The Dr. Ardis Show | Protecting your Kidneys | Episode 03.11.2026

Hi, everybody. I'm Dr. Brian Artis and this is the Dr. Artis Show. In this entire presentation,

this podcast is titled Protecting Your Kidneys. Chronic kidney disease, acute kidney disease,

including UTIs, kidney stones, hyper-tension. You name it. There's all kinds of issues with

the kidneys that affect millions around the world in this broadcast. This episode is for you. Remember,

if this applies and this information to you or anyone you know or love that has acute or chronic

kidney disease of any kind, forward this link to this show to them, also you can go to the resources tab

at thedoctorartisshow.com. And you can actually download this entire PowerPoint. I'm about to walk

you through. I'm going to show you what the medical profession declares are the most common acute

and chronic kidney disease scenarios, what causes them, what are the drugs they prescribe for them,

all their horrible side effects. And then I'm going to walk you through what are the natural

antidotes to all things kidney disease. And you should be blown away because there's natural antidotes

to help prevent most of these issues that you're an effrologist. Your cardiologist don't even know

about. That's why the Dr. Artis Show exists. And I'm excited to present this to you today. So,

for anybody affected by kidney disease, worried about kidney disease. If that runs in your family,

this one's for you. So, let's dive in. All right, this is protecting your kidneys. This is my

PowerPoint presentation. We will walk you through this. You can scan the QR code. If you are not

a current follower of the Dr. Artis Show, just scan the QR code and we will notify you after you

put in your email of all of our upcoming shows, which are once a week on somehow topic. All right,

WebMD states kidney disease causes and symptoms and treatment. What is kidney disease?

Kidney disease can affect your body's ability to clean your blood, filter extra water out of

your blood and help control your blood pressure. It can also affect red blood cell production,

and vitamin D metabolism needed for bone health. Not sure you knew this, but there are cells in your

kidneys that produce a substance that helps build red blood cells. When your kidneys are damaged,

waste products and fluid can build up in your body that can cause swelling in your ankles,

nausea, weakness, poor sleep, and shortness of breath. Anybody out there got any of those?

Because you most likely have kidney disease. Without treatment, the damage can get worse,

and your kidneys may eventually stop working. That is serious, and it can be life-threatening.

You know anybody on dialysis? That's because their kidneys have failed.

All right, healthy kidneys. What is their job? This is their key functions.

According to WebMD, they keep a balance of water and minerals, such as sodium, which is salt,

potassium, and phosphorus in your blood. Your kidneys remove waste from your blood after digestion,

muscle activity, and exposure to chemicals or medications.

Also, your kidneys make rennen, which your body uses to help manage your blood pressure.

Kidneys also make a chemical called a rethropoetin, which promotes your body to make red blood cells.

Your kidneys also make an active form of vitamin D. Did you know that? Everyone's told you

you'll get vitamin D from the sun, or you have to supplement it. Did you know your kidneys

activate a form of vitamin D? They make it needed for bone health and bodily functions.

Your kidneys also filter all your blood in your body every 30 minutes.

What are types of kidney disease per WebMD?

Chronic kidney disease is a condition where your kidneys can't filter toxins or extra fluid from

your body as well as they should. CKD is the abbreviation for chronic kidney disease. Usually

it's worse over time. They say, if left untreated, chronic kidney disease may lead to kidney failure.

At this stage called in-stage renal disease, the condition must be treated by dialysis or kidney

transplant. It's estimated that one in seven adults, everybody listen to me watching this show.

One in seven adult Americans have this condition, but 40% of those with serious chronic kidney

disease aren't even aware they have the condition. How's that possible? Do they not know they have

nausea? The parts of the body are swelling. They can't sleep. Here's a list of other common forms

of kidney disease and pay attention. This might be you. Polycystic kidney disease, this genetic

disorder causes cysts to grow in your kidneys. It's actually usually parasites, but that's what the

WebMD tells you. Lupus nephritis, one of my favorite designated chronic kidney diseases. Lupus is

an autoimmune disease, meaning your immune system attacks healthy cells. All right, hold on,

everybody. I just need to listen to me. There are three primary drugs they prescribe to all

lupus patients. Methotrexate, plaquanal, and prednisone. All of them cause kidney damage,

but what they call the damage of the side effects of those three drugs most commonly prescribed

to every lupus patient causes lupus nephritis.

