TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘TBI Caregiver’

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.)

Survivors SPEAK OUT! Peter Corfield

Survivors  SPEAK OUT!  Peter Corfield

by

Donna O’Donnell Figurski

Peter Corfield - Brain Injury Survivor - 2010

Peter Corfield – Brain Injury Survivor – 2010

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

Peter Corfield

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

Marcilly En Bassigny, France      petercorfield3@gmail.com

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

My brain injury happened on June 1, 2010. I was 55 years old.

4. How did your brain injury occur?

I had a stroke caused by bleeding of an AVM (arteriovenous malformation).

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

After returning from an art course, my wife found me on the floor.

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

I was stabilized, and then I was helicoptered to Dijon Hospital. There they did a craniotomy and repaired the vein.

Peter Corfield - Brain Injury Survivor 2010

Peter Corfield – Brain Injury Survivor – 2010

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

Yes. I was put into a coma for about two and a half weeks.

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

I was sent to a rehab centre. There I had rehab for five and a half months.

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

I was hemiplegic (paralysis of one side of the body) with left-side paralysis, and I had an anxiety problem in the form of overactive bladder.

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

My life has changed a great deal. In some ways, it is better; in others, much worse.

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

I miss being able to sleep in a normal bed with my wife. I also miss playing my guitar and driving.

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

I like being able to help others who have had the same experience.

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

I dislike the lack of normality.

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

My wife’s support has helped. Also my writing has been important.

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

It has. My wife and I sleep apart. But, my stroke has made me more thoughtful towards others. I think I am a better person.

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

Yes. My anxiety affects our going out in the dark. The anxiety also makes it awkward to sit on chairs with no arms.

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

My wife is my caregiver. I fully understand how hard it is for her. It drives me on to recovery.

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

I am determined to be recovered enough to look after my wife and to be helping other 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 survivors with your specific kind of injury.

Keep a diary to realise just how much you have improved, as recovery is slow.

Corfield, Peter  Leg Push

Peter Corfield – Brain Injury Survivor – 2010

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

I have written Kindle stroke-experience books. I donate all royalties to The ARNI (Action for Rehabilitation from Neurological Injury) Institute (http://www.arni.uk.com) to try to help other stroke-affected people.

 

Thank you, Peter, 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 Peter.)

 

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

Michael Flusche (survivor)

I am who I am – a survivor of brain injury. Some say I am acting or I am forgetful, impulsive, weird, lame, FLushche, Michael Survivor 031015crazy, etc. I get lost easily. I have short attention at times.Flusche, Michael Survivor 030515 I run into things, stumble, spill food, trip, and do other stupid stuff, but I like me this way. I hope you can too.

 

Melinda Murphy (survivor)

Murphy, Melinda 1I am just over four years post injury. I was a home health nurse in my Murphy, Melinda 2autistic client’s home when it happened. I fell down the basement steps. Wood and concrete are not a good mix. Because it was a work injury, I was caught up in the workers’ comp system, and I was not treated for several months. Only then did I find out that I had a basilar skull fracture. Only 5% of those who suffer from them survive. I did! I’m still progressing. Don’t give up.

Ginger Pickering (caregiver of her son, Bob)

On July 1, 2014, my youngest son, Bob, who is eight, and I were in a car accident. He suffered a severe TBI and other injuries. He had a sucker in his mouth when we hit, and the air bag pushed it into his Pickering, Ginger & Son 1throat. He went a very long time without oxygen, which contributed to the severiPickering, Ginger Son 2ty of the TBI. Our lives changed in that moment, and they will never be the same. He was flown three hours to the primary children’s hospital in Salt Lake City, Utah, and put into a medically induced coma for fourteen days. We were told that, if he survived, we would have to place him into a home. He had no gag reflex, no responses – nothing. I was devastated and in shock. For three months, Bob was in a medical rehab hospital, where he received outstanding care and intense therapy daily. I can’t say enough about his progress. It’s an absolute miracle! We are just so grateful. It’s a struggle, but we’re doing whatever we need to do.

(Clip art compliments of Bing.)

(Photos compliments of contributors.)

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.

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.)

Caregivers SPEAK OUT! . . . . . Jessica Fell

Caregivers SPEAK OUT! – Jessica Fell

by

Donna O’Donnell Figurski

 

Jessica Fell – Caregiver

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

Jessica Fell

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

Mobile, Alabama, USA     chrissmomi05@gmail.com

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?

