TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘Brain Injury Radio Network’

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.

Alicia Gilman (survivor)…Five years out from my stroke, I’m again trying occupational therapy for my hand. The neurologist actually discouraged me from trying and said not to expect any improvement, but I’m trying anyway. I picked up 25 foam balls and put them into a crate with e-stim (electrical muscle stimulation) assistance, but still it’s more than I’ve done in 5 years. Yay, me! I like my neurologist a lot. I’m sure he meant well when he told me that, but I’ve decided that no one will put limits on me – not even an awesome doctor with lots more education than I’ll ever have. I would rather hope for the best, expect the best, and receive what the good Lord decides He wants for me, than not to try and fall victim to apathy – just because my doctor said it’s not worth the effort. It is ALWAYS worth the effort! Thank you for doing what you’re doing here. It is great encouragement.

Debbie Madison (survivor)…I allowed myself a break during the craziness! Took a nap when I became overwhelmed. I think my Itty-Bitty Giant Step is to remember to listen to my body and give it a break. If I don’t, the results can be catastrophic!

Lessia G. Malloy  (survivor)…My new doctor actually added some fish oil to my diet. I do feel better.

Tracy McDonald (caregiver)…I told you all several months ago that my 27-year-old son, Charles, decided to get off the Duragesic pain patches. Well, before he discontinued the patches, he weighed 118 lbs. on his 6 ft. 1 in. frame – very underweight. He just weighed himself before showering and hollered, “Mom! My weight is now 135!” The worry of his low weight had been a great concern of his doctors. To know that Charles made the choice to stop taking that patch and now endures more pain – I am very proud of him. He wears long thermal underwear under his jeans to help with pain. He meditates. He is able to walk for hours out in the woods with his dog Cali. His agitation is less now too! I just wanted to share with my friends here. It has been 5 years since his accident. A big accomplishment – always believe!!

Lc Sossaman  (survivor)…Today I had two things to do – one was for my husband. I didn’t write them down and didn’t take a note, but I remembered them, so it was a good day. I got goat food, but that was an easy one to remember. I could remember goats – it was easy – they are my pets. My husband asked me to get a certain bucket and remember to get the lid. I did. Woo, hoo! I know it sounds so small, but not writing it down and actually doing it was good for me. Just a piddly thing, I know.

Kimberly June West (survivor)…I have been working on the “ab and butt” challenge. One of the exercises is lunges. Two years ago, I could not have done one lunge without losing balance and falling. I did 15!!! Yay, me!!

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

Survivors SPEAK OUT! . . . . . . . Deb Angus

SPEAK OUT! – Deb Angus

by

Donna O’Donnell Figurski

 

Deb Angus & her book

Deb Angus with Regaining Consciousness

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

Deb Angus

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

Alberta, Canada

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

July 2001   Age 44

4. How did your TBI occur?

We were rear-ended at a red light by a distracted driver.

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

It was realized I had a brain injury about one week afterwards.

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

None

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

No

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

My rehab was all outpatient: physical therapy, January-March 2002; vestibular therapy, March-April 2002; occupational therapy, April-May 2003; and speech therapy, May-June 2003.

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

I have light-sensitivity (pain from bright sunlight, photo flash, strobe lights, etc.), double vision, depth-perception problems, tinnitus, pain from loud noises, speaking problems (word-finding, stuttering, and stammering), memory problems, concentration and attention problems, a balance problem and dizziness, left-side weakness, sleeping problems, and spatial-coordination problems. I had constant debilitating head pain for the first three weeks and shooting head-pains from August 2001 until about 2010, which have dissipated quite a lot over the years. They still occur once in a while, but they’re much milder than earlier in my recovery. In 2005, I developed an extreme sensitivity to perfumes and colognes. It started as the result of olfactory and trigeminal nerve damage.

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

My life is worse. I cannot do many activities anymore (e.g., riding a bicycle or ice-skating). Parties, large crowds, and loud noises are difficult or impossible. Light-sensitivity is still an ongoing issue. It affects my driving, watching certain movies and TV programs, and attending certain events.

