TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘brain injury survivor’

Another Fork in the Road . . . . . . NFL Player, Kyle Turley, Brain Injury, Football, and Music

YOU ARE INVITED!

NFL Player, Kyle Turley, Brain Injury, Football, and Music

with host Donna O’Donnell Figurski

putthis_on_calendar_clip_artKyle Turley, former football player for the New Orleans Saints, the Saint Louis Rams, and the Kansas City Chiefs, will join me to discuss life after football while living with brain injury. As an offensive tackle, Kyle has had more than his share of concussions – leading to seizures and various Kyle-Turleybrain-injury complications, which have adversely affected his life. Kyle is picking up the pieces and assembling his life-puzzle by speaking out about brain injury. He does this through his music, The Kyle Turley Band, and his recent documentary, “The United States of Football.”12821083-standard

You can hear one of Kyle’s songs here. “Fortune and Pain.” It’s powerful!

Come One! Come ALL! 

What:        NFL Player, Kyle Turley, Brain Injury, Football, and Music

Why:        Kyle Turley SPEAKS OUT! about how brain injury affects his life.

Where:     Click: Brain Injury Radio Network

When:       Sunday, October 18th, 2015

Time:         5:30p PT (6:30p MT, 7:30p CT, and 8:30p ET) 80 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” Show Menu.

(Clip Art compliments of Bing.)

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 Step

Dee Farrell 2 011415Dee Farrell (survivor)For the first time in a very long time, I am very proud of myself. I am two years post car accident, and I never thought it would be possible for me to ever get back on a horse after my injuries. Well, with a lot of hard work and encouragement from my family and caregivers, I recently achieved my dream of riding again. I still can’t believe it myself! I’m sure you know the roller coaster that comes with a traumatic brain injury, and there have been times I was close to just throwing the towel in because it was all too hard. For me, this is the moment when all my hard work paid off. A big “Thank You!” goes to Oliver for being a true gentleman the whole time.

YOU did it!

Congratulations to contributor!

(Clip Art compliments of Bing.)

As I say after each post:anim0014-1_e0-1

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.

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.

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! . . . . . 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.

SPEAK OUT! . . . . . . . . . . . . . . . . . Faces of Brain Injury . . . . . . . . . . . Tony Hernandez-Frazione

SPEAK OUT! Faces of Brain Injury – Tony Hernandez-Frazione

presented by

Donna O’Donnell Figurski

 Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718

It 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.

Hernandez,-Frazione, Tony Survivor 070715Tony Hernandez-Frazione (survivor)

This is my six-month anniversary. Here’s a bit of my story. Six months ago, I started a new job. It was my first day – I put a starter on a Ford F350 to show the bossman I knew what I was doing. I finished up and left the house where I was at, made a right onto Beach Blvd. to get to South Side Blvd. It was an ordinary day like any other. Right before I got to South Side, a school bus pulled out right in front of me and changed my life and others’ lives forever. I collided with that bus, and a bigger part of me was killed in the process. Life as I knew it was changed forever. I know some of you don’t care and won’t read all this, but my message is this: Count every day and moment like it’s your last. Hernandez,-Fragione, Tony Survivor 070715Hug and kiss your children and loved ones every day, even if you’re upset at each other, because it could be your last. I thank God every day that I see my daughter, and I breathe again. I thank God too for the few true friends that were there and still are, when so many have left because of the “new” me. But, I don’t look at “me” any differently.

(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.

SPEAK OUT! . . . . . . . . . . . . . . . . . Faces of Brain Injury . . . Marc Tima

SPEAK OUT! Faces of Brain Injury – Marc Tima

presented by

Donna O’Donnell Figurski

 Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718

It 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.

Marc Tima (survivor)

Marc Tima 1 Survivor 090715Traumatic brain injury (TBI) is a crazy, life-changing event. When I was fourteen years old, I was in a pretty bad car accident, in which I suffered a TBI. I was life-flighted to Allegheny General Hospital in Pittsburgh. I was in a coma for about three weeks. My doctors prepared my parents for my remaining in a vegetative state. God, my family, and I had other plans. At one point, the doctor told my parents that if she were a betting woman, she would not bet on my chances. My mother was in tears and began to weep. My father, on the other hand, said, “I’ll take that bet, and my son will prove you wrong.”

