together with the now 4 cases of stiff man syndrome that Petros has brought back to life, the case shown here of a regeneration of BSE = Creutzfeldt-Jacob (CJD) = Mad Cow Disease is simply mind-blowing! Unimaginable! Simply shifts the perception of possibilities!
If I hadn’t seen it and seen it myself, I simply wouldn’t believe it!
Petros had repeatedly told me on the phone or when we met about this patient here in recent months.
He has personal experience with BSE because around 10 years ago the wife of a good friend of his died of it in 3 months and he was able to observe this but at that time he had not yet known about the power of neuromodulation.
Now – after 9 months the case is going so well that he can show it here.
Creutzfeld Jakob is a horrific disintegration of the brain, in a few months those affected deteriorate completely and die. The cause is known, there is no treatment, you can only watch. Terrible!
Petros says that the patients age by 10 years within a week and you can watch them turn 70-80-90 years old and finally deteriorate and die.
Case report
Petros has written permission from the family to publish this data including the findings.
The patient was successfully operated on for a meningioma (benign brain tumor) and was in good condition post-op.
Sudden deterioration in hospital, increasing hallucinations, unable to eat, within 30 days finally “moribund” (unconscious).
Prions were detected twice, once in a Cypriot laboratory and once in a university clinic laboratory in Germany – so the diagnosis is fixed.
Relatives took her home to die and called Petros again, who drove there and started brain stimulation. Miraculous regeneration within several months so that she was finally able to attend her granddaughter’s wedding and dance!
Patient before neuromodulation
Patient after several months of neuromodulation
I have edited together a few short sequences from the approximately 30 videos that Petros made during the course of the treatment.
German lab report
yes – the CFD protein was low – but that was also at the beginning of the illness, the patient continued to deteriorate until she showed the picture above in the video
Discharge report
Dear people
I have been in clinical practice for over 30 years, after this time you have seen almost everything and know what is possible and impossible.
for example, here are the possibilities for improvement in cases of severe spastic paralysis (from birth). This is also just as unbelievable, just as fantastic and here I have shown my own case here and Petros has several cases of spastic cerebral palsy that have been very clearly improved.
This is such an “impossible case” that I have only experienced once before with a “miracle colleague”:
Miracle Doctor Dr. Prafull Vijayakar - Homeopath in India
during the courses completed around 20 years ago with the sadly deceased Indian ultra-homeopath Dr. Prafull Vijayakar, where I also saw long-term video courses where Prafull documented the patients on video every 1-2 months and you could “watch live” the course of the treatment:
a 12-year-old boy blind/deaf from birth with brain defects (including corpus callosum defect and occipital defects) who was completely “lifeless” began to see and respond to being spoken to within a year: In the video, his mother lets him choose different colored pencils, and he picks up the right ones. You have to imagine the parents’ euphoria, that’s what makes these videos so believable
a 24-year-old boy with trisomy 13 (Down syndrome) started to speak and write within a year and his mother was able to send him shopping alone: “come on Ravi, come on, show the doctor how you can write now! Isn’t that fantastic, may God bless her and her whole family!” (I can still remember something like that – 20 years ago – but yesterday’s patients are quickly fading from my memory)
a boy with spastic paralysis caused by a congenital genetic disease (confirmed by genetic testing) where blood vessel tumors destroy the brain “Morbus Hippel-Lindau” who recovered within a year and the repeat genetic testing showed that the genetic disorder had disappeared, so it was carried out a second time with confirmation that the genes were “cured”.
a doctor – neurologist – who woke up after 17 years in a coma after cerebral tuberculosis and said in a video interview that he is working again and does not feel that he has any deficits, he is back to how he was before (homeopathic remedy was methylene blue C200)
a man who suffered from severe carbon monoxide poisoning in an Indian well shaft with “brain death” (no more brain activity in the functional MRI) – who, after a 1-year coma, was recovered with a homeopathic remedy (Oxygenium C200 – administered 3 times this year) to the extent that he was able to do housework at that time
a 10-year-old girl with agenesis of the hand, where the hand that had been missing since birth grew back within a year (we watched monthly videos)
those were simply unforgettable impressions. Vijayakar homeopathy is probably the most masterful form of therapy there is, but for me it is “too advanced” because my memory is not good enough for it. Prafull had a photographic memory and repertorized fantastically in his head.
He also sometimes 10,000 people treated in one month with his 10 assistants (free of charge, they traveled for weeks from all over India) – who knows how many he had these incredible effects on. The Indians are also very, very compliant:
I remember an Indian case with primary biliary cirrhosis who, based on his doctor’s recommendation, drank ONLY and EXCLUSIVELY camel milk for 1 year. After a year, everything was just as bad, the doctor simply said “one more year”.
