Alex.C

1.6K posts

Alex.C

Alex.C

@claudechen16

well

Katılım Ocak 2019
534 Takip Edilen4.1K Takipçiler
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Alex.C
Alex.C@claudechen16·
从了解病毒,疫苗的问题,学习了解羟氯喹,伊维菌素,青蒿素。发现除了治疗covid还可以治癌症,最后发现这一百年来的医学被控制,癌症早就被攻克,其实就是寄生虫和其排泄物,甚至大部分疾病都是如此,但是一直被ds掌控了,从此百年医疗体系再无任何突破,癌症手术放化疗,治愈率不到3%(接下)
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Dr. Pat Soon-Shiong
Dr. Pat Soon-Shiong@DrPatrick·
So the Thymus produces T cells. IL-15 is a T cell growth factor. When the Thymus is removed, there is a 2x higher chance of dying earlier of all causes according to this report. These findings are consistent with the JAMA paper that shows when ALC is less than 1,500 (low T cells) longevity is decreased with increased mortality risk from all causes. The data is consistent: IL-15 is a T cell growth factor and they called T cells because of the T in Thymus. And IL-15 was ranked #1 by NCI and FDA to "cure" cancer as far back as 2007. Now this report links the Thymus (which produces T cells) to longevity - consistent with the JAMA report that 52 million Americans suffer from low T cells, called lymphopenia. IL-15 to treat cancer, enable longevity and to overcome sepsis - Immunotherapy 2.0. Stay tuned. Are the dots connecting that ALC matters? JAMA Zidar 2019: "Association of Lymphopenia With Risk of Mortality Among Adults in the US General Population" jamanetwork.com/journals/jaman… WaPo Gift Link: "The body's most mysterious organ may play a key role in longevity and cancer. What to know about the incredible shrinking thymus"
Dr. Pat Soon-Shiong tweet media
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AusMini
AusMini@aus_mini·
🧐Wilcock 解释说:Illuminati(光明会)或 Kabbalist(卡巴拉)团体在“精神规则”下运作。 他们必须通过音乐视频、颁奖典礼等公开媒体提前披露自己的计划。 这样才能获得公众的“默许同意”,从而合法化他们的行动。 这被视为一种“黑魔法”或精神层面的协议:负面力量需要邀请或同意才能充分运作。
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Inty News
Inty News@__Inty__·
马斯克:让瞎子看见东西只是开始
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Camus
Camus@newstart_2024·
Dr. Patrick Soon-Shiong drops a paradigm-shifting take on cancer treatment in this clip: For 50 years, we've fought cancer like a war—using poisons (chemo) and radiation to shrink tumors temporarily—while unknowingly wiping out the very immune cells that could remember the enemy and deliver long-term survival. He compares it to the gastric ulcer breakthrough: Doctors ridiculed the idea that an ulcer was caused by infection (treatable with antibiotics) until the science proved it right. Same story here? Core insight: The root cause of cancer (and even limited longevity) is immune system collapse. Maintain robust protective cells → you don't just survive cancer, you thrive into old age. He cites the world's oldest person (lived to 122) whose only standout feature was an exceptionally active immune system. It's a call to rethink: Stop treating symptoms with war-era weapons; focus on restoring and protecting the immune system as the real battlefield. Mind-blowing or overhyped? Have you seen cases where immune-focused approaches changed outcomes—or are we still too locked into the old paradigm? Share your thoughts below.
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Yasin Aslan
Yasin Aslan@YasinAslanTrk1·
Suudi Arabistan Gıda ve İlaç İdaresi, Mesane ve Akciğer Kanseri Tedavisi İçin Kanseri Kemoterapisiz Yok Eden 'Anktiva' Adlı Çığır Açan Yeni Kanser İlacına Hızlandırılmış Onay Verdi. Anktiva, vücudun kendi savunma sistemini harekete geçiren yeni nesil bir immünoterapi ilacıdır. Yani kanseri doğrudan zehirlemek yerine, vücudun kanserle savaşan askerlerini güçlendirerek etki gösterir. Bu ilaç, bağışıklık sistemimizin kanserli hücreleri tanıyıp yok edebilenen önemli savaşçıları olan NK hücrelerini ve kanseri tanıyıp hatırlayan T bağışıklık hücrelerini çoğaltıp daha aktif hâle getirir. Böylece bağışıklık sistemi, kanser hücrelerini daha kolay bulur ve hedef alır. Klasik kemoterapiler çoğu zaman sağlıklı hücrelere de zarar verir ve bağışıklığı zayıflatır. Anktiva ise tam tersine, bağışıklık sistemini güçlendirmeyi amaçlar. Bu nedenle daha hedefli etki, daha az yan etkive daha uzun süreli bir bağışıklık cevabı sunma potansiyeline sahiptir. Bu yaklaşımın ne kadar güçlü olabileceğini gösteren çarpıcı bir örnek de klinik çalışmalarda rapor edilmiştir: Kemik iliğinin %95’i kanser hücreleriyle dolmuş, standart tedavilere hiç cevap vermeyen bir lenfoma (kan kanseri) hastasında, hastadan ya da uygun bir bağışçıdan alınan bağışıklık hücreleri laboratuvar ortamında kanseri tanıyıp saldıracak şekilde güçlendirilmiş ve tekrar hastaya verilmiştir. Sonuçta kemik iliği tamamen temizlenmiş ve hastada 15 aydır hastalığa dair hiçbir bulguya rastlanmamıştır. Bu örnek, bağışıklık sistemini doğru şekilde yönlendirmenin kanserle mücadelede ne kadar etkili olabileceğini göstermektedir. Yapılan klinik çalışmalarda, özellikle standart tedavilere cevap vermeyen zor vakalarda, bağışıklık sisteminin yeniden toparlandığı, hastaların hayat süresinin uzadığı ve başta akciğer kanseri olmak üzere farklı kanser türlerinde umut verici sonuçlar elde edildiği bildirilmektedir. Anktiva’nın geliştirildiği şirketin kurucusu, dünyaca tanınmış milyarder cerrah ve bilim adamı Dr. Patrick Soon-Shiong’dur. Şirket, kemoterapisiz bağışıklık temelli tedaviler üzerinde uzun süredir çalışmalar yürütmektedir. Suudi Arabistan’ın, Anktiva’yı yetişkin mesane ve akciğer kanseri hastaları için onaylaması, bağışıklık sistemi temelli kanser tedavilerinde önemli ve öncü bir adım olarak görülmektedir. Bu onay, tedavi için ülkeye hasta akını başlatması ihtimalini de güçlendirmiştir.
Yasin Aslan tweet media
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redpillbot
redpillbot@redpillb0t·
