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Military health-related problems due to combat exposure are not purely military problems, DoD problems, or VA problems. They are national problems and we need to be thinking about national solutions in order to address them.
Children have a unique experience of PTSD and TBI -- they're young, they may not fully understand what is going on, and they are usually are not provided the information they need. Dr. Stephen Cozza discusses the different ways a parent's brain injury and/or PTSD may affect children.
Family life after brain injury? It’s complicated. People walk out of your life without explanation, without just cause, leaving you to wonder what the heck happened.
I feel like I have mastered the face-to-face challenges I used to confront when asked about my health. But it’s my written work that still often causes me angst. Like a human-sized pendulum, I swing back and forth about how much I should share. How transparent is too transparent?
Gretchen Rubin, once wrote, “The days are long, but the years are short.” She was writing about parenting and not traumatic brain injury, but as I reflect on this poignant quote, I realize that as a caregiver, even those seemingly endless days have passed with such speed that I can hardly account for the last three years of my life.
The more we try to look backward and wish for what was, the harder it becomes to move forward and away from the incident or accident that caused all the grief in the first place. Yoga is not a cure, but it’s a catalyst.
It’s well documented that stress affects our ability to concentrate, remember, and sleep, and I don’t think there are many stresses equal to the days and weeks immediately following a severe traumatic brain injury...
It’s easy for us to think people could do better after they look better, to want to say, “Please try harder!” But when we see all the needs that must be fulfilled before a person moves from one level to the next, the picture becomes clearer.
Looking back with the benefit of hindsight, I now see that my family was not fractured. It was slowly being rebuilt as a new kind of family — a survivor family.
Sometimes I wonder if I’m underestimating Jack’s awareness of the situation. Perhaps it’s not so much that he doesn’t notice, as he doesn’t let it bother him.
I know there will always be days when I cry my face off because of what happened to my dad, but I have learned that the best remedy for the unfairness is meeting the daughters and sons and wives and brothers and friends of others who have been where I have been.
Today I live an unfiltered life as my brain injury has essentially wiped away my emotional and verbal filters. No longer does anyone say, “So David, can you tell me how you really feel? These days, I am learning, often the hard way, to say less. ne times.
Of all the things I was warned about following TC’s brain injury diagnosis, no one suggested the idea of mistrust or suspicion. I didn’t anticipate waking up one day, twelve exhausting and painstaking months into his recovery, to find myself on trial, accused of harboring ulterior motives and secret plans...
Life changes in a million small ways that others cannot see when a loved one is suddenly brain injured. Few understand why caregiving spouses are grieving. After all, you should be grateful that your loved one is still with you. Right? Of course…and yet….
We’ve arrived. It’s taken two and half years to get here, but I now cautiously declare that our family has reached that elusive, indeterminate state of being otherwise known as the “new normal.” What I didn’t expect, however, is that it would take so long for the new normal to finally take hold. Or, like I wrote last month, that it would be so fragile.
March is brain injury awareness month. It’s the dead of winter in these parts and about the time of year when my dad starts to get bored. And when my dad gets bored, he gets in trouble. I feel all the heat and sorrow of this brain injury pour over me yet again.