TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Another Fork in the Road’

Survivors SPEAK OUT! Bonnie Weikel

Survivors SPEAK OUT!  Bonnie Weikel

presented by

Donna O’Donnell Figurski

Bonnie Weikel – Brain Injury Survivor

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

Bonnie Weikel

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

New Bethlehem, Pennsylvania, USA

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

I was 47. My brain hemorrhage was in 2004.

4. How did your brain injury occur?

I had a subarachnoid hemorrhage (blood leaking into the space between two of the membranes that surround the brain; mine was from a ruptured brain aneurysm). I always like saying the correct medical terminology because I can actually remember how to spell it. For the majority of the time, I refer to it as “My head blowing up.” I also had a stroke during my craniotomy.

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

I was aware of my problems after I woke up from surgery. (The doctor wasn’t able to guarantee what kind of shape I would be in if I survived the surgery.)

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

First, the hospital ruled out a stroke, and, because I complained of “the headache from hell,” they did a CT (computerized tomography) scan and found the bleed on my brain. They packed me up and transported me to Allegheny General Hospital in Pittsburgh, where I had my brain surgery done.

operating-theatre-illustration-surgeon-patient-hospital-41734906.jpg7. Were you in a coma? If so, how long?

No, thank God. I recognized everyone when I came out of surgery. I just couldn’t remember who was there to visit from one minute to the next. My daughter took pictures of me with everyone who came to see me.

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 was in inpatient therapy for a month and then in outpatient therapy for about five weeks. I had to learn to do everything all over again – starting with feeding and dressing myself.

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

I have short-term memory loss and issues with balance, vision, and hearing. I have worked very hard over the past ten years to get to where I am today, and I did it all by myself.

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

My life has changed dramatically. It is better. I love the “new” me much better than the old version. I also found out who my true friends are.

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

I did lose one thing I used to love to do. I used to sew for hours. I had my own sewing business. I made anything from window treatments to wedding gowns, and I was good at it. I lost all desire to sew; it is no longer something I love to do. It is more of a chore.

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

I like that I am back in school. I am taking college courses online. It is the biggest challenge I have taken on since the TBI (traumatic brain injury).

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

I have an invisible disability, and some people think I am faking it and living off the system.

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

Yes. Changing my attitude about people and life in general has helped. One day, I decided I could sit and cry for the rest of my life about all that I have lost, or I could be happy with my new life and live it.

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

My home life has been affected, but in a positive way.

I take pride in myself and in my accomplishments. Relationship-wise, it’s been a curse.

I haven’t been able to find people who can deal with my issues because they just do not understand. I am thankful they don’t understand how life is for a TBI survivor because, if they did, it would mean they also suffered a TBI. (The only way anyone can truly understand what life is like for a survivor is to live it themselves.)

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

Yes. My social life has changed a lot. During the first year, I found out who my real friends are. Now I have a small circle of friends who I know I can trust. I go out dancing once a week with friends. I do this because I still can.

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

After living with my daughter for about a year, I am now on my own. I do everything myself – I am even back to driving. I will say this much: I thank God for my GPS! Ha, Ha! Yes, I understand what it is to be a caregiver, and it takes a special kind of patience for a caregiver of someone with a TBI.

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

I am working on a Communications degree and changing to Community Service and Social Work. My goal is to work with other survivors as a life-coach/advocate. I am getting better grades now than I ever did in high school. I can only handle two classes a semester, so it will take twice as long as normal to get my degree. But, I will see it through to the end.

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.

It didn’t take me as long as it does for some others, but learning to love your new self and accept your new life is, I believe, the secret to moving on. Love and acceptance of yourself is the base you can grow from.

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

I highly recommend that brain-injury survivors seek out other survivors. It was such an awesome feeling the first time I spoke to someone who “Gets it.” It was like someone turned my light back on. I felt free and almost normal again. I was no longer alone. I have a motto I live by. It was written from one of the first survivors I met – in a Yahoo health and wellness chatroom. I think he went by “Rhino.” Anyway, here it is. “Mourn what you lost. Use what you have. Anyone can quit.” My strongest advice to other survivors is “NEVER GIVE UP!”

 

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

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SPEAK OUT! . . . . . . . . . . . . . . . Faces of Brain Injury . . . . . . . . Ina M. Dutkiewicz (survivor)

SPEAK OUT! Faces of Brain Injury – Ina M. Dutkiewicz (survivor)

presented

by

Donna O’Donnell Figurski

Brain Injury is NOT Discriminating!

bigstock-cartoon-face-vector-people-25671746-e1348136261718It can happen to anyone, anytime, . . . and anywhere.

