury occur?

A drunk driver crossed the center lane as we were turning a corner in our Ford F250 Power Stroke. We were pulling a 26-foot travel trailer. There was a cliff on the other side of us. We should have gone over the cliff, but instead we crossed all lanes of traffic and ended up in a ditch. We should have jackknifed, but we didn’t. The truck that hit us also went through the length of our travel trailer. He ended up in the lane opposite to the one he was traveling in and facing in the opposite direction. We all should have died. The details of the accident are many. It sounds like a made-for-TV movie. We are all alive, but we’re not OK.

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

I first learned of my son’s brain injury when I took him to a neurologist. His primary care physician wanted a follow-up because my son was sleeping so much and his balance was off a bit. We made him rest all summer. When he went back to school, he went from an A-B student to one who got Ds and Fs. I was really focused on my son, but the neurologist diagnosed me too. The diagnosis shocked my primary care provider and me. I didn’t really believe her until I lost my job as a Special Education teacher.

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

I lost consciousness. I was taken to the Emergency Room. I don’t remember babbling to the sky, but that is what my kids said. They told me this several weeks after the accident. They didn’t know I didn’t know. That’s when my husband knew something wasn’t right. But he thought I would get over it. We all rested that summer. I seemed to be doing well – no headaches, etc. – until I went back to work.

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

No

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 have been to two ten-day sessions of speech therapy, vestibular therapy, cognitive behavioral therapy, and exposure therapy. I also attended Carrick Brain Injury Center, a multidisciplinary brain rehab center.

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

I am still struggling to work. My memory is still affected to the point of frustration for my family members. I struggle with headaches, dizziness, and confusion when people speak to me. I have given up being a youth group-leader. I tried to go back to work, but, due to the fact that educational systems do not accommodate, I cannot work as a teacher – not even online. I really want to run and work out like I used to, but I don’t. That is the biggest change. I never used to drink coffee or alcohol. I don’t abuse either, but now I drink both. I never used to eat chips or anything unhealthy, but I eat those things now. I used to garden, but now I don’t. I do want to return to the way it was with those things, but it is hard while I’m keeping up with my kids and their needs since the accident.

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

I think my life is worse, but can get better. It is worse because I can’t work in a job where I can get full-time benefits. My health care needs have increased, and my income has decreased. I am trying to help my husband start a new business in construction. He is being patient with me, but it is not easy. Our kids are different, and we really struggled with their behavior until we went to Carrick Brain Injury Center. We still struggle with one kiddo, but I think it is a grief process that he is going through.

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

I miss running. (I ran a half marathon and was training for a full marathon when we were hit.) I miss having the energy to do anything I wanted. I miss remembering everything. I miss being able to find a job whenever I wanted. (I have been working since I was eight. I started working for my dad and got my first out-of-family job at the age of fourteen. I paid for the first four years of college by working, and I sent myself to Europe – some people in my church helped me to play basketball internationally.)

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

Nothing really. I wish I could say something different. But, my life is so limited from what it once was, and I look so normal. People expect me “to do better,” “to not give up,” or “to stop making excuses.”

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

I dislike that I cannot be independent and that people expect more from me than I can do. If a person had a broken leg, that person would receive accommodations until it healed. Accommodations are not given when one has an invisible traumatic brain injury (TBI). It doesn’t work that way. But I will not give up.

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

I was actually helped by the fact that I can’t work no matter how hard I try. Working came easily to me, just like sports. Now, working and sports are the hardest things for me to do. I will keep trying though. I can’t do them now, but that doesn’t mean I won’t be able to do them forever. I won’t give up. I will do them someday.

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

Yes, immensely. My kids get really frustrated with me, and so does my husband. I used to be unorganized and forget things, but now it is ten times worse. I really have to rely on notebooks and repeat myself several times. That is what is so frustrating for my family. They also don’t understand my need for rest or my light-sensitivity to the TV. There are many things to list, but I will keep it short!

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

I don’t visit with anyone anymore. I used to go to bible studies, but they scare me now. (I am afraid I will say the wrong thing.) I can’t go see my mom because I can’t drive that long at one time (it takes two days for me to get there), and it’s just too long to be gone. Plus, I have a huge family, which is hard to be around. My sisters don’t understand my brain injury. I just stay away. It’s better for all of us.