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

I miss the spontaneity – just going out and doing whatever whenever.

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

I have more compassion and understanding. I’m more aware of concussions and their impact on brain health.

13. What do you like least about your TBI?

I realize our fragility in life.

14. Has anything helped you to accept your TBI?

I have been helped by time, a lot of inner work on acceptance, and learning about TBI.

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

Many people have given up on me; good friends have stood by me; many more new friends have entered my life. Only I and my husband are here – I have no contact with my family back east. It wasn’t until halfway through my rehab that I realized what a brain injury was and how much it had affected me. I was then able to recognize the symptoms in my husband when he was rear-ended at red light by a drunk driver in ’92. He was never diagnosed. He hasn’t worked outside the home in 22 years. His injury is more depressive than mine, and he dislikes being around people now.

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

I don’t go out as much as I used to. A small circle of friends, who understand what I’ve gone through and what I still contend with, invite me out for lunches, etc. No more drinking; no more music events; no large-crowd events, like the Calgary Stampede or fireworks.

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

My caregiver is just me, my husband, and patience.

Book Cover-FINAL-6x9-web3

Regaining Consciousness: My Encounter with Mild Brain Injury — The Silent Epidemic

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

I still continue to work full-time. It took 10 years of writing and research, but I finally published my book on mild brain injury in 2014. I am now out delivering talks on concussions and brain injuries to raise awareness. I’m hoping to be able to retire in next 3-5 years and to concentrate more on promoting my book and delivering talks. I’m hoping that this work will help change the paradigms in the medical, legal, and insurance industries for recognition of these injuries, the recovery process involved, and the fact that many survivors need support for employment, housing, and medical issues that may crop up due to TBI – especially as we age.

19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other TBI survivors with your specific kind of TBI.

I wish I would have known how easily concussions occurred and that repeated concussions lead to permanent brain injury. And to deal more effectively with stress, which can wear the body and spirit down to dust. I am currently dealing with kidney failure due to a rare autoimmune response to a virus. My general practitioner is convinced that this occurred because of the stress I’ve endured working through brain injury, having a job that was uncertain from year to year, and having to move six times in four years, due to problem tenants, a rodent problem, and a job transition in 2012.

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

Deb Angus winter

Deb Angus

Be patient with yourself. Be gentle and nurturing with lots of self-care. Keep strong, be determined to improve, and be willing to explore all kinds of healing modalities. Keep trying to find the right doctors and the right therapists who will listen to you and help you.

 

Thank you, Deb, 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 Deb.)

Speak OUT! NewsBit . . . . . . . . . Major News About Football-Caused Concussions

Major News About Football-Caused Concussions

Newsboy thYou’ve probably heard of Kosta Karageorge, the senior on the Ohio State University football team who apparently committed suicide. He enjoyed hitting his opponents. He had several known concussions, and probably several more that were unreported. It’s now very clear that concussions injure the brain. Kosta complained about his concussions in his last text message to his mother, saying “…but these concussions have my head all f—ed up.” His tragic case is still being investigated, but because he played on a major football team and because he had a history of brain trauma, his case has highlighted the need to know more about concussions and the need to better protect players, particularly young players, whose brains are still developing. (Full stories 1 and 2)

Both the National Football League (NFL), a league of professional players, and the National Collegiate Athletic Association (NCAA), a national organization that oversees most college football, have settled class-action lawsuits about concussions. (The NFL settled for $765 million, and the NCAA, for $70 million, but judges are likely to rule that more is needed.) High school football is not regulated by a national organization, but rather by the individual states. Now the first class-action lawsuit has been filed against the athletic association of a state – Illinois. The attorney is the same one that filed the NCAA lawsuit. This is the first lawsuit for high school football, and the attorney believes that high school athletic associations need to be sued in every state to affect the sport nationally. He is representing a former high school quarterback who suffered several concussions. The objective of the lawsuit is to make the sport safer. (Full stories 3 and 4)

A star high school football player has written a poignant essay about why his concussion landed him in the hospital fighting for his life. He definitely enjoyed being one of the “elite,” but now he writes that football wasn’t worth shattering his life and dreams (“…was playing football worth it? The answer is no. Not by a long shot”). He hopes to warn other youths of the incredible danger. (Full story)

(Clip Art compliments of Bing.)

