Remission My Way. No Hydrogel Rubber Clot in My Blood. Other Ways to Get There.

I have posted in the past how I have seemingly eradicated the hydrogel rubber clot by using ivermectin, fibrin proteases, a particular EDTA product and nutricuticals with unknown benefit toward this.

Most recently I have heard of several others achieving remission by other protocols. I think it is helpful to identify the components and hopefully find a safe and repeatable treatment.

I have been in conversation with Dr David Nixon MD from Australia via Zoom meetings. He has adopted the blood collection via vacutainer and centrifuge of the specimen to identify the hydrogel rubber clot that I had called gel/plastic (g/p) in prior posts. I recommend you follow davidnixon.substack.com for details.

Well, Michael Merrick has a protocol using the essential oils and in particular thieves oil (blend of clove, cinnamon, eucalyptus, lemon, rosemary). He also takes activated charcoal. He has a Telegram channel LAC microscopy https://t.me/+TxtC1NOznXw0YTZh

I will let Michael and Dr David Nixon explain the process on their channels as well as the precautions since 3 of the oils listed in thieves oil have toxicities (clove, eucalyptus, rosemary). It seems using the oils topically or to vaporize them is not effective in obtaining remission. Michael was applying the oil to his oral cavity in particular to his gums.

Well, another interesting finding by Dr Nixon is that when the vacutainer tube after showing no initial hydrogel rubber clot following the centrifuge proceedure does show what appears to be a hydrogel develop in the tube after several days after doing the thieves oil treatment. So after the thieves oil treatment the vacutainer tube appears clear of hydrogel rubber clot after being centrifuged but when allowed to rest (I assume refrigerated) for 3 to 4 additional days a gel develops in the serum region of the tube. I have not tried letting a negative tube set undisturbed for more than 24 hours and that will be addressed later in the post.

Another individual that participates in Dr Nixon's Zoom is William from the USA. By the way, you can participate in the Zoom if you are a paid subscriber to Dr Nixon's substack and if you have the time especially on Sat at 2 pm central for about 2.5 hrs you can hear from William and Michael. Back to William's story, his wife is a CRNA and was required to be vaccinated and likely explains William's exposure. He and his wife tested negative using the centrifuge method while taking many nutraceuticals. When he stopped his treatment the hydrogel rubber clot returned. I am sorry but the list of compounds may not be complete since I might have missed something but he was taking: methylene blue (20 drops), vit C 5000 mg, NAC 1000mg, glutathione, fish oil, aspirin 81mg, CoQ10 100mg, Calcitrate 250mg, vit D3 4000u, Centrum Silver 50 plus, glucosamine DS 1500mg, chondroitin 1200mg, B17 1000mg, zinc, humic acid, nano curcumin, nattokinase, boswellia,bromelain, quercetin, Immune Supplement Support, MedFive twice a day. It should be noted that his wife did not add the MedFive product to her similar regimen and still tested negative for hydrogel rubber clot. It seems William lives a rural life in Alabama that may also contribute to his findings.

On the Zoom call a few suggestions to him were made by naturopaths to stop the aspirin, cal citrate, and possibly Centrum Silver. I will be looking forward to his future findings.

Since my last post I tried decreasing and even stopping briefly the ivermectin. I tried adding thieves oil to my morning drink (2 drops) and 2 drops topically along with coconut oil as a carrier oil to decrease irritation. Remember Michael said this would not be effective but I thought to confirm. I then decided to try and see if using my ivermectin protocol a hydrogel would present itself in the tube after 3 or 4 days if refrigerated undisturbed.

Let me go through the procedure for the new folks. I draw blood via venipuncture into a plain red top vacutainer tube. Plain tubes do not contain an anticoagulant such as EDTA, citrate, or heparin. Full anticoagulation in a vacutainer tube prevents the development of the hydrogel as does normal body temperature. Please see prior posts for details. After the blood draw the tube is inverted x 10 to gently mix and allow to clot for 30 min as per normal routine in most clinics drawing blood. The tube is then centrifuged for 30 min at ~3K rpm at room temp (near 75°F). I do a visual exam of the tube contents and discard a tube if hemolysis is present. Hemolysis is the disruption of the red blood cells that will leave a red tint to the normally straw colored serum and this will prevent hydrogel rubber clot formation. If hydrogel is present it leaves a cloudy appearance above the packed cells in the tube. I take the tube and refrigerate overnight and the next day empty the tube contents on a plate. The hydrogel can be separated from the normal currant jelly clot and if the hydrogel is rinsed in water and given about 5 min it will firm up, shrink, and become whiter taking on the calamari appearance.

