I have Mollaret's meningitis. After six bouts in seven years, I am positive there are after effects. I have experience fatigue and have had issues with disequilibrium for the past two years.
But for me, that's not the worst part. It's the not knowing that troubles me. As in not knowing when I will experience another bout of meningitis and / or if the next bout will lead to additional nerve damage.
Thanks for letting me know. People here have made suggestions about boosting immunity: lysine, astragalus, olive leaf, red algae. There are many other things for that. I've tried some. Best of luck.
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