They’ll lose. They be laughed out of the public square. The passionate 2% amongst them won’t be platformed anymore. They won’t gain traction, not even the appearance of it.

Will they awaken from their slumber? Get off the blue pill habit?

The left is slowly loosing their secular neo-fascist religion. There will be die hards but they will be hiding in their safe spaces where they belong.

Are we going to let them get away with feigning victimhood? What about all the pain and suffering they’ve caused? They absolutely deserve to be shamed and ridiculed for what they’ve done.

Should we forgive them, however?

Absolutely.

Perhaps after we have some fun tho… :)

#WWG1…

Thoughts?

🤝🛕👁

Anyone else have this problem?

Edit:

Thanks for the replies, frens :) ✝️

The fact of the matter is that pathogens including viruses and bacteria are beneficial—as they challenge our immune systems forcing us to evolve adaptations that thwart any encountered pathogens and all of their possible variants—if we maintain the following:

1. Regular high quality Stage IV REM sleep (the deep restorative phase of sleep during whence dreams occur)

2. Low stress or at least not regular/prolonged periods of high stress

3. Regular interval and/or weight training

4. Proper inputs: this includes everything that goes into our bodies via respiration including of beneficial particles in forest air while excluding pollution, everything absorbed through skin (avoid parabens, pthalates, etc.), and digestion of properly raised animals and animal products like eggs and dairy but also a variety of raw or barely cooked fruits, nuts, vegetables, mushrooms, etc. (using supplements when necessary) and also includes regular fasting to induce autophagy which is a process where the body recycles it’s broken, toxic, and scar tissues, cells, organelles, etc.*

5. Proper vitamin D levels via direct skin contact with sun rays and/or supplementation and/or diet.

Being deficient in meeting just one of these health requirements for too long will not only affect your ability to maintain the others but will result in immunodeficiency which if left unchecked for too long will result in any number of chronic illnesses including cancers, coronavirus illnesses including flus/covids, other infections, etc.

If you generally maintain most of these health requirements even with frequent—not sustained/long-term—deficiencies, the work of divine evolutionary creation that is your body will handle anything that comes it’s way sans severe physical injuries including those resulting from harmful injections.

So chill the fuck out (avoiding the idiot box and antisocial media reap yuge benefits), eat well and fast often, avoid pollution, sleep well, catch some rays, pump iron, and take a hike.

*Autophagy kicks in a after 16 hours of zero caloric input. This is easy to do if you do strict keto for a few days prior and then sleep off the first eight hours by starting your fast after dinner and not eating again until the next dinner. You’ll get almost 8 hours of autophagy this way in a 24 hour period. This should be done as often as tolerable. Personally, I try to do this at least once per week.

Now go and do the things, King.

“The plant is reported to possess anti-oxidant, anti-inflammatory, anti-cancer, anti-diabetic, anti-bacterial, anti-obesity, and immunomodulatory activities. The plant extract inhibits cancer cell growth by inducing apoptosis, cell cycle arrest, autophagy and inhibiting cancer stem cells. The plant is rich in bioactive chemical constituents like cucurbitane type triterpenoids, triterpene glycosides, phenolic acids, flavonoids, essential oils, saponins, fatty acids, and proteins. Some of the isolated compounds (Kuguacin J, Karaviloside XI, Kuguaglycoside C, Momordicoside Q–U, Charantin, α-eleostearic acid) and proteins (α-Momorcharin, RNase MC2, MAP30) possess potent biological activity. In the present review, we are summarizing the anti-oxidant, anti-inflammatory, and anti-cancer activities of Momordica charantia along with a short account of important chemical constituents, providing a basis for establishing detail biological activities of the plant and developing novel drug molecules based on the active chemical constituents.”

“MC has been cultivated traditionally in developing countries like India, China, Brazil, Colombia, Cuba, Ghana, Haiti, Mexico, Malaya, New Zealand, Nicaragua, Panama, and Peru, and is commonly used for the treatment of diabetes and colics [12–13]. MC is also used as antiviral, anti-malarial, and anti-bacterial agent, while it is applied for wound healing and treatment of peptic ulcers in Traditional Turkish medicine. In Indian medicinal systems, MC is reported to possess anti-diabetic, abortifacient, anti- helminthic, anti-malarial, and laxative properties, while it is also used for treatment of dysmenorrhea, emmenagogue, eczema, gout, galactagogue, kidney (stone), jaundice, leucorrhea, leprosy, pneumonia, piles, rheumatism, and psoriasis [14].”

