TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘MVA’

SPEAK OUT! Faces of Brain Injury Jenn Von Hatten

SPEAK OUT! Faces of Brain Injury – Jenn Von Hatten

presented by

Donna O’Donnell Figurski

 Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718On Valentine’s Day 2011, I went to work only for a meeting. (I was a nurse at a long-term mental health facility.) Freezing rain struck during the meeting. The treacherous road condition was responsible for my car’s being T-boned at highway speed. That’s how I acquired my traumatic brain injury. The paramedics found me “clinically dead.” Obviously, I was alive. The pressure on my brain was monitored to see if I needed to have surgery. Also my liver was lacerated. Fortunately I did not need surgery for either. I was put into a medically induced coma because, in addition to my brain injury, I fractured a rib and three vertebrae. I was in a coma for over seven weeks. I managed to develop pneumonia and had to have a tracheotomy. I was discharged on July 14th. I Jenn Von Hatten Emma, & Hannasurvived to see my oldest children graduate from high school. Emma graduated in June 2013, and Liam, in 2014.

Spastic muscles affected my speeJenn Von Hatten & Liamch, so I went to physiotherapy, occupational therapy, and speech therapy. My balance was severely affected. I used to be in a wheelchair, due to the fractured vertebrae. I since “graduated” to a walker, then to a quad cane, and eventually to a mini quad cane. Now I’m a fall risk. My life has definitely changed. I am no longer able to work as a nurse. I cannot say if my life is better or worse. All I can say with certainty is that my life is different.  I enjoy my time with Hanna, my 7-year-old daughter and youngest child. (I have joint custody. I remind myself that not many relationships survive a TBI.) I now have a cat, Spunkster, which I got from the local SPCA. When Hanna’s not with me, I hang out with Spunkster. I miss most my being able to work as a nurse. But as much as I would like to a work as a nurse, I know I would not be safe – physically (because I am a fall risk) as well as mentally Jenn Von Hatten & Hanna(in terms of remembering if I gave a client his or her medication or treatments). I had graduated as a nurse only seven months before my 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 driver’s license has not been revoked, but my rehabilitation doctor says I still cannot drive, as my reflexes are not up to snuff. My plan is to help others that are TBI survivors or caregivers. I can provide info and support.

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

(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 Comment” below this post.

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SPEAK OUT! Faces of Brain Injury Dale Christianson

SPEAK OUT! Faces of Brain Injury Dale Christianson

presented by

Donna O’Donnell Figurski

Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718It can happen to anyone, anytime, . . . and anywhere. The Brain Trauma Foundation states that there are 5.3 million people in the United States living with some form of brain injury. On “Faces of Brain Injury,” you will meet survivors living with brain injury. I hope that their stories will help you to understand the serious implications and complications of brain injury. The stories on SPEAK OUT! Faces of Brain Injury are published with the permission of the survivor or designated caregiver. If you would like your story to be published, please send a short account and two photos to me at neelyf@aol.com. I’d love to publish your story and raise awareness for Brain Injury – one view at a time.

Dale Christianson (survivor) Christianson, Dale 1 050815Thirty years ago, my family was hit by a carload of drunken teens. My life slowly fell apart after that. I nearly gave up. For a long time, I thought that the guy who hit my car was the lucky one. He died in the accident, along with my stepdaughter. The only compensation that I got was $7,000. I have had a hard time holding a job or maintaining a relationship since then. My most successful relationship just ended. My fiancée of five years just gave up on me. She said it was too hard to live with me. My sisters and other family members won’t talk to me. They treat me like I don’t exist, or they wish that I didn’t. I am at another breach in my relationships, and I don’t have a job. I have anxiety and panic attacks. I take Paxil, and it helps tremendously. I understand that I’m difficult, but I haven’t given up on myself.

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

(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 Comment” 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.

“Another Fork in the Road” . . . Brain Injury Radio Network . . . Interview: Lisabeth Mackall

You Are Invited

Lisabeth Mackall: Caregiver, Therapist, Author

putthis_on_calendar_clip_art

When Lisabeth Mackall opened her front door at 2:30am on January 2, 2012, it changed her life forever. She learned that her husband, Police Officer Frank Mackall, had been in a serious motor vehicle accident while on duty, and had been airlifted to a hospital. When Lisabeth opened her front door, she unknowingly entered the world of brain injury. She had to follow “Another Fork in the Road.” Lisabeth will share how she and her family picked up the remnants, pieced them together with patience, persistence, and love, and forged a new life.

