TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘TBI’

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.

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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!

Feel free to “Like” my post.


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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(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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On the Air . . . . . . . . . . . . . . . . . . . Brain Injury Radio “Another Fork in the Road”  “Where Have All My Friends Gone?”

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

with

Panelists: Caregiver, Lisabeth Mackall and Survivor Troop, Juliet Madsen

Topic: Where Have All My Friends Gone?

presented

by

Donna O’Donnell Figurski

Mackall, Lisabeth with Book

Lisabeth Mackall joined other caregivers when her husband and police officer, Frank, was in a serious car accident on the way to an emergency call. The accident left him with a brain injury.

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.”

Losing relationships, both family and friends, is a common result of brain injury and it is devastating to survivors and their caregivers, as well. Troop and survivor, Juliet Madsen, and Lisabeth Mackall, therapist and caregiver for her husband, join me to discuss the topic of “Where Have All My Friends Gone.” We’ll examine the reasons why some people just can’t stick it out and try to shed some light on how folks can keep their relationships alive with their brain-injured friends.

If you missed this show on “Another Fork in the Road” on September6th, 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” Where Did All My Friends Go? with panelists, Caregiver, Lisabeth Mackall and Survivor Troop, Juliet Madsen

(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.

 

About Me and My Blog!

SPEAK OUT! for Brain Injury 

Donna O’Donnell Figurski

Writer, Blogger, Radio Host, Speaker

1 Donna Featured PhotoWRITER

My completed memoir, “Prisoners Without Bars: A Caregiver’s Story,” starts the minute my husband, David, had his brain injury. He was exercising. He did one more chin-up than his normal twelve. That dreaded thirteenth changed our lives forever. The story carries the reader through three unwanted brain surgeries – none of which David was expected to survive and which reduced him to an infantile state. “Prisoners Without Bars: A Caregiver’s Story” portrays David’s first eighteen months of struggles through recovery, therapy, and rehabilitation, while heralding his strength and persistence. I have included an epilogue to bring the reader up to date on David’s recovery and David added his flair to the story and his personal touch by writing the afterword. “Prisoners Without Bars: A Caregiver’s Story,” documents my dedication to helping David recover and details how we picked up the pieces and glued our lives back together. The story will make you laugh. No – brain injury is not funny, but life without humor during recovery from brain injury would be unbearable. It will also make you cry. No doubt! But, mostly it will offer hope to brain-injured survivors, their caregivers, and their family and friends. “Prisoners Without Bars: A Caregiver’s Story” is my completed memoir currently searching for an agent

I have four stories published for children in three books with Scholastic in their Education Department. Also, three biographies about notable Native Americans are scheduled for publication in two anthologies in early 2016.

BLOGGER2 Donna Collage

My blog, Surviving Traumatic Brain Injury, was the brainchild born from my realizing how many people are living with brain injury. At least 5.3 million people, just in the United States alone, are affected by brain injury. That is an astounding number! After being a part of this huge community for almost ten years, I knew I had to raise my voice, and I realized I could use my writing skills to reach a large audience.  Social media was not yet a part of folks’ lives when David had his brain injury, so we invented our own wheel. But now, with so many social media sites where brain-injury survivors, their caregivers, and their family and friends can search for information, I felt it was senseless for them to invent their own wheels. I wanted to help. The blog began with the Survivors SPEAK OUT! interviews, which gave survivors a voice, using my blog as their stage. That venue became hugely successful, and soon the Caregivers SPEAK OUT! interviews evolved. Soon after, many more categories followed as I saw a demand for them. The categories are listed below with a brief description.

BLOG CATEGORY DESCRIPTIONS3 Donna Collage

Brain Injury Resources

The Brain Injury Resources category houses various informational topics, including books, movies, documentaries, facts, and research about brain injury.

Caregivers SPEAK OUT! Interviews

Read interviews from caregivers of brain-injured survivors. If you are a caregiver, this is where you can tell your side of the story. Look for the Caregivers SPEAK OUT! Questionnaire below.

 Caregivers SPEAK OUT! Questionnaire

This is the Caregiver Questionnaire. It’s easy – just fill out the 20-question template. (All the directions are on the page.)4 Donna Collage

SPEAK OUT! Faces of Brain Injury

Meet brain-injured survivors and their caregivers on “Faces of Brain Injury.” Their candid and heart-wrenching stories will help readers understand the serious implications and complications of living with brain injury.

 If you’d like to share your story on “Faces of Brain Injury,” please send it to me at neelyf@aol.com. I’d be happy to consider it. (Please put “Faces of Brain Injury” in the subject line.)

 SPEAK OUT! Guest Bloggers

Everyone has a story. In this section, Guest Bloggers can SPEAK OUT! about topics relevant to brain injury and special to them.