“Various extracts of MC are studied for biological activities, including anti-oxidant [15], anti-diabetic [16], anti-cancer [17], anti-inflammatory [18], anti-bacterial [19], antifungal [20], anti-viral [21], anti-HIV [22], anti-helminthic [23], anti-mycobac-terial [24], hypotensive [25], anti-obesity [26], immunomodulatory [27], anti-hyperlipidemic [28], hepatoprotective [29], and neuropro-tective [30] activities. Several chemical constituents such as cucurbitane type triterpenoids, cucurbitane type glycosides, triterpene saponins, phenolic, and flavonoid compounds, and some protein fractions have been isolated from MC [31]. In the present review, we are summarizing some of the important reports dealing with anti-oxidant, anti-inflammatory, and anti- cancer activities of MC along with its reported chemical constituents and their biological activities.”

https://draxe.com/nutrition/bitter-melon/

• Managing blood sugar levels and diabetes

• Reducing respiratory infections such as pneumonia

• Lowering inflammation and raising immunity

• Treating abdominal pain, peptic ulcers, constipation, cramps and fluid retention

• Increasing cancer-protection

• Reducing fevers and coughs

• Lowering menstrual irregularity

• Treating skin conditions including eczema, scabies and psoriasis

• Antiviral, antibacterial and anthelmintic properties (including those that can be used to prevent or treat parasites, HIV/AIDS, malaria and even leprosy)

• Treating gout, jaundice and kidney stones

• Managing symptoms of autoimmune disorders including rheumatoid arthritis

https://www.healthline.com/nutrition/bitter-melon

“6 Benefits of Bitter Melon (Bitter Gourd) and Its Extract”

https://www.healthline.com/health/diabetes/bitter-melon-and-diabetes

“Bitter Melon and Diabetes”

Best product I found considering price/performance is called Jarrow Glucose Optimizer:

https://jarrow.com/products/glucose-optimizer-120-tablets

(You can find it for about $20 elsewhere)

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/

“Ivermectin has powerful antitumor effects, including the inhibition of proliferation, metastasis, and angiogenic activity, in a variety of cancer cells. This may be related to the regulation of multiple signaling pathways by ivermectin through PAK1 kinase. On the other hand, ivermectin promotes programmed cancer cell death, including apoptosis, autophagy and pyroptosis. Ivermectin induces apoptosis and autophagy is mutually regulated. Interestingly, ivermectin can also inhibit tumor stem cells and reverse multidrug resistance and exerts the optimal effect when used in combination with other chemotherapy drugs.”

“IVM can inhibit the replication of flavivirus by targeting the NS3 helicase [17]; it also blocks the nuclear transport of viral proteins by acting on α/β-mediated nuclear transport and exerts antiviral activity against the HIV-1 and dengue viruses [18]. Recent studies have also pointed out that it has a promising inhibitory effect on the SARS-CoV-2 virus, which has caused a global outbreak in 2020 [19]. In addition, IVM shows potential for clinical application in asthma [20] and neurological diseases [21]. Recently scientists have discovered that IVM has a strong anticancer effect.”

“After treatment with IVM, the proliferation of multiple breast cancer cell lines including MCF-7, MDA-MB-231 and MCF-10 was significantly reduced.”

“IVM regulates the tumor microenvironment and mediates immunogenic cell death, which may be a new direction for research exploring anticancer mechanisms in the future.”

“Nambara’s study showed that IVM could significantly inhibit the proliferation of gastric cancer cells in vivo and in vitro and that the inhibitory effect of IVM depended on the expression of Yes-associated protein 1(YAP1)[39].”

“In a study that screened Wnt pathway inhibitors, IVM inhibited the proliferation of multiple cancers, including the colorectal cancer cell lines CC14, CC36, DLD1, and Ls174 T, and promoted apoptosis by blocking the Wnt pathway [41].”

“IVM could inhibit the development of hepatocellular carcinoma by blocking YAP1 activity in spontaneous liver cancer Mob1b-/- mice [43].”

“Experiments confirmed that IVM could significantly inhibit the proliferation of five renal cell carcinoma cell lines without affecting the proliferation of normal kidney cells, and its mechanism may be related to the induction of mitochondrial dysfunction [48].”

“In Nappi's experiment, it was found that IVM could enhance the drug activity of the anti-androgen drug enzalutamide in the prostate cancer cell line LNCaP and reverse the resistance of the prostate cancer cell line PC3 to docetaxel [50]. Interestingly, IVM also restored the sensitivity of the triple-negative breast cancer to the anti-estrogen drug tamoxifen [36], which also implies the potential for IVM to be used in endocrine therapy. Moreover, IVM was also found to have a good inhibitory effect on the prostate cancer cell line DU145 [51].”

