TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Traumatic Brain Injury Survivor’

SPEAK OUT! . . . . . . . . . . . . . . . . . Guest Blogger: Sue Hannah “Bittersweet TBI”

Bittersweet TBI

by

Sue Hannah

presented by

Donna O’Donnell Figurski

Girl Blogger cartoon_picture_of_girl_writingI once had a client whose words have stayed with me: “How could this happen? Why would God allow it?” The man who said this was very religious, and he genuinely was confused as to how such agony could affect his family. The incident he spoke of was about a cruel betrayal that a dear family member had endured. After much reflection and therapy with him, one thing became very clear. He and I believed that in order to see God’s grace, there must be challenge.

Let me take this a step further. The traumatic brain injury I have came from violence very early in my life. Throughout growing up and in school, a very clear split emerged. Verbal skills came very easily to me. I was able to do well in spelling and in any class that involved interaction or debate. Then there was the other side of my life. I struggled to learn to tie my shoes. Don’t ever ask me to tie a bow, and please don’t ever ask me to give you directions or to read any public transit schedule. While we’re at it, don’t ask me to get you one of those luggage carts at the airport either. I am also very sensitive to light, sound, and movement. In fact, I am so sensitive to light and color that party shops and fabric stores cause me to feel faint and the color to drain from my face.

Sue Hannah

Sue Hannah – TBI Survivor

Everything that ever involved spatial processing, like horseback riding, dog sports, exercise, or any sport, was so not my thing. I struggled to get on a horse. The fear of not knowing where I was in space was so scary and then was critiqued because most people don’t have that issue. Dog sports, like agility, obedience, and herding, require you to know where you and your dog are in space, and herding involves knowing where the obstacles and livestock are as well. I participated in these things but struggled horribly with them. Aerobics, swimming, dodge ball, softball, tennis, or any other sport showed how impaired my visual and vestibular processing was. It took me years to get beyond my motion sickness in all vehicles, and please, I beg of you, don’t ask me to go to an amusement park because for me there is no enjoyment in it.

When you’re “normal-looking,” the last thing people think of is that you are disabled. Because I was bright, there was no testing in school. I was just told I was lazy, sloppy, and careless. I could learn the theory of lots of topics, but I struggled to understand the physical application of things. Until I was a middle-aged adult and my husband taught me how to do a puzzle, I was without the skills of matching and understanding how things fit together. I even had a neuropsychologist tell me that I couldn’t possibly be a therapist because I didn’t have the neurological skills to do the job. This occurred during the end of my 20-year career!

Her comment of “You can’t!” is probably the core of what I believe about traumatic brain injuries. Many experts and well-meaning people, licensed or otherwise, often mean well and want to stop those of us “disabled” not to set our hopes too high, so we, and they, don’t get disappointed. It is my very strong belief that no one can know what any of us is capable of achieving. Whether we appear outwardly disabled or not, those of us who know traumatic brain injury know what it’s like to question yourself: “Can I do it today? Will I be able to do it? I could do it yesterday! What’s wrong with me?” TBI, like all disabilities, causes us to have good days and bad. Some days our brains click along with few glitches; other days we literally cannot put a sentence together. Perhaps that’s why I am as spiritual as I am. On those days when I can be productive, I want to do as much as I can. On the days when I can’t, I work to remember that my worth is defined because I have the light of God within me. Regardless of what my struggles are, I matter. Life matters.

The stories of those whose lives have been forever changed by TBI can rock someone to his or her core. Truly my client’s words – “How could this happen?” – is exactly what so many of us feel. Personally, I don’t believe in coincidences. I believe all things have significance in our lives. Every time we survivors do what the professionals said we couldn’t, we remember. Every time a professional is caring and kind, we remember. Each moment we are blessed to feel love and gentleness in our lives, we remember. What is it that we remember, you may ask? I believe we remember that our lives matter. Les Brown, speaker and motivator, often spoke of how only we can give life and power to our dreams.

Just when we question our importance – our reason for being, God shows us how much we matter. Sometimes we are so lost in our pain that only hurt is released from our hearts and minds. Even within the deepest, darkest night of the soul, there is light. It may be small, dim, and weak, but it is there. It is up to us to remember it exists and to allow it into our lives.

