Recent Findings

Sorry that I've not posted in a while but now I have some interesting findings.

In my latter posts I recommended that you not test for detection of blood hydrogels using the centrifuge since it can readily show the normal fibrin hydrogel that all living humans should express. I did conclude that a new and foreign hydrogel maybe present but masked within the normal fibrin hydrogel. It seemed to me that blood collected in plain red top vacutainer tubes when allowed to sit for 30 min prior to centrifuge will form a fibrin mesh around the red blood cells as well as around the white cells and platelets and even the foreign hydrogel if present. I had recommended waiting 30 min prior to centrifuge since that was the time advised by phlebotomists for serum samples in red top tubes. Since blood clotting in a tube can have a normal range of time to clot, the fibrin hydrogel net may or may not have netted everything in the 30 min prior to centrifuge. If the fibrin net formed in time, then the spin in the centrifuge might show no hydrogel (normal or abnormal type) to be present (only a currant jelly clot) plus serum. This might give a false negative result and could also give a false positive result if clotting was delayed. Due to this confusion I went back to collecting blood in plain plastic vacutainer tubes and allowing at least 4 hours to clot and no centrifuge use. This was analogous to the 30 ml of blood in a large syringe that Dr Ana Mihalcea uses to show the abnormal rubber clots. See anamihalceamdphd.substack.com.

I collected my blood by venipuncture into a 8 ml plain red top vacutainer tube and allowed it to sit for 4 hrs at room temperature. I examined visually the tube and did not see any abnormal gel above the currant jelly clot after 4 hrs but placed the tube in refrigerator overnight.

I subsequently fully examined the contents of the tube by dumping the contents on a paper plate. No abnormal gel above the currant jelly clot was seen.

I repeated the test again with an added variation in that I severely agitated the tube after blood collection to cause red cell rupture (hemolysis). This did not alter the findings and no gel above the currant jelly clot was seen after 4 hrs.

Full exam of the tube’s contents was done after refrigeration overnight. No gel was seen above the currant jelly clot.

Overall this would be good news that I did not show an abnormal gell in my blood at this time. If you look at my more recent post, you can see what the abnormal gel looks like when present.

As a further possible proof that the abnormal gel may not be present in my blood, I saved the blood collection tubing to see if rubber clot would also be absent there after 24 hrs. The following pictures show the tube’s contents after cutting off the ends and blowing out the contents.

As a contrast, the following photo shows the rubber clot that formed in tubing from my blood drawn in 3/4/2024.

Here are a few pictures of my blood from 8/26 using a dark field scope at 250x to 1000x.

My impression on the dark field pics is there are some areas of rouleaux (stacking of red cells), some bubble appearance areas (not sure of an artifact or abnormal organizing center), no obvious fibers, and no flashing particles. I’m unsure about abnormal crystal formations.

Summary and Discussion.

At this time I cannot detect abnormal hydrogel in my blood. It was not seen in a plain plastic red top vacutainer tube when allowed to sit for 4 hrs and overnight. The gel was also not seen in the collection blood tubing. I feel the exam of the collection tube contents might be an easy test to detect this rubber clot. I would keep the tube overnight at room temp and then cut off the tube’s ends and gently expell the blood and look for rubber clot.

What is this abnormal hydrogel or rubber clot? The late German pathologist, Dr Arne Burkhardt felt this gel contained some products of blood vessel breakdown (endothelialitis) as well as fibrin, spike protein and amyloid. Here is a link to a lecture he gave January this year: https://rumble.com/v2bnvdm-pathologist-dr.-arne-burkhardt-autopsies-show-the-mrna-vaccine-shreds-peopl-html.

Further information to the story is from Dr Douglas Kell that explains the fibrin of clotting may be changed to a fibrinaloid nature that forms a clot that is hard to breakdown and giving rise to long covid symptoms. If you have not seen this recent video from Vejon Health on YT make sure you watch it. https://www.youtube.com/live/ySMqoy0Nc00?si=lW33Al8HVMwbcdY1

I have been following Dr Peter McCoullough's recommendations and taking nattokinase, quercetin, bromelain, NAC. I also follow Dr Ana and take vit C, oral EDTA, methylene blue, fulvic humic acid, lemon oil, grapefruit oil, cinnamon oil. Adding lumbrokinase and serrapeptase digestive enzymes seems helpful. I have decreased oral ivermectin to only 20 mg weekly. I am healthy at 68 yo with stable chronic hypertension treated with a single drug that is unchanged for 20 yrs (beta blocker, atenolol). I don't know if the above products always work but go with the experts named above recommendations (it seems to have improved my blood findings).

For God so loved the world that he gave his only begotten Son, that whoever believes in Him should not perish but have everlastinglife. John 3:16.