Well maybe that’s a bit of an overstatement. She probably won’t cause post-viral illnesses have historically not received the attention they deserve. And long covid probably will fall into that pattern.
I would love to hear the implications for vaccines and vaccine long haulers discussed... It feels like everyone is too scared to even touch the topic. Despite the acknowledgement this is caused so efficiently by spike proteins Dr. Asan Khan also discussed his significant worsening after vaccination leading to PEM pots etc all getting unbearable
I agree. The vaxxed have microclotting and stroking going on as well as neurological and heart issues...they have been given a shot that produces the spike protein. The Harvard study proved in rats that the spike protein even without the virus produced awful results ,(spring of 2021)
They are afraid to touch the topic of vaccine injury because their funding might abruptly stop. Read the book The Real Anthony Fauci by Robert F. Kennedy Jr. He explains what happens behind the scenes.
Too many with Long Covid, especially those with extreme cases, never had the vaccine. Also, Corona viruses attach to cells with spike proteins. Those spikes on the virus give it it's 'Corona' (crown) name. So spike proteins are literally how the virus itself functions.
Thank you both so much for taking the time to share this amazing insight into the research you are carrying out. As an ME patient for nearly three years I cannot express my gratitude for the hope you are giving me and others in my community. You are 2 extraordinary ladies.
Thanks so much for your work on the long covid research I started crying at the end when you said don't give up. I have dealt with long covid almost a year and still have so much of these symptoms. It gave me hope and asking my doctor about the test for checking the microclotting as you discussed. I have done so much research on this and probably know more than most doctors around the USA LoL. I hope here they can take this and help people here in the USA. I also have small fiber neuropathy as discussed it's crazy everything you talked about sounds like myself. Only one issue I have that might be nerve related is I have bladder issues ever since I got covid. Getting a nerve test done on bladder and see what they say. Keep my fingers crossed for something on this test. I still also have chest pain and problems with exercising it just flares everything up and I get so fatigued. I just pray and hope that your next test results will even help us even more thanks again for your help and let's hope the grant will go through to help the research.
@@rockywigg7882 I really don't know I woke up last week and felt like i could get a deeper breath that I have not felt for 14 months a feeling money can't buy I found a steroid Inhaler helped with my extreme fatigue. Hoping I can build my stamina up now.
@@davidrobinson8947 wow that's great news. My heart doctor said he had patient that just got better after 18 months. Hopefully I will get better over time. I take inhaler as well if I don't get chest pain. Wake up with it lately. Crazy. Still can't exercise with out having issues. Having neurologic issues. Been a year today since I had covid. Might go to a covid clinic nearby soon. Not sure what they do but worth looking into. Good luck on your health.
@@rockywigg7882 my taste has also came back last week aswell as it was disoriented. Yeah hopefully they can do testing and find a cure for it. As it feels like we are being left behind. All the best
Thank you for this. I’m a 33 y/o male who has LC for 14 months. I thought I had amyloidosis in the beginning and I got every test to rule that out first. Interestingly I had a UPEP done and there was globulin fractions in the urine (which aren’t supposed to be there). One of the things this could be is amyloidosis! I have no doubt I’m suffering from micro clot issues due to these amyloid fibrin clots. I can’t find any Drs to help me. They’re just clueless. My fatigue is horrible and just can’t get over it. Please help!!
I've had a huge improvement in my fatigue levels after taking 1 litre of gutilthione /vitB3 mix. Via IV injection It got rid of all my soreness from inflammation.
@@samhouston1483 hey did you do the IV? If u did how u feel at the moment? I did another one this morning, all my chest and back pains dissappeared so now I'm gonna take it really slow and try not over exert myself and end up at square 1 again
It is first a respiratory disease damaged Gas Exchange then BECAUSE of this damage in Gas exchange links into vascular disease which you describe so brilliantly. Things are linked.
Year 4 for me. I got covid when I was 36. Still battle miscle fatigue and weakness exercise intolerance. Got lapband surgery to help me loose weight and live life to the fullest. Many gains with amny setbacks. But I stay active as I can.
Thanks for sharing your experiences and insights! Glad you mentioned the general circulation of microbes in the blood. Afaik there's not been a lot of normative whole genome sequencing data of microbial content in healthy "sterile" blood.
thanks for this. I am a 18 months long hauler and suspect blood clots. Still struggling with compromised lung function and buildup of mucus in my lungs and throat. any recommendations to dissolve the blood clots. naturally
In Waldenstrom macroglobulinemia high monoclonal antybody can increase blood hiperviscousity, erytrocyte aggregation and amyloid precipitate(?) Cysteine was used to decrease blood viscousity.
Great work but I can’t see any of us having access to this treatment… I’m hoping the NAD+ deficiency theory are the treatment with Niacin is going to help my condition improve
Research nattokinase and serrapeptase. I was infected 2/20, took me 6 months of study to figure out most of what they are discussing here, and started dosing around 8/20. I’m still here! I could literally feel it working when I first started dosing, but I was in really bad shape. I don’t feel it working anymore. It wasn’t a permanent solution but a band aid to keep me alive until the medical community catches up. I’m looking to trypsin supplementation now, or possibly increase serrapeptase to mimic trypsin.
This is so cool but I would have been interested to know her criteria for diagnosing Long Covid as everyone keeps talking about the heterogeneity of the disease.
I find it interesting that you discuss leaky gut, I had some tests done and it was determined that I have the leakiest gut they had ever seen. I am 1 year Long Covid sufferer, preciously very fit and healthy.
