TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Donna O’Donnell Figurski’

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.)

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On The Air: Brain Injury Radio “Another Fork in the Road” “Depression and Suicidal Thoughts”

On The Air: Brain Injury Radio “Another Fork in the Road” 

with

Panelists: Survivor, Melissa Cronin and Survivor Troop, Juliet Madsen

Topic: Depression and Suicidal Thoughts

presented

by

Donna O’Donnell Figurski

Depression is a state of mind that can cause mental mood disorders. It is devastating and can affect every aspect of daily living. It can affect people in so many different ways and it is pure agony resulting from desperation and the need to escape. Depression is not an unfamiliar state for those who live with brain injury.

Juliet Madsen and Melissa Cronin, both survivors of brain injury, join me to discuss depression and suicide – two common, yet serious, repercussions of brain injury.

Melissa Cronin Head Shot 2When a car went rogue careening through 2 1/2 blocks of the Santa Monica, California Farmer’s Market it left Melissa Cronin with not only broken bones and a ruptured spleen, but also with a Traumatic Brain Injury. Melissa is the author of “Invisible Bruise” and “Silencing the Boom.” Both stories are published in “Chicken Soup for the Soul” books.

Juliet Madsen Uniform

Troop, Juliet Madsen, got her brain injury while serving her country in Iraq. Juliet is a member of the Board of Directors of R4 Alliance and is a master quilter. You can see some of her work at “Stroke of Luck Quilting.”

If you missed this show on “Another Fork in the Road” on October 4th, 2015, don’t fret. You can listen to the archived show here. Click the link below.

See you “On the Air!”

On The Air: Brain Injury Radio “Another Fork in the Road” Depression and Suicidal Thoughts with panelists, Survivor, Melissa Cronin and Survivor Troop, Juliet Madsen

Sources I used for this show:

  1. Everyday Health – 8 Unconventional Ways to Ease Depression

http://www.everydayhealth.com/depression-pictures/unconventional-ways-to-ease-depression.aspx

  1. Health – 7 Types of Therapy That Can Help Depression

http://www.health.com/health/gallery/0,,20310354,00.html

  1. Mayo Clinic – Psychotherapy

http://www.mayoclinic.org/tests-procedures/psychotherapy/basics/definition/prc-20013335

  1. Mental Health Foundation – Depression

http://www.mentalhealth.org.uk/help-information/mental-health-a-z/D/depression/

  1. The Guardian – Robin Williams, depression and the complex causes of suicide

http://www.theguardian.com/science/blog/2014/aug/18/robin-williams-depression-causes-suicide

  1. WebMD – Psychologist or Psychiatrist: Which Is Right for You?

http://www.webmd.com/mental-health/features/psychologist-or-psychiatrist-which-for-you

  1. WebMD – Symptoms of Depression

http://www.webmd.com/depression/guide/detecting-depression

Hotlines:

If you or someone you know needs immediate help, don’t waste time on the web, call 9-1-1 immediately.

There are many depression and suicide hotlines. Here are some I located. I am NOT endorsing them, but if you have concerns about depression or suicide, I might want to look into them in advance of any crisis.

 

  1. National Suicide Prevention Lifeline (1-800-273-8255) Suggested by the Mayo Clinic

http://www.suicidepreventionlifeline.org/

  1. Samaritans 24-Hour Crisis Hotline (212) 673-3000

http://samaritansnyc.org/24-hour-crisis-hotline/

  1. 24/7 Crisis Support 775-784-8090  

http://crisiscallcenter.org/crisisservices.html

  1. Most states have mental health hotlines. Here is a site that has links to most states.

Suicide Hotlines

http://www.suicide.org/suicide-hotlines.html

(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.

