Whistleblower from Berlin nursing home: the terrible dying after COVID vaccination
WHISTLEBLOWERS
For the first time, there is an eyewitness report from a Berlin nursing home on the situation after the vaccination. It comes from the AGAPLESION Bethanien Havelgarten retirement home in Berlin-Spandau. There, within four weeks after the first vaccination with the BioNTech/Pfizer vaccine Comirnaty, eight of 31 seniors, who suffered from dementia but were in good physical condition according to their age before the vaccination, died. The first death occurred after only six days, and five other seniors died approximately 14 days after vaccination. The first symptoms of the disease had already appeared shortly after the vaccination. From information available to 2020News the patients
have not been duly informed about the risks of this vaccine. One reason being that no detailed information about the novelty of this mRNA vaccine which has only conditionally been certified in the European Union have been provided.Attorney at Law Viviane Fischer and Attorney at Law Dr. Reiner Füllmich of the Corona Committee spoke in a video interview with the whistleblower about the closer circumstances of the vaccination, the symptoms that occurred and the different nature of the deaths in temporal connection with the vaccination.
On January 3, 2021, 31 female and male residents of the dementia ward “ground floor/protected area” had been vaccinated with Comirnaty. Relatives of another three seniors had objected to vaccination, and two residents were in terminal care, so no vaccination was given.
The residents of this ward are very active, “self defending” dementia patients who are physically in good condition. They are allowed to move around the ward all day without restriction. The day before the vaccination, the 31 vaccinated persons were all in good health. A few days earlier, all had tested negative for Corona, according to the whistleblower report.
According to the whistleblower, the first vaccination event with Comirnaty on January 3, 2021, took place in such a way that all residents were gathered in the recreation room of the first floor area. A vaccination team consisting of an aged vaccinator, three aides and two federal soldiers in camouflage uniforms performed the vaccinations. The home staff as well as the home physician assisted in the process. The role of the soldiers, who at no time moved away from the vaccine, has not been conclusively determined.
What the whistleblower was able to establish, however, was that the presence of the uniformed men greatly intimidated the seniors. The group, which normally shows a “strong defensive behavior” in the case of unfamiliar treatments, was hardly recognizable, so predominantly “lamblike” they had let the vaccination with Comirnaty pass over them. The whistleblower suspects that this could also be related to the fact that the elderly seniors, who had still experienced the war, could not properly assess the role of the soldiers and possibly felt reminded of war-traumatic circumstances.
During the first vaccination, a resisting senior citizen was detained by a nurse under the watchful eyes of the German soldiers, the eyewitness reported. A judicial decision for the detention, which as such represents a coercion and therefore requires in principle a judicial evaluation in the individual case, had not been issued.
According to the whistleblower’s account, the administration of the second vaccination dose took place without warning always on the spot where the person to be vaccinated was found. For example, an elderly lady lying unsuspecthe ingly in bed who began to resist the second dose was restrained by two members of tnursing staff in order to overcome her resistance – again without the necessary court order. The swabbing for the PCR test, which some seniors tried to resist, is also regularly done with the use of physical force against the seniors resisting the unwanted treatment, the whistleblower said.
According to the whistleblower, the vaccination education of the caregivers and relatives – the seniors are unable to effectively consent to vaccination due to their dementia – was based on outdated information sheets from the RKI/Grünes Kreuze. In particular, the information required by Regulation (EC) No. 507/2006 on the fact the vaccine Comirnaty has only been granted conditional marketing authorization and why this is the case is missing. In particular, the information should have been provided that from the point of view of the regulatory authority EMA, the data situation still needs to be improved with regard to various aspects, e.g. the interaction of Comirnaty with other drugs.
Already on the day of vaccination, four of the vaccinated seniors began to show unusual symptoms. In the evening of that day they were fatigued and extremely tired, some of them fell asleep at the table during dinner. A sharp drop in blood oxygen saturation was noted. In the further course, the leaden fatigue continued, the oxygen saturation in the blood remained insufficient, in some cases gasping breathing occurred, and fever, edema, skin rash, a yellowish-gray discoloration of the skin, and a (characteristic) muscle tremor of the upper body and arms occurred.