The Brain Trauma Foundation states that there are 5.3 million people in the United States living with some form of brain injury.

On “Faces of Brain Injury,” you will meet survivors living with brain injury. I hope that their stories will help you to understand the serious implications and complications of brain injury.

The stories on SPEAK OUT! Faces of Brain Injury are published with the permission of the survivor or designated caregiver.

If you would like your story to be published, please send a short account and two photos to me at neelyf@aol.com. I’d love to publish your story and raise awareness for Brain Injury.

Ina M. Dutkiewicz (survivor)

Dutkiewicz, Ina M. Survivor 2 041316

Ina M. Dutkiewicz- Brain Injury Survivor

I had a near-fatal car accident on my way to work on February 3, 2010. I was immediately put into a coma from the violent crash, and I stayed in that coma for over four weeks. My pelvis was broken on both sides from my seat belt. When I woke up, I was classified as “not weight bearing” (wheelchair-bound). I slowly moved to a walker, and then to a cane. Now I can navigate without the cane if the weather is nice and not snowy or icy. I had to learn to walk again (I still have gait problems), as well as relearn to swallow and eat. (They started me out with ice cream! 🙂 ) I also had to do disability driving lessons before I could drive again.

It has been a long, scary road these past seven years. I was not willing to give up on myself, and I gave my all and then some to my recovery. I am hoping to someday return to work part-time.

Thank you Ina M. Dutkiewicz for sharing your story.

(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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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.

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David Smith – Brain Injury Survivor

David Smith (survivor) … Today’s Itty-Bitty Giant Step is going to be to just get out of bed and to stay up.

bed

 

 

bonni-villarreal-1

Bonni Villarreal – Caregiver for Husband

Bonni Villarreal (caregiver) … My husband had a stroke in 2012, so he has an acquired brain injury (ABI). It has been a long, hard road as is most of what you post about. But, I do have wonderful news to report. After almost five years of having a G-Tube (gastrostomy a332i0_185tube), Mike is now able to drink fluids! (He’s been eating for a long time, but we didn’t think he would ever get back the ability to swallow liquids.) So, DON’T EVER GIVE UP! It’s almost five years later, and Mike is proving doctors wrong every day. He is going for a swallow test, so the tube can come out for good … best present ever!

YOU did it!

Congratulations to contributors!

(Clip Art compliments of Bing.)

(Photos compliments of contributors.)

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

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

Feel free to “Like” my post.

Survivors SPEAK OUT! Mark Moore

Survivors SPEAK OUT!  Mark Moore

presented by

Donna O’Donnell Figurski

moore-author-photo

Mark Moore – Bran Injury Survivor & Author

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

Mark Moore

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

McLean, Virginia, USA     mark@mbmoorefoundation.org

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

2007   At age 46

4. How did your brain injury occur?

I had two strokes.

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

I was coaching my son’s baseball practice, and I began to lose my balance.

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

I had a craniectomy (brain surgery in which a piece of the skull is removed, but, unlike a craniotomy, is not returned to its original location) to relieve the pressure on my brain.

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

Yes. I was in a coma for four weeks.

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?

Yes. I had physical therapy, occupational therapy, and speech therapy as an inpatient for two weeks and then as an outpatient for two months.

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

Initially I had significant diminished use of my left side and loss of peripheral vision in my left eye. I couldn’t walk or speak.

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

Having a stroke was the worst day AND the best day of my life. It was the worst day because it was scary and it was one of the first times I realized that I had no control over the outcome. It was scary for my wife and my family. When I found out that I had basically been “asleep” for nearly six weeks, I was scared all over again. I had to face the fact that I might not walk, talk, or think like Mark Moore ever again. In fact, I had to recognize that the “old” me might actually be gone. At that moment, it felt like the worst thing I could imagine.

Mark & Brenda Moore with Obamas.jpg

Mark & Brenda Moore with President & Mrs. Obama

As I struggled with those concerns though, I remembered my mother’s words – words I had forgotten, words she had spoken to me during her own health crisis. She said, “Mark, God will never give you more than you are able to handle.” Those words impacted me and turned me around. I was slowly able to stop thinking just of myself. I started thinking about God and what He could do and would do with my life now. He could pick up the pieces of this broken version of me and heal me – create in me the person he meant for me to be. That thought began to work in me, and though I knew it wouldn’t be easy, I also knew that, with God’s help, I could let go of the old Mark and become a new man.