I guess it's all related. While I'm not a medical professional and perhaps not that insightful, I'm noting that researchers have found traces of COVID still residing in the intestines, even though one might not pick it up in a PCR test. Maybe it's doing damage to the gut while there. Lots of luck and health to you in any event. (Mecfs person since 11 years here ;)
Thank you for this very insightful talk. This is on the cutting edge of solving long covid. The only thing left seems to be to find what is causing the clotting in the first place. Or why LC patients are not able to clear the clots themselves.
Things to think about taking supplementary wise in combination with a pro metabolic diet and healthy lifestyle limiting unnecessary stress. 1-Methylene Blue 1-2grams daily 2-Nattokinase/Serrapeptase 3-Aspirin 4-Vitamin D3/K2 applied topically 5-Vitamin C (ascorbic acid) 6-Red Light Theray/Sunlight frequently 7-Vitamin E 8-Magnesium All supplements must be of high quality
69, very healthy, very active, no co-morbidities, BMI 22, lowcarb/keto plus intermittent fasting, unvaxxed. COVID bout at Christmas now debilitated by what I'm convinced is Amyloid Clotting. Only symptoms are slight dizziness and extreme fatigue if I try and exercise. HELP!
No answer here, but I have nearly the same situation as you described for yourself. I had infection the same month as you, too. (Contracted it from a vaxxed family member, I believe). I just hike for seven weeks, 635 mile in the mountains. I noticed changes in my symptoms during the hike. Cardiopulmonary symptoms deceased, tinnitus and neuropathy increased. I did take aspirin daily as a precaution since I believed clotting was an issue with covid. Hydration, activity and anticoagulants may be a start. I actually felt better after two weeks of hiking, I peaked at about four weeks and felt worse when I got back home to “relax”. I have a continuous head pressure and low interest in being active, which not normal for me.
@@youflatscreentube I took a couple of ivermectin tablets after 3 months of the CFS. Instant fix. Must have been spike protein build up in my gut. Back to full match fitness now, some 3 months later. Maybe try it if you're still suffering at all?
I have long haul 9 months now from a mild case of covid in January . Heart palps ,severe insomnia and tinnitus . I’m doing better but I can’t get back to any form of exercise ( I use to exercise 5 days a week ) . Now even walking fast makes me feel ill .Vacuming my house makes me feel ill . My co morbidities are chronic Lyme , mold toxin illness , celiac disease . I have a very good Lyme doctor trying to help me . Do you have any advice because as far as my abilities to exercise I feel I’m getting worse. I was doing well and in remission from . PLEASE help if you can . Thank you
Is there a way we could contact doctor Pretoria to work out how we can bring tests to the UK? We are trying to at least get people the chance for a diagnosis that could potentially follow the clinical trial that will take place after this
Have you heard anything about getting surgery with long covid? Given the clotty nature of our blood, I’m debating whether a surgery should be avoided? Any information here would be greatly appreciated. Thanks!
Sounds great except for the fact that it's not available or affordable for most people suffering from long covid. I was totally dismissed from my Doctor's office and my complaints not addressed as I am sure any doctor I try to get to listen will treat me exactly the same.
I totally share your frustration. I’m slowly developing a disrespect for Western medicine. However, I believe we can have this simple blood spinning done at any LabCorp office. Plus- You need to find a really good functional medicine doctor. They will listen to you and try to help.
This disturbs me . Had Covid Long 2 times and my physician says because I have no large clots and blood samples show I do not have clotting factors . Not sure how I can get accurate information and treatment for long term effects ! 😠
This is March 2024. What can be done during the acute phase? Im 3 weeks in , not getting better. After 4 days fever broke , then bad cough and sore throat, loss of taste and smell. Then Uticaria hives, angioedema, exhaustion. Painful icy feet and hands. Im on prednisone cause headaches and on pepsid and zyertec. I have heart disease and neurological problems from previous TBI. In ohio OSU no help so far....
She deserves a Nobel prize 🇿🇦 proud of you doc! could these micro- clots lead to complications in pregnancy and when we want to test, do we test the same as the general population given that fibrinogen is more abundant in pregnancy, would microscopy imaging be the best option than drawing blood?
"mild" covid was always wrong and this was known very early in the pandemic. All, including children, need appropriate early covid treatment to prevent acute covid severity, long covid and long "slow kill" covid.
The docter that's doing the tests and treatment is based in stellenbosch, South Africa, he's working with this lady. I went to him yesterday and I got to see my blood slides! Plus he gave me a script to try out, called the triple protocol. He mentioned he's able to talk people through the process from overseas provided they can get a docter on their side to actually do the test which is very easy to do actually. Good luck
@@FullSend27 hey I had an IV of gutilthione and vit B3 last week, I'm feeling absolutely amazing with my chest pain gone, but it comes back here and there still but very faint. My titnitis is frikken gone! I can go for a small run and my hr stays low instead of jumping into the high 100s. Im gonna do another session of it next week. I'm sure the gultithione reserves get depleted with a NAD+depletion somehow linked to it as well. Funny thing is I couldn't get it through my normal gp, as he couldn't even find glutathione on his system to order it. I had to go to these trendy IV vitamin bars to get it. Of all the things I've tried so far, I've made the MOST PROGRESS with the IVs to date!
