When Pushing Through Stops Working

Brain injury, the pressure to be strong, and learning that recovery sometimes requires the opposite of everything we’ve been taught.

There's something interesting about the way we're taught to handle difficult situations. Work harder. Stay focused. Don't complain. Figure it out. If something isn't working, try harder until it does. For many of us, that approach becomes so ingrained that we hardly recognize it as a choice anymore. It's simply how we operate.

And for much of our lives, it probably worked reasonably well.

Then something happens to the brain, and suddenly the rules aren't quite the same.

After a traumatic brain injury, the very strategies that once helped us succeed can sometimes become obstacles. Pushing through exhaustion may make symptoms worse. Ignoring sensory overload doesn't necessarily make us more tolerant of it. Trying to concentrate harder when our cognitive resources are depleted can leave us frustrated, confused, and wondering why something that used to be so simple has become so difficult.

But what I find particularly interesting is that we don't always recognize this change right away. We continue approaching problems the way we've always approached them, assuming that enough determination will eventually produce the results we're accustomed to seeing.

And when it doesn't, we start questioning ourselves.

Why can't I do this anymore? Why am I so tired? Why am I getting emotional over something that wouldn't have bothered me before? Why can I accomplish something perfectly well on Tuesday and struggle with that exact same activity on Thursday?

Those are difficult questions, particularly when we don't yet understand what's happening neurologically.

When strength becomes a complicated idea

I think our understanding of strength deserves some reconsideration after brain injury.

We're accustomed to associating strength with endurance, independence, and perseverance. Those qualities aren't inherently bad. In fact, they can be valuable throughout rehabilitation. But there's a difference between perseverance that helps us improve and persistence that repeatedly pushes us beyond our available capacity.

Consider someone who can comfortably exercise for an hour but struggles to manage an afternoon of paperwork, phone calls, and appointments. To someone looking from the outside, that might seem contradictory. If you're physically healthy enough to work out, why can't you handle a few administrative tasks?

The answer may involve how differently the brain processes those demands.

Physical activity, cognitive concentration, emotional regulation, sensory processing, and multitasking place different demands on the nervous system. They can interact, of course, but the ability to perform well in one area doesn't guarantee the same capacity in another.

And that brings us to something we discuss frequently at Project TBI: the Fluctuating Energy Economy, or FEE.

FEE is a developing framework for understanding why cognitive capacity can vary after brain injury and why activities that appear relatively simple can become unexpectedly expensive in terms of mental effort. It isn't an established medical diagnosis or a validated clinical measurement system. It's a way of organizing observations and questions about what many survivors experience.

The basic idea is that we need to consider both how much capacity is available and how much an activity costs.

A quiet conversation with one person might be manageable. Put that same conversation in a crowded restaurant, with music playing, dishes clattering, and several people talking at once, and the cognitive cost may increase dramatically.

The activity is still a conversation. But the conditions have changed.

The same principle can apply to driving, reading, shopping, working, or even spending time with family. We may be capable of doing something, but the environment, timing, duration, and competing demands can determine how much it takes out of us.

And when the cost exceeds what we can comfortably sustain, determination alone may not solve the problem.

The emotional side of brain injury

There's another part of this that deserves more attention, and that's what happens emotionally.

Brain injury can affect emotional regulation in ways that are difficult to predict or explain. Someone who rarely cried before an injury may suddenly find themselves becoming emotional over seemingly minor things. Frustration can appear more quickly. Background noise that was once tolerable may become overwhelming. A simple disagreement might require far more effort to navigate than it did before.

That can be particularly confusing for people who have spent their lives trying to maintain control over their emotions.

And while men may face certain cultural expectations about toughness and emotional expression, these experiences aren't limited to men. Anyone who has built their identity around independence, responsibility, or being the person others rely upon may struggle when those familiar roles become harder to maintain.

What's important is recognizing that emotional changes following brain injury aren't necessarily failures of character or self-discipline.

Neurological changes, fatigue, stress, pain, sleep disruption, and the ongoing effort of adapting to a different life can all contribute to how we respond emotionally.

Sometimes the frustration isn't just about what happened in a particular moment. It's about the accumulated effort of trying to function in a world that still expects us to operate the way we did before.

And there's a certain irony in trying to overcome emotional dysregulation by getting angry at ourselves for having it.

That approach probably isn't going to help much.

What if rest is part of the strategy?

For people accustomed to measuring progress through productivity, rest can be surprisingly difficult to accept.

We understand rest when it follows obvious physical exertion. Run five miles, lift weights, spend the afternoon doing yard work, and nobody questions why you might need to recover.

But spend two hours reading documents, participating in a meeting, or navigating a noisy environment, and the exhaustion can be harder to explain.

You might not have moved from your chair.

Yet the cognitive effort was substantial.

After brain injury, certain activities may require more attention, compensation, or processing effort than they previously did. Research has examined altered neural recruitment and increased cognitive effort in some people following TBI, although the patterns differ across individuals and tasks.

This is part of why I think it's useful to distinguish between doing more and functioning better.

If we can complete an activity with fewer symptoms, better pacing, or less recovery time afterward, that may represent meaningful progress even if the total amount of work hasn't increased.

Sometimes improvement means recognizing the early signs of fatigue and stopping before the situation becomes unmanageable.

Sometimes it means dividing a task into shorter sessions.

Sometimes it means changing the environment rather than expecting ourselves to tolerate everything in it.

And sometimes it means accepting that today isn't the day for a particular activity.