Sue Hannah - TBI Survivor

Sue Hannah – TBI Survivor

Because I have TBI: I have intuition that others do not.

Because I have TBI: I can hear what others aren’t saying.
Because I have TBI: I can “see” people and places in a bold and global way.

Because I have TBI: I can feel touch and connection in a way that is uniquely mine.
Because I have TBI: I can hold the space for others in pain in a courageous way.
Because I have TBI: I have been able to see how strong I truly am.
Because I have TBI: I have seen the suffering in others in a kind and compassionate way.
Because I have TBI: I have the opportunity to make an impression on this world that is my own.

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

Thank you, Sue Hannah.

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

(Clip Art compliments of Bing.)

Survivors SPEAK OUT! Lessia Malloy

Survivors  SPEAK OUT!  Lessia Malloy

by

Donna O’Donnell Figurski

Lessia Malloy - Survivor

Lessia Malloy – Survivor – Pre-Brain Injury

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

Lessia Malloy

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

Doyline, Louisiana, USA

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

Age 51

4. How did your TBI occur?

My TBI resulted from a motorcycle accident. I wasn’t wearing a helmet.

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

I don’t know. I was knocked unconscious upon impact.

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

I had a tracheotomy. I was given CPR (cardiopulmonary resuscitation). Then I had surgery to remove my skull plate.

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

Yes. I was in a coma thirty days.

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 thirty days of rehab – both in- and outpatient.

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

I have short-term memory issues.

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

I’m no longer totally independent.

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

I miss being independent and working.

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

I have less stress, since I don’t take on more than I can handle.

13. What do you like least about your TBI?

I dislike that my TBI makes me second-guess myself.

14. Has anything helped you to accept your TBI?

I came to accept my TBI because I had to rebuild my life in every way.

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

My TBI put an end to an already rocky marriage. But, I came out a winner on that.

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

My injury has made me very wary of people. I’m not as outgoing, and I watch and listen more.

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

My husband helps me.

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

Maybe I’ll be working in something that fulfills me.

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.

Don’t push it. Let yourself heal. Accept what you went through. Then tackle the world. Learning stuff all over again is good for the soul in so many ways. Have fun.

Lessia Malloy - Survivor

Lessia Malloy – Survivor – Post-Brain Injury

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

Take it one day at a time. Do what you can with what you have. Work with that and build on it.

 

Thank you, Lessia, 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.)

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.

(Photos compliments of Lessia.)

 

SPEAK OUT! Faces of Brain Injury

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 donnaodonnellfigurski@gmail.com. I’d love to publish your story and raise awareness for Brain Injury.

Allegra Merzlock  (caregiver for her son)

Allegra Merzlock and son, Gibson

 

This is my hero, Gibson – my mirMerzlock, Gibsonacle baby. On August 21, 2013, he was kicked in the head by a horse. He has a severe TBI, but he is doing well. We still have a long road ahead, but he is still here with us.

Joanne SmithSmith Joanne 030515

I’m almost eleven months out. I was assaulted fromSmith, Joanne behind with a metal handle while at work in a prison. I am a survivor. I am a Phoenix. I am proud. ♡

 

 

(Clip art compliments of Bing.)

(Photos compliments of contributors.)

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

SPEAK OUT! Itty-Bitty GIANT Steps

 

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 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.

Karie Jacobson Collins (caregiver)…Today’s victory was that my husband initiated saying “I love you” to me. He i_love_you_by_pambahas responded in kind when I have said it to him. But, this is the first time since the morning he had his accident that he initiated it. My cup runneth o’er.

Jonathan Curtis (survivor)…I just bought myself art paper and colored pencils for the first time. It’s an Itty-Bitty Giant Step that could lead to great things.Writing+and+art+supplies

Michael Montepara (survivor)…My Itty-Bitty Giant Step for this week: I kept all appointments, did chores like Hazel thehappy-pill-sparkling-bottle housekeeper, twice shopped for snowstorms, got a much-needed haircut, refilled meds that I was nearly out of, filled my truck with gas, reached out to an old friend, wrote a letter to my Ex and sent it, contacted a lawyer for advice, sent faxes for a hearing, and managed to piss off several Facebookies! It’s been a busy week so far, and it’s only hump day!