“In an experiment designed to screen potential drugs for the treatment of leukemia, IVM preferentially killed leukemia cells at low concentrations without affecting normal hematopoietic cells [51].”

“The majority of cervical cancers are caused by human papillomavirus (HPV) infection [54,55]. IVM has been proven to significantly inhibit the proliferation and migration of HeLa cells and promote apoptosis [56]. After intervention with IVM, the cell cycle of HeLa cells was blocked at the G1/S phase, and the cells showed typical morphological changes related to apoptosis.”

“In a study by Hashimoto, it found that IVM inhibited the proliferation of various ovarian cancer cell lines, and the mechanism was related to the inhibition of PAK1 kinase [58]. In research to screen potential targets for the treatment of ovarian cancer through the use of an shRNA library and a CRISPR/Cas9 library, the oncogene KPNB1 was detected. IVM could block the cell cycle and induce cell apoptosis through a KPNB1-dependent mechanism in ovarian cancer [59].”

“In a study that screened drugs for the treatment of nasopharyngeal cancer, IVM significantly inhibited the development of nasopharyngeal carcinoma in nude mice at doses that were not toxic to normal thymocytes [69]. In addition, IVM also had a cytotoxic effect on a variety of nasopharyngeal cancer cells in vitro, and the mechanism is related to the reduction of PAK1 kinase activity to inhibit the MAPK pathway.”

“Lung cancer has the highest morbidity and mortality among cancers [70]. Nishio found that IVM could significantly inhibit the proliferation of H1299 lung cancer cells by inhibiting YAP1 activity [43]. Nappi's experiment also proved that IVM combined with erlotinib to achieved a synergistic killing effect by regulating EGFR activity and in HCC827 lung cancer cells [50]. In addition, IVM could reduce the metastasis of lung cancer cells by inhibiting EMT.”

“Gallardo treated melanoma cells with IVM and found that it could effectively inhibit melanoma activity [73]. Interestingly, IVM could also show activity against BRAF wild-type melanoma cells, and its combination with dapafinib could significantly increase antitumor activity. Additionally, it has been confirmed that PAK1 is the key target of IVM that mediates its anti-melanoma activity, and IVM can also significantly reduce the lung metastasis of melanoma in animal experiments. Deng found that IVM could activate the nuclear translocation of TFE3 and induce autophagy-dependent cell death by dephosphorylation of TFE3 (Ser321) in SK-MEL-28 melanoma cells [74]. However, NAC reversed the effect of IVM, which indicated that IVM increased TFE3-dependent autophagy through the ROS signaling pathway.”

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835698/

“So far, at least 235 clinically-approved, non-cancer drugs have proven antitumor activity either in vitro, in vivo, or even clinically. Among these, ivermectin, an antiparasitic compound of wide use in veterinary and human medicine, is clearly a strong candidate for repositioning, based on the fact that i) it is very safe, causing almost no side-effects other than those caused by the immune and inflammatory responses against the parasite in infected patients, and ii) it has proven antitumor activity in preclinical studies. On the other hand, it is now evident that the use of very selective “unitargeted” drugs is commonly associated to early development of resistance by cancer cells, hence the use of “dirty” or “multitargeted” drugs is important to explore. In this sense, ivermectin has this potential as it modulates several targets such as the multidrug resistance protein (MDR), the Akt/mTOR and WNT-TCF pathways, the purinergic receptors, the PAK-1 protein, certain cancer-related epigenetic deregulators such as SIN3A and SIN3B, RNA helicase activity, while stimulates chloride channel receptors leading to cell hyperpolarization, and down-regulates stemness genes to preferentially target cancer stem-cell like population, at least in breast cancer. Importantly, the in vitro and in vivo antitumor activities of ivermectin are achieved at concentrations that can be clinically reachable based on the human pharmacokinetic studies done in healthy and parasited patients. Thus, existing information on ivermectin could allow its rapid move into clinical trials for cancer patients.”

https://www.sciencedirect.com/science/article/pii/S1043661820315152

“• Ivermectin effectively suppresses the proliferation and metastasis of cancer cells and promotes cancer cell death at doses that are nontoxic to normal cells.

• Ivermectin shows excellent efficacy against conventional chemotherapy drug-resistant cancer cells and reverses multidrug resistance.