 

SPEAK OUT! Itty-Bitty GIANT Steps

SPEAK OUT! Itty-Bitty GIANT Steps

Itty-Bitty GIant Steps for Blog

 

 

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

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

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

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

 

Here are this week’s Itty-Bitty Giant Steps.

Bart Boughner (survivor)…I found my old horse this past month. I haven’t seen him since 2004. Today (yeah!) I remembered I can scan pictures to send to the new owner. Yesterday I tried the camera – not so good. I love days like today!

Bart Boughner, 2 months after TBI, poses with his horse.

Bart Boughner, 2 months after TBI, poses with his horse.

Ever So Dirty, aka Hannah and Rightly Zipped, aka Bubba

Ever So Dirty, aka Hannah and Rightly Zipped, aka Bubba

The big one is my old mare, Ever So Dirty, aka Hannah. She had two babies for me. The one I just found is the little one, Rightly Zipped, aka Bubba.  I still have the sister, and – funny thing – they were born on the same day, two years apart, and with the same parents.

Olivianjeana Collazo (caregiver)…Our biggest accomplishment has been finding fish oil and other things to help our son with his brain injury, which happened in July. All that the doctors could say was the worst. I can’t wait to show them our son now. He is doing half the things they said he wouldn’t! Thanks for reading.

Peter Cornfield (survivor)…Peter uses innovative measures to move a basket of firewood to the fireplace using only one hand. See his inspirational video on You Tube. Moving Wood With My Stick.

Jamie Fairles (survivor)…Hi, Donna. As of yesterday, I’m off for four weeks from my B SW (Bachelor of Social Work) field practicum placement until my second term begins in the new year. I have the rest of this practicum to finish, a second field placement, and only two more full courses until I’m a social worker!

 Heather Sivori Floyd (caregiver)…BIG NEWS to share! Kinda nervous to share but really excited! Had a meeting with a few people from Brain Injury Alliance of Kentucky today. They have written something for bicycle helmet legislation for children. It will be called TJ’s law!! Very exciting! Now to get the right people involved to get this thing passed.

William Jarvis (survivor)…Donna, a big step for me was moving. Five months ago, I thought it would be impossible, due to my TBI and walking with a cane. However, I am now in my new home in Myrtle Beach. I got a lot of support from family and friends. You can do more than you think! Don’t be afraid to try things.

Debbie Madison (survivor)…I went to my first Christmas party, and I didn’t hide in the bathroom! It wasn’t so bad, and I had a nice time with my husband.

Debbie Madison (survivor)…I finished the shopping, and I sent out cards without losing addresses or the list.

Julie-Ann Manners (survivor)…It’s Wednesday here in Oz (Australia). I just got out of the hospital on Monday. [I was in due to my epilepsy from my ABI (acquired brain injury).] And this is HUGE FOR ME. I have finally been put on the list for rehab for fine motor control, speech, walking, reading, and writing!! Eventually I will be able to start being me again!! I’m so super excited!! My injury happened this year in February, and I have had no help, and now after Christmas, I am finally going to be able to get some! YAY!!!!

Michael Montepara (survivor)…Okay, here’s one of my Itty-Bitty Giant Steps: I am thankful that this week I did not have to sleep in my truck in the cold. AMEN.

Shanna Wolf Heart Powell‎ (survivor)…I accomplished grocery shopping tonight with out a break down, except for the pig head they were selling at the store!!! I broke down and cried in Walmart!!!

YOU did it!

Congratulations to all contributors!

(Clip Art compliments of Bing.)