Come One! Come ALL! 

What:        Interview with Lisabeth Mackall, caregiver to spouse, Frank Mackall

Why:        Lisabeth will take us on a harrowing journey of how her husband got a brain injury and how her family is coping with this new “normal.”Mackall, Lisabeth with Book

Where:     Brain Injury Radio Network

When:       Sunday, May  3rd, 2015

Time:         5:00p PT (6:00p MT, 7:00p CT, and 8:00p ET) 90 minute show

How:         Click: Brain Injury Radio Network

Call In:    424-243-9540

Call In:     855-473-3711 toll free in USA

Call In:    202-559-7907 free outside USA

or SKYPE

If you miss the show, but would like to still hear the interview, you can access the archive on On Demand listening. The archived show will be available after the show both on the Brain Injury Radio Network site and on my blog in “On the Air.”

(Clip Art compliments of Bing.)

(Photo compliments of Lisabeth Mackall.)

Survivors SPEAK OUT! Kristin Russo

Survivors  SPEAK OUT!  Kristin Russo

by

Donna O’Donnell Figurski

Russo, Kristin December 2014 After

Kristin Russo – Post-TBI Dec. 2014

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

Kristin Russo

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

Annandale, Virginia, USA

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

July 22, 2013 – I was 28.

4. How did your TBI occur?

My TBI was caused by a collision with a tractor-trailer. Read about it. “Kristin Russo accident.”

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

It was realized about 2-3 days into my stay in the ICU (Intensive Care Unit).

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

I have no memory of the accident, the month in the hospital, and even the first 5-6 months at home under 24-hour care.

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

Yes. My coma was induced.

8. Did you do rehab? What kind of rehab (i.e., inpatient or outpatient and occupational and/or physical and/or speech and/or other)? How long were you in rehab?

I had occupational, physical, speech, and recreational therapies for a month as an inpatient. I had therapy as an outpatient until May 2014 when all but physical therapy ended. I’m still in physical therapy for physical injuries.

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

I have moderate to severe diminished visual memory, mild to moderate decreased attention span, diminished executive function, and mildly diminished speech and language function. Those are the significant findings as per my neurological addendum. It was also noted that I am likely to have significant permanent neurocognitive dysfunction due to the TBI. This problem with the physical brain injury is further complicated due the fact that I have significant PTSD (post-traumatic stress disorder). I have a college degree, yet I had to learn how to do things as simple as double-digit subtraction. My entire education has been wiped away. Since I graduated with honors, it was easy to get accepted to Liberty University. But, I can’t retain information anymore, so I’m not sure if I’m going to go back to try and learn everything all over again. My neurologist has diagnosed me with ADD (attention deficit disorder) due to the TBI. I’m not allowed to use anything hot without supervision, etc.

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

Some things are better because I now have an excuse for being directionally challenged or for when I mess up (haha). 😉 Things are worse because I am dependent and I HATE IT! (I am an independent girl.) I was such an intelligent woman. I was still paying off my degree when the accident happened. Not being able to use ANY of the knowledge really made me unhappy. Not being able to work has been horrible because that is all I have ever known. I have been working since the day I turned 14. (My first day of work was on my 14th birthday). I worked at the same place until I graduated high school and went to college. I hate that I can no longer drive. I miss being able to do what I want to do when I want to do it. 😦 I live about eighty miles from where I grew up, so it’s not often that someone comes to visit me. The accident caused me to lose my family because my own father was stealing my pain pills for his sick addiction. I’ve lost some of my friends because I’m a totally different person personality-wise. I’m 100% honest, and I have dedicated my life to Jesus Christ. The girl in the accident died. She wasn’t the best wife. (I’d give more details, but those things are better kept between husband and wife. 😉 ) But, that’s why my accident happened, and I know it. God was showing me what was in front of me, and the same, for my husband. God was bringing us closer together, and that’s exactly what my accident did. So, that’s what I do like about the TBI. Another thing that I like about the TBI is that I don’t remember the accident or being in the hospital or even the 5-6 months after it. I also don’t remember my surgeries up to July. I remember the ones on Black Friday and December 1st. But, yeah, the girl I was before was a girl who drank a lot and went to clubs and acted like she was a single 21-year-old female. Since I’m not her anymore, I’ve lost a couple friends who were just like that girl. I don’t need those girls anyway!

