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Posts by vividrider7

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Benign brain tumor - cavernoma in Health ·
Hello everyone. I’ve started this thread so we can exchange experiences and offer recommendations to one another. Specifically, I’m talking about cerebrovascular malformations—in my case, a cavernoma. I’ll share my story first, and hopefully, others will feel comfortable doing the same.

I am 23 years old. Back in January 2019, I had a nasty fall while skiing on my very first day in France. I tumbled down a slope for quite a while, though fortunately, I didn't suffer any immediate physical injuries. However, shortly after, I started noticing what felt like flickering lights in my peripheral vision while staying in the apartment. I asked the others if they saw anything, but nobody else noticed a thing. Once I got back home to New York City, the flickering stopped entirely, so I just chalked it up to the lighting in the rental.

Then, in the summer of 2019, the light flickering returned. I realized it was triggered by spending extended periods in dark rooms, and these symptoms have persisted ever since—yes, even a year and a half later. I saw several ophthalmologists, but my eyes were perfectly healthy, so the next logical step was a neurologist. Finally, this past May, my neurologist ordered an MRI, which revealed a frontotemporal cavernoma.

The flickering lights haven't stopped, and sometimes I experience flashes in my eyes as well. I am still undergoing a battery of tests to confirm whether the cavernoma is indeed the culprit behind these visual disturbances.

One thing I found absolutely fascinating happened during the MRI scan itself. At one point, I felt a tingling sensation on one side of my face, running from my jawline up toward my forehead. Every time that tingling occurred—let’s say it happened five times—the lights would flicker in that exact same pattern I usually experience. Then, when the tingling shifted to the other side of my face, the lights flickered again.

Another strange detail: the tumor isn't located in the occipital lobe, which is the brain's visual processing center, yet my visual disturbances remain constant.

My follow-up appointment with the neurosurgeon is scheduled for December, and that’s when we’ll decide on the next steps. Personally, I’m optimistic that things will turn out fine, especially since I am under the care of Robert.

Now, I would like to hear your stories, your thoughts, or any recommendations you might have. Anything helps. 😁
Small fiber neuropathy (SFN) experiences in Health ·
Jacob Lopez51 said:Don't mention it. 🙂
It really depends on the specific pill, but you should probably get a prescription for it...

Thanks. My doctor finally wrote me the script today. I just took my first dose right before bed, so fingers crossed it actually does something.
Small fiber neuropathy (SFN) experiences in Health ·
Jacob Lopez51 said:It’s just Xanax or Helex... look, Ashwagandha helps lower cortisol, so things feel slightly better, but you really need actual anxiolytics. Honestly, I don't think an antidepressant would even touch this; if an anxiolytic targeting GABA receptors resets everything to what should be a "normal" state, then there's no point in SSRIs—besides, I don't even feel depressed... just incredibly anxious, probably because of the 10g. Currently, I'm taking Ashwagandha, dosing dopamine with Tyrosine when my energy bottoms out, and using Helex as needed. Let’s be clear: I should probably be taking it daily, but that’s dangerous because of the addiction risk, so I just try to tough it out. It's always worst at night.
That has everything to do with muscle twitching from a neurological standpoint or BFS, whereas from a psychological perspective, it's a psychosomatic disorder.
Best,

thanks Jacob Lopez51. You’ve been a huge help. Is Helex prescription-only? Can I ask a primary care physician for it, or do I strictly have to go through a psychiatrist?
Small fiber neuropathy (SFN) experiences in Health ·
Jacob Lopez51 said:I couldn't care less about the foot issues because I've already learned how to live with those. But this sensation in my head? It feels like a swarm of ants. It’s like being on some kind of drug. It’s easy to blame anxiety or hypochondria, sure, but I haven't heard of anyone dealing with head tingling for two years straight just because they're anxious.

I don't have any muscle weakness or cramping.

God, I was actually starting to think I was losing my mind. I've had this tingling sensation for the last four months, and every doctor tells me it's just anxiety. The thing is, I feel happier than I ever have. What are you taking to make this tingling stop? I don't even notice it during the day when I'm moving around; it only hits at night once I lie down and settle in. Then I can't sleep. It happens every single night. :/