TBI – Survivors, Caregivers, Family, and Friends

Archive for the ‘Faces of Brain Injury’ Category

SPEAK OUT! . . . . . . . . . . . . . . Faces of Brain Injury – Evonia with her Mom, Amber Baxley

SPEAK OUT! Faces of Brain Injury –

Amber Baxley (caregiver for her two-year-old daughter, Evonia)

presented

by

Donna O’Donnell Figurski

 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.

 

 

Evonia

Evonia – Brain Injury Survivor

(Note: Today, May 19th, 2016 marks Evonia’s first anniversary of her brain injury. She has a long road ahead, but she has a very loving and supportive mother who will help her through)

Baxley, Amber 2 Caregiver of Evonia

Amber Baxley – Mother of Evonia – Survivor

I’m feeling emotional. Today is the one-year anniversary of my daughter’s brain injury. (My daughter, Evonia, will be three next month.) Evonia’s life was forever changed a year ago today. At 3:00 pm on May 19th, 2015, my now two-year-old daughter was shaken and got her traumatic brain injury (TBI). There is not a day that goes by that I don’t wish I could go back to that day and stop it from happening. I made a huge mistake that day. I chose to leave my daughter and her big brother with a man I thought I could trust – a man I thought loved his family, especially his children, more than anything in the world. Man, was I wrong! I wish I had taken my children with me. That day, not only did my daughter’s life forever change, but also I learned that you cannot always trust those who are supposed to be the ones you can trust.

Baxley, Amber 2 Caregiver of Evonia 3

Evonia – Brain Injury Survivor

Evonia spent three weeks in a coma fighting for her life because of him. She spent three months in the Pediatric Intensive Care Unit trying to recover some. My daughter had bleeding of the brain caused by her having been shaken. The blood tried to clot and caused a stroke. As of now, my little girl has had a total of five brain surgeries. She’s also had surgery to place a feeding tube into her stomach and another to remove it. Evonia will likely need to have other surgeries as she gets older. Before everything happened, Evonia was a bright, bubbly little girl – full of life. Because she was always exploring, she was always getting into things. Evonia was perfectly healthy. Now she has to fight to regain every milestone she had already surpassed.

Baxley, Amber Caregiver of Evonia 1

Evonia – Brain Injury Survivor

I so wish I could go back and do that day over again. She would have never had to go through this. If I could, I would do it in a heart beat.

 

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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SPEAK OUT! . . . . . . . . . . . . . . . Faces of Brain Injury Beth Kidd Koziol (survivor)

SPEAK OUT! Faces of Brain Injury Beth Kidd Koziol

presented

by

Donna O’Donnell Figurski

 

 

Beth Kidd Koziol

Beth Kidd Koziol – Survivor

My brain injury happened in 2005 from being a passenger on the back of a motorcycle. I had a traumatic brain injury (TBI)/closed-head brain bleed, a fractured clavicle, five fractured ribs, a lung contusion, many fractures in my left hand, including a fractured scaphoid bone. (I was told that, if the blood supply could not get to it, I would lose the use of my hand. Thank God, it healed!) I also had a badly fractured pelvis and several torn ligaments in my left shoulder. I was airlifted to a trauma unit, where I stayed for three days. I was then transferred to a rehab hospital for about two months. There I got extensive occupational, physical, and speech therapies. I had a neuropsychologist, a neurologist, an orthopedic specialist, and a pain-control specialist. After I left the rehab hospital (in a wheelchair), I visited three times a week for an additional three to six months. I had to learn how to eat, swallow, talk, and walk. I had taste and smell issues with food, plus I couldn’t swallow normal foods. I got dizzy when I moved my head. It was determined that I had shattered microscopic bones in my left ear (the side of all my injuries). After about three weeks of physical therapy, I had a treatment that corrected that problem and reset those little microscopic bones.