With Petros you learn scientific study-based modulation of the brain. This method is currently still Level 2 EBM and not yet in accordance with guidelines, so we cannot speak of “treatment” because it is not yet an official “therapy”. But it will certainly become a standard therapy accepted worldwide in the next few years, patients are already making sure of that – because doctors also get old and get neurological diseases.
If you want to be critical …..
you would of course doubt the diagnosis. 2 positive CJD laboratory tests in 2 independent laboratories, the almost prototypical course that would undoubtedly have led to death – I’m not sure whether we have the right to diagnose any post-OP (meningioma surgery preceded) brain stem disorder with failure of the reticular system (formatio ret)
these days it is easy to get an overview of this and ChatGPT agrees with the discharge diagnosis.
ChatGPT about the clinical symptoms
The symptoms described – increasing confusion, hallucinations, refusal to eat and drink, unconsciousness and a moribund state – indicate a global dysfunction of the brain in which various brain regions can be involved. Here is an overview of possible structures involved and their functions:
Involvement: Confusion and hallucinations could be caused by disorders of the cerebral cortex, especially in the association areas of the parietal and temporal lobes.
2. Limbic system (including hippocampus and amygdala)
Function: Emotions, memory, and behavior.
Involvement: Hallucinations and behavioral changes can be triggered by a dysfunction of the limbic system.
3. Thalamus
Function: Filtering of sensory information, regulation of consciousness and alertness.
Involvement: Disorders in the thalamus can lead to confusion and loss of consciousness.
4. Hypothalamus
Function: Regulation of hunger, thirst and autonomic functions.
Involvement: Dysfunction could explain food and fluid refusal.
5. Reticular formation (in the brain stem)
Function: Maintaining the state of alertness and vital functions.
Involvement: Loss of consciousness and transition to a moribund state could be due to impairment of the reticular formation.
6. Basal ganglia and prefrontal cortex
Function: Control of movements and complex behavior.
Involvement: Behavior and decision-making, such as refusing to eat, could be influenced by dysregulation of these structures.
Pathophysiological mechanisms:
Metabolic causes: Hypoglycemia, electrolyte disturbances, uremia (especially in cases of impaired renal function such as a GFR of 42), hepatic encephalopathy.
Toxic causes: Medications, alcohol, drugs or endogenous toxins.
Neurodegenerative processes: Alzheimer’s, Parkinson’s or other dementias.
Infections: encephalitis, meningitis, or systemic sepsis.
Structural damage: ischemia, bleeding, or tumors.
For an accurate diagnosis, imaging procedures (e.g. MRI/CT) and laboratory tests are essential to identify the underlying cause.
If two independent laboratory tests for Creutzfeldt-Jakob disease (CJD) are positive, this indicates a very high probability that this is indeed the disease. The symptoms described (confusion, hallucinations, refusal to eat, loss of consciousness) fit well with the typical clinical picture of CJD, especially in the advanced stages.
Pathophysiology and brain regions involved in CJD
CJD is a prion-related neurodegenerative disease caused by misfolding of the prion protein (PrP^Sc). This leads to:
Rapid neuronal loss (spongiosis, gliosis) in various brain regions.
Diffuse involvement of the central nervous system, in particular:
Unconsciousness: Progressive loss of brain function.
Prognosis
CJD usually progresses rapidly and is usually fatal within a few months of the onset of symptoms. There is no curative therapy; treatment is purely symptomatic and palliative.
A thorough neurological assessment, based on test results and imaging procedures, is essential to confirm the diagnosis and plan further care.
About Creutzfeldt-Jakob: cause and progression
Creutzfeldt-Jakob disease (CJD) is a rare and serious brain disease. It is caused by so-called prions – misfolded proteins that also cause healthy proteins in the brain to misfold.
These prions damage the brain and cause it to literally “break down”, become full of holes and completely dissolve.
Cause of prions? Spontaneous (possibly genetic) through infection with prions (e.g. via contaminated tissue or medical interventions).
Known as Mad Cow Disease – was transmitted to humans via infected hamburgers.
The disease begins slowly, with symptoms such as memory problems, confusion or unusual behavior.
As the disease progresses, the symptoms worsen quickly:
Those affected lose their mental abilities, have movement disorders and fall into a coma.
Unfortunately, the disease is always fatal, usually within a few months to a year.
There is currently no cure. Treatment focuses on alleviating the symptoms and supporting the patient as best as possible. Scientists continue to conduct intensive research to better understand the disease and one day find an effective therapy.
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