As another Lame Cherry exclusive in matter anti matter.
We are finally finding the silver thread or threat which flows through these mRNA vaxes which is beyond the prions, to something more genocidal, and the rot of this is that Moderna and Pfizer, created their gene programming in the mRNA from DNA fragments, which are left over in the vaxes. The reason this matters is these fragments are Monkey Cancer Virus, and the reality that damaged DNA or parts of it, infused into cells causes something we are familiar with, cancer and HIV. Yes the very VANCERS and VAIDS which have appeared are due to these DNA fragments corrupting the healthy cell structures in a body.
Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes because problems, including the possibility of insertional mutagenesis that could lead to the activation of oncogenes or the inactivation of tumor suppressor genes."
"FDA says they're not aware of any concerns, but Moderna in its own patent lays out exactly the same concerns that exist about DNA in insertional mutagenesis and genotoxicity.
The big words above mean mutant cell replication and gene poisoning. They have in these vaxes inserted mutation genetics into DNA, to cause this prion to mass produce quickly as a spike protein of the coronavirus, the problem is that the contaminating fragments are corrupting cells in this quick replication, causing illnesses.
I bothered to look up some diseases which appeared when the DNA is being contaminated. As you can read by the links below, the manifestations are rapid aging, senility, hand shaking in Parkinsons.
Defects in DNA damage repair have been linked to several human diseases including promoting oncogenesis, heritable neurodegenerative and neuromuscular diseases caused by unstable DNA repeats, neuropathies and myopathies caused by mutations and rearrangements in mitochondrial DNA, neuropsychiatric disorders, and heritable premature aging syndromes.
As you can read, this is exactly what is manifesting in people now in mass. What we can discern in this is, that these diseases are from the damaged DNA replication. Other diseases which have appeared as clots, hardening of blood vessels are not damaged DNA, but something completely different.
As TL noted, we are starting to see people with intestinal problems show up, in operations to cut out intestinal tracts which are no longer viable, This is not even mentioned yet in any of the current data.
The Lame Cherry will publish below the listed corrupt DNA diseases which are known. In reading this list, I'm seeing things people we know who have been vaxed are experiencing, including a form of hyper cateract growth that degenerated so quickly the person they needed emergency surgery.
| Disease | Affected DDR Mechanism | Affected Gene(s) | Disease Prevalence | Phenotype |
| (1) Cancer syndromes | ||||
| Ataxia-Telangiectasia[43,152] | DSB repair | ATM | 1 in 40,000-100,000 live births | Lymphomas, leukemias, breast cancer |
| Ataxia Telangiectasia-Like Disorder[153] | DSB repair | MRE11 | Rare | Leukemias |
| Bloom Syndrome[96,97,154] | HR repair | BLM | Overall prevalence is unknown; estimated 1 per 48,000 births in the Ashkenazi Jewish population | Carcinomas, leukemias, lymphomas |
| Fanconi Anemia[30,32,155] | ICL repair, HR | FANCA-C, FANCD1, D2, FANCE-G, FANCI, J, L-N | 1 in 136,000 newborns, varies from 1 in 100,000 to 250,000 births | Leukemia, myelodysplasia, squamous cell carcinoma |
| Hereditary Breast and Ovarian Cancer Syndrome[156,157] | HR repair | BRCA1, BRCA2 | Estimated 1 in 333 to 500 individuals have a BRCA1/2 mutation | Breast and ovarian cancers |