Pam McClurg Richardson (survivor)…Sometimes I OVERTHINK things. I am MY OWN worst enemy! I need to learn not to be so hard on myself. After all, each of us is human with human flaws (with or without a brain injury). 🙂 I came to a point where I realized that Girl_thinking_ct_smI was a different person now than I was before my TBI. It’s OK for me to be a “different” me now and to grieve the loss of the “old” me. Besides, in some ways, I am a BETTER me. 🙂

JR Vigil (survivor)…I moved back to the U.S after Christmas. I was in Orlando in January for a month while I was being fitted for a new prosthetic socket. At the urging of my dad, I searched for a job. (I was actually offered a job, but I turned it down.) When the other job prospects weren’t looking so great, I thought, “Who do I know that I can stay with?” I’ve been in Seattle a little over two weeks, and today I had an interview at a temp agency that offers benefits. This temp agency is paid by companies looking for temp-to-hire workers, so it did not cost me a thing. A few hours after the interview, I bought a car for the first time in my life. I still can’t believe it! I will be applying to business us_map-736562schools in the following months. Driving around in the U.S. is definitely interesting with a brain injury. It’s a good thing we have map apps now because I have gotten lost so many times. There was one time where I had to make five U-Turns – no joke! On the other hand, after about two weeks, I didn’t need the apps for the places I frequented, so there is hope.

 

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

SPEAK OUT! Faces of Brain Injury

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 donnaodonnellfigurski@gmail.com. I’d love to publish your story and raise awareness for Brain Injury.

(Clip art compliments of Bing.)

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

SPEAK OUT! Itty-Bitty GIANT Steps

 

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 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.

Yourself-Hugged-John Bell (survivor)…I hugged three of my four kids – the oldest couldn’t make it to dinner. (There is no school tomorrow for the two still in grade school because of the weather conditions.) I got in a pre-lunch run, and I plan another run tomorrow night with a run group. (The temperature is predicted to be in the low single digit range; with wind chill, it should feel like -25.) Firewood use has been nonstop. I’m trying to replenish the stock, but I need help to try to keep up with the demand. I just got back from skiing in Colorado with an old friend, but now it’s time to get back to work.

April Snyder Bomysoad (caregiver)…My husband went from having pneumonia to being more aware – all in a week. I am amazed! I can talk to him about my day, and the next day, he would ask me about it. The aide told me about how aware my husband is and how well he is doing. I said you would know, since I see him only once a week. My car has died, so I’ve got to save money to fix it. My husband asked me about it and instructed me on what I should do. It’s so weird – I feel like my husband has returned!

Jonathan Curtis (survivor)…Got friends, got a job, got dates, got transportation, got a nice view of the city, got spending money. I am loving life! I also got a past that22072823-origpic-ba2d02 I find to be remarkable – reminds me that I’m capable of so much more.

Jonathan Curtis (survivor)…I was given a tremendous blessing this morning. I was reunited with a wonderful ex-girlfriend. I haven’t communicated with her for twenty years, yet we chatted like we just dated yesterday!

Joshua Edward Daniel (survivor)…I joined a gym today. I have a hard time running now. I get lightheaded, but it should get better. 🙂

Michael Montepara (survivor)…I’ve had a few nice Itty-Bitty Giant Steps this week.graphics-laundry-basket-181953 I scheduled a follow-up with the vision surgical team for Friday morning. I washed clothes, swept floors, did some shopping, tried several times to contact my Ex, and kept sane for another week! Yippee!

Cindy McFaden Samartino (caregiver)…Good news today! My husband and I won a Cindy McFaden Samartinosweetheart photo contest with this picture from our December wedding. And, I had a preliminary part-time job interview, with a follow-up on Sunday. AND, I was finally able to get the stubborn stain off the shower floor.

