TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Brain Injury’

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

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 – one view at a time.

 

Cam Compton (survivor)

11056773_804796876222530_117254145_nOn March 21st, I celebrated my “strokaversary.” Three years ago, I suffered a stroke. It has changed my life dramatically. I am still “me” – still Cam – but at the same time, I am not. I have learned to live and to love this new me. I have had fun. Whatever I was before (like fun or nerdy), I am still that, but three times more so now. I have met many new friends. I have done things that I would never have done if I had not had my stroke: my billboards, the talks, facilitating a stroke support-group, the stroke walk (mark April 18th on your calendar), and my newest – Brain Injury Radio host. I will be hosting my own show on the second Friday of every month. I’m happy to be here alive and on this side of the dirt.

 

Lindsey Dunn (survivor)

Dumm, Lindsey Survivor 032015 10686800_10101531483831264_2468134818312325958_nYesterday was two years ago that I fell about sixty feet on a spiral staircase in Valencia, Spain. I hit my Dumm, Lindsey Survivor 032015 10407045_10101650526873054_7173077641176124389_nhead on the way down (on one of the metal spindles), causing me to get a traumatic brain injury. I am actually very happy that this happened to me. I’m lucky that people have Dumm, Lindsey Survivor 032015  11043033_10101641035463914_6164584326813463685_nstuck by my side through this trial. Maybe my story will give hope to people and God can use it to help others.

 

Marcel’s moms (caregivers)

10711_356648177855326_33065405394910668_nWhen our son, Marcel, was eleven months old, he suffered a severe TBI. The doctors told us that he would never eat, walk, see, or talk – basically that he would be a vegetable. It’s been eight months, and his vision is starting to come back, he’s smiling and laughing, and he’s getting neck strength back. His limbs are getting stronger and starting to move a lot. MarcelHe’s learning how to eat again. And he babbles like a baby. Marcel has come so far, but he still has a long way to go. Obviously, God has plans for Marcel because he is a fighter. He was so close to dying, but he fought to stay here. A lot of people, doctors, and nurses told us all the things that our son would never do. Our boy will continue to fight and prove to everyone that he can. He’s doing many of them already.

 

Daniel Wondercheck (survivor)

Wondercheck, Daniel Survivor 0311815On July 23, 1991, I was involved in a construction accident that was serious enough to smash my hardhat, crack my skull, and knock me out for six days. I spent 85 days in the hospital, 95 days as an inpatient in a rehabilitation hospital, and another 186 days in rehabilitation as an outpatient. Now – twenty-three years and nearly eight months later, I still use a wheelchair, I talk funny, I have involuntary movements in my extremities, my left eye moistens itself approximately half as much as it should, and my right eye does not moisten itself at all. For 26.5 hours per week, I have a personal assistant who helps me with daily-living activities. (My personal assistant is also my best friend and “guardian angel.”) But, I do have enough mental ability to be a top-rated Power Seller on eBay and to be an administrator for an online support-group for traumatic brain injury survivors (Traumatic Brain Injury – TBI – Terrific Beyond Injury).

 

(Clip art compliments of Bing.)

(Photos compliments of contributors.)

Brain Injury Resources . . . . . . Fatigue and The Spoon Theory

Fatigue and The Spoon Theory

Brain th-2Every brain injury is different. Yet, the survivor interviews on this blog have shown that fatigue is a common effect of a brain injury. Once the survivor was energetic – able to do many things. Now the survivor is often tired or worried about getting tired.

Have you ever tried to explain chronic fatigue to someone healthy? Usually he or she doesn’t get it. Christine Miserandino, who has Lupus – a chronic disease, invented The Spoon Theory to show her healthy friend why she is so concerned with the energy cost of doing anything. Christine’s Spoon Theory 309_1_is a simple way to show the difference between being healthy and energetic and being worried about fatigue by having a chronic condition – like Lupus or a brain injury. In The Spoon Theory, Christine writes, “I explained that some days were worse than others; some days I have more spoons then most. But I can never make it go away, and I can’t forget about it. I always have to think about it.”

Christine’s Spoon Theory can be found HERE.

(Clip Art compliments of Bing.)