@@boknows1355 is the eliquis the anti clotters? the doc put me on disprin for last 2 months prior to this and drew 2 blood samples as well but now i gotta go in and get some meds he says.
@@alexandrecouture2462 sure. I went off the protocol in June or July. Felt good until about November when I got the flu. Found out I have a condition which makes me prone to stokes or heart attack so I am back on blood thinners and medication to remove and possible clots.
Thank you for this very informative video. One reason why micro-clotting is still occurring in 2024 is that many people who took the Covid-19 vaccines, even those whose last injections were way back in 2021, could still have modRNA producing the spike protein in their bodies today. Just as the spike protein from the virus can cause the formation of micro-clots, so too can the much larger amounts of spike protein continually produced by the vaccine. I have conducted two "Worldwide Embalmer Blood Clot Surveys." In my latest survey, I asked the embalmers two questions about the micro-clots, which they describe as what looks like "coffee grounds" in the blood as it is draining out of the corpse. A stunning 79% of embalmers (212 out of 269) saw the "micro-clotting" in 2023. And they saw the "micro-clotting" in an even more stunning 1 out of every 4 corpses (25%)! Previous to the years of Covid and the vaccines, embalmers saw micro-clotting in less than 5% of their corpses. th-cam.com/video/4rAoqhTUU0g/w-d-xo.html
I am having a surgery Is it possible to get a spike protein through blood transfusion? I am unvaccinated and I am getting anxious and thinking about not having the surgery
Does anyone have experience with Inuspherese already? What about clotting and autoantibodies with this form of Apherese? Does someone with LC or ME/CFS have experience with this already?
I have been reading a lot about this microclots finding in long haulers, btw I am one of those. I had covid in middle April 2021, and some of my symptoms are still not going away including mild chest pain, SOB, a little feverish feeling in the morning, and an extremely dry nose. So I have a few questions if anyone could answer that: 1. If the researchers say due to microclots, our blood is not able to carry oxygen efficiently as it used to, and leaving some of the tissues/organs oxygen-deprived. Then how come oximeters are showing normal, i have my readings always between 96 to 98. 2. Why can't we simply remove some portion of blood, like we do in blood donation and our body again regenerated it? Will the regenerated blood still be having these mircoclots?
I am not a medical professional so this is my lay understanding: 1. Blood pulse ox is normal because the blood does have normal oxygen saturation. The hypoxia is due to the microclots "clogging up the pipes" which deliver blood to the tissues. In this case the "pipes" are very small (capillaries, etc). 2. Either viral fragments still in the body or some other mechanism is continuing to produce new blood clots, so removing blood via blood donation will only cause new blood to be reproduced with new clots. Bruce Patterson has mentioned this in several interviews: th-cam.com/video/El1rdF8XET4/w-d-xo.html For what it's worth, I'm hopeful that I am wrong about the blood donation part. If it helped, blood donation would be a very convenient and safe therapy.
@@vanjacalantropo Hi, looks like my recovery has just stopped at 70%, neither has it dropped nor increased. Though I am not quite sure if i had omicron, but i had fever a few weeks ago.
@@hardyismyname I don’t know how you determine percentage? Are you 70% of your previous health or are your symptoms improved by 70%? You might platough but you can still improve after awhile.. don’t do too much.
my oximeter was just like that as well, id be breathless and id stick it on and it would read at 98% . i think the problem is that the oxygen is good say in your arm but there's clots constantly developing and breaking down all over your body . So suddenly a clot develops that's related to your kidneys but not your arm, that's gonna make you feel terrible for a bit, but its not affecting your arm so while your oximeter is checking 98% for the blood flow in your finger its NOT a good indication of what's happening on ALL OF THE BLOOD FLOW IN THE BODY. I think that's the misconception/confusion. In a NORMAL medical environment a doctor will monitor a patients oxygen with a oximeter and, it'll be a very good indication as to the oxygen levels in the body overall. With the blood clotting in LC its a not a true representation and the oximeter actually belongs in the bin I'm afraid. I've had it the other way too , I've had readings of 72% and I've felt absolutely fine. I'm 2 years in ,I've found using a infrared lamp whenever I sit On the computer seems to have had a good effect on me as well. ( its linked to nitric acid production )
Dr. Patterson at InCellDx uses Pravastatin alongside Maraviroc to inhibit CCR5 and Fractalkine receptors to stop the endothelial inflammation that is causing the blood clots
not much, all its going to do is reduce the normal lcl, the deformed bad lcl that are floating around in the blood - its not gonna touch them. I think those are the real problem cause they the ones really getting stuck in the blood vessels and causing a lot of inflammation. I'm not a doctor , I've just been forced to do my own research as my doctor is not so interested in long covid:(
Theres many athletes like myself who are suffering from long covid that were fit,healthy,dont smoke,drink,drugs ,sunshine warriors.Docter said i had anxiety wtf. I never had any time in my day to be anxious before this! lol. i bet its gonna be down to genetics that they find in years to come.
Shortness of breath at times and I can't push myself with excersise otherwise Ill become breathless the next day, sleeplessness nights and anxious, sore chest
I’m a psychotherapist and no sh!t people have anxiety. They don’t feel themselves, don’t know when or if they’ll feel better, they have been isolated for several years and ostracized if they feel differently. Anxiety is a byproduct of all of this not a pathology.
