Remission Again, No Gel/Plastic, Rubber Clot in My Blood.

I have tried to reduce the number of compounds to achieve remission of gel/plastic (g/p), rubber clot in my blood but still unable to do it with a single compound.

In prior posts I have stopped expression of g/p in my blood by taking oral ivermectin, plus multiple oral fibrin proteases, plus oral and topical EDTA. I tried daily ivermectin (ivm) as a single ingredient to suppress g/p but did not achieve this at 2 ml/ day (0.32 mg/kg) for one week. If the half life of ivm is 12- 66 hrs then maybe a week was not long enough time to achieve a steady state (10 days better). Still I have heard of two others by a first hand witness that have achieved remission with ivm alone.

Briefly the vacutainer test uses a 10 ml plain tube ( no added anticoagulants), blood collected by venipuncture, tube gently inverted × 10, allowed to rest upright for 30 min, centrifuged × 30 min, grossly examined for cloudiness above the packed red cells, refrigerated overnight in the upright position, and fully examined about 24 hrs later by dumping out the tube contents for exam.

The following picture shows the appearance of g/p after rinsing in tap water and given 5 minutes to dry.

Nevertheless I did add back nattokinase 12,000 FU to the ivm for 5 days and did a vacutainer tube blood test and g/p was present so I doubt ivm alone would have changed the result.

The following picture is 5 min after rinsing g/p.

I then added lumbrokinase 30,000 FU to the ivm for 4 days and repeated a vacutainer tube blood test and again g/p was present. The picture is 5 min after rinse.

I then added oral EDTA (Med Five, Inc. product) for 5 days to the daily ivm, plus daily lumbrokinase x 8 days and chlorine dioxide 30 ppm x 8 ounces for 2 days and achieved remission. The following picture shows a clear straw colored serum without evidence of g/p.

The following picture shows full examination of the tube contents. No g/p, rubber clot, is seen.

I will add a darkfield microscope picture of my blood. I needed to add it to a drop of normal saline in order to spread out the cells.

Summary and Discussion. I will again refer to the work from the late German pathologist Dr Arne Burkhardt that did an analysis of g/p and found 137 proteins and 5 were specific to the innermost lining of blood vessels (endothelium) and were present as a result of inflammation (endotheliitis) from spike protein.

Here is a link to Dr Burkhardt's video. https://rumble.com/v2bnvdm-pathologist-dr.-arne-burkhardt-autopsies-show-the-mrna-vaccine-shreds-peopl.html

I don't know what spike really is or where it comes from but something appears to be causing an inflammatory destruction of vessels and the after effect appears to be g/p, rubber clot. In theory you have two types of treatment for g/p in the blood. You can treat the inflammation from spike with ivm and I assume chlorine dioxide. Again this is not medical advice. Consult your health care provider on any new treatments. In a prior post I stated that chlorine dioxide did not help to achieve remission and this maybe the case but needs to be confirmed or refuted by more testing. I am looking at this compound for this reason plus I had a report of others having good results using it. One issue with adding or removing a compound to your personal testing is the delayed effect issue. Did you give enough time to see an effect? In regards to ClO2, I am taking 30 ppm for 8 ounces of water which is 3.6 mg/ day. This is much less than Andreas Kalcker uses in his epidemic protocol of 30 ppm for 1 liter/ day which is 30 mg/ day. ClO2 interrupts the synthesis of a pathogen's cell wall proteins via selective oxidation per Noszticzius 2013. If this is the case then it might decrease vessel wall destruction. Further testing needs to be done.

In this trial I took a single protease, lumbrokinase. I posted a report in the past that lumbrokinase was 40 x more potent than nattokinase but I can't say this by my testing this is the case. All I can conclude is it was part of a regime that achieved remission. I had remission in the past by taking all 4 proteases (with other compounds) throughout the day (lumbrokinase, serrapeptase, bromelain, nattokinase). I think proteases can work to denature spike prior to any inflammation as well as after creation so I personally think they are useful.

In this trial I used EDTA in the product Med Five Inc. but I have used topical and oral forms in the past. I plan to stop this product and see the effect on holding onto remission it has. This should be in next post. I am not sure how EDTA or other chelators affect overall prognosis if they are working to prevent expression of g/p after vessel wall destruction has occured.

So in summary, you can stop the expression of g/p in the blood but what combination of compounds is most effective in changing the prognosis still needs to be determined.

I will praise You, For You have answered me, And have become my salvation. Psm 118: 21.