 

 

On the Air: Brain Injury Radio Another Fork in the Road . . . . . Joshua Puckett and wife, Tatiana

On the Air: Brain Injury Radio

Another Fork in the Road

with Brain Injury Survivor, Joshua Puckett and his wife, Tatiana

images-1

Joshua Puckett was just minding his business in his own front yard when he was attacked by a “random
drunk person” causing his brain injury. Now he says he has a “memory of a fish.”Joshua Puckett - TBI Survivor 2013
Memory problems combined with balance issues, anger, and confusion have become the “new norm” in his new life.

But, Joshua is overcoming his deficits by directing his attentions to his art and his music. Both are opening new doors in this talented young man’s life.

If you missed his interview on “Another Fork in the Road” on March 15th, you are in luck. You can listen to the archived show here.Joshua Puckett & Tatiana Puckett

Click the link below to listen to Joshua Puckett, his wife, Tatiana, and me.

See you “On the Air!”

On the Air: Brain Injury Radio – Another Fork in the Road

with Brain Injury Survivor, Joshua Puckett and his wife, Tatiana

Click here for a list of all “Another Fork in the Road” shows on the Brain Injury Radio Network.

Caregivers SPEAK OUT! . . . . . Karie Collins

Caregivers SPEAK OUT! – Karie Collins

by

Donna O’Donnell Figurski

 

Karie Collins - Caregiver

Karie Collins – Caregiver

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

Karie Collins

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

Green River, Wyoming, USA     mrskarie@q.com

3. What is the TBI survivor’s relationship to you?

The TBI survivor is my husband, Danny.

How old was the survivor when he/she had the TBI?

He was 50.

What caused your survivor’s TBI?

Danny was in a golf cart accident. The foursome he was in had finished golfing, and they were racing each other back to the truck. The wind blew the driver’s hat off, and the driver made a sharp U Turn to go get it. Danny was the passenger. He hit his head on the cart and fell out. Danny landed on his feet, but he instantly fell face-first onto the pavement. They had been drinking all day.

4. On what date did you begin care for your TBI survivor?

Karie Collins - Caregiver Danny Collins - TBI Survivor

Karie Collins – Caregiver
Danny Collins – TBI Survivor

Danny’s accident was on August 16, 2014. He was taken to our local hospital by ambulance. He was then airlifted to Salt Lake City, Utah. He came home from the hospital/rehab on September 24. I was with him from the beginning, but I took on the role of sole caregiver on the 24th, when we came home from the University of Utah Hospital/rehab.

Were you the main caregiver?

Yes

Are you now?

Danny is high-functioning now. He has returned to driving and working, so the need for a full-time caregiver has mostly passed. I still help him manage and remember things as needed. We remain a team and have been for over 30 years.

How old were you when you began care?

I was 50.

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

Our children are all grown now. They are on their own, except for our youngest son. However, Danny’s mother had to be placed in a care center at the beginning of September – while we were still in the hospital. So, we began caring for her, as Danny is her only living biological child.

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

I was in the process of making a job change – certifying to be a substitute teacher. I opted to put that on the back burner to be able to care for the love of my life. Now that Danny is doing so well, I am updating my résumé so that I can return to work. We need additional steady income to get our financial security back.

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

I did have some help off and on – from our children and from some friends as well. They were good about giving me breaks. They came to be with Danny or even sometimes to take Danny “out” so I could get things done at home. (Danny always wanted me to be right by him or to be playing cards with him.)

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

My support began immediately. Actually, you could say that my support of Danny began on April 7, 1985, when we married. 😉

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

Danny was in a coma for several days and in a state of confusion for several weeks after. Overall, Danny spent two weeks in the Neuro Critical Care unit. He then spent another three and a half weeks in the rehab unit. The first few days were low to no contact days, so I mostly hung out in the waiting room with family and friends and prayed. After that, I was pretty much in his room with him. I continued to pray. Also I asked questions and learned all I could to support and assist him.

Karie Collins - Caregiver Danny Collins - TBI Survivor

Karie Collins – Caregiver
Danny Collins – TBI Survivor

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)?

In addition to the three and a half weeks of physical, occupational, and speech therapies in the hospital, Danny continued with all three therapies on an outpatient basis at our local hospital after we came home. He finished with physical therapy in December. He “graduated” (that’s how he puts it) from speech and occupational therapies on February 23rd.

How long was the rehab? Where were you when this was happening?

