TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Brain Awareness’

Trike Treks – David Figurski

Trike Treks – David Figurski

presented

by

Donna O’Donnell Figurski

David Figurski 2004 Pre-Brain Injury

David Figurski – pre-brain injury

My husband, David, bought a Catrike 700 in April 2015.  He rides three days each week, 15 miles each day. David loves his trike. Despite not being able to walk outside unassisted because of a balance problem, he feels “normal” when he rides. He has found that people have a lot of curiosity about the trike. People have stopped him to ask questions. One woman talked to him from her car when they were at a Stop sign.

David is excited because he just broke 2,500 miles. But he still has a ways to go before he equals the 5,390 miles ridden by Dan Zimmerman and Catherine Brubaker on their cross-country trek.

David’s cumulative mileage as of 10/13/16               2,580 mi

Miles to reach 5,390* miles                                          2,810 mi

UPDATE:

David’s cumulative mileage as of 09/04/117               3,727 mi

Miles to reach 5,390* miles                                          1,663 mi

*done by both Dan Zimmerman and Catherine Brubaker on their cross-country ride

Figurski, David Trike

David Figurski – post-brain injury on his Catrike 700

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Brain Injury Resources CTE & Football (chronic traumatic encephalopathy )

Brain Injury Resources . . . CTE & Football

presented

by

Donna O’Donnell Figurski

 

Brain th-2The regular season of the NFL (National Football League) begins this week. Although American football can be exciting, we in the brain-injury community are very aware of the havoc that both concussive and sub-concussive head impacts play not only on the brain health of the pros, but also on the brain health of college and high school players (1). We are especially sensitive to the high risk of the trusting and still-developing young players in Pop Warner leagues (2, 3).th

There has been a growing public awareness of the brain disease CTE (chronic traumatic encephalopathy), which can develop from hits to the ctehead and lead to “memory loss, confusion, impaired judgement, impulse control problems, aggression, depression and progressive dementia.” Some players have retired early (4, 5). Former players have sued or are suing the NFL (6). There is still a great deal of ignorance about CTE, but much research has been done and is being continued vigorously. This article tells us some basic facts that we should know.

Here is a brief outline from the article:

“Concussions in the NFL are more widespread than we thought

“An estimated 96 percent of deceased NFL players had CTE

“Researchers are working on a test for living players

“The NFL has donated $0 to this important new brain injury study”

I urge you to read the article for the details.

 

(Clip Art compliments of Bing.)

 

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SPEAK OUT! . . . . . . . . . . . . . . Itty-Bitty GIANT Steps

SPEAK OUT! Itty-Bitty GIANT Steps

presented by

Donna O’Donnell Figurski

 

Itty-Bitty GIant Steps for BlogSPEAK OUT! Itty-Bitty Giant Steps will provide a venue for brain-injury survivors and caregivers to shout out their accomplishments of the week.

If you have an Itty-Bitty Giant Step and you would like to share it, just send an email to me at neelyf@aol.com.

If you are on Facebook, you can simply send a Private Message to me. It need only be a sentence or two. I’ll gather the accomplishments and post them with your name on my blog approximately once a week. (If you do not want your last name to be posted, please tell me in your email or Private Message.)

I hope we have millions of Itty-Bitty Giant Steps.

 

Here is this week’s Itty-Bitty GIANT Steps

 

Janice Tindle - Survivor

Janice Tindle – Survivor

Janice Tindle (survivor)…My accomplishment is getting published after my TBI (traumatic brain injury). I have a blog (janicetindle.com), where you’ll find all my links. I’m on Facebook, Twitter, and LinkedIn. I’ve been published in Caregiver magazine, Fearless Caregiver, and TBI Hope and Inspiration magazine. I’m also a contributor to TheMighty.com. I raise awareness about TBI and dystonia (a neurological movement disorder). I recently won the 1pg. Short Screenplay Contest. My entry, entitled Galicia’s Granite, was performed at the Novel Writing Festival. It’s on YouTube. I just fought two spam sites and got them to remove my article, 7 Ways to Support a Loved One with a Traumatic Brain Injury, off their sites. kids-hand-writing-clip-art-hand_with_pencil_5CAnnie Ricketts has it posted (with my permission) on her site, biglobalpicnic.org. I’m very proud of that article. I’m working on a several books and hope to become a PAID writer very soon!

