Survivors SPEAK OUT! Jordan Fallert
Survivors SPEAK OUT! Jordan Fallert
by
Donna O’Donnell Figurski
1. What is your name? (last name optional)
My name is Jordan Fallert.
2. Where do you live? (city and/or state and/or country) Email (optional)
I live in St. Louis, Missouri, USA.
3. On what date did you have your brain injury? At what age?
I got my brain injury on February 5th, 2021. I was 23 years old.
4. How did your brain injury occur?
I got my TBI (traumatic brain injury) from a car crash around 5:30 on a Friday. I had just left work to go home to study for a test for my master’s degree. 
5. When did you (or someone) first realize you had a problem?
What saved my life was that a fire truck had responded to a fire on that same road. They were told their backup was no longer needed. Their captain (who was in an SUV, not the fire truck) saw the crash happen. I was unconscious on impact, and they had to use the “Jaws of Life” to get me out of the car. After I was rescued, they took me straight to the hospital to have emergency surgery. I was in a coma for six weeks. I slowly gained consciousness and became aware pretty quickly that I was in the hospital, but I had no idea why. That was my biggest indication that something was wrong. Also, I couldn’t walk, and I had extreme right-side weakness.
6. What kind of emergency treatment, if any, did you have?
After I was rescued from my car and in the ambulance, the firemen realized very quickly I was having extreme difficulty breathing. I was hit on a road that had a speed limit of 45 mph. I was turning onto the road and going about 12 mph, and the other driver was speeding and going over 60 mph. Even though I was going so slowly, the force of the impact caused my diaphragm to rupture, my lungs to push on my stomach, and my stomach to push on my heart. Once I was at the hospital, I was immediately taken to the trauma floor. I was in surgery for about six hours.
7. Were you in a coma? If so, how long?
I was in a self-induced coma for about six weeks.
8. Did you do rehab? What kind of rehab (i.e., inpatient or outpatient and occupational and/or physical and/or speech and/or other)? How long were you in rehab?
Yes. I did a lot of rehab. I was in the hospital for about four months. As soon as I was conscious, they began putting me into rehab. I did speech, occupational, and physical therapies. After I was released from the hospital, I stayed with my mom in a house on the hospital campus and did intense outpatient therapy. And when I came home, I did more therapies at a hospital near me. It’s difficult to say how long I was in rehab, but I would guess about nine months.
9. What problems or disabilities, if any, resulted from your brain injury
(e.g., balance, perception, personality, etc.)? 
My vision is one of my biggest problems so far. I go to a neuro-ophthalmologist to help combat my double vision. I have had some personality changes that my mom would probably agree with. But I would consider a lot of these “personality changes” to be normal for a very intelligent 24-year-old who had the whole world going for her. Someone else’s actions took that away. I also lost my independence.
10. How has your life changed? Is it better? Is it worse?
My life has changed, but I wouldn’t say it’s better or worse; it’s just different. (I personally have really tried my best to think like that.) My life has changed in that I have to rely on people a lot more than I am comfortable with. I got a car for my 16th birthday (almost ten years ago), so I’ve always been able to go places and do things without having to ask other people for rides and things like that. It feels like I was knocked down a peg or two.
11. What do you miss the most from your pre-brain-injury life?
This is a bit of a complicated question for me. My life was in such a weird place when my crash happened. Courses all went online because of COVID. I had to come home–exactly from my undergrad degree. I continued with a job where I had my internship at, but I hardly saw my friends because of COVID. They were all in different cities in the US, and we couldn’t really travel. So I guess what I really miss are my college years because those are the most recent and foremost in my mind. Because of the accident, I have retrograde amnesia. So I don’t remember anything from about two years before.
12. What do you enjoy most in your post-brain-injury life?
Before my accident, I was on a breeder list to get a cavapoo puppy. I was sixth on the list, and a litter was born in May 2021. Some people skipped on this litter of two (the Tom and Jerry litter), so I was able to have my choice. I chose Tom and renamed him Brew. He has been my saving grace after my brain injury. He’s my best friend and constant companion. I don’t know what I’d do without him.
13. What do you like least about your brain injury?
I don’t like feeling weak. This right-side weakness has been an uphill battle to deal with. But it’s getting better.
14. Has anything helped you to accept your brain injury?
My parents have really been my saving grace. They have never given up on me and never make me feel like I am limited. If I want to do something, they encourage me and help me do it.
15. Has your injury affected your home life and relationships and, if so, how?
I continue to live with my parents since my brain injury. I was living with them before due to COVID. My parents have been nothing but great. But I have had a lot of friendships wither and decay, which has been hard in and of itself.
16. Has your social life been altered or changed and, if so, how?
Yes and no. I didn’t have a social life before the accident because of COVID. After the crash and when I came home, I had some friends come see me at my house, but they slowly drifted away. It’s hard when you can’t drive, so you are always having to ask others to drive up to see you or drive you somewhere.
17. Who is your main caregiver? Do you understand what it takes to be a caregiver?
My main caregivers are my mom and my dad. I do not understand–and hope to never understand–what it takes to be a caregiver. I just know that they are the strongest individuals I know.
18. What are your plans? What do you expect/hope to be doing ten years from now?
My plans are very fluid and always changing. I recently (less than a month ago) got my license, and last week, I was able to buy my own car. With these changes, my attitude and outlook have drastically improved. I feel like I can conquer the world if I have this outlook. A Traumatic Brain Injury won’t keep me down and will not limit me. I won’t let it! 
19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other survivors with your specific kind of brain injury.
I was always angry that my brain couldn’t heal faster, but my mom kept reminding me that it’s not like a broken bone. It’s an organ that controls your entire body, so give it time to heal.
20. What advice would you offer to other brain-injury survivors? Do you have any other comments that you would like to add?
Don’t take your anger out on your caregiver(s). They want to help you get your life back. Hug everyone tighter, and tell them you love them. A brain injury will only limit you if you let it.
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I dislike how easily I forget stuff and having to constantly ensure I’m eating right – so my brain is working at its optimal capacity.
19. Are you able to provide a helpful hint that may have taken you a long time to learn, but which you wished you had known earlier? If so, please state what it is to potentially help other survivors with your specific kind of brain injury.
My family didn’t understand – it took a lot of time. Now, I get a lot of understanding and support.
In some cases, there were several weeks of good health. But weeks or months later, they showed new symptoms. (Adult symptoms include fatigue; fever; cough; sore throat; chest pain; shortness of breath; neurocognitive problems with memory, concentration, processing, or finding words; diarrhea; headaches; insomnia; dizziness; heart palpitations; abdominal cramps, rashes; tinnitus; joint pain; depression; and anxiety.) The symptoms may last weeks or months, and some people still have symptoms after several months.
I haven’t seen the data, but I suspect that the 10-13% number came from people who either had an obvious symptom or tested positive. If we include the number of asymptomatic infections, the percentage of infected children who get long COVID will likely go down significantly. If you and your children are using masks and social-distancing, then you’re already at a low risk of even getting infected. 
I am incredibly excited to announce that I have been recognized as a Book Excellence Award Finalist for my book, 
The book was released in 2018 and is about me, a “forever” caregiver for David, my high school sweetheart, best friend, and spouse after he had a traumatic brain injury. David was not expected to survive his three brain surgeries in January 2005, but he DID! Triple YAY!
know. I have Severe Anxiety Disorder and huge panic attacks. Strangers are a HUGE trigger; letting them into my home is even bigger! I handled it all – no anxiety; no nothing!
It can happen to anyone, anytime, . . . and anywhere.
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