 

Jim Ward (survivor)…Friday I had the second interview for a job. The position is with an environmental consulting company in the Madison, Wisconsin area. The interviewGot a Job lasted a whole fifteen minutes! It took longer to drive there through the drifting snow! I was asked a few questions. The last question was, “When can you start?” I almost blurted out, “Where is my office?” :} (LOL) I didn’t though. I start next week! I feel so blessed, and I am very thankful. I want to thank everyone for the prayers, the good wishes, and the positive thoughts to help with the outcome. People told me after I left the hospital, “You won’t be able to work again.” Well, thankfully, they were wrong! Work hard at it, have faith, and believe in yourself!

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

 

 

 

Survivors SPEAK OUT! Justin Phillips

Survivors  SPEAK OUT!  Justin Phillips

by

Donna O’Donnell Figurski

 

Justin Phillips - TBI Survivor

Justin Phillips – TBI Survivor

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

Justin Phillips

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

Annapolis, Maryland, USA

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

My TBI happened on November 11, 2010. I was 30 years old.

4. How did your TBI occur?

My TBI occurred because I was in a bad car accident on my way to work one morning.

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

Immediately

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

I was given a tracheotomy. I had a feeding tube. A DVT (deep vein thrombosis) filter was put into my vena cava.

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

Yes. I was in a coma ten days.

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 was given five months of therapy as an inpatient and another five months as an outpatient. I had physical, occupational, and speech therapies.

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

My balance/equilibrium was thrown off for two to three years. My temper is worse. I lost my sense of smell. I also make poor decisions.

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

My life is better than it was immediately post accident. I appreciate family and life much more. Small, insignificant issues don’t bother me or my family as much. What my family went through was awful. When something stressful is bothering us, we like to say, “We’ve been through worse.” Life is different now. I wouldn’t say “worse” because I’m still alive, but it’s definitely been changed.

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

Before my TBI, I felt young. I feel a lot older now. I miss not questioning EVERY activity I do to see if I can handle it.

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

I like how much more I appreciate everything.

13. What do you like least about your TBI?

I dislike questioning almost every activity I do to see if I can handle it or if it’s dangerous.

14. Has anything helped you to accept your TBI?

Time has helped me. It took almost two years before the injury wasn’t my first thought after waking up and wasn’t constantly in my thoughts until I went to bed. It’s nice not living in the past.

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

My son was only seven when the accident happened, so it was really tough on him. But, he handled it all like a champion. I’m married, and my wife had to be my caregiver after I moved home for five months, as I couldn’t drive and was still “off.” We pushed through it all and are still together.

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

I still have friends, but I don’t go out much to visit or anything. I had social anxiety for about a year. I would rather just spend my time with my family.

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

I am my caregiver now, but I still need my wife for lots of things. For example, I make poor decisions. My wife was my caregiver for about five months after I moved home. It was hard on her. Rehab was two hours from home. She and my son would come up to visit every weekend. My accident was in November, so my wife spent all winter driving through snow to come visit.

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

I plan on opening a kitchen-remodeling company within the next few months. I would like for that to be successful, and in ten years, to be well established.

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.

Time is your friend. A lot of my issues took a long time to heal. Brain injuries are terrible to overcome. You might choose to apply the adjective “blessed,” “lucky,” or “fortunate.” I’m actually all of them.

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

TBI is the hardest thing I’ve ever been through. Having my son to focus on was a HUGE motivator for my recovery. Time was essential for me, as many of the issues took a long time to heal. I’m blessed, lucky, and fortunate that everything turned out so well. Positive thoughts are also a great help. Being down emotionally makes everything seem more difficult. Take breaks; get plenty of sleep; and eat well.

Justin Phillips – 6 months pre-TBI

 

Thank you, Justin, 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.)

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.

(Photos compliments of Justin.)

 

Survivors SPEAK OUT . . . . . John May

Survivors  SPEAK OUT!  … John May

by

Donna O’Donnell Figurski

May, John E. 1

John May TBI Survivor since 2007

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

John May

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

Boston, Massachusetts, USA     johnmay@mindless.com

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

My brain injury occurred in 2007. I was 49.

4. How did your TBI occur?

This is a question that confuses me. My brain injury was not due to an accident, but to an infection.

