Dear Traumatic Brain Injury,
You came into our home almost three years ago and decided to enter with no invitation, no introduction, and no preparation for your never-ending presence. I have since learned that this is how you operate; you just show up in some series of unexpected events. There is no protocol for when you arrive. One moment we don’t have any clue of your existence and the next you are all we know, and it feels as if knowing you has been eternal.
Thanksgiving Eve of 2012, we did not know your name, and we were not well acquainted enough to recognize your face. You waltzed in silently and escorted my bright, strong, beautiful, full of life, 21-year-old son down a flight of stairs in his home, where he was supposed to be safe. You all but destroyed him.
A fall down thirteen stairs in close to thirteen seconds would forever alter the person we knew and loved, the person we ultimately needed. Our introductions to you were made with words like devastating, coma, brain bleeds, fractures, skull plates, swelling and the most horrific words of them all, “He may not survive.”
In that first night, within those initial moments, you stole many of our hopes, dreams, and chances at the things we used to take for granted. In place of them you gave challenges, frustrations, and endless new maps to navigate.
You would also bring out something else in us: unyielding fight, determination, and hope.
I still remember the first time I saw Taylor’s eyes after you entered his brain. Your cracks, unimaginable bumps, breaks and bruises had an effect on him that caught me unprepared. I searched for my son, but instead found a person who was void of Taylor’s light, his spark, and the love that connected us. Where was our Taylor and would he ever return? I knew none of this was going to be easy, and yet I was thankfully unaware of just how grueling it would become.
Together, our family would spend months in the ICU, inpatient rehab, and endless days of physical, cognitive, occupational and speech therapies. In the beginning, all of the therapies were sponsored by specialists, but as time moved on, and insurance approval grew slim, creativity was forced in charting the continued course. All the while, missing my son, I tried to explain to people that even though Taylor was here, so was something else that had taken so much of him, and that would be you, Traumatic Brain Injury.
I have hated you since the day we met. You have made me sadder than I ever imagined. You have made me weaker and more exhausted than I ever conceived. You have made me angry and bitter, and you have taken not only bits and pieces of the son I love so very much but huge parts of my own heart as well. In reality, you have taken something from every single person in our family. You have changed the course of our lives, and we are still adjusting.
After nearly three years, I still find myself trying to make peace with you. I have screamed at you, and at times you produced an endless flow of tears that left my face raw with irritation from how many have fallen. You have brought me to my knees, and yet made me stand taller than I ever thought I could. I have felt your defeat and agony, and I have felt the victories that come from witnessing the powerful implications of a recovery that takes place one moment at a time.
I have grown as a mother, as an advocate, and as a person. I have learned how to work with what I cannot change or fix. I have learned that letting go of some expectations of our survivor and ourselves is not only crucial but also necessary. I have learned that I really don’t have to be afraid of you, traumatic brain injury, because at the end of each day, you may have taken us for another wild ride, but we have been victorious.
How do I accept your unwanted and unwelcome presence? I try to work with you, and not against you. I remain certain that you are not stronger than the force of love, family, and friends that encircle us. I try my best to work within the parameters that you have set while knowing that there is a fierce fire within us that is greater than the devastation you brought.
Dear traumatic brain injury, you have made my sons, my husband and myself, warriors, and I believe that in the end, we will be better human beings because you are here.
Comments (45)
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Jenny replied on Permalink
You write so well about this journey of ours . Thankyou, so very similarly to my sons story ❤️
Anonymous replied on Permalink
Your story brought tears to my eyes, mostly because it has so many similarities to mine. My son suffered a TBI on Jan 2016, he was 24. He was in a coma for 3 months and the Dr's said, if he recovered he'd be in a vegetative state. Miraculously my son is not in a vegetative state. He cannot walk but his brain has recovered, no where near to what it was but he is no vegetable. He is not the same, but I am looking forward to many more miracles. Keeping the faith!!
David Bruce replied on Permalink
I was also the victim of that devil. Each case is different, so do not give up it takes time. I had a bruise on my brain left after surgery for a total of five years. Everything looked fine on the outside, but Trust Me, Jesus, it affected me and everyone I came in contact with for many years in one way or another. It's been ten years now, it made me wiser to all of those around me and allowed me to show tremendous compassion for others I do not even know, because I have no idea what they are experiencing in life. Have Faith and Patience, it takes Both to make the time pass just a little faster.
