Dr Markov CBIS Theory of ME/CFS - General Discussion

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12
hi Civicko -
you will need to enable conversations invites in your profile

are you undergoing the Markov Treatment at the moment ?
What about now?

No, not yet, but I'm inclined to think that I have a streptococous overgrowth so it might be worth trying.
 

Atlas

"And the last enemy to be destroyed is death."
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142
Location
New Zealand
I began the fourth and final 10 injection course within the second 6mo cycle of treatment last week.

The first intradermal gave me a reasonable red inflammatory reaction, but unlike last cycle, the subcuts of this polyvalent vaccine are so far no longer giving me a large red swelling. There is only a barely noticeable invisible swelling and bruise.

Last time this lack of visible reaction only happened on the very last injection (the largest dose). So this progression suggests to me that my body is getting quicker at clearing the antigens. It could also be that it's getting better at ignoring them haha, but one would hope not.
 
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Dear ME/CFS-patients on PhoenixRising,

Markov clinic, Kiyv, Ukraine, and Dr.-med.Igor Markov inform you that despite the current known events in Ukraine, the remote (per Email/messengers/etc.) ME/CFS-for-CBIS (Chronic Bacterial Intoxication Syndrome) full diagnostics and treatment with anti-ME/CFS-CBIS autovaccines, individually for a patient prepared from autostrains of bacteria, isolated&idendified in urine cultured on dip slides, and delivered to a patient,
have been continuing as before.

Please welcome Markov clinic:
www.vitacell.com.ua
admin@vitacell.com.ua
 

kewia

Senior Member
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244
Would interest me likewise.

Is there already an overview, who has improved to what extent?
 

Blazer95

..and we built castles in the Sky.
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425
Location
Germany
Chronic bacterial intoxication is a posibility I kinda suspect being prevalent in me aswell. So this is kinda interesting.

If its as easy as getting a urine culture and doing an autovaccine From that is doubtful however. What if the bacteria sits Not in the urigential tract?
 

Atlas

"And the last enemy to be destroyed is death."
Messages
142
Location
New Zealand
@MonkeyMan as far as I know I am the only forum member still actively trying the treatment. Some other members have done a single 6-month cycle but stopped due to various reasons. At least 2 of those had temporary symptom improvements, but no full remissions. However, since the full treatment protocol is usually 4-6 cycles over 2-3 years, I'm hopeful that we just need more people to try for longer.

If there are others who expressed interest in trying the treatment and went ahead but have not posted, I am also interested to hear from them. (Please! :) )

...

Here's my update from August which I wrote in the private thread:

Update: I'm still doing treatment and my third vaccine cycle is currently being shipped to me.

I finished my last cycle mid March so it's been about 5 months off and though I could have restarted after ~3-4 months, Dr Markovs prescription did suggest a wait of 3-6 months before next cycle so not sure whether to record that as any time off or not. Probably to be consistent with last time will mark July as no treatment, because I would have restarted in July if not for long shipping times to get my dipslides there and get the vaccines back.

I'm not sure exactly when it happened but I have definitely been doing more than last year, although my brain does feel slightly more derealised right now because of overdoing it, I have been able to do a lot more daily cognitive activity than in previous years before my brain shuts down completely.

Actually it doesn't usually shut down the same any more with the same sort of brain fog, I just get "long" pem where I generally feel more derealised and less "conscious", instead of my brain becoming so fogged that I can't think. Which can still happen if I concentrate too much but less rapidly. Which makes it harder to pace because the punishment is not as obvious or rapid-onset.

But I think overall considering how much I have been doing I do have relatively more energy on average than last year. I don't know if this is relevant to the treatment or not.

I'm not sure it's a full or half level change but relatively it feels like something. Physically I'm still bedbound all day but do go out to the kitchen on a rollie stool and have been making my own fried eggs when my Mum is gone. I've also gone to the back door a couple times to put the cat out.

My absolute limits are still not much, like I was washing my earmuffs in the kitchen sink and it became painful pretty quick and my arms/wrist muscles literally fatigued to exhaustion before I could finish washing them.

But I don't know, I think there is some difference from before it's just maybe a 5% to a 7% so not a full half level I don't think.

And it is hard to tell because my energy levels fluctuate anyway.

