Red pill alert needed. I think I need a drink, I feel as I did after reviewing the myriad ways to initiate autoimmune disorders and the consequences. Crashed CD34 out to 300 days with no uptick. RSV in kids you say? No sh!t.
Pure evil, thanks John. I've shared of course with Genervter.
Measles appears milder long term, but the consequences of CD34+ suppression are of interest here:
Targeting and Hematopoietic Suppression of Human CD34+ Cells by Measles Virus†
...Herein we present evidence that measles virus (MV) disrupts hematopoiesis by infecting human CD34+ cells and human bone marrow stroma. MV infection does not affect the hematopoietic capability of hematopoietic stem cells (HSCs) directly; rather, the infection impairs the ability of stroma to support development of HSCs. These results suggest that MV-mediated defects in hematopoiesis contribute to the long-term immunosuppression seen in measles.
..One hallmark of MV immunosuppression is profound lymphopenia (including that involving CD4+ T cells, CD8+ T cells, and B cells), monocytopenia, and neutropenia that persists following virus clearance (2, 20, 33). Interestingly, young children with the highest level of BM output (24, 28) recover most quickly from MV-induced lymphopenia and immunosuppression. Older children and adults with a less robust BM reconstitution capacity require longer periods of time for recovery from MV immunosuppression.
...Other immunosuppressive viruses, such as human cytomegalovirus, dengue virus, murine leukemia virus and human immunodeficiency virus type 1, have been reported to target BM stroma and inhibit hematopoiesis by reducing expression of supportive cytokines such as stem cell factor and/or increasing expression of suppressive cytokines such as transforming growth factor β (1, 4, 21, 22, 27, 30, 41). Thus, stromal cell targeting may be a common mechanism used by immunosuppressive viruses to induce hematopoietic suppression.
I have been re-reading this hard science (for me), which only amplifies the horror.
And, once again, thank you, Doorless Carp, for your inimitable contributions. It is so painful to think about cancer patients who have already been through radiation treatments and were vulnerable to the blandishments of their oncologists, etc. to get the jabs.
My vaccinated relative just got giant cell arteritis, an "autoimmune" or inflammatory problem in which Interferon Gamma is implicated. I don't think that's a mere coincidence.
Now I'm not saying this is to the same degree, it's not ionising radiation, but potential recovery periods are somewhat alarming.
And now relate this to Dr Paul Alexander, who stated that they expected peak immunosuppression to take...5-6 years:
Hematopoietic bone marrow recovery after radiation therapy: MRI evaluation
F Casamassima et al. Blood. 1989.
...Bone marrow recovery was observed only when patients were treated with doses lower than 50 Gy. The earlier radiation-induced modifications of the bone marrow MRI pattern occurred 6 to 12 months after irradiation, and they were most evident 5 to 6 years after the treatment. From 2 to 9 years after radiotherapy, we observed partial recovery. Complete recovery, when it occurred, was observed only 10 to 23 years after the treatment. Our results indicate that MRI studies are likely to be useful in the assessment of radiation-induced injuries.
Galectin approach to lower covid transmission - Drug Development for clinical use
Conclusion PL-M is safe and effective for clinical use in reducing viral load and promoting rapid viral clearance in COVID-19 patients by inhibiting SARS-CoV-2 entry into cells through inhibition of Gal-3.
Is there anything a pregnant woman can do to protect the fetus short of becoming a hermit for the duration of the pregnancy? My daughter is pregnant now, second trimester, but had an active covid infection in April 2022, prior to conception. If she gets covid again, would early treatment help the end results for the fetus? Treatment with supplements (although not sure safety of larger doses in pregnancy) or IVM?
Red pill alert needed. I think I need a drink, I feel as I did after reviewing the myriad ways to initiate autoimmune disorders and the consequences. Crashed CD34 out to 300 days with no uptick. RSV in kids you say? No sh!t.
Pure evil, thanks John. I've shared of course with Genervter.