Interstitial nephritis, this condition happens when you've had a bad reaction to a medicine that

limits your kidney's ability to filter toxins. Glimmeriolo nephritis. Well, what is that?

Glimmeri are the thousands of tiny filters that remove waste from your blood and your kidneys,

and this condition damages them, and your kidneys can't function as well. That is also a very

common prescription drug side effect. Apol-1, mediated kidney disease. Normally, apol-1 gene helps

make an immune system protein, but if you inherit a mutated version of the gene from your parents,

you may be more at risk for this type of kidney disease. And then there's long-lasting viral

illnesses. HIV and AIDS, hepatitis B, hepatitis C may cause kidney disease. And then all of you

have most likely had this at one point in your life. You just didn't know they called it this

pylonephritis. This is a urinary tract infection. So you've heard the term UTI, but in the medical

profession, they call it pylonephritis. Kidney disease causes for acute kidney conditions or

causes or diseases. If your kidneys suddenly stop working, doctors call it acute kidney injury or

acute renal failure. The main causes are they don't even list them. Drugs are number one prescription

drugs. Not enough blood flow to your kidneys, they say direct damage to the kidneys, my drugs.

You're in backed up in the kidneys. Alcohol would be no. Those things can happen when one,

you have a traumatic injury with blood loss, such as being in a car wreck.

Acute kidney injury can happen when you're dehydrated or your muscle tissue breaks down,

sending too much kidney toxic protein in your bloodstream, or at the bottom,

have complications during pregnancy, such as eclampsia or preeclampsia. However, we want to star

these three for you. You can have acute kidney injury if you go into shock because you have a

severe infection called sepsis. Number two, you have an enlarged prostate or kidney stones that

block your ear and flow can cause acute kidney disease. And the one I mentioned a second ago,

certain drugs or are around certain toxins that directly damage the kidney can cause acute kidney

injury. Now let's go to chronic kidney disease. Per the Cleveland Clinic, kidney disease means your

kidneys aren't working properly and are beginning to lose their function. Chronic kidney disease,

CKD, worsens over time, high blood pressure and diabetes are two common causes of chronic kidney

disease. Do you know what both high blood pressure and diabetes have in common? Lots of prescription

drugs. Therefore, you will see a lot of chronic kidney disease being diagnosed after those

conditions are diagnosed because when you're diagnosed with diabetes or high blood pressure,

you're immediately prescribed prescription drugs that cause acute and chronic kidney disease.

Now read, there's no cure for chronic kidney disease. Do you know why? You're taking drugs

most of the time that are creating it and you've been told to take them for life. Notice the two

conditions they're saying, proceed chronic kidney disease. High blood pressures, anybody ever told you

just take high blood pressure drugs for a few months and then you're done? No, they tell you you have

to take it for life. This is why you don't cure it. Diabetes, are you told you can cure diabetes?

No, you're told you need insulin, glucophage, metformin, it's an inherited disease. You have to

take these drugs for life, even though it's an epicomagovia or lifelong prescriptions for diabetes.

So there is no cure as long as you're injecting yourself and taking drugs that causes.

What are the symptoms of chronic kidney disease? Let's highlight some of these for you.

They need to pee more often. Tireness, weakness, low energy, loss of appetite, swelling of your

hands, feet and ankles, shortness of breath, foamy or bubbly pee, fluffy eyes, puffy eyes, swollen

eyes. Sorry, I couldn't read that far. It's a little far that monitor for me. Drying itchy skin,

trouble concentrating, trouble sleeping, numbness, nausea or vomiting, muscle cramps, high blood

pressure, darkening of your skin. And here's an infographic from Cleveland Clinic. I'm just showing

you some images of the most common symptoms of chronic disease, which I just read.

What are common symptoms of disease or chronic, sorry, what are common treatments for chronic

kidney disease? And you can see it on the list. High blood pressure, hypertension and diabetes

are the most common causes. Sorry, most common causes of chronic kidney disease.

We'll marry a little nephritis, polycystic kidney disease. We've read through some of these

lupus you see at the bottom, diabetes, nephrodic syndrome that's kidney failure, kidney infections,

obstruction by stones. What are the complications of chronic kidney disease? Well, here they are.

Anemia, brittle bones, gout, metabolic acidosis, heart disease and blood vessel diseases,

hyperchlamia, which is high potassium, high phosphorus, nerve damage, neuropathy,

high risk of infection due to a weak immune system, fluid build up near ankles and hands.

