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#BREAKING Ivermectin as a Potential Hazard? While ivermectin is widely used in both veterinary and human medicine, misuse or overdose can result in serious toxicity—especially in genetically sensitive individuals or animals. Toxic effects may affect the nervous system, digestive tract, and cardiovascular functions. General Risks Include: Neurological Effects: Seizures,...

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Jack Straw

335,388 subscribers

27,055 görüntüleme • 1 yıl önce •via X (Twitter)

Sağlık & İyilikHaberler & PolitikaBilim & Teknoloji#BREAKING
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10 Yorum

Exhausted profil fotoğrafı
Exhausted1 yıl önce

What substance misused and overdosed, does not have a negative impact? Applesauce will kill you if I drown you in it...

Jack Straw profil fotoğrafı
Jack Straw1 yıl önce

true...

ConservativeDeadHead 🇺🇸 profil fotoğrafı
ConservativeDeadHead 🇺🇸1 yıl önce

Sounds like big Pharma is getting their propaganda Machine fired up.

Mikey profil fotoğrafı
Mikey1 yıl önce

Not buyin' this one even on double coupon day.

Jack Straw profil fotoğrafı
Jack Straw1 yıl önce

just exercise caution...that's all

"WE THE PEOPLE" profil fotoğrafı
"WE THE PEOPLE"1 yıl önce

Been Used for 6 Decades. How many deaths from Ivermetin vs How many cancer Cures?

ScarletBaker🅾️ profil fotoğrafı
ScarletBaker🅾️1 yıl önce

Sorry but I don’t believe this for a second. However any medication you take can be toxic. Now they want to scare people away from Ivermectin.

Nicholas Tre acc#7 profil fotoğrafı
Nicholas Tre acc#71 yıl önce

Calling bs they don't tell you about the other 1,000's of drugs and chemicals they are sneaking into everything even our clothes and fabrics are infused with these chemicals @SecKennedy knows exactly what they are doing 🙏🏻

Rick Stevenson profil fotoğrafı
Rick Stevenson1 yıl önce

Same guy that told us aliens are coming

Mr. Charles Dotson profil fotoğrafı
Mr. Charles Dotson1 yıl önce

Jack. I recently conducted a 6-month experiment with daily ivermectin. The dosage schedule was designed to ensure the amount of bioavailable ivermectin in the blood was maintained at peak bodyweight levels continuously for 180 days. I'm too old to even want to 'reproduce.' But the regimen worked SO WELL, it cured tremors I'd been having for decades after prolonged stimulant use. It reversed the neurological ravages of prolonged cocaine and alcohol use. A worthy gamble if you've already had your kids.

Benzer Videolar

The truth about vaccines causing disease is two fold: 1. Massive toxicity 2. Genetic alteration • Aluminum: Used as an adjuvant to boost immune response; concerns about potential central nervous system effects and accumulation in the body. • Thimerosal: A mercury-containing preservative; linked to worries about mercury exposure and neurotoxicity. • Formaldehyde: Used in processing to inactivate toxins or viruses; noted for its carcinogenic properties in higher doses. • 2-Phenoxyethanol: A preservative; potential toxicity concerns, including effects on the nervous system. • Tween 80 (polysorbate 80): An emulsifier; animal studies cited showing possible reproductive effects. • Triton X-100 (octylphenol ethoxylate): A detergent used in manufacturing; environmental and reproductive toxicity concerns. • Hydrocortisone: Occasionally present; potential for immune suppression. • Lactose: A milk-derived sugar; allergen concerns. • Bovine serum albumin: From cow’s milk; risk of allergic reactions. • Ovalbumin: Egg protein; common allergen. • Nanoparticles: Used in some modern vaccines • MSG (monosodium glutamate): Stabilizer; neuroexcitatory effects. • Gelatin: Stabilizer derived from animal sources; linked to anaphylactic reactions. • Squalene: An adjuvant; associated with autoimmunity in some studies. • Antibiotics (e.g., polymyxin B, streptomycin, neomycin): To prevent bacterial contamination; allergy risks. • Fetal bovine serum: Used in manufacturing; potential for introducing contaminants. • Human cell strains (aborted fetal stem cells): Used in development and production; ethical and contamination concerns, including DNA from other humans containing both male and female genetics. • Insect cells: Used in production for certain vaccines like flu shots. • Live viruses or virus-vectored components: The active parts in live vaccines; risks of shedding or mutation. Strands of DNA, RNA, or mRNA that alter genetics of infected cells. • Yeast: Used in some recombinant vaccines; allergen potential.
16:16

The truth about vaccines causing disease is two fold: 1. Massive toxicity 2. Genetic alteration • Aluminum: Used as an adjuvant to boost immune response; concerns about potential central nervous system effects and accumulation in the body. • Thimerosal: A mercury-containing preservative; linked to worries about mercury exposure and neurotoxicity. • Formaldehyde: Used in processing to inactivate toxins or viruses; noted for its carcinogenic properties in higher doses. • 2-Phenoxyethanol: A preservative; potential toxicity concerns, including effects on the nervous system. • Tween 80 (polysorbate 80): An emulsifier; animal studies cited showing possible reproductive effects. • Triton X-100 (octylphenol ethoxylate): A detergent used in manufacturing; environmental and reproductive toxicity concerns. • Hydrocortisone: Occasionally present; potential for immune suppression. • Lactose: A milk-derived sugar; allergen concerns. • Bovine serum albumin: From cow’s milk; risk of allergic reactions. • Ovalbumin: Egg protein; common allergen. • Nanoparticles: Used in some modern vaccines • MSG (monosodium glutamate): Stabilizer; neuroexcitatory effects. • Gelatin: Stabilizer derived from animal sources; linked to anaphylactic reactions. • Squalene: An adjuvant; associated with autoimmunity in some studies. • Antibiotics (e.g., polymyxin B, streptomycin, neomycin): To prevent bacterial contamination; allergy risks. • Fetal bovine serum: Used in manufacturing; potential for introducing contaminants. • Human cell strains (aborted fetal stem cells): Used in development and production; ethical and contamination concerns, including DNA from other humans containing both male and female genetics. • Insect cells: Used in production for certain vaccines like flu shots. • Live viruses or virus-vectored components: The active parts in live vaccines; risks of shedding or mutation. Strands of DNA, RNA, or mRNA that alter genetics of infected cells. • Yeast: Used in some recombinant vaccines; allergen potential.

Dr. C

34,173 görüntüleme • 9 ay önce

🚨Dr. William Makis: Ivermectin Dosing for Cancer Explained In one of his recent talks, Dr. William Makis shared what he considers the most important dosing guide for using Ivermectin in cancer. According to Dr. Makis, the starting dose for most cancers is 1 mg per kilogram of body weight per day For example, a person weighing 60 kg would take 60 mg daily, that’s five 12 mg pills or roughly one teaspoon (6 ml) of liquid ivermectin. He mentioned that Ivermectin has shown positive effects in many types of cancer, including: - Breast cancer - Colon cancer - Lung cancer - Pancreatic cancer - Gastric cancer - Renal cell carcinoma - Leukemias He noted that there is very little research on lymphomas, but that doesn’t mean it won’t work, it simply hasn’t been studied much yet. Important points from Dr. Makis: 1) The anti-cancer effect of Ivermectin appears to be dose dependent. 2) Higher doses may offer better results in more aggressive cancers. 3) For very aggressive cancers (such as pancreatic, leukemia, or brain cancers), he suggests considering 2 mg/kg or even up to 2.5 mg/kg per day. Some patients have used these higher doses for many months with only temporary side effects (such as mild visual disturbances that usually resolve within a few days). Real-world examples include a prostate cancer patient whose PSA dropped from 89 to 11 on 45 mg daily, and a terminal gallbladder cancer case that resolved after 14 months on 2 mg/kg. Dr. Makis emphasizes that Ivermectin is a very safe drug with no reported long-term side effects at 1 mg/kg. He recommends starting at this dose and adjusting upwards depending on the individual case and cancer type. He also stresses that people can safely stay on Ivermectin for months as long as there is active disease. If you're researching Ivermectin for cancer protocols, many people are choosing GENIX MEDS for clean, pharmaceutical-grade Ivermectin with straightforward worldwide delivery. #Ivermectindosage #MakisMD #Genixmeds
5:47

🚨Dr. William Makis: Ivermectin Dosing for Cancer Explained In one of his recent talks, Dr. William Makis shared what he considers the most important dosing guide for using Ivermectin in cancer. According to Dr. Makis, the starting dose for most cancers is 1 mg per kilogram of body weight per day For example, a person weighing 60 kg would take 60 mg daily, that’s five 12 mg pills or roughly one teaspoon (6 ml) of liquid ivermectin. He mentioned that Ivermectin has shown positive effects in many types of cancer, including: - Breast cancer - Colon cancer - Lung cancer - Pancreatic cancer - Gastric cancer - Renal cell carcinoma - Leukemias He noted that there is very little research on lymphomas, but that doesn’t mean it won’t work, it simply hasn’t been studied much yet. Important points from Dr. Makis: 1) The anti-cancer effect of Ivermectin appears to be dose dependent. 2) Higher doses may offer better results in more aggressive cancers. 3) For very aggressive cancers (such as pancreatic, leukemia, or brain cancers), he suggests considering 2 mg/kg or even up to 2.5 mg/kg per day. Some patients have used these higher doses for many months with only temporary side effects (such as mild visual disturbances that usually resolve within a few days). Real-world examples include a prostate cancer patient whose PSA dropped from 89 to 11 on 45 mg daily, and a terminal gallbladder cancer case that resolved after 14 months on 2 mg/kg. Dr. Makis emphasizes that Ivermectin is a very safe drug with no reported long-term side effects at 1 mg/kg. He recommends starting at this dose and adjusting upwards depending on the individual case and cancer type. He also stresses that people can safely stay on Ivermectin for months as long as there is active disease. If you're researching Ivermectin for cancer protocols, many people are choosing GENIX MEDS for clean, pharmaceutical-grade Ivermectin with straightforward worldwide delivery. #Ivermectindosage #MakisMD #Genixmeds