Measles appears milder long term, but the consequences of CD34+ suppression are of interest here:
Targeting and Hematopoietic Suppression of Human CD34+ Cells by Measles Virus†
...Herein we present evidence that measles virus (MV) disrupts hematopoiesis by infecting human CD34+ cells and human bone marrow stroma. MV infection does not affect the hematopoietic capability of hematopoietic stem cells (HSCs) directly; rather, the infection impairs the ability of stroma to support development of HSCs. These results suggest that MV-mediated defects in hematopoiesis contribute to the long-term immunosuppression seen in measles.
..One hallmark of MV immunosuppression is profound lymphopenia (including that involving CD4+ T cells, CD8+ T cells, and B cells), monocytopenia, and neutropenia that persists following virus clearance (2, 20, 33). Interestingly, young children with the highest level of BM output (24, 28) recover most quickly from MV-induced lymphopenia and immunosuppression. Older children and adults with a less robust BM reconstitution capacity require longer periods of time for recovery from MV immunosuppression.
...Other immunosuppressive viruses, such as human cytomegalovirus, dengue virus, murine leukemia virus and human immunodeficiency virus type 1, have been reported to target BM stroma and inhibit hematopoiesis by reducing expression of supportive cytokines such as stem cell factor and/or increasing expression of suppressive cytokines such as transforming growth factor β (1, 4, 21, 22, 27, 30, 41). Thus, stromal cell targeting may be a common mechanism used by immunosuppressive viruses to induce hematopoietic suppression.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC136250/
Brilliant point made. As allways I "enjoyed" (maybe not the right word) your work. Thank you dear John.
Per usual, thank you!
I have been re-reading this hard science (for me), which only amplifies the horror.
And, once again, thank you, Doorless Carp, for your inimitable contributions. It is so painful to think about cancer patients who have already been through radiation treatments and were vulnerable to the blandishments of their oncologists, etc. to get the jabs.
How horrifying.
A sobering breakdown. Well done
My vaccinated relative just got giant cell arteritis, an "autoimmune" or inflammatory problem in which Interferon Gamma is implicated. I don't think that's a mere coincidence.
Thanks once again.
The most uplifting in your post was the album. I like it.
... in medium and long run we are now more in FUNERAL DOOM territory.
(https://bellwitch.bandcamp.com/album/mirror-reaper?from=hp) ;)
Now I'm not saying this is to the same degree, it's not ionising radiation, but potential recovery periods are somewhat alarming.
And now relate this to Dr Paul Alexander, who stated that they expected peak immunosuppression to take...5-6 years:
Hematopoietic bone marrow recovery after radiation therapy: MRI evaluation
F Casamassima et al. Blood. 1989.
...Bone marrow recovery was observed only when patients were treated with doses lower than 50 Gy. The earlier radiation-induced modifications of the bone marrow MRI pattern occurred 6 to 12 months after irradiation, and they were most evident 5 to 6 years after the treatment. From 2 to 9 years after radiotherapy, we observed partial recovery. Complete recovery, when it occurred, was observed only 10 to 23 years after the treatment. Our results indicate that MRI studies are likely to be useful in the assessment of radiation-induced injuries.
https://www.sciencedirect.com/science/article/pii/S0006497120789755?via%3Dihub
We are screwed
Do you think a ’vaccinated’ man’s sperm will affect the immune system of the baby in the same way? Or just the exposure in utero?
New PrePrint Alert:
https://www.medrxiv.org/content/10.1101/2022.11.09.22282151v1
Galectin approach to lower covid transmission - Drug Development for clinical use
Conclusion PL-M is safe and effective for clinical use in reducing viral load and promoting rapid viral clearance in COVID-19 patients by inhibiting SARS-CoV-2 entry into cells through inhibition of Gal-3.
Is there anything a pregnant woman can do to protect the fetus short of becoming a hermit for the duration of the pregnancy? My daughter is pregnant now, second trimester, but had an active covid infection in April 2022, prior to conception. If she gets covid again, would early treatment help the end results for the fetus? Treatment with supplements (although not sure safety of larger doses in pregnancy) or IVM?