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! . . . . . . . . . . . . . . . . . Guest Blogger: Miki Mashburn-Bailey “Awareness: TBI Survivor Advocate”

Awareness: TBI Survivor Advocate

by

Miki Mashburn-Bailey

presented by

Donna O’Donnell Figurski

Girl Blogger cartoon_picture_of_girl_writingIt has been twenty years since my husband’s traumatic brain injury (TBI). Unawareness has been our enemy and hurt us tremendously. Awareness has found its place in our home just this past year, and it has brought along with it forgiveness, acceptance, and understanding.

Awareness has turned our life around. And, everyone who suffers from a TBI deserves to understand this life he or she lives. So obviously, awareness is important to me. It has become my passion. I ask you to help me prevent further damage by making the world aware. Your response could save a life – a marriage – a family.Miki Mashburn-Bailey 1

My husband was hit in the head by a brake drum that had flown off an eighteen-wheeler. The brake drum was traveling at highway speed. It wasn’t actually a “car accident,” but it was an unnecessary and unfortunate accident. (It’s for a reason such as this that you can receive a ticket for “failure to maintain your vehicle.”) My husband’s car veered to the left. The barrier between the highway lanes slowed him to a stop, as he was combative and lost all control of his being. An ambulance just happened to be driving by soon after, and the EMS (Emergency Medical Services) team just happened to look down into my husband’s vehicle. They saw him and took immediate action.

I am thankful for this EMS team because they helped save my husband’s life. They responded quickly and effectively, and my husband was rushed to the nearest trauma center. The team there responded quickly, and the surgeon was able to do what was necessary to prevent further damage. This man and the trauma center team saved my husband’s life. I am forever grateful to them. They did their jobs, and they did them well. Had the EMS team not responded in the manner they did, it would’ve made the trauma center’s job more difficult.

Miki Mashburn-Bailey and Jay Bailey 3My husband survived an incident he should not have. He improved much sooner than expected. He recovered miraculously and was discharged earlier than expected. I am thankful to everyone. They did their jobs well.
 HOWEVER, there was still a job that was necessary. There was still work to do. There was still much-needed therapy. There was still much-needed counseling.
 A life was saved, but it was forever changed, and no one was there to help make sense of it. No one was there to guide my husband and me to the next step. No one was there to warn of the subtle changes that have huge impacts. No one was there to enlighten and give insight as to what to expect next. 
EMS did a great job and sent us on to the next step – the trauma center. The trauma center did a great job and sent my husband on into surgery. The surgeon did a great job.

But, the only place left to pass my husband on to was home. “No more treatment necessary” written on discharge papers means “There is no more left for us to do on our end,” but, to the sufferer of a TBI, it reads as, “You’re fine. You will heal right up!”
 My husband and I go home. We expect things to be different. We adjust. We assume time is all that’s needed. Time marches on, and things don’t improve, or we begin to notice this and that here and there. By the time we recognize things aren’t healing cognitively as well as they are physically, we go to a doctor confused and try to communicate our concerns. My husband is brushed off because he “looks fine.”

Trauma centers need to have a “TBI Survivor Advocate” to hold the survivor’s hand into the next step of the TBI journey – not to hand out written material that will be lost in all of the other paperwork given at discharge. TBI Survivor Advocates would sit down with survivors and their families and/or friends and help them understand that, while EMS and the hospital saved the survivors’ lives, there are others who will help survivors LIVE their lives. TBI Survivor Advocates could direct and guide survivors to find therapists and counseling that will help transition and adjustment to their “new normal.” 
A disservice was done to my husband – to his future, to the company he worked for, to our relationship, and to our family.
 We were denied effective help and expected to carry on, due to my husband’s “miraculous” physical healing. Because of that, the cognitive damage that affected his being never got the attention or therapy it desperately needed.

Awareness of the reality of TBI as often being an invisible disability is vital in the health of the world we all live in. TBI is a thief in the night and has no prejudice. It can happen to anyone of any status. Please help me make others aware. Miki Mashburn-Bailey 4We can be that hand that guides others to their next steps in their journeys. The world we live in is full of those who have influence. A difference CAN be made in the way a brain-injured individual adjusts to his or her new life. All it takes is ONE person to make a difference. The more we help one another, the better our world becomes.