The survivor was my boyfriend of four years, now my husband. We just got married on New Year’s Eve, his birthday.
 Daniel was 29 when he got his TBI. He was driving to work on his motorcycle, and a truck turned into a driveway without yielding. Daniel had no time to stop, slow down, or swerve. He collided with the truck.

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 never left the hospital. There wasn’t a single day in the two months Daniel was in the hospital that I didn’t stay the night with him. Initially I was waiting for him to “wake up” from his coma. I am, and have been, Daniel’s only caregiver. We lived together with my two little girls. I stopped working to take care of him at home, instead of having him go to a rehab hospital. I was 27 when he was injured. I turned 28 while he was in the hospital.

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

I was caring for my two children. I still do now.

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

I continued to work until a few days before Daniel was released from the hospital. I do not work now.

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

I had no help at all. Daniel’s family came into town every weekend, but they did not stay at our home.

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

Immediately

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

Daniel was in a coma for nineteen days. I stayed by his side constantly waiting for him to wake up.

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?

Daniel had rehab in the two-month period that he was in the hospital. He only had physical therapy afterwards – once a week. He has not yet started any other therapy.

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

The only thing Daniel needs me for now is driving. I did have to help with his walking, showering, and getting dressed. But, he’s fully capable of those things now.

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

I have had to grow up a lot and learn to be more patient. It’s not better because I would like to be working now and to still be doing outgoing things with him. But, I am hopeful that he’ll get back there soon. It’s not worse because our relationship is so much better than it’s ever been.

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

I miss Daniel’s crazy, spontaneous personality. I miss his being so full of life. He’s still very funny, and he loves to laugh. But, he can’t hang for long, and he gets very anxious and worried so easily.

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

I enjoy that our loyalty to each other is so much stronger. I am happy that Daniel has calmed down some.

15. What do you like least about TBI?

I dislike the anxiety Daniel has, his memory’s not being as good, and sometimes his temperament.

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

I believe I have come to accept Daniel’s TBI through God and family and by trusting each other. I’ve come a long way.

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

Daniel and my mom no longer speak because she doesn’t understand. It makes it difficult for me to balance their time together and ours.

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

I can’t leave the house without worrying that Daniel is going to be OK or wants me to come home. I feel guilty that he’s not with me.

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

I hope that we are both back at work and in our own home, which we hope to purchase one day. I hope we have a child together.

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

Jessica Fell

Jessica Fell – Caregiver

My main advice is to never, ever give up. Don’t let TBI take away your life. Don’t let it destroy your relationship. It shouldn’t just be the survivors who are forced to change. The survivors might not have control, but you can change how you handle yourself when it comes to certain things. We have to adapt to this new person and learn to love him or her again. The survivor deserves love and needs it. Be dedicated. Be a believer in yourself and in your survivor because spirituality does take you a long way in this journey. God puts you in situations for a reason – to learn from them. Find out your reason; learn from it; let go and let God. He will get you through any situation he places you in. Trust and believe in that and in yourself.

 

Thank you, Jessica, 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 Jessica.)

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

 

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.)

 

 

 

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.)

Caregivers SPEAK OUT! . . . . . Kristina Hopkins

Caregivers SPEAK OUT! – Kristina Hopkins

by

Donna O’Donnell Figurski

 

Kristina Hopkins - Caregiver Tom Hopkins- TBI Survivor

Kristina Hopkins – Caregiver
Tom Hopkins- TBI Survivor

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

Kristina Hopkins

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

Blum, Texas, 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?

The survivor, Tom, is my husband. He was 25 years old when he got a moderate to severe TBI.

Tom was on his last of four deployments to Iraq. His camp came under attack, and the building he was working in shook because it was hit. He got hit in the head, we believe, and they found him on the floor. He has damage to the occipital and frontal lobes of his brain. His autonomic and limbic systems were also damaged. Those are the systems that make the body feel and move. Tom does not feel over 60% of his body, and he is losing the use of his legs.

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 taking care of Tom in early 2008. I am the main and only caregiver. I believe I was 31.

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

I was caring for two daughters, one with Asperger’s Syndrome.

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

I was working, but that changed.

