In my previous post, I explored how brain fog in acoustic neuroma (AN) is more than just a side effect of stress—it’s a genuine neurological phenomenon. Many of you shared your stories, and one theme stood out: “Now that I understand what’s happening, what can I do about it?”
While you may be waiting for surgery—or finding that your symptoms linger or even worsen afterward—mental fog can feel like an unwelcome and persistent companion. It affects focus, memory, and emotional well-being, making everyday life more challenging.
This post is your next step.
Let’s explore practical strategies to cope with mental fog—so you can live more clearly, even while navigating the complexities of AN.

1. Rule Out Treatable Causes First
Before diving into cognitive strategies, start with the basics: ask your Doctor for a full blood test and a thorough medical review. Sometimes, what feels like mental fog from acoustic neuroma is being made worse by underlying, treatable conditions.
Ask your doctor to exclude other possible contributors, such as:
- Vitamin D and B12 deficiencies
- Thyroid dysfunction
- Iron deficiency or anemia
- Hormonal imbalances
“After months of fog, I found out I had a severe vitamin D deficiency. Once I started supplementing, my energy and clarity noticeably improved
Also don’t say absolute No to Antidepressants. While antidepressants can’t cure brain fog caused by the physical presence of an acoustic neuroma, they can still play a meaningful role in recovery—especially when the fog is made worse by emotional exhaustion.
Living with AN takes a psychological toll. There’s the shock of the diagnosis, the fear of treatment outcomes, the grief of losing “how you used to function,” and the strain of trying to explain invisible symptoms to others. All of this can lead to chronic stress, anxiety, or low mood—which in turn, can deepen the fog.
You might be sleeping poorly, feeling disconnected, or constantly “on edge”—even if your MRI looks stable. That’s the mind-body loop in action: emotional distress makes cognitive symptoms heavier, and the heavier they feel, the more emotionally drained you become.
So if your doctor suggests antidepressants as a supportive tool, it’s not because they’re dismissing the neurological reality of your condition. It’s because they understand that emotional suffering and cognitive fog often coexist, and treating one can ease the weight of the other.
In this context, antidepressants aren’t a cure—they’re a layer of support. They may help restore balance in your nervous system, reduce the background noise of anxiety or low mood, and give your brain more breathing room to adapt and recover.
Think of it not as a fix, but as a tool in a larger healing strategy—one that includes medical care, therapy, lifestyle adjustments, and a whole lot of self-compassion.
2. Conserve Your Mental Energy
Your brain is working hard to compensate for hearing loss, balance issues, and spatial confusion. Don’t overload it.
Try this:
- One task at a time (no multitasking)
- Use reminders, checklists, and memos
- Break tasks into small, manageable steps
- Schedule frequent breaks
Think of it as cognitive pacing—like physical therapy for your brain.
3. Move Gently, Breathe Deeply: Regulate Brain and Body
Movement and calmness might seem like opposites—but together, they are powerful tools to reduce brain fog. Movement boosts blood flow and supports neuroplasticity, while calming your nervous system reduces the anxiety that often makes brain fog worse.
Try this:
- Vestibular rehabilitation therapy (ask your ENT or neurologist)
- Gentle yoga
- Daily walks, especially in nature
I used to walk with my daughters—and I still do. Those quiet, outdoor moments not only help my body but clear my mind. Even something as simple as playing outside with kids or pets can re-engage the senses and ground you in the present moment.
Combine movement with calming practices:
- Guided meditation or breathwork (apps like Calm or Insight Timer)
- Box breathing: Inhale 4 – Hold 4 – Exhale 4 – Hold 4
- Grounding techniques: focus on textures, sounds, or colors around you
A calm, gently moving body helps create a clearer, more focused mind
4. Lean Into Support Systems
You don’t have to do this alone. Isolation worsens fog—connection lightens it.
Ways to find support:
- Acoustic Neuroma Association (ANA) forums
- Facebook or Reddit support groups
- Let trusted friends or family read this blog for insight
Talking to everyone is not the same as talking to someone who truly understands your situation. Find your people—those who get it. It can be incredibly grounding to speak with others who have walked a similar path.
Sharing what you’re going through helps others understand—and gives you emotional space to heal.
5. Use Your “Clear” Windows Strategically
Brain fog can come and go. Use your good windows wisely.
Tips:
- Do mentally demanding tasks during peak clarity (often mornings)
- Use “foggy” periods for rest or low-stakes activities
- Track your fog patterns in a journal or app
Understanding your rhythm allows you to work with your brain, not against it.
6. Practice Compassionate Self-Talk
Progress isn’t always linear. Some days, brain fog wins—and that’s okay.
Learning to speak to yourself with kindness can feel awkward at first. It’s easier said than done, especially when you’re used to pushing through or measuring your worth by how much you get done.
Many of us blame ourselves for not being as “productive” as we used to be—or for not performing certain tasks as easily as others seem to. That quiet self-criticism feeds both depression and mental fog, keeping us stuck in a loop of guilt and fatigue. Try replacing:
“Why can’t I think straight?”
With: “My brain is working hard right now—I’ll take it slow.”And remember:
Resting is not doing nothing.
Healing is a task.
It takes energy, patience, and resilience. If all you did today was rest, you still did something meaningful—something necessary.You wouldn’t criticize a friend for needing time to heal. Offer yourself the same grace.
Now it’s my turn to ask you.
Do you experience mental fog with AN? What’s helped you cope?
What was your strategy? What worked for you?
Share your story in the comments below, I would love to hear from you.
Very informative! I shared this post with someone going through similar circumstances, and they told me it was really helpful. Please keep sharing—this can truly make a difference in many lives. Thumbs up!
Thanks for sharing, Amir! It’s very helpful indeed.
Walk, walk, walk. Before my AN surgery and even before diagnosis I would walk to clear my wonkiness (brain fog, feeling like I was half hungover and half drunk at the same time). After a while during the walk I could feel the fog lift and started to feel better.
I take chinese mushrooms, especially Lions mane helps with brain fog. It works like a charm 100%. The hardest thing about AN is that no one in my family or friends has really done anything or said much. When my dad got sick he got so much support. I think there is a stigma to getting sick in youth or middle age, people are more judgemental that you aren’t working than concerned you have a brain tumor. I don’t have much that is holding me back. I get migraines every once in awhile, but migraine medicine works like a charm, I feel sinus medicine also works well and is implicated in my migraines. I decided not to treat my AN. i dont trust doctors because I had another medical condition which I decided to use alternative treatment and they came down really hard on me, espeically after my alternatives worked. So now I don’t really trust medicine and I did my homework and other countries wouldn’t treat me until much later anyway. This will make you appreciate all the time left you have in life. I’m every once in awhile nervous because I was told I would eventually faint or stop respirating. I’m not scared to faint, I’ve fallen off plenty of horses and thats way worse than falling on the ground when your already standing on the ground. But I sometimes worry about what it will feel like when I stop respirating, will I struggle to breath, like will I be gasping for breath, will it be scary, how long will it take. But luckily with the Chinese mushrooms I’m just fine as far as brain fog goes. They can be bought at Walmart for 15 dollars a month, and they’re good enough for me, no side effects, only thing I don’t appreciate having to swallow three pills a day, but I used to have a lot of brain fog every day, and I feel swallowing three pills is easier than feeling like a zombie.