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Profile picture for wilsonanderson @wilsonanderson

I tried LDN c.6 years ago, before I got LC, and was probably still taking it into LC since I had numerous chronic diseases then said to benefit from it, including fibromyalgia but though I slowly titrated to full dose didn’t obviously get any better. I might well give it another go! I have tried to do a one drug/ supplement change at a time … it’s so slow going it’s quite easy to spend 2 years getting back to where you were, as I am with antihypertensives… I have to try to think which drug is responsible for making me more breathless, reduces BP but increases HR, and which is preferable as my medics not very concerned ( in Uk)…

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Replies to "I tried LDN c.6 years ago, before I got LC, and was probably still taking it..."

Being five years post long Covid, I totally understand you. Current studies with long Covid users are showing some of us react well to extremely low-dose naltrexone such as .01 or .05 MG… while others need to get up around three or 4.5 mg to see some improvement. My sweet spot was 3 mg per day for about the first four months and then I titrated slowly up to 4.5 and feel better than I have in years. Hoping it works for you too!