TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘survivingtraumaticbraininjury.com’

“Another Fork in the Road” . . . Brain Injury Radio Network with Julie Kintz and Mark A. Ittleman, M.S., CCC/SLP

YOU ARE INVITED!

 

putthis_on_calendar_clip_artJulie Kintz of “Quantum Leap” will be substituting for Donna O’Donnell Figurski of “Another Fork in the Road” on the Brain Injury Radio Network.

Julie’s guest will be Senior Speech Language Pathologist-Author Mark A. Ittleman, M.S., CCC/SLP. Mark Ittleman will discuss speaking difficulties and tell how loved ones can help improve the speech of their survivor at home in a fun and easy way.

Come One! Come ALL!

(NOTE: New Day, Sunday – Same Time)

What:        Host, Julie Kintz of “Quantum Leap” substitutes for “Another Fork in the Road” host, Donna O’Donnell Figurski.

Why:         Hear Mark A. Ittleman, M.S., CCC/SLP discuss speaking difficulties.

Where:     Brain Injury Radio Network

When:       Sunday, October 19th, 2014

Time:         5:00p PDT (6:00p MDT, 7:00p CDT, and 8:00p EDT) 90 minute show

How:         Click: Brain Injury Radio Network.

Call In:    424-243-9540

Call In:     855-473-3711 toll free in USA

Call In:    202-559-7907 free outside US

or SKYPE

If you miss the show, but would like to still hear the interview, you can access the archive on On Demand listening. The archived show will be available after the show both on the Brain Injury Radio Network site and on my blog in “On the Air.”

(Clip Art compliments of Bing.)

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

SPEAK OUT! Itty-Bitty GIANT Steps

Itty-Bitty GIant Steps for Blog

SPEAK 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 donnaodonnellfigurski@gmail.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.

David Figurski…I assembled Donna’s new office chair. It came as 12 pieces with 13 screws. The Allen screws made it possible to use my non-ataxic left hand. Because the instructions were written with two good hands in mind, I sometimes had to devise my own way of assembling the parts. It took me twice as long, but I felt good about doing it.

Jodi Mannon…I was hit and thrown down stairs in January by my ex-roommate. I don’t remember a lot in the past 8 1/2 months. Yesterday I became friends with a lot of people who also have a TBI. I spoke with one on Facebook Messenger for a couple of hours. We chatted for a moment today, and he is going to call me tonight. I was shocked! He made me truly happy for once because we were able to talk the way we did and share our lives. I haven’t done that with anyone because I’ve never even thought about it before. I just had a lot of issues in dealing with getting better. It’s the greatest feeling to have people who have been through the same thing understand me!! Not that my parents and friends haven’t been nice, but they just don’t understand the things I go through. My new friends do. I feel so blessed to have them in my life, and I look forward to keeping these new friendships for the rest of my life!!!

Carmen Gaarder Kumm…I passed the test that allows me to keep my job!!! I needed a 70, and I got 73.7 – not much, but I PASSED! Better yet, I found my car after going out a different door than the one I went in. (Also, I was parked on the street in a college city that I’ve only been to once before.) I walked around for a half an hour looking for it – but I was still within 2 hours! LOL!

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

Survivors SPEAK OUT! David Villarreal

SPEAK OUT! – David Villarreal

by

Donna O’Donnell Figurski

David Villarreal

David Villarreal

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

David Villarreal

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

Temple, Texas, USA

3. When did you have your TBI? At what age?

1st and 2nd – 2012 (age 50), 3rd – 2013 (age 51), and 4th – 2014 (age 52)

4. How did your TBI occur?

I’m not sure…I really don’t remember.

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

It was realized when I hit the floor and did the best I could do to call for help.

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

A coworker called 9-1-1. I was rushed to the Emergency Room and given some kind of med that broke up the clot (note: possibly tissue plasminogen activator, tPA) and saved my life.

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)? How long were you in rehab?

Yes. I had physical therapy and occupational therapy for 6 months.

It wasn’t until my 3rd stroke that I finally got help. It was from the Central Texas VA (Veteran’s Administration) in Temple, Texas. They have made everything possible for me. I credit all my progress to them.