@@Kellykpw62 spot on, as an update, I've made a huge improvement as time has gone by, my sleep pattern is almost resolved, the breathless has gone to the point where I work most days AND I can drive again( I couldn't drive as it felt as if I got information overload every time to the point of an absolute dander on the road ?!?! My problems now revolve around me going back to sport and my mental outlook of myself which I see as a very sick person incapable of doing much and how my sports peers are light years ahead of me, I cringe to go back and fear the inevitable defeat when ill have to compete again. Basically you end up with zero confidence in your ability and have to start from scratch:(
I will also add to this discussion, that Covid is entering the mitochondria of cells everywhere which is where our energy comes from (ATP). This is another possible reason for the sheer exhaustion.
May be ,,low temperature agglutinine,,trigger by increasing blood viscousity and ischemic effect, endotelial inflamation especially at perifereal circulation ,where blood have low temperature.?
Interesting. I have never been diagnosed with covid. However, after running a d dimer after delivery of my baby, my level was over 5,000 or 7.3, even after a month post pardum. I just had another test to check if the level has dropped any. Waiting on results.
If a dropp of blood of some patients after SARS COV2 infection was put on a cold glass lamela agglutinate before coagulate. At microscope can be seen erytrocyte aggregation like coin rolls.(not at normal body temperature) Like in Waldenstrom macroglobulinemia may be increasing level of some antybody induce that. That can increase blood viscousity, damaging capillary blood flow. Did N- acetylcysteine decrease blood viscousity? Did Dextran40 decrease blood viscousity?
Latex reaction for detection of rheumathoid factor indicate that some antybody complex neutralizeze electrostatic forces that maintain suspension ,and adsorbtion forces induce aggregation.(?)of particles of polistiren covered with latex
At TWiV Nr 659 at min29 virologist Christian Drosten indicate very low tissue temperature better to replicate SARS COV2 in lab.(septembrie 2020) Avoiding persistent infection with SARS COV2,we avoid to hiperstimulate specific immune system. May be ,,mask wearing,,not only filtrate but also increase upper mucoseal respiratory temperature.? May be oxigenotherapy must use more warmed oxigen mix.?If SARS COV2 infect respiratory tract.
I’ll bet this woman receives a Nobel prize in science.
Well maybe that’s a bit of an overstatement. She probably won’t cause post-viral illnesses have historically not received the attention they deserve. And long covid probably will fall into that pattern.
Two brilliant women doing brilliant work. Thank you!!!
I would love to hear the implications for vaccines and vaccine long haulers discussed... It feels like everyone is too scared to even touch the topic. Despite the acknowledgement this is caused so efficiently by spike proteins
Dr. Asan Khan also discussed his significant worsening after vaccination leading to PEM pots etc all getting unbearable
I agree. The vaxxed have microclotting and stroking going on as well as neurological and heart issues...they have been given a shot that produces the spike protein. The Harvard study proved in rats that the spike protein even without the virus produced awful results ,(spring of 2021)
Good Question.
They are afraid to touch the topic of vaccine injury because their funding might abruptly stop. Read the book The Real Anthony Fauci by Robert F. Kennedy Jr. He explains what happens behind the scenes.
Is there any credible source that is focusing on this question?
Too many with Long Covid, especially those with extreme cases, never had the vaccine. Also, Corona viruses attach to cells with spike proteins. Those spikes on the virus give it it's 'Corona' (crown) name. So spike proteins are literally how the virus itself functions.
Thank you both so much for taking the time to share this amazing insight into the research you are carrying out. As an ME patient for nearly three years I cannot express my gratitude for the hope you are giving me and others in my community. You are 2 extraordinary ladies.
Thanks so much for your work on the long covid research I started crying at the end when you said don't give up. I have dealt with long covid almost a year and still have so much of these symptoms. It gave me hope and asking my doctor about the test for checking the microclotting as you discussed. I have done so much research on this and probably know more than most doctors around the USA LoL. I hope here they can take this and help people here in the USA. I also have small fiber neuropathy as discussed it's crazy everything you talked about sounds like myself. Only one issue I have that might be nerve related is I have bladder issues ever since I got covid. Getting a nerve test done on bladder and see what they say. Keep my fingers crossed for something on this test. I still also have chest pain and problems with exercising it just flares everything up and I get so fatigued. I just pray and hope that your next test results will even help us even more thanks again for your help and let's hope the grant will go through to help the research.
I have just recovered from long covid after 14 months it is a illness that put my life on hold hope you get well soon
@@davidrobinson8947 thank you. How did you recover after 14 months
@@rockywigg7882 I really don't know I woke up last week and felt like i could get a deeper breath that I have not felt for 14 months a feeling money can't buy I found a steroid Inhaler helped with my extreme fatigue. Hoping I can build my stamina up now.
@@davidrobinson8947 wow that's great news. My heart doctor said he had patient that just got better after 18 months. Hopefully I will get better over time. I take inhaler as well if I don't get chest pain. Wake up with it lately. Crazy. Still can't exercise with out having issues. Having neurologic issues. Been a year today since I had covid. Might go to a covid clinic nearby soon. Not sure what they do but worth looking into. Good luck on your health.
@@rockywigg7882 my taste has also came back last week aswell as it was disoriented. Yeah hopefully they can do testing and find a cure for it. As it feels like we are being left behind. All the best
Thank you for this. I’m a 33 y/o male who has LC for 14 months. I thought I had amyloidosis in the beginning and I got every test to rule that out first. Interestingly I had a UPEP done and there was globulin fractions in the urine (which aren’t supposed to be there). One of the things this could be is amyloidosis! I have no doubt I’m suffering from micro clot issues due to these amyloid fibrin clots. I can’t find any Drs to help me. They’re just clueless. My fatigue is horrible and just can’t get over it. Please help!!