GENIX MEDS

19,733 görüntüleme • 25 gün önce

When I caught Covid, my friends rushed doses of Ivermectin to me — kicked Covid in 24 hours. Here’s a cancer surgeon revealing her discoveries about the impact of Ivermectin on CANCER… 9 min. must see: Also — Compelling Evidence for Ivermectin in Treating Covid: · Front Line COVID-19 Critical Care Alliance Review — This review, which summarized findings from 27 studies, concluded that ivermectin demonstrates a strong signal of therapeutic efficacy against COVID-19. This includes both prevention and treatment aspects. · Meta-Analysis on Ivermectin — A meta-analysis covering 96 studies and over 135,000 patients suggests that ivermectin has shown effectiveness in combating COVID-19. This analysis points towards ivermectin's role in reducing severity and improving health outcomes. · Antiviral Effect Study — A study aimed at assessing the antiviral effect of high-dose ivermectin found it to have an impact on viral load, suggesting its potential in reducing the severity of the disease by decreasing the viral replication. Evidence for Ivermectin in Treating Cancer as summarized by Dr. William Makis, Radiologist, Oncologist, Cancer Researcher. NEW ARTICLE: IVERMECTIN and Protocols for CANCER Ivermectin has a dozen anti-cancer mechanisms but they can be summarized into two main ones: 1. Inhibits cancer proliferation signaling pathways (Akt, mTOR, Wnt) 2. Inhibits Cancer Stem Cells IVERMECTIN will act against regular CANCER as well as Pfizer and Moderna COVID-19 mRNA Vaccine Induced TURBO CANCER (which is highly resistant to chemo) Here are recent studies on IVERMECTIN use in certain types of cancer: BLADDER CANCER - (2024 Fan et al) - Ivermectin Inhibits Bladder Cancer Cell Growth and Induces Oxidative Stress and DNA Damage LUNG CANCER - (2024 Man-Yuan Li et al) - Ivermectin induces nonprotective autophagy by downregulating PAK1 and apoptosis in lung adenocarcinoma cells GLIOMA - (2024 Xing Hu et al) - Ivermectin as a potential therapeutic strategy for glioma MULTIPLE MYELOMA - (2024 Yang Song et al) - Gene signatures to therapeutics: Assessing the potential of ivermectin against t(4;14) multiple myeloma OVARIAN CANCER - (2023 Jawad et al) - Ivermectin augments the anti-cancer activity of pitavastatin in ovarian cancer cells PROSTATE CANCER - (2022 Lu et al) - Integrated analysis reveals FOXA1 and Ku70/Ku80 as targets of ivermectin in prostate cancer COLON CANCER - (2022, Alghamdi et al) - Efficacy of ivermectin against colon cancer induced by dimethylhydrazine in male wistar rats PANCREATIC CANCER - (2022 Lee et al) - Ivermectin and gemcitabine combination treatment induces apoptosis of pancreatic cancer cells via mitochondrial dysfunction MELANOMA - (2022 Zhang et al) - Drug repurposing of ivermectin abrogates neutrophil extracellular traps and prevents melanoma metastasis IVERMECTIN has proven anti-cancer activity against some 20 cancer types, although these are pre-clinical studies. We will never see clinical studies because Ivermectin is off patent and cheap. Merck, which used to have a patent on Ivermectin, has partnered with Moderna on mRNA Cancer Vaccines. IVERMECTIN is so safe, that in much of the civilized world, it is available over the counter, no prescription needed. Ivermectin is annually taken by close to 250 million people.
9:41

When I caught Covid, my friends rushed doses of Ivermectin to me — kicked Covid in 24 hours. Here’s a cancer surgeon revealing her discoveries about the impact of Ivermectin on CANCER… 9 min. must see: Also — Compelling Evidence for Ivermectin in Treating Covid: · Front Line COVID-19 Critical Care Alliance Review — This review, which summarized findings from 27 studies, concluded that ivermectin demonstrates a strong signal of therapeutic efficacy against COVID-19. This includes both prevention and treatment aspects. · Meta-Analysis on Ivermectin — A meta-analysis covering 96 studies and over 135,000 patients suggests that ivermectin has shown effectiveness in combating COVID-19. This analysis points towards ivermectin's role in reducing severity and improving health outcomes. · Antiviral Effect Study — A study aimed at assessing the antiviral effect of high-dose ivermectin found it to have an impact on viral load, suggesting its potential in reducing the severity of the disease by decreasing the viral replication. Evidence for Ivermectin in Treating Cancer as summarized by Dr. William Makis, Radiologist, Oncologist, Cancer Researcher. NEW ARTICLE: IVERMECTIN and Protocols for CANCER Ivermectin has a dozen anti-cancer mechanisms but they can be summarized into two main ones: 1. Inhibits cancer proliferation signaling pathways (Akt, mTOR, Wnt) 2. Inhibits Cancer Stem Cells IVERMECTIN will act against regular CANCER as well as Pfizer and Moderna COVID-19 mRNA Vaccine Induced TURBO CANCER (which is highly resistant to chemo) Here are recent studies on IVERMECTIN use in certain types of cancer: BLADDER CANCER - (2024 Fan et al) - Ivermectin Inhibits Bladder Cancer Cell Growth and Induces Oxidative Stress and DNA Damage LUNG CANCER - (2024 Man-Yuan Li et al) - Ivermectin induces nonprotective autophagy by downregulating PAK1 and apoptosis in lung adenocarcinoma cells GLIOMA - (2024 Xing Hu et al) - Ivermectin as a potential therapeutic strategy for glioma MULTIPLE MYELOMA - (2024 Yang Song et al) - Gene signatures to therapeutics: Assessing the potential of ivermectin against t(4;14) multiple myeloma OVARIAN CANCER - (2023 Jawad et al) - Ivermectin augments the anti-cancer activity of pitavastatin in ovarian cancer cells PROSTATE CANCER - (2022 Lu et al) - Integrated analysis reveals FOXA1 and Ku70/Ku80 as targets of ivermectin in prostate cancer COLON CANCER - (2022, Alghamdi et al) - Efficacy of ivermectin against colon cancer induced by dimethylhydrazine in male wistar rats PANCREATIC CANCER - (2022 Lee et al) - Ivermectin and gemcitabine combination treatment induces apoptosis of pancreatic cancer cells via mitochondrial dysfunction MELANOMA - (2022 Zhang et al) - Drug repurposing of ivermectin abrogates neutrophil extracellular traps and prevents melanoma metastasis IVERMECTIN has proven anti-cancer activity against some 20 cancer types, although these are pre-clinical studies. We will never see clinical studies because Ivermectin is off patent and cheap. Merck, which used to have a patent on Ivermectin, has partnered with Moderna on mRNA Cancer Vaccines. IVERMECTIN is so safe, that in much of the civilized world, it is available over the counter, no prescription needed. Ivermectin is annually taken by close to 250 million people.

Bobby

159,980 görüntüleme • 1 yıl önce

Micro-dosing GLP-1 receptor agonists (drugs like semaglutide/Ozempic) could offer meaningful benefits while minimizing harmful side effects. There’s no doubt these drugs are incredibly effective for weight loss. But the high doses currently being used might be too much of a good thing. For example, high-dose GLP-1 receptor agonist use has been linked with a near doubling in the risk of suicidal behavior and a tripling in the risk of depression, as well as a two-fold increase in the risk of age-related macular degeneration. However, these drugs may still have utility when used strategically. According to Dr. Ben Bikman (Benjamin Bikman), micro-dosing GLP-1 receptor agonists intermittently may be a beneficial strategy to manage hunger, reset eating behaviors, and encourage healthier dietary patterns. Specifically, Bikman proposes that using low doses for about 90 days could fundamentally shift one's relationship with food. There is even some speculation that these medications may have pro-longevity benefits, independent of their effects on weight loss. To learn more, check out the new FMF episode with Dr. Ben Bikman. You can find it on YouTube, Spotify, and Apple Podcasts. Links in the comments.
1:49

Micro-dosing GLP-1 receptor agonists (drugs like semaglutide/Ozempic) could offer meaningful benefits while minimizing harmful side effects. There’s no doubt these drugs are incredibly effective for weight loss. But the high doses currently being used might be too much of a good thing. For example, high-dose GLP-1 receptor agonist use has been linked with a near doubling in the risk of suicidal behavior and a tripling in the risk of depression, as well as a two-fold increase in the risk of age-related macular degeneration. However, these drugs may still have utility when used strategically. According to Dr. Ben Bikman (Benjamin Bikman), micro-dosing GLP-1 receptor agonists intermittently may be a beneficial strategy to manage hunger, reset eating behaviors, and encourage healthier dietary patterns. Specifically, Bikman proposes that using low doses for about 90 days could fundamentally shift one's relationship with food. There is even some speculation that these medications may have pro-longevity benefits, independent of their effects on weight loss. To learn more, check out the new FMF episode with Dr. Ben Bikman. You can find it on YouTube, Spotify, and Apple Podcasts. Links in the comments.

Dr. Rhonda Patrick

47,267 görüntüleme • 1 yıl önce

IVERMECTIN: FULL DOSAGE SCHEDULE FOR CANCER & PREVENTION 1000s of people use Dr. William Makis MD’s IVERMECTIN dosing chart. Here’s a clear, categorized breakdown based on body weight (mg/kg per day). LOW DOSE: ≤ 0.5 mg/kg/day **Best for:** - Cancers in remission - Strong family history or genetic predisposition - Prophylaxis (preventive) **Side effects:** No long-term side effects reported. **Example:** Dr. Tess Lawrie reported a Stage 3 ovarian cancer case treated with chemo + 12 mg ivermectin daily. Tumor marker CA125 dropped from 288 to 22 after 2 months and the tumor vanished. MEDIUM DOSE: 1.0 mg/kg/day **Best for:** Starting dose for **most cancers** (lung, pancreatic, renal cell, gastric, etc.). **Side effects:** No long-term side effects reported. **Example:** Dr. Shankara Chetty’s 70-year-old prostate cancer patient (PSA 89) took 45 mg/day (plus lactoferrin). After two months PSA fell to 10.9. HIGH DOSE: 2.0 mg/kg/day **Best for:** Very aggressive cancers (leukemia, pancreatic, brain cancers). **Side effects:** No long-term side effects reported. **Example:** Dr. Allan Landrito’s Stage 4 gallbladder cancer patient took 2 mg/kg daily for 14 months — cancer disappeared. VERY HIGH DOSE: ≥ 2.5 mg/kg/day **Best for:** Extensive metastatic disease, extremely poor prognosis, or certain brain cancers. **Side effects:** Possible short-term & transient visual effects (usually resolve in a few days). **Example:** Dr. Shankara Chetty treated a patient with 2.5 mg/kg/day — no side effects reported. **Quick conversion example (for a 60 kg / 132 lb person):** - Low: ≤30 mg/day - Medium: 60 mg/day (≈5×12 mg tablets or 1 teaspoon liquid) - High: 120 mg/day - Very High: ≥150 mg/day Many anecdotal reports exist of long-term daily use (months to over a year) with no serious toxicity, but individual responses vary. Always work with a knowledgeable clinician, especially if you have pre-existing conditions (e.g., vision issues or glaucoma). This is for educational purposes only. Share to spread awareness — information is power. 💊
5:47

