White Clots and POTS: A New Path to Recovery?
A few days ago, I spent two hours discussing with Willem, a reader of “The Needle’s Secret” who was severely injured by the COVID vaccines.
Willem is a father of two, an accomplished sportsman who was severely harmed three years ago by the anti-COVID vaccine shots. During our conversation, Willem listed the many conditions he suffered after the shots: a stroke, Guillain-Barré, cognitive issues, loss of hair, thrombosis and the need for surgery to remove the clots, POTS or postural orthostatic tachycardia syndrome (you faint when you try standing up), bowel disorders, psoriasis, infections, Covid toes or blue toes with, more recently, black shards emerging from his toes…a nightmare that the medical authorities and community of his country, New Zealand, have been trying to downplay and to hide.
Several months ago, Willem contacted me to tell me he had read my Substack and “The Needle’s Secret”. He mentioned the Bolus Theory made all the sense in the world to him. He had recently bought a mild-HBOT system (see picture below), and within 10 sessions had started feeling much better, better than he had ever felt for over 2 years. In this long battle, this message gave me a feeling of hope for once…
Here’s what Willem wrote me:
“Bonjour Marc, I hope you’re well and enjoying the interviews that have accompanied the launch of your book. As one of the many vaccine injured, I thought I’d give you an update on the mHBOT therapy. I’ve been using my 1.5 Atmospheric Pressure with 100% oxygen mask for ten days consequently since it arrived. Various changes have happened with my POTS symptoms. One is that I don’t always have the tachycardia response, my heart rate is lowering and no longer spiking so high. This is a good sign, yet vascular constriction still isn’t working and I have had several fainting episodes. I’m not worried, I’m persistent. I am concurrently doing swimming every second day and have had very rapid improvements in endurance gain, without having the debilitating post-exertion fatigue. Something that wasn’t possible before the oxygen therapy.”
Overall, these past few months, Willem’s condition has been improving steadily. Even though an infection seems to have put him back some, his hair has come back, his toes are back to normal, the brain fog is gone, and his cognitive issues have disappeared. Friends compliment him on his pristine skin. His condition had significantly improved, but somehow, despite the visible reconstruction operated by his stem cells throughout his body, his POTS is still happening. Lower limb constriction is still not happening…
Even though the exchange was via video, we were both excited to finally meet face-to-face. I had originally hoped his POTS would disappear with OT, that body repair would take place, and I was intrigued by the fact he still had tachycardia and wanted to get to the bottom of it.
Willem and I spent two hours exchanging like old friends, his young sons occasionally peaking in to say friendly “hello”. The forty-year-old family man told me about his ordeal, about how an MRI scan had shown restricted diffusion in the left cerebellum, a known sign of a recent stroke, was dismissed as a machine error by an oblivious radiologist (!), and how he’d already spent 200+ hours in the mild-HBOT tent. Obviously, Willem has been very seriously injured. He is lucky to be alive. Did his repair needs exceed the norm (typically, 40 hours solve a lot of conditions, including advanced Parkinson’s)? Why was Willem still sick? Yes, his recent staph infection could explain going backward some. But, something was off…
My first hypothesis was that some kind of degenerative disease was at play, but given the number of hours in the mild-HBOT tent, his capillary leakage had to be mended. All the signs showed that stem cell repair had happened. That hypothesis didn’t make sense. What was I missing?
It is obvious that a large bolus of vaccine nanoparticles stormed through his body three years ago, in the intestines, the brain, the skin... The toe damage indicates the bolus went through the leg’s arteries. Mentally, I returned to the Bolus Theory map, and it hit me: White clots! Oxygen therapy couldn’t and wouldn’t solve white clots.
Of course! How could arteries in the legs constrict if a thick cast of white fibrin binds them?
To instantly constrict, our blood vessels need to be unhindered, and given the symptoms shared by Willem, the probability is very high that his endothelial walls have been damaged widely and would be covered with fibrin. I have covered at length in chapter 15 of “The Needle’s Secret”.
Only high-doses of fibrinolytics (Nattokinase, Bromelaine…) over months can progressively and safely erode the fibrin. Oxygen therapy wouldn’t do much good to sort this, and the body’s own fibrinolytic processes can’t deal with such a large surface area with day-to-day plasmin levels.