17. Who is your main caregiver? Do you understand what it takes to be a caregiver?12202566_895719670463583_794991146_n

Me. I am my own caregiver. My husband tries, but he is focused on the business. I submit insurance claims and speak to the doctors. I am even filing claims with Disability Rights of Idaho, so I know I can be organized and I can do something!

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

I plan to be working in construction until I put myself through college again to finish my counseling degree and/or get a certification in TBI so I can educate teachers about it. There is the need for special education to have a different evaluation process. I also plan to use online settings to sell lessons that target students with TBI in the secondary school classroom.

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.

I wish I knew more about Disability Rights of Idaho and more about the complaint process for educators. (Parents are at such a loss!) The biggest tip I can give other survivors is not to listen to negative comments or to employers who tell you that you can’t do the job. Listen to your heart and your soul. Fight for yourself and others. It will keep you going.

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

Never, ever give up! If you can’t realize your dream one way, find another way to do it. It may take you longer, but do it. Henry Winkler (the Fonz) applied to sixty-eight different colleges before one accepted him. He was not diagnosed with dyslexia until his son was. He never gave up. We can’t either!

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it with your enemies. I don’t care!

Feel free to “Like” my post.

Survivors SPEAK OUT! Brandy Hunter

Survivors SPEAK OUT! Brandy Hunter

presented

by

Donna O’Donnell Figurski

1 Brandy Hunter1. What is your name? (last name optional)

Brandy (Denise) Hunter

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

Blountsville, Alabama, USA (about an hour north of Birmingham and an hour south of Huntsville)

Email (optional)

BrandyDHunter@Gmail.com

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

January 13, 2004

At what age?

I had just turned 24 years old. (My 24th birthday was November 20, 2003.)

4. How did your brain injury occur?

I was driving to work to a local restaurant (Ruby Tuesday). The highway on which I was driving is a four-lane. I was in the left (“fast”) lane. (I was driving a four-door Plymouth Neon.) The driver of a full-size pickup truck moved in front of me. He then slammed on his brakes, stopping his truck abruptly in front of my car. I swerved into the right (slow) lane so I could avoid hitting his pickup truck. I assume that I panicked – I either did not see the 18-wheeler driving in the lane I was “escaping” into or I thought I would be able to “beat” the truck. The pickup-truck driver did not stop or even look behind at the devastation he had caused. Witnesses say that that he sped up and went through the next 4-way stop.

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

The driver of the 18-wheeler truck ​climbed out of his rig ​to check on me. I was unresponsive, so he climbed into the car with me. (I “remember” seeing him cradling me – but I’m not sure that is possible because he THANKFULLY did not move me.) ​He began praying audibly. I recall this happening. I remember seeing it from above. I refer to it as an “out of body experience.” (DISCLAIMER: I believe in God, but I am not religious.)

6. What kind of emergency treatment, if any, did you have?4 Brandy Hunter

Paramedics and fire fighters were quickly on the scene. (The accident happened close to where a volunteer firefighter lived – thankfully.) I had a chest tube inserted for a collapsed lung. A “Life-Saver” helicopter transported me to UAB Hospital in Birmingham, Alabama (at the University of Alabama). The accident occurred around an hour (driving time) away from the hospital. When I was admitted into the hospital, it was determined that I had a traumatic brain injury (TBI). (The first responders had thought I had a TBI, as we were told months later, because I had what is referred to as “doll’s eyes” at the scene.) In the Emergency Room and in the hospital, a breathing tube was inserted, and two tubes were inserted into my right frontal lobe to drain fluid. I had a C2 fracture of the spine. Therefore, I had a brace placed around my neck to keep me from breaking the vertebrae. I wore the neck-brace for about six months.

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

I was medically induced into a coma, and, of course, I fell into one soon after. I remained comatose for approximately five weeks. My score on the Glasgow Coma Scale was 7 or 8, if I am recalling correctly. I know it was a dangerous score.

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?

As a patient, I had occupational, physical, and speech rehab for about two months. After I was released from the hospital, the therapies then continued at an outpatient facility for around two years. I also had a couple of months of voluntary speech therapy about three ​years after my outpatient therapies ended.

