Hello,
My wife is about to try valacyclovir for her ME/CFS. I am curious to hear about your experiences of starting dose and titration. I know the studies have shown 1g q6h have worked however some people have mentioned it causing insomnia which for ME is one of the major issues already so we do not want to make it worse. We are thinking of starting 500 mg BID. Any help or insight would be appreciated.
And I know alot of people feel worse at first before getting better after months of treatments. Has anyone felt better without getting worse at first?
Thank you so much in advance
My wife is about to try valacyclovir for her ME/CFS. I am curious to hear about your experiences of starting dose and titration. I know the studies have shown 1g q6h have worked however some people have mentioned it causing insomnia which for ME is one of the major issues already so we do not want to make it worse. We are thinking of starting 500 mg BID. Any help or insight would be appreciated.
And I know alot of people feel worse at first before getting better after months of treatments. Has anyone felt better without getting worse at first?
Thank you so much in advance