Then again, there are other symptoms which have gotten worse, like myoclonic jerks which only showed up in the last ~year.


My sense of smell is still much improved.


Since then I have started the 3rd cycle. No big changes but I did seem to get a decent energy boost for a few days after the most recent injection group. E.g. I found myself able to work on my tax returns for a lot longer than usual, without hitting a brain fog wall. The energy boost has subsided somewhat now after I overdid it :/
 

Atlas

"And the last enemy to be destroyed is death."
Messages
142
Location
New Zealand
(Second part of the update from August)

These are some of the reasons I know the vaccines are acting in a positive way against ME/CFS however:

1. After the 8th polyvalent vaccine in last cycle, I woke in the night and it seemed like all my life memories had come back and I could remember things much more easily. Then I couldn't sleep and the next morning woke up head "hungover" feeling crashed again as usual. Prior to this experience, the same evening, I had experienced diarrhoea and a sense of stomach burning/stomach ache (on the day after that vaccine. The same thing happened last cycle). This ease of memory recall did not return again.

2. The feeling of being able to "see in 3d" the world again returned again for some mornings after the end of treatment, but then went back to how it was before. (To be precise it is not that my eyes changed, I can see in 3d, but brain is sluggish so usually feels derealized). In other words, derealization temporarily improved noticeably. [This happened again in October around the same time I got the "energy boost"]

3. My sense of smell which returned after the previous treatment cycle is still good. My nose is definitely clearer on average than it was before.
 

MonkeyMan

Senior Member
Messages
425
Thanks Atlas.
Unfortunately, my conclusion is: Markov's approach is virtually useless, at least for most patients.
 
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82
Location
Amsterdam, NL
Maybe it’s just a simple that the auto vaccines create a feverish immune reaction,
That can shortly reverse the low hypometabolic state our mitochondria and immune system are in.
- just like many patients have experienced improvements after a strong immune reaction (high fever) to an infection (Covid, bacteria) or Sometimes the Covid-vaccine
 
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Atlas

"And the last enemy to be destroyed is death."
Messages
142
Location
New Zealand
I have completed the 3rd vaccine cycle in early January. I am now cultivating new cultures both from urine and then from nose/throat.


Here is my update:

The 3rd cycle gave me energy boosts during the vaccination period where I felt considerably more energy than usual, although I was still severe, in bed most of the day, I found:

- more energy to talk — I could now often have 15min-30min and sometimes even longer conversations with my Mum or others without serious deterioration afterwards.

- Felt my voice naturally had energy to speak louder. I.e. I naturally without realising started projecting my voice again in conversations instead of the usual whisper talk that I do

- I found I had energy to sing

- more energy for going to get lunches. I usually roll on a stool to get my lunch now. I just naturally feel hungry to go get my own lunch, and feel enough energy to do it, instead of before always waiting for it to be brought. I even made dinner once, partly standing up (although this caused after effects, but not as severe as I would normally expect).

- I find I have energy to shower sitting down now most days. Showers do not usually make me wiped out for the rest of the day any more.

- Brain fog/cognitive stamina for some time, was considerably improved


Now, these effects started a little during each vaccine course, but most noticeably occurred and the highest energy boost I received was shortly after the nasal bacterial autovaccine (the last one, Staphylococcus haemolyticus 1 from the nose and 2 from urine).

Over time, these benefits declined as I did significantly more than usual and probably overdid it a little, and post-exertional effects declined me, to the point my brain fog was worse again, but when I rest for a day or two it improves and it is still not worse than before I started the last cycle.

My physical (not cognitive) energy is still more on average. (~3 months later)


All this to say, I found a more noticeable positive effect this time, and am hoping to continue treatment soon. Particularly I think the autostrains from nose/urine in the last vaccine seemed particularly noticeable in effect.

(This cycle I took nose/throat swabs to send to the clinic and the autovaccine which included bacteria from my nose seemed to give me the biggest boost)


I would say for 2 months after treatment ended I went up a half level according to the Phoenix Rising severity scale. Presently I'm in a crash and have declined back down about a quarter level.

I say a half level because on the scale I consider 1 to be where I go outside, and on a few of the better days I went outside to rest in the sun. That is not trivial at my level because requires going down and up a few steps and walking around the side of the house, and it did not cause a crash afterwards during those 2 months.
 

