MRNA Injection


Please be advised that to support the wellbeing of the men and women that work and come to Back Door Spa property, we will not be accepting people who have taken the experimental MRNA Covid injection within 30 days of their appointment.


This decision is based on the fact that the manufacturers have not accepted any financial liability for compensating any adverse events of their MRNA Covid injections, in fact in New Zealand they have been granted indemnity by the government. In New Zealand the injection has only been given provisional approval by MedSafe with 58 provisions. Furthermore we have taken into account the lack of animal trials (especially long term safety studies), lack of long-term human trials and a lack of comprehensive trials which include a true representation of the population (not just the healthy) as well as lack of reporting the effects of the injection on human reproduction. Many of these concerns are shared by MedSafe in their Summery of Risk Management for the Covid injection.  We are also aware of past animal trials in 2012 with MDNA injection technology where animals suffered from pulmonary immunopathology on challenge with the SARS virus. Finally, we are considering worldwide vaccine adverse reaction reporting systems such as this one which according to this government report (page 6, third paragraph) only represent 1% of the actual numbers and yet already show alarming rates of adverse reactions.


The purpose of this law is to protect men and women at Back Door Spa from possible spike protein viral shedding (which according to this study impairs endothelial function via down regulation of ACE 2) prevent overall transmission from injected persons to non injected persons according to this Pfizer document (bottom of page 67) and also to prevent possible contraindications of our services with the possible negative side effects of the experimental injection. A new article explaining spike proteins and possible reasons for so many of the following side effects including links to studies, can be found here. Reported side effects that concern us include and are not limited to; flu symptoms, miscarriages, still births, infertility, seizures, blood clotting disorders, autoimmune disorders, neurological damage, prion disease, encephalitis, brain damage, Bell's Palsy, myocarditis and pericarditis (according to this FDA document page 7) and death. These effects and more can be found in this FDA document on page 17 already in October 2020.


We apologize for any inconvenience and we will re-evaluate the situation when clinical trials of the experimental injections are completed in 2023 (see Pfizer study with beginning date April 29th, 2020 to completion date May 2nd, 2023) or when new information comes to light. 


Thank you for your understanding.