Post viral syndrome peripheral nerve hyperexcitability

Posted by josh701 @josh701, Apr 6, 2025

Hi everyone,
I’m a 36-year-old navigating recovery from what’s been described as post-viral small fiber involvement and motor nerve hyperexcitability.

How It Began:

It started after a viral illness in August 2024, during a time when my whole family had upper respiratory symptoms.

I developed fever, diffuse headache, and left-sided temple pain, which later localized and became persistent.

By January 2025, I began to experience:

Burning sensations

Pins and needles

Odd wet or sunburn-like skin feelings

Muscle fasciculations (twitches) across my body

Migratory muscle pain and intermittent joint discomfort

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Workup So Far:

MRI of brain and cervical spine: Normal

Autoimmune workup: Negative

Skin biopsy: Normal epidermal nerve fiber density

Nerve conduction studies & EMG (lower extremities): Normal

CBC, CMP, CRP, ESR, CK, aldolase, B12: All normal

No evidence of large fiber neuropathy or motor neuron disease

No clinical weakness or atrophy

---

Current Working Diagnosis:

Post-viral small fiber sensitization

Motor nerve hyperexcitability (likely benign fasciculation syndrome or similar)

Significant health anxiety, especially due to my medical background and profession

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What’s Helping Me:

Gabapentin (600 mg at night)

Supplements:

Magnesium glycinate

CoQ10

Alpha-lipoic acid (ALA)

Omega-3

Curcumin

B-complex

Vitamin D3 + K2

Ashwagandha, glycine, apigenin (for calming and sleep)

Exercise: Strength remains intact and working out reinforces my confidence

Mind-body tools:

Headspace and Curable app

Weekly visits with a psychologist

Gratitude journaling

Somatic calming techniques (breathing, grounding, mantra work)

New mantra I use daily:

> “One in a million. I am strong. This will pass.”

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Biggest Lessons:

Even with scary symptoms like widespread twitching or burning, the body can be in a state of hyperawareness, not disease.

I’ve learned the importance of regulating fear and stress to support nervous system healing.

Benign doesn’t mean painless—but it does mean hopeful.

Working with a neurologist, psychologist, and staying grounded in scientific reasoning has helped me reclaim my peace.

---

Happy to connect with anyone navigating something similar. You're not alone—and your body is capable of calming, rewiring, and healing.

Interested in more discussions like this? Go to the Neuropathy Support Group.

Profile picture for fryski43 @fryski43

Hi @josh701

I wanted to say thanks for sharing, your history sounds very similar to my own. In Dec 2024 I caught the flu from my young son and after a hefty chronic cough developed tingling and burning on my tongue, constant tingling back and top of the head and ears, tinnitus, constant ear fullness, electric shocks in my toes and localized constant myalgia in the anterior neck muscles. Apparently my nervous system is triggering the muscle pain.

My health anxiety dialled things up, on reflection Dr Google and doomscrolling forums left me catastrophizing to the point it was borderline inducing panic attacks. It's reassuring to hear the strategies that are working for you and that you are remaining to stay strong. Likewise I'm using Cureable, supplements and therapy to navigate through this. Luckily I have no fatigue so physical therapy is massively helping.

Officially I'm diagnosed with localized sensitization (primarily neck and head) resulting in myofascial pain. My nervous system is on constant high alert and needs to reset. I'm on a medium dose of Amitriptyline, bloods all came back normal along with ANA panel and vitamin testing. In a strangely reassuring way my neurologist (who has expertise in long Covid) said that disruption of the nervous system is becoming more common, often triggered now by sinus infections, flu and even hefty colds. What is reassuring is that my neurologist said most people recover with the right strategies and time, I was even given a ballpark timeframe for recovery.

I was curious if your neurologist also gave you a timeframe for recovery and if you've found anything that particularly helped with the anxiety?

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@fryski43 Hi, thank you for sharing the story. What is the timeframe for recovery of hyperexcitable nerves, according to your Neuro? Best of health! Ivana

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Profile picture for josh701 @josh701

You can certainly send me a message if you would like. Just an update so my appointment got moved up due to a cancelation. Saw a neuromuscular specialist. He also had time for me to get a repeat emg. All normal. Symptoms still evolving things that were bugging no longer are such as aches in my leg and now its aches to my right hand and wrist. Going on 6 weeks with new wrist hand symptoms. He gave me the analogy my circuit breaker (Brain and spinal cord) are fine its just my wiring got fried likely after a virus and anxiety is making things take longer to heal.

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@josh701 That is what my doctor says - anxiety makes it harder and longer to heal. I hope we all feel better. My doctors don't believe that estrogen or hormonal imbalance can do this to you but I think it can.

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Profile picture for ivce @ivce

Hi, I wanted to check with you how you are feeling now? I hope the twitching went away. I would really appreciate it if you could let me know. All the best, Ivana

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@ivce still have body wife fasiculations, more focal in my right calf but they are elsewhere as well. My right hand symptoms seem to be improving. Now im dealing with right lower extremity tightness aches. My twitches started 7 days after starting SNRI (coincidence??) So im reluctant to trial any other serotonin regulating meds

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Profile picture for josh701 @josh701

@ivce still have body wife fasiculations, more focal in my right calf but they are elsewhere as well. My right hand symptoms seem to be improving. Now im dealing with right lower extremity tightness aches. My twitches started 7 days after starting SNRI (coincidence??) So im reluctant to trial any other serotonin regulating meds

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@josh701 Oh my God. Thank you for that information. I thought it started after a viral infection. So, your twitching started after SNRI? But if it was a side effect, it should stop after stopping the meds. What did the doctor say? Is it listed as a side effect of SSRI? Thank you so much for this information.

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Profile picture for josh701 @josh701

@ivce still have body wife fasiculations, more focal in my right calf but they are elsewhere as well. My right hand symptoms seem to be improving. Now im dealing with right lower extremity tightness aches. My twitches started 7 days after starting SNRI (coincidence??) So im reluctant to trial any other serotonin regulating meds

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@josh701 Which medication did you try? Sertaline/Zoloft? Please let me know so I don't use the one that caused your twitching. I used Sertaline two years ago and I was ok. It did not give me any twitching. My doctor told me that I need to take care of the anxiety first and then the twitching will go away.

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