STOP NORMALIZING asthma, chronic ear infections, eczema, food/seasonal allergies, and neurocognitive delays. What are we doing to our immune systems that is causing these OVER-REACTIONS in our children?
Vaccines contain adjuvants that are designed to create an immune RESPONSE. Perhaps these doses of adjuvants are creating an OVER response? With any pharmaceutical there is a possibility of overt action…
》too much blood pressure medication = low BP
》too much insulin = low sugar
》too much antibiotic = bye-bye biome balance, hello opportunistic virulent and resistant organisms
》too much immune system suppression = no immune response, risk for illness
What about too much immune system stimulation? What happens when your immune system is on high alert and you eat an allergenic food at the same time? What happens when you’re given this stimulation repeatedly as a newborn with an IMMATURE immune system that still prioritizes Th2 (inflammatory) response over a Th1 (antibody) response?
That sounds like chronic inflammation. Alike… asthma, chronic ear infections, eczema, and food/seasonal allergies. The neurologic disorders may be a byproduct of heavy metal exposure (we see this with Alzheimers and aluminum in brain tissues as well as brain disorders with Cobalt hips). There is potential here, too!
Newborn immune systems lack memory and are tolerant of antigens for a reason. Babies are born sterile. They are still learning boundaries and creating the flora in their bowels that will become a major component of their immune system for their lifetime. If their body created a Th1 response to every foreign substance, they wouldn’t survive in this world… as we live in symbiosis with the microbes on our skin, in our airway, and in our bowels. Newborns must be colonized with these organisms and build up those systems. How does chronic stimulation of the immune system fit into this matrix?
It does not make sense. Vaccines are given in several doses to “create antibodies” though we know that more are added because they are ineffective in doing that in the first 2-3 doses… probably due to lack of the Th1 response, eh? So, now we give these tiny bodies several doses of adjuvant along with a fragment of a genetic component or microbe without considering what complexes are made between those simultaneous IM exposures, nor do we even study them.
The ACIP, advisory council for immunization practices, does not perform nor require adequate studies! They STATE that fact in these meetings.
So, if you still think that the voice of several thousand concerned mothers and fathers is horsebalogna, your cognitive dissonance is strong. We don’t do this to create drama. We do this to create safer practices for future generations. Mothers and fathers should not have to prove that these practices are harmful. Robust scientific evidence (not industry jargon) should prove interventions to be SAFE before subjecting our most vulnerable populations to them. Concerns should be addressed with valid studies (again, not industry jargon).
Pharmaceutical studies are done on adult populations and medications are recalled for adverse events… I think it is time for a recall, but “biologics” are not considered ‘medications’ for that exact reason…
Are we trading short-term infection for long-term disease?
Are we damaging immune systems by overstimulating them in their development?
When do we start paying attention to the parents that witness their children’s struggle to breathe, eat, and feel well? A normal child should not battle painful skin, constant stomach disturbances, nor frequent episodes of intense ear infections. This was not our (parents born before 1995) reality of childhood and must be questioned.
Shalom, light, and love.