RFK Jr: "The polio vaccine contained a virus called SV40." "It's one of the most carcinogenic materials that is known to man." "But it was in that vaccine. 98 million people... in my generation got it." "And now you've had this explosion of soft tissue cancers in our generation that kill many, many, many, many, many more people than polio ever did."
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Dr Dave Cartland BMedSc MBChB Ex-MRCGP
🚨 FOUR Independent Sources Confirm Pfizer/Moderna mRNA Can Integrate Into the Human Genome 📌 Aldén et al: Pfizer mRNA reverse-transcribed into DNA in liver cells—within 6 hours 📌 Kyriakopoulos et al: showed genome integration may happen via: LINE-1, Polymerase theta (Polθ), Defective DNA repair pathways. These routes could trigger cancer, autoimmunity, or inheritable DNA damage. 📌 InModia Lab (Germany): Spike + SV40 found in human tissue years later 📌 Neo7Bioscience + Univ. of North Texas: Persistent synthetic RNA, SV40, and cancer-linked gene dysregulation in vaccinated blood Some may become permanent spike factories—driving chronic inflammation, immune collapse, and cancer. As regulators remain silent, we will continue to study these deeply worrisome findings. Join ➣ 👉@COVID19VACCINEVICTIMSANDFAMILIES
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墓碑科技
墓碑科技@mubeitech·
治寄生虫的药,怎么就能治癌症? 这听起来像天方夜谭。 但世界顶尖的癌症生物学家,托马斯·塞弗里德,给出了答案。 答案就两个字:能量。 癌细胞和寄生虫,它们俩的能量来源,竟然是同一条路! 它们都依赖一种特殊的代谢途径,叫“线粒体底物水平磷酸化”。 你看,芬苯达唑、甲苯咪唑这些药,本来是干嘛的? 杀寄生虫的。 它们攻击的就是这条能量通路。 结果呢? 药物根本不在乎攻击的是寄生虫,还是癌细胞。 只要你用这条能量通路,它就干掉你。 所以,药到病除的奇迹就发生了。 这根本不是因为“癌症是寄生虫”。 别搞错了。 而是因为它们共享了同一个致命的弱点。 更有意思的是什么? 当身体进入一种叫“营养性生酮”的状态时, 这些老药,会变得“超级有效”! 这给了一个全新的思路: 把那些被扔掉的、被认为无效的药物,重新捡回来。 在新的身体状态下,它们可能就是奇迹。 至于那个备受争议的伊维菌素呢? 塞弗里德教授的实验室因为政治原因没去碰它。 但他也指出了,伊维菌素走的是另一条路 它直接启动了癌细胞的“死亡程序”。 你看,捅破了那层窗户纸,原理就这么简单。
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Liz Churchill
Liz Churchill@liz_churchill10·
How TF is this not a War Crime? “We found that vaccinated children had 54% HIGHER CANCER RATES compared to the unvaccinated in our peer-reviewed reanalysis of the Henry Ford birth-cohort study...”
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Dr. Pat Soon-Shiong
Dr. Pat Soon-Shiong@DrPatrick·
Working to explain to the world how and why Bioshield works. T cells and NK cells kill cancer, that’s irrefutable. Low NK cells and T cells means cancer grows, that’s irrefutable. So if there is a drug available to boost NK and T cells then there is better chance to kill the cancer cell of any tumor type – That’s the how and it is that simple. 1. NK and T cells (lymphocytes) kill cancer… causation 2. Anktiva proliferates, grows and activates NK and T cells in the body... causation (and in the FDA approved label) 3. Adding Anktiva to current standards of care have shown prolonged survival in patients with cancer across multiple tumor types since it is treating the immune system... causation. That is the HOW! Anktiva the Bioshield is the first immunotherapy in history of medicine that is FDA approved with a mechanism of action to grow and supercharge NK and T cells in the body, generate memory T cells and restore the immune system without stimulating immunosuppressive T cells. Now what's next? We can measure low NK and T cells (lymphopenia) with a simple blood test (ALC). This is no different than the same test measuring low red blood cells (anemia) or low neutrophils (neutropenia). Low NK and T cells are called lymphopenia. Ask your doctor what is my ALC? (absolute lymphocyte count) Today, FDA has approved EPOGEN to treat anemia regardless of cancer type and has approved NEUPOGEN to treat neutropenia regardless of cancer type. So, based on the mechanism of action of ANKTIVA and the irrefutable causation that NK cells and T cells kill cancer, ANKTIVA should be enabled to treat patients with low NK and T cells (lymphopenia) regardless of tumor type. Especially since ANKTIVA, by activating NK and T cells (reversing lymphopenia) is the only FDA APPROVED mechanism of action in the label to generate MEMORY T CELLS. This supercharging of the immune system happens regardless of the cancer type and we have now shown in completed clinical trials across multiple tumor types including lung cancer (NSCLC), small-cell lung cancer (SCLC), urothelial carcinoma, head and neck cancer, melanoma, colorectal cancer, cervical cancer, renal cell carcinoma, gastric cancer, and hepatocellular carcinoma (manuscript in progress) that by increasing NK and T cells, we induce prolonged survival in patients who have failed all standards of care including current immunotherapy with checkpoint inhibitors. This mechanism of action has already been approved showing long term complete responses, but approved only for an orphan state of a subset of bladder cancer. So, if ANKTIVA could receive the same consideration as EPOGEN and NEUPOGEN as an immune supportive agent, many patients could benefit now without having to fly to LA. I hope we can change that quickly and change the lives of countless of desperate patients in which all standards of care have failed. Working hard to change the course of cancer everyday. The paradigm change is we are treating the immune system, regardless of its cancer type. Cancer is the symptom and the collapse of the immune system is the root cause.
Dr. Pat Soon-Shiong tweet media
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Thomas Sowell Quotes
Thomas Sowell Quotes@ThomasSowell·
RFK Jr: "You have in New York City Bill Gates hosting a coronavirus pandemic simulation. His co-host is Avril Haines, the Deputy Director of the CIA."
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Nicolas Hulscher, MPH
Nicolas Hulscher, MPH@NicHulscher·
PATHWAY TO AUTISM 💉 Multiple Vaccines → 🤒 Fever/Seizure → 💊 Tylenol → 🧠 Developmental Regression (AUTISM) Tylenol is an amplifier — VACCINES are the trigger.
Nicolas Hulscher, MPH@NicHulscher