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

I miss being able to drink alcohol sometimes – at least to drink socially. I miss being able to drive. I miss being able to do what I want when I want. I miss working. What I do now is to constantly go to appointments – it’s nuts! I am still in physical therapy – several months post accident. I just got yet another MRI scan (magnetic resonance imaging). I had surgery number eight on January 27th. I began speech therapy in January since insurance started paying again. I miss sleeping like a normal person. I miss being skinny. (I was a size 2 when I was married on July 7th, 2011, and I’m not that size anymore.) I hate being on so many damn medications. I loathe people’s not understanding invisible disabilities. I also have CRPS (complex regional pain syndrome) that was caused by the accident. It’s a chronic pain disease that has no cure.

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

I enjoy the fact that the Trauma Survivors Network Next Steps program taught me to find the positive in everything, so I do. When my legs hurt, I remind myself that I shouldn’t have any, so I thank God for letting me keep my legs! When I have my chronic headaches, I thank God for not making the swelling be so bad that I need to have surgery!

13. What do you like least about your TBI?

I don’t like that I sleep every other day sometimes. I dislike the chronic headaches and the fact that a headache is invisible. I don’t like having memory issues and being confused so often.

14. Has anything helped you to accept your TBI?

God

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

My husband gets rather upset when I forget that I’m not supposed to use a curling iron, and I fail to remember to turn it off. I no longer speak to my parents – my father makes fun of my TBI and acts like I’m making it up. (A*^#@~! ! I guess that’s what drugs do to ya.)

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

I don’t really have a social life anymore. Things are so much louder now. People annoy me more. 😦 I have NO filter. I just want to be home with my husband or alone with my dogs. I haven’t watched TV since the accident.

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

My husband is my main caregiver.

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

I’ll be running a photography business. 🙂 And, I better be a mommy to more than just my fur babies!

Russo, Kristin Before Accident

Kristin Russo Pre-TBI

19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other TBI survivors with your specific kind of TBI.

I urge people to try to make a positive out of everything. Depression is so ugly. I wish that I never hit that stage. Having a positive attitude has helped me SOOO much.

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

I give back now by volunteering at the hospital where I did my outpatient therapy. I got one of my dogs certified as a therapy dog, and we visit patients. I also visit patients in the trauma unit. My visits help others, and they also help me!

 

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

(Disclaimer: The views or opinions in this post are solely that of the interviewee.)

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

(Photos compliments of Kristin.)

As I say after each post:

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

Feel free to follow my blog. Click on “Follow” on the lower right corner of your screen.

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.

 

Caregivers SPEAK OUT! . . . . . Christina WIlliams

Caregivers SPEAK OUT! – Christina Williams

by

Donna O’Donnell Figurski

Christina WIlliams1. What is your name? (last name optional)

Christina Williams

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

Pine, Colorado, USA

3. What is the TBI survivor’s relationship to you? How old was the survivor when he/she had the TBI? What caused your survivor’s TBI?

The TBI survivor was my fiancé. His TBI was caused by a motor vehicle accident. He was 37. I want to add that it was in 2008, so it happened more than six years ago.

4. On what date did you begin care for your TBI survivor? Were you the main caregiver? Are you now? How old were you when you began care?

I was at the scene of the accident. I was his main caregiver; I still am now. I began care as soon as I could. I was 47 when the accident happened.

5. Were you caring for anyone else at that time (e.g., children, parents, etc.)?

No

6. Were you employed at the time of your survivor’s TBI? If so, were you able to continue working?

I worked with my fiancé in our own business – building custom homes, decks, basements, bars, etc. We also designed and created log furnishings on the side. When he got hurt, I was unable to continue working. I lost my job because I assisted him. We lost both businesses.

7. Did you have any help? If so, what kind and for how long?

No

8. When did your support of the survivor begin (e.g., immediately – in hospital, when the survivor returned home, etc.)?

Never.

9. Was your survivor in a coma? If so, what did you do at that time?

Yes, my fiancé was in a coma. I sat at his bedside, cried, and prayed a lot. I NEVER left the hospital for 72 days. I finally did after he was transferred to the rehab hospital.