IVERMECTIN: FULL DOSAGE SCHEDULE FOR CANCER & PREVENTION 1000s of people use Dr. William Makis MD’s IVERMECTIN dosing chart. Here’s a clear, categorized breakdown based on body weight (mg/kg per day). LOW DOSE: ≤ 0.5 mg/kg/day **Best for:** - Cancers in remission - Strong family history or genetic predisposition - Prophylaxis (preventive) **Side effects:** No long-term side effects reported. **Example:** Dr. Tess Lawrie reported a Stage 3 ovarian cancer case treated with chemo + 12 mg ivermectin daily. Tumor marker CA125 dropped from 288 to 22 after 2 months and the tumor vanished. MEDIUM DOSE: 1.0 mg/kg/day **Best for:** Starting dose for **most cancers** (lung, pancreatic, renal cell, gastric, etc.). **Side effects:** No long-term side effects reported. **Example:** Dr. Shankara Chetty’s 70-year-old prostate cancer patient (PSA 89) took 45 mg/day (plus lactoferrin). After two months PSA fell to 10.9. HIGH DOSE: 2.0 mg/kg/day **Best for:** Very aggressive cancers (leukemia, pancreatic, brain cancers). **Side effects:** No long-term side effects reported. **Example:** Dr. Allan Landrito’s Stage 4 gallbladder cancer patient took 2 mg/kg daily for 14 months — cancer disappeared. VERY HIGH DOSE: ≥ 2.5 mg/kg/day **Best for:** Extensive metastatic disease, extremely poor prognosis, or certain brain cancers. **Side effects:** Possible short-term & transient visual effects (usually resolve in a few days). **Example:** Dr. Shankara Chetty treated a patient with 2.5 mg/kg/day — no side effects reported. **Quick conversion example (for a 60 kg / 132 lb person):** - Low: ≤30 mg/day - Medium: 60 mg/day (≈5×12 mg tablets or 1 teaspoon liquid) - High: 120 mg/day - Very High: ≥150 mg/day Many anecdotal reports exist of long-term daily use (months to over a year) with no serious toxicity, but individual responses vary. Always work with a knowledgeable clinician, especially if you have pre-existing conditions (e.g., vision issues or glaucoma). This is for educational purposes only. Share to spread awareness — information is power. 💊

Valerie Anne Smith

958,643 görüntüleme • 2 ay önce

IVERMECTIN: FULL DOSAGE SCHEDULE FOR CANCER & PREVENTION 1000s of people use Dr. William Makis MD’s IVERMECTIN dosing chart. Here’s a clear, categorized breakdown based on body weight (mg/kg per day). LOW DOSE: ≤ 0.5 mg/kg/day **Best for:** - Cancers in remission - Strong family history or genetic predisposition - Prophylaxis (preventive) **Side effects:** No long-term side effects reported. **Example:** Dr. Tess Lawrie reported a Stage 3 ovarian cancer case treated with chemo + 12 mg ivermectin daily. Tumor marker CA125 dropped from 288 to 22 after 2 months and the tumor vanished. MEDIUM DOSE: 1.0 mg/kg/day **Best for:** Starting dose for **most cancers** (lung, pancreatic, renal cell, gastric, etc.). **Side effects:** No long-term side effects reported. **Example:** Dr. Shankara Chetty’s 70-year-old prostate cancer patient (PSA 89) took 45 mg/day (plus lactoferrin). After two months PSA fell to 10.9. HIGH DOSE: 2.0 mg/kg/day **Best for:** Very aggressive cancers (leukemia, pancreatic, brain cancers). **Side effects:** No long-term side effects reported. **Example:** Dr. Allan Landrito’s Stage 4 gallbladder cancer patient took 2 mg/kg daily for 14 months — cancer disappeared. VERY HIGH DOSE: ≥ 2.5 mg/kg/day **Best for:** Extensive metastatic disease, extremely poor prognosis, or certain brain cancers. **Side effects:** Possible short-term & transient visual effects (usually resolve in a few days). **Example:** Dr. Shankara Chetty treated a patient with 2.5 mg/kg/day — no side effects reported. **Quick conversion example (for a 60 kg / 132 lb person):** - Low: ≤30 mg/day - Medium: 60 mg/day (≈5×12 mg tablets or 1 teaspoon liquid) - High: 120 mg/day - Very High: ≥150 mg/day Many anecdotal reports exist of long-term daily use (months to over a year) with no serious toxicity, but individual responses vary. Always work with a knowledgeable clinician, especially if you have pre-existing conditions (e.g., vision issues or glaucoma). This is for educational purposes only. Share to spread awareness — information is power. 💊
5:47

IVERMECTIN: FULL DOSAGE SCHEDULE FOR CANCER & PREVENTION 1000s of people use Dr. William Makis MD’s IVERMECTIN dosing chart. Here’s a clear, categorized breakdown based on body weight (mg/kg per day). LOW DOSE: ≤ 0.5 mg/kg/day **Best for:** - Cancers in remission - Strong family history or genetic predisposition - Prophylaxis (preventive) **Side effects:** No long-term side effects reported. **Example:** Dr. Tess Lawrie reported a Stage 3 ovarian cancer case treated with chemo + 12 mg ivermectin daily. Tumor marker CA125 dropped from 288 to 22 after 2 months and the tumor vanished. MEDIUM DOSE: 1.0 mg/kg/day **Best for:** Starting dose for **most cancers** (lung, pancreatic, renal cell, gastric, etc.). **Side effects:** No long-term side effects reported. **Example:** Dr. Shankara Chetty’s 70-year-old prostate cancer patient (PSA 89) took 45 mg/day (plus lactoferrin). After two months PSA fell to 10.9. HIGH DOSE: 2.0 mg/kg/day **Best for:** Very aggressive cancers (leukemia, pancreatic, brain cancers). **Side effects:** No long-term side effects reported. **Example:** Dr. Allan Landrito’s Stage 4 gallbladder cancer patient took 2 mg/kg daily for 14 months — cancer disappeared. VERY HIGH DOSE: ≥ 2.5 mg/kg/day **Best for:** Extensive metastatic disease, extremely poor prognosis, or certain brain cancers. **Side effects:** Possible short-term & transient visual effects (usually resolve in a few days). **Example:** Dr. Shankara Chetty treated a patient with 2.5 mg/kg/day — no side effects reported. **Quick conversion example (for a 60 kg / 132 lb person):** - Low: ≤30 mg/day - Medium: 60 mg/day (≈5×12 mg tablets or 1 teaspoon liquid) - High: 120 mg/day - Very High: ≥150 mg/day Many anecdotal reports exist of long-term daily use (months to over a year) with no serious toxicity, but individual responses vary. Always work with a knowledgeable clinician, especially if you have pre-existing conditions (e.g., vision issues or glaucoma). This is for educational purposes only. Share to spread awareness — information is power. 💊

Dr. Zakaria MD

133,235 görüntüleme • 18 gün önce

Who is to blame? The authorities for giving permission and allowing OTC sale, or the pharmacist handing them out without the prescription, or the parent? Victim is the baby, finally! If you ask me, if a medicine is not to be given to some one below 4 years of age, permission should not be given in the first place for these drops. If it is a schedule H drug, OTC sale should not be allowed. Ministry of Health #maxtradrops #sinarestAFdrops #solvincolddrops #zyrtecdrops #sinarestdrops There is nothing like 'cough syrup'. Cough can be because of a lot of congestion,bronchospasm, bronchiolitis, acid reflux, allergy or infection. It can be a habit cough, or due to inflammation of the throat or stress related. Address the underlying cause. Syrups available in India in the name of cough syrups contain either decongestants like phenylephrine (whose side effects are mostly due to overdosing or wrong dosing - increase in heart rate, increase in blood pressure, and arrhythmias), or anti allergy medications like chlorpheniramine and cetirizine (overdosing can cause sedation and respiratory depression- less with Levocetirizine, though), mucus breaking drugs like ambroxol and guaifenesin, bronchodilators like levosalbutamol and Terbutaline(overdosing can cause tremors, increased heart rate and arrhythmias) and cough suppressants like dextromethorphan and codeine(which can cause severe respiratory depression when overdosed). We should not suppress the cough, as it might even help in expelling the germs out. For every medicine there is a minimum age before which we can't give the medicine to the child, especially without the paediatricians's advice. For phenylephrine in India, it is now four years, though most guidelines say it is 2 years. For cetirizine, it is 6 months. In India the combination of Phenylephrine and Chlorpheniramine should not be used below 4 years of age. If a medicine is prescribed by a doctor, If the right dose is given by a mother for a right indication, problems usually don’t happen. The problem of overdosing happens when the parents go and buy over-the-counter medications, and give them randomly without knowing the doses. So, don’t buy the so called cough syrups on your own and decide to give them to the children. If they have a cough, paediatricians are there to address the underlying cause for cough and prescribe the treatment depending on the age group, symptoms, and the etiology. Stick to the doses, read expiry date. Doctors should write the prescriptions clearly, mention composition and tell the parents not to repeat the prescription, explain to them about dangers of wrong dosing, overdosing and repetition of prescription. First aid for cough mainly is compression with a warm cloth. In India many of them give steam directly. That is dangerous. If steam should be given, then the bathroom should be filled with the steam and the kid should be made to sit there.Don't give vicks,eucalyptus oil, Zindatilismath etc. In younger children they can cause seizures, and can worsen the cough and asthma symptoms. If the nose is blocked, put one to two drops of saline nose drops (from the pharmacies) in each nostril. If the cough is severe, the kid is vomiting or coughing continuously, consult the doctor. Drug regulators should avoid giving permission for drops and syrup with the same brand name, for unscientific combinations of medicines, for formulations with different components but the same brand name with a suffix or prefix. We need to have only a few standard brands or generic medicines with strong quality control. Form a panel of paediatricians for the same. Also, Terbutaline and Levosalbutamol shouldn't be part of the combinations. We have specific indications for these medicines. Safer route of administration for Levosalbutamol is using a nebulizer or MDI with or with out spacer, only if advised by the paediatrician when the child has bronchospasm. INFACT, AVOID COMBINATIONS! Dr Sivaranjani Santosh
1:30

Who is to blame? The authorities for giving permission and allowing OTC sale, or the pharmacist handing them out without the prescription, or the parent? Victim is the baby, finally! If you ask me, if a medicine is not to be given to some one below 4 years of age, permission should not be given in the first place for these drops. If it is a schedule H drug, OTC sale should not be allowed. Ministry of Health #maxtradrops #sinarestAFdrops #solvincolddrops #zyrtecdrops #sinarestdrops There is nothing like 'cough syrup'. Cough can be because of a lot of congestion,bronchospasm, bronchiolitis, acid reflux, allergy or infection. It can be a habit cough, or due to inflammation of the throat or stress related. Address the underlying cause. Syrups available in India in the name of cough syrups contain either decongestants like phenylephrine (whose side effects are mostly due to overdosing or wrong dosing - increase in heart rate, increase in blood pressure, and arrhythmias), or anti allergy medications like chlorpheniramine and cetirizine (overdosing can cause sedation and respiratory depression- less with Levocetirizine, though), mucus breaking drugs like ambroxol and guaifenesin, bronchodilators like levosalbutamol and Terbutaline(overdosing can cause tremors, increased heart rate and arrhythmias) and cough suppressants like dextromethorphan and codeine(which can cause severe respiratory depression when overdosed). We should not suppress the cough, as it might even help in expelling the germs out. For every medicine there is a minimum age before which we can't give the medicine to the child, especially without the paediatricians's advice. For phenylephrine in India, it is now four years, though most guidelines say it is 2 years. For cetirizine, it is 6 months. In India the combination of Phenylephrine and Chlorpheniramine should not be used below 4 years of age. If a medicine is prescribed by a doctor, If the right dose is given by a mother for a right indication, problems usually don’t happen. The problem of overdosing happens when the parents go and buy over-the-counter medications, and give them randomly without knowing the doses. So, don’t buy the so called cough syrups on your own and decide to give them to the children. If they have a cough, paediatricians are there to address the underlying cause for cough and prescribe the treatment depending on the age group, symptoms, and the etiology. Stick to the doses, read expiry date. Doctors should write the prescriptions clearly, mention composition and tell the parents not to repeat the prescription, explain to them about dangers of wrong dosing, overdosing and repetition of prescription. First aid for cough mainly is compression with a warm cloth. In India many of them give steam directly. That is dangerous. If steam should be given, then the bathroom should be filled with the steam and the kid should be made to sit there.Don't give vicks,eucalyptus oil, Zindatilismath etc. In younger children they can cause seizures, and can worsen the cough and asthma symptoms. If the nose is blocked, put one to two drops of saline nose drops (from the pharmacies) in each nostril. If the cough is severe, the kid is vomiting or coughing continuously, consult the doctor. Drug regulators should avoid giving permission for drops and syrup with the same brand name, for unscientific combinations of medicines, for formulations with different components but the same brand name with a suffix or prefix. We need to have only a few standard brands or generic medicines with strong quality control. Form a panel of paediatricians for the same. Also, Terbutaline and Levosalbutamol shouldn't be part of the combinations. We have specific indications for these medicines. Safer route of administration for Levosalbutamol is using a nebulizer or MDI with or with out spacer, only if advised by the paediatrician when the child has bronchospasm. INFACT, AVOID COMBINATIONS! Dr Sivaranjani Santosh