“Another Fork in the Road” . . . Brain Injury Radio Network Interview with Christian Jungersen, author of “You Disappear”

YOU ARE INVITED!

putthis_on_calendar_clip_art

Christian Jungersen, author of “You Disappear” takes his readers on the twisted journey of Frederick, a headmaster at a prestigious school; Mia, his wife and a reputable schoolteacher; and their teenage son, Niklas as they are caught in the web of brain injury.

 

Come One! Come ALL!

What:        Interview with Christian Jungersen, author of “You Disappear”

Why:        Hear Christian talk about his book, “You Disappear” and take a glimpse into the life of a TBI Survivor and his family as they maneuver through the TBI maze.

You Disappear by Christian Jungersen

You Disappear
by
Christian Jungersen

Where:     Brain Injury Radio Network

When:       Sunday, December 7, 2014 (Special Announcement: It’s my birthday. Bring thumbnail-1

Time:         5:00p PT (6:00p MT, 7:00p CT, and 8:00p ET) 90 minute show

How:         Click: Brain Injury Radio Network

Call In:    424-243-9540

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

Call In:    202-559-7907 free outside US

or SKYPE

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

(Clip Art compliments of Bing.)

Survivors SPEAK OUT! – Bob Bernardi

SPEAK OUT! – Bob Bernardi

by

Donna O’Donnell Figurski

 

Bob Bernardi

Bob Bernardi

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

Bob

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

Wheeling, West Virginia, USA

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

My TBI happened in 1992 at the age of 35.

4. How did your TBI occur?

Car accident

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

It was first realized while I was in the ICU (Intensive Care Unit).

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

I was put on a respirator at the scene of the accident because I stopped breathing. My chest was crushed, and my back was broken in half at my T6 vertebra. My spine was bruised, and I had a traumatic brain injury. My lung collapsed three days later.

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

I was in a semi-coma for about six 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 was in the hospital for almost 7 weeks. Then I was in outpatient rehab from May until February. In that time, I had physical, work, and speech therapies.

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

My whole life changed on that terrible morning. I had to relearn all of my simple math skills and redevelop my short-term memory. I slowly regained my ability to walk. My attention span has been diminished, and I go into a deep depression at times.

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

Bob Bernardi

Bob Bernardi

My life is much worse. I was never able to regain my executive skills or my position as a Regional Human Resources Manager. I am 100% disabled today and feel as if I am a warehoused individual. A diabetic hypoglycemic reaction caused my car accident, and since my accident, my condition has worsened to the point that I am now very brittle. In 2009, I applied for 100% disability, and, in 2010, it was granted. I now depend on a small Social Security check and my wife’s pay. Our whole lifestyle has changed because my earning potential was eliminated. Seven years ago, I was diagnosed with celiac disease and also with brain meningiomas. In May of 2014, it was determined that I needed Gamma Knife brain surgery to stop the growth of the meningioma. So far, the surgery has been deemed a success. I now live day-to-day and do my best to enjoy life the best way that I can. I feel that my best therapy is talking to friends on the Brain Injury Awareness Group on Facebook and giving and taking advice on making our lives more bearable. I try as often as I can to inform and educate people on Traumatic Brain Injuries, how best to avoid them, and, if they do occur, how to deal with this tragic occurrence in life.

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

Work. I was diagnosed with having a Type 1 personality, and so my mind is always trying to work at accomplishing things.

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

I enjoy helping others cope and giving encouragement to others who have injured their brains.

13. What do you like least about your TBI?

I dislike the stigma attached to me that I am slow or stupid.

14. Has anything helped you to accept your TBI?

Not really, but, when I look at others who have suffered this terrible happening in their lives, I feel lucky at times because I came out better than a lot of my survivor friends.

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

My injury has put all of our financial burden on my wife, who is in constant worry both for me and in handling her “management” position. She is stressed to the maximum.

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

My social life is not too bad because when others look at me, they really do not know. I have some scars on my forehead, but you really have to look, and I have no problems with speech. I may repeat myself at times, but I know how to keep my conversations in check. I have no problems today walking or doing physical activities, but I will tire more easily. Many have no idea what my physical body has gone through. I have always kept a small circle of friends. Probably the worse aspect of my TBI is that many have left me because they all want the “Old Bob” back. I would love for the “Old Bob” to come back, but he is gone forever.