I spent three months in the Rehabilitation Institute of Pittsburgh. After my rehab, I was barely able to start my tenth-grade year of high school. Instead of getting As and Bs like I used to, I scraped by with Cs and Ds. During my coma, my entire body atrophied. Instead of being a top football and basketball player, I was made a team manager for football and basketball. I spent much of high school crying because of my shortcomings. But, I cried to myself in my room. I also spent every free second I had working out and getting stronger. By my junior year, I was able to get back on the football team. My coaches were worried about my getting injured again, so they would not let me play in the varsity games. I spent my eleventh-grade football career on the scrub team. During practice, I would outplay all the seniors who were able to play varsity. My grades were still very poor, but my short-term memory was improving little by little. By the time I was a senior, I was a starter for football and a top defensive player in western Pennsylvania. My grades were still poor, but they were improving. I got recruited to play football for Duquesne University. Though my high school grades were poor, they let me into Duquesne Marc Tima 2 Survivor 090715because of my football and some heavy pleading from my mother.

Anyway, the hits in college football were too hard for my head. So, I had to give up football. I stayed at Duquesne, though, and earned my degree. I worked extremely hard in high school to earn Cs and Ds. At Duquesne, I worked just as hard, but now I was getting As and Bs. In fact, when I graduated from Duquesne on the Dean’s List, my parents contacted that doctor who bet against my father on my recovery. He showed her my academic record at Duquesne. And, she took my parents out to dinner as payment for losing the bet she made with my dad.

I now have a Master’s degree in Exercise Science, own an “Anytime Fitness” in Ohio, and am a personal trainer. Several of my clients are TBI survivors, whom I help with their recoveries.

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Survivors SPEAK OUT! . . . . . . Anonymous

Survivors  SPEAK OUT! – Anonymous

(survivor requested anonymity for personal reasons)

presented by

Donna O’Donnell Figurski

th-11. What is your name? (last name optional)

Anonymous

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

Ohio, USA

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

I was 28 years old.

4. How did your brain injury occur?

My ex-boyfriend pushed me over a balcony, and I hit my head on concrete.

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

People called 9-1-1, so it was within a few minutes.

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

I had two craniotomies (removal of part of the skull to expose the brain). A pic line (also “picc line,” peripherally inserted central catheter) was added in my arm. I had a G-PEG (gastric tube inserted by percutaneous endoscopic gastrostomy; the tube leads directly to the stomach and allows direct feeding).

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

I was in a coma for four days. The coma was medically 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)?

I had occupational, physical, and speech therapies.

How long were you in rehab?

I did six weeks of inpatient therapy, followed by ten months of outpatient therapy.

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

I’m half deaf. I have problems with muscle weakness, memory loss, double vision, balance, discoordination, and loss of the brain’s executive function.

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

My life is better now. I’m more loving to my family and my son. It seemed impossible at the time – I thought I’d be crippled.

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

I was in college to be an RN. At the time, I already had a good job helping people with their everyday needs.

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

I have a new appreciation for life. I know that life can end at any time, so I cherish each day. I don’t drink anymore. Therefore, I can now provide my son with whatever he needs.

13. What do you like least about your brain injury?Brain Street Sign th

I dislike forgetting words and names. I have a hard time with what I want to say to people. Often, I have short-term and long-term memory loss. Those things can be the hardest.

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

My son and my family have helped me to accept my new changes by being caring and patient.

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

My brain injury has affected my home life by my having to find new ways to get around things. I have also learned that, while a relationship would be nice, I don’t have to be in one.

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

My social life is now limited to walking in my small town and the occasional visit to the grocery store or department store to get only what I need

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

My mom is my main caregiver. She handles all of my finances, plus she’s been an Occupational Therapist for over twenty years.

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

I would like to continue talking to people about the effects of alcohol, the effects of abuse, and how we can change all of that.

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’ve known what real abuse is – not only the physical aspects, but emotional and psychological abuses as well. Had I been aware of those, I would not have been injured in a way that completely altered my life.

