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Do you believe viral infections undiagnosed cause SFN?

Neuropathy | Last Active: Aug 5, 2023 | Replies (14)

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@emo

I’m so sorry this is happening to you.

I have small fiber neuropathy as well, believed to be triggered by a viral infection because I had a horrible cold (underwhelming, I know, but I was really sick) two weeks before onset of symptoms. And that started a cascade of other issues and diagnoses, including an autoimmune arthritis.

Yes, small fiber neuropathy can affect heart rate. The small fiber nerves influence sensation, temperate, and pressure in sensory neuropathy. But small fiber nerves also run your autonomic processes: heart rate, digestion, breathing, etc. I have both small fiber sensory and autonomic neuropathy. So I don’t think it’s a matter of believing whether or not it can; it’s one iteration of small fiber neuropathy.

I don’t have links to research to back this up, but it’s my understanding viral infections are a known trigger for several neurological conditions, including small fiber neuropathy.

Just like with other autoimmune conditions, something acts as a trigger (we don’t always know what) that flips a switch in the immune system, whether it’s an environmental factor, chronic stress, covid, etc. It’s one reason for those of us who’ve long had chronic pain/illness/fatigue, that long covid exists and has similar consequences and treatments doesn’t feel surprising, at least it wasn’t for me and seemingly with others on my care team.

Are you seeing a neurologist in addition to the person you’re seeing for MCAS?

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Replies to "I’m so sorry this is happening to you. I have small fiber neuropathy as well, believed..."

I don't have team of drs just get tests and no treatment. Cant find drs here treat neuroinflammatio in nyc area are booked until next year. Dr tested liver thats it -- she got ebv elevated antigen & fatty liver. Blame me for fatty liver. No further testing i read many diseases associated w ebv. I feel really sick, plus to know that i could have other diseases undetected that could be life threatening likr cancer and not able to find dr for further testing. My primary care refer me to drs not available until next year!! no appointments someone pls help

No, I do not have a neurologist that is helping me with this pain. The MCAS dr recommended IVIG and Mestonin, but he did not prescribe it since he is an allergist. IVIG is somehow specific for my diagnosis of -- HATS/SFN/MCAS. I have not found any effective treatment for SFN pain, it's there everyday since Sept 2020. I very open to any neurology reommendations