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

Riding rollercoastersroller-coaster-thought-of-the-day-jewels-art-creation-clip-art

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

I enjoy my relationship to God.

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

I dislike the constant scanning to drive

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

Having a stroke meant I had to learn to surrender. I had to face the fact that my abilities as a “fix-it guy” were not going to come to the rescue. I had to do something that was hard for me to do. I had to be willing to give up my illusions of who Mark Moore was and hold on for dear life to who God is. That’s surrender! That’s where everything you thought you knew comes to a halt and God finally has enough of your attention to help you become what He planned all along.

When I first looked at what was going to be required of me in the recovery process, I did not want to do it. I thought it would simply be easier if God just shut me down, packed me up, and sent me back to His house. But, He didn’t do that! He kept me in the hospital for several weeks and then sent me back to my house. He showed me that recovery meant I had to totally trust Him and my wife, Brenda, and the therapists, who would bring me back to good health.

mark-moore-brain-injury-survivor-dc-marathon

Mark Moore – Brain Injury Survivor – 5K Race

Starting therapy looks daunting. It is daunting, and it’s even frightening! Everything in me resented that I had to be there and that I had to learn all over again things I’d known all my life. If you’re facing therapy and recovery now, all I can tell you is to do what you’re told to do. Make the effort. Try harder than you’ve ever tried in your life, and lean on the people who love you. Open your heart and mind to all that can still be possible for you. That’s what surrender requires. That’s what trusting God is all about. You’ll be in recovery for a long time (maybe the rest of your life), but you’ll be in good hands in the process.

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

One day (May 12, 2007), I had a stroke, which was followed by another one. I was fine one minute and fighting for my life the next. In the process of recovering from those strokes, I discovered something I had not fully realized before. God had a plan for my life. He had a purpose for me, and I was not on the path He preferred. In one day, my life changed, and my purpose changed with it. To be honest, when I discovered God wanted something more from me, I was relieved. Clearly, there was more I could do, and it didn’t always revolve around the work I had carved out for myself. I was relieved to know that I could step back from the life I designed and be far more comfortable in the one He designed.

basketball-clipart17My friends were amazed when I did not show any interest in simply going back to work. They thought it was strange that I did not want to play basketball, a game I had loved playing all my life. What I did want to do was to please God. What energized my spirit and resonated with my soul was to do the things God wanted – to fulfill His purposes in me.

What a difference a day makes! What joy it is to my heart that God was with me through the strokes and is with me now to guide me into being the Mark Moore He always knew I could be. What a joy it is to live more intentionally and more fully awake to the places He would have me go.

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

Not really

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

I don’t have or need a caregiver.

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

When God had my attention as I lay in a hospital bed, He asked me a new question. Whose job is it to help others? Whose job is it to make a difference? Whose job is it to spread the gospel? The answer was the same in every case. It was MY job! God had blessed my work and made it possible for me to bless others. He took me out of the race in which I’d driven laps for twenty years and said, “I have something new for you. I want you to slow down and hear what I have to say.” I stopped then and listened.

God didn’t “give me a stroke.” He used the stroke to give me a new purpose. He used the situation to help me hear His voice more clearly and to understand the job He had in mind. Whose job is it … to do good, to help others, to lend a hand? It’s mine, and it’s yours! Let’s use whatever resources we have been blessed with to help those around us. It will fulfill our life-purpose like nothing else can do.

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.

It was interesting to me after my stroke experience to discover that I did not want to be “naked” in front of my family – in front of the people who knew me the best. Like Adam and Eve, I wanted to hide so they would not discover my fear and sense my weakness.

As I looked back at my initial reactions to my strokes, I realized we can’t hide from the people who know us well and love us any more than we can hide from God.

mark-brenda-moore

Mark & Brenda Moore

My wife did not want me to hide from her. She was ready to help me – ready to stand beside me and offer me her strength. My friends were like that too. Caregivers and hospital personnel were set to help me, but I had to be willing to be “naked.” I had to be willing to let them see my weaknesses and my vulnerability. I was not the person I had been; I needed their strength.

Another thing that was extremely helpful during my stroke recovery was that I began to regularly put on my headphones to listen to gospel music. The effort to re-establish my fine-motor skills was sometimes grueling, and I wasn’t always sure I could do it. Gospel music comforted me and helped me get through the ordeal. It reminded me over and over again of what Jesus did to give me life, to lift me up, and to restore my soul. It also reminded me that there was nothing I was going through that Jesus did not experience. He paid the price so that I could be restored eternally, spiritually, and physically to this day.