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

My memory was impaired for several years after the injury occurred. I would forget the things that happened two minutes prior. Then it was five minutes prior – then fifteen minutes – then hours – and then days. Slowly, I began to recall things more easily. I still get days mixed up. I might believe something occurred several weeks ago, when in reality it happened one or two days ago. I wasn’t able to remember much of the 3-6 years prior to the accident because my brain injury was so severe. It’s now hazy, but I can remember those incidents when my memory is triggered by a smell, a sound, or something else that is considered minor. (The brain is an amazingly complex, yet simple thing.)

Although it has been eleven years since I sustained brain damage, I still have trouble with my balance. I almost always have to hold onto a handrail when climbing and, especially, descending a set of stairs. My balance isn’t nearly as troublesome for me as it was, though. When I am shaky, when I run into things (due to a problem in spatial reasoning), when my speech is slurred, or when dysplasia occurs (saying one thing, but meaning another – usually substituting for the correct word another word that has absolutely nothing to do with what is being said), it is because I am tired. Mom says my brain is overworked and needs to rest. Dad compares my brain to a computer and says that it needs to “reboot.”

My perception is altered a bit (but not enough to hinder my ability to drive a vehicle legally).

My personality is sometimes dramatically changed. I express anger differently. I no longer find certain things humorous like I did before. However, when I do find something funny, it is difficult for me stop giggling. Before the TBI, I would cry “at the drop of a hat.” I rarely cry now. I believe it is because I unintentionally “taught” myself to hold back emotions like that because my speech is very difficult to understand if I am crying when I talk. My always-short patience seems to have been negatively affected. I would once say, “I don’t want (it) yesterday; I want (it) the day before yesterday!” Since the accident, I want (it) three days before yesterday!

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

My life has changed for the better in some ways. (Maybe the reason is also due to maturing.) I have done things I never would have done before. I moved to Long Island for three years. I’ve learned who my TRUE friends are. I’ve accepted and admitted (to myself and others) romantic feelings for “old” friends. I’ve given one man “a chance” that I never did before (and now we are planning to marry one another).

My life is also worse in some ways because I have a hard time controlling my emotions. (For example, I succumb to anger much more easily.) I hate that I am able to control my once-considered “soft heart” where other people are concerned. Also, I am now much more sensitive. I take things personally more often than I once did – I no longer let things “roll off of my back.”

11. What do you miss the most from your pre-brain-injury life?5 Brandy Hunter

I miss my voice.

I miss being able to multitask.

I miss being able to work as a “deejay” and have a radio show (sort of the same as my previous answers).

I miss being able to accomplish more than one thing per day. It is tiring for me if I try to go to the store AND go see my grandparent. Add another task in there, and I am spent!

I miss the way I didn’t have such a “wild-eyed” look in photos.

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

I enjoy that I am more willing to accept that I am wrong. Honestly, I like the feeling I get when I admit that I’m wrong. I like that I’m more apt to say, “I’m sorry,” as opposed to allowing my pride to win.

I am grateful that I no longer take little things for granted.

I am grateful that I now enjoy the company of dogs. I was once a “cat person.” I still love cats, but I truly do not know how I would have gotten through the past several years (finishing my college degree, etc.) without the love of my “babies,” Coco and Whiskey. I am not as keen on having children as I once was. I used to say that I wanted a house FULL of kids. Now I am happy with my “chi-weenies” as my only children.

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

As previously mentioned, I dislike how much my voice has changed. I do not like that, due to dexterity issues, my handwriting is sloppy. I don’t really enjoy having to wear glasses for more than reading. But, it is what it is. At least I’m here and able to complain (and understand why I am complaining).

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

I now accept the differences in my life since the TBI. I have learned to accept the difficulties I have now (and will always experience). I finally (and regrettably) accepted that my life will never again become the life I had before the TBI. Knowing that other people (some of them, anyway) understand how my personality is NEVER going to be the same allowed me to learn to accept my new personality too. I was always a proud, strong girl and having my plans (or really “lack of plans” – remember, I expected things to just “fall into my lap”​) altered so severely fueled my desire to become a prouder, stronger WOMAN.