I left the rehab hospital in a wheelchair. It took me another three to four months before I could walk with a walker and then with a cane. Now I use nothing. After six to nine months of continued outpatient sessions of physical therapy and occupational therapy, I was called “Wonder Woman” and “Miracle Child” because no one knew how determined I was in my recovery. I was my own caregiver because I was 3,000 miles away from family. Rather than alarm them, I did not tell them of my accident until I was well enough to travel back to the East Coast and tell them in person, so they could see that I was OK on the outside. My family still doesn’t understand the damage and changes on the inside that I endure daily. I have short-term memory problems, I can no longer multitask, and I have to talk in detail as if I were writing a book or describing a picture. I’m told I talk too much; that hurts. If I am doing anything, including talking, and I am interrupted, I cannot remember what it was that I was going to say or do. This is commonly the new normal for many brain injury survivors.

Beth Kidd Koziol 2 survivor 051616

Beth Kidd Koziol – Survivor

The best thing I can suggest is to find materials – books to read to get informed or educated and websites that help you understand what a TBI-person goes through. It helps the survivor when you understand and are patient with him or her. After ten years for me, I still find areas in which I am still healing.
My motto is “Never Give Up!” [smile emoticon]

 

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SPEAK OUT! . . . Guest Blogger Tanya Dallas

One Day at a Time

by

Tanya Dallas

presented

by

Donna O’Donnell Figurski

Girl Blogger cartoon_picture_of_girl_writingI am new to this diagnosis of brain injury. For the last few years, I have had several unexplained symptoms – my life was spinning out of control. No one was listening to me. No one was asking the right questions. A few weeks ago, my father took me to the Emergency Room. He was desperately seeking help because I had no control of my emotions. I was placed in a locked-down psychiatric unit.

Dallas, Tanya Survivor 2 050716

Tanya Dallas – Brain Injury Survivor

A very nice doctor asked me if I’ve ever had a head injury. I began to tell my story. At 11 years old, I had a bike accident. I had no helmet, and I was unconscious for two minutes. At 12 years old, I took a softball to the face. I was unconscious for a few seconds. At 18 years old, I was in a car accident. I was unconscious for an unknown amount of time. Once I was struck in the head with a rock. I was also hit in the head with a ten-pound dumbbell (working with juveniles means risks). I experienced five years of domestic violence. I have no idea which of these things caused my brain to work differently.

Dallas, Tanya Survivor 1 050716

Tanya Dallas – Brain Injury Survivor

It’s hard for me to process. I was always so independent, and now I am unable to even hold a job. I learned what “flooding” was yesterday. I cried as I watched the video. For the first time in years, I felt understood. I felt like I wasn’t completely losing my mind.

It’s hard because my family still doesn’t understand. And they can’t see the injury, so they don’t think it’s there. I’m just taking one day at a time at this moment.

 

Thank you, Tanya Dallas.

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

(Clip Art compliments of Bing.)

(Photos compliments of Tanya Dallas)

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

SPEAK OUT! Faces of Brain Injury Charles Ross  (survivor)

presented by

Donna O’Donnell Figurski

 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.

 

Charles Ross (survivor)

Ross Jr., Charles Survivor 112415 copy

Charles Ross Jr. – Brain Injury Survivor

It has been just over thirty years since I had my traumatic brain injury (TBI) in November 1985. I remember nothing of the accident at all. What I say of the accident is what I learned after the fact. I had the paddles put on me before I got on the helicopter to fly to the larger hospital in St. Louis. The doctors even told my parents they were removing me from Intensive Care to make room for someone who might live. I was in a coma for fifty days. I spent over ten months in the hospital. I was in a wheelchair for one and a half years. And, I had seven summers of surgery to make it to where I can now walk with a cane.

I have severe memory problems. My short-term memory was, and still is, bad. I had been having what I called “spells,” during which I would get a feeling like a chill in my spine. My parents noticed the staring while I was in the hospital. The doctors took me off seizure medicine because they did not believe I was having seizures. I know those spells increased in frequency after that. I could go days with no spells, but other days, I could have hundreds. They usually seemed to last a few seconds, but Mom thought they sometimes lasted longer.