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

Wow…I have problems with my speech, vision, balance, strength, and control of my bodily functions. I could not eat or drink. I still do not have use of my right side. I am right-handed, so that is a problem. I have to learn to do everything again with my left hand.

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

Oh my goodness! My life has changed so much. I was a studio musician before all of this happened. I’ve heard many of the CDs that I am on. I went from playing several instruments to not being able to play any. That led to some very, very deep depression.

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

My musician life

12. What do you enjoy most in your post-TBI life?Villarreal, David Handcycle

That I now race a handcycle

13. What do you like least about your TBI?

That I get tired too fast

14. Has anything helped you to accept your TBI?

I got up one day and remembered I was a Marine. I decided to do what Marines do best, and that is save others. So now, I ride this handcycle with the one hand that works to let other stroke survivors know we can still have a good, normal life.

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

Well, after my first stroke, my wife of 10 months filed for divorce three days after I had it. I met my current wife a year later – after my 3rd stroke. She was my therapist. We got married about a month ago.

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

For the longest time, I would not leave my home. I didn’t want anyone to see me like this. Now I go out more often, but I’m not really at ease with it.

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

I have been taking care of myself from the start. Now I am having a very hard time allowing my wife to do anything for me. She wants to help me so badly, but I have a hard time letting go.

18. What are your future plans?

I really don’t know.

    What do you expect/hope to be doing ten years from now?

I hope to be helping stroke survivors.

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 TBI survivors with your specific kind of TBI.

Ok, it happened (the stroke). Get over it…Cry…Get mad…OK, now that is out of the way…Get to work, and work harder than you have ever worked. It will be worth it if you can do it. Life is so good when you get through it all.

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

DON’T GIVE UP. YOU CAN DO WHATEVER YOU WANT TO DO. Don’t let anyone tell you different. I have been told I am supposed to be dead…I am supposed to be paralyzed from my neck down. BY THE GRACE OF GOD I AM NOT!!!!!!!!

David Villarreal - 1st of 4 strokes (Not expected to survive) He DID!

David Villarreal – 1st of 4 strokes (Not expected to survive.) He DID!

 

Thank you, David, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

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

(Photos compliments of David.)

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.

Survivors SPEAK OUT! Melissa Cronin

SPEAK OUT! – Melissa Cronin

by

Donna O’Donnell Figurski

 

Melissa Cronin Head Shot 2

Melissa Cronin

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

Melissa Cronin

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

South Burlington, Vermont, USA

3. When did you have your TBI? At what age?

Age 36

4. How did your TBI occur?

In 2003, when visiting the Santa Monica Farmers’ Market, an elderly driver confused the gas pedal for the brake and sped through the market. I was thrown forward, and my head hit the pavement. The force of the impact resulted in a ruptured spleen and multiple fractures, including my pelvis.

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

Fourteen months after the accident, when I returned to part-time work as a public health nurse, I experienced increased fatigue, difficulty concentrating, and multitasking. My boss threatened to fire me, so I resigned and attempted part-time work in a pediatrician’s office (bad idea for someone with a TBI), but I struggled to keep up in a fast-paced environment. In May 2006, I finally saw a neuropsychiatrist for testing, and the results proved to be consistent with a TBI.

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

I did not have emergency treatment for a TBI. The CT (computerized tomography, also known as “CAT”) scans showed no bleeding (typical for a “mild” TBI). I did have emergency surgery, though, to remove my ruptured spleen.

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)? How long were you in rehab?

I had physical and occupational therapy at Cedars Sinai Hospital in Los Angeles to help regain muscle mass and strength after being hospitalized for nearly one month. I would be in a wheelchair for four months while my fractures healed, so rehab taught me ways to navigate through my day.

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

Fatigue, difficulty multitasking and concentrating, occasional irritability, depression; and difficulty processing verbal, auditory, and visual information

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

My life is both better and worse. It’s better because my TBI, and other injuries, opened up a path for me to writing. And my husband, whom I met only three weeks prior to the accident, has been my strongest support. It’s worse because I eventually had to give up my 20-year nursing career.

