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Roy Bell

Army Staff Sergeant Roy Bell on Life After a TBI

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My name is Staff Sergeant Roy Bell. I'm in the United States Army. I've been in the Army for 12 years. I'm from Charleston, South Carolina. I suffered a traumatic brain injury incurred through multiple IED blasts and rocket blasts attack on our living areas. I wasn't immediately evacuated because there was no loss of consciousness nor was I aware of the possible brain injuries that incur from blasts, and I didn't start getting treatment until I returned back home my last time. I started incurring treatment through the symptoms that I was showing that for me were completely blind. I didn't notice any of my symptoms. I didn't know what they were. I thought I was just being me. I was having problems remembering things and putting things together--sentences, words, trying to figure things out, what I wanted to do. I would have chronic migraines all the time, almost every day. It would be so bad, but I just had to push through. My balance is messed up. I could just be walking and all of a sudden I'd go off to the left. At one time that could happen at any time. You get up out of the bed at night to use the bathroom and you all of a sudden run into a wall because you can't control where you're going. And the migraines--I could just wake up with migraines. Light sensitivity--bright lights would hurt my eyes and cause a headache. Through some of the therapy that I've been going to I've noticed improvements in concentration and remembering things. I'm not like I used to be. I don't know if I ever will be. But the therapy helps. I do speech pathology here at Walter Reed, I do physical therapy, I've done occupational therapy, I've done balance therapy through the CAREN unit. Between the physical therapy and the CAREN therapy it really helps me with my balance, trying to help my brain retrain to what's right with my injuries because there's not a way you can fix your balance except just to retrain your brain. It also helps my back because I have a tear in one of my discs. The speech therapy and occupational therapy helps me with my concentration, teaches me ways how to think again and try to concentrate and really focus on doing what I've got to do. In my opinion, I feel it's hard to determine the emotional side of things with a TBI because with my experiences I have been diagnosed with PTSD. And TBI and PTSD have some of the similar psychological symptoms. But it's different for everybody. I do some therapy with my psychologist, and he teaches me ways to try to deal with things, but I've learned that a lot of the ways that I have adapted into are ways that my brain just kind of threw into a survival technique. It's how I live now. There's not really a way you can change that. I've been dealing with it for so long I've just learned to control it a lot better than other people. The biggest thing that really helps me try to keep on track and remember things is I've got a PDA. There's a company that really cares about TBI patients, and if they qualify, they help them and give them some of this stuff. The biggest thing I could tell other TBI patients that are recently injured is just not to give up hope and try to stay calm and not get frustrated about everything. It's tough. It's real tough. But there's light at the end of the tunnel. Just don't give up. Stay focused. Be patient and you'll get better. You'll get better than what you are now.

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“Stay focused and patient and you'll get better," says Army Staff Sergeant Roy Bell.

 

Produced by Victoria Tilney McDonough and Brian King, BrainLine.

Comments [1]

Thank you for this post! I am a marriage and family therapist, and I work spcifically with survivors of traumatic brain injury. I would love to know more about the PDA tool you find helpful. Thanks!

May 31st, 2013 2:35pm

 


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