Thank you, Miki Mashburn-Bailey.

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

(Clip Art compliments of Bing.)

(Photos compliments of Miki Mashburn Bailey)

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SPEAK OUT! . . . . . . . . . . . . . . . . . Faces of Brain Injury . . . Alexis Turcotte

SPEAK OUT! Faces of Brain Injury – Alexis Turcotte

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.

0092415 Alexis Turcotte Survivor 1Alexis Turcotte (survivor)

So many people ask me how I can be so positive after all that I’ve been through. Well, the answer is that I’m not going to dwell on the crash. I don’t say, “I almost died, so I’m going to sit here and be worthless.” Instead, I’m going to show that I’m better than all the labels I’ve been given. So many people have said, “Oh well, since your hospital papers say … then you can’t do ….” My response has always been, “Can I please prove you wrong before you say I can’t do it?” I make an effort to change the negative to a positive. Why? Because there’s so much to be positive about – so much to be grateful for.

092415 Alexis Turcotte Survivor 2
For crying out loud, I was given a second chance to live! The crash happened two days after my birthday. (One photo is from my birthday. I’m uninjured. The other is of me in the hospital in a coma.) I was in the passenger seat of the vehicle. The firefighters had to cut the door off to get to me, since I was unconscious at the scene. My skull was fractured in two places; my left foot was shattered; my left leg was broken in half (the bone was sticking out); and my nose, jaw, left shoulder, and pelvis were broken. The firefighters were told that I wouldn’t make it. The crash happened September 20, 2014. I awakened from the coma in late October, and I left the hospital on December 4.
I was told by doctors not to return to school, but I wanted to go back. I did return on January 5. I continued my courses, including my college-prep course and my two AP (advanced placement) courses. I earned As in all but one of my courses. I was also told that I wouldn’t graduate on time, but I pushed myself to do so with hours of online schooling to make up for the semester of school I missed. I wanted to show that, just because I have a label, I’m not a nothing.
I am good now. I’m still in pain due to the screws restricting my foot, but soon my doctor will remove them. Then I should be able to work out and run again. I also want to return to my team in girls’ flag football. (My coach will only allow me to play if I get written consent from my doctor and a parent. My doctor said I should be OK to play in six months.)

11734112_1057605137584263_505801146_oMy story shows that miracles do happen.

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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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.)

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On The Air: . . . . . . . . . . . . . . . . . . Brain Injury Radio “Another Fork in the Road” Janiece Naber Martindale “Caregivers Need Care Too”

On The Air: Brain Injury Radio “Another Fork in the Road” 

with

Janiece Naber Martindale

Topic: Caregivers Need Care Too

presented

by

Donna O’Donnell Figurski

Martindale, Janiece NaberJaniece Naber Martindale knows a lot about caregiving. She is a two-time caregiver – first for her husband, then for an elderly friend. Janiece says that her caregiving responsibilities were very different for each person. Janiece and I examined what it takes to be a good caregiver.

If you missed this show, “Caregivers Need Care Too” on “Another Fork in the Road” with Janiece Naber Martindale anoon September 20, 2015 don’t fret. You can listen to the archived show here. Click the link below.

See you “On the Air!”

On The Air: Brain Injury Radio “Another Fork in the Road” with Janiece Naber Martindale: “Caregivers Need Care Too”

(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.

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

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

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Survivors SPEAK OUT! . . . . . Debra Cody

Survivors SPEAK OUT! Debra Cody

presented

by

Donna O’Donnell Figurski

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

Debra Cody

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

Ailsa Craig, Ontario, Canada     debcody63@gmail.com

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

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

4. How did your brain injury occur?

I suffered four concussions over a five-year span.

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

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

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

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

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

No

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

Yes. I was in an outpatient treatment program.

How long were you in rehab?

I have been in the program for three years now.