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

My wife has always been there for me. After 22 years, she is worn out, and her health is beginning to fail.

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

I do not plan ahead anymore. I do one day at a time. Ten years from now is just too far away. I keep getting all of these health challenges, and that keeps me busy enough.

19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other TBI survivors with your specific kind of TBI.

I have learned that, if I need to remember something, then I must tell myself to remember it. I almost curse myself to remember and not to forget. So far it has worked. I also would like for people who have suffered with TBI, or BI in general, to not always write in stone what the doctors tell you. The human brain is more capable than even they know, and the healing process never really stops. I just had cognitive tests done, and I only scored “fair” on almost all of them. I was somewhat down, but I started thinking how I handle things in real life situations, and I can do a lot. I even do our own taxes every year. I am an avid reader, and I do word puzzles to keep my brain active. I refuse to give up. The bottom line is DO NOT GIVE UP ON YOURSELF!

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

I honestly think that TBI is one of most evil happenings that a person can go through because it alters how one thinks, one’s personality, and his or her life in general. I would suggest for anyone who has gone through this personal hell to hook up with others – either online or in personal groups – so as to talk about your different problems and to share feelings – both negative and positive – so as to help one another cope.

Bob Bernardi

Bob Bernardi

 

Thank you, Bob, 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 Bob.)

Survivors SPEAK OUT! – GeorgeAnna Bell

  SPEAK OUT! – GeorgeAnna Bell

by

Donna O’Donnell Figurski

10570970_836853459658124_752128615_n1. What is your name? (last name optional)

GeorgeAnna

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

San Tan Valley, Arizona, USA

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

My first was at the age of 6 years old. I have had multiple concussions as a child. I had yet another head injury in 2001 and another concussion from another car accident on June 25, 2014. I am now 40 years old.

4. How did your TBI occur?

My first brain injury was from a bicycle accident – I lost control of my bike. I flipped over the handlebars and landed on the right side of my head, cracking my skull. The concussions were from falls; sports; an ATV (all terrain vehicle); motor vehicle accidents; rapes; abuse; falls; and being young, foolish, and idiotic.

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

My parents realized I was a different child the day they brought me home from the hospital.

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

I’ve been treated by the ICU (intensive care unit). I’ve had eye/vision therapy and cognitive behavior therapy. I attended specialized schools – junior high school and senior high school – that were for children with mental, emotional, physical, and developmental disabilities.

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

Yes     72 hours

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 did not go to a rehab center. I got everything from schools, specialized doctors, etc.

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

I have a balance problem, dizziness, seizures, short- and long-term memory loss, mental illness (anxiety, depression, mood disorder, personality disorder), cognitive issues, social issues and social anxiety, headaches and migraines, numbness and tingling in my extremities, ringing in my ears (the ear, nose, and throat specialist calls it tinnitus), insomnia, vision and hearing issues (optic and audio nerve damage), and blurred vision (on and off). I am easily confused and distracted. (For example, I cannot multitask. I have to do one thing at a time. Otherwise, I get flustered and stressed out.) I am sensitive to lights, sounds, or distractions. I developed fibromyalgia, tremors, and speech issues, all of which the doctor thinks are the result of my head injury. I also have arthritis (rheumatoid arthritis and osteoarthritis). I have a developmental disability (due to the age at which I sustained my first head injury) and learning disabilities. I attended a special educational school from 7th grade until my senior year because I could not stay mainstream in a public school.

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

I honestly do not know because I was so young when my first head injury occurred. However, over the years, I have sustained multiple head injuries. (For example, because of a short-term coma and concussions, I have increased mental, emotional, and physical issues.)

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

I wouldn’t remember what it was like before because I was only 6 years old when I sustained my first head injury.

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

I am grateful for my Significant Other – the ONLY person I personally know who is supportive of me and tries to be understanding.