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

I lived in Ft. Lauderdale at the time; I owned a house; I was a decorative painter; and I owned a tattoo shop. I, with the help of a partner (a world famous tattooist), did all the bookwork and the management of our employees. This was all possible due to my having ADHD (attention deficit hyperactivity disorder) because I needed only three or so hours of sleep a night. I got lost driving to the supermarket less than a mile from my home. That night, I went to sleep and never woke up.

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

I was taken to the hospital in an ambulance. After a few days, my skull was opened. Most of my left temporal lobe and other areas on the left side of my brain had disintegrated. They cut out areas of my brain that were infected. My friends and family were told that probably I would never regain consciousness and that, if I did, I would never walk or talk again.

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

Yes. My coma was for a few months. I was kept alive only because my family and my friends were fighting a legal battle over who had the authority to make the decision to end life-support. One court had given my family the authority to disconnect me, but my friends appealed this ruling because my business stated that I had given them the authority to make that decision, until there was a second option. While they waited for a new court date, I woke up with no past memory and with the intelligence of a three-year-old.

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?

Once out of my coma, I drove the hospital crazy due to my constant curiosity and the fact that I laughed at everything. I was put into a rehab hospital for about nine months. There I was taught the basics of life. I’m proud that, although I didn’t even know how to shave or brush my teeth, I never dirtied my diaper.

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

My mostly always being happy was thought to be a symptom of brain damage, but it was eventually discovered that I’d been that way since birth. It was as though I was mentally challenged as a baby because I never cried.

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

The struggle over me and my property went on. At the same time, the value of my real estate crumbled with the recession. I’m lucky enough not to remember my life before my injury. I have no clue as to what I owned, but it was battled away. I no longer speak with my family. They sucked me dry of my money and then put me into a homeless shelter. I have learned much in only seven or eight years. It’s not clear whether I have relearned things or whether I have simply remembered what I know now. As long as I have a hat on to cover the huge dent in my head, people wouldn’t know I had brain injury.

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

I don’t know my pre-brain-injury life.

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

I enjoy knowing I have people in my life like Ali.

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

I wouldn’t know.

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

My true friends stuck by my side, but I kept a distance for a time while I relearned the basics of life. I now live in Boston and have a group of friends that never knew the old John May.

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

I don’t have many people to interact with. As such, I spend a lot of my time alone.

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

I am proud to state that I am my main caregiver.

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

One effect of my brain injury is that I have no conception of time. I might think that it is the 4th of July one minute and Christmas, the next.

18. 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 brain-injury survivors with your specific kind of brain injury.

I read all the brain injury sites and communicate with some.

May, John E. 3

John May – TBI Survivor (since 2007)

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

Don’t get angry with those who love you. They are having a hard time understanding brain injury. They need as much help as we do!

Thank you, John, 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.)

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.

(Photos compliments of John.)

 

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

SPEAK OUT! Itty-Bitty GIANT Steps

 

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 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.

Debra Cody (survivor)…I am so grateful to have my husband Phil by my side. I know that his life has been forever holding_hands_1changed by my injury and that he could walk away and have a much easier life, but he chooses to stay. I thank God for giving Phil the love in his heart and the strength of character to continue to hold my hand every day!

Karie Jacobson Collins (caregiver)…It has been a busy weekend here. On Friday night, we attended the service-awards banquet for my hubby’s work. He received an award for 25 years of service. Award 515wwJCwmXLWhile we were there, he repeatedly told me to be quiet – loudly. It was a bit embarrassing. Fortunately, we sat with people whom we are close to, and they helped to smooth things over. It still hurt, though. Then today, we went to a local event, called “The Crystal Classic,” with our daughters and grandsons. Then we washed his truck and vacuumed it out. (It has been unseasonably warm here, so he has been wanting to do that for a week now.) Then we went to dinner with our youngest daughter and her family before going to watch our oldest grandson ride mini-broncs in a rodeo. As we were leaving the restaurant after dinner, my husband apologized for being rude to me the night before. I almost passed out! This is the first acknowledgement of his bad behavior. Miracles never cease! It may never happen again, but I will take it for today. It was a great day.