 

 

Raine Turner - Caregiver & Author

Raine Turner – Caregiver & Author

Raine Turner (caregiver)…I am going to brag – big huge momma brag! My son [my brain-injured son, who was not supposed to survive, never mind thrive; my drug-dealing son, with a federal criminal record; my son, who is now at the University of Calgary studying a dual degree in Business and Actuarial Science (I said I was going to brag) and getting 80s (yes, on a reduced course load and with tutors)] is thriving against all odds. congrats-you-did-itThis same young man was actually the KEYNOTE speaker at the Brain Injury conference in Ottawa, which is supported by the federal government! So, if you think you cannot achieve, cannot fight, or cannot rise up to be at a higher level than the one on which you are at, you should put on your “big boy” or “big girl” underpants and work hard. You WILL rise up to be at a level higher than the one you are at now. It will not be easy; it will not be fun; but you will improve your life. If you need, I can always “kick your ass” to achieve more, as I did for my son! I am so excited; I am so proud of him! He has worked so hard for so long. My son is my HERO!

Raine Turner, the author of “Only Son… Only Child,” will be a guest on my show, “Another Fork in the Road” on Sunday, August 21, 2016, at 5:30pm Pacific Time, with her son, Ryan. I hope you will join us.

 

Matthew Vickers - Survivor

Matthew Vickers – Survivor

 

Matthew Vickers (survivor)…A huge feat for a traumatic brain injury survivor tubshower11who can’t walk or stand and only has the use of his right arm and hand … For consecutive weeks, I have independently showered, and that includes completing all necessary transfers.

 

 

YOU did it!

Congratulations to contributors!

(Clip Art compliments of Bing.)

(Photos compliments of contributors.)

 

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Survivors SPEAK OUT! . . . Abi

Survivors SPEAK OUT! Abi

presented

by

Donna O’Donnell Figurski

 

Abigail

Abi – brain injury survivor

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

Abi

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

Columbia City, Indiana, USA

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

I had my TBI (traumatic brain injury) at age 20.

4. How did your brain injury occur?

I was hit by a freight train in a suicide attempt.

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

I knew I had a problem when I started speaking, as my voice pitch changed quite a bit. Also, when I was asked to remember things from the day before, I had trouble doing so.

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

I was taken to a hospital right away. In addition to the problems noted above, I also had a messed up back and an amputated right arm, so those were tended to right away. I was also immediately given stitches to close up a wound on my head.

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

I don’t think I was in a coma, but I don’t recall very well the two days after my incident.

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

I had occupational therapy, physical therapy, and speech therapy both as an inpatient and as an outpatient. I was in the rehab inpatient therapy for at least six weeks. I was in outpatient therapy even longer, but the outpatient therapy focused more on my missing arm. I also had in-home therapy.

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

I have poor balance and slurred speech. I experience personality changes.

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

I believe my life has changed for the better, as I’ve met so many who are worse off than me.

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

I miss nothing from my pre-brain-injury life, as my personality changed for the good. But I do miss people understanding me.

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

Abigail 2

Abi – brain injury survivor

I like to meet others with a TBI and other disabilities.

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

I dislike my slurred speech and sounding different than I used to.

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

Yeah – meeting those worse off

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

I’m much better, as I’m more social.

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

Yeah. I went from being deathly shy to a social butterfly.

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

My mother is my main caregiver. Yeah, I do understand what it takes. It’s hard work.

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

I plan to have a family and to be a counselor helping suicidal people.

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

Don’t give up.Don't Give Up

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

My advice is Don’t give up, and be you.
(Disclaimer: The views or opinions in this post are solely that of the interviewee.)

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

(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.

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SPEAK OUT! . . . . . . . . . . . . . Faces of Brain Injury . . . . . . Paige Matis (caregiver for her boyfriend, Bryan Carpenter)

SPEAK OUT! Faces of Brain Injury

Paige Matis (caregiver for her boyfriend, Bryan Carpenter)

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.

 

Bryan Carpenter 1

Bryan Carpenter – Survivor & Marine

In honor of this recent Memorial Day, I want tell you about my Marine and my hero – and my better half, Bryan.

Bryan enlisted in the United States Marine Corps in 2004. He went to fight for our country in the war in Iraq in 2006. Luckily, that year he survived not one, but two IEDs (improvised explosive devices often used as roadside bombs).

In the second incident, Bryan was the driver of the Humvee he was in. He suffered the worst injuries of the four Marines involved in the explosion. Bryan was knocked unconscious from the impact of the bomb. In the field, a military doctor did an emergency tracheotomy, but he nicked Bryan’s artery. Bryan also had a shattered pelvis, which cut his abdomen and caused him to bleed internally. Bryan only had moments to live. He underwent a transfusion with six units of blood. Nobody thought Bryan would make it out of his medically induced coma.