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

One thing I tell everybody is that you can’t recover from a stroke or any debilitating illness without the help of your family, your friends, and your faith. It can take days, weeks, or months to see any real change in the things you are able to do physically. That means that mentally and emotionally you have to lean on the things that boost your morale and make a difference in your attitude. When it comes to the kind of help your family, friends, and faith can give in your recovery, it all depends on YOU!

I say it depends on you because you are the only one who can let others in to help make a difference. Your spouse can come to your aid every day and cheer you on and encourage you, but it won’t do any good unless you’re willing to receive it. I can admit that there were times when I didn’t really let my wife, Brenda, in. I was scared, and I didn’t want her to know it. I didn’t want to have to tell her that I didn’t think I could do what it took to recover. She had known me as a guy who was a go-getter – someone who rose to the occasion to get things done. After the stroke, though, I didn’t always believe that I had that same courage.

Friends stood beside me as well and helped me get the message that a lot of people cared and were rooting for me. They wanted me to get better and to become the old Mark again.

 

(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 SPEAK OUT! Survivors Interview Questionnaire for a copy of the questions and the release form.

(Clip Art compliments of Bing.)

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

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.

Daniel Bellmore - Brain Injury Survivor

Daniel Bellmore – Brain Injury Survivor

Daniel Bellmore (survivor) … I graduated from grad school with my Master’s Degree in mental health counseling, specializing in trauma and addictions.mental-health

David Smith (survivor) … In the past week, I’ve been working for a guy I met in town. I have been cleaning out his basement, 16358690_1201798153189065_1370881325_nthe entire house, etc. Yesterday, I began painting a bedroom, and I plan to finish this morning. I went to a TBI (traumatic brain injury) workshop – an art-therapy group. I also went to a “celebrate-recovery” group – I’ve been trying to help a friend.

clip-art-painting-314011I have difficulty staying focused on these accomplishments and others, since I woke out of a coma eight months ago. I’m glad that I can do these things.

YOU did it!

Congratulations to contributor!

(Clip Art compliments of Bing.)

(Photos compliments of contributors.)

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

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

Feel free to “Like” my post.

Survivors SPEAK OUT! Jordan Emerson

Survivors SPEAK OUT!  Jordan Emerson

presented by

Donna O’Donnell Figurski

jordan-emerson-2

Jordan Emerson – Brain Injury Survivor – Race Car Driver

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

Jordan Emerson

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

Windham, Maine, USA

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

I had my brain injury at 13 years young.

4. How did your brain injury occur?dan Emerson

Jordan Emerson - Brain Injury Survivor - Race Car Driver

Jordan Emerson – Brain Injury Survivor – Race Car Driver

I was driving a fully-safety-equipped racecar.

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

When I was unconscious

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

I was given a trach. I had emergency procedures for a cracked left hip, brain stem, seizures, a crushed left arm, paralyzed vocal chords, and paralyzed stomach.

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

Jordan Emerson - Brain Injury Survivor

Jordan Emerson – Brain Injury Survivor

Yes. Almost 3 months

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

I have occupational and physical therapies as an outpatient. I was also helped by a speech-language pathologist.

How long were you in rehab?

I’m still attending OT and PT as an outpatient.

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

I still have awful trouble going to the bathroom. Being in crowded areas makes me tired. (It’s “overstimulation,” but instead of overstimulation, it feels like a “draining of my energy.”)

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

My life is neither better nor worse. It’s just different.

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

I miss being able to run around outside with my dogs.

th-112. What do you enjoy most in your post-brain-injury life?

I like that everybody seems to offer to help more often.

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

I dislike that I’ll be thinking so hard about something, and then, *poof* it’s gone.

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

Talking with other survivors has helped.

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

Before I developed a filter, I said things to friends, and over time, those friends disappeared.

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

Yes. I have lost friends.friends

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

My mom is my main caregiver. I’m thankful for her every day.

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

I plan to be driving, living in my own apartment, married, etc.

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.

Hard work really does pay off.

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

Jordan Emerson and Mom & Dad

Jordan Emerson – Brain Injury Survivor and Mom & Dad

I owe a lot of my journey to my loving parents – I couldn’t have done this without them. I ♡ them!
Please feel free to reach out to me (#Believe). I enjoy helping whenever I am able. Believe!