I've had a huge improvement in my fatigue levels after taking 1 litre of gutilthione /vitB3 mix. Via IV injection It got rid of all my soreness from inflammation.
@@marky5493 i will actually be doing an IV w these in it tomorrow ha
@@samhouston1483 nice! Let me know how u feel in a couple of days, I'm trying to see if it was just me or is it really a thing:)
@@samhouston1483 hey did you do the IV? If u did how u feel at the moment?
I did another one this morning, all my chest and back pains dissappeared so now I'm gonna take it really slow and try not over exert myself and end up at square 1 again
@@marky5493 unfortunately didn’t do anything for me :(. I’ll be doing a stellate ganglion block next to see if that could help
I believe in you I am from the states do you take patients from far away
It is first a respiratory disease damaged Gas Exchange then BECAUSE of this damage in Gas exchange links into vascular disease which you describe so brilliantly. Things are linked.
Year 4 for me. I got covid when I was 36. Still battle miscle fatigue and weakness exercise intolerance. Got lapband surgery to help me loose weight and live life to the fullest. Many gains with amny setbacks. But I stay active as I can.
Thanks for sharing your experiences and insights! Glad you mentioned the general circulation of microbes in the blood. Afaik there's not been a lot of normative whole genome sequencing data of microbial content in healthy "sterile" blood.
Amy you're the best! Thank you for your commitment to finding a cure for ME/CFS
thanks for this. I am a 18 months long hauler and suspect blood clots. Still struggling with compromised lung function and buildup of mucus in my lungs and throat. any recommendations to dissolve the blood clots. naturally
Research Umcka....very amazing on mucus
Research serrapeptase and nattokinase
@@thetube4p yes correct
In Waldenstrom macroglobulinemia high monoclonal antybody can increase blood hiperviscousity, erytrocyte aggregation and amyloid precipitate(?)
Cysteine was used to decrease blood viscousity.
Thanks Amy and Reisa! Amazing and very important research results which will have ramifications for the research into a wide range of diseases.
Does Nattoinkase help
It seems like it does. Along with serrapeptase.
Fantastic interview, fantastic work. My wife helps her with her lab design.
Great work but I can’t see any of us having access to this treatment… I’m hoping the NAD+ deficiency theory are the treatment with Niacin is going to help my condition improve
Research nattokinase and serrapeptase. I was infected 2/20, took me 6 months of study to figure out most of what they are discussing here, and started dosing around 8/20. I’m still here! I could literally feel it working when I first started dosing, but I was in really bad shape. I don’t feel it working anymore. It wasn’t a permanent solution but a band aid to keep me alive until the medical community catches up. I’m looking to trypsin supplementation now, or possibly increase serrapeptase to mimic trypsin.
@@thetube4p how are you doing?
Is this with or without the CV shots and boosters?
Great discussion! What about trying antiviral drugs to remove the viral fragments from the microclots? Thanks
Dr Patterson actually is using Maraviroc and Ivermectin for that purpose
I tried Paxlovid for my Long COVID.
No success
This is so cool but I would have been interested to know her criteria for diagnosing Long Covid as everyone keeps talking about the heterogeneity of the disease.
Me too.................its the freaking jabs. Why are people this dim?
this video is 2 yrs ago. What is the current state of the apheresis method of removing the clot load? Is the Dr. in Germany still doing this?
I find it interesting that you discuss leaky gut, I had some tests done and it was determined that I have the leakiest gut they had ever seen. I am 1 year Long Covid sufferer, preciously very fit and healthy.
I guess it's all related.
While I'm not a medical professional and perhaps not that insightful, I'm noting that researchers have found traces of COVID still residing in the intestines, even though one might not pick it up in a PCR test.
Maybe it's doing damage to the gut while there.
Lots of luck and health to you in any event.
(Mecfs person since 11 years here ;)
Which test please ? I have IBS so probably leaky gut
@@jacquie42800 it was just a stool test I did with my holistic doctor, checking for zonulin levels
@@0521coxy thank you for your answer!
@@0521coxy how do we fix leaky gut?
Thank you for this very insightful talk. This is on the cutting edge of solving long covid. The only thing left seems to be to find what is causing the clotting in the first place. Or why LC patients are not able to clear the clots themselves.
Things to think about taking supplementary wise in combination with a pro metabolic diet and healthy lifestyle limiting unnecessary stress.
1-Methylene Blue 1-2grams daily
2-Nattokinase/Serrapeptase
3-Aspirin
4-Vitamin D3/K2 applied topically
5-Vitamin C (ascorbic acid)
6-Red Light Theray/Sunlight frequently
7-Vitamin E
8-Magnesium
All supplements must be of high quality
When do we find out whether the microclots come back after being cleared out....?
69, very healthy, very active, no co-morbidities, BMI 22, lowcarb/keto plus intermittent fasting, unvaxxed. COVID bout at Christmas now debilitated by what I'm convinced is Amyloid Clotting. Only symptoms are slight dizziness and extreme fatigue if I try and exercise. HELP!
No answer here, but I have nearly the same situation as you described for yourself. I had infection the same month as you, too. (Contracted it from a vaxxed family member, I believe). I just hike for seven weeks, 635 mile in the mountains. I noticed changes in my symptoms during the hike. Cardiopulmonary symptoms deceased, tinnitus and neuropathy increased. I did take aspirin daily as a precaution since I believed clotting was an issue with covid.