 If you have a Guest Blog you’d like to share, please contact me at neelyf@aol.com. I’d be happy to consider it. (Please put Guest Blogger in the subject line.)

SPEAK OUT! Itty-Bitty GIANT Steps

When you are living with a brain injury, no accomplishment is too small. ibGs provides a platform for brain-injury survivors and their caregivers to shout out their BIGGEST (or smallest) recent accomplishment. Share yours now!

Send it to me at neelyf@aol.com. I’d be happy to consider it. (Please put Itty-Bitty GIANT Step in the subject line.)

My Book: “Prisoners Without Bars: A Caregiver’s Story”

You can read about my book under “Writer” above.

SPEAK OUT! NewsBits

NewsBits is the place to go to find out the latest in the news about brain injury. 5 Donna Collage(Well, it was the “latest” when I published it. I’m sure it’s still interesting, though.)

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

My radio show, “Another Fork in the Road,” airs the first and third Sundays of each month at 5:30pm Pacific Time. The show features brain-injury survivors and/or their caregivers. It also delves into the problems and issues that survivors and caregivers live with each day. Professionals, including therapists, are also interviewed on the show. If you can’t tune in to the live show, don’t fret. You can listen to the show anytime. It’s archived. Just find the show you want to hear and click the link. (“On The Air Show Menu” in the sidebar of my blog has a list of all my shows and provides their links.)

On the Air! Show Menu

This is the place to go if you are looking for a great show about brain injury. All of my shows are listed here with a link that will carry you directly to the station to listen. So, sit back, relax, and learn.6 Donna Collage

So, Whaddya Think?

Is there something you are passionate about in this brain-injury world? Do you want to be heard? Your opinion matters! You can SPEAK OUT! on “So, Whaddya Think?

Send your opinion piece to me at neelyf@aol.com. I’d be happy to consider it. (Please put So, Whaddya Think? in the subject line.)

Survivors SPEAK OUT! Interviews

Read interviews from brain-injured survivors from all walks of life. Brain injury is NOT discriminating. If you are a brain-injured survivor, this is where you can tell your side of the story. I’d be happy to consider it. Look for the Questionnaire Template below.

Survivors SPEAK OUT! Questionnaire

This is the Survivor Questionnaire. It’s easy! Just fill out the 20-question template. (All the directions are on the page.)

TBI Tales7 Donna Collage

The stories that are shared here by a variety of survivors and caregivers will make you laugh and cry – sometimes at the same time. They may delight you or they may shock you, but I can guarantee that the stories will offer you courage and hope.

If you have a TBI Tale you’d like to share, please contact me at neelyf@aol.com. I’d be happy to consider it. (Please put TBI Tale in the subject line.)

and Explore More …
You’re just going to have to click to find out. Go ahead! You know you want to.

RADIO HOST

Becoming a radio host had never entered my mind and may be just about the biggest surprise in my life. When I was approached to join the Brain Injury Radio Network on blogtalk radio, I was hesitant. Probably more like…are you kidding me? It took some convincing and a lot of soul-searching before I said, “Yes.”

I wondered what skills I had for this job, and I began to think – always dangerous. I had been a teacher for more than three decades, entertaining my audience of more than four hundred six- to eight-year-olds – teasing them into learning to “read, ‘rite, and do ‘rithmetic.” Believe me, teachers nearly stand on their heads to keep their little “twerpsters” entertained – a must, if you are going to keep their attention.8 Donna Collage

I am also in the theater and periodically climb onto the stage to cavort with other actors in front of hundreds of play-goers, so I thought maybe this radio-host thing might work. After all, if I can speak in front of hundreds of people who are directly in front of me, speaking to thousands of invisible listeners should be a cinch. So, yes, I decided to join the network.

Well, it’s not a cinch, and I still get the butterflies before each show, but as soon as my intro music plays, I am in the zone. My 80-minute show flies by, and when I invite my audience to tune in again in two weeks and the mics shut down, I savor the satisfaction of a job well done.

Since I’ve lived in the brain-injury world for more than ten years as the caregiver for my husband, David, I’ve learned a lot and was eager to share my knowledge with others. I’ve been with the network for more than a year now, and I have hosted more than twenty-seven shows.

You can listen to my radio show, “Another Fork in the Road,” on the Brain Injury Radio Network. My show airs the first and third Sundays of each month at 5:30pm Pacific Time. On my 80-minute show, I interview guests in the brain-injury world, including survivors and/or their caregivers, delving into their lives to better understand how they cope with daily living after brain injury. I invite folks from the medical professions, such as therapists, who are willing to offer suggestions and hope to survivors. I talk with folks in brain-injury communities, such as troops from the combat zones of recent wars and athletes from the battlegrounds of the playing fields. I address many topics pertinent to brain injury with my panel of brain-injury survivors and caregivers.