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

Running and skiing, and the babies I cared for in the neonatal intensive care unit where I worked before my injury

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

Writing, playing the Irish fiddle, going for walks, and, of course, my husband’s unwavering support

13. What do you like least about your TBI?

I’m much slower at getting things done. I often sleep in until 9:30 or 10:00 am, and I feel as if I’ve wasted much of the day. Also, I often fail to understand concepts others seem to grasp so easily.

14. Has anything helped you to accept your TBI?

I’ve been helped by the neuropsychiatrist who diagnosed me with a TBI and by the cognitive therapist who treated me. Also, my therapist – he continually reminds me that my brain has been rewired.

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

Definitely my home life has been affected. I rely on my husband to do much of the “heavy” lifting, like cooking, grocery shopping, and driving, because I am easily distracted.

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

Absolutely. I do not socialize as much as I did before my injury because it doesn’t take much for me to become fatigued.

9781611592399_p0_v3_s260x420

“Invisible Bruise” Chicken Soup for the Soul: Recovering from Traumatic Brain Injuries. June 2014

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

I am my own main caregiver, though my husband does much of the cooking. I do not know what it takes to be a caregiver, though my father is living with Alzheimer’s, and I help out as much as I can.

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

Writing and traveling

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 TBI survivors with your specific kind of TBI.

I wish I understood much earlier the truth about TBIs before I re-entered the workplace and had to face the threat of being fired. For example, I wish someone had warned me that I might have actually suffered a TBI, and that the initial presentation of milder injuries does not mean the consequences are mild.

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

Persevere. Try not to compare yourself to non-brain injured individuals – you’ll only get frustrated. Pay attention to what your body and brain are telling you, and give yourself permission to take naps. Exercise your brain, in moderation, by doing crossword puzzles or learning a new skill. Whatever you accomplish, even if it’s getting out of bed by 7:00 am, is an accomplishment.

Melissa is the author of “Invisible Bruise,” published in Chicken Soup for the Soul: Recovering from Traumatic Brain Injuries.

Melissa playing fiddle

Melissa Cronin with her fiddle

To learn more about Melissa, please visit her website/blog at Melissa Cronin.

 

Thank you, Melissa, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

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

(Photos compliments of Melissa.)

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.

“Another Fork in the Road” . . . Brain Injury Radio Network: “Triking Across America – diagonally,” with Catherine (Cat) Brubaker

YOU ARE INVITED!

 

putthis_on_calendar_clip_art“Another Fork in the Road” on Brain Injury Radio Network invites you to meet Catherine (Cat) Brubaker who is “Triking Across America – diagonally.” Cat looks like your normal, everyday, young woman. But what you don’t know about Cat, by just looking at her, is that she is living with not one, but two, traumatic brain injuries. But, Cat does not let her brain injury tie her down. No, she is on a 5,200 mile trike trip across America – diagonally – to raise awareness for TBI. Come hear Cat.

Come One! Come ALL!

(NOTE: New Day, Sunday – Same Time)

What:        “Another Fork in the Road” . . . Brain Injury Radio Network presents “Triking Across America – diagonally” with Catherine (Cat) Brubaker

Why:         Hear Cat’s amazing story of how she is pedaling into her future on he recumbent trike despite two traumatic brain injuries..

Where:     Brain Injury Radio Network

When:       Sunday, October 5th, 2014

Time:         5:00p PDT (6:00p MDT, 7:00p CDT, and 8:00p EDT) 90 minute show

How:         Click: Brain Injury Radio Network.

Call In:    424-243-9540

Call In:     855-473-3711 toll free in USA

Call In:    202-559-7907 free outside US

or SKYPE

If you miss the show, but would like to still hear the interview, you can access the archive on On Demand listening. The archived show will be available after the show both on the Brain Injury Radio Network site and on my blog in “On the Air.”

(Clip Art compliments of Bing.)

Survivors SPEAK OUT! . . . . . . . . . . Lisa Parker McGreggor

SPEAK OUT! – Lisa Parker McGreggor

by

Donna O’Donnell Figurski

McGreggor, Lisa Parker1. What is your name? (last name optional)

Lisa Parker McGreggor

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

Tampa Bay, Florida, USA    parkermcgreggor@yahoo.com

3. When did you have your TBI? At what age?

July 24, 2000     I was 15 – only two weeks shy of 16.

