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#covid19

50 posts38 participants4 posts today

Heute vor vier Jahren, am 15. April 2021, war ich sehr froh: Ich konnte den Termin für meine erste Sars-CoV-2-Impfung buchen!

Die erste Tranche von Terminen, für die ich in Frage gekommen bin, wurde damals freigeschaltet. Die Termine waren ab Montag, ich hab quasi sofort reagiert, und trotzdem war mein Termin am Dienstag Nachmittag, so groß war damals die Nachfrage.

Meine Eltern (Gruppe 65+) hatten zu dem Zeitpunkt bereits die erste Teilimpfung, und meine Großmutter (90+) beide. Davor war die Phase mit den Bürgermeistys, erinnert ihr euch? Szenen haben sich abgespielt, weltweit! Es wurde gelogen und betrogen, um schneller an die Impfung zu kommen.

"Sie haben soeben beim Impfservice Wien Ihre Termine für die zwei Teilimpfungen der Corona-Schutzimpfung vereinbart. Dieses Mail enthält alle Termininformationen zur *ersten Teilimpfung* der Corona-Schutzimpfung. Die
Termindetails zur zweiten Teilimpfung erhalten Sie zeitgerecht in einem weiteren Mail vom Impfservice Wien..."

Die ersten Impfungen waren alle im Austria Center, im Untergeschoß unter dem Vorplatz, mit der Voranmeldung oben an Containern unter dem Flugdach. Memories!

From Germany:

Abnormal Coronary Vascular Response in Patients with #LongCOVID Syndrome – a Case-Control Study Using Oxygenation-Sensitive Cardiovascular Magnetic Resonance

sciencedirect.com/science/arti

Image is from latest Science for ME weekly update

Hashtags:
@longcovid
#PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC

@covid19 #Coronavirus
#COVID19 #COVID #COVID_19 #COVIDー19 #SARSCoV2 #CovidIsNotOver
@auscovid19 #auscovid19

1/

You know when the Wall Street Journal starts publishing news stories on #COVID19 brain damage, it might be time to pay attention. Don't use your brain? No problem, then!

"Studies have found that older people who have Covid-19 are at increased risk of developing Alzheimer’s sooner than if they haven’t had it... It doesn’t look in older adults that this is a reversible process.”

Link to WSJ article: wsj.com/health/wellness/is-cov

Link for those without WSJ access: archive.today/WxF2Z

Replied in thread

@pathfinder @cesarpose @actuallyautistic And what they never seem to get is that such behavior can remove the WISH to associate with them. They can't imagine that anyone who can enjoy socializing would ever lose the desire for it. They assume that the motivation for seclusion must be fear. No, it's anger and disgust. I no longer CARE whether I would be able to defend myself from #COVID19 in public. I simply don't want to socialize with them anymore, whether I would be able to do so safely or not.

Replied in thread

@pathfinder @cesarpose @actuallyautistic Except for work, and my immediate household, I've been avoiding people since the start of #COVID19. The lack of full solidarity against the disease has been intensely alienating. Why should I want to associate with those who would happily infect me with a disease that could leave me maimed or dead?

By comparison, here is a photo taken by my wife in December 2019 — one of the last few times we dined out. I don't think I look much like a misanthrope by nature. But the public reaction to #COVID19 has made me one.

With the LP.8.1.* variant on the way to dominance in most places, it is time to ponder which variant might drive the next wave.

The leading contenders at this point are LF.7.7.2, LF.7.9, NB.1.8.1, NY.9 (new), XEC.25.1, XFG and XFJ.

I show them here using a log scale, so you can compare their growth rates vs the most common LP.8.1.* sub-lineage: LP.8.1.1. Note the recent sample volumes are quite low, so the right side of this chart might not be a representative picture.