10. Did your survivor have rehab? If so, what kind of rehab (i.e., inpatient and/or outpatient and occupational, physical, speech, and/or other)? How long was the rehab? Where were you when this was happening?

My fiancé was accepted to Craig Hospital in Denver, Colorado, (one of the top ten rehabilitation facilities in the US for spinal cord and brain injuries) for intensive physical, occupational, and speech therapies. He also had group therapy, recreational therapy, and swim therapy. I was with him every day. I had to be there before breakfast to help dress and feed him and to get him to his daily “classes.” He remained an inpatient for three and a half months. He then became an outpatient. I took him to therapy three times a week at first. Over time, it decreased to one or two times a week. After about sixteen months, we no longer went. We still continue to go back to Craig Hospital for specialized therapies for issues he has had since the accident. The last one was vestibular therapy for vertigo symptoms. But, they couldn’t treat it, so they worked on his balance issues.

11. What problems or disabilities of your TBI survivor required your care, if any?

He has epilepsy due to his TBI, so he requires supervision 24/7. He can never be left alone. Because of seizures and balance issues, he has frequent falls and injuries that require medical attention and trips to the Emergency Room. He can’t drive or work. He requires prompting for many of daily living skills, including hygiene, which is a huge issue.

12. How has your life changed since you became a caregiver? Is it better? Is it worse?

Both our lives have changed drastically. Our lives are worse, since we can’t have the “normal” life together that we expected. We now realize that we took our lives for granted. Buying a home or a new car and taking vacations are no longer possibilities in our lives.

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

I miss the freedom and having hope for the future.

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

I enjoy spending time with him every day. Every day is NOT “sunshine and roses,” but we make the best that we can out of every day. He is simply amazing. I look at him and watch him in awe, as he does whatever he does. I have a saying: “Let’s just hope today is better than yesterday.” It helps us focus on the positives in every day.

15. What do you like least about TBI?

I dislike that the TBI has destroyed such a good person and his future. We also lack the money and the ability to do whatever we want.

16. Has anything helped you to accept your survivor’s TBI?

Yes. God.

17. Has your survivor’s injury affected your home life and relationships and, if so, how?

We were officially engaged two days before the accident. We were SO in love and excited to be planning our future. Since his injury, his emotions (or I should say “ his lack of emotions”) and his poor judgment have caused us many, many problems.

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

We have no social life. ALL our “friends” vanished after he was hurt. Our social life is whatever we do in our day. When he has a doctor or therapy appointment, we plan a whole day in the city together.

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

I don’t have any hopes or plans anymore. We just take it a day at a time. In ten years, I imagine that we will still be doing what we’re doing now, but perhaps in a different house.

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

Turn to Facebook for support, especially the TBI pages. You may not know the people, but they have been a constant and great support not only to me, but also to so many others – survivors, caregivers, and their families and friends. It’s nice to read the stories of others and to share comments and advice. When my fiancé was hurt, I wasn’t using Facebook. It would have been so nice just to know that I wasn’t alone in my journey. Facebook is my “human” outlet for support. I have also come to find out that I can help others. That is more rewarding to me than I can say.

I think what I would want people to know that they aren’t prepared for is that it is VERY common for TBI survivors to start having seizures a year or so after the injury. It was something we weren’t prepared for, or even thought could happen. He was on anti-seizure meds while in rehab, but there was “no seizure activity.” So, they took him off the medication, and I thought it would never be a concern. Boy, was I wrong!Christina Williams 2012

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

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

(Photo compliments of Christina.)

Disclaimer: The views or opinions in this post are solely that of the interviewee.


SPEAK OUT! . . . . . . . . . . . . . . . . . Guest Blogger: Melissa Cronin Stages of Forgiveness

Stages of Forgiveness

by

Melissa Cronin

 

Girl Blogger cartoon_picture_of_girl_writingMore than eleven years ago, eighty-six-year-old George Russell Weller confused the gas pedal for the brake and sped through the Santa Monica Farmers’ Market. He struck seventy-three pedestrians. Ten people died.

I sustained life-threatening injuries, including a ruptured spleen and multiple fractures. Due to the nature of my traumatic brain injury, it wouldn’t be until three years after the accident when a neuropsychiatrist diagnosed me with a TBI.