Plus, let it be noted that no two traumatic brain injuries (TBIs) are ever the same.

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

I am a TBI survivor. We are all TBI survivors in our own ways. We don’t need to be in abusive relationships; we deserve all of the care in the world. My advice – don’t become a statistic of horrible abuse that could harm you. Everyone has the capacity to be stronger. I realize that now, and I hope that everyone does.

 

(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.)

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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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!

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SPEAK OUT! . . . . . . . . . . . . . . . . . Faces of Brain Injury . . . . . . . . . Shanna Wolf Heart Powell

SPEAK OUT! Faces of Brain Injury – Shanna Wolf Heart Powell

presented by

Donna O’Donnell Figurski

 Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718

It 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.

Shanna Wolf Heart Powell (survivor)

Powell, Shanna Wolf Heart Survivor 062715 3This was me three years ago. I was in this truck when it flipped and rolled at 60 mph. I had a shattered face and a shattered shoulder. And, I spent some time in a coma. This was the final nail – the one that pushed my PTSD (post-traumatic stress disorder) into full mode and gave me a TBI (traumatic brain injury). I am not the same me. I am the “new” me. God chose me to still be here. I see it too many times – people are in wrecks and they don’t make it. Powell, Shanna Wolf Heart Survivor 062715 2My survival just makes me even more thankful. (I now make a horrible passenger, as every time the driver swerves, a car looks like it’s going to hit us, or it appears that it is not going to stop, I freak out.) I forget things a lot. I loose what I am saying in the middle of a conversation. I get flustered easily. I have many depressed days and cannot do all the things I used to. I panic for people when I see them getting flown by Care Flight (as I was a “passenger” once). All I can do is say, “God, please help them.”

One day, I had taken my boys to a hospital’s Emergency Room for something, and they wheeled a trauma patient past us. Covered in blood, she was badly hurt from an automobile accident. She was screaming, confused, and scared. They were taking her out to put her on Care Flight. I cried for her and panicked. That was one of the first-known PTSD triggers for me. I have no recollection of the wreck that almost killed me. But, I relived a horrible moment in my life through her. I could only imagine what it was like for me.

Those who care enough to read through my story will read this and then go on with life. But, I live this every day. My TBI (though not as bad as some, and for that I say, “Thank you, God”), my PTSD, and my bipolar disorder will never go away. So, I just have to live with them every day. I cannot do a simple task without issues. For example, I may not understand things when I go to places, like the cell phone store. I don’t understand how to put the airtime cards in my new phone. Instead of telling the clerk, “I have a TBI and don’t understand,” I just say, “Oh, OK.” 😦

Almost every day, something triggers my PTSD, and I fight to stay afloat. People say, “Get over it.” 😦 There is no getting over it! It’s not an easy battle, so please do not tell me to “get over it.” I have lost the memory of a lot of things in my life. I may forget things you just told me. I get confused to the point that I just say, “Forget it. If you try to explain any further, I will just get mad because I don’t get it.” And, I have no filter. I tend to say what I think. So, if I say something and it offends you, move along or unfriend me. It’s not personal.

Powell, Shanna Wolf Heart Survivor 062715 1So “Happy Three-Year Survival” to me! This is why I’m getting the “;” tattoo. And, my story is not over.

To those who think I am stupid and annoying, “Please don’t let the door hit ya where the good Lord split ya.” And, to those who stayed by my side, stayed my friends, or have become my new friends – “Thank you! Love to all!”

(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

SPEAK OUT! . . . . . . . . . . . . . . . . . Guest Blogger: Sue Hannah “Different Path”

A Different Path

by

Sue Hannah

presented by

Donna O’Donnell Figurski

Girl Blogger cartoon_picture_of_girl_writingMy traumatic-brain-injury story is different from some. I didn’t have a wonderful life that suddenly was transformed by tragedy. I had violence in my early life that forever changed me. Because no one spoke of my damage or the violence that caused it, decades passed until I was finally able to understand what had happened. In the meantime, I spent years painfully searching for an answer. I wanted to know why my handwriting was not only not neat, but how it seemed regressed to an age much earlier than my actual age. I sought to understand why spatial concepts were so difficult for me to comprehend. I yearned to know why colors and patterns made me sick to my stomach and why motion sickness affected me in vehicles, rides, and even something as gentle as a swing. After years of doctor visits, neuropsychological testing, therapists, alternative practitioners, and even nutritionists, I finally found an answer.