As the spells increased, the feelings I had changed too. I began to notice a feeling like I needed to have a bowel movement, but I never did that, I remember. I would get extremely hot, and sometimes the sweat would just pour out of me for a few seconds. Mainly at night, I would wake with a spell and have a horrible taste in my mouth. After I got my license back, I sometimes had these spells while I was driving. I could have them in class or while I was watching TV or walking or sleeping – it did not matter. I never noticed anything that triggered them. Four years after the accident, in my sleep on New Year’s Eve night 1989, I had a tonic-clonic (grand mal) seizure. It was determined that the “spells” were petit mal seizures. Treatments finally began for traumatically incurred epilepsy, which the doctor finally said I had.

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After I started on medication, the spells decreased dramatically. I would still have one, and my neurologist would increase my dose. That helped for some time, but the spells never stopped completely. Even though I had severe memory and physical problems along with the seizures, I managed to get two Associate Degrees over nine years. However, because of my memory problems, I failed to get my Bachelor’s Degree. I started working with my last degree, but the stress was too powerful to maintain the job. I had many jobs though, mainly contract jobs without benefits.

I began to have blank spells. Maybe I had them before, but I never remembered them or realized it. Why I knew I had them was because I was driving again and I would have an accident in which I hit someone in the back end. I would come out of any blank spell immediately, but I never remembered what had happened, other than that I hit someone. I figured that they hit the brakes quickly in rush-hour traffic and I could not stop.

Over the years, I would have an accident every year or two. Finally, I realized that, before each accident, I had that strange feeling also. So, then I knew what the real cause of the accidents was. After fifteen years of work, I lost my job. I moved in with my parents again. The new neurologist started me on a second medication, and that helped. It did not stop the spells though.

Ross, Charles Survivor

Charles Ross Jr. – Brain Injury Survivor

I moved again and got another neurologist. She put me on two more medicines. One was the same brand, just a different strength. That medicine with such a heavy dosage made me have mood swings sometimes. Altogether, it was over twenty-two years after treatment began and twenty-seven years after the accident before the right mixture was found and I felt in control again. I moved back in with my parents again in late 2014. I helped my parents the best I could with my three hospital stays and two operations. I drove my dad for cancer treatments before his death in September 2015. I am with my mom now. We help each other during the grieving process.

I hope my story serves as a source of strength, encouragement, and determination for others with TBIs to never give up. I was never supposed to live! If I did, they said I would be no more than a being in a chair, unable to do anything for myself.

Never Give UpI am writing my story, I drive, I went to college, I got two Associate degrees, and I worked for fifteen years. There is so much more, but anyone who reads this story should know that anything is possible. You may not accomplish as much as I did, or you may accomplish more. Just know that you should never give up on yourself. Feel proud of your body. If they had been in your shoes, they could never have done what you did, and that is to survive! Be proud!

 

(Clip Art compliments of Bing.)

(Photos compliments of contributor.)

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SPEAK OUT! . . . . . . . . . . . . . . . Faces of Brain Injury . . . . . . . . . . James Thomas (survivor)

SPEAK OUT! Faces of Brain Injury James Thomas  (survivor)

presented by

Donna O’Donnell Figurski

 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.

Thomas, James survivor 111115James Thomas  (survivor)…I’m a traumatic-brain-injury (TBI) success story. I had three brain surgeries to remove three blood clots in my head. After the third surgery, I fell into a coma for three days. When I woke up, I lost the ability to walk and talk, and I wasn’t able to take care of myself. I had to learn every life-skill again, including how to write. I had to wear a diaper for seven months.

I was in the hospital for a month. When I was released, I went to one of best rehab centers in the state of New Jersey. There I had occupational, physical, and speech therapies twice a week. I was able to go home after three months, and my ex-girlfriend nursed me back to good health. I improved 150% in two years. I work now as a teacher assistant with Special Needs students.