The seniors also showed a change in demeanor, were partially unresponsive, and refused to eat or drink. One vaccinated senior, who had previously been “in great shape” for her age and suffered from no serious previous illnesses, died as early as January 9, 2021, just six days after vaccination. Deaths among vaccinated seniors and senior citizens occurred on January 15, January 16, January 19 (2 deaths), January 20, February 2, and February 8, 2021. The most recently deceased senior citizen was a former opera singer who had been playing the piano the day before vaccination. The whistleblower reports on the state of health that the old gentleman regularly went jogging, danced, played music and was otherwise very dynamic and active.
Of the seniors who tested negative before vaccination, various suddenly showed a positive test result after vaccination. However, all of these seniors did not show any of the known COVID-19 symptoms, i.e., symptoms of colds such as cough, cold, loss of sense of smell and taste, etc.
On January 24, 2021, the second dose of Comirnaty was applied to 21 seniors. After this vaccination, according to the whistleblower, eleven seniors are now showing persistent extreme fatigue, partially gasping for breath, partially edema, skin rash, and the yellowish-grayish skin discoloration. As of February 10, 2021, none of the seniors who received the second dose of Comirnaty has died, but the health of some of the seniors in this group is steadily deteriorating.
The whistleblower impressively describes the different nature of the dying process of the vaccinated. Normally, the person dying would eventually accept their approaching death and – perhaps after seeing a loved one for the last time – go in peace. Dying as after vaccination, however, was different, he said. It is “inhumane.” The old people he had seen dying had breathed heavily, trembled strongly, and seemed as if inwardly they had passed away already. It seemed to him like a lonely, futile struggle against death, as if “the people knew that their time had not yet come, and therefore they had not yet been able to let go.”
The AGAPLESION Bethanien Havelgarten senior citizens’ residential home was requested to comment on the events on February 3, 2021 by Attorney at Law Viviane Fischer, in the name and on behalf of two journalists researching the topic, but has still not received a response.
Attorney at Law Viviane Fischer filed a criminal complaint with the public prosecutor’s office on February 3, 2021, 12:04 a.m., and informed the police as well as Prof. Klaus Cichutek, the head of the Paul Ehrlich Institute, which is responsible for recording vaccination side effects, and the Senator for Health of Berlin, Dilek Kalayci, about the events. The health department was also informed, as well as the office of the senate administration responsible for nursing homes.
Lawyer Fischer requested the public prosecutor’s office to secure the body of the last deceased old gentleman, She alerted the officials to the imminent death of the eighth death victim, which was to be feared at that time promptly. In the meantime he succumbed to his illness.
Upon telephone inquiry on February 8, 2021, the file could not be found in the registry at the public prosecutor’s office. Such a registration, so it was communicated, can in Corona times take up to six weeks.
On February 8, 2021 Attorney a Law Fischer has therefore additionally filed a criminal complaint via the Internet guard of the Berlin police.
A press inquiry with view of initiated investigations, seizure of the corpses and possible similar occurrences in the past examined by the authorities, which Attorney at Law Fischer had placed again in agency of the two journalists on February 8, 2021, answered the police in the evening of February 9, 2021, as follows: “So far the Berlin police led no investigations in connection with the deaths described by you. Such investigations are always initiated when a doctor certifies a non-natural cause of death when issuing the death certificate. The two deaths you mentioned are also not known to the Berlin police. In this respect, no investigations were conducted nor has the body of the deceased been seized. The criminal charges filed by you are available to the Berlin police and are currently being investigated by a specialist department of the criminal police or by the Berlin public prosecutor’s office. Information for this can be received from the press office of the public prosecutor’s office in Berlin.”
The investigation behavior of the police presenting itself at present as little engaged stands in contrast to the legality principle and pursuit obligation for criminal offences, to which police and public prosecutor are subject, Attorney at Law Dr. Fuellmich states. A violation of this could justify the reproach of an obstruction of justice in the office pursuant to § 258 a StGB.§ Section 160 (I) sentence of the Code of Criminal Procedure stipulates: “As soon as the public prosecutor’s office becomes aware of the suspicion of a criminal offense through a report or by other means, it must investigate the facts of the case in order to decide whether to file a public complaint.” Section 163 (I) sentence 1 of the Code of Criminal Procedure stipulates: “The authorities and officers of the police service must investigate criminal offenses and issue all orders that do not permit any delay in order to prevent the case from becoming obscure.
