Time markers:
01:09 What are agonistic autoantibodies (AAB)?
05:16 Clinical pictures and their autoantibodies (i.a. Alzheimer, high blood pressure, vascular diseases, glaucoma)
9:18 IgG immunoadsorption
10:17 How does a immunoadsorption proceed
12:28 Alzheimer
15:38 subsidy from health insurance?
18:21 Diabetes
20:28 Precis
23:54 Conclusion
post-viral syndrome - post-covid/-vaccination - CFS - vascular and Alzheimer dementia - Diabetes Mellitus - thromboangiitis obliterans - heart failure - therapy resistant hypertension etc.
Engineer Mrs. Marion Bimmler is a biochemist and Engineer for laboratory technology. She did research on the AAB for decades and especially published her studies with vascular and Alzheimer dementia. She owns two patents for AAB determination - control measurements show a 100% consensus.
Here is a German overview article, opening as PDF.
These AAB have a prevalence of 3% in the German population, which has been discovered by a blood bank analysis.
90% of people who send their blood to the E.R.D.E.-AAK-Diagnostik GmbH, because after a covid infection or vaccination they didn’t return to their previous health condition, were tested AAB-positive.
For such a percentage of discrepancy there has to be a connection - an infection, as well as a vaccination with currently in Germany common covid vaccines can cause a buildup of AABs.
The connection to different diseases, that are connected to AAB, hint long-term consequences we couldn’t detect in previous massive short-term observations.
But there is hope, because AAB can be removed within five consecutive days by the IgG immunoadsorption apheresis. A filter that paid off is the Fresenius’s GLOBAFFIN. This therapy takes 3-5 hours. For old people with vascular problems, it makes sense to insert a central vein catheter. Because healthy antibodies are removed as well, in the following 4-6 weeks one is extra prone to infection. This should be endured by quarantine and wearing a FFP2-mask. Administering immunoglobulins can once again lead to a vaccination of AAB, because products are not examined in that context yet. Observation periods of 18 years have shown that these AAB nearly don’t ever return. However, the used filter that provides 19 exertions is kept cool , so that in the worst case another apheresis is possible.
This apheresis also removes other substances that could be separately detected in the eluate.
Using this, the agAAB status of the following diseases can be inspected:
- DCM, myocarditis ( β1- & M2-AAK )
- Hypertension ( α1- & AT1- & ET-AAK )
- Type 2 diabetes ( α1- & AT1- & ET-AAK )
- Dementia ( α1- & β2-AAK )
- Transplantation rejection ( α1- & AT1- AAK )
- Dialysis associated diseases ( α1- & AT1-AAK )
- Glaukom ( β2- AAK )
- TAO, thrombangiitis obliterans ( α1- & ET- & PAR-AAK )
- POTS (pdf), postural orthostatic tachycardia syndrome ( α1- & AT1- & β1- & β2- & M2- & ET- AAK )
- Post-covid-19 ( α1- & AT1- & β1- & β2- & M2- & ET- & ACE2-AAK )
This also applies to post-viral syndromes , such as CFS - I've even found it in Asperger's Syndrome and psychosis - literature also refers to anxiety and depression.
Everyone who’s got these AAB should know it’s not about titres but about yes or no. The dangerous AABs are the ones we can’t see, because they bind to the receptors over weeks and cause a continuous stimulus which in the end leads to a deficit of the mitochondria’s function, so only ADP but no ATP can be built anymore.
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The presented information and recommendation is only for general information and not for advertising or advising purposes. They under no circumstances replace the individual advice from a doctor in person and are no medical help. Treatments in this special field without consulting a doctor - especially with known previous diseases and unclear symptoms - are particularly not recommended.
Негізгі бет Ғылым және технология Self-destruction through one's own immune system - long-covid, hypertension, Alzheimer's and more?
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