4. How did your TBI occur?

Car accident

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

When I didn’t get up at the scene

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

I had a G (gastrostomy) peg (feeding tube). My spleen was removed.

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

Yes. I was in a coma for three 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)? How long were you in rehab?

Yes. I had rehab at the hospital for six months. Afterwards, I was still going, but insurance would only pay every three months.

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

I have a problem with my balance. My mood is an issue. My right arm is drawn up.

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

My life may be better, but it’s lonelier.

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

My freedom

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

Food

13. What do you like least about your TBI?

The fact that it exists

14. Has anything helped you to accept your TBI?

Reality

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

Yes. It made me reliant on my parents. I hardly ever go out, so I don’t have a boyfriend.

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

Most of my friends left.

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

My mom is my main caregiver. Yes, I understand what it takes.

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

I don’t have any plans.

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 TBI survivors with your specific kind of TBI.

You can never “quit.”

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

Be strong.

Enjoy the ride. Life is shorter than you think!McGreggor, Lisa Parker 2

Thank you, Lisa, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

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

(Photos compliments of Lisa.)

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.

Caregivers SPEAK OUT! . . . . . Trisha

SPEAK OUT! – Trisha

by

Donna O’Donnell Figurski

 

Trisha

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

Trisha

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

Rural western Oklahoma, USA

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

My son fell asleep while driving to work. The pickup left the roadway and rolled several times, and he was thrown through the window. It was ten days after his 20th birthday.

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

I began immediately – the morning of November 3, 2011 – as soon as I got the phone call from the Highway Patrol telling us what had happened and that my son was being medevacked to a hospital in Oklahoma City. I called my husband; he left work, and we headed that way. I stayed in Oklahoma City the entire four months. I am still his main caregiver, but my husband, my son’s girlfriend, and my other sons help.

5. Were you caring for anyone else at that time (e.g., children, parents, etc.)?

I had two younger sons, ages 16 and 11, at home. (They’re still at home.) My stepdaughter, her husband, and their four children had just moved in with us about three weeks before the wreck. They moved out about three weeks after we came home from the hospitals. And I was about six months pregnant.

6. Were you employed at the time of your survivor’s TBI? If so, were you able to continue working?

I was running my own photography business, and I still am.

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

Every church, countless people in our area, and family not only prayed, but also made it financially possible for me and my sister to stay in Oklahoma City the entire time my son was in the hospitals and also for my husband to be there whenever he had time off work. My husband’s bosses also were also able to get him extra time when it first happened, so he was able to stay for several weeks before he had to go back to work.

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

Immediately, at all the hospitals

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

Yes. My son was in an induced coma. We stayed by his side and prayed, until they’d make us leave at night. Then we’d be right back in the morning.

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 this was happening?

My son was at Oklahoma University Medical Center first. Then he went to Select Specialty Hospital for a few weeks. From there, he was at Valir Rehabilitation Hospital from the middle of December until we came home in February. He had about 8 weeks of therapy at Elk City Hospital as an outpatient after we came home. Since then, we’ve continued doing therapy ourselves at home. I was with him the entire time, except at night, when we’d go to the motel.

11. What problems or disabilities of your TBI survivor required your care, if any?

Trisha's Son after TBI

Trisha’s Son after TBI

My son suffers from short-term memory problems, lack of balance and coordination, problems with fine-motor skills, and incontinence. One of our biggest battles has been depression. He is in a wheelchair, but he is able to use a walker for short periods of time.

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

Everything is pretty much centered around my son. He can be home alone, but only for a couple hours at a time. If I have to leave, I need to make sure either someone else is here or will be here.

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

The active and outdoor lifestyle we had

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

This is actually a difficult question to answer. Post-TBI for us is also the start of our daughter’s life. She was born one week after my son and I got home from Valir.

15. What do you like least about TBI?

Even though it is going on three years, there are still times that I feel like it’s a bad dream, and I’m waiting to wake up. I’m distressed by the fact that my son had a ton of friends before, and now he will go weeks, sometimes months, at a time without seeing or hearing from any of them.