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

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

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

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

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

“Me”

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

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

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

My limitations

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

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

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

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

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

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

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

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

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

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

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

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

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

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

 

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

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

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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

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

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

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

Feel free to “Like” my post.

Caregivers SPEAK OUT! . . . . . Janiece Naber Martindale

Caregivers  SPEAK OUT!  Janiece Naber Martindale

presented by

Donna O’Donnell Figurski

Martindale, Janiece Naber1. What is your name? (last name optional)
Janiece Naber Martindale

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

Chickasaw, Alabama, USA

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

My husband, James Martindale, was 61 when he was diagnosed with multiple system atrophy (MSA, a progressive neurodegenerative disorder that affects the brain). In December 2008, my husband and I drove an empty semi-tractor to Calexico, California, to our drop yard. We were to pick up a loaded trailer for our trip home. Because of rain, the drop yard was extremely muddy. The semi got stuck in the mud, so James walked through the muddy yard looking for our loaded trailer, when he fell in the mud. James hurt his back at that time, and he began to complain of dizziness. He also complained of a nasty headache. I believe that that was the beginning of James’ MSA.

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

I began my husband’s care in June 2009. I was 45. I was his main caregiver. I am not now because my husband passed away on October 16, 2014.

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 brain injury? If so, were you able to continue working?

Yes, we were working at the time. But, we had to quit.

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

My husband had hospice care for the two years before he passed away.

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

For the first three years, I was the only caregiver, and I didn’t really have any help. But, I had a lot of help in the final two years with hospice care coming into the house.

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

No

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 your survivor was getting therapy?

My husband had no rehab.

11. What problems or disabilities of your brain-injury survivor required your care, if any?

My husband had problems with his balance and his gait. He couldn’t write. He wasn’t able to drive a car. Eventually, he lost all ability to move. He had an upper respiratory infection.

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

My life is better because I now have the knowledge to help other people

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

I miss being able to go out and ride around the Gulf coast together.

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

It’s hard to enjoy life, since I have to start over all by myself.

15. What do you like least about brain injury?

My husband died too soon.

16. Has anything helped you to accept your survivor’s brain injury?Martindale, Janiece Naber 2 091515

I just accepted it. It was the way of life.

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

I had to stay at home a lot. I realized that I could change that when I had the help of hospice workers.

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

My social life was affected at the time. Now I’m trying to put my life back together again with a husband.

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

I plan to help someone who is living in this situation – I may even start a support-group, so people have a place to go and chat.

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

Keep a positive attitude. Hold your head high. Be patient. Encourage the survivor.

(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!

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Thank you, WORLD!

Thank You, World

by

Donna O’Donnell Figurski

blogI started my blog, “Surviving Traumatic Brain Injury,” in March 2014 when I saw a need to connect with other survivors and caregivers in the brain-injured community. I saw people struggling as I had as I tried to make sense out of this new life that visited us when my husband had his brain injury in 2005. At that time, I had no community to turn to. There were no social media. I felt lost and alone. I didn’t know there were other people living with many of the same problems that we were battling. But now, because of the rise of social media, there are many places for people to find information about brain injury, and I wanted to be one of those places.

In the more than ten years that my husband, David, has lived the brain-injured life, I have learned a lot, and I want to share my information with newcomers to this unexpected life. I want to provide a place where they can go to obtain information, but mostly I want to provide survivors and caregivers a platform to SPEAK OUT! I want them to share their stories and their thopinions, and I want others to draw hope and courage and inspiration from those who are traveling a similar path.

This page was created to say THANK YOU to the survivors and caregivers who have so graciously shared their stories here with the hope of raising awareness of brain injury.

It was created to say THANK YOU to everyone in the WORLD who stops by to read it. In the year and a half since I created my blog, thousands of folks have stopped by from all over the world (nearly 50,000 at this point).Thank-you-post-it
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Welcome to Harmony Kent Online

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TBI - Survivors, Caregivers, Family, and Friends

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