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

My home life is different, since I no longer live with my parents (partly due to an angry outburst I had). My relationship with my mom has been forever changed. My inability to have a strong hold over my reactions/words when I’m angry enabled Mom to see a side of me that I always kept to myself. I regret the reasons things have changed, but I think the ways in which they did are for the better – in BOTH our lives. I am unable to “think before I speak.” Therefore, I often say words I do not mean to people I love, so that I can be “heard.”

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

Yes, my social life was altered greatly. I was once a very popular person with multiple invites to different places, often happening at the same time. I would have to turn off the ringer on my phone in order to take a nap, or even to get a little sleep. People would show up at my house unannounced at any hour.

When I got out of the hospital, people only wanted to visit me out of curiosity. They were curious as to how a brain-injured person looked. I don’t have any scars from the accident. I look exactly the same – luckily. I only have scars from the people who worked so diligently to save my life. Those scars are minor, too. My visitors assumed that, because I was home and looked the same, I was completely “normal” again or that I was the same person they so fondly remembered.

3 Brandy Hunter17. Who is your main caregiver?

My mom was my primary caregiver, with help from my (step)dad when he wasn’t at work. I have lived with a roommate since September 2006, including my current boyfriend since August 2011. The two of us traveled to England, where we lived together for three months.

Do you understand what it takes to be a caregiver?

Yes. I understand that my parents had to halt their own lives so I could have a semi-“normal” one myself. I will never be able to aptly express my gratitude to either of them for their unwavering love.

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

I would like to begin writing on a regular basis.

I do not wish to work outside the home; I am no longer able to prioritize my time. [I have tried to disprove doctors and family and actually work with the public. At one job, I was a cashier at the busiest grocery store on Long Island. The store worked with me and allowed me to have four-hour shifts because my brain would tire out. I worked for almost one year before I was fired for my cash-register drawer coming up short a few times. I had a caseworker come in and fight for me to at least still have a job with the company. I tried working in the floral department (no cash was handled), but I had to quit after about one month. Also, while on Long Island, I worked at Macy’s. I ran a register for three days. I informed the woman who hired me that the job was far too “fast-paced” for me, and regrettably I would have to quit. (I sincerely thanked her for her giving me a chance. She understood because her husband was a TBI survivor.) She gave me a job as a “recovery specialist.” I moved items from the storage rooms to the sales floor. I would put products that were moved by customers back into the correct places. I did that for four hours a day. In both aforementioned jobs, I would work Mondays and Tuesdays for four hours a day. I would have Wednesdays off and then work four hours a day on the following Thursday and Friday. I moved back home to Alabama after I finished my degree online. (I began it while living in New York.) I got a job working as a “pizza maker” at Papa John’s. (I had that job years before the accident.) Apparently, I was not working quickly enough, so I was fired from that job. I had never been fired from a job until the grocery store in New York and later Papa John’s in Alabama. A few months later, I began to look after a 3-year-old boy while his parents worked. That little boy was rambunctious! But for some reason, I was very patient with him. For example, he would tell me he needed to go to the bathroom. So, I would get him situated and walk outside the room to give him privacy. He normally would go without a problem. One particular day, he refused to go after telling me that he needed to. I would not allow him to leave the bathroom until he used the toilet. He got so tired that I made him sit down until he decided to go. My tenacity proved to be a positive thing with this child. We also went through the same thing after he got up and I told him to wash his hands. It wasn’t nearly as difficult because he KNEW I was not giving up. I mostly despise how my brain gets focused on something, but with this child, my focus was a good thing. I also worked at Babies-R-Us for five months. Again, I worked in BOH (back of house). I would run a register occasionally. I quit that job after five months because my now-fiancé took me to Bristol, England, for three months. That was an opportunity that I could not pass up.] When we returned to the States after living in England, my boyfriend said I could be a housewife if I did not wish to work outside of our home. I once never would have imagined that sort of thing bringing me happiness. Now, I am so uberly happy and oh-so-lucky to have his love and understanding.

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.

Accept the challenges you now face daily. Don’t think you will become who you were pre TBI. (As one of my doctors in the hospital would constantly say, “THIS IS NOT TV.”) Difficult as it is, strive to acknowledge that you are no longer exactly like the person you were. You have differences. Learn how it is best for you to handle them and share what you’ve learned with those who are in your everyday life. Acceptance of the “new you” is crucial to being happy in your future. Also, allow the help that people offer. At the same time, do as much independently as you are able.