It would therefore be contrary to current law for the police to take action only when the family doctor, emergency physician or even the vaccinator himself filling out the death certificate confirmed an unnatural cause of death. It was already questionable whether an external physician, who in case of doubt could not know the medical history in detail, would at all be able to assess the situation and the dying process correctly. According to Dr. Fuellmich, the lawyer, there is undoubtedly a considerable initial suspicion that the extraordinary accumulation of deaths – otherwise only one or two seniors die per month in the respective department of the nursing home – was not due to natural causes.
With regard to the eleven seniors whose health condition had deteriorated after administration of the second dose of Comirnaty, there was also imminent danger.
The police, the health offices and the senate administration have a guarantor position to avert danger for the population. If the persons installed to fend off danger from the public do not follow their obligation, a punishability of the acting persons because of active assistance and/or assistance by omission to the body injury (possibly even with death consequence) – committed while in office – comes into consideration, Attorney at Law Fischer states. Also a negligent act participation must be examined. In order to avoid dangers for possible future victims the police is obligated to immediately start professional investigations. Post-mortem examinations must be carried out. A retreat to a possible theoretical assessment of police experts, as this was indicated to Attorney at Law Fischer by the police department in charge (LKA 115, offenses against humans), could not be accepted. The question, which symptoms develop after a vaccination and possibly cause the death of the patient can at present not be answered by any expert simply because up-to-date no study exists for instance regarding the endangerment of old humans by the vaccine. In particular no interaction studies regarding other medicines have been performed. After deaths in Norway following the Corona vaccination, the vaccination of very old, fragile people is no longer recommended in Norway.
The causal relationship between vaccination and the accumulation of deaths, especially among the elderly, is such that government action is urgently needed to protect the health and lives of all those willing to be vaccinated and those who have already received a dose of Comirnaty. The precautionary principle may include temporarily suspending the use of this vaccine for the duration of a full and transparent investigation into any role it may have played in the deaths of the elderly whose fates are the subject of this article.
These governmental measures should also be taken, in particular, for the benefit of those who wish to visit vaccination centers, are residents of retirement or nursing homes, or have a job in health care with contact with patients.
Comirnaty seems by no means as safe as one might think based on the government’s vaccination campaign and the many public statements by politicians and experts who support the government’s lockdown course.
Comirnaty is a so-called mRNA (messenger ribonucleic acid) vaccine. The mRNA contains the “blueprint” for a protein on the surface of SARS-CoV-2. Through vaccination, this blueprint enters the body cells of the vaccinated person via tiny fat particles (fat nanobodies). These are then supposed to produce a protein that is found on the surface of the virus. This is intended to induce a response in the immune system that will in turn cause an appropriate immune response to occur in the event of subsequent infection with SARS-CoV-2.
Because of the unusually short duration of clinical testing on humans, it is obvious from the point of view of 2020news.de that not all possible negative effects of this vaccine could be researched. In particular, experts believe there is a risk of the formation of antibody-dependent enhancement (ADE). This is the term used to describe antibodies that bind to the surface of viruses but do not neutralize them, instead leading to enhanced uptake of the virus into a cell and thus promoting the spread and multiplication of the virus. Infection-enhancing antibodies promote immunopathogenesis and constitute a long-known potential hazard of certain vaccines.
The occurrence of this hazard has been well documented for previous unsuccessful attempts to develop vaccines against coronaviruses (such as SARS-CoV). In some preclinical animal studies, test animals became severely ill or even died after encountering the wild virus because of the appearance of infection-boosting antibodies.
Experts also fear that the occurrence of autoimmune diseases and an impairment or endangerment of fertility, pregnancy, unborn life, breastfeeding with breast milk and children whose mothers were vaccinated during pregnancy cannot be ruled out. In their view the probability of the occurrence of these negative consequences could not – or not sufficiently – be investigated due to the design of the clinical trials in humans, which BioNTech/Pfizer conducted before the conditional approval of Comirnaty.
