A few people have asked me to write up all the things I did in order to become a remote patient of the Markov Clinic (like where to buy dipslides, urine testing with dipslides, how to ship the dipslides to the Markov Clinic by Category B using Fedex, and so forth).
I've been working on a comprehensive write up, and when it's ready, I will put it online, probably in a few weeks. It's already nearly 6000 words. I hope to get the write up ratified by the Markov Clinic, to ensure everything in it is accurate.
Although rather than putting these instructions online, I was actually debating whether I should only give these instructions to ME/CFS patients who request them. This is because it would be best for the ME/CFS community to hear progress reports of any patients who get the Markov autovaccine treatment, so that we can all assess the effectiveness of the treatment.
If I put the instructions online, anonymous people might use them to become a remote patient of the clinic, but not actually take the time to inform everyone of their progress, so we lose useful data. Whereas if patients contact me to get the instructions, then at least I can ask them for progress reports every say 3 months, even if they do not post these details online themselves.
I can't see that any research group is going to rush to replicate Dr Markov's treatment in a clinical trial; so the only way for the moment that we are going get some sort of replication is via the anecdotal accounts of ME/CFS patients who try the autovaccine treatment. If we then get a handful of very positive results from patients, this might then prompt researchers to try to replicate the results.