20. What advice would you offer to other brain-injury survivors?

Don’t dwell on the way life WAS; make the best of the life you still have. Create what is “normal” for you – a survivor. Never accept the “normal” for other survivors. Admit it when you realize that you are wrong. “I’m sorry” is a phrase that will help you with your relationships (be they familial, romantic, or even friendly).

Do you have any other comments that you would like to add?2 Brandy Hunter

Pre TBI, I took life for granted. Even though I was grateful for the life I was given/chosen, I did not actively pursue the things that I wanted. Rather, I expected everything to just “fall into my lap.” Post TBI, it’s taken me almost ten years to realize that there’s no shame in having to work harder at something that WAS simple pre TBI. [I have since attended a traditional university – thanks to my mom and dad, who drove me to classes taught at a university that is ​25 minutes from our home. I made As and Bs studying Broadcast Communication. (Before the injury severely affected my speech, I was an on-air personality for a large-market FM radio station. I was also a producer for a popular morning-show team. My on-air name for that show was “1/2 Pint.”) I finished my degree online through Ashford University, and I obtained a Bachelor of Arts degree in Communication Studies when I finished my education online at Ashford. (I lacked one semester and an internship in order to graduate from the original university.) I made the Dean’s List each semester I was enrolled at Ashford, and I graduated college with a 3.79 GPA.​]

Read Brandy’s Guest Blog post on my blog at, “I Am Blessed.”

Click here to learn more about Brandy Hunter.

Click here to read Brandy’s blog, Brandy’s Brain.

For the sweetest video about Brandy and her Mom, click here. Because She Loved Me . . .

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

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If you don’t like my blog, “Share” it with your enemies. I don’t care!

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Survivors SPEAK OUT! . . . . . Pam Richardson

Survivors SPEAK OUT! Pam Richardson

presented

by

Donna O’Donnell Figurski

Richardson, Pam McClurg 11. What is your name? (last name optional)

Pam Richardson

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

Louisville, Kentucky, USA    pamr1672@yahoo.com

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

My brain injury happened in 2004. I was 46.

4. How did your brain injury occur?

I had a colloid cyst removed. It’s a benign brain tumor located in the third ventricle of the brain. Not much is known about a colloid cyst. It is thought to be something one is born with, but symptoms occur later in life.

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

I had headaches and dizzy spells for years. I went to all the appropriate doctors. I was diagnosed with sinus headaches and Meniere’s disease (an inner ear disorder causing dizziness).

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

I was passing out and falling down. A CT scan (computerized tomography, also known as a CAT scan – computerized axial tomography) showed that the tumor was cutting off my CSF (cerebrospinal fluid) in my brain. I was urgently scheduled for removal of the tumor the next day. I had a ten-hour surgery with a craniotomy (surgical opening of the skull) for the complete removal of the tumor.

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

I was not in a coma. However, I had no memory.

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 no rehab. After a year, I realized there had to be help for people like me, and I started getting on the computer. However, my short-term memory was terrible. I found the Brain Injury Alliance of Kentucky, and they changed my life! But I don’t remember. 😦

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

I have short-term memory loss, although my memory is (thankfully) getting better all the time. I made terrible decisions. I divorced my husband and don’t remember it. When people say, “Live in the moment” – that is what I did. It is a HORRIBLE PLACE TO LIVE! I have no concept of the past to be able to reference, and I have no ability to think of the consequences of my decisions for the future. I bought cars for both of my sons. I bought clothes I would never wear. I couldn’t remember what kind of food I liked to eat … and lots more I can’t think of right now. Oh, I tried to go back to work, but I couldn’t remember what I used to do.

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

My life is completely turned around. I was married to a physician. We would travel. We had a good time. We had a great life. I screwed everything up. I divorced him – don’t know why. I came to a realization a few years ago that I had to accept the NEW ME because that is the life I have now. No looking back. Accept where I am now. Live forward from today.

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

I miss being married. But it’s OK, and I’m still young. 🙂

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

I like that I have the ability to relate to others about traumatic brain injury (TBI). I love to help others. I am much more “healed” than I was when I started on this journey. Of course, each year I thought I was feeling much better. What I have learned is that it is a life-long journey.

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

I dislike my short-term memory issues.