Atlas

"And the last enemy to be destroyed is death."
Messages
142
Location
New Zealand
I received some new info related to my current prescription and these vaccines in general if anyone is interested:

...

I had sent my latest samples to the Markov clinic and this time they only found Enterococcus Faecalis from urine samples and Staph Aureus in the nose.

Every prior time they found E. Coli in the urine samples, but not this time. They also found Streptococcus last time, but not this time.

1. Despite not finding these two bacteria any longer, Dr. Igor has still prescribed bivalent vaccines containing prebanked pathogenic strains of these bacteria species which were previously identified.

I asked if this was because he suspects these may still be present in the body even though they were not identified in this round of cultures. He confirmed this to be the suspicion.

He says that E. Coli frequently tends to hide "behind" the others, presumably in the biofilm. (I.e. even when not detected it is often identified later once the "front row" of other bacteria are killed off). If I understand correctly he suggests that Streptococci often do the same thing when in the nose. That's why my prescription is to continue to take vaccines made from those bacteria in addition to the autostrains identified.

1. Me: My question is, is the reason for continuing to take these bivalents because you suspect there is still a possibility that those bacteria (Strep and E. Coli) might still be present even though not detected?
1. Dr. Markov: You have understood everything correctly. The most part of diseases are caused by one pathogen. For example, measles, diphtheria, chickenpox, etc. In your case, Nephrodysbacteriosis in kidneys and the focus in the nasopharynx are polyetiological diseases caused by a team of bacteria. During culturing/isolation of bacteria, we “catch” the dominant strains that are currently “sitting in the front row of the parterre/stall”. But our experience has shown that behind them are just streptococci (in the nasopharynx) and E.coli (in the kidneys). Therefore, we confidently introduce them into the vaccine to speed up the treatment process. At subsequent stages of treatment, we use polyvalent vaccines that include the isolated strains as well as up to 15 different types of bacteria that we previously detected in similar cases. These are rhinodentavaccine, pneumovaccine and urovaccine. In your case, we have not yet reached this stage of treatment.

2. I asked if people have recovered when treated using only their identified autostrains, and he said yes, they did that starting 25 years ago, but about 10 years ago they found it sped up the process significantly when they started adding to the vaccines prebanked strains of the most pathogenic bacteria which had been previously identified (presumably in previous patients).

Since the vaccines consist of antigens from the bacteria, not the whole bacteria, they find that adding the banked strains to the process increases the immunogenicity of the vaccine.


2. Me: I remember you wrote somewhere that combining deposited vaccines with autostrains is more effective — is that correct? But do some people recover using only autostrains? How major is the benefit of the deposited strains in addition?
2. Dr. Markov: About 25 years ago, we used only strains of bacteria isolated from a patient. But the process of recovery moved slowly, with long intervals. Therefore, within about last 10-12 years, we began to use a combination of own bacteria (autostrains of bacteria) with a large set of deposited/deponited strains. We established our own museum of deposited strains and placed about 100 strains of the most pathogenic bacteria in the National Depository of Microbial Strains of Ukraine as reference samples for industrial production of vaccines (if it comes to that). Since vaccines contain only a set of antigens from destroyed bacteria, the vaccine becomes much more immunogenic (and gives a better clinical result of use), while remaining completely non-virulent (non-infectious). There are no living bacteria in vaccines, only their fragments. Just this is the basis for our patents, which we had received in 2018, for 9 mono-, bivalent- and polyvalent vaccines. Just their consistent/consecutive use ensures the best clinical result.


3. I also asked about the two Staphylococcus vaccines that I'm taking and if the Staph component is different in each of them.

The two vaccines are Staphylo-Primavac,
And a Staph-Strep bivalent which also contains my autostrains.

Dr. Markov's reply:
3. Me: Is there a difference in Staph bacteria between Staphylo-Primavac and Staphylococcus-Streptococcus Bivalent, i.e. is the Staphylococcus component in the bivalent also a revaccination?
3. Dr. Markov: No, there is no difference in the set of deposited staphylococci in monovalent and bivalent (with streptococci) vaccine. Both each have 80 strains of the same staphylococci. Simply, in the bivalent vaccine we necessarily/surely introduce autostrains that are absent in the purely staphylococcal vaccine. The dosages, schemes and place of administration also differ.
 
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