TBI – Survivors, Caregivers, Family, and Friends

Posts tagged ‘hyperbaric chamber’

SPEAK OUT! NewsBit . . . . . . . . . . . . Joe Namath – Football – Brain Injury

Joe Namath Speaks OUT About Brain Injury and Football

presented by

Donna O’Donnell Figurski

Newsboy thJoe Namath, former star quarterback for the New York Jets and football legend, said that, now knowing the sport’s likely danger to the brain, he wouldn’t have played football.joe namath large

Namath’s wake up call happened when he saw a problem with his brain in a brain scan. It revealed that the right side was not getting enough oxygen, whereas the left side was normal. He was worried about the several concussions he had had, but he thought his growing forgetfulness was caused by old age.

Fortunately, after several months of rigorous treatment alg-joe-namath-jpg(1-hour sessions, 5 days a week) in a hyperbaric chamber, in which he was subjected to a high pressure of oxygen, a new scan indicated that both sides of Namath’s brain were normal. (Full story 1 and Full story 2 – with video)

(Clip Art compliments of Bing.)

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SPEAK OUT! Faces of Brain Injury Richard Johnson

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.

Richard Johnson (survivor) 

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Hello, I’m a TBI (traumatic brain injury) survivor. In October 2003, I was cleaning the gutters on my house. The ladder slipped, and down I went, hitting my head on a concrete slab. I was admitted to HCMC (Hennepin County Medical Center), and I spent the first month there. I was placed into a medically induced coma and had a craniotomy, one session in the hyperbaric chamber, multiple MRI (magnetic resonance imaging) scans and/or CAT (CT, computerized tomography) scans, and a tracheotomy. A feeding tube was inserted. And, I was given a protective helmet.

During the second month, I was sent to Bethesda Hospital to help me “wake up” from my coma. There I had cognitive and physical therapies.  For my third month, I was transferred to Regions Hospital. I continued with speech, physical, and occupational therapies on a daily basis (two sessions a day, 45 minutes each).  In January 2004, I was released from the hospital and was able to return home. In February 2004, I went back to HCMC, where they placed my bone back onto my skull (and I was able to throw away my helmet). During January through September, I had daily outpatient sessions for speech and occupational therapies. In October 2004, I was able to start working again full-time at my “pre-injury” job.

My main “post injury” side effects are aphasia and a short-term memory issue. To “heal” my ongoing aphasia, to help other survivors (and their families), and also to inform the general public about brain injuries, I am a co-facilitator for a brain injury support-group in the Courage Kenny Rehabilitation Center and a member of the Minnesota Brain Injury Alliance Speaker Bureau. To help me recover from my short-term memory issue, I bought myself a mandolin.  I didn’t just buy it to play some tunes, but to remember the notes, chords, and lyrics for those songs hour-to-hour, day-to-day, and month-to-month. To me, playing my mandolin is self-help therapy and perhaps the best idea I’ve had after my injury.

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

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

As I say after each post:

Please leave a comment by clicking the blue words “Leave a Comment” below this post.

Feel free to follow my blog. Click on “Follow” on the upper right sidebar.

If you like my blog, share it with your friends. It’s easy! Click the “Share” buttons below.

If you don’t like my blog, “Share” it with your enemies. I don’t care!

Feel free to “Like” my post.

Survivors SPEAK OUT! . . . . . William

SPEAK OUT! – William

by

Donna O’Donnell Figurski

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

William

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

Eastern Tennessee, USA

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

Age 43

4. How did your ABI occur?

I was subjected to 334 ppm (parts per million) of carbon monoxide for six days.

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

At 6:00 am on the seventh day, I was found unconscious outside my apartment door.

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

A hyperbaric chamber was used on three occasions while I was in a coma.

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

I was in a coma 32 days.

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

I had physical and speech therapies for two years – first, inpatient; then outpatient.

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

Pre-injury, I was a retired Marine Colonel on discharge leave. After my injury, I developed a pronounced hyperkinetic motion disorder, with severe spasticity, a short-term memory disorder, and slow-awakening problems. I cannot walk, type, write, or do anything requiring either fine-motor control or large muscle use.

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

I went from an active Marine to an inactive thinker. From one perspective, my life got significantly worse – about the worst it could. In another perspective, it became rather better. I have a better logical process; I am more understanding of others; and I have the dubious privilege to be unable to use any pharmaceutical drug. To combat this odd aspect of my disability, I studied to be an herbalist, and I live quite well. I cannot have many food chemicals, so I eat better too.

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

I miss being a Marine Corps Colonel.

What do you enjoy most in your post-ABI life?

12. I enjoy knowing how to help people who cannot yet cope with their disability. I help anyone who asks.

13. What do you like least about your ABI?

My brain injury turned me into a burden on everyone in my circle. I can do very little. Whenever I try to use my muscles, hyperkinesia starts up, followed by severe spasticity. It makes doing most things impossible.

14. Has anything helped you to accept your ABI?

I eventually realized that this was what I had left in my life. I could either mope about lost opportunity, or I could grasp any opportunity that came my way. I chose the latter – I cannot change anything, so I willingly accept it.

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

My life has been affected in every conceivable way. Everything is different. Relationships are far harder – people do not wish to know the twitching cripple in the fancy wheelchair. Physical relationships are completely different – I cannot be an active partner, so I must be passive. It takes a special person to be able to cope with that.

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

Able-bodied people do not like to see severely disabled people. It embarrasses them. This makes socializing rather difficult. People will say “Call me” and give me the wrong number. Or, they will shudder at the thought of seeing me again. In stores, I am apparently invisible.

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

Caregivers come and go. Some are good; some are perverts; some are thieves. They are necessary, so I lose things, get humiliated, or get assaulted. I have a friend who takes time to look after me once or twice a month. My friend works away and is home infrequently.

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

It would be nice to still be breathing. I have lived as I do now for twenty years. I hope to live for longer.

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 ABI survivors with your specific kind of ABI.

Accept it as it develops. It takes time to reach the level you will live at. Accept that, and it will be easier.

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

It is easy to be angry at the condition you find yourself in. You were not supposed to get disabled in any way, and you probably think that it is horrifically unfair. That is completely true in every case, but it does not help you go on with living. To do that, you have to look at what you have been given, what you still have, and what you can do. Take that inventory slowly and carefully because it is important. When you know what you have to work with and what you can do, don’t try getting anything else. Just accept what you have and adapt to live at that level. When you have done that and you can live calmly at that level, you could try to do more, but not until you are calm with your disability. So many people spend all of their time trying to fight the un-fightable. They are constantly miserable because it does not seem fair. I know it isn’t. I lost nearly everything three months after I retired from the Marines. All my dreams, hopes, and expectations died along with some of my brain. I really do not need to make worse what I have left by being miserable about it. That is foolish. I have to go on living. I had, and still have, no alternative, so I must make the very best of what I have. You will enjoy a better standard of living if you do the same.

 

Thank you, William, 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.

(Clip Art compliments of Bing.)

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No memory of the day that changed my life

My name is Michelle Munt and this is my story about surviving a brain injury and what I continue to learn about it. This is for other survivors and their loved ones, but also to raise awareness of what can happen to those in an accident. This invisible injury too often goes undiagnosed and it can be difficult to find information about it. I will talk about things that have helped me as I continue to recover and invite others to see if it works for them too.

Everything and nothing. GM1123 😊

Bienvenue. I’m thinking this is the spot where I am to write a witty, flowery personal section that pulls you in......I got nuthin’

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