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

I didn’t have any help. Tom does have a TBI service-dog. The dog, Duke, let’s him know every morning whether he will be walking or rolling in his wheelchair.

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

Tom started receiving partial help in 2008, and then he received full-time medical help in 2009.

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

No

10. Did your survivor have rehab? If so, what kind of rehab (i.e., inpatient and/or outpatient and occupational, physical, speech, and/or other)? How long was the rehab? Where were you when this was happening?

Tom received physical therapy, memory therapy, and occupational therapy. All therapies were outpatient, except for the physical therapy. For that therapy, the therapists came into our home. Since moving to Texas two and a half years ago, I have taken over all of Tom’s therapy.

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

I assist Tom on all his ADLs (Activities of Daily Living). Tom cannot cook, so I do that. I handle the finances, with Tom’s help. I am the main driver. I am his therapist, whether it is physical or occupational therapy. I handle all appointments, i.e., I’m Tom’s “personal assistant.” (LOL)

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

My life has changed. I cannot say if it’s for the better or for the worse. We have learned to overcome Tom’s injuries and to adapt to them. It’s a lonely life at times, but I would not change my life. I am truly honored to be married to my husband.

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

I miss making plans a month or more into the future. We can’t do that now.

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

EVERY day is different. It can be exciting. Case in point – our Thanksgiving this year.

15. What do you like least about TBI?

I don’t like that people look at Tom as if nothing is wrong. They need to walk a day in his shoes or mine. Then they can decide.

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

I had to accept Tom’s TBI right away. There was no time not to.

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

Yes. We don’t go “out” as much. We cannot make plans for the distant future. We just take one day at a time.

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

What’s a “social life”? (LOL) We do get out now and then, but not often.

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

I cannot answer this question about my plans for ten years from now. I have no clue. We don’t plan that far in advance. In ten years, hopefully our daughters will be in college or in the military or just getting out. As for the two of us, my hope is to be where we are at now – taking it one day at a time.

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

Good question. I guess to answer that question would depend upon whom I am talking with. Not every caregiver is at the same stage. So my advice varies. I guess all I can say now is this: YOU ARE NOT ALONE.

 

Kristina Hopkins - Caregiver

Kristina Hopkins – Caregiver

Thank you, Kristina, 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 Kristina.)

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

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.

Dan Gregory  (caregiver)…I want to share some wonderful news. My wife, Nichole Gregory, after suffering a TBI due to a motorcycle accident in 2010, has just finished an accelerated course in drug and alcohol counseling and behavioral science. She was able to make the Dean’s List and graduate after only eighteen months of school. huge.61.305531She now has her Bachelor’s Degree, and she is getting a job with the State of Nebraska. She will be working with high-risk, troubled youth in a crossover youth position. (The program is designed to keep young people from “crossing over” into the judicial system.) I am so very proud of her. She does what she can in spite of her TBI. She is an amazing woman and an inspiration, not just to me, but also to everyone around her. Unfortunately, long hours at school leave her emotionally and physically drained, but I am proud of her for not giving up the fight.

Timothy Guetling (survivor)…I want to tell you about my greatest TBI survival success. I had my TBI at 16. Next was acceptance; the fog lifted at 25. I adopted the vegan/vegetarian lifestyle at that time, and I was receptive to what that did to keep me healthy and to be alert to compassion for myself and all life. At 32, I was given the opportunity to realize the Master/Soul/God/Self-Inside through daily meditation of the Light/Sound principle. Since my acceptance, receptivity, and realization, though I have the repercussive effects of my TBI and always will, my life has been nothing but blissful “recovery evolution,” and it continues.

Sophia Hill Kusderci  (caregiver)…I have an incredible, happy moment I want to share. Anyone who knows us 11954302561011212002liftarn_Pillows.svg.hiunderstands that pillow-arranging was a huge thing in our marriage. It was our nightly ritual. My husband, Ahmet, did it to show me that he cared, even when he was angry. For twelve years, he did it. It stopped after the accident, and I just accepted it as another change about Ahmet. I simply thought that it was something I couldn’t have anymore. But…in the past couple of weeks, he’s been randomly doing it. It’s become a habit again – arranging my pillows only for ME to show me HIS love. I’m blessed by life’s small gifts. This, I believe, is a huge part of the lesson from his accident. Thank you.

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

 

 

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