Spike detoxifying formulation with fibrinolytic Nattokinase may provide you the support needed post COVID mRNA technology gene injection vaccine; as the science matures & develops, consult with your
doctor on using this cheap, available, safe formulation from The Wellness Company (Foster Coulson); be sure to factor in allergies, if you are a bleeder (this is a blood thinner) or have intolerances
See link to product here:
https://www.twc.health/collections/covid19/products/long-haul-formula?ref=Paul
Vaccinated or not, toxic spike proteins pose a long-term threat to your health.
This revolutionary Spike Support Formula is the only product that contains nattokinase and dandelion root, researched to block and dissolve spike proteins inside your body.
Buy daily Spike Support and protect you and your family against the effects of COVID, vaccines, and shedding.
Top Recommendation by Health Consumer's Nattokinase.com!
From
$65.99/ Members $54.99
HOW SPIKE SUPPORT HELPS YOU
Spike Support Formula contains all natural, non-GMO, scientifically-supported ingredients:
Nattokinase has been researched to dissolve spike proteins and blood clots. Plus, it's soy-free.
Dandelion root may prevent spike protein from binding to your cells.
Selenium to help reduce stress, aiding in helping the body repair itself and recover.
Black sativa extract may facilitate cellular repair.
Green tea extract provides added defenses at the cellular level through scavenging for free radicals.
Irish sea moss is mineral-rich and could help rebuild damaged tissue and muscle.
https://www.twc.health/collections/covid19/products/long-haul-formula?ref=Paul
I have written about the Spike Recovery formulation in my substack and provide the link above for further consideration should you wish to examine it further for use (especially for long-COVID symptoms that are likely due to the impact of the constant spike protein production and its inflammatory effects on the vasculature as an example; it should be noted that Nattokinase has emerged as having a potential beneficial effect in the Prevention and Treatment of Atherosclerotic Cardiovascular Disease; additional research is urgently needed (comparative effectiveness research, large sample size, large event number, robust trustworthy methodologies) and the science is maturing and developing and refining but existing reports are quite favorable). The same can be said about the Spike Recovery formulation out of The Wellness Company.
See link again:
https://www.twc.health/collections/covid19/products/long-haul-formula?ref=Paul
I also draw your attention to a 2018 paper by Chen et al. on the role of nattokinase as a promising alternative in prevention and treatment of cardiovascular diseases.
SOURCE:
Abstract:
‘Nattokinase (NK), the most active ingredient of natto, possesses a variety of favourable cardiovascular effects and the consumption of Natto has been linked to a reduction in CVD mortality…
Recent research has demonstrated that NK has potent fibrinolytic activity, antihypertensive, anti-atherosclerotic, and lipid-lowering, antiplatelet, and neuroprotective effects…
This review covers the major pharmacologic effects of NK with a focus on its clinical relevance to CVD. It outlines the advantages of NK and the outstanding issues pertaining to NK pharmacokinetics. Available evidence suggests that NK is a unique natural compound that possesses several key cardiovascular beneficial effects for patients with CVD and is therefore an ideal drug candidate for the prevention and treatment of CVD. Nattokinase is a promising alternative in the management of CVD.’
Our argument is that with advisement by your doctor, and the fact that people are suffering now due to the effects of the spike protein (virus and devastatingly the vaccine), then the Spike Recovery formulation may hold benefit. We ask that persons who are breast feeding, who are on blood thinning anti-thrombotic medications, and persons under 18 years of age do not take this and always consult your physicians.
‘In summary, compared with traditional antithrombotic and antihypertensive drugs, NK is characterised by high safety, low cost, simple production process, oral availability, and long in vivo half-life. As such, it is expected to become a new-generation drug for thrombotic disorders or CVDs. Although human trials and clinical studies demonstrate the clinical benefits of NK in the clinical settings, there remain a number of limitations. However, all the available data are encouraging and promising and further clinical trials are needed to fully examine the prospect of NK as an alternative medication to tPA, aspirin, warfarin, or newer anticoagulants in the management of CVD. In the near future, it is possible that patients with CVD may need only a single NK pill to replace multiple drugs administered for the prevention and management of CVD, including tPA, antihypertensives, statins, aspirin, and warfarin.’
I draw your attention to a prior substack by me:
THere is only 2000 FUs of Nattokinase per two caps of this product. That seems on the low side if someone is dealing with a spike issue.... I would think 4000 FUs at a min per day, but the therapeutic dose for destroying the spike protein may be 4000s FU three times a day/// Does anyone really know?
I have started on Natto NKCP, mainly due to age + possible spike contamination via shedding. But, in the same paper referenced here it states:
One key question that has not been adequately addressed is the mechanism by which NK is absorbed into the bloodstream after oral administration. There is no current convincing data available to demonstrate the bioavailability and metabolism of NK administered as an oral dose.
In fact, several groups have pointed out that the molecular size of NK is considered to be generally too large for oral absorption through the GI tract. It is recognised that NK may be susceptible to chemical oxidation and subsequent inactivation, or denaturation, in the GI tract. Thus, further studies are required to fully understand the pharmacokinetics of NK.
-Since the molecular weight of the Nk molecule is 28 kDa, yet drug absorbtion of molecules heavier than around 500 Da is poor in the intestinal tract - how does it get into the body???