#COVID19 #LF_7_7_2 #LF_7_9 #NB_1_8_1 #XEC #XFG #XFJ
🧵

RT @EckerleIsabella@x.com: »My opinion & I will die on this hill: The current anti-vaccine movement will have a major impact on women and will reverse women's rights. When women have to produce extra babies because 1 in 5 will not survive, they will not have energy or time to fight for equality anymore.

While being pregnant, postpartum, caring for many children, caring for a sick child, grieving deceased ones & fearing their siblings dying as well, women will be drained of energy & will not fight oppression. Without vaccines, a lot of healthy children will not survive their early childhood period.

In addition, not providing vaccines will disproportionally affect vulnerable children: While many perfectly healthy children will die, those with underlying conditions are even at higher risk. Not protecting them will shorten their life. We've seen it already during Covid.

I just want to stress this: Most of society is not aware in which a luxury situation vaccines has put parents in only the last few decades, that is, not seeing your young children die. If you don't believe me, read books about the polio period, or visit an old graveyard. It's all there.«

STUDY finds that the Novavax #COVID19 vaccine may provide more robust protection against medically attended COVID-19, compared to Pfizer.

medrxiv.org/content/10.1101/20

So, of course, our HHS secretary is casting doubt on the Novavax vaccine effectiveness and its likelihood of approval this year.

reuters.com/sustainability/boa

medRxiv · Effectiveness of NVX-CoV2373 and BNT162b2 COVID-19 Vaccination in South Korean AdolescentsPurpose: Adolescents can have severe/chronic outcomes from COVID-19. Real-word data on relative vaccine effectiveness (rVE) between mRNA- and protein-based vaccines are limited, and more data are needed on disease outcomes in this age group. Methods: The K-COV-N database, COVID-19 vaccine registry, and health insurance claims were retrospectively reviewed to identify adolescents (12–18-year-olds) in South Korea who received a homologous primary series of NVX-CoV2373 or BNT162b2 and a heterologous or homologous third vaccine dose. Vaccine recipients were propensity score matched to reduce confounding baseline factors. Adjusted hazard ratios (aHRs) for any medically attended COVID-19 post vaccination (starting 14 days post primary series and 7 days post third dose) were calculated to assess rVE every 30 days through a 180-day risk window. Results: From February to December 2022, 3174 and 6253 doses of NVX-CoV2373 and BNT162b2, respectively, were administered to South Korean adolescents. Individuals who received NVX-CoV2373 tended to be older, have a disability, and/or have a prior SARS-CoV-2 infection. Propensity score matching resulted in 107 individuals in each primary series group and 701 and 1417 individuals in the NVX-CoV2373 and BNT162b2 third-dose groups, respectively. The aHR (95% CI) for NVX-CoV2373 compared with BNT162b2 for medically attended COVID-19 in the 180-day risk window was 0.57 (0.31–1.05) for the primary series and 0.68 (0.54–0.84) for the third dose. Discussion: These results suggest that NVX-CoV2373 may provide more robust protection against medically attended COVID-19, compared to BNT162b2, both as a homologous primary series and as a homologous or heterologous third dose. ### Competing Interest Statement E.G., S.-A.C., K.K., E.B., and Y.J.C. are study investigators and do not have any conflicts of interest to report. M.H.G., J.F., and M.D.R. are salaried employees of and may own stock in Novavax, Inc. M.V. was a salaried employee of Novavax, Inc., and may own stock. ### Funding Statement The study was funded by Novavax, Inc. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The study received ethical approval from the Korea University Anam Hospital institutional review board (IRB No. 2023AN0124). I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes The data used in this study are from the K-CoV-N cohort, which is not publicly available. Researchers can apply for access to these data through the National Health Insurance Service (NHIS) and Korea Disease Control and Prevention (KDCA) data linkage system. Applications can be submitted via the Health Care Data Linkage (HCDL) website (https://hcdl.mohw.go.kr/) and are subject to review by the relevant authorities.