Hydration, activity and anticoagulants may be a start.
I actually felt better after two weeks of hiking, I peaked at about four weeks and felt worse when I got back home to “relax”. I have a continuous head pressure and low interest in being active, which not normal for me.
@@youflatscreentube I took a couple of ivermectin tablets after 3 months of the CFS. Instant fix. Must have been spike protein build up in my gut. Back to full match fitness now, some 3 months later. Maybe try it if you're still suffering at all?
How are u now?
@@shaft657 fully fit 2 days after the ivermectin tablets (end March). I take 1 a week now. (Thanks for asking!).
@@mikehardwicke23 what were your symptoms?
I have long haul 9 months now from a mild case of covid in January . Heart palps ,severe insomnia and tinnitus . I’m doing better but I can’t get back to any form of exercise ( I use to exercise 5 days a week ) . Now even walking fast makes me feel ill .Vacuming my house makes me feel ill . My co morbidities are chronic Lyme , mold toxin illness , celiac disease . I have a very good Lyme doctor trying to help me . Do you have any advice because as far as my abilities to exercise I feel I’m getting worse. I was doing well and in remission from . PLEASE help if you can . Thank you
Dr Bryan ardis...nicotine gum..research hin
Is there a way we could contact doctor Pretoria to work out how we can bring tests to the UK? We are trying to at least get people the chance for a diagnosis that could potentially follow the clinical trial that will take place after this
I too am very interested (Brit in Malaysia).
@@adrenalinejunkie3828 have you managed to find anyone in the UK that can help please?
Merci pour ce travail , espérons que ça arrive en Europe et comme vous dites : « don t give up »
Have you heard anything about getting surgery with long covid? Given the clotty nature of our blood, I’m debating whether a surgery should be avoided? Any information here would be greatly appreciated. Thanks!
Cancer is the biggest concern....thick blood triggers cancer...research MDM2. Research P53 and how to turn it back on.
same here...i am considering shoulder replacement surgery and not sure
Anything on vaccine-related vascular injury?
See doctors4covidethics
Sounds great except for the fact that it's not available or affordable for most people suffering from long covid. I was totally dismissed from my Doctor's office and my complaints not addressed as I am sure any doctor I try to get to listen will treat me exactly the same.
I totally share your frustration. I’m slowly developing a disrespect for Western medicine. However, I believe we can have this simple blood spinning done at any LabCorp office.
Plus- You need to find a really good functional medicine doctor. They will listen to you and try to help.
Thank you for keeing us informed. It's very hopeful. It would be useful if you could add closed captions to the videos. Thank you.
I wont give up! Thanks for all you do
This disturbs me . Had Covid Long 2 times and my physician says because I have no large clots and blood samples show I do not have clotting factors . Not sure how I can get accurate information and treatment for long term effects ! 😠
Many many thanks for this!
Brilliant work and scientific outreach
This is March 2024. What can be done during the acute phase? Im 3 weeks in , not getting better. After 4 days fever broke , then bad cough and sore throat, loss of taste and smell. Then Uticaria hives, angioedema, exhaustion. Painful icy feet and hands. Im on prednisone cause headaches and on pepsid and zyertec. I have heart disease and neurological problems from previous TBI. In ohio OSU no help so far....
How can I get treated by Dr Pretorius? Her contact info please 🙏 I’m really sick, 3 years now
She deserves a Nobel prize 🇿🇦 proud of you doc! could these micro- clots lead to complications in pregnancy and when we want to test, do we test the same as the general population given that fibrinogen is more abundant in pregnancy, would microscopy imaging be the best option than drawing blood?
"mild" covid was always wrong and this was known very early in the pandemic. All, including children, need appropriate early covid treatment to prevent acute covid severity, long covid and long "slow kill" covid.
Thank you. Do you know any laboratory in Europe for. egz.Germany, that could check the microclots?
The docter that's doing the tests and treatment is based in stellenbosch, South Africa, he's working with this lady. I went to him yesterday and I got to see my blood slides! Plus he gave me a script to try out, called the triple protocol. He mentioned he's able to talk people through the process from overseas provided they can get a docter on their side to actually do the test which is very easy to do actually.
Good luck
@@marky5493 would you mind giving us more details of the name of the doctor please and how we can access overseas. Thank you
Hi Joanna, I live in Germany too and was wondering whether you have found a doctor or hospital where they test people for microclots. Thanks!
Wonderful Interview, thank you. LarryC #mylongcovidrelief
Interesting work ! Have you considered correlations with glutathione levels for the cause of these microclots ?
I have #LongCovid type symptoms and raising glutathione actually has helped me a good bit. Curious why you had a hunch this would be helpful? 🙏
@@FullSend27 hey I had an IV of gutilthione and vit B3 last week, I'm feeling absolutely amazing with my chest pain gone, but it comes back here and there still but very faint. My titnitis is frikken gone!
I can go for a small run and my hr stays low instead of jumping into the high 100s.
Im gonna do another session of it next week.
I'm sure the gultithione reserves get depleted with a NAD+depletion somehow linked to it as well.
Funny thing is I couldn't get it through my normal gp, as he couldn't even find glutathione on his system to order it. I had to go to these trendy IV vitamin bars to get it.
Of all the things I've tried so far, I've made the MOST PROGRESS with the IVs to date!