Tune in! Click on Brain Injury Radio and look for “Upcoming Broadcasts.” (My show will be advertised about two days before the first or third Sunday of each month.)

You can listen to the shows anytime. They’re archived. Just click on On the Air! Show Menu on my blog. See you “On the Air!”

SPEAKER9 Donna Collage

If you’ve read the section above about my being a radio host, you will already understand why I have chosen to become a spokesperson for brain injury. Though brain injury has been around for forever, it seems that it is finally coming to the forefront as our troops arrive home with traumatic brain injury – what the world is calling the “signature” wound of the Iraq and Afghanistan wars. Recently too, there is a lot of attention to the head traumas that many football players have received, resulting in serious repercussions for them, such as memory loss, unrestrained anger, and even early dementia. Sadly, many players have completely lost hope and have resorted to suicide. Of course, with the baby boomers reaching their “golden” years (and some not so golden), they are finding that many of them and their loved ones are requiring caregivers in their lives simply to manage day-to-day living. And that’s where I come in. With my knowledge and experience of being a caregiver for my husband, David, for more than ten years, I have learned a fair bit and would like to share my knowledge to help others.

Need a speaker? My 90-minute PowerPoint Presentation, “What Caregivers Need to Know,” is for anyone with a brain injury, anyone who is caring for a brain-injured person, or anyone with any interest in learning more about brain injury. For details or to schedule me for your event, please contact me at neelyf@aol.com.

Below is my brochure.

Click on photos to enlarge.

10 Brochure 111 Brochure 2

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.

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

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SPEAK OUT! . . . . . . . . . . . . . . . . . . Faces of Brain Injury Chelsea Rolph

SPEAK OUT! Faces of Brain Injury

Chelsea Rolph

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.

Chelsea Rolph (survivor)

Chelsea Rolph 3 Survivor 061415Four summers ago, I did not know what I was going to do after leaving high school. I had suffered multiple concussions, and I spent my summer in concussion rehab. I was sent for a test or results at least once a week. I had a neuropsychological exam. It was a full, exhausting day of random tests. The results of this exam really gave me some answers. Essentially the doctors were telling me that I have a lot of problem areas. If I decided to go to school, I would need:
– a note-taker
– a private room for exams
– extra time for exams
– take-home, open-book exams, if possible
– formulas for any possible math classes
– extended time for assignments
– to be given assignments right away
– exam reviews from the profs
– the use of a computer

I had a lot of problems, and I needed a lot of help. The doctor told me that, because I was trying to choose between college and university, I should choose college. I was told that college is more hands-on, but it was suggested that I take time off and not even consider going to school. I decided that I would go to McMaster University and see if I can get the accommodations. When I sat down with one of the guidance counselors, I was told that they have had people with my problems before. The counselor suggested that I take one, maybe two, classes a semester. Basically I left that meeting feeling discouraged. I didn’t think I would be going to school at all.Chelsea Rolph 1 Survivor 061415

As the school year approached and I had to make a final decision on school, I decided that I was going to go to school. I decided that I wanted to prove everybody wrong.

Four years later, I GRADUATED! I did it without the help of any doctors and without any accommodations from Mac. It wasn’t easy, but I walked across that stage and became an official “Graduate of 2015.”

Chelsea Rolph 2 Survivor 061415I would like to thank everybody that made it possible, and I want to thank everybody I have met along the way to make these past four years some of the most memorable. Among the Vanier Cup win in first year, Homecoming, meeting the love of my life, beer pong Tuesday, and even a flash mob, I have made some unforgettable memories.

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

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

As I say after each post: Please leave a comment by clicking the blue words “Leave a 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 Erin Lea Beville & Evelyn Pumarejo-Justiniano

SPEAK OUT! Faces of Brain Injury

Erin Lea Beville & Evelyn Pumarejo-Justiniano

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.

A special shout out to two special nurses.nurse_0515-0911-1420-0746_SMU

Breville, Erin LeaErin Lea Beville (survivor)

I’m a sixteen-year survivor. I got my bachelor’s degree in nursing from Florida State University in May (2014) and my RN license last October. Having a traumatic brain injury (TBI), I needed a bit of rest following the hell that is nursing school. I was fried!

I recently started a job as an Integrated Health Wellness Coach and Peer Support Specialist at Community Mental Health. It’s perfect because they want me to share my story and pay me for it. My brain injury is finally an asset rather than a liability. So, hooray for patience, Breville, Erin Lea & nieceperseverance, and determination! I’ve done it – not in spite of my TBI, but because of it. Together, we can be the difference, for each other and for others. Go out there and inspire people. Be the person only you can be – yourself. Then own it. You rock!

