There are the acyclovir responders like me and there's herpes abortive lytic reactivation theory and acyclovir has a very good activity against EBV early phase "mise-en-place" work of virus replication.I see it the other way: it leaves the door open. But I only see it this way because it literally always happens like this. It should be banned entirely from this program, for the same reasons why faith healing and any other form of pseudoscience would be, on grounds of validity and quality of proposals alone.
I have zero doubt that plenty of resources will be wasted on psychosomatic nonsense, because it's always disguised, and this language easily allows it. Plus there is all the pressure that will happen in secret, behind closed doors, which is where 99% of decisions are made.
The emphasis on clinical trials is also problematic. Clinical trials are not viable without a plausible mechanism to address a known pathophysiology, and we don't have that yet. Given everything that's happened with the debacle of LC research, it's very clear that money spent on clinical trials is entirely wasted at this stage. This is especially problematic because trials take years to slowly cruise from one end of the pool and back. They are one of the least effective and efficient processes known to humanity, and almost never work out, even when we know what to target. Which we don't.
If someone has a plausible mechanism for a drug that might work, it would be far more efficient to do basic research to validate this mechanism, rather than trying anything that might affect it. It's faster and cheaper, while actually serving the purpose.
This is not encouraging at all.
I feel not taken seriously with these ideas on this forum since months because half of the forum is obsessed with fighting PBW nonsense like you and the other half with the hypes around the drug study of Fluge and the genetics and machine learning project at Edinburgh.
I agree with you at least on the emotional plane. Yes, it's very frustrating.