My first experience with vision therapy was helpful and did improve my handwriting, but it did not eliminate my issues. Syntonics (phototherapy) and prism glasses made huge differences in my life! My spatial orientation changed dramatically, my coordination improved, and even my tolerance for colors and patterns improved. I had no idea how powerful the visual system was or how Sue Hannahmuch of the brain was involved in causing my visual system to fully function. My traumatic brain injury (TBI) had done damage to areas of my visual system, which cascaded into my motor functioning as well as into my proprioception and tactile senses. Syntonics, or light therapy, gently and consistently shifted, and continues to shift, major obstacles for me. There are many optometrists in the US who do vision therapy, but I’d like to think mine is someone quite special. Her down-to-earth manner and genuine kindness radiate to her patients, as well as to her team of professionals in her office. Dr. Amy Thomas, located in Tucson, Arizona, has shown me amazing paths to my healing. She would never choose to take credit for healing anyone. She would, I believe, be willing to accept responsibility for helping patients heal themselves.

For the neuro-typical people of the world, let me say that few things are more annoying to lots of us with TBI than the following: “You don’t look like you’re brain damaged. You seem so normal. I know exactly how you feel.” Um, no you don’t! Everyone’s walk with TBI is a unique one, in my opinion. I had doctor after doctor tell me that my sensitivity was something I just needed to get over and deal with if I were to get along in life. My teeth still grate over that one! The reluctance of so much of our society to acknowledge sensitivity, neurological challenges, intensity, and deep emotions pains me. There are times for me when even sunlight can cause a round of irritability or other intense emotions. Medical professionals who discount the feelings and experiences of their patients are missing a huge amount of information that, if they allowed, could change their practices.

Hannah, Sue 2My life-path has not been easy, but it has caused me to not take little things for granted. I lost the ability to drive for a brief time, and, because of my new therapies, I am slowly getting my independence back. It’s interesting to note that as we get more reflective, we often begin to see what is most important to us. One of my strongest passions is to never give up. I was determined to find an answer to what happened to me and, even more so, to improve the quality of my day-to-day life. The second is one I continue to pursue. On days that seem filled with grief and loneliness, I remember that there are still wonderful people in the world. For me, these people have helped me to get up when I fall and to remember that tomorrow is another day.

To learn more about Sue, please visit her website/blog at Platypus Expressions.

Thank you, Sue Hannah.

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

(Clip Art compliments of Bing.)

(Photos compliments of Sue Hannah)

SPEAK OUT! . . . . . . . . . . . . . . . . . Faces of Brain Injury – Linda Wells

SPEAK OUT! Faces of Brain Injury – Linda Wells

presented by

Donna O’Donnell Figurski

 Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718

It 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.

Linda Wells (survivor)

2 565047_3919814115943_1697366413_nI am a brain-injury survivor of twenty-three years. I went through five years of intense speech and physical therapies. I could not walk or talk. Now I am a speaker for the Brain Injury Center of Ventura County, California. Our group started in a living room with me, my dear late husband, Rex, and six other people. I am very proud that last year there was an attendance of 300+ people. I work very hard to educate the community about traumatic brain injury. This year at our event, I will be receiving the Honoree Award for a Survivor. I often say, “One foot in front of the other.” I try very hard to do just that – to say, “I can, I will, I did.” I enjoy family, my friends, and my dog; and I have three great caregivers.

Also, I am now a watercolor artist.

4 Linda Wells 10960117_10203992863724065_7194897410358730162_o

10301184_10202793038249178_5470330639061493067_n5 Linda Wells6 Linda Wells 1604838_10201545679825997_791510895_n

(Artwork compliments of contributor. They are copyrighted and may only be used with express permission of Linda Wells. )

Clip Art compliments of Bing.)

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

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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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