The fact that I am having very mild viruses is indicative of the fact that I'm getting zinc into my cells. Maybe I could get even more but it appears that I have been nipping the viruses in the bud.
Speaking of zinc and copper I have always been mystified by the serum ranges that they use in testing. If you take the highest end of the zinc range and compare it to the lowest and of the copper range the ratio is only about 2 to 1. I believe the optimum ratio for zinc to copper is between 8 and 10 to 1. What am I missing here?
I think this whole Covid 19 bullshit would be over if big Pharma had not deep-sixed hydroxychloroquine. I have heard that QUERCITIN also works just as well

 

@brookway17 Have you considered -> Chitosan?

It is a derived from the shells of crustaceans such as crabs, shrimp, and lobster.

The use of chitosan in intranasal delivery of an influenza vaccine to healthy human volunteers produces systemic (IgG) protection.

Chitosan alone elicits both Th1 and Th2 responses, whereas alum triggers strong Th2 and very weak Th1 responses. In general, the Th1 response plays a dominant 27 role in adaptive immunity (a.k.a. acquired immunity) to viral infections, and is responsible for cellular immunity and killing of infected cells by cytotoxic T lymphocytes (CTL), whereas Th2 is humoral and promotes antibody production. Ideally, both Th1 and Th2 processes are elicited by appropriate antigens and adjuvants, and which to target by vaccination are likely to be pathogen specific. Spike protein stimulation of peripheral blood mononuclear cells (PBMC) of SARS-CoV-2 patients results in secretion of high levels of primarily Th1 cytokines, and elevated but much lower levels of Th2 cytokines. This suggests that SARS-CoV-2 infection provokes a primarily Th1 T-cell response, and a protective vaccine should similarly produce a primarily Th1-based prophylactic response.

Model of chitosan nanoparticle (CSP)-induced NLRP3 inflammasome activation and cross-presentation: Ag together with CSP (via adsorption or encapsulation) was internalized by APCs. The protonation of the amino groups (“proton sponge effect”) leads to an extensive inflow of ions and water into the lysosome, which causes the osmotic swelling and deconstruction of the lysosome. The entrapped components (CSP and Ag) are released and finally presented onto MHC I, by cytoplasm degradation (with proteasome and ER involved); After the rupture, lysosome enzymes, cathepsin B, was also leaked into the cytoplasm, which induced the assembly and activation of NLRP3 complex. The capacity of TLR4 stimulation of CSP also played an important role in the intracellular synthesis of pro IL-1β and triggered the secretion of IL-1β and inflammatory responses, together with NLRP3 activation. (Ag: antigen; CSP: chitosan particle.)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185844/


https://radvac.org/wp-content/uploads/2020/07/White-Paper-SARS-CoV-2-vaccine-ver-2-3-2.pdf

 

hey @JanSz,You were talking about some liquid selenium solution you were using. What was the name?

 

I always eat my shrimp with the shell on
I take IMUMRAN to manage my auto immune condition, it suppresses the production of T cells in my bone marrow. Therefore vaccines are not very effective with me, I do not believe in them anyway I am one of those wacky anti-vaxers. I think hydroxychloroquine and zinc is a much better approach to dealing with viruses since it works at a very fundamental level of the cell. If you do than you don't need to invoke your immune system

 

I used 20 drops/day first.
Now, after Spectracell analysis
I raised to 40 drops/day

https://www.amazon.com/BodyBio-Sele...ywords=bodybio+selenium&qid=1597881903&sr=8-1

 

Thanks Jan, so you are taking 1 mL per day

 

40 drops/day

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Did this unit work for you? Any metering done?