None of those decisions automatically means we've given up.

Starting over doesn’t mean starting from nothing

There's a tendency to compare our current abilities with what we could accomplish before the injury. That's understandable, but it can become a frustrating way to measure progress.

If we once worked long hours, managed multiple projects, traveled constantly, or exercised intensely, beginning with ten minutes of an activity can feel almost insulting.

But rehabilitation frequently involves identifying an appropriate starting point and gradually building capacity or developing compensatory strategies from there.

Consider physical exercise. Someone recovering from a neurological injury might begin with short walks, a few carefully selected exercises, or brief periods of activity followed by rest. Over time, and with appropriate medical guidance, they may be able to increase their activity.

The same gradual approach may be useful when thinking about cognitive tasks, although physical conditioning and cognitive rehabilitation are not interchangeable.

The important part is understanding that progress isn't always linear.

There may be days when an activity feels easier and others when the same activity becomes difficult again. Sleep, pain, stress, illness, sensory stimulation, and prior exertion can all influence the experience.

A good day doesn't necessarily establish a new permanent baseline.

And a difficult day doesn't automatically erase the progress we've made.

That's an important distinction, because we can become so focused on whether we're improving that we overlook the circumstances affecting our performance.

Can we change the way we approach a challenge?

This brings up another interesting question.

What happens when we change the language we use to describe our expectations?

Imagine approaching a new activity with the thought, I probably can't do this anymore.

Now consider approaching that same activity with a slightly different question: What if I can do some version of this, under the right circumstances?

That doesn't mean ignoring symptoms, dismissing medical advice, or assuming that confidence can overcome neurological injury.

It means leaving room for the possibility that the conditions, strategies, or abilities involved may have changed.

In psychology, this kind of shift is related to cognitive reframing, which involves examining an interpretation and considering a more useful or balanced perspective.

There's also a connection worth exploring with neuroplasticity, the nervous system's ability to change through experience, learning, and repeated practice. Learning different cognitive and behavioral responses involves processes supported by neural plasticity, although we shouldn't assume that changing a thought automatically repairs damaged brain tissue or restores lost neurological function.

Still, I find the relationship interesting.

If we repeatedly tell ourselves that an activity is impossible, we may become less willing to explore whether an adaptation could make it manageable. If we approach it with curiosity instead, we might discover an alternative strategy.

Or we might discover that the limitation is still there.

Either result gives us information.

And information is useful, particularly when we're trying to understand a brain that doesn't always behave predictably.

Learning to accept help

Another part of adapting to brain injury involves recognizing that independence doesn't always mean doing everything ourselves.

Sometimes it means finding ways to accomplish what matters using the resources available.

A person with memory difficulties might use photographs, reminders, or voice recordings. Someone who struggles with writing or screen sensitivity might dictate their thoughts and use transcription software. Someone with auditory processing difficulties may benefit from quieter environments, written instructions, or conversations with fewer competing voices.

Artificial intelligence is becoming another tool in that collection. It can help organize notes, transcribe spoken ideas, create outlines, and reduce the administrative work involved in completing certain tasks.

These tools don't cure a brain injury, and they come with limitations involving accuracy, privacy, and the need to verify important information.

But they may reduce the amount of effort required to participate in activities that remain meaningful.

I think that's an important way to understand assistive technology. It isn't necessarily about doing something the easy way. It's about recognizing that the original way may now carry a cost that isn't worth paying when a practical alternative exists.

The same applies to rehabilitation professionals, family members, friends, and peer-support communities.

Accepting assistance doesn't eliminate independence. In many circumstances, it's what makes independence possible.

Maybe we’re asking the wrong question

I've been thinking about how often we measure recovery by comparing ourselves with who we were before the injury.

Can I work the same hours? Can I handle the same workload? Can I tolerate the same environment? Can I get through the day without resting?

Those questions are understandable, but they may not always tell us what we need to know.

Perhaps we should also be asking whether we're learning to recognize our limits earlier, whether we've developed better strategies for managing cognitive fatigue, whether we can participate in activities with less discomfort, and whether we're finding ways to maintain the parts of life that matter to us.

Those changes may not be as visible as lifting heavier weights or working longer hours, but they can have a substantial effect on quality of life.

And maybe the idea of strength needs to evolve along with our understanding of recovery.

Strength might mean knowing when to stop. It might mean admitting that something is difficult. It might mean asking for help, trying a different approach, or allowing ourselves to experience emotions without interpreting them as weakness.

I don't think brain injury requires us to abandon determination. But perhaps it does require us to reconsider how we use it.

Because the goal isn't necessarily to push harder.

It's to understand what we're working with, make informed decisions, and find a way forward that doesn't require us to fight our own brains every step of the way.

And that leaves me with a question I've been turning over for a while.

What if adapting to a brain injury isn't about becoming less determined, but about learning where our determination can actually do some good?

I'd be interested in hearing how others have approached that question. Have you found yourself trying to push through symptoms because that's how you've always handled difficult situations? Has learning to rest, ask for help, or approach an activity differently changed the way you think about recovery?

Sometimes hearing how somebody else figured something out gives us an idea we wouldn't have considered on our own.

And that seems like a pretty good reason to keep having these conversations.

Project TBI  •  Remember less. Capture more. Heal together.

Project TBI explores traumatic brain injury through lived experience, emerging research, practical tools, and the questions that don’t always have easy answers. Our discussions are educational and aren’t a substitute for individualized medical advice.


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