The following pic is of the tube showing the cloudy hydrogel above the packed red cells after the centrifuge process.

I waited 5 days after collection to see what additional effect this would have on the hydrogel present. I saw no additional effect and performed the full exam by emptying the tube. The following pic shows the separated hydrogel with initial measurements of 10x10x3 mm.

The following pic shows the hydrogel rubber clot taking on the calamari appearance after rinsing in tap water plus 5 min and rolling between fingers.

I decided to increase the oral ivermectin to 3 ml /day from the 2 ml/day. This would be 3ml of the 10 mg/ ml solution that recommends 1 ml solution per 110 lbs cattle weight (not a recommendation to you). This would be about 0.3 mg/ kg for my weight of 140 lbs. Remember the early dosing during the pandemic was 0.2 mg/kg but inc. to 0.6 mg /kg during to delta strain per FLCCC. I continued the proteases (nattokinase, lumbrokinase, bromelain, serrapeptase) as well as the MedFive EDTA product and oral (in a drink) and topical thieves oil. This resulted in remission. Let me list the “lesser" products I take daily: 5 drops methylene blue, 4 drops fulvic humic acid, vit d with k2, nascent iodine, vit c, zinc, quercetin, NAC, fish oil, turmeric, activated charcoal. Here is a pic of the clean serum without hydrogel when taking the above compounds.

I placed the tube in refrigerator for the next 3.5 days with no change in appearance and no new hydrogel appearing. I also drew an EDTA vacutainer tube and over the next 5 days no new appearance of a hydrogel appeared in the tube. This finding is consistent with prior finding that full anticoagulation prevents hydrogel rubber clot formation.

I was thinking about a comment, I believe the embalmer Richard Hershman made on a podcast about a drain placed in a body that showed the calamari like clot. I have been showing that the blood banks can only stay in business these days because full anticoagulation prevents expression of the hydrogel rubber clots. The last post I showed the hydrogel rubber clot is a temperature sensitive hydrogel that is in its soluble form (dissolved) when at body temp. but when the temp is lower than body temp (how much cooler than body temp I do not know) you may form hydrogel rubber clot in a tube if at room temp and normal blood coagulation can occur (i.e. no anticoagulant present). I surmised that I should see a linear calamari like clot (even like those seen by embalmers) in my blood collection tubing so I took my tubing from a few days ago and cut the ends off and blew with my mouth the tube contents on a plate. The following is a pic showing a tiny string of what appears to be calamari clot!

Here is a picture of my blood drawing tubing from the specimen that was negative for hydrogel rubber clot. I do not see the white strings but I assume normal currant jelly clot. Interesting!

Summary and Discussion. I again refer to the late German pathologist Dr Arne Burkhardt that felt the blood findings consistent with an autoimmune disease where there is destruction of the blood vessels. https://rumble.com/v2bnvdm-pathologist-dr.-arne-burkhardt-autopsies-show-the-mrna-vaccine-shreds-peopl.html

To me, two definite types of therapy are possible. One therapy would stop or at least inhibit the tissue destruction (maybe ivermectin) and other therapy would be to dissolve the destroyed tissue byproducts (fibrin proteases and other treatments). One type would be superior to the other in health prognosis, I assume. For an excellent review of ivermectin and a great researcher of the literature you should subscribe to ohbaby.substack.com. Here is a link to Dr Philip McMillan and several doctors discussing calamari clots, hydrogel, vasculitis, amyloid. https://www.youtube.com/live/mIXMoPwKqEo?si=0nVLmefhkki0XYd2

As far as the appearance of a hydrogel after the initial negative finding when Dr Nixon used thieves oil, I have no explanation except any protein when denatured (disrupted by temp, pH, proteases, reducing agent, etc) may go from a globular and “dissolved” form to a fibrous and potential hydrogel form. I will say I do not see the appearance of a new hydrogel using ivermectin plus protocol. I will keep the tube for further observation.

What is needed are more individuals with the ability to draw blood or have someone capable of doing it and acquiring a centrifuge and test tubes and butterfly needles with tubing (23 gauge is best) and testing compounds.

Not much logic here but ivm and thieves oil as well as boswellia (frankincense) are oils so I think I will test frankincense next.

For guaranteed eternal life remember John 3:16. For God so loved the world He gave his only begotten Son, that who ever believes in Him should not perish but have everlasting lfe.