The CDC wrote its own elitaph by sneering, condescending at & ultimately dismissing #covid19 & airborne viral transmission advocates, letting Delta Airlines set public health policy, & ultimately being an agency captured & purposed to be subservient primarily to the ruling class.

Walensky et al can roast in hell.

This isnt a good thing of course -- millions will suffer.

But it was in large part because of their actions that it is so.

And yeah, I recall all those houses at Halloween in Atlanta mocking citizens for "doing their own research".

After tacitly suggesting we do just that -- "do your own risk assessment".

Another passage that speaks volumes for me since #covid19. Way before really, Iraq War probably; but never so explicitly conclusive.

"None of us got here overnight. There are stages to the process of being betrayed by your society. One is jolted from complacency by the discovery of difference, by hypocrisy, by inexplicable or incongruous ill treatment.

What follows is a time of confusion -- deconstructing & unlearning what one thought to be the truth. Immersing oneself in the new truth. And then a decision must be made.

Some accept their fate. Swallow their pride, forget the real truth, embrace the falsehood for all they're worth -- because, they decide, they cannot be worth much. If a whole society has dedicated itself to their subjugation after all, then surely they deserve it. Even if they dont, fighting back is too hard, too painful, too impossible. At least this way, there is peace of a sort. Fleetingly.

The alternative is to demand the impossible. To change society [& the prevailing unjust world order]. There can be peace this way too.

But not before conflict."

- NK Jemisin

Continued thread

that Blood Advances paper aligns with earlier autopsy results, and confirmed

SARS-CoV-2+ megakaryocytes are present in lung and brain autopsy tissues from deceased donors who had COVID-19

But heck! We already knew MKs were long-term impacted. This from 2024 ashpublications.org/bloodadvan - though in mice gives what I guess should be an obvious outcome, since the immune system isn't open-loop:

Megakaryocytes (MKs), integral to platelet production, predominantly reside in the bone marrow. [...] at peak SARS-CoV-2 viremia, when the disease primarily affected the lungs, MKs were not significantly different from those from healthy mice. Conversely, a significant divergence in the MK transcriptome was observed during systemic inflammation, although SARS-CoV-2 RNA was never detected in the BM, and it was no longer detectable in the lungs. Under these conditions, the MK transcriptional landscape was enriched in pathways associated with histone modifications, MK differentiation, NETosis, and autoimmunity

and autoimmunity

The breadcrumbs are everywhere.

fin/🧵

Issue Cover
American Society of HematologySARS-CoV-2 infection modifies the transcriptome of the megakaryocytes in the bone marrowIn a mouse model of SARS-CoV-2 infection, cytokines in the bone marrow are different from those in blood and lungs.SARS-CoV-2–mediated inflammation promote
Continued thread

That aligns with results from 2022-2023 like ashpublications.org/bloodadvan which found

Using peripheral blood, we show that megakaryocytes are increased in the systemic circulation in COVID-19

peripheral blood - circulating!!

SARS-CoV-2–containing megakaryocytes are a strong risk factor for mortality and multiorgan injury

2/🧵

Issue Cover
American Society of HematologyCirculating SARS-CoV-2+ megakaryocytes are associated with severe viral infection in COVID-19Key Points. To our knowledge, we provide the first evidence implicating SARS-CoV-2+ peripheral blood megakaryocytes in severe disease.Circulating megakaryo

So. How about this careful result demonstrating viral replication inside megakaryocyte immune cells?

transmission electron microscopy pointed to the presence of viral particles inside bone marrow MK. Immunolabeling confirmed the presence of two SARS-CoV-2 proteins, spike and Orf3a, as well as double-stranded RNA suggesting a potential viral replication cycle.

Note this study is from last month, but it's from hospitalized 2020-2021 patient data. It's existence proof, not population statistics.

That said:

bone marrow MK infection is not a strict determinant of mortality. However, all survivors experienced post-acute sequelae SARS-CoV-2 condition (PASC) diagnosed during post-intensive care follow-up

short 🧵