Dr.Sivaranjini

105,892 görüntüleme • 5 ay önce

Europe just banned gel nail polish. The highly popular product is worshipped for its ability to create a long-lasting, no-chip manicure. It boasted a market value of nearly $6 billion in 2024. But the EU banned one of its key ingredients, trimethylbenzoyl diphenylphosphine oxide (or TPO), after it was classified as “carcinogenic, mutagenic, or toxic-to-reproduction" substance. The EU cited studies that found animals experienced fertility and reproductive health issues after ingesting high levels of TPO. But people getting a gel manicure don’t ingest TPO, putting them at minimal risk of harmful effects, experts told PBS News. Why isn’t this banned in the U.S.? EU standards take a hazard-based approach, looking at the intrinsic harm of a chemical or product in isolation. The U.S. takes a risk-based approach, taking into account both the risk and exposure, experts said. What does this mean for you? Michelle Wong, a chemistry P.h.D and science communicator at Lab Muffin Beauty Science, told PBS News that 1% of TPO is left after curing and if you go into the sun afterwards, the TPO is going to be gone altogether. But there are risks with at-home gel nail kits, including painting outside of your nails or not curing the paint correctly.
2:54

Europe just banned gel nail polish. The highly popular product is worshipped for its ability to create a long-lasting, no-chip manicure. It boasted a market value of nearly $6 billion in 2024. But the EU banned one of its key ingredients, trimethylbenzoyl diphenylphosphine oxide (or TPO), after it was classified as “carcinogenic, mutagenic, or toxic-to-reproduction" substance. The EU cited studies that found animals experienced fertility and reproductive health issues after ingesting high levels of TPO. But people getting a gel manicure don’t ingest TPO, putting them at minimal risk of harmful effects, experts told PBS News. Why isn’t this banned in the U.S.? EU standards take a hazard-based approach, looking at the intrinsic harm of a chemical or product in isolation. The U.S. takes a risk-based approach, taking into account both the risk and exposure, experts said. What does this mean for you? Michelle Wong, a chemistry P.h.D and science communicator at Lab Muffin Beauty Science, told PBS News that 1% of TPO is left after curing and if you go into the sun afterwards, the TPO is going to be gone altogether. But there are risks with at-home gel nail kits, including painting outside of your nails or not curing the paint correctly.

PBS News

20,059 görüntüleme • 10 ay önce

Did you know 128hz is a penetrative frequency that goes through the tissues into the bones and helps release nitric oxide into your cells? Grok: Nitric oxide (NO) is a naturally produced signaling molecule in the body that plays a critical role in many physiological processes. It acts primarily as a **vasodilator**, relaxing and widening blood vessels to improve blood flow, deliver oxygen and nutrients more efficiently, and support overall cellular communication. Here are the key benefits of nitric oxide in the body, based on its established physiological functions: ### 1. Cardiovascular Health and Blood Pressure Regulation Nitric oxide helps relax the smooth muscles in blood vessel walls, leading to vasodilation. This increases blood flow, reduces vascular resistance, and helps maintain healthy blood pressure levels. It also protects the endothelium (the inner lining of blood vessels), reduces arterial stiffness, inhibits platelet aggregation (lowering clot risk), and may decrease inflammation and plaque buildup. Low NO levels are linked to endothelial dysfunction, hypertension, and higher cardiovascular disease risk. ### 2. Improved Exercise Performance and Muscle Function By enhancing blood flow to working muscles, nitric oxide improves oxygen and nutrient delivery while helping remove waste products like lactate. This can boost endurance, increase exercise tolerance (especially in less-trained individuals), reduce muscle soreness, and support better recovery. It may also influence muscle contraction speed and mitochondrial efficiency in cells. ### 3. Support for Erectile Function and Sexual Health Nitric oxide is a primary mediator of penile erection, as it promotes relaxation of smooth muscle in blood vessels, allowing increased blood flow. Supplements that boost NO (such as L-arginine or L-citrulline) have shown potential benefits for mild to moderate erectile dysfunction (ED) in some studies. It may also support sexual arousal more broadly. ### 4. Immune System Defense Nitric oxide acts as a key player in immune responses. It helps immune cells (like macrophages) kill bacteria, viruses, and even some cancer cells by producing higher levels during infection or inflammation. It also modulates inflammation—providing anti-inflammatory effects at normal physiological levels while aiding targeted defense at higher concentrations. ### 5. Brain and Nervous System Function As a neurotransmitter and neuromodulator, nitric oxide facilitates communication between brain cells. It supports cerebral blood flow, learning, memory, and other neurological processes. Adequate levels may help protect against cognitive decline by improving brain oxygenation and circulation. ### 6. Other Potential Benefits - **Wound healing and tissue repair**: Enhanced blood flow and signaling support recovery processes. - **Respiratory support**: In medical settings, inhaled NO helps relax lung blood vessels in certain conditions (like pulmonary hypertension in newborns). - **Anti-aging and metabolic effects**: By supporting circulation, reducing oxidative stress in balanced amounts, and aiding hormone regulation, it contributes to overall vitality. It may also play roles in reducing risks associated with diabetes complications or arthritis inflammation. Note that nitric oxide has a dual nature: beneficial at physiological (low-to-moderate) levels, but excessive production (often in chronic inflammation) can contribute to tissue damage or pro-inflammatory effects. The body produces NO via enzymes (nitric oxide synthase) from precursors like L-arginine, or through nitrate-nitrite pathways from diet. **Natural ways to support nitric oxide levels** include eating nitrate-rich foods (beets, leafy greens like spinach/arugula, garlic), consuming antioxidants (to preserve NO), regular exercise (which stimulates production), nose breathing, and maintaining good sleep and cardiovascular habits.
0:57

Did you know 128hz is a penetrative frequency that goes through the tissues into the bones and helps release nitric oxide into your cells? Grok: Nitric oxide (NO) is a naturally produced signaling molecule in the body that plays a critical role in many physiological processes. It acts primarily as a **vasodilator**, relaxing and widening blood vessels to improve blood flow, deliver oxygen and nutrients more efficiently, and support overall cellular communication. Here are the key benefits of nitric oxide in the body, based on its established physiological functions: ### 1. Cardiovascular Health and Blood Pressure Regulation Nitric oxide helps relax the smooth muscles in blood vessel walls, leading to vasodilation. This increases blood flow, reduces vascular resistance, and helps maintain healthy blood pressure levels. It also protects the endothelium (the inner lining of blood vessels), reduces arterial stiffness, inhibits platelet aggregation (lowering clot risk), and may decrease inflammation and plaque buildup. Low NO levels are linked to endothelial dysfunction, hypertension, and higher cardiovascular disease risk. ### 2. Improved Exercise Performance and Muscle Function By enhancing blood flow to working muscles, nitric oxide improves oxygen and nutrient delivery while helping remove waste products like lactate. This can boost endurance, increase exercise tolerance (especially in less-trained individuals), reduce muscle soreness, and support better recovery. It may also influence muscle contraction speed and mitochondrial efficiency in cells. ### 3. Support for Erectile Function and Sexual Health Nitric oxide is a primary mediator of penile erection, as it promotes relaxation of smooth muscle in blood vessels, allowing increased blood flow. Supplements that boost NO (such as L-arginine or L-citrulline) have shown potential benefits for mild to moderate erectile dysfunction (ED) in some studies. It may also support sexual arousal more broadly. ### 4. Immune System Defense Nitric oxide acts as a key player in immune responses. It helps immune cells (like macrophages) kill bacteria, viruses, and even some cancer cells by producing higher levels during infection or inflammation. It also modulates inflammation—providing anti-inflammatory effects at normal physiological levels while aiding targeted defense at higher concentrations. ### 5. Brain and Nervous System Function As a neurotransmitter and neuromodulator, nitric oxide facilitates communication between brain cells. It supports cerebral blood flow, learning, memory, and other neurological processes. Adequate levels may help protect against cognitive decline by improving brain oxygenation and circulation. ### 6. Other Potential Benefits - **Wound healing and tissue repair**: Enhanced blood flow and signaling support recovery processes. - **Respiratory support**: In medical settings, inhaled NO helps relax lung blood vessels in certain conditions (like pulmonary hypertension in newborns). - **Anti-aging and metabolic effects**: By supporting circulation, reducing oxidative stress in balanced amounts, and aiding hormone regulation, it contributes to overall vitality. It may also play roles in reducing risks associated with diabetes complications or arthritis inflammation. Note that nitric oxide has a dual nature: beneficial at physiological (low-to-moderate) levels, but excessive production (often in chronic inflammation) can contribute to tissue damage or pro-inflammatory effects. The body produces NO via enzymes (nitric oxide synthase) from precursors like L-arginine, or through nitrate-nitrite pathways from diet. **Natural ways to support nitric oxide levels** include eating nitrate-rich foods (beets, leafy greens like spinach/arugula, garlic), consuming antioxidants (to preserve NO), regular exercise (which stimulates production), nose breathing, and maintaining good sleep and cardiovascular habits.