🚨BREAKING: White House Announces Tylenol–Autism Link, Opens Door to Vaccines The pathway to developmental regression begins with VACCINES, NOT acetaminophen. As Trump said: “They pump so much stuff into those beautiful little babies, it’s a disgrace.” But the spotlight fell on Tylenol. The evidence is clear: it is NOT the root cause. At most, it weakens defenses and amplifies risk. The true trigger — then and now — is VACCINES. 📍THE EVIDENCE: • Prada et al. (2025): 27 studies linked prenatal Tylenol to ↑ NDD risk; autism never at birth, emerges ages 2–8 — the vaccine years. None accounted for vaccination. • Schultz (2008): Tylenol after MMR = 6× autism risk; 8× in severe post-vax reactions. Ibuprofen showed no link. • Yengst (2025): 674k kids — repeated fevers/illness = 2.5–4× autism risk. These fevers often follow vaccines. Tylenol depletes glutathione, the body’s master antioxidant, just as the brain faces fever, seizures, and inflammation. Some pediatricians even recommended it before vaccines — priming kids for worse outcomes. 📍Confounding by Indication: Tylenol use is rarely random — it’s given because a child is feverish or seizing, often post-vaccine. That means the reason for Tylenol (a vaccine reaction) is already risky. 📍Timeline Reality: Tylenol hit the market in the 1950s. Autism rates stayed flat. The surge began in the late 1980s–90s, when the vaccine schedule doubled and tripled. If Tylenol were the cause, the spike would’ve started decades earlier. 📍Missing Evidence: No case reports show regression from Tylenol alone. But thousands of parental reports + multiple peer-reviewed studies document regression after vaccination. Nonetheless, today’s announcement cracks the door to an official investigation into the glaring link between vaccines and autism. At the McCullough Foundation, we are finalizing one of the most comprehensive analyses ever conducted on autism’s causes — untainted by fraud, bias, or corruption. All risk factors will be included, INCLUDING VACCINES. No stone will be left unturned — and no protected interest will be spared.