During the early days and weeks of my recovery, weighed down by pain and the unthinkable – that others died while I survived – my brain lacked space for anything heady like the notion of forgiveness. Years later, when I possessed enough emotional fortitude to unearth the new articles I had collected about the accident, I decided I needed to find a way to forgive Russell Weller. I’ve been told that forgiveness is overrated, that you don’t have to forgive to heal. While that might very well be true, my want to forgive others for any wrong committed is part of my constitution. So I had to at least make an attempt to forgive Russell Weller. Otherwise, I’d be infected with a case of chronic bitterness and cynicism and worried I’d be contagious. Who wants to hang out with someone with a transmittable illness she has the capacity to heal?

To forgive, one must first assign blame. But, as in Russell Weller’s case, if there is no act of intentional harm, where do you place blame and, therefore, how do you forgive? To add an additional elusive layer, how do you forgive someone you’ve never met? Is it even possible to forgive someone you don’t know? I reached out to Russell Weller’s family years after the accident, but they refused my request to visit him. In 2010 he died.

The following year, I enrolled in an MFA program. During my third semester, still befuddled as to how to forgive Russell Weller, I wrote my critical thesis on the topic: The Face of Forgiveness. I examined how a particular writer, who had sustained life-threatening injuries after a car struck him, navigated the indeterminate nature of forgiveness on the page. Because each circumstance varies, forgiveness cannot be defined in absolute terms. *Since forgiveness is a process, I arrived at the conclusion that it can be charted in stages:

1) Understanding of the accident/incident

2) Transference of anger and other emotions

3) Self-pity

4) Awareness of others’ suffering

5) Avoidance

6) Surrender

Melissa Cronin leaves

Melissa Cronin

These stages don’t necessarily occur sequentially. Like Elisabeth Kübler-Ross’ stages of grief – denial/isolation, anger, bargaining, depression, acceptance – the stages of forgiveness may overlap, or one may become stuck in a particular stage. For me, I became stuck in one or two and skipped another one or two altogether. It’s also worth noting that the stages of forgiveness may not occur in a defined timeframe.

Stage 1: Understanding of the accident/incident

I dedicated months to reading news articles and investigative reports, parsing out the details of the accident: What Russell Weller was doing in the moments before he sped through the market, his medical history, his driving history, what bystanders witnessed at the scene of the crash. Somehow, I believed by reading those articles I would get to know Russell Weller and, therefore, be able to forgive him, or not. But written words weren’t enough – they seemed static on the page. Even though some articles included his apology – “I’m deeply sorry for any pain that everyone went through” – I could not hear his voice, hear his remorse, anger, or fear. And with all the contradicting statements about Russell Weller’s character and what people saw or didn’t see, I only became more confused. I felt like a pendulum – swaying dizzily between sadness and anger.

Stage 2: Transference of anger

As I read articles about the role the local entities had to play in running the market, any anger I harbored for Russell Weller quickly transferred to city officials who were responsible for ensuring the safety of pedestrians. I wondered why they didn’t have sturdy barriers in place, rather than wooden sawhorses. But, similar to my confusion regarding how to feel about Russell Weller, my feelings and emotions swayed – from judgment to understanding, from contempt to submission.

Stages 3 and 5: Self-pity and Avoidance

I did not become victim to self-pity – perhaps the perpetual warring dialogue in my head thrust self-pity aside. For the same reason, I skipped avoidance.

Stage 4: Awareness of others’ suffering

As I continued my dogged search to find meaning within the chaos, I could not help but be lured into an awareness of others’ suffering.  I imagined the physical and emotional pain the other injured pedestrians endured and the rage and anguish that tore into the families of the deceased. I viewed Russell Weller as injured, too – emotionally, mentally, psychically. I imagined Russell Weller’s grief: plagued by nightmares, isolated behind drawn window shades, sallow from regret.

The judge who presided over Russell Weller’s trial said he “lacked remorse” Because he didn’t cry? Why is it that we have a tendency to forgive others only if they exhibit unequivocal remorse: falling to their knees, drooping, sobbing? But a display, or physical showing, of remorse is not necessarily what matters to those harmed. Of course, a sincere apology does not negate the harm done, but sincerely spoken words of remorse are what matter. The quality of the voice matters: is it harsh, tense, creaky?