@@marky5493 What is IV?
@@jhonybraavo IV - intrevenous vein
So I am about to go on the triple protocol. Any idea how long this will take to resolve?
Are u on it still? I'm about to start it tomorrow
@@marky5493 I am off Eliquis but still on Plavix and aspirin for another month or so.
@@boknows1355 is the eliquis the anti clotters? the doc put me on disprin for last 2 months prior to this and drew 2 blood samples as well but now i gotta go in and get some meds he says.
Hi! Can you do an update? Thank you!
@@alexandrecouture2462 sure. I went off the protocol in June or July. Felt good until about November when I got the flu. Found out I have a condition which makes me prone to stokes or heart attack so I am back on blood thinners and medication to remove and possible clots.
My sister acutally has a microscope. How do the blood microclots look like? How can we detect them?
IT seem that low blood temperature enhance erytrocyte aggregation.
May be hypothermia must be avoided in Covid19?
Even SARS COV2 seem to replicate better at low tissue temperature (a year ago atTWiV Nr 659 at min29 Christian Drosten indicate that)
After some viral infection and after Mycoplasma infection, at some patients ,,low temperature agglutinine,, occur
Thank you for this very informative video. One reason why micro-clotting is still occurring in 2024 is that many people who took the Covid-19 vaccines, even those whose last injections were way back in 2021, could still have modRNA producing the spike protein in their bodies today. Just as the spike protein from the virus can cause the formation of micro-clots, so too can the much larger amounts of spike protein continually produced by the vaccine.
I have conducted two "Worldwide Embalmer Blood Clot Surveys." In my latest survey, I asked the embalmers two questions about the micro-clots, which they describe as what looks like "coffee grounds" in the blood as it is draining out of the corpse. A stunning 79% of embalmers (212 out of 269) saw the "micro-clotting" in 2023. And they saw the "micro-clotting" in an even more stunning 1 out of every 4 corpses (25%)! Previous to the years of Covid and the vaccines, embalmers saw micro-clotting in less than 5% of their corpses.
th-cam.com/video/4rAoqhTUU0g/w-d-xo.html
I am having a surgery Is it possible to get a spike protein through blood transfusion? I am unvaccinated and I am getting anxious and thinking about not having the surgery
Please read about Serapeptase.
19:53 : Wenzel et al’s result about Mpro cleaving NEMO comes to mind.
Does anyone have experience with Inuspherese already? What about clotting and autoantibodies with this form of Apherese? Does someone with LC or ME/CFS have experience with this already?
This guy does th-cam.com/video/xuR10FxmTDI/w-d-xo.html
I have been reading a lot about this microclots finding in long haulers, btw I am one of those. I had covid in middle April 2021, and some of my symptoms are still not going away including mild chest pain, SOB, a little feverish feeling in the morning, and an extremely dry nose.
So I have a few questions if anyone could answer that:
1. If the researchers say due to microclots, our blood is not able to carry oxygen efficiently as it used to, and leaving some of the tissues/organs oxygen-deprived. Then how come oximeters are showing normal, i have my readings always between 96 to 98.
2. Why can't we simply remove some portion of blood, like we do in blood donation and our body again regenerated it? Will the regenerated blood still be having these mircoclots?
I am not a medical professional so this is my lay understanding:
1. Blood pulse ox is normal because the blood does have normal oxygen saturation. The hypoxia is due to the microclots "clogging up the pipes" which deliver blood to the tissues. In this case the "pipes" are very small (capillaries, etc).
2. Either viral fragments still in the body or some other mechanism is continuing to produce new blood clots, so removing blood via blood donation will only cause new blood to be reproduced with new clots. Bruce Patterson has mentioned this in several interviews: th-cam.com/video/El1rdF8XET4/w-d-xo.html
For what it's worth, I'm hopeful that I am wrong about the blood donation part. If it helped, blood donation would be a very convenient and safe therapy.
@@vanjacalantropo Hi, looks like my recovery has just stopped at 70%, neither has it dropped nor increased. Though I am not quite sure if i had omicron, but i had fever a few weeks ago.
@@hardyismyname I don’t know how you determine percentage? Are you 70% of your previous health or are your symptoms improved by 70%? You might platough but you can still improve after awhile.. don’t do too much.
@@vanjacalantropo i am 70% of my previous health.
my oximeter was just like that as well, id be breathless and id stick it on and it would read at 98% . i think the problem is that the oxygen is good say in your arm but there's clots constantly developing and breaking down all over your body . So suddenly a clot develops that's related to your kidneys but not your arm, that's gonna make you feel terrible for a bit, but its not affecting your arm so while your oximeter is checking 98% for the blood flow in your finger its NOT a good indication of what's happening on ALL OF THE BLOOD FLOW IN THE BODY. I think that's the misconception/confusion.
In a NORMAL medical environment a doctor will monitor a patients oxygen with a oximeter and, it'll be a very good indication as to the oxygen levels in the body overall.
With the blood clotting in LC its a not a true representation and the oximeter actually belongs in the bin I'm afraid.
I've had it the other way too , I've had readings of 72% and I've felt absolutely fine.
I'm 2 years in ,I've found using a infrared lamp whenever I sit On the computer seems to have had a good effect on me as well. ( its linked to nitric acid production )
What impact, if any, might a statin course have on microclotting?