16. Has anything helped you to accept your survivor’s TBI?

I honestly don’t know if I have actually accepted it yet. To me, acceptance pretty much means we give up, and he hasn’t given up. In fact, this week, for the first time ever, he has walked on a treadmill. For the first time since the day before his wreck, I saw him make full strides with both feet! He didn’t do his normal “step with one foot, catch up with the other” like he does when he uses his walker.

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

Yes. We had to remodel one of our bathrooms to make it accessible for a wheelchair. His younger brothers help out with some of his needs.

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

My son and I both have friends who no longer come around. People, including his own grandfather, get upset with us because he refuses to go to their houses. Yet, their homes don’t have access for a wheelchair – let alone have a bathroom that he could get into if needed.

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

I take things day-by-day, with a lot of prayers going up.

Trisha's Son before TBI

Trisha’s Son before TBI

20. What advice would you offer other TBI survivor caregivers? Do you have any other comments that you would like to add?

Fight for answers from all doctors or “teams.” Insist on seeing each one. When the accident first happened, my son had “teams” of doctors for his different injuries. We never saw the neurology team. They always came through before we were allowed into his room. His brain injury was made out to us like it was a secondary injury – not that bad. In reality, it was his worst injury, but that’s not what we were told.

 

Thank you, Trisha, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

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

(Photo compliments of Trisha.)

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

Survivors SPEAK OUT! Luke R. Hostetler

SPEAK OUT! – Luke R. Hostetler

by

Donna O’Donnell Figurski

 

Use This Hostetler, Luke

Luke R. Hostetler

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

Luke R. Hostetler

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

Woodburn, Indiana, USA     Lrhostetler@gmail.com

3. When did you have your TBI? At what age?

September 10, 2010     Age 26

4. How did your TBI occur?

I fell down stairs.

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

Friends looked for me when they realized I was absent from the party for too long. The doctors diagnosed the TBI!

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

I had a tracheotomy, and a feeding tube was inserted. My jaw was wired shut. 😦

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

I think I was, but I don’t think it was for an extended period of time.

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 rehab (occupational therapy, physical therapy, and speech therapy – maybe others), both as an inpatient and an outpatient. Rehab was maybe two years?

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

My right optic nerve is damaged. I have a problem with short-term memory. 😦

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

I’ve met many new people, so that’s a very good thing!

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

I miss my occupation and driving!

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

A new friend whom I met because of my TBI. 🙂

13. What do you like least about your TBI?

My short-term-memory is junk. 😦

14. Has anything helped you to accept your TBI?

My new friend. She also has a TBI!

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

Home life: At 30 years old, I still live with my mom, and I depend on others for most everyday activities.

Relationships: I’ve made countless new friends. That’s ALL GOOD. 🙂

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

I am much more of a social being.

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

My Loving Mother, Vicki Rose Hostetler, is my caregiver. I know and understand it’s hard work, and I appreciate that!

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

I hope to be able to live independently. I’d like to have had found the love of my life!

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 TBI survivors with your specific kind of TBI.

Patience is a virtue!

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

Live your life in stride. Good things come to those who wait. God has a perfect plan. 🙂

Hostetler with Muskie 10639383_10204875651152455_5899253425922197294_n

Luke R. Hostetler & Muskie

 

Thank you, Luke, for taking part in this interview. I hope that your experience will offer some hope, comfort, and inspiration to my readers.

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

(Photos compliments of Luke.)

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.

 

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

SPEAK OUT! Itty-Bitty GIANT Steps

Itty-Bitty GIant Steps for Blog

SPEAK 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 donnaodonnellfigurski@gmail.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.

(Though we’ve only two contributors, their accomplishments are great.)

DuWayne Hall…I got a job! My baby step this week is working for a non-profit organization that works with TBI survivors.

Carmen Gaarder Kumm…A giant step. I taught high-school Spanish for 23 years, but I had to resign because I couldn’t do it post accident. Tuesday I taught 20 adults how to tell their name, age, and condition and how to count to 100. I can hardly wait until next week.

DuWayne Hall…I’ve just been offered another job! It provides a paid apartment, full salary, and profit sharing. And that is in addition to the job I was offered on Monday, in which I would be working with military survivors who have PTSD (post-traumatic stress disorder)! Wow! Life is funny and God is Great!

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

TBI Tales: Can Music Rewire Brain?