Melissa Cronin desert

Melissa Cronin

In 2011, I finally obtained and viewed a copy of the videotape of Russell Weller speaking with police officers soon after the accident. I slid the video into the CD player, inched close to the television screen, so close I felt as if he and I were together in the same room. Though he did not cry, his full-toned voice quivered as he said, “I’m in trouble with my heart and soul.” His voice then quieted to a whisper, as if he were in church mourning over the dead: “God almighty, those poor, poor people.”

That’s when I forgave Russell Weller. That’s when I surrendered – to Russell Weller’s remorse.

*Stages of forgiveness conceived by Melissa Cronin

 

9781611592399_p0_v3_s260x420Melissa is the author of “Invisible Bruise,” published in Chicken Soup for the Soul: Recovering from Traumatic Brain Injuries

forgiveness

 

Melissa also penned the essay, “Silencing the Boom,” which is published in Chicken Soup for the Soul: The Power of Forgiveness

 

To learn more about Melissa, please visit her website/blog at Melissa Cronin.

Thank you, Melissa Cronin.

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

(Clip Art compliments of Bing.)

(Photos compliments of Melissa Cronin)

Survivors SPEAK OUT! . . . . . Tracy Johnson

SPEAK OUT! – Tracy Johnson

by

Donna O’Donnell Figurski

Tracy Johnson Pre-TBI

Tracy Johnson
Pre-TBI

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

Tracy Johnson

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

Hogansville, Georgia, USA    lacigurl1@gmail.com

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

November 18, 1990    Age 20

4. How did your TBI occur?

Motor vehicle accident

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

It was noticed that I had a problem as I was slowly coming out of my coma. From then on, it was noticed daily.

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

I was life-flighted to the trauma center at Georgia Baptist Medical Hospital, which is now Atlanta Medical Center. The life-flight EMTs (emergency medical technicians) performed a tracheostomy. As they arrived, I was hanging outside the driver’s door having seizures, with lots of blood coming out of my mouth due to a busted spleen and a lacerated liver. At the trauma center, I received 37 pints of blood. Mom stopped asking about me after this because the situation looked grim. I even had docs (twelve of them) telling my mom there was nothing else they could do. They even made her sign some documents to this effect. On top of all the blood loss and trauma, I developed a bleeding stomach ulcer and required a PPI drip (proton-pump inhibitor). I had severely bruised my heart. My brain swelled to where my ears were set two inches deep within the swelling. The steering wheel had broken and jammed my front teeth up into my gums. My top teeth bit through my lower gums, so stitches were required. I had emergency surgery to my legs. I had broken my left hip. Three screws were required. (It healed, but at 23, I had to have a left hip replacement due to the dying of the blood vessel to the femur head.) My left femur was repaired (a rod was put in). It had also ripped through the skin. I had a left pelvic fracture. My left knee was broken in three places and required three screws. My left tibia and fibula were broken, but they’re okay now. My right knee was broken in four places. It was thought it may have been crushed, but an Emory specialist was able to save it. However, right knee arthroscopy a year ago yielded no good results, so I’m waiting for right knee replacement.

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

Yes. I was in a coma for five and a half weeks. I was on a breathing machine for four weeks. My heart stopped at the scene of the accident due to all the trauma my body was already in, but drugs were used to restart it.

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 rehab as an outpatient because my mother refused to let me go and stay at the Shepherd Center in Atlanta. I can’t remember how long I was at Georgia Baptist’s physical therapy. I know my mother was busy working at the time. This rehabilitation was for my multiple lower broken extremities, pelvis, and left hip. Nobody cared about the injury to my brain, except for me. And, I have just found my fellow sister and brother survivors via the Brain Injury Network. Praise God! 😉