 

(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 Commentanim0014-1_e0-1 below this post.

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SPEAK OUT! . . . . . . . . . . . . . Faces of Brain Injury – Amy Zellmer

SPEAK OUT! Faces of Brain Injury – Amy Zellmer

presented by

Donna O’Donnell Figurski

 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.

Amy Zellmer (survivor)

Amy Zellmer 3 Survivor 101015They say a picture says a thousand words. It’s been nineteen months since I fell on a patch of ice and landed full-force on the back of my skull. I suffered a traumatic brain injury (TBI) plus whiplash, torn muscles in my neck, shoulder, and chest, and I also dislocated my sternum. What the photo doesn’t show is how I wasn’t able to do any exercise – even mild – for the first year. Just walking around the grocery store was enough to leave me spent for the rest of the day – let alone carrying in the bags of groceries. I am not exaggerating when I tell you that I lived pretty much in my bed or on the couch for over a year. I would do photography sessions a few times a week (because that’s my only form of income, and I had bills to pay) and pay the price for two days – icing my body and popping ibuprofen like it was candy. Even just six months ago, I couldn’t properly stand up straight – let alone do strength training. And let’s not forget about the horrible vertigo and balance issues that came with the TBI. But I finally decided that ENOUGH IS ENOUGH! It was time to DO SOMETHING – anything! So I started doing yoga for 10-15 minutes a day. At first it was hard – really hard. I could do only very basic, simple stretching poses. I would hold onto a chair for any pose that required standing so that I didn’t lose my balance. But you know what? IT HELPED! It started me on a path to gaining back my strength and endurance.Amy Zellmer Survivor 1 101015

AND NOW LOOK AT ME! I am working with a fab trainer. We are using weights and resistance to get my body back to pre-injury status. It feels so good to be able to walk standing fully upright, and have the strength to carry my groceries into the house. I feel absolutely amazing, and my symptoms are subsiding (the physical ones; Amy Zellmer 2 Survivor 101015the neurological ones are still present). I know it seems impossible when you’re in the darkest days after a TBI. I’ve completely been there. But, man, you take back control of your life when you finally start to step out of it and say, “F… Y.., TBI!” If I can do this, I know you can too!

(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 Commentanim0014-1_e0-1 below this post.

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

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

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

Feel free to “Like” my post.

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

SPEAK OUT! Faces of Brain Injury – Jen Swartz

presented by

Donna O’Donnell Figurski

 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.

Jen Swartz (survivor)

Jen Swartz Survivor

Jen Swartz

One incredible fact that I have learned after sustaining a traumatic brain injury (TBI) is that really simple things in life bring me happiness. I

Jen Swartz 2

Jen Swartz

don’t require spending tons of money on a house, on a car, or on an extraordinarily expensive vacation to find happiness. Being with my awesome friends or my family or enjoying the smaller things in life really brings so much joy to my heart. Because I survived something that could have easily taken my life, I know I still have purpose. As do all of you!

(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 Commentanim0014-1_e0-1 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.

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

SPEAK OUT! Faces of Brain Injury – Sarah Robinson

presented by

Donna O’Donnell Figurski

 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.

Sarah Robinson (survivor)

Robinson, Sarah Survivor

Sarah Robinson – I’m proud of how far I’ve come.

I sustained a traumatic brain injury (TBI) when I was a teenager. It drastically changed my personality as well as my life. I experienced rejection from people in my family because of my condition, and it is devastating. I have an important message for people who have a survivor in their family. Please never give up on him or her. My mother selflessly gave me so much of her time in order to help me recover. Her belief in me saw me through my traumatic experience and into adulthood, where I recovered dramatically. I have a brain injury, but it is my little secret. People don’t know if I don’t want them to. I want to share my story because I am proud of how far I have come, and I also want to inspire others.

(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 Commentanim0014-1_e0-1 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.

