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Chronic EBV

Infectious Diseases | Last Active: Jan 1 10:42am | Replies (3)

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@kenforce
I appreciate the input. I believe my situation has also been a slow decline since 2020 that was then put into hyperdrive in 2024. Did you take any supplements or change your diet/activity level? I understand it is going to be a slow recovery; however, how long did it take you to function well enough to return to work/have a semblance of a life? I think I can probably “deal” if I can get 20% improvement. I know I won’t be firing on all cylinders but not being able to do more than one task a day without severe exhaustion and pain is doing a number on my mental health.

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Replies to "@kenforce I appreciate the input. I believe my situation has also been a slow decline since..."

@bbj2009 There is an article on Phoenix Rising called, "The reason why antivirals like Valtrex and Valcyte take such a long time to work in ME/CFS (or don't work at all), according to Dr Martin Lerner."

I caught mine early as my EBNA was climbing up to 600 and was able to see it start dropping. I attached a chart of my data. If your EBNA is over 600 then it's difficult to know if your having any improvement.

One thing I can tell you is even though my numbers where improving I found it more difficult to walk long distance. I kept making myself walk around the block. Before it got better I could hardly walk to the end of the driveway without being out of breath. I was really scared and even had my heart check but everything was ok. One day I started feeling better. It was like a switch flipped. I describe the whole situation to when I was younger and you had to exercise a lot and you get that pain in your side but if you push past that you feel fine.

Anyway, the only number that I can see that shows your on the right track is the EBNA, in my case. Maybe I was lucky to start early...I don't know. Remember, it was not a cure in my case. I still take 1 to 2 grams of valacyclovir every day to maintain but I'm fine.