𝒦𝑒𝓁𝓁𝓎࿎☽

21,956 görüntüleme • 3 ay önce

In my most recent Q&A on marathon training, I talked about all of the supplements that I use to support performance and recovery. Here’s the list: 🥤 Whey Protein Dose: 20–30 grams mixed with almond milk. Why: Used as a convenient meal or post-run recovery option, especially when appetite is low after hard workouts in the heat. High-quality protein source. 🌱 Greens Supplement (Bloom Greens) Why: For prebiotic/probiotic support and general wellness. You enjoy the taste (berry flavor) and feel good taking it. Often added to morning smoothies. 🧬 L-Glutamine Dose: 10 grams/day (5g twice daily). Why: Added recently for immune and gut health support, particularly to help prevent upper respiratory infections in endurance athletes after stressful events like marathons. 💪 Creatine Monohydrate Dose: 5 grams/day; 10 grams on hard training or long run days. Why: Supports strength, recovery, muscle hydration, and potentially endurance performance. No significant side effects noted. May slightly increase body weight via hydration, but not enough to negatively affect performance. 🧠 Omega-3 Fatty Acids Why: For cardiovascular health and to reduce inflammation and muscle soreness after intense workouts. Taken daily due to limited fish intake in diet. 🩸 Iron (Thorne Ferrasorb) Why: To address low ferritin levels found in recent blood tests. Supports red blood cell production and oxygen transport—important for endurance performance. ☀️ Vitamin D3 Dose: 5,000 IU daily. Why: Despite living in sunny Austin, blood tests showed low-normal levels. Supplementing to boost levels for overall health and performance. 🌿 Ashwagandha Why: Used occasionally for stress reduction and performance support. Known as an “adaptogen,” possibly aids in stress resilience. Taken on hard training or high-stress days; avoided on weekends to prevent potential cortisol suppression.
5:05

In my most recent Q&A on marathon training, I talked about all of the supplements that I use to support performance and recovery. Here’s the list: 🥤 Whey Protein Dose: 20–30 grams mixed with almond milk. Why: Used as a convenient meal or post-run recovery option, especially when appetite is low after hard workouts in the heat. High-quality protein source. 🌱 Greens Supplement (Bloom Greens) Why: For prebiotic/probiotic support and general wellness. You enjoy the taste (berry flavor) and feel good taking it. Often added to morning smoothies. 🧬 L-Glutamine Dose: 10 grams/day (5g twice daily). Why: Added recently for immune and gut health support, particularly to help prevent upper respiratory infections in endurance athletes after stressful events like marathons. 💪 Creatine Monohydrate Dose: 5 grams/day; 10 grams on hard training or long run days. Why: Supports strength, recovery, muscle hydration, and potentially endurance performance. No significant side effects noted. May slightly increase body weight via hydration, but not enough to negatively affect performance. 🧠 Omega-3 Fatty Acids Why: For cardiovascular health and to reduce inflammation and muscle soreness after intense workouts. Taken daily due to limited fish intake in diet. 🩸 Iron (Thorne Ferrasorb) Why: To address low ferritin levels found in recent blood tests. Supports red blood cell production and oxygen transport—important for endurance performance. ☀️ Vitamin D3 Dose: 5,000 IU daily. Why: Despite living in sunny Austin, blood tests showed low-normal levels. Supplementing to boost levels for overall health and performance. 🌿 Ashwagandha Why: Used occasionally for stress reduction and performance support. Known as an “adaptogen,” possibly aids in stress resilience. Taken on hard training or high-stress days; avoided on weekends to prevent potential cortisol suppression.

Brady Holmer

20,024 görüntüleme • 1 yıl önce

The Dangerous Cult of 'Fasting' Influencers. Fasting has its anecdotal benefits, yes. But it is overrated. And water fasting is highly overrated. But this video featuring a Cardiologist is amusingly nonsense. There is no study from Boston (from a "University?" - how vague!) that says 7-days water fasting reduces risk of cancer (what cancer?) by 70%. And there is no proof that fasting kills cancer cells in humans. Here is what fasting does to cancers in humans. Nothing. Fasting is now become a sort of religion-like cult for wellness influencers to rake in views and engagement. From a scientific standpoint, there are no realistically good human studies to prove anything from fasting that benefits cancers. I know, I know, "autophagy" and all that. Autophagy: Autophagy is the natural, conserved degradation of the cell that removes unnecessary or dysfunctional components. Yes, its a legit term and all. But in the context of cancer reduction and fasting in humans, it sounds like "immunity boosting," another wellness fraud term. The effects of fasting on cancer cells are all based on MOUSE studies, and none explicitly translated to humans. See this paper: everything is based on cells and tissues and small animal experiments: "While research on the subject is tantalizing, there’s little clinical evidence involving humans to substantiate the claims. Studies on the potential impacts on cancer treatment from various forms of fasting or calorie restriction, including the possibility that they reduce side effects, have been limited." "Fasting may not be appropriate for malnourished individuals or those with cancer cachexia, which results in a continuing loss of skeletal muscle mass, or for people with chronic diseases. Those with diabetes need to be very careful, because of the risk of hypoglycemia." "Based on our systematic review and meta-analysis, there is currently no evidence supporting the superiority of therapeutic fasting over non-fasting in preventing chemotherapy toxicity." - see here: Even intermittent fasting (IF) is overrated in cancer. "IF may be considered in adults seeking cancer-prevention benefits through means of weight management, butwhether IF itself affects cancer-related metabolic and molecular pathways remains unanswered. See here: Also this: "Fasting for short periods does not have any beneficial effect on the quality of life of cancer patients during treatment. Evidence on fasting regimes reducing side effects and toxicities of chemotherapy is missing." See here: The whole aspect of "fasting reducing cancer incidence" in the real world is just due to weight loss. Obesity is associated with at least 13 types of cancers and reversing obesity reduces risk of cancer - nothing to do with fasting killing off cancers cells in the body. And one can lose weight even without fasting. See here: Everything from prevention of adverse events of cancer, to reduction in side effects from chemotherapy, to slowing cancer growth by reducing glucose levels, to promoting cell regeneration by affecting autophagy is all LAB BASED MOLECULAR LEVEL HYPOTHESIS that has not been proven conclusively in humans. See here: Cancer patients must not starve. They must remain hydrated and they must eat a well balanced diet because cancer condition is highly demanding. And dont water fast for 7 days. Easy for people to make reels on it, but in real life, it may prove disastrous. Water fast does make you lose weight (because of starvation) but it is not at all a healthy way to lose weight. Stop with this fasting and cancer madness already.
0:21

The Dangerous Cult of 'Fasting' Influencers. Fasting has its anecdotal benefits, yes. But it is overrated. And water fasting is highly overrated. But this video featuring a Cardiologist is amusingly nonsense. There is no study from Boston (from a "University?" - how vague!) that says 7-days water fasting reduces risk of cancer (what cancer?) by 70%. And there is no proof that fasting kills cancer cells in humans. Here is what fasting does to cancers in humans. Nothing. Fasting is now become a sort of religion-like cult for wellness influencers to rake in views and engagement. From a scientific standpoint, there are no realistically good human studies to prove anything from fasting that benefits cancers. I know, I know, "autophagy" and all that. Autophagy: Autophagy is the natural, conserved degradation of the cell that removes unnecessary or dysfunctional components. Yes, its a legit term and all. But in the context of cancer reduction and fasting in humans, it sounds like "immunity boosting," another wellness fraud term. The effects of fasting on cancer cells are all based on MOUSE studies, and none explicitly translated to humans. See this paper: everything is based on cells and tissues and small animal experiments: "While research on the subject is tantalizing, there’s little clinical evidence involving humans to substantiate the claims. Studies on the potential impacts on cancer treatment from various forms of fasting or calorie restriction, including the possibility that they reduce side effects, have been limited." "Fasting may not be appropriate for malnourished individuals or those with cancer cachexia, which results in a continuing loss of skeletal muscle mass, or for people with chronic diseases. Those with diabetes need to be very careful, because of the risk of hypoglycemia." "Based on our systematic review and meta-analysis, there is currently no evidence supporting the superiority of therapeutic fasting over non-fasting in preventing chemotherapy toxicity." - see here: Even intermittent fasting (IF) is overrated in cancer. "IF may be considered in adults seeking cancer-prevention benefits through means of weight management, butwhether IF itself affects cancer-related metabolic and molecular pathways remains unanswered. See here: Also this: "Fasting for short periods does not have any beneficial effect on the quality of life of cancer patients during treatment. Evidence on fasting regimes reducing side effects and toxicities of chemotherapy is missing." See here: The whole aspect of "fasting reducing cancer incidence" in the real world is just due to weight loss. Obesity is associated with at least 13 types of cancers and reversing obesity reduces risk of cancer - nothing to do with fasting killing off cancers cells in the body. And one can lose weight even without fasting. See here: Everything from prevention of adverse events of cancer, to reduction in side effects from chemotherapy, to slowing cancer growth by reducing glucose levels, to promoting cell regeneration by affecting autophagy is all LAB BASED MOLECULAR LEVEL HYPOTHESIS that has not been proven conclusively in humans. See here: Cancer patients must not starve. They must remain hydrated and they must eat a well balanced diet because cancer condition is highly demanding. And dont water fast for 7 days. Easy for people to make reels on it, but in real life, it may prove disastrous. Water fast does make you lose weight (because of starvation) but it is not at all a healthy way to lose weight. Stop with this fasting and cancer madness already.

TheLiverDoc™

269,452 görüntüleme • 2 yıl önce

"Ivermectin's Miraculous Results For Neurological Conditions Of Parkinson's & Alzheimer's." Dr William Makis Buried Research, Deleted From Google, Has Been Found, Proving Ivermectin Reverses Alzheimer's. Neurological Disease Improves In Only A Few Days On Ivermectin Therapy... Dementia affects more than 55 million people globally, with Alzheimer’s disease (AD) being the most prevalent subtype. These neurodegenerative disorders, including debilitating Parkinson's Disease, progressively impairs memory, cognition, daily functioning, muscle & body control. As interest grows in repositioning known compounds for neurodegenerative applications, ivermectin—a macrocyclic lactone with FDA-approved antiparasitic use—has surfaced as a candidate for neurological disease therapy. Deleted Research Study That Google Scrubbed... I Found It Last Week After Hours Of Research. Here Is A Paraphrased Summary In 'Non Scientific' Regular Language: 70 male Wistar rats were used in the research study. At baseline the rats had cognitive ability to do a task session at the rate of 2.8 minutes with 1.3 errors. Alzheimer's Disease (AD) was induced by injecting them with ALUMINUM CHLORIDE until their cognitive ability to do the same task session regressed to the slow rate of 6.5 minutes with 4.4 errors. These rats were then given IVERMECTIN for 4 consecutive weeks. The same task session improved drastically from 6.5 minutes back to only 3.6 minutes. And the rate of errors improved from 4.4 back to only 1.4 errors. Almost back to baseline in only 4 weeks at 3.6 minutes with 1.4 errors. Recent studies have explored its effects on neuroinflammation, neurotransmission & synaptic protection. Ivermectin’s Effects On Neurological Disease: 1. Anti-Inflammatory Effects: A 2023 study published in Inflammation demonstrated that ivermectin mitigates neuroinflammatory damage in encephalomyelitis. Ivermectin reduced inflammatory cytokines. 2. Stabilizes Neurotransmission: A 2019 study in PLOS Pathogens found that ivermectin restores balance in synaptic neuro pathways. 3. Cholinergic Transmission: A 2024 study published in Cell & Bioscience reported that ivermectin increased activity of striatal cholinergic interneurons, enhancing dopamine release via nicotinic receptor modulation. Conclusion: Ivermectin is emerging as more than an antiparasitic agent. Its anti-inflammatory, synaptic & cholinergic effects are beneficial in neurodegenerative disorders like Dementia, Alzheimer's & Parkinson's. Dosages suggested by Dr William Makis: Parkinson’s: Patients on high-dose ivermectin (60-72mg) saw dramatic improvements in movement & symptoms. - Multiple cases of symptom reversal—where tremors, stiffness & rigidity significantly improved. Alzheimer’s: Patients on low-dose ivermectin (12-24 mg for 4-5 days) brought back memories, recognition & cognitive function in patients. Why Isn’t This Everywhere? - A preclinical Alzheimer’s study proving ivermectin’s healing ability was SCRUBBED from Google. - Big Pharma doesn’t profit from a safe, cheap, Nobel Prize-winning drug that reverses neurodegeneration. This isn’t theoretical—it’s happening NOW in real patients. Decades of suffering could be reversed by a few pills. If you have a loved one with Parkinson’s or Alzheimer’s—TRY IT. The results could be LIFE-CHANGING. 👇Ivermectin Reverses Alzheimer's (Deleted Study)👇 👇Ivermectin For Autoimmune & Neurological Ills👇 👇Ivermectin Increases Choline & Dopamine👇 Speaker: Dr William Makis, Nuclear Medicine Physician & Cancer Researcher
3:57