According to the assessment of the Paul Ehrlich Institute, the polyethylene glycol (PEG)-containing lipid nanoparticles contained in Comirnaty may, too, be possible triggers of observed serious reactions in connection with the vaccination. This is also troubling because in numerous preclinical studies, PEG liposomes have been shown to transport substances across the blood-brain barrier. Certain liposomes have also been linked to the death of specific cells in the liver and lungs in animal studies. For more details, see the recording of Corona Committee Meeting #37 (starting at 03:55:00).
According to the EMA Dashboard, as of February 12, 2021, 54,828 adverse vaccine reactions have already been reported. As of January 31, 2021, there were 26,849.
Because of the multiple concerns about the vaccine, a withdrawal request against the approval has already been submitted to the EMA. According to lawyer Fischer, Attorney at Law Dr. Renate Holzeisen will file an action against this approval, including summary proceedings, with the European Court of Justice (ECJ) in due time on behalf of clients residing in Italy. Such an action and such an application is possible within a period of two months after the conditional approval of Cominarty had been granted. According to lawyer Fischer, these proceedings will now also be accompanied by an international network of lawyers and scientists, to which the members of the Corona Committee also belonge. The judgment in the main proceedings and the decision in the summary proceedings will have an impact in all member states of the EU for which the conditional approval of Comirnaty has effect.
On February 12, 2021, the public prosecutor informed Attorney at Law
of the European Union (EU) of the European Commission (EU) of the
European Commission’s decision in the matter of the European
Commission’s decision in the matter of the European Commission’s
decision in the matter. This, in turn, is intended to induce a response
in the immune system that will cause an appropriate immune response to
occur in the event of subsequent infection with SARS-CoV-2.
Because of the unusually short duration of clinical testing on humans, it is obvious from the point of view of 2020news.de that
not all possible negative effects of this vaccine could be researched.
In particular, experts believe there is a risk of the formation of
antibody-dependent enhancement (ADE). This is the term used to describe
antibodies that bind to the surface of viruses but do not neutralize
them, instead leading to enhanced uptake of the virus into a cell and
thus promoting the spread and multiplication of the virus.
Infection-enhancing antibodies promote immunopathogenesis and constitute
a long-known potential hazard of certain vaccines.
The occurrence of this hazard has been well documented for previous unsuccessful attempts to develop vaccines against coronaviruses (such as SARS-CoV). In some preclinical animal studies, test animals became severely ill or even died after encountering the wild virus because of the appearance of infection-boosting antibodies.
Experts also fear that the occurrence of autoimmune diseases and an impairment or endangerment of fertility, pregnancy, unborn life, breastfeeding with breast milk and children whose mothers were vaccinated during pregnancy cannot be ruled out – in particular because the probability of the occurrence of these negative consequences could not be investigated or not sufficiently investigated due to the design of the clinical trials in humans, which BioNTech/Pfizer conducted before the conditional approval of Comirnaty.
According to the assessment of the Paul Ehrlich Institute, the polyethylene glycol (PEG)-containing lipid nanoparticles contained in Comirnaty may also be possible triggers of observed serious reactions in connection with the vaccination. This is also troubling because in numerous preclinical studies, PEG liposomes have been shown to transport substances across the blood-brain barrier. Certain liposomes have also been linked to the death of specific cells in the liver and lungs in animal studies. For more details, see the recording of Corona Committee Meeting #37 (starting at 03:55:00).
According to the EMA Dashboard, as of February 4, 2021, 41,140 adverse vaccine reactions have already been reported. As of January 31, 2021, there were 26,849.
Because of the multiple concerns about the vaccine, a withdrawal request against the approval has already been submitted to the EMA. According to attorney Fischer, attorney Dr. Renate Holzeisen will file an action against this approval, including summary proceedings, with the European Court of Justice (ECJ) in due time on behalf of clients residing in Italy. Such an action and such an application would be possible within a period of two months after the conditional approval of Cominarty had been granted. These proceedings would now also be accompanied by an international network of lawyers and scientists, to which the members of the Corona Committee also belonged. The judgment in the main proceedings and the decision in the summary proceedings will have an impact in all member states of the EU for which the conditional approval of Comirnaty has effect.
On February 12, 2021, the public prosecutor informed attorney Viviane Fischer in writing: “Your criminal complaint is already known here, but not yet recorded in our system, so I cannot provide you with any further information on this at present. However, within the scope of the permissible investigations, everything necessary will be arranged with the necessary acceleration.”
2020News will report on further developments.
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