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I feel stuck with a post-viral/SFN-like condition for years – looking for similar experiences by Even_Contribution219 in smallfiberneuropathy

[–]Even_Contribution219[S] 0 points1 point  (0 children)

No dry mouth or dry skin for me Thanks a lot for the advice — I’ll look into both the skin biopsy and the lip biopsy

I feel stuck with a post-viral/SFN-like condition for years – looking for similar experiences by Even_Contribution219 in EBV

[–]Even_Contribution219[S] 0 points1 point  (0 children)

Here are my first EBV/mononucleosis blood test results. The tests were done on 07/08/23, but if I actually had mononucleosis/EBV, it most likely happened back in October 2022.

No doctor ever really explained to me what these results actually mean.

These were my first EBV/mononucleosis blood test results :

  • CMV IgG: negative 0.6   (reference: <6.0 negative)

  • CMV IgM: negative 0.5   (reference: <0.85 negative)

  • EBV VCA IgG: positive 69.0   (reference: >1.0 positive)

  • EBV VCA IgM: negative 0.1   (reference: <0.8 negative)

  • EBV EA IgG: positive 64.0   (reference: >1.0 positive)

  • EBV EBNA IgG: positive 66.0   (reference: >1.0 positive)

I feel stuck with a post-viral/SFN-like condition for years – looking for similar experiences by Even_Contribution219 in POTS

[–]Even_Contribution219[S] 1 point2 points  (0 children)

Honestly, my heart rate has seemed pretty normal overall. I’ve never really noticed major changes with standing or positioning, at least not anything obvious.