Erica Renee Gilliam-Chiles (caregiver)…Today I saw my husband run. Fourteen months ago, he couldn’t move his left side. Being an active duty Marine, he had as one of his top goals to be able to run again, and he did!

15278739Kayla Bradberry Knight (caregiver)…Last year on February 13, my husband, Wyatt, took me out for a Valentine’s Day dinner. He and the kids gave me cards that morning. I was on cloud nine. Who would have thought that five days later my husband would be fighting for his life and our families would be turned upside down? God has taught me many lessons this year. Most of all, I’ve learned that earthly possessions mean nothing. Sure, they make one happy for a while. But no gift, flower bouquet, or box of chocolates could take the place of what I have today. My husband is still here! Oh, how happy it makes me to be able to say that! He may not realize that it’s even Valentine’s Day. Nor will he walk through the door with a gift, BUT I still get to hug him. The kids and I still get to tell him how much we love him. That, my friends, is irreplaceable. Don’t just sign that sweet card or have those beautiful flowers delivered. Show that person how much he or she means…not just today, but every day!

Sophia Hill Kusderci (caregiver)…My husband knows that I’m sad a lot living isolated in Germany. This past week, he said to me, “I try to talk to you. It’s why I ask you, ‘What are you doing?’ and ‘What are you reading?’ ” It was such a surreal moment that he “got it,” and I realized he’s trying very hard to make me happy. It’s nearly fourteen months, and I’m thankful for where we are right now. It’s not perfect, but it’s so far from where we were last year. It seems so small in real life, but for me, it is huge.cartoon-love-u-187615

Shelley Lawrence (caregiver)…My husband and I were in a shop today, and we walked past a huge Valentine’s Day stand. He stopped, looked at it, turned to me, and said, “I’d forgotten, but do you know that I love you so very much anyway?” I just grinned and said, “Yes!” How simply AWESOME is that!

Darcy Clarkson Leslie (caregiver)…Valentine’s Day – another gift-giving holiday with my brain-injured husband. I’m getting to hate this day because either he forgets or gives me a gift that his former wife would have liked. Last year at Christmas, he picked out a very large and bulky bracelet and watch set that was full of rhinestones. “You need a heart_&_key_2watch because you’re a nurse,” he said. I don’t do big. I don’t do bling. I am not a nurse. Today he gave me a necklace – a heart with a small key. “Now you really have the key to my heart,” he said. He picked this out himself. This is the first sign that my husband is really starting to get to know me again, and that is the best gift of all! Thanks for listening.

Lynn Sandoval (caregiver)…Today was a great Valentine’s Day for us! I had run to the gas station to get gas to mow the lawn, and I left my husband at home with his sister. When I returned home, I went into the kitchen and there was my husband – walking all by himself without his walker! It was the first time. thHe hadn’t realized that he did it at first. He just turned to walk over and try the chili that his sister had just made. When he got to the sink, he realized what he had done. He started walking back the other way, and that’s when I walked in. I began crying, and he walked over and hugged me. It was amazing!!! Best Valentine gift I’ve ever gotten!

 

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

TBI TALES . . . . . . . . . . . . . . . . . . . . What’s Really Important

What’s Really Important

 by

 Kayla Bradberry Knight

(presented by Donna O’Donnell Figurski)

 

Kayla Bradberry KnightLast year on February 13, my husband, Wyatt, took me out for a Valentine’s Day dinner. He and the kids gave me cards that morning. I was on cloud nine. Who would have thought that five days later my husband would be fighting for his life and our families would be turned upside down?valentine-s-day-clip-art

God has taught me many lessons this year. Most of all, I’ve learned that earthly possessions mean nothing. Sure, they make one happy for a while. But no gift, flower bouquet, or box of chocolates could take the place of what I have today. My husband is still here! Oh, how happy it makes me to be able to say that!

He may not realize that it’s even Valentine’s Day. Nor will he walk through the door with a gift, BUT I still get to hug him. The kids and I still get to tell him how much we love him. That, my friends, is irreplaceable. Don’t just sign that sweet card or have those beautiful flowers delivered. Show that person how much he or she means…not just today, but every day!Love Every Day

 

(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.

 

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