| Hereditary Nonpolyposis Colorectal Cancer[158-160] | MMR | MSH2, MSH6, MLH1, PMS2 | 2%-5% of the Caucasian population | Colorectal cancer, carcinomas |
| Li-Fraumeni Syndrome[161,162] | DSB repair | TP53 | Not well established, one group reported prevalence at 1:3,555 to 1:5,5476 | Gliomas and breast cancers, sarcoma |
| MYH-Associated Polyposis[163-165] | BER, oxidative damage repair | MYH | Responsible for 7% of attenuated adenomatous polyposis and 6.6% of classic polyposis cases | Colorectal cancer |
| Nijmegen Breakage Syndrome[117,166,167] | DSB repair | NBS1 | 1 in 100,000 newborns worldwide | Lymphomas |
| Rothmund-Thomson Syndrome[101] | BER, HR? | RECQL4 | Prevalence is unknown; about 300 cases have been reported in the literature | Osteosarcoma |
| Werner Syndrome[99,168,169] | BER, HR, telomere maintenance | WRN | 1 in 200,000 in the US, estimated 1 in 30,000 people in Japan and Sardinia | Various cancers (thyroid, melanoma, soft tissue sarcoma, osteosarcoma) |
| Xeroderma Pigmentosum[2,170,171] | TC-NER | XPA-G, POLH | 1 in 1,000,000 in US and Europe, about 1 in 22,000 in Japan | UV-induced skin cancers |
| (2) Neurologic syndromes | ||||
| Aicardi Goutieres Syndrome[172,173] | Damage signaling | RNASEH2, TREX1 | 1 to 5 per 10,000 live births | Cerebral atrophy, intracranial calcifications, microcephaly, neurodegeneration |
| Ataxia Telangiectasia[43,152] | DSB repair | ATM | 1 in 40,000-100,000 live births | Cerebellar ataxia, neurodegeneration, oculomotor apraxia |
| Ataxia Telangiectasia-Like | DSB repair | MRE11 | Rare | Cerebellar ataxia, neurodegeneration, oculomotor apraxia |
| Ataxia with Oculomotor Apraxia Type 1[64,77] | SSB repair | APTX | A rare disease, most frequent in Portugal and Japan | Cerebellar ataxia, neurodegeneration, oculomotor apraxia |
| Ataxia with Oculomotor Apraxia Type 2 | SSB repair, R-loop resolution | SETX | Estimated 1 in 900,000 individuals worldwide | Cerebellar ataxia, neurodegeneration, oculomotor apraxia |
| Cerebro-Ocular Facio-Skeletal syndrome[176,177] | TC-NER | CSB, XPD, XPG, ERCC1 | Rare - fewer than 20 cases confirmed | Brain calcification, hypomyelination, microcephaly, neurodegeneration |
| Cockayne Syndrome[87,178] | TC-NER | CSA, CSB, XPB, XPD, XPG | Less than 1 case per 250,000 live births in the US | Microcephaly, demyelination, neurodegeneration |
| Dyskeratosis Congenita[179] | Telomere maintenance | DKC1, TERC | Prevalence is unknown; more than 400 families were reported in the world | Microcephaly, cognitive impairment, developmental delay |
| Microcephaly, Intractable Seizures, and Developmental Delay | NHEJ, SSB repair | PNKP | Rare, prevalence unknown | Microcephaly, seizures, growth defects |
| Seckel Syndrome[139,183] | DSB repair, replication fork repair | ATR, PCTN, SCKL2, SCKL3 | Less than 1 in 1,000,000 | Microcephaly, cognitive impairment, developmental delay |
| Spinocerebellar Ataxia with Axonal Neuropathy[75] | SSB repair | TDP1 | Rare | Cerebellar ataxia, neurodegeneration |
| (3) Aging syndromes | ||||
| Ataxia-Telangiectasia[43,152] | DSB repair | ATM | 1 in 40,000-100,000 live births | Premature bone marrow exhaustion, early-onset diabetes, neurodegeneration |
| Alpers-Huttenlocher Syndrome[184] | Mitochondrial DNA replication and repair | POLG1 | 1 in 100,000 individuals | Neurodegeneration, liver failure |
| Bloom Syndrome[96,97,154] | HR repair | BLM | Overall prevalence is unknown; estimated 1 per 48,000 births in the Ashkenazi Jewish population | Early-onset diabetes, pulmonary disease, increased cancer risk |
| Cockayne Syndrome[86,87,178] | TC-NER | CSA, CSB, XPB, XPD, XPG | Less than 1 case per 250,000 live | Cataracts, muscle atrophy, neurodegeneration |