13. What do you like least about your TBI?

I dislike how people treat me. People act as if I am some kind of idiot because I am slower than others, and then they look at me as if I have serious issues. I hate being judged. I want people to treat me as I would treat them. I don’t want them to judge me and look at me and say, “Well, you look fine.”

14. Has anything helped you to accept your TBI?

People’s ignorant behaviors and idiosyncrasies

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

My parents did not want to deal with my issues. They did not allow me to speak of my issues to anyone because it embarrassed them that they had a child with a disability. They still do not like my talking about my disabilities and TBI. However, I tell them I am a full-grown adult now, and I say to them, “If you do not like it, do not listen.”

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

I have issues keeping friends. People tend to easily get annoyed with me. I tend to get frustrated easily, too. As for relationship with guys, I was always told I am a very taxing person – annoying, weird, and psychotic. I have had nicknames given to me by guys over the years: pain-in-my-ass, crack baby, wacko, weirdo, dumbass, stupid, idiot, retarded, sensitive bitch, nagging bitch, crazy, worthless.

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

My main caregiver is my boyfriend. No, I do not understand what it takes to be a caregiver.

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

I would love to open a 501c3 animal shelter and help unwanted animals – mainly dogs. I would like to extend the knowledge I currently have on animal studies and have better knowledge and understanding of the animal behavior.

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.

Do not stop trying. Eventually it will work out.

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

I encourage you to just try your best and keep trying. Do not give up. Once you give up, you lose everything, and it is not easy to get everything back again – even if you are able to get things back again.10695279_836854542991349_1216029697_n

 

Thank you, GeorgeAnna, 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 GeorgeAnna.)

On the Air: Brain Injury Radio Interview with Melissa Cronin

On the Air – Brain Injury Radio

Interview with Melissa Cronin, author of “Invisible Bruise”

in “Chicken Soup for the Soul: Recovering From Traumatic Brain Injuries”

Melissa CroninMelissa shares her life both before and after her TBI. She said she was an energetic child who loved to run and play. In college she became a serious student as she pursued her career as a pediatric and a neonatal nurse, a career she loved. But, Melissa’s nursing career ended on that fateful day when a car went rogue careening through 2 1/2 blocks of the Santa Monica, California Farmer’s Market leaving Melissa with not only broken bones and a ruptured spleen, but also with a Traumatic Brain Injury.Melissa playing fiddle

Melissa has picked up the pieces and has found new loves. Her Irish fiddle; her husband, John; and her new career as a writer are just some of her newly adopted loves (NOT in that order).

If you missed Melissa’s interview, don’t fret. You can always listen to the archived show. I’ve included the link below.9781611592399_p0_v3_s260x420

Please SHARE!

I hope you’ll tune in to my show, “Another Fork in the Road,” which airs the 1st and 3rd Sunday evenings of every month. The show starts at 5:00p Pacific Time and runs for 90 minutes. On the fifth Sunday in a month, Julie Kintz, Host of “Quantum Leap,” and I team up to cohost a show called “Another Quantum Leap in the Road.”

See you “On the Air!”

Interview with Melissa Cronin, Author of “Invisible Bruise”

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

“Another Fork in the Road” . . . Brain Injury Radio Network Interview with Melissa Cronin, Author of “Invisible Bruise” in “Chicken Soup for the Soul: Recovering From Traumatic Brain Injuries”

YOU ARE INVITED!

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Melissa Cronin was strolling through the Santa Monica Farmer’s Market when an elderly man lost control of his car and barreled into the crowd. That changed her life forever. Now Melissa lives with an ‘invisible bruise.’ But Melissa picked up the pieces and is embarking on a new life. Hear how she copes and thrives after her Traumatic Brain Injury.

Come One! Come ALL!

(NOTE: New Day, Sunday – Same Time)

What:        Interview with Melissa Cronin, Author of “Invisible Bruise” in “Chicken Soup for the Soul: Recovering From Traumatic Brain Injuries”

Why:        Hear Melissa’s perspective of living with Traumatic Brain Injury

Where:     Brain Injury Radio Network

When:       Sunday, November 16, 2014

Time:         5:00p PT (6:00p MT, 7:00p CT, and 8:00p ET) 90 minute show

How:         Click: Brain Injury Radio Network

Call In:    424-243-9540

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

Call In:    202-559-7907 free outside US

or SKYPE

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

(Clip Art compliments of Bing.)