Bryan Carpenter 5 Survivor

Bryan Carpenter – Survivor

Two and a half weeks later, Bryan woke up. He was told by doctors that his dream of serving in the military as his lifelong career was over. The chances of Bryan’s ever walking “normally” again were close to zero. He was also told that he would suffer from this explosion for the rest of his life. Bryan said his dreams literally shattered right before his eyes.

Bryan never gave up. He was determined to beat the odds the doctors gave him. So far, he has done his best to achieve that goal. I know he still struggles every day with his PTSD (post-traumatic stress disorder), his traumatic brain injury, and the pain from his physical injuries. But, he still pushes forward. Bryan learned to walk again on his own. He has dedicated his life to physical therapy, and he never misses a day at the gym. After the incident, Bryan was a 120-pound man and was barely able to stand on his own two feet. He is currently walking independently, and he weighs 230 pounds (all healthy body mass and muscle).

Bryan Carpenter 2

Bryan Carpenter – Survivor

Bryan strives every day to help others. He has been an inspirational speaker, speaking to school-shooting victims, middle-school students, open events, etc. He is a gym trainer and an MMA (Mixed Martial Arts) coach. He was a bouncer at night clubs; he went to the Fire Academy; he threw out the ceremonial Opening Pitch in 2012 for the Cleveland Indians; he was even the Grand Marshall in his hometown parade. I know Bryan tries to accomplish everything he puts his mind to, especially when he knows that it will benefit someone. He is trying his hardest to help people achieve their goals after suffering pain like the pain he has gone through. Although he may struggle with the effects of his injuries from the explosion, he never lets them limit him.

Bryan Carpenter 3

Bryan Carpenter – Survivor

Bryan has put all his focus and attention into his new dream and reality – his book. He wrote the book not only as therapy, but also to inspire others that the unbelievable is always possible. In his book, Bryan talks about his dream to be in the military – from when he enlisted and went through boot camp to being deployed and injured. He has written about his recovery and the inspirational things he has done with his life as of now.

Holidays, like Memorial Day, remind me of what Bryan has overcome. Thankfully, and miraculously, he has beaten death. He has gone on to beat the odds. He wrote a book on his recovery to continue to serve and better his country.

 

Bryan Carpenter 4

Bryan Carpenter – Survivor

Many people have paid the ultimate price in the military. Those men and women will never be forgotten. … I am very thankful to have the chance to hug my Miracle a little tighter and a little longer on Memorial Day.

 

To learn more about Bryan Carpenter, please visit his website, Battle After Iraq.

You can also see Bryan’s book about his recovery. “Never Ending Battle After Iraq: A Marine’s Road to Recovery.”

 

Thank you to Paige Matis for sharing this story about her boyfriend, Bryan.

 

(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.

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Feel free to “Like” my post.

 

 

 

Survivors SPEAK OUT! . . . . . . Bart Goldstein

Survivors SPEAK OUT! Bart Goldstein

presented

by

Donna O’Donnell Figurski

Bart Goldstein 2

Bart Goldstein – Survivor

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

Bart Goldstein

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

Delmar, New York, USA

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

My brain injury happened on December 29, 2001. I was almost 17.

4. How did your brain injury occur?

I was riding with friends in an auto, and we had an accident. I was in the back seat. We were just teenagers clowning around. There were no drugs or alcohol.

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

I was in a coma after the accident.

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

I was airlifted to emergency surgery. Later I was given a trache and a G-peg (feeding tube inserted directly into the stomach by percutaneous endoscopic gastrostomy).

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

Yes. I was in a coma for a month.

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?

Bart Goldstein & Dog

Bart Goldstein – Survivor

I had speech therapy, physical therapy, and occupational therapy as an inpatient for three months at Helen Hayes Hospital. Then I had five more months of therapy as an outpatient at the hospital.

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

I have problems with walking, my speaking sensibly, control of anger, partial blindness, and memory.

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

I am much more of a planner now than I was prior to accident. An article, “The Journey Back,” from Brain Injury Awareness Month a couple of years ago answers this question and most of the others: http://spotlightnews.com/uncategorized/2014/03/20/journey-back/

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

See the Spotlight article (address given in the answer to the question 10).

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

See the Spotlight article (address given in the answer to the question 10).

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

See the Spotlight article (address given in the answer to the question 10).

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

I’ve been helped by my Christian faith, my parents, and my sense of humor.

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

See the Spotlight article (address given in the answer to the question 10).

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

See the Spotlight article (address given in the answer to the question 10).

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

My folks are my main caregivers. Caregiving takes a lot of love and more.