Playing a Mandolin

 by

 Richard Johnson

(presented by Donna O’Donnell Figurski)

 

mandolin-for-gloggtserMy traumatic brain injury took place in October 2003. I did survive (fortunately), but one of the main side effects from my injury is short-term memory loss.

Years ago, I was in a local coffee shop drinking a cup of coffee and thinking – not “Why me? Why me?” but “What can I do to help my short-term memory loss?” The coffee shop had two people playing guitars. One person put down his guitar and picked up a mandolin. They then played three of my favorite songs. What they triggered was like a bolt of lightning had gone through me! I knew right away that learning how to play an instrument, how to read sheet music, and, most importantly, remembering what I just practiced would be the best memory therapy in the world.

When the musicians took a break, I asked about the mandolin. I told the mandolin-player that I had never played any instrument before. I asked if I could chord with less than four fingers (I only have about two-and-a-half usable fingers), and on and on we talked. He showed me a couple of mandolin chords and said to search on Google for two-finger mandolin chords. He told me to buy a beginner’s mandolin to start and to have fun. And that’s exactly what I did. I bought a good-enough beginner’s mandolin from a friend of a friend, found a great local music store that gives mandolin lessons, bought a couple of books and DVD’s, and started playing.

Well, it’s been a few years now, and I play at least one hour every day. It seems to take a month to learn a song. I’m taking the old “practice, practice, practice” route. I’m able to remember and play (most of) those songs without reading the sheet music. If I haven’t played one of those songs in a couple of weeks, I may need to read the sheet music to remember a measure or two.

I wake up in the morning thinking about the songs I practiced and played the day before. I think about the songs I will practice and play that day by “singing” the songs in my head (not the lyrics, but how they’re fretted and picked). When I’m playing, I’m in a whole different world, and the daily toils just slide away.  I’m sure I could refer to my playing-time as “therapy,” but, for me, it’s pure bliss.

In short, playing a musical instrument is one of the main keys I have gained for rewiring my brain. I truly think that beginning and learning a new hobby or new skill is very important, as it makes us think, think, and think. I also believe that playing music, any type of music, all the time helps my brain find those broken nodes and, with its neuroplasticity, “fixes” them. And most importantly, my short-term memory problem is less and less pronounced. Sure, I can still forget what I had for lunch an hour after eating it, but I can bring that memory back a few seconds later. I can still forget who called me earlier today or why, but again it’s easier to make that connection again.

I would like to continue talking, but my mandolin is calling me.

(Richard Johnson’s experience is an excellent example of something I thought might be true – using the playing of a musical instrument to stimulate the brain and thereby help heal an injured brain.)

 

RJohnson-PortraitThank you, Richard, for sharing your story in TBI Tales. I hope that your experience will offer inspiration to my readers.

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

 

If you have a story to share and would like to be a part of the SPEAK OUT! project, please submit your TBI Tale to me at donnaodonnellfigurski@gmail.com. I will publish as many stories as I can.

(Pictures compliments of Richard.)

(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

Please follow my blog. Click on “Follow” on the lower right corner of your screen. (It’s nice to know there are readers out there.)

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.

 

diemodi jewelry

uniquely hand-crafted jewelry by donna

Welcome to Harmony Kent Online

The home of all things books

Pete Springer

Passionate Teacher and Future Children's Author

HOPE TBI

Helping Other People Excel - To Be Independent

For the Love of Books, Old and New

Katie Fischer, Writer and Reader of Stories

Charlie Bown

Children's Author

Jessica Hinrichs

“We write to taste life twice, in the moment and in retrospect.” ― Anais Nin

VIVIAN KIRKFIELD - Writer for Children

Picture Books Help Kids Soar

Mindy’s Writing Wonderland

For authors, parents, teachers & everyone who loves children’s books.

Kaitlyn Leann Sanchez

Literary Agent

Surviving Traumatic Brain Injury

TBI - Survivors, Caregivers, Family, and Friends

The Care Factor

Loving someone with a Traumatic Brain Injury

Brain Injury Support Group of Duluth-Extension

Brain Injury Information and SUPPORT

Brain Aneurysm Global Insight

Brain Aneurysm, cerebral hemorrhaging, hemorrhage stroke