Nicole replied on Permalink
Thanks for your insight, David. ~ Nicole
David replied on Permalink
I know its Now November Nichole, but You are Delightfully Welcome, i Hope and Pray that the Journey with Your Son has taken You All on a better road as of now. Don't Give Up, Not that there is Any Doubt that You Would, as You Wouldn't have had the Insight to Share Your Initial Story.
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Your words are a gift to me this day marking the third year of our family's intro. TBI land. Thank you thank you. Onward and upward!
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Nicky replied on Permalink
Amen
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Beautiful, simply beautiful words! My brain injury was almost 11 years ago. I was 25, a college graduate and newlywed. Instead of starting a career I started life all over again learning to walk, talk, read, read and write. I had my degree in Education and was "supposed" to be teaching these things to others! I write a blog about my experiences to help with the language deficits I struggle with! Walkingtalkingmiracle.blogspot.com ! Thank you for sharing your story, I can't wait to read your book!
-Lisa W
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I was severely concussed almost four years ago by getting hit in the left forehead by a line drive while playing ball. I was paralyzed for three months. I have suffered 3-4 more concussions since then because of my post concussion syndrome symptoms. I can no longer do day to day activities and docs believe I have developed CTE. Mood swings are horrible and a lot of the time I do not want to live anymore. Help is hard to get. I hope everyone else who may suffer a TBI will get the help they need
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I have had a difficult time focusing on reading since my brain surgeries (Two in 2007, One in 2014) to solve my epilepsy caused by my TBI on April 16, 1996. Well, I have trouble with memory and focus on just about everything, but reading is especially difficult. I skimmed this article and took away enough to know this strikes the heartbeat of TBI. This year is the 20th Anniversary of my TBI. My #SurvivalDay20, as it were. I owe my mother SO MUCH! If it was not for her insistence I go to a rehabilitation facility, I would never have progressed to this level! I obtained a paralegal certificate and learned German post-injury, pre-surgery.
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I completely broke down reading this...as a care giver I'm sooooo tired and seems like I'm fighting a losing battle..we are in about 20 months...my 18 suffered a TBI from an Atv accident....things were going fairly well til about 6 weeks ago when he started a muscle relaxer..basically lost his mind and became violent.....I'm now a prisoner in my own home and wonder if this is the day he might actually kill me..this has been by far the hardest part and I'm trying to find solutions or just even a bit of help....feel like I'm falling apart at every seem....thanks for your story...I feel your pain and hope we all can find the strength xoxo
Anonymous replied on Permalink
I am so sorry for what you are going through. I remember my son went through rages like that after he woke up from his coma. The Drs and therapist advised me that it was one of the stages of TBI. Thank God that he did move past it. I pray that things have gotten better for you.
Anonymous replied on Permalink
Oh, this is so true. TBI took my husband. I have my husband but I don't. Our lives have changed so much not only he will never be the same as he once was, my family and I will never be the same. Our friends never understand that. Everybody sees him and says he is doing so good. Well, he is for what he has gone through but they don't see or live with this TBI. He struggles daily with just understanding. People don't understand when I say that I want my husband of thirty-one years back. I was told at the hospital in the first few days that this will be harder for you as his wife because he won't remember but you will. Oh so true! I do love my husband dearly but this TBI world is so hard.
Corinne replied on Permalink
A TBI stole my husband from me 4 years ago. I love that he is still here beside me but I hate that he isn't. He was my strength and now I've had to learn to be his. His strength and tenacity help me to find my strength. He helps me not give up, I mean, how can I if he won't? He's remarkable and incredible and my love and admiration for him has soared as has my heartache. Thank you for sharing so we all know we are not alone.
Nicole replied on Permalink
Corinne, I am so sorry about your husband. He is fortunate to have you. Sending love. ~ Nicole
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Nicole replied on Permalink
Sweet mom, I am sending you my best regards as well. And lots of love. I am very sorry about your daughter. ~ Nicole