During outpatient therapies, I would drive Danny to and from his appointments. I did this until the end of January, when Danny’s driving privileges were restored. Usually I sat and waited for him, but on some days, I took advantage of the three hour sessions to go run errands or do other tasks. Occasionally, I would go visit the teachers and students at the school I used to work at. It was my “therapy.”

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

Well, Danny couldn’t drive, so I drove him. I handled and organized his medications, and initially I gave them to him. Now I load his pill organizer, and he takes them. Danny was diagnosed with diabetes during all of this, so monitoring his blood sugar was my task at first. He now takes care of it. Other difficulties Danny has are looping, fixation, frustration, outbursts, over-stimulation, anger, anxiety, etc. He has no filter; he has difficulties with memory loss; and he is easily tired. I/we deal with it as it comes along. Through therapy, we have learned some new coping skills and some strategies to use to compensate for what was damaged and lost. Danny has always been very independent and determined, so while in the beginning these qualities caused great stress, once the corner was turned to where Danny began to understand he had had a serious injury, they became the driving force to his recovery. He HAD to drive, and he HAD to go back to work. If that meant therapy, meds, and no drinking, then that’s what had to be done – even if he didn’t think he needed it.

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

Our life changed dramatically. We went from being spontaneous and outgoing to being very routine-oriented. Danny is not as affectionate as he once was, nor is his tolerance for things and people what it was. He says what he thinks, no matter whom it hurts. Some things are better, as we have a new appreciation for life, our family and friends, and the blessings of greater faith. For a while, things were bad, but thankfully, they improved. While I don’t wish this on anyone, I wouldn’t trade what we have gained for anything.

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

I miss Danny’s affection. In April, we will have been married 30 years, and I miss my affectionate man. Fortunately, more and more now, he is showing affection to our grandsons, so I am hopeful his affection will come back to the kids and me with time. Somethings, I think, are a matter of relearning them.

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

I enjoy how much closer my family has become. I also enjoy how my faith and testimony have grown. I have become calmer and more tolerant of things because in the big picture WHAT REALLY MATTERS?

15. What do you like least about TBI?

I dislike how one moment things seem fine/normal, and then, out of the blue and for no real explainable reason, it all gets turned upside down and inside out.

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

Yes. Love, faith, and reality. I mean, it is what it is. You either accept it, move on, and make the best of it, or you don’t. If it were cancer or some other disease, you would do all you could to overcome it. No different here.

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

How can it not? Some struggles exist because of Danny’s difficulties, so we have learned to choose our battles. We also choose to accept that life changes and people change, and so we choose to accept Danny’s injury and to try to understand all that we can. Overall it has brought us closer together and has given us a new respect for life and how truly fragile it is.

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

This all changed Danny in ways he doesn’t understand. He acknowledges that he has a brain injury. But, he thinks he is the same as he was before the accident, so he thinks life should be as it was before. You see, Danny was very social and what I would call a “social alcoholic.” So much of what we did socially was tied to drinking – drinking to get fall-down drunk. So, while we have still socialize with our friends, it is different because Danny cannot drink (or at least shouldn’t). So far, he hasn’t, but he says that it isn’t as much fun because he cannot drink.

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

Wow! Ten years from now…I hope that Danny has better clarity, that he can show affection again, that he can again filter what not to say in certain situations, and that financially we are again back to where we were headed, so we can travel and enjoy time with each other and with our family and friends.

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

First, take time for you – no matter what. Even ten minutes a day can make a huge difference.

Ask for help. On some of the worst days, I reached out to say I need help. I was never let down. Someone always came through. Even if it was just a phone call, it helped.

Find and join a support-group for yourself. They will get it when no one else does.

Cut yourself some slack. It’s okay to be mad, cry, grieve, and mourn. We always think we have to be brave or strong, but sometimes we NEED to let it out and let go.

Try to stay positive.

Choose your battles wisely. At the end of the day, this is what will be most important.

You can only control so much. Give your survivor information and your opinion or reason, and then let him or her decide things as much as you can. Where respect is given, respect will be returned.

Karie Collins - Caregiver

Karie Collins – Caregivers

Lastly, never give up. There is always HOPE.

 

Thank you, Karie, 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 Karie.)