| Fanconi Anemia[30,32,155] | ICL repair | FANCA-W | 1 in 136,000 newborns, varies from 1 in 100,000 to 250,000 births | Premature bone marrow exhaustion, increased cancer risk |
| Hutchinson-Guilford Progeria Syndrome[185,186] | DDR, DSB repair, chromatin organization | LMNA | Approximately 1 in 20,000,000 | Alopecia, atherosclerosis |
| Werner Syndrome[99,168,169] | BER, HR, telomere maintenance | WRN | 1 in 200,000 in the US, estimated 1 in 30,000 people in Japan and Sardinia | Growth retardation, short stature, premature graying of hair, alopecia, arteriosclerosis, atrophic skin, bilateral cataracts, type II diabetes |
| (4) Immunodeficiencies | ||||
| Hyper-IgM Syndrome[112] | CSR | AID, UNG | Fewer than 1 in 1,000,000 | Increased IgM levels, lymphoid hyperplasia |
| Immunodeficiency with Microcephaly[1,187] | NHEJ | XLF | Less than 1 in 1,000,000 worldwide | Hypogammaglobulemia, lymphopenia, microcephaly |
| Ligase IV Syndrome[82,188] | NHEJ | LIG4 | Prevalence is unknown; globally only 28 cases are described | Hypogammaglobulemia, lymphopenia[188] |
| Radiosensitive Severe Combined Immunodeficiency[187] | NHEJ | ARTEMIS | Rare | Agammaglobulinemia, lymphopenia |
| Schimke Immuno-Osseous Dysplasia | Replication fork repair | SMARCAL1 | 1 in 1,000,000 to 3,000,000 people in North America | T cell deficiency |
| Severe Combined Immunodeficiency Syndrome[154,187] | NHEJ | Rag1, Rag2 | 1 in 100,000 in US | Agammaglobulinemia, lymphopenia |
This is now confirmed in these vaxes in cause and effect. There is not a cure for prions. Ivomec appears to arrest some of this in the replication, but there is not any cure but a miracle from God for damaged DNA.
TL and I have had numerous discussions about this the past years, as I kept harping ON THE PLATFORM, as I knew that was the key part in I knew from experience that we could be exposed to prions which would replicate in us, but in a few weeks flush out literally with diarrhea.
I knew there had to be something in the vax which was the replication factor which did this as the platform which separated the vaxed from the pure bloods.
This platform has to be in injected or enter through the blood barrier, which would include sex or contamination from body fluids or excrements.
What we are witnessing though is two parts in two different disease orders. The one platform is the hyper reproduction of prions for immunity from the coronavirus as the spike protein. The other is this corrupt DNA, which just happens to be fused into the prion replication platform. That is what is manifesting this array of debilitating diseases.
The reason that the Ivomec like TB vaccines work is there is a fragment of some critter or TB spliced into the sequence. If it interferes with the replication, it is a viable treatment.
Honestly, the treatment for damaged DNA is what the medical community has been using to treat specific illnesses. Those treatments are working, but some things like aging do not have a treatment in this trans human portfolio.
We are learning what was deliberately engaged in with this serum. Protocols were violated and it was known what would happen, as it was supposed to happen, and that is why the Pharms were all given legal protection.
We are dealing with two if not three manifestations of mass disease, off the one platform of hyper replication. What this is, is just accelerated degenerative diseases which can be treated, and death for which only a hole in the ground is the cure.
The vaxed were scared and enjoyed tormenting those unvaxed. I just feel sad for the vaxed.
This is another Lame Cherry exclusive in matter anti matter.
Nuff Said
agtG