Some of you might argue this is speculative. Of course, the hypothesis requires further confirmation, but it makes sense from a physical standpoint, it is because vasoconstriction doesn’t happen that the heart needs to accelerate its rate to provide blood to the brain. It’s indeed possible other causes, like neuronal necrosis, are to blame. Nevertheless, given the high number of occurrences - I found 1,001 symptoms of POTS in VAERS - systemic hit on the arteries versus specific harm to nerves is much more probable, statistically speaking.
The high number of white clots found by embalmers suggests this hypothesis is highly likely. That could very well explain why so many are suffering from POTS…
Willem told me he had taken for nearly two year 2,000 FU of Nattokinase twice a day, which probably saved his life. But indeed, 4,000FU per day isn’t enough to clear up the white fibrin: the research paper I shared on Nattokinase in “The Needle’s Secret” states that 3,600 is ineffective.
The study also shows Nattokinase is a safe and well-tolerated treatment.
If my hypothesis is right, high-dose fibrinolytics open up a promising therapeutic avenue for people who suffer from POTS post-vaccine.
I would encourage people to discuss this therapeutic avenue with their doctor, and researchers to start getting to work.
On the safety side, I would suggest anyone with POTS considering Nattokinase, or any other fibrinolytic, to ensure that all vascular repair has occurred before using fibrinolytics. Oxygen therapy, whether normobaric or hyperbaric, can help to mend any holes. But, before taking away a BandAid (fibrin is a natural BandAid), one needs to ensure there’s no risk of bleeding. My friend, Steve Kirsch, was unaware of that risk when he started Nattokinase a few months ago, and, according to him, he lost vision in one eye because of that.
In any case, once again, face-to-face discussion, observation and attention to detail makes all the difference in the world. I want to thank Willem for his openness, his trust and his honesty. I hope this can be helpful to many POTS patients who have been suffering these past few years. Feel free to share this article widely.
I apologize for my silence recently. I am translating “The Needle’s Secret” into 5 other languages and trying to get traction in France, which has been time-consuming. My personal situation is still very complicated and stressful on the financial side, so feel free to subscribe, or to support my work on PayPal, and don’t hesitate to read “The Needle’s Secret” and share it widely.
A big hug to you all.
Marc
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This is frightening. My 18 yo grandson has POTS and is no doubt highly vaxxed. My daughter will hear absolutely nothing from me about any part of this nightmare. Nor will he. He is damaged by the HPV jab I’m sure. Neural injuries but of course that possibility is a no go topic. I dread phone calls from them as they are all jabbed. I 🙏🏻.
I have read your book, twice, and it is the only explanation for so many diseases that makes any sense. I am disgusted with a large portion of the “alternative” medical world who generally refuse to entertain that your thesis is plausible, and urgently needs to be explored further. Their ego, and being “right” is more important to them than getting the word out to help as many people as possible.
Your work has been the only thing that has given me hope with my wife’s recurrent miscarriage problem. Early in life she had a forced vaccination in Kenya of something which immediately and permanently changed her menstrual cycles. We think that she may have been affected by a Bolus of whatever was in that shot. Only one blood test comes back “bad” for her, which is Protein S…she has a deficiency. The doctors are undecided whether she clots too much or doesn’t clot enough, since they have blamed recent pregnancy losses on both of those things. The last loss was a partial molar pregnancy which was a horror for her.
Anyway, after reading your book, we looked into oxygen therapy and we have gotten a home unit with a concentrator that is supposed to be used while exercising. The thought is that is you get your heart rate up enough, your body will call for more oxygen while exercising, and it will be distributed more efficiently than through passive inhalation in a MBOT chamber. They also have a feature where you can “starve” your body with low oxygen for a few minutes, and then flood it with highly concentrated oxygen.
We just got it and have used it a few times. If it doesn’t work, we will try a home MBOT system. Hopefully something will allow her to have another child so our daughter will have a sister.
Thanks so much for all you do. I subscribe, but am not in a position to do anything else. We are living close to the edge with all the medical bills and others.
Joe