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

God – and my family and friends

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

Yes, as mentioned above. Also, you really learn who your true friends are. People just don’t understand TBI.

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

My social life has changed completely. When you don’t “remember” to call your friends back time after time, there is a time when they don’t call you back.

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

At first, my main caregiver was my husband. But after I left, it was my sister. She still is there whenever I need her.

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

I don’t really know what the future holds for me. I now have grandchildren who are the love of my life. I take one day at a time.Richardson, Pam McClurg 2

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.

I wish I would have known more about what would really happen AFTER my surgery. I was told I might have a few memory problems – but nothing like what I have experienced. Of course, I had no time to prepare, nor would I have remembered it. Nevertheless, my family would have been more educated and informed. Physicians need to be educated about brain injury!

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

YOU WILL MAKE IT! Think positive! Have a good support system! Go to support-groups. Get online to support-groups. There are resources in your state and in your community. Never, ever give up. YOU ARE WORTH IT!

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it with your enemies. I don’t care!

Feel free to “Like” my post.

Survivors SPEAK OUT! . . . . . Debra Cody

Survivors SPEAK OUT! Debra Cody

presented

by

Donna O’Donnell Figurski

Deb Cody Post accident1. What is your name? (last name optional)

Debra Cody

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

Ailsa Craig, Ontario, Canada     debcody63@gmail.com

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

I was 47 when I was diagnosed, but I was 42 when I had my first concussion.

4. How did your brain injury occur?

I suffered four concussions over a five-year span.

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

It was clear I had a problem about four months after my last concussion in 2010, but my mother and my husband say they noticed a difference in me about two years before that.

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

I was assessed in the Emergency Room after the first, second, and fourth concussions. I was always told to go home and rest for a couple weeks for the concussion. I opted not to go to the hospital after the third one because I knew I would just be told to go home and rest. For the fourth one (after the car accident), I was taken to the hospital by ambulance, as the concussion (according to the doctor) was “the least of my worries.” I had other injuries that needed surgery, a tracheotomy, and a G-PEG (gastric tube that leads directly to the stomach for feeding).

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

No

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)?

Yes. I was in an outpatient treatment program.

How long were you in rehab?

I have been in the program for three years now.

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

I have headaches. I tire easily. My personality was affected. I have issues with perception, hearing, anxiety, depression, confusion, and vertigo.

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

I like to say that “life is my oyster and my brain injury is the pearl.” My life started out as worse, but it has slowly gotten better. My life is quieter now. I am less socially active than I was before, but I am finding (TBI). I am careful about how I choose to spend my time, as I have so little “functioning” time to spend.

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

“Me”

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

I enjoy having the awareness of how valuable time truly is.

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

My limitations

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

Counseling and the love and support of my husband and children have helped me to accept my TBI.

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

My home is quieter, and we have gotten rid of a lot of things. I get over-stimulated easily, so we streamlined our home. My relationships have changed greatly. There are fewer people in my life – I found that family and friends stopped coming around and calling. Slowly, over that past eight months, I am seeing some of “The Lost” coming back. Over all, people found the changes in me hard to understand and accept.

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

I go out less, and I am careful about the events I attend. It takes a lot of planning and preparation for me to go somewhere. The spontaneity is gone from my life.

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

My husband is my main caregiver. I don’t go far without him. I truly do understand what it takes to be a caregiver. (It helps the understanding that I am the mother of four children.)

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

My plans are to keep moving forward. I look back to where I was four years ago, and I know that I never want to go back there. The only way to prevent that is to keep “getting better.” As for ten years from now, I don’t know. I have become a “one-day-at-a-time” person. What I can say is that I hope to see that I have been able to reclaim some of my independence.

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.

My advice is to be gentle with yourself. I lost a lot of time trying to “force” myself to be who I once was.

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

Planning, preparation, and pacing are huge in my life now. On days when I think I am “Superman” and can “fly” by the seat of my pants, the “kryptonite” (my brain injury) “defeats” me every time! The three things above will make your life so much easier. Look for something good in every day. Remember to celebrate your accomplishments, no matter how small they may seem to others. And, be gentle with yourself. It takes time to create something as amazing as you are going to be!

 

(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.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it with your enemies. I don’t care!

Feel free to “Like” my post.

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