 

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

SPEAK OUT! Faces of Brain Injury – Jessica Taylor

presented by

Donna O’Donnell Figurski

 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.

Jessica Taylor (survivor)

One day in 1969, I was out on business for my Merle Norman Cosmetic Studio in Toronto, Canada, and I fell headfirst down an unlit flight of stairs. My head hit against a steel-plated door at the bottom. It caused me to become severely concussed, and I was put into a semi-comatose state. I also had a hemorrhage behind my right 581530_373670692710673_622315000_neye and a contusion of my back. My life hung on a thread. Later when I woke up, I did not recognize my husband or my two very young daughters. My personality change distanced me from everyone I previously knew.

Determined to survive, however, I activated my neurons by writing down sentences, as well as short poems, and memorizing them. I also made a journal of everyday events, as my recent recall was totally shot. I began to study various subjects by going to a research room at a library. The subjects Science and The Supernatural fascinated me, so I studied the works of many writers. I read writings of the Greek writers Plato and Aristotle. I also read Galileo, Einstein, and many others. Subsequently, I found myself to be on a different vibration. I now believe that intensive study activates the dormant neurons of brain-injured survivors so that these neurons then take over for the dead or injured ones. The studying, however, may need to be of a long duration for some survivors.

I have since written my life-story, which is entitled “From Tragedy to Triumph: Journey Back From the Edge.” 456164_373685366042539_2053049192_o(The information is on my website.) I have given talks at brain-injury conferences and at social gatherings in Ireland, UK, Canada, and the US. Also, I have been on many radio shows. Recently, I completed a manuscript based on my years of research. I have been told by many readers that, when it is published, the manuscript will go to universities as a teaching book about the science of religion and the supernatural.

I would like brain-injured survivors to know of my achievements, so that they can have hope and encouragement and think positive. It was, after all, positive thinking that got me to where I am today.

Jessica E. Taylor, author and activist

To learn more about Jessica Taylor, click the following links.

Jessica Taylor Website

Jessica Taylor Facebook

Jessica Taylor Twitter

Jessica Taylor LinkedIn

Jessica’s interview with George Lewis on his show, “Spiritual But Not Religious Show

(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 Commentanim0014-1_e0-1 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.

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

SPEAK OUT! Faces of Brain Injury – Melanie Goodman

presented by

Donna O’Donnell Figurski

 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.

Melanie Goodman (survivor)

I had an AVM (arteriovenous malformation), a birth defect. No one knows he or she has one until it ruptures. Mine was about having weak veins where an artery was supposed to be. The weak veins were under constant high pressure. AVMThe AVM finally exploded at home one night. My love and best friend rushed me to the hospital, where they life-flighted me to Missoula, Montana. They said to let her die because she’s just going to be a vegetable for the rest of her life. My boyfriend fought them to get me to the best hospital on the West Coast, which was all the way in Seattle, Washington. Harborview Medical Center saved my life.

(Clip Art compliments of Bing.)

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Welcome to Harmony Kent Online

The home of all things books

Pete Springer

Passionate Teacher and Future Children's Author

HOPE TBI

Helping Other People Excel - To Be Independent

For the Love of Books, Old and New

Katie Fischer, Writer and Reader of Stories

Charlie Bown

Children's Author

Jessica Hinrichs

“We write to taste life twice, in the moment and in retrospect.” ― Anais Nin

VIVIAN KIRKFIELD - Writer for Children

Picture Books Help Kids Soar

Mindy’s Writing Wonderland

For authors, parents, teachers & everyone who loves children’s books.

Kaitlyn Leann Sanchez

Literary Agent

Surviving Traumatic Brain Injury

TBI - Survivors, Caregivers, Family, and Friends

The Care Factor

Loving someone with a Traumatic Brain Injury

Brain Injury Support Group of Duluth-Extension

Brain Injury Information and SUPPORT

Brain Aneurysm Global Insight

Brain Aneurysm, cerebral hemorrhaging, hemorrhage stroke