Bart & Joel Goldstein

Bart Goldstein – Survivor with Father, Joel Goldstein (author of “No Stone Unturned”)

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

I hope to continue to heal and to find a good woman and settle down.

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.

Learn patience. It’s a long haul.

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

Keep your faith and your sense of humor. Try alternative therapies.

 

(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!

On the Air: . . . . . . . . . . . . “Another Fork in the Road” Panel: Cognitive & Memory Deficits After Brain Injury

On the Air: “Another Fork in the Road”

Panel: Lisabeth Mackall and GeorgeAnna Bell

Cognitive & Memory Deficits After Brain Injury

presented

by

Donna O’Donnell Figurski

images-1Memory loss and cognitive deficits are both prevalent for many survivors after brain injury. Memory loss literally leaves many folks feeling a loss of control over their lives. Cognitive deficits can leave one feeling less than whole.

Lisabeth Mackall Book 061215

Lisabeth Mackall – Caregiver, Author, Speech Therapist

 

My panel, caregiver, Lisabeth Mackall and survivor, GeorgeAnna Bell joined me to discuss how memory loss and cognitive deficits affect them personally and how the deficits hinder their family dynamics. They offered suggestions that have worked for them.

Click on the link below to listen to the show.

GeorgeAnna Bell - Survivor

GeorgeAnna Bell – Survivor

 

 

See you “On the Air!”

On the Air: “Another Fork in the Road”

Cognitive & Memory Deficits After Brain Injury

(Clip Art compliments of Bing.)

(Photos compliments of panelists.)

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.

SPEAK OUT! Guest Blogger . . . GeorgeAnna Bell . . . . . . . . . . . . . How My Brain Injury Affected My Life

How My Brain Injury Affected My Life

by

GeorgeAnna L. Bell

presented

 by

Donna O’Donnell Figurski

 

Girl Blogger cartoon_picture_of_girl_writingI was diagnosed as being moody at nine years old. I still have that diagnosis to this very day: “mood disorder due to brain injury.” I also have anxiety and panic attacks. I still have today most of the same problems I had back then, just in an expanded manner.

GeorgeAnna Bell - Survivor

GeorgeAnna Bell – Survivor

I remember one thing that always frustrated me – Before my head injury, I was able to read, comprehend, and retain what I was reading. I remember having A to A+ grades and never getting into trouble. But, as soon as I had my head injury, I remember being hit a lot with a ruler by the nuns, being called “demon child,” not being able to read out loud, and having issue after issue trying to remember what we just learned or read five minutes ago and being told that I was lazy. (Oh, that one always got my goat.) I could not keep quiet or shut my mouth for more than five seconds, and I would speak out of turn. I could not sit still in my seat, and I was constantly moving around and around. These are some of the things I personally remember.

Kids_smiling_girl_cartwheelI know my parents wondered why I acted out, and they took me to multiple specialists during my youth. I was diagnosed with optic nerve damage, but no other problems resulting from my head injury were identified. Each doctor gave my parents the same answer: “There is no logical explanation as to why she is doing this now when she did not do it before the head injury.

I was extremely impulsive and still am to this day. In addition to the moodiness, this has been one of the hardest things for me to overcome. I experience emotions very quickly and intensely. As a child and into my teen years, I was very moody and got aggravated very quickly over the littlest things. I always felt anxious without exactly knowing why most of the time. It still happens to me to this very day. I will have an anxiety/panic attack, and I cannot explain why it happened. Recently, I went to a friend’s house, and I had to leave soon after I got there because I started to have an anxiety attack. I get anxious easily still today because I am so afraid people are going to make fun of me and tease me because I am different. I do not tend to keep friends very long because they tend to find something that is strange or I say something weird and they run from me.

I have absolutely no tolerance for change. I have no patience when it comes to waiting – I have to have everything NOW, NOW, NOW. I am always told I have indiscreet ways for making my feelings known to others. So many people take my statements out of context. I feel that I am acting appropriately, but others do not see me that way. When I change my way of saying something or going about something, I am told I am coming off as hostile or aggressive. I do not see it that way, nor do I mean it in that way either. I try to explain my head injury to others, but they tell me to shut up and act normal and stop giving excuses. Yet, it is not an excuse; it is the truth.gg66852714

As a child, as a teenager, and even in my adult years, I lacked awareness of my own personal deficits. It was only about five years ago that I started to realize the things I do that cause these issues, and I personally have tried to change them.

I would verbally lash out, cry, become depressed, and literally throw temper tantrums. This went on into my early 30s. I realized that, if I do not change, I will never have anyone in my life because all I do is find a way to push everyone out of my life. It wasn’t until maybe a year ago that I started to try to change things on my own.