 

 

 

(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 SPEAK OUT! Survivors Interview Questionnaire for a copy of the questions and the release form.

(Clip Art compliments of Bing.)

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

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 is this week’s Itty-Bitty GIANT Step

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Ric Johnson – Brain Injury Survivor

Richard Johnson (survivor) … With two new grandsons, my wife and I decided we needed a baby crib in our house. So, we went to a store, bought one, drove it home, and then had to put it together. It should have been easy, but not so much after a traumatic brain injury.crib

First, it was hard to focus in the store – too much noise and too many lights. Then, having short-term memory issues and only two hands, I took four hours to put it together.

YOU did it!

Congratulations to contributor!

(Clip Art compliments of Bing.)

(Photos compliments of contributors.)

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Caregivers SPEAK OUT! . . . . . Lori Strauss Heckman

Caregivers  SPEAK OUT!  Lori Strauss Heckman

(caregiver for her son, Bartholomew Wayne Nathaniel),

presented by

Donna O’Donnell Figurski

lori-strauss-heckman-caregiver-012017Three years ago, our lives were turned upside down when my then 21-year-old son had his accident. It has been a long road with many hurdles to overcome, but I am so proud of him. He is my hero and my greatest blessing. And, proof to never give up. We were told that he would probably not make it that night. We were also informed that, if he did, he would not have any quality of life. But, he proved everyone wrong! Many prayers were prayed and many tears were shed, and my son is still with us – and doing very well. The first and second photos are of my son after the accident; the third is him wearing a helmet in recovery; and the fourth photo is of him with his car. (Yes, my son is driving, and his seizures are under control.)

Meet Bartholomew Wayne Nathaniel

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(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 SPEAK OUT! Caregiver Interview Questionnaire for a copy of the questions and the release form.

(Clip Art compliments of Bing.)

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

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

SPEAK OUT! Itty-Bitty GIANT Steps

presented by

Donna O’Donnell Figurski

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

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

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

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

 

Here is this week’s Itty-Bitty GIANT Step

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David Figurski, PhD – Brain Injury Survivor

David Figurski (survivor) … Because my speech has been affected by partly paralyzed vocal chords and tongue, I was worried that my comments at my father’s funeral Mass would not be understood. On top of that, I was beginning to lose my voice from speaking with so many people the day before at the funeral parlor. But, with Donna’s support as she balanced me, I walked to the podium, and I gave my comments. For ten minutes, I gave them – careful to speak slowly and enunciate every sound.

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David Figurski at Podium

Several people came up to me afterward and said that they had no problem understanding me. It’s something I had wanted to do to honor my 95-year-old father. I was happy and proud that I did.

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Hank Figurski 1921 – 2017

 

YOU did it!

Congratulations to contributors!

(Clip Art compliments of Bing.)

(Photos compliments of contributors.)

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.

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TBI Tales . . . . . . . . . . . . . . . . Twelve Years, But Who’s Counting?

Twelve Years, But Who’s Counting?

by

Donna O’Donnell Figurski

1242232191169820850212_white,_green_rounded_rectangle.svg.med.pngTwelve years! Twelve years ago today, I came as close as a breath to losing my husband and best friend, David. While exercising (a thing he did every day to stay in shape), David did thirteen chin-ups, one more than he had done every other day. That was the proverbial “straw that broke the camel’s back,” or in David’s case, the “chin-up that caused his subarachnoid hemorrhage.” That day, as I rode with him in the ambulance to the hospital, I never realized what lay ahead for us. I never dreamed that this blip would be life-altering. I thought we’d be home by the end of the day, carrying on with life as usual. I was wrong!

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David H. Figurski, Ph.D. – Brain Injury Survivor

David remained in the hospital in the Neuro-Intensive Care Unit (NICU) and the step-down unit at Columbia Presbyterian Hospital (now New York Presbyterian Hospital) for three weeks. While he was there, he was treated to two more brain surgeries – one for an aneurysm and the other for an arterial venous malformation (AVM). He then became a guest at a local rehab hospital for another two months, until insurance wrongly said he was fine to go home.th-1

I am grateful that David is still with me. He wasn’t expected to be. Each surgeon gave me little hope that he would survive any of his surgeries. I’m glad that David proved them all wrong. I’m glad that we have had twelve more years together, and I hope to spend many more with this man whom I have loved since I was sixteen years old.

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Hopefully, in the sometime future, you will be able to read David’s whole story in my book-in-manuscript, titled “Prisoners Without Bars: A Caregiver’s Tale.”

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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