Billy_Bob
Diamond Member
From the top, I am not "anti-vax". So please do not go there. I am posting this as a person with extensive knowledge in the medical field and simply posting empirical observations.
Modified RNA vaccines (mRNA) are designed to look for common parts of a virus. This makes creating a quick vaccine very easy but it also has negative problems that we are now having to deal with.
Modified RNA vaccines look for "parts" of the virus, not the virus itself. While they will lessen the severity if you do become infected, once the antibodies are gone its the same as never having seen the virus, as you body did not have to heal and create B and T cells in your bone marrow. The antibodies were triggered by a part of a virus and not the virus, in this case, the "spike proteins". You gain no long term protections.
This is also why you can become infectious to others. The virus grows unabated until there are sufficient "spike proteins" to trigger a response from your immune system. This is why people get ill, become infective, but have very mild cases. It is the lack of healing and the trigger by spike proteins which stops the body from creating long term immunities in B and T cells. Once your antibodies are gone from this mRNA vaccine your body has never seen or reacted to the actual virus, you are now a walking time bomb again to have a very sever case.
In summary;
* The "trigger" for your immune system is the spike proteins and not the virus. The human bodies immune system never trains itself to look for the virus. No long term immunity is formed.
* Once the active antibodies are gone from a mRNA virus you are again at risk to become ill. Without the formation of long term immunities in your bone marrow which look for the virus you do not gain these.
* Because the mRNA vaccine trains the body to look for the 'spike proteins', the virus will run rampant until it creates sufficient mass to trigger the antibody response from the spike proteins. This time period allows the viral load to amass and the person to become infective to others. The body never responds to the virus as a threat. The antibodies will attack anything that has the spike proteins present so it kills the infection.
* mRNA antibodies rapidly decrease at 3-4 months. By 5-9 months they are insufficient to foster further protections.
* mRNA vaccines cause swelling of cardiac tissues in persons under the age of 25 and blood clots in women.
The studies coming out about the efficacy of the mRNA vaccines is stunning. Problems, like viral transmission, were not foreseen by the creator of the method. While this method does make early vaccine intervention possible, it is not a long term solution to endemic viruses such as COVID-19. Using identifiable parts of a virus can give some protection to mutation outbreaks, if the right part is used, but it can also have unforeseen bad outcomes.
In My Opinion, the fact that mRNA vaccine are incapable of creating long term memory and immunities makes them a stop gap measure until a more suitable vaccine can be created which does. Now Europe is seeing its third wave because of waning vaccine antibodies. Something needs to change fast or this will cycle never stop. I am glad that I have had the virus and have acquired (non-vaccine) driven immunities. My body has long term memory cells so my problem is over as far as COVID 19 is concerned.
References:
pubmed.ncbi.nlm.nih.gov
Modified RNA vaccines (mRNA) are designed to look for common parts of a virus. This makes creating a quick vaccine very easy but it also has negative problems that we are now having to deal with.
Modified RNA vaccines look for "parts" of the virus, not the virus itself. While they will lessen the severity if you do become infected, once the antibodies are gone its the same as never having seen the virus, as you body did not have to heal and create B and T cells in your bone marrow. The antibodies were triggered by a part of a virus and not the virus, in this case, the "spike proteins". You gain no long term protections.
This is also why you can become infectious to others. The virus grows unabated until there are sufficient "spike proteins" to trigger a response from your immune system. This is why people get ill, become infective, but have very mild cases. It is the lack of healing and the trigger by spike proteins which stops the body from creating long term immunities in B and T cells. Once your antibodies are gone from this mRNA vaccine your body has never seen or reacted to the actual virus, you are now a walking time bomb again to have a very sever case.
In summary;
* The "trigger" for your immune system is the spike proteins and not the virus. The human bodies immune system never trains itself to look for the virus. No long term immunity is formed.
* Once the active antibodies are gone from a mRNA virus you are again at risk to become ill. Without the formation of long term immunities in your bone marrow which look for the virus you do not gain these.
* Because the mRNA vaccine trains the body to look for the 'spike proteins', the virus will run rampant until it creates sufficient mass to trigger the antibody response from the spike proteins. This time period allows the viral load to amass and the person to become infective to others. The body never responds to the virus as a threat. The antibodies will attack anything that has the spike proteins present so it kills the infection.
* mRNA antibodies rapidly decrease at 3-4 months. By 5-9 months they are insufficient to foster further protections.
* mRNA vaccines cause swelling of cardiac tissues in persons under the age of 25 and blood clots in women.
The studies coming out about the efficacy of the mRNA vaccines is stunning. Problems, like viral transmission, were not foreseen by the creator of the method. While this method does make early vaccine intervention possible, it is not a long term solution to endemic viruses such as COVID-19. Using identifiable parts of a virus can give some protection to mutation outbreaks, if the right part is used, but it can also have unforeseen bad outcomes.
In My Opinion, the fact that mRNA vaccine are incapable of creating long term memory and immunities makes them a stop gap measure until a more suitable vaccine can be created which does. Now Europe is seeing its third wave because of waning vaccine antibodies. Something needs to change fast or this will cycle never stop. I am glad that I have had the virus and have acquired (non-vaccine) driven immunities. My body has long term memory cells so my problem is over as far as COVID 19 is concerned.
References:
Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine - PubMed
The mRNA-1273 vaccine showed 94.1% efficacy at preventing Covid-19 illness, including severe disease. Aside from transient local and systemic reactions, no safety concerns were identified. (Funded by the Biomedical Advanced Research and Development Authority and the National Institute of Allergy...
pubmed.ncbi.nlm.nih.gov