Survivor’s SPEAK OUT! – Daniel Mollino

SPEAK OUT! – Daniel Mollino

by

Donna O’Donnell Figurski

 

 

Daniel Mollino - TBI Survivor & Cyclist

Daniel Mollino – TBI Survivor & Cyclist

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

Daniel Mollino

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

Ringwood, New Jersey, USA     Daniel@mollino.net

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

August 11, 2010     Age 27

4. How did your TBI occur?

At work, I fell from a ladder on a telephone pole.

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

Right away. The emergency response was fast.

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

I was in a medically induced coma. I had a craniotomy, and a shunt was inserted.

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

I was in the medically induced coma for about three 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)?

I had speech therapy as an inpatient. As an outpatient, I had physical therapy and therapy for executive skills.

How long were you in rehab?

Three months as an inpatient; a little over a year as an outpatient.

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

I have deafness of and ringing in my right ear. I have issues with fatigue, memory, balance, personality, pain, and finding words. (See my website below for more details.)

Daniel Mollino - TBI Survivor in hospital

Daniel Mollino – TBI Survivor in hospital

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

Things became harder. It is in some ways better and in others, worse.

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

My memory

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

That I got back to being able to ride

13. What do you like least about your TBI?

The problem with my memory; also the public’s understanding of how a TBI impacts a person

14. Has anything helped you to accept your TBI?

My family’s being there helped. My strong headed, never-give-in mentality stuck and resulted in the support and the joining in of larger groups in my 2015 cross country bike ride to get brain injury addressed and donations to research groups. I am also on a calling basis with the offices of federal politicians from my district trying to get them to fix a system I saw fail. Hopefully the ride will get more people calling their politicians.

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

My home life changed in some ways. My wife and I switched roles – but not in a bad way.

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

My social life hasn’t really changed that much. But, my deafness is an issue, and I don’t like loud environments.

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

My wife is my main caregiver. Thankfully, I am not as bad off as some.

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

My future plans are in motion. I am biking coast to coast in hopes of getting attention for brain injury and donations flowing to research groups. I also hope I can get the media involved and possibly get more sponsors, so I can continue on that path for years to come. A book would be nice. However, my English is really bad, so I am looking for a ghostwriter. My hope is that I can keep going and prove that “disabled” does not mean that someone is incapable of great things. That aspect is aimed at all those who give up.

19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other TBI survivors with your specific kind of TBI.

I have to say no, but I may be wrong. As I have said to others, when you accept “broken” as a status, you will always be broken. You need always to push for a want. Nothing is impossible, but life is a pathway of obstacles. You will at times just have to step back and find another way. For when you give up trying, that is the point in the life that you have willfully chosen to be in the broken state.

20. What advice would you offer to other TBI survivors?

Fight for what you want. Ask others for help, and keep your eyes on the goal. Never give in to defeat. My personal view is that I will do this or die trying. Not to sound morbid, but the idea is that if you try your entire life, you are living life – not letting life live you.

Do you have any other comments that you would like to add?

I hope that some of you see my ride as I post my routes and progress in 2015 and show up if you’re near. Nothing is better than seeing others involved and having the support. I will be personally calling media stations I can find numbers to, but getting calls from others, sharing photos on Facebook, etc. would be a great help. The more exposure and media I get, the more we can educate the public and force the politicians to move on fixing the issues.

 

You can learn more about Daniel at the following sites.

TBI to Victory

TBI Rider

Double Cross-Country Bicycle Ride Will Challenge New Jersey TBI Athlete

 Stroll ‘N Roll With Kessler Foundation at Verona Park

Daniel Mollino - TBI Survivor & Sky Diver

Daniel Mollino – TBI Survivor & Sky Diver

 

 

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

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

(Photos compliments of Daniel.)

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.

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