I have also tried to seek professional help, even going as far as intentionally getting myself diagnosed as being “severely mentally ill” just to get the help. But, nothing worked. Actually, getting that diagnosis set me back years.

I had NO assistance from the mental health system. They were actually making my problems worse. Now I try to address the fact that there is an issue, and I doggedly try to understand what the physical, emotional, and psychological effects are upon my daily day. I try to rectify those effects that I deem as a hindrance to my social well-being by forcing myself to change the way I interact with others. I started by intentionally going to bars, not to drink, but to interact with others so I could watch how people reacted to certain behaviors. Honestly, this was hard and long. I lost people from my life, but those people were not the people I truly wanted in my life anyway.family-clip-art

I have a problem keeping people in my life as a result of my inability to function properly in certain social situations. The majority of family and/or friends that choose to maintain their relationship with me either ignore or downplay any behaviors that I portray. Only a select few recognize and respond well when my behaviors are considered outside social normality. When people start to see the social abnormalities in my personality, most either ask what is wrong with me, why I am acting like a crazy person, or just never speak to me again by cutting me out of their lives. (Almost always, they cut me out little by little.)

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

Amber GeorgeAnna Bell's Service Dog

GeorgeAnna Bell’s Service Dog, Amber

Within the last year, I have found one of the best outlets to cope with the changes in my behavior. I now fall back on crocheting. I make things for others who are in need of certain things more than I. For years, I would fall back a lot on my dogs and my boyfriend. Honestly, one of the dogs – my service dog, Amber – helped me break free from my isolation. The attention that people placed on her made me break free of the isolation I had restricted myself to. I interacted with people just by talking. I learned how to cope with my anxiety and my expression around other people.

 

Thank you, GeorgeAnna Bell.

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

(Clip Art compliments of Bing.)

(Photos compliments of GeorgeAnna Bell.)

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.

 

SPEAK OUT! . . . Guest Blogger Tanya Dallas

One Day at a Time

by

Tanya Dallas

presented

by

Donna O’Donnell Figurski

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

Dallas, Tanya Survivor 2 050716

Tanya Dallas – Brain Injury Survivor

A very nice doctor asked me if I’ve ever had a head injury. I began to tell my story. At 11 years old, I had a bike accident. I had no helmet, and I was unconscious for two minutes. At 12 years old, I took a softball to the face. I was unconscious for a few seconds. At 18 years old, I was in a car accident. I was unconscious for an unknown amount of time. Once I was struck in the head with a rock. I was also hit in the head with a ten-pound dumbbell (working with juveniles means risks). I experienced five years of domestic violence. I have no idea which of these things caused my brain to work differently.

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Tanya Dallas – Brain Injury Survivor

It’s hard for me to process. I was always so independent, and now I am unable to even hold a job. I learned what “flooding” was yesterday. I cried as I watched the video. For the first time in years, I felt understood. I felt like I wasn’t completely losing my mind.

It’s hard because my family still doesn’t understand. And they can’t see the injury, so they don’t think it’s there. I’m just taking one day at a time at this moment.

 

Thank you, Tanya Dallas.

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

(Clip Art compliments of Bing.)

(Photos compliments of Tanya Dallas)

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Brain Injury Resources . . . . . “Jump on the Bumper” to Raise Awareness of Brain Injury

“Jump on the Bumper” to Raise Awareness of Brain Injury

presented

by

Donna O’Donnell Figurski

Kidd Koziol, Beth Survivor 2

Beth Kidd Koziol – Brain Injury Survivor – NASCAR enthusiast

If you have a NEED for Speed, then “Jump on the Bumper” with our own Beth Kidd Koziol. Beth’s name and photo will be on the bumper of driver Joey Gase’s racecar as he races around the Charlotte Motor Speedway (in North Carolina) in search of a win in the Xfinity Race on Memorial Day weekend.

Joey Gase

Joey Gase – NASCAR Driver

 

Joey lost his mother to a brain aneurysm when he was eighteen. Joey donated his mother’s organs, and today 66 people are alive because of them. Joey’s goal is to raise awareness for “Donate Life” and traumatic brain injury groups of North Carolina.

Beth, a NASCAR enthusiast, invites other brain injury survivors to take the ride of their life with her on the bumper of Joey’s car and help her fulfill her dream of raising awareness for brain injury.

Joey Gase and Car

Joey Gase – NASCAR Driver

All I can add is “Beth, hang on tight!”

Please click the link below for details.

“Jump on the Bumper” with Beth Kidd Koziol

 

 

 

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 with your friends. It’s easy! Click the “Share” buttons below.

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