"Ivermectin's Miraculous Results For Neurological Conditions Of Parkinson's & Alzheimer's." Dr William Makis Buried Research, Deleted From Google, Has Been Found, Proving Ivermectin Reverses Alzheimer's. Neurological Disease Improves In Only A Few Days On Ivermectin Therapy... Dementia affects more than 55 million people globally, with Alzheimer’s disease (AD) being the most prevalent subtype. These neurodegenerative disorders, including debilitating Parkinson's Disease, progressively impairs memory, cognition, daily functioning, muscle & body control. As interest grows in repositioning known compounds for neurodegenerative applications, ivermectin—a macrocyclic lactone with FDA-approved antiparasitic use—has surfaced as a candidate for neurological disease therapy. Deleted Research Study That Google Scrubbed... I Found It Last Week After Hours Of Research. Here Is A Paraphrased Summary In 'Non Scientific' Regular Language: 70 male Wistar rats were used in the research study. At baseline the rats had cognitive ability to do a task session at the rate of 2.8 minutes with 1.3 errors. Alzheimer's Disease (AD) was induced by injecting them with ALUMINUM CHLORIDE until their cognitive ability to do the same task session regressed to the slow rate of 6.5 minutes with 4.4 errors. These rats were then given IVERMECTIN for 4 consecutive weeks. The same task session improved drastically from 6.5 minutes back to only 3.6 minutes. And the rate of errors improved from 4.4 back to only 1.4 errors. Almost back to baseline in only 4 weeks at 3.6 minutes with 1.4 errors. Recent studies have explored its effects on neuroinflammation, neurotransmission & synaptic protection. Ivermectin’s Effects On Neurological Disease: 1. Anti-Inflammatory Effects: A 2023 study published in Inflammation demonstrated that ivermectin mitigates neuroinflammatory damage in encephalomyelitis. Ivermectin reduced inflammatory cytokines. 2. Stabilizes Neurotransmission: A 2019 study in PLOS Pathogens found that ivermectin restores balance in synaptic neuro pathways. 3. Cholinergic Transmission: A 2024 study published in Cell & Bioscience reported that ivermectin increased activity of striatal cholinergic interneurons, enhancing dopamine release via nicotinic receptor modulation. Conclusion: Ivermectin is emerging as more than an antiparasitic agent. Its anti-inflammatory, synaptic & cholinergic effects are beneficial in neurodegenerative disorders like Dementia, Alzheimer's & Parkinson's. Dosages suggested by Dr William Makis: Parkinson’s: Patients on high-dose ivermectin (60-72mg) saw dramatic improvements in movement & symptoms. - Multiple cases of symptom reversal—where tremors, stiffness & rigidity significantly improved. Alzheimer’s: Patients on low-dose ivermectin (12-24 mg for 4-5 days) brought back memories, recognition & cognitive function in patients. Why Isn’t This Everywhere? - A preclinical Alzheimer’s study proving ivermectin’s healing ability was SCRUBBED from Google. - Big Pharma doesn’t profit from a safe, cheap, Nobel Prize-winning drug that reverses neurodegeneration. This isn’t theoretical—it’s happening NOW in real patients. Decades of suffering could be reversed by a few pills. If you have a loved one with Parkinson’s or Alzheimer’s—TRY IT. The results could be LIFE-CHANGING. 👇Ivermectin Reverses Alzheimer's (Deleted Study)👇 👇Ivermectin For Autoimmune & Neurological Ills👇 👇Ivermectin Increases Choline & Dopamine👇 Speaker: Dr William Makis, Nuclear Medicine Physician & Cancer Researcher

Valerie Anne Smith

634,679 görüntüleme • 11 ay önce

ADDERALL...We Are Giving Children This Toxic Drug Created By Nazi Germany. If People Read The Package Insert, No One In Their Right Mind Would Ever Give It To their Children Or Take It Themselves. Adderall Causes 5X Increase In Mania Psychosis & Is Totally Toxic To The Heart. ---Warnings--- Serious Cardiovascular Events: Sudden deaths, stroke & myocardial infarction have been reported in patients taking stimulant drugs at usual doses for ADHD. Psychiatric Adverse Events: Treatment emergent psychotic or manic symptoms, e.g., hallucinations, delusional thinking, aggression, or mania in patients without prior history of psychotic illness or mania can be caused by stimulants at usual doses. Long-Term Suppression of Growth: 36 month clinical studies showed height stunted 2cm & weight stunted 2.7kg per year. Children who are not growing or gaining weight should stop treatment with Adderall. Seizures: Clinical evidence shows possible convulsive adverse events. Peripheral Vasculopathy, Including Raynaud’s Phenomenon: Decreased blood flow in fingers, toes, nose, ears & lips causing cold, numbness & swelling. Serotonin Syndrome: Adderall should not be taken with an SSRI antidepressant. Serotonin syndrome symptoms include mental status changes (e.g., agitation, hallucinations, delirium & coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Manufacturer Term Of Use: Adderall should be prescribed sparingly. There are no long term systematic clinical trials or studies. Amphetamines may cause sudden death & serious cardiovascular adverse events. Manufacturer Listed Side Effects: Palpitations, Tachycardia, Hypertension, Sudden death, Myocardial infarction, Psychotic episodes at recommended doses, Overstimulation, Restlessness, Irritability, Euphoria, Dyskinesia, Depression, Tremor, Tics, Aggression, Anger, Logorrhea, Vision Injuries, Mydriasis, Intestinal ischemia (injury to the large or small intestine occurs due to not enough blood supply), Other gastrointestinal disturbances, Urticaria (hives), Rash/hypersensitivity reactions including angioedema and anaphylaxis, Serious skin rashes including Stevens-Johnson syndrome & toxic epidermal necrolysis have been reported, Impotence (failure of sexual power in the male), Changes in libido, Frequent or prolonged erections, Alopecia (baldness), Rhabdomyolysis (damaged skeletal muscle breaks down rapidly. 👇Adderall Package Insert👇 👇Adderall Causes 5 Fold Increase In Psychosis👇 👇Amphetamines Are Neurotoxic👇 Speaker: Calley Means Video: TCN
1:00

ADDERALL...We Are Giving Children This Toxic Drug Created By Nazi Germany. If People Read The Package Insert, No One In Their Right Mind Would Ever Give It To their Children Or Take It Themselves. Adderall Causes 5X Increase In Mania Psychosis & Is Totally Toxic To The Heart. ---Warnings--- Serious Cardiovascular Events: Sudden deaths, stroke & myocardial infarction have been reported in patients taking stimulant drugs at usual doses for ADHD. Psychiatric Adverse Events: Treatment emergent psychotic or manic symptoms, e.g., hallucinations, delusional thinking, aggression, or mania in patients without prior history of psychotic illness or mania can be caused by stimulants at usual doses. Long-Term Suppression of Growth: 36 month clinical studies showed height stunted 2cm & weight stunted 2.7kg per year. Children who are not growing or gaining weight should stop treatment with Adderall. Seizures: Clinical evidence shows possible convulsive adverse events. Peripheral Vasculopathy, Including Raynaud’s Phenomenon: Decreased blood flow in fingers, toes, nose, ears & lips causing cold, numbness & swelling. Serotonin Syndrome: Adderall should not be taken with an SSRI antidepressant. Serotonin syndrome symptoms include mental status changes (e.g., agitation, hallucinations, delirium & coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Manufacturer Term Of Use: Adderall should be prescribed sparingly. There are no long term systematic clinical trials or studies. Amphetamines may cause sudden death & serious cardiovascular adverse events. Manufacturer Listed Side Effects: Palpitations, Tachycardia, Hypertension, Sudden death, Myocardial infarction, Psychotic episodes at recommended doses, Overstimulation, Restlessness, Irritability, Euphoria, Dyskinesia, Depression, Tremor, Tics, Aggression, Anger, Logorrhea, Vision Injuries, Mydriasis, Intestinal ischemia (injury to the large or small intestine occurs due to not enough blood supply), Other gastrointestinal disturbances, Urticaria (hives), Rash/hypersensitivity reactions including angioedema and anaphylaxis, Serious skin rashes including Stevens-Johnson syndrome & toxic epidermal necrolysis have been reported, Impotence (failure of sexual power in the male), Changes in libido, Frequent or prolonged erections, Alopecia (baldness), Rhabdomyolysis (damaged skeletal muscle breaks down rapidly. 👇Adderall Package Insert👇 👇Adderall Causes 5 Fold Increase In Psychosis👇 👇Amphetamines Are Neurotoxic👇 Speaker: Calley Means Video: TCN

Valerie Anne Smith

312,760 görüntüleme • 1 yıl önce

🚨 Vaccines may not be appropriate for Humans now? Reallly? Major Safety Concerns with Covid Vaccines amid the Discovery of Billions of DNA Fragments in both Pfizer and Moderna Vaccines 🔴 How do these “Vaccines” Impact Humans? — Healthy human genes are being transformed into cancerous cells — Causes chromosomal instability — It effects of other parts of the body, such as the heart, brain, lungs, and the injection site 🔴 The Explosion of Cancer — Cancer in young people have exploded — Young people dying of cancer at explosive rates — 2024– more than 2 million new cancer cases expected 🔴 FL Surgeon General, Joseph Ladapo sent these concerns to the CDC & FDA in a letter. The FDA and the CDC has completely ignored him and these findings. — “if the risks of DNA integration with Covid Vaccines cannot be addressed, the vaccines are not appropriate for the use in humans.” 🔴 LISTEN closely to what a “Doctor” says….. “We’ve introduced new medications that we were told it’s very safe and very effective, and they’ve turned out not to be safe or effective… there’s a lot of birth defects, things like that…” This should tell you that the majority of doctors don’t have a damn clue and you should not listen to a thing your they say if it involves prescription drugs or vaccines… These are not doctors… these are drug dealers for big Pharma who blindly prescribe things to their patients operating off the checklists the NIH, FDA, and CDC provide. Video: TexasLindsay™
4:49