• Ivermectin combined with other chemotherapy drugs or targeted drugs has powerful effects on cancer.

• The structure of crosstalk centered on PAK1 kinase reveals the mechanism by which ivermectin regulates multiple signaling pathways.

• Ivermectin has been used to treat parasitic diseases in humans for many years and can quickly enter clinical trials for the treatment of tumors.”

https://pubmed.ncbi.nlm.nih.gov/32474842/

“Purpose:

Ivermectin is an antiparasitic drug that exhibits antitumor effects in preclinical studies, and as such is currently being repositioned for cancer treatment. However, divergences exist regarding its employed doses in preclinical works. Therefore, the aim of this study was to determine whether the antitumor effects of ivermectin are observable at clinically feasible drug concentrations.

Methods:

Twenty-eight malignant cell lines were treated with 5 μM ivermectin. Cell viability, clonogenicity, cell cycle, cell death and pharmacological interaction with common cytotoxic drugs were assessed, as well as the consequences of its use on stem cell-enriched populations. The antitumor in vivo effects of ivermectin were also evaluated.

Results:

The breast MDA-MB-231, MDA-MB-468, and MCF-7, and the ovarian SKOV-3, were the most sensitive cancer cell lines to ivermectin. Conversely, the prostate cancer cell line DU145 was the most resistant to its use. In the most sensitive cells, ivermectin induced cell cycle arrest at G0-G1 phase, with modulation of proteins associated with cell cycle control. Furthermore, ivermectin was synergistic with docetaxel, cyclophosphamide and tamoxifen. Ivermectin reduced both cell viability and colony formation capacity in the stem cell-enriched population as compared with the parental one. Finally, in tumor-bearing mice ivermectin successfully reduced both tumor size and weight.

Conclusion:

Our results on the antitumor effects of ivermectin support its clinical testing.”

https://jeccr.biomedcentral.com/articles/10.1186/s13046-019-1251-7

“These findings demonstrated that ivermectin significantly enhanced the anti-cancer efficacy of chemotherapeutic drugs to tumor cells, especially in the drug-resistant cells. Thus, ivermectin, a FDA-approved antiparasitic drug, could potentially be used in combination with chemotherapeutic agents to treat cancers and in particular, the drug-resistant cancers.”

1. Recall that initially Trump was anti vax/anti lockdown/pro therapeutic (ivermectin, hcq, etc.)

2. The mass psychosis was overwhelming

3. Facing re-election, brainwashed boomers/millennials, powerful Pharma cartel, etc. he changed his tune but..

4. In the same breath he appeared to shill for Pharma, he always said there should be choice

5. He moved to Florida and worked closely with Gov. DeSantis where they are anti mask, anti vax, anti lockdown, pro therapeutic

6. Competing nations were developing mRNA tech which is primarily a defense/weapons tech and therefore our mRNA injections must be injected into more arms than their mRNA injections

7. States were left to choose tyranny versus freedom and there has been an exodus from tyrannical states to free states, moving us towards a shift in electoral college representation

8. The vaxxofascists thus carried forth their crippled plans for multi year global lockdowns, mass forced vax, and global CCP takeover while fully exposed and only the weakest and most brainwashed faggots are still falling for it while the rest of us know better and he knows we know better partially thanks to his initial seeding of the truth

9. “Vax” being optional allows the sheeple to select themselves and their offspring out of the gene pool—which is sad but necessary for what’s coming—but everyone else can reject it and move to a based red state if they have to which they’re only likely to do if they’re based enough which is a good filter, at least electorally, if people are moving from blue counties/cities to based red states

10. He still blames the CCP who everyone owes a lot of money to and he’s now saying we don’t owe the CCP anymore and instead CCP owes $60T for damages and if re-elected (again lol) he can lead the charge to bankrupt the CCP by getting everyone to agree to not pay the CCP back.

This war will go hot at some point. How hot and for how long? It doesn’t fucking matter because only the based will be fighting it and only we shall repopulate the earth. SO BUCKLE THE FUCK UP AND PREPARE TO…

MAKE EARTH GREAT AGAIN

So DON’T get the fucking jab and make LOT’S babies and DON’T let them inject the kids and RAISE them properly, and HAVE A MERRY FUCKING CHRISTMAS, FAGGOTS. ✝️🎄🎅 🎁

AND

✝️🇺🇸 GOD BLESS AMERICA. 🇺🇸✝️

Edit:

For trollzies, say, “I didn’t like Trump until he saved hundreds of millions of lives by fast tracking his Trump vaccines. So cool!”