jk600

u/jk600



r/MyastheniaGravis•

For those who had an MG relapse due to Covid or other virus, did your weakness improve itself as you recovered from the infection? Or did MG symptoms stick around long after?

I'd been virtually symptom free for 2 years, but MG symptoms have come back since I acquired Covid a couple weeks ago. I finished Paxlovid 5 days ago and viral symptoms are well gone but my MG weakness is still slowly worsening. I was hoping the MG would improve as my immune system settled back down. Maybe wishful thinking, so I'd like to hear others' experiences.

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