🚨 Vaccines may not be appropriate for Humans now? Reallly? Major Safety Concerns with Covid Vaccines amid the Discovery of Billions of DNA Fragments in both Pfizer and Moderna Vaccines 🔴 How do these “Vaccines” Impact Humans? — Healthy human genes are being transformed into cancerous cells — Causes chromosomal instability — It effects of other parts of the body, such as the heart, brain, lungs, and the injection site 🔴 The Explosion of Cancer — Cancer in young people have exploded — Young people dying of cancer at explosive rates — 2024– more than 2 million new cancer cases expected 🔴 FL Surgeon General, Joseph Ladapo sent these concerns to the CDC & FDA in a letter. The FDA and the CDC has completely ignored him and these findings. — “if the risks of DNA integration with Covid Vaccines cannot be addressed, the vaccines are not appropriate for the use in humans.” 🔴 LISTEN closely to what a “Doctor” says….. “We’ve introduced new medications that we were told it’s very safe and very effective, and they’ve turned out not to be safe or effective… there’s a lot of birth defects, things like that…” This should tell you that the majority of doctors don’t have a damn clue and you should not listen to a thing your they say if it involves prescription drugs or vaccines… These are not doctors… these are drug dealers for big Pharma who blindly prescribe things to their patients operating off the checklists the NIH, FDA, and CDC provide. Video: TexasLindsay™

MJTruthUltra

748,881 görüntüleme • 2 yıl önce

Based on thousands of victim testimonies and detailed medical record reviews from across the country, we have uncovered the most common tactics used in the deadly COVID hospital protocols. This was the hospitals’ modus operandi during COVID — a systematic, coordinated approach that turned patient care into patient harm. Download PDF 👇👇👇 Refused Outpatient Treatment — Family doctors, clinics, urgent care physicians refused to see patients or provide early treatment, instructing patients to “do nothing” until oxygen levels dropped requiring hospitalization. Isolation tactics — Upon being admitted to the hospital victims were denied access to family, friends, advocates, pastors, priests, or clergy. Even in death, last rites and family access were refused. Denial of rights — Admission and consent forms were left unsigned or marked by staff as “unable to sign.” Staff falsely claimed “verbal” consent to treatments was provided. No informed consent — Victims/POA received no information on risks or side effects of medications, intubation, or procedures as evidenced by no formal documentation in medical records and testimony by family or survivors. Vaccination Discrimination — Victims faced mockery, verbal abuse, and neglect based on vaccination status. Often receiving lower levels of care and different treatment options. Rapid oxygen escalation — Oxygen levels increased aggressively (often via BiPAP), causing anxiety and lung damage that led to mechanical ventilation. Forced protocol drugs only — Victims were limited to heavily incentivized and harmful hospital protocol drugs: Remdesivir/Veklury, Baricitinib/Olumiant, Tocilizumab/Actemra — often forced even when refused. Denied other treatments — Requests for vitamins, Ivermectin, Budesonide, Hydroxychloroquine, etc., were refused or ridiculed. Families were falsely told these were “not FDA approved” or “ineffective.” Gaslighting — Constantly told they would “die without compliance to protocol” or ventilation; families and victims told repeatedly they were “a very sick woman or man.” Communication cut-off — Call lights, glasses, phones, or devices were removed or placed out of reach. Families were falsely told patients didn’t want to speak. Refusal to communicate — Doctors, nurses, and administrators ignored family and advocate inquiries, often disregarding valid medical and durable POA documents. Sedation and overdose — Heavy use of Ativan, Midazolam, Haldol, Lorazepam, Precedex, Morphine, and Fentanyl, impairing breathing and leading to overdoses requiring reversal drugs. Non-emergency ventilation — Victims were pressured into early or unnecessary ventilation “to let the lungs rest,” despite no emergency need. Manipulated DNR orders — Pressure to sign Do Not Resuscitate (DNR) orders, misrepresentation of Do Not Intubate (DNI) as DNR, or outright falsification and disregard of existing directives. Starvation and dehydration — Victims were denied food, water, or any nutrition and given diuretics or laxatives instead. Physical and chemical restraints — Used without legal justification or proper documentation. Bathroom denial — Forced catheterization or use of rectal tubes without need or consent. Neglect of basic care — Hygiene, oral care, bathing, grooming, and dirty linens are often ignored. Dehumanization — Victims described as being treated like animals, stripped of dignity. Intuition of wrongdoing — Families and victims overwhelmingly felt “something was terribly wrong.” End of Life Care pushed — Pressured into palliative care, comfort care or hospice early on; often covertly ordered. Security enforcement — Police or security used to enforce isolation and institutional policies; families threatened with arrest when advocating for their loved one. Refusal of new doctors or facility transfer — Denied requests to change doctors or transfer hospitals; rapid decline or hastening of death when transfers were attempted. Secondary infections — Hospital-acquired infections like Sepsis or MRSA; severe wounds, injuries, necrosis, blood clots and pressure sores developed. Unqualified or transient staff — Treatment by foreign, travel, FEMA, or inadequately qualified medical personnel. #BetrayalProjectUSA Betrayal Project USA 🌟 aka Huckleberry (Brad) Huckleberry's Wife Genny Health Warrior MI-Betrayal Project: Exposing Insti. Betrayal VinnDogg Radio USA🇺🇲✝️🇮🇱 JusticeForJamieKay @welcometheeagIe Michelle Spencer Lisa Butler Intentional w/ Mic Meow Robert F. Kennedy Jr Mary Talley Bowden MD James Thorp MD Donna Spakes Matt Youngblood🇺🇸🇺🇸🇺🇸 James Bradley DALILA GAITAN Laura Bartlett - I DO NOT CONSENT FORM™ Ronald F. Owens, Jr. Julie4Butte5
10:11

Based on thousands of victim testimonies and detailed medical record reviews from across the country, we have uncovered the most common tactics used in the deadly COVID hospital protocols. This was the hospitals’ modus operandi during COVID — a systematic, coordinated approach that turned patient care into patient harm. Download PDF 👇👇👇 Refused Outpatient Treatment — Family doctors, clinics, urgent care physicians refused to see patients or provide early treatment, instructing patients to “do nothing” until oxygen levels dropped requiring hospitalization. Isolation tactics — Upon being admitted to the hospital victims were denied access to family, friends, advocates, pastors, priests, or clergy. Even in death, last rites and family access were refused. Denial of rights — Admission and consent forms were left unsigned or marked by staff as “unable to sign.” Staff falsely claimed “verbal” consent to treatments was provided. No informed consent — Victims/POA received no information on risks or side effects of medications, intubation, or procedures as evidenced by no formal documentation in medical records and testimony by family or survivors. Vaccination Discrimination — Victims faced mockery, verbal abuse, and neglect based on vaccination status. Often receiving lower levels of care and different treatment options. Rapid oxygen escalation — Oxygen levels increased aggressively (often via BiPAP), causing anxiety and lung damage that led to mechanical ventilation. Forced protocol drugs only — Victims were limited to heavily incentivized and harmful hospital protocol drugs: Remdesivir/Veklury, Baricitinib/Olumiant, Tocilizumab/Actemra — often forced even when refused. Denied other treatments — Requests for vitamins, Ivermectin, Budesonide, Hydroxychloroquine, etc., were refused or ridiculed. Families were falsely told these were “not FDA approved” or “ineffective.” Gaslighting — Constantly told they would “die without compliance to protocol” or ventilation; families and victims told repeatedly they were “a very sick woman or man.” Communication cut-off — Call lights, glasses, phones, or devices were removed or placed out of reach. Families were falsely told patients didn’t want to speak. Refusal to communicate — Doctors, nurses, and administrators ignored family and advocate inquiries, often disregarding valid medical and durable POA documents. Sedation and overdose — Heavy use of Ativan, Midazolam, Haldol, Lorazepam, Precedex, Morphine, and Fentanyl, impairing breathing and leading to overdoses requiring reversal drugs. Non-emergency ventilation — Victims were pressured into early or unnecessary ventilation “to let the lungs rest,” despite no emergency need. Manipulated DNR orders — Pressure to sign Do Not Resuscitate (DNR) orders, misrepresentation of Do Not Intubate (DNI) as DNR, or outright falsification and disregard of existing directives. Starvation and dehydration — Victims were denied food, water, or any nutrition and given diuretics or laxatives instead. Physical and chemical restraints — Used without legal justification or proper documentation. Bathroom denial — Forced catheterization or use of rectal tubes without need or consent. Neglect of basic care — Hygiene, oral care, bathing, grooming, and dirty linens are often ignored. Dehumanization — Victims described as being treated like animals, stripped of dignity. Intuition of wrongdoing — Families and victims overwhelmingly felt “something was terribly wrong.” End of Life Care pushed — Pressured into palliative care, comfort care or hospice early on; often covertly ordered. Security enforcement — Police or security used to enforce isolation and institutional policies; families threatened with arrest when advocating for their loved one. Refusal of new doctors or facility transfer — Denied requests to change doctors or transfer hospitals; rapid decline or hastening of death when transfers were attempted. Secondary infections — Hospital-acquired infections like Sepsis or MRSA; severe wounds, injuries, necrosis, blood clots and pressure sores developed. Unqualified or transient staff — Treatment by foreign, travel, FEMA, or inadequately qualified medical personnel. #BetrayalProjectUSA Betrayal Project USA 🌟 aka Huckleberry (Brad) Huckleberry's Wife Genny Health Warrior MI-Betrayal Project: Exposing Insti. Betrayal VinnDogg Radio USA🇺🇲✝️🇮🇱 JusticeForJamieKay @welcometheeagIe Michelle Spencer Lisa Butler Intentional w/ Mic Meow Robert F. Kennedy Jr Mary Talley Bowden MD James Thorp MD Donna Spakes Matt Youngblood🇺🇸🇺🇸🇺🇸 James Bradley DALILA GAITAN Laura Bartlett - I DO NOT CONSENT FORM™ Ronald F. Owens, Jr. Julie4Butte5

CA Betrayal Project USA

30,535 görüntüleme • 4 ay önce

In 1993 CNN warned against pregnancy ultrasound and had the FDA admit it was aware of its dangers. Remarkably, the FDA raised the maximum allowable ultrasound dose by 8 times (despite data showing the old dose was too high) and all those dangers were forgotten. Ultrasound causes a dose dependent injury to the organs and cells that fetuses are particularly susceptible to (especially early in life when ultrasounds have no medical value). Those harms include: •Genetic damage, significant damage to cellular structures (e.g., mitochondria, microtubules and the nucleus). •Initiating programmed cell death. •In mice and monkeys, significantly impaired learning, memory, activity, and sociability. •Fetal death. •Hemorrhages. •A wide range of congenital malformations. The Chinese in turn conducted a series of studies showing the low doses of ultrasound created those injuries in the placenta, pituitary gland, eyes, immune system, kidneys, liver, ovaries, testicles (and sperm), and the brain’s neurons and glial cells. Additionally, in humans, ultrasound has also been linked to miscarriages, premature ovulation, male infertility, fetal growth restrictions, altered neurological function, developmental delays. Conversely, ultrasound has not been proven to improve pregnancy outcomes (rather it just leads to more frequent C-sections, prenatal testing, anxiety for the parents, abortions and neonatal distress) Rather, all it can do most of the time is (sometimes erroneously) tell parents to abort their baby or subject it to invasive (and harmful tests), all of which creates immense unnecessary anxiety and anguish for the parents. I complied the 200+ studies proving all of this in the article below.
11:21

In 1993 CNN warned against pregnancy ultrasound and had the FDA admit it was aware of its dangers. Remarkably, the FDA raised the maximum allowable ultrasound dose by 8 times (despite data showing the old dose was too high) and all those dangers were forgotten. Ultrasound causes a dose dependent injury to the organs and cells that fetuses are particularly susceptible to (especially early in life when ultrasounds have no medical value). Those harms include: •Genetic damage, significant damage to cellular structures (e.g., mitochondria, microtubules and the nucleus). •Initiating programmed cell death. •In mice and monkeys, significantly impaired learning, memory, activity, and sociability. •Fetal death. •Hemorrhages. •A wide range of congenital malformations. The Chinese in turn conducted a series of studies showing the low doses of ultrasound created those injuries in the placenta, pituitary gland, eyes, immune system, kidneys, liver, ovaries, testicles (and sperm), and the brain’s neurons and glial cells. Additionally, in humans, ultrasound has also been linked to miscarriages, premature ovulation, male infertility, fetal growth restrictions, altered neurological function, developmental delays. Conversely, ultrasound has not been proven to improve pregnancy outcomes (rather it just leads to more frequent C-sections, prenatal testing, anxiety for the parents, abortions and neonatal distress) Rather, all it can do most of the time is (sometimes erroneously) tell parents to abort their baby or subject it to invasive (and harmful tests), all of which creates immense unnecessary anxiety and anguish for the parents. I complied the 200+ studies proving all of this in the article below.