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Ethical Skeptic ☀
Ethical Skeptic ☀@EthicalSkeptic·
Summary (4:45pm, 22 Feb 2025) Autism = 1 in 31 (1 in 12 for boys) - Hyperpandemic Multifactorial Causes: A. Vaccines B. Acetaminophen supra-additive interaction C. Folate deficiency FDA will notify physicians that 1. vaccine schedules are too aggressive / excessive / bundled 2. the use of acetaminophen should be eliminated as a treatment for vaccine reactions 3. the use of acetaminophen should be eliminated during pregnancy 4. An end to silencing and demonizing mothers (parents) who cite vaccine injury 5. "We will perform the studies which should have been done 25 years ago."
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Chief Nerd
Chief Nerd@TheChiefNerd·
TRUMP: “We have already taken out and are in the process of taking out mercury and aluminum … You know what aluminum is? Who the hell wants that pumped into a body? … We're having them taken out of the vaccines.”
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Secretary Kennedy
Secretary Kennedy@SecKennedy·
Some 40-70% of mothers who have children with autism believe that their child was injured by a vaccine. President Trump believes that we should be listening to these mothers instead of gaslighting and marginalizing them like prior administrations.
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Nicolas Hulscher, MPH
Nicolas Hulscher, MPH@NicHulscher·
We documented the first-ever direct evidence that mRNA “vaccine” genetic code integrates into the human genome. In a young stage IV bladder cancer patient, chromosome 19 now carries a Spike-encoding gene sequence. PERFECT 20/20 bp match — 1 in a TRILLION chance of coincidence.
Nicolas Hulscher, MPH@NicHulscher