Tracy Johnson - TBI Survivor

Tracy Johnson – TBI Survivor

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

I had a problem with all my memory at first, but the doctors said I would remember as my life took place. I had just given birth to my one and only child not even a month before my accident, and I know he belonged to me because this is what my family told me. Today he is 24, and I am 43. Our relationship has always been as “best friends” since my accident. My family often spoke of my deficits and of my inability to raise a child. My memory has greatly improved over the years. I repeated myself continuously, and I still do to this day. My emotions are all out of whack – I feel too happy, too sad, or too mad. I’ve been told by physicians that I am called a cycling bipolar manic depressive. But, I never knew a day of depression until I started being prescribed drugs. My anger goes to extremes. I guess it has something to do with growing up with a violent, alcoholic father and two brothers older than I. Hence, it was suggested that I was suffering from being left behind and of being deprived of parental love. My dad chased us around with shotguns. He beat my mom and brothers. He would point and shoot guns all the time. Oh yeah, I would be noticed and would be told to run and hide. My dad was always damaging things, causing me to have PTSD (post-traumatic stress disorder) along with the PTSD I already had from the auto accident. I also have PTSD from a carjacking and kidnapping/rape back in 2005, due to my being too trusting. Now it leads me not to trust anyone and to be very suspicious. I walk with a limp, due to one hip replacement and worn out right knee. I’m beginning to be aphasic in speech and can’t deliver my thoughts into the proper wording.

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

I feel my life is better because I was very judgmental. Having this injury occur and being out of this world for that length of time made me realize that the world keeps spinning around and people go on with their lives whether you’re here or not. Jeez, I was naïve. I now know that one’s life and recovery is what that person makes of it – NO ONE else. After the accident, I was, by the grace of God, very compassionate, nonjudgmental, and indeed touched by an Angel.

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

I miss the ability to think cognitively. I miss my memory. I only remember bits and pieces from my early childhood and preteen years. I don’t have much memory of my high school years – I guess because those memories were made so close to my coma days. (I was in high school from ages 16 to 19.) I guess as I’m thinking this through now, my traumatic dysfunctional childhood explains my issues with anger.

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

I like having the ability of not staying angry at someone for long, having the ability to forgive easily, and being able to experience things (always) as though they are the first experiences. Some of the learned knowledge of first experiences can lead to better outcomes, like relationships.

13. What do you like least about your TBI?

I can no longer think cognitively or remember as I did before. Oh, and almost all people have trouble relating. For example, people sometimes say I am making up my injury and symptoms, or I use it as an excuse.

14. Has anything helped you to accept your TBI?

I have been helped by my belief that Jesus Christ died on the cross for me. That is the gift of Grace from my heavenly Father above.

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

Yes, oh yes! It has caused distrust, dishonesty, and fighting. It has broken some of my most meaningful, close family relations to where I know they still love me, but they feel they have to love me from a distance.

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

I had friends, but they could not cope with such a tragic event happening so close to them, so they are not around anymore. I try to isolate myself now because I am rather paranoid of people and their motives.

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

My caregiver is my fiancé. I have been engaged for 7 years. Please don’t laugh – I just find it hard to trust anyone after being hurt by people time and time again, including my own mother. I know what is entailed in being the caregiver of someone with Alzheimer’s, as I, just this week, have made arrangements for my dad to go to a nursing home. I cared and assisted him for three years.

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

I stopped chemical prescription drug therapy, except for 1200 mg of a medicine for mental seizures until I can become part of protein therapy at Emory University Hospital in Atlanta, 53 miles from where I live. I would like to help others. I want to devote my time to helping motivate others by decreasing the negativity in their lives, even if it is just one person. I want to find a way to counsel young folks. I want to transform their lives if their parents feel they are too busy with work or if their parents just didn’t have anyone in their lives to show or explain to them.

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.

To control my emotions, I had to learn, study, and meditate on the Word of God. In doing so, I realized there are no set rules for being a child of God or to be loved by God. We all walk different paths with different hurdles, and all sins are different because of such. Therefore, our Father in Heaven does not judge each of us to the same measure or degree. We are CHILDREN of God, and we are learning each and every day. So, unlike the legal system, we shall not be punished for NOT knowing something.

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

Be your own unique, strong self – the one who made you a survivor. Do not be too hard on yourself. Take each step in stride knowing Jesus walks right there beside you. Know that family and friends do not intentionally mean to shift blame by calling you names or cutting you down – it’s just their way, however, of dealing with an injury of such scope and magnitude to their loved one. Learn to laugh it off, and if you can’t laugh it off, well then, smile it off. Humor and inner peace are always the best medicine. Sorry, docs. 🙂

Tracy Johnson, Tbi-Survivor

Tracy Johnson, Tbi-Survivor

 

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

(Disclaimer: The views or opinions in this post are solely that of the interviewee.)

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

(Clip Art compliments of Tracy.)

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