A Midwestern Doctor

781,645 görüntüleme • 1 yıl önce

Humacyte is proud to announce that the FDA has granted full approval for Symvess™, a first-in-class, universally implantable, bioengineered human vessel for extremity vascular trauma replacement and repair. This approval is a significant milestone in regenerative medicine, offering a new treatment option for patients with severe arterial injuries. Congratulations to our incredible team and partners who made this possible! Learn more at See the Prescribing Information, including Boxed Warning: INDICATION SYMVESS is an acellular tissue engineered vessel indicated for use in adults as a vascular conduit for extremity arterial injury when urgent revascularization is needed to avoid imminent limb loss, and autologous vein graft is not feasible. IMPORTANT SAFETY INFORMATION BOXED WARNING: GRAFT FAILURE -Loss of SYMVESS integrity due to mid-graft rupture or anastomotic failure can result in life threatening hemorrhage. CONTRAINDICATIONS DO NOT use SYMVESS in patients who have a medical condition that would preclude long-term antiplatelet therapy (such as aspirin or clopidogrel) after resolution of acute injuries. WARNINGS & PRECAUTIONS -Graft Rupture: Vascular graft rupture has occurred in patients treated with SYMVESS. Advise patients that arterial bleeding can be life-threatening and to seek emergent medical evaluation for any signs or symptoms of graft rupture such as bleeding, pain and swelling in the extremity, or signs of extremity ischemia. Follow appropriate procedures for handling and administering SYMVESS. -Anastomotic Failure: Anastomotic failure has occurred in patients treated with SYMVESS. In clinical studies of SYMVESS, anastomotic failure occurred within the first 36 days post-implantation. Monitor patients for signs of anastomotic failure such as pain and swelling at the surgical site, decreasing hemoglobin or other signs and symptoms of bleeding. Advise patients to seek urgent medical evaluation if they have any signs or symptoms that may be indicative of anastomotic failure such as bleeding, swelling or worsening pain at the surgical site or changes in color of overlying skin. Follow appropriate procedures for handling and administering SYMVESS. -Thrombosis: Thrombosis has occurred in patients treated with SYMVESS. In clinical trials of SYMVESS, patients received antiplatelet therapy following implantation of SYMVESS to reduce the risk of thrombosis. The risk of thrombosis may increase in patients who discontinue antiplatelet therapy. Anti-platelet therapy is recommended following treatment with SYMVESS. -Transmission of Infectious Diseases: SYMVESS is manufactured using cells and reagents that may transmit infectious diseases or infectious agents. The cells used in the manufacture of SYMVESS are derived from a donor who met the donor eligibility requirements for transmissible infectious diseases. Animal-derived reagents are tested for animal viruses, bacteria, fungi, and mycoplasma before use, but this does not eliminate the risk of transmitting these or other transmissible infectious diseases and disease agents. No transmissible agent infections have been reported during clinical testing. ADVERSE REACTIONS The most common adverse reactions (≥3%) were thrombosis, fever, pain, anastomotic stenosis, rupture or anastomotic failure, and infection. USE IN SPECIFIC POPULATIONS Pediatric Use: The safety and effectiveness of SYMVESS in pediatric patients (0 to 17 years old) have not been established. Geriatric Use: Two patients out of the 54 Extremity Group implanted with SYMVESS as a conduit in Study 1 were aged ≥65 years. The number of patients aged ≥65 years was not sufficient to determine whether they responded differently than younger patients to SYMVESS. #Humacyte #FDAApproval #RegenerativeMedicine #Innovation #Biotech #Firstinclass $HUMA
0:35

Humacyte is proud to announce that the FDA has granted full approval for Symvess™, a first-in-class, universally implantable, bioengineered human vessel for extremity vascular trauma replacement and repair. This approval is a significant milestone in regenerative medicine, offering a new treatment option for patients with severe arterial injuries. Congratulations to our incredible team and partners who made this possible! Learn more at See the Prescribing Information, including Boxed Warning: INDICATION SYMVESS is an acellular tissue engineered vessel indicated for use in adults as a vascular conduit for extremity arterial injury when urgent revascularization is needed to avoid imminent limb loss, and autologous vein graft is not feasible. IMPORTANT SAFETY INFORMATION BOXED WARNING: GRAFT FAILURE -Loss of SYMVESS integrity due to mid-graft rupture or anastomotic failure can result in life threatening hemorrhage. CONTRAINDICATIONS DO NOT use SYMVESS in patients who have a medical condition that would preclude long-term antiplatelet therapy (such as aspirin or clopidogrel) after resolution of acute injuries. WARNINGS & PRECAUTIONS -Graft Rupture: Vascular graft rupture has occurred in patients treated with SYMVESS. Advise patients that arterial bleeding can be life-threatening and to seek emergent medical evaluation for any signs or symptoms of graft rupture such as bleeding, pain and swelling in the extremity, or signs of extremity ischemia. Follow appropriate procedures for handling and administering SYMVESS. -Anastomotic Failure: Anastomotic failure has occurred in patients treated with SYMVESS. In clinical studies of SYMVESS, anastomotic failure occurred within the first 36 days post-implantation. Monitor patients for signs of anastomotic failure such as pain and swelling at the surgical site, decreasing hemoglobin or other signs and symptoms of bleeding. Advise patients to seek urgent medical evaluation if they have any signs or symptoms that may be indicative of anastomotic failure such as bleeding, swelling or worsening pain at the surgical site or changes in color of overlying skin. Follow appropriate procedures for handling and administering SYMVESS. -Thrombosis: Thrombosis has occurred in patients treated with SYMVESS. In clinical trials of SYMVESS, patients received antiplatelet therapy following implantation of SYMVESS to reduce the risk of thrombosis. The risk of thrombosis may increase in patients who discontinue antiplatelet therapy. Anti-platelet therapy is recommended following treatment with SYMVESS. -Transmission of Infectious Diseases: SYMVESS is manufactured using cells and reagents that may transmit infectious diseases or infectious agents. The cells used in the manufacture of SYMVESS are derived from a donor who met the donor eligibility requirements for transmissible infectious diseases. Animal-derived reagents are tested for animal viruses, bacteria, fungi, and mycoplasma before use, but this does not eliminate the risk of transmitting these or other transmissible infectious diseases and disease agents. No transmissible agent infections have been reported during clinical testing. ADVERSE REACTIONS The most common adverse reactions (≥3%) were thrombosis, fever, pain, anastomotic stenosis, rupture or anastomotic failure, and infection. USE IN SPECIFIC POPULATIONS Pediatric Use: The safety and effectiveness of SYMVESS in pediatric patients (0 to 17 years old) have not been established. Geriatric Use: Two patients out of the 54 Extremity Group implanted with SYMVESS as a conduit in Study 1 were aged ≥65 years. The number of patients aged ≥65 years was not sufficient to determine whether they responded differently than younger patients to SYMVESS. #Humacyte #FDAApproval #RegenerativeMedicine #Innovation #Biotech #Firstinclass $HUMA

Humacyte

26,873 görüntüleme • 1 yıl önce

🚨 President Donald Trump, next to Joe Rogan and RFK JR, signed an executive order today “Accelerating Medical Treatments for Serious Mental Illness.” Primarily Including psychedelics. It directs the FDA to fast-track reviews of certain psychedelic drugs—primarily focusing on ibogaine (a substance derived from the African iboga plant), along with others that have received Breakthrough Therapy designations (such as some forms of psilocybin or MDMA-related compounds). Reported/potential benefits: • PTSD and Trauma (Especially Veterans): Ibogaine has shown promise in reducing PTSD symptoms, intrusive thoughts, and emotional numbness in small studies and anecdotal reports from veterans. It may “reset” brain pathways disrupted by trauma, offering rapid relief after one or few sessions (unlike weeks/months of traditional meds or therapy). • Depression and Anxiety: Certain psychedelics (e.g., psilocybin) can promote neuroplasticity—helping the brain form new connections—which may lead to lasting improvements in mood for treatment-resistant depression. Effects can be profound and quicker than standard antidepressants. • Addiction (Opioids, Alcohol, etc.): Ibogaine is noted for potentially interrupting addiction cycles, reducing cravings and withdrawal in some users, by affecting brain reward systems. • Traumatic Brain Injury (TBI): Early research suggests benefits for cognitive and emotional recovery in veterans with head injuries. • Overall Mental Health Crisis: Proponents argue this could provide new tools for severe, persistent cases, potentially lowering suicide rates and long-term healthcare costs by offering alternatives to lifelong pharmaceutical dependence.
1:12

🚨 President Donald Trump, next to Joe Rogan and RFK JR, signed an executive order today “Accelerating Medical Treatments for Serious Mental Illness.” Primarily Including psychedelics. It directs the FDA to fast-track reviews of certain psychedelic drugs—primarily focusing on ibogaine (a substance derived from the African iboga plant), along with others that have received Breakthrough Therapy designations (such as some forms of psilocybin or MDMA-related compounds). Reported/potential benefits: • PTSD and Trauma (Especially Veterans): Ibogaine has shown promise in reducing PTSD symptoms, intrusive thoughts, and emotional numbness in small studies and anecdotal reports from veterans. It may “reset” brain pathways disrupted by trauma, offering rapid relief after one or few sessions (unlike weeks/months of traditional meds or therapy). • Depression and Anxiety: Certain psychedelics (e.g., psilocybin) can promote neuroplasticity—helping the brain form new connections—which may lead to lasting improvements in mood for treatment-resistant depression. Effects can be profound and quicker than standard antidepressants. • Addiction (Opioids, Alcohol, etc.): Ibogaine is noted for potentially interrupting addiction cycles, reducing cravings and withdrawal in some users, by affecting brain reward systems. • Traumatic Brain Injury (TBI): Early research suggests benefits for cognitive and emotional recovery in veterans with head injuries. • Overall Mental Health Crisis: Proponents argue this could provide new tools for severe, persistent cases, potentially lowering suicide rates and long-term healthcare costs by offering alternatives to lifelong pharmaceutical dependence.

MJTruthUltra

15,984 görüntüleme • 2 ay önce