Evelyn Pumarejo-Justiniano 2 Survivor 082315Evelyn Pumarejo-Justiniano (survivor)

I suffered a traumatic brain injury (TBI) almost twenty years ago. I had to learn how to walk and talk and to relearn the basic things we take for granted in life. Yet, I feel I am blessed. I overcame all the obstacles and unforeseen Evelyn Pumarejo-Justiniano Survivor2 082431jpgcircumstances put in my life. I returned to school after my injury and had a GPA of 3.79 in nursing school. Today I am a nurse – going on a year now. I am planning to go for the degree of Bachelor of Science in Nursing. And, I thank God for my good husband, who has been by my side the past 29 years.

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

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

As I say after each post: Please leave a comment by clicking the blue words “Leave a 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! . . . . . . . . . . . . . . . . . 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 are this week’s Itty-Bitty GIANT Steps

drivers-license-621806Cory Edmondson (survivor)…Two years ago, I was told that I would never drive again. That didn’t sit too well with me. My mom told me I could accept it or I could continue to work hard and, one more time, prove somebody wrong. I am now one excited dude – I got my license back! Never give up. Always believe in yourself.

washdishesclipsahoyCory Edmondson (survivor)…I’m pretty proud of myself right now. I stood at the sink, washed and wiped the supper dishes, and put away 98% of them. I walked around the kitchen with just one hand on the cupboard. This was a BIG accomplishment for this fella. Never give up! 🙂

Jo Emery & DaughterJo Emery (caregiver)…This week in Australia, it is Brain Injury Awareness Week. For donations, we have BangOnABeanie and BangOnABarbie (“Barbie”=BBQ). I am so very proud of my beautiful twelve-year-old, who organised the BangOns with her local girl-guide unit. She talked about why they were doing them and a little bit about her dad. She also played a memory game with them. She raised about $30, which was really great. I’m a very proud mummy!

Minion Puzzle for Kyle F.Kyle F. (survivor)…This puzzle took me ALL day. It may seem rather easy, with its being only forty-eight pieces and all, but I get distracted extremely easily – a heck of a lot more easily than before my TBI. So…score one for me. Also, this puzzle is as cute as heck with all the minions.

blood_donors_1Kristina Hopkins (caregiver)…I’m about ready to donate blood again. I feel so honored to be able to do this every eight weeks. I’m a universal donor with my O-negative blood type, and it’s a blessing to be able to help so many. I challenge you all to donate if you can and are able.

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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.

SPEAK OUT! NewsBit . . . . . . . . . . . . Simple Blood Test For Traumatic Brain Injury

Simple Blood Test For Traumatic Brain Injury

presented by

Donna O’Donnell Figurski

Newsboy thA simple and convenient test for the existence and severity of a traumatic brain injury (TBI) is badly needed. Currently the only test for a TBI appropriate for use in the Emergency Room is the CT (computerized tomography, often referred to as “CAT”) scan. However, a CT scan can only determine if there is bleeding in the brain. If there isn’t a hemorrhage, the patient is likely to be sent home. Also, a CT scan cannot determine the existence of a concussion. Concussions (even those that do not cause loss of consciousness) are brain injuries that can be harmless and heal, or they can be fatal or cause major life-altering problems. Until now, there has been no way to measure brain damage.

Exciting new results show that the amount of a blood protein (BDNF, brain-derived neurotrophic factor) correlates with the existence of a TBI, when measured within 24 hours of the trauma. Patients with a blood-tube-cartoonTBI had less than one-third the amount of BDNF in their blood than did non-TBI patients. The researchers also found that patients with a TBI who had very low levels of BDNF recovered poorly. This is an exciting beginning because it will be routine to tell if there is brain damage in a person who may have been in an event that could lead to a concussion. A person who has experienced any trauma (like a motor vehicle accident, a sports-related injury, or domestic violence) can now be assessed for brain injury. Appropriate therapies can be considered immediately, instead of waiting for symptoms to appear.

Of interest to current TBI survivors is the possibility that continued BDNF measurements may correlate with the speed of recovery. This correlation needs to be tested – is a BDNF measurement taken months later still meaningful? Also, researchers urgently need to learn the molecular mechanism behind the lowering of BDNF with TBI. Do things that raise the BDNF level allow a patient to recover faster from a TBI? (Interestingly, omega-3 fatty acids and exercise raise BDNF levels.) (Full story)

(Clip Art compliments of Bing.)

As I say after each post:

Please leave a comment by clicking the blue words “Leave a Comment” below this post.anim0014-1_e0-1

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

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

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

Feel free to “Like” my post.

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Welcome to Harmony Kent Online

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Pete Springer

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TBI - Survivors, Caregivers, Family, and Friends

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Loving someone with a Traumatic Brain Injury

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Brain Aneurysm, cerebral hemorrhaging, hemorrhage stroke