It seems that a small minority of the medical community is admitting the existence of problems associated with Covid infection with or without mRNA Covid injections. If you mention it happened after Covid, you will get sympathy; if you say your problems began after a vaccination, you will be shown the door.

Once purely the realm of conspiracy theorists, I have had patients tell me they have visited established academic medical centers for so-called Long Haulers or Long Covid.  Although the literature showing possible problems from autoimmune-like reactions to spoke protein exists, most clinicians don’t dare learn more about it because they personally, their families, and their patients are all potentially affected by the implications. Some current theories are that spike proteins can cause autoimmune reactions, increase blood-brain permeability, cause micro-clotting of small vessels, and therefore also engender nerve damage.

Trying to convince people that there many be adverse reactions to the very widely adopted mRNA therapies is difficult because of the cognitive dissonance surround science which became political in a climate where politics itself was religious. I actually had a mother tell me her 14-yo could no longer walk but that the consulting neurologist, instead of running imaging or lumbar puncture tests, insisted that it was psychosomatic after the mom suggested symptoms began after mRNA vaccination.

Sadly, nearly every week, I am contacted by a patient who believes their problems began with an mRNA shot or a Covid infection, but usually it is both. They usually have similar stories insofar as their problems began shortly after a vaccination, then lingered, then worsened after a natural Covid infection. The most common symptoms are 1) tinnitus with or without hyperacusis, 2) lethargy, headache, and brain fog, and 3) occasionally chest pain with or without palpitations, and rare dizzyness with standing (postural orthostatic tachycardia syndrome). Not surprisingly, they have all seem multiple doctors who insist that their symptoms couldn’t be related to the vaccines but they get a sympathetic ear if they only mention Covid because that supports the doctor’s beliefs that Covid is horrible.

My own 19-yo was given three doses that were mandated by his schools and was having chest pains for six months, especially when flying in a plane. After administration of IV exosomes twice, he has been without complaints for over six months. Even my brother, who is a pediatrician, thought my son had low grade myocarditis from the shots; it was right there on page one of the consent for those who bothered to read the consent, which I did. 

I attended medical school at Columbia University’s College of Physicians and Surgeons, which has since been renamed the Vagelos School of Medicine after an alumnus and benefactor, the CEO and Chairman of Merck. One of their blockbuster drugs was the much-maligned 2015 Nobel Prize winning Ivermectin, used to treat parasites and river blindness. Ironically, one of Dr. Vagelos’s proteges came to see me after experiencing brain damage from Long Covid. He had received three Pfizer mRNA shots, contracted the Delta variant of Covid, then took another two Moderna mRNA shots. After severe cognitive decline, he went to the Mayo Clinic’s Long Covid clinic where they confirmed his cognitive decline and brain damage were due to Long Covid and a neuroautoimmune condition. They only offered nutritional supplements, saying that the anecdotal use of MSC exosomes was not indicated.

In Contrast, Yale has a Long Covid Clinic which is openly treating long Covid with exosomes. This is a scientific article explaining the practice (which is inhaled nasal). Here is an excerpt of an article about their practice: https://researchfeatures.com/using-stromal-cell-exosomes-treat-long-covid-syndrome/

Administering MSC-exosome therapy via the nose, where they pass through the tiny spaces between the descending olfactory (smell) nerves and the skull of the cribriform plate, should allow these extracellular vesicles to move into the brain. This is a method already used in previous studies, that showed successful nasal administration of exosomes for other inflammatory conditions, such as multiple sclerosis, Alzheimer’s and Parkinson’s disease. Coupled with existing evidence that shows how MSC-derived exosomes can be used against acute COVID-19 infections, and in a variety of systemic inflammatory disease models and neuropathology models of Alzheimer’s and Parkinson’s disease in animals, it is postulated that it may also be possible to harness this approach for nasal administration of MSC-exosomes for treatment of the neuro psychiatric aspects of LCS