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

Survivors SPEAK OUT! Amanda Parten

Survivors  SPEAK OUT!  Amanda Parten

by

Donna O’Donnell Figurski

 

Amanda Parten - TBI Survivor

Amanda Parten – TBI Survivor

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

Amanda Parten

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

Grove Hill, Alabama, USA     amanda.parten@yahoo.com

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

Age 29

4. How did your TBI occur?

My Jeep was hit by a Mack Truck. I was sitting in the median, and a Brand Energy Mack Truck jackknifed me in the driver’s door.

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

The EMS (Emergency Medical Service) technicians realized I had a problem as soon as they were on the scene.

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

I was life-flighted south to the Medical Center at The University of South Alabama in Mobile. I suffered a broken hip, a crushed pelvis, and a lacerated spleen. Transverse processes were broken off my spine. I had a “mild to moderate” parietal TBI. I was in a coma, and I remained in the hospital for a few weeks after I woke up. I was in physical therapy for six weeks after I was released from the hospital.

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

Yes. I was in a coma for eleven days. Technically, I was still in my coma for an additional 4-6 months after the wreck – according to the Rancho Los Amigos coma scale.

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 had physical therapy as an outpatient.

How long were you in rehab?

Six weeks

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

I am mostly plagued by short-term memory loss. I experience hip pain, mood swings, and personality changes. I have difficulty sleeping. I had a year of depression.

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

Everything about my life has changed. Sometimes I feel like my life is better; sometimes I feel like it’s worse.

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

I miss my awesome memory. I could remember things from every moment – no matter how long ago. I never had to write anything down.

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

I appreciate little things more now. For example, when I wake up and remember a dream, it’s like a gift! This has happened maybe six times in six years.

13. What do you like least about your TBI?

I dislike the fact that I really have to warm up to new people. New people tend to make me nervous.

14. Has anything helped you to accept your TBI?

Time…knowing that there is nothing that will undo the accident and that I must press on.

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

I feel like people don’t want to stay around for more than a few months once they see what an impact the TBI has had on me. I was living with my boyfriend at the time of the accident. We broke up two years later. I was married a couple years after that – but for only four months.

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

It has. I don’t go out anymore. I’m no longer spontaneous. Everything has to be very scheduled.

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

I am my own caregiver. I also take care of my two children.

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

Ten years from now, I expect one daughter to be graduating from college. The other will be in middle school. I will still be a therapist.

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.

If you cannot accept your new self, then try to compensate. When I stopped thinking that I would “wake up” and be back to normal, accepted myself, and started putting compensatory strategies into place, life stopped being such a struggle.

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

Get into a group, whether it is on Facebook or somewhere else on the Internet. Having access to others who are going through the same thing as you can be such a help. Sometimes knowing that you aren’t the only one who has ever felt a certain way or that the same thing that happened to you has happened to someone else can make a huge difference.

Amanda Parten - TBI Survivor

Amanda Parten – TBI Survivor

 

Thank you, Amanda, 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 Amanda.)

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.

 

Chorn, Jennifer Girouard & SpouseJennifer Girouard Chorn (survivor)

I am a TBI (traumatic brain injury) survivor. I fell from the second story of my house onto a tile floor in August 2010. I was life-flighted to the shock and trauma center of the Chorn, Jennifer Girouard & Kidshospital. I was in a coma for almost a month. I broke my arm, back/sacrum, and eye socket. But, the most serious invisible injury is my TBI. Apparently God wasn’t yet done with me. So I’m very thankful for my family, who helps me overcome my TBI every day.

West, Kimberly JuneKimberly June West (survivor)

I am the face of TBI (traumatic brain injury). In 2001, I had a sagittal sinus thrombosis, a clot in the main vein of my brain. Three weeks after I gave birth to my last baby and with only a 10% chance to live, I had several strokes. In 2013, I had a frontal lobe stroke that changed me completely.

Michael - TBI Survivor

Michael – TBI Survivor

Sandy Cutshall Williams (caregiver of son, Michael)

My survivor is twenty months post injury. We visited his neurosurgeon Friday. The doctor stopped mid-sentence with a tear in his eye and said, “Wow, Michael! I just cannot believe you are the same kid I thought would never make it through surgery. I never in a million years thought you would survive and be as well as you are.” Michael walks, talks, and has a part-time job. He still cannot remember much from the previous day, and it’s obvious his speech is a problem. He is more than my survivor and my hero; he is MY son. I am so glad that God gave him back to me.

 

(Clip art compliments of Bing.)

(Photos compliments of contributors.)

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.)

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.

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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.)

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