Dr. Patterson at InCellDx uses Pravastatin alongside Maraviroc to inhibit CCR5 and Fractalkine receptors to stop the endothelial inflammation that is causing the blood clots
not much, all its going to do is reduce the normal lcl, the deformed bad lcl that are floating around in the blood - its not gonna touch them. I think those are the real problem cause they the ones really getting stuck in the blood vessels and causing a lot of inflammation. I'm not a doctor , I've just been forced to do my own research as my doctor is not so interested in long covid:(
Low dosed atorvastatin is on the FLCCC’s treatment plan. So I’d give it a shot if I were you. It didn’t work for me, but every body is different.
Theres many athletes like myself who are suffering from long covid that were fit,healthy,dont smoke,drink,drugs ,sunshine warriors.Docter said i had anxiety wtf. I never had any time in my day to be anxious before this! lol.
i bet its gonna be down to genetics that they find in years to come.
what symptoms u have
Shortness of breath at times and I can't push myself with excersise otherwise Ill become breathless the next day, sleeplessness nights and anxious, sore chest
You are correct. My brother and I had nearly identical symptoms, and that was infection one year apart.
It looks to be designer level virology
I’m a psychotherapist and no sh!t people have anxiety. They don’t feel themselves, don’t know when or if they’ll feel better, they have been isolated for several years and ostracized if they feel differently. Anxiety is a byproduct of all of this not a pathology.
@@Kellykpw62 spot on, as an update, I've made a huge improvement as time has gone by, my sleep pattern is almost resolved, the breathless has gone to the point where I work most days AND I can drive again( I couldn't drive as it felt as if I got information overload every time to the point of an absolute dander on the road ?!?!
My problems now revolve around me going back to sport and my mental outlook of myself which I see as a very sick person incapable of doing much and how my sports peers are light years ahead of me, I cringe to go back and fear the inevitable defeat when ill have to compete again.
Basically you end up with zero confidence in your ability and have to start from scratch:(
I will also add to this discussion, that Covid is entering the mitochondria of cells everywhere which is where our energy comes from (ATP). This is another possible reason for the sheer exhaustion.
May be ,,low temperature agglutinine,,trigger by increasing blood viscousity and ischemic effect, endotelial inflamation especially at perifereal circulation ,where blood have low temperature.?
May be N-acetylcysteine by decreasing blood viscousity can stop pathogenesis of endotelial damages
I'm using an infrared body lamp and I'm feeling ALOT better after i sit Infront of it everyday. maybe there is something to this low temperature idea
Dr Mary Fowkes did autopsies and found micro blood clots and inflammation
Interesting. I have never been diagnosed with covid. However, after running a d dimer after delivery of my baby, my level was over 5,000 or 7.3, even after a month post pardum. I just had another test to check if the level has dropped any. Waiting on results.
I had PE 5 years ago as well, with Hashimoto's in remission, fibromyalgia
Very interesting, thank you!
Have either of you Drs seen this type of abnormal clotting in snake venom!
Sorry to ask but if anyone will know you will 🙏
I have had keloids for a couple of months and then healed on it`s own. Long covid is just too long.
Hi..tell me please what is keyloids?
If a dropp of blood of some patients after SARS COV2 infection was put on a cold glass lamela agglutinate before coagulate.
At microscope can be seen erytrocyte aggregation like coin rolls.(not at normal body temperature)
Like in Waldenstrom macroglobulinemia may be increasing level of some antybody induce that.
That can increase blood viscousity, damaging capillary blood flow.
Did N- acetylcysteine decrease blood viscousity?
Did Dextran40 decrease blood viscousity?
Latex reaction for detection of rheumathoid factor indicate that some antybody complex neutralizeze electrostatic forces that maintain suspension ,and adsorbtion forces induce aggregation.(?)of particles of polistiren covered with latex
Thank you so much for this!
Does omicron cause micro clots in long Covid? Thank you!
May be ,,low temperature agglutinine,, occur after SARS COV2 infection?
Its not the spike protein doing the damage, they are oxalates, use large doses of vit k, and ozonated oil/ozone therapy to clear them out.
I’m long covid patients my spike protein igg antibody is 4000 ug so high
At TWiV Nr 659 at min29 virologist Christian Drosten indicate very low tissue temperature better to replicate SARS COV2 in lab.(septembrie 2020)
Avoiding persistent infection with SARS COV2,we avoid to hiperstimulate specific immune system.
May be ,,mask wearing,,not only filtrate but also increase upper mucoseal respiratory temperature.?
May be oxigenotherapy must use more warmed oxigen mix.?If SARS COV2 infect respiratory tract.
Thx
its crazy how covid just can give us problems we never had
I dont think you scientist know how desperate us Long Covid folks are..we cant wait another fucking year..trial smiile..let's get this done
Well people have had ME for decades and are bedbound or worse so hopefully this will help us ME patients
welcome to the club, I've been waiting 23 years with the same symptoms due to ME, nobody ever cared
@@olmo4767 what symptoms do u have?
@@ThànhTrần-333 extreme lack of energy, pain in every muscle and joint, cognitive deficit, nausea, lightheadness, postural tachycardia, etc
@@olmo4767 sounds like a case of endotheliitis
May be,,latex reaction,it,is pozitive?
why arent they talking about vaccines causing clotting?
🙏
here for the hot drs staying fir the info 😎😉
All talk no treatment! 🤷♀️
Her grandfather helped create Frankensteins Bride
coupla babes.
Spike is a trojan
This doesnt really make any sense..
What doesn't make sense ?