🚨BREAKING STUDY: First Direct Evidence of mRNA "Vaccine" Genomic Integration Identified in Stage IV Cancer Patient We found a vaccine DNA plasmid–derived Spike gene sequence integrated into chromosome 19 with PERFECT 20/20 bp identity — accompanied by widespread genomic dysfunction ⬇️ We describe a previously healthy 31-year-old woman who developed rapidly progressive stage IV bladder cancer within 12 months of completing a three-dose Moderna mRNA injection series. Bladder cancer is exceedingly rare in young women, and such aggressive presentations are almost unheard of. To investigate, we performed comprehensive multi-omic profiling, including plasma-derived circulating tumor DNA, whole-blood RNA, and urine exosome proteomics. What we uncovered was striking: ⚠️DIRECT GENOMIC INTEGRATION EVENT: Within circulating tumor DNA, a host–vector chimeric read mapped to chr19:55,482,637–55,482,674 (GRCh38), in cytoband 19q13.42, positioned ~367 kb downstream of the canonical AAVS1 safe harbor and ~158 kb upstream of ZNF580 at the proximal edge of the zinc-finger (ZNF) gene cluster. This sequence aligned with perfect 20/20 bp identity to a segment (bases 5905–5924) within the Spike open reading frame (ORF) coding region (bases 3674–7480) of the Pfizer BNT162b2 DNA plasmid reference (GenBank accession OR134577.1). Although the patient received only Moderna injections, the sequence aligned to Pfizer’s published BNT162b2 plasmid reference because Moderna has never deposited its proprietary plasmid in NCBI. Crucially, both Pfizer and Moderna vaccines encode the same prefusion-stabilized SARS-CoV-2 Spike protein and therefore share identical stretches of nucleotide sequence within the Spike ORF coding region. It is within one of these conserved regions that the integration was captured, producing the perfect 20/20 bp match to the Pfizer reference. The probability of a random 20-base sequence perfectly matching a predefined target is ~1 in a trillion. This makes accidental artifact virtually impossible. Multi-omics profiling revealed: – Oncogene activation (KRAS, NRAS, MAPK1, PIK3CA, CHD4, SF3B1) – DNA repair collapse (ATM, MSH2) → genomic instability – Transcriptomic chaos across plasma, blood, and urine The convergence of (i) close temporal proximity to vaccination, (ii) genomic integration of a vaccine plasmid–derived spike gene fragment, and (iii) consistent transcriptomic and proteomic instability across biospecimens represents a highly unusual and biologically plausible pattern. These findings demand urgent genomic surveillance, orthogonal validation with long-read sequencing, and large-scale cohort studies to fully assess the genomic and oncologic risks of synthetic mRNA technology. This evidence compels the immediate withdrawal of all COVID-19 mRNA products from the market. Humanity now confronts the unprecedented threat of vaccine-induced genomic disruption—a danger too great to ignore. @Docjohnc @neo7bioscience @P_McCulloughMD @McCulloughFund

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