What are the medications for chronic kidney disease? And remember, if I go too fast to this

PowerPoint, you can download it for free at the resources tab. The whole thing, the whole thing's

there for you. Look up preventing kidney disease. Medications for kidney disease. Number one,

I highlighted angiotensin converting enzyme called ACE inhibitors. All right, so ACE inhibitors

of high blood pressure, but the most prescribed drugs for kidney disease.

Chronic kidney disease. Phosphate binders, a diuretic like lasex, hydrochlorothiocide,

medications to lower cholesterol levels, or ethropoetin to build red blood cells. If you're anemic,

vitamin D and calcittral to prevent bone loss. All right, so those are those drugs. Now,

ACE inhibitors, which was the first one we just highlighted for chronic kidney disease.

I can't wait to share this with you. ACE inhibitors, angiotensin. We read that to you just

I go. Here we go. The number one ACE inhibitors prescribed for kidney disease are captopryl,

analopryl, fosinopryl, lusinopryl, and ramopryl, then with pril. First one ever is the first one

on the list. Captopryl and all the other ones are just similar molecules to captopryl.

So exciting. I want to tell you where captopryl comes from. Number one prescribed drug for

kidney disease. Let's read it together. This is from neoscienceclub.com. How a Brazilian

viper's venom became the first ever ACE inhibitor. Oh my god, which one is that? Look at that. I

mean, anybody with high blood pressure in chronic kidney disease, don't you think you most likely

have chronic kidney disease because you're deficient in this snake's venom. Look at him. Any pretty?

Yeah, I think God intended all of you to have a little bit of this guy's venom inside of you to

lower your blood pressure. Okay, let's read it together. You've seen my clips in social media all

around the world about this topic. So I'm just going to show you the story of modern hypertension

treatment began, high blood pressure treatment began not in a pharmaceutical laboratory,

but in the Brazilian rainforest with a deadly pit viper. In the 1960s Brazilian drug maker,

Sergio Henrique Ferrarra was studying the venom of the Bothrop Storacus Viper, a snake whose bite

causes victims blood pressure to plummet catastrophically, meaning it kills you. Ferrarra identified

a peptide, a little piece of a protein from that snake's venom that he called Brady Kainan

Potentiating Factor, BPF, that enhanced the blood pressure lowering effects of Brady Kainan.

When he brought this venom extract to Nobel laureate John Vane's laboratory in London,

the team discovered that this Brady Kainan Potentiating Factor from the venom of this viper

selectively inhibited angiotensin converting enzyme, the key regulator of blood pressure.

Let's keep reading. The discovery launched a rational drug design program at what is now Bristol

Myersquib. After 60 components and 18 months of optimization, Captapril emerged as the first

orally active ACE inhibitor in 1977. Captapril's mechanism elegantly mirrors the viper's natural

strategy, oh, that ends with catastrophic death, approved by the FDA 1981 Captapril revolutionized

cardiovascular medicine. It became the cornerstone for hypertension, heart failure, and post-heart attack

care, spawning an entire drug class that now includes Lucinapril, Enalapril, and Ramapril.

How many of you knew you were swallowing dried snake venom in a pill to lower your blood pressure?

ACE inhibitors, they say, have prevented millions of strokes, heart attacks, and deaths worldwide.

Really, I'd like to know why since 1981, when the FDA approved a snake venom in a drug called

Captapril. Now, Lucinapril, Enalapril, and Ramapril, I'd like to know why these are the most

prescribed for ACE inhibitors for chronic kidney disease and high blood pressure. I'd like to know

why. Why is heart disease still the number one or two, number two killer world wide to this day?

22 million Americans, by the way, woke up this morning and swallowed this viper's venom,

called Lucinapril. And yet, heart disease is still the number one killer among Americans.

Amazing. Ask your doctor if snake venom from Brazil is right for you if you've been

prescribed an ACE inhibitor, because I keep talking about it. It perfectly mirrors the snake

venom of the viper that catastrophically kills people. There's much safer ways to prevent

chronic kidney disease than swallowing either synthetic or crude snake venom from a viper in Brazil.

I promise. And don't even get me started. If you swallow anything that looks like is from a viper's

venom, it is published in 1956 and 1961 to cause rapid forming cancer in any mammal who ingested

or put it on their skin. So, ask your doctor if an ACE inhibitor made to mimic and mirror snake

venom from a Brazil viper that causes cancer proven and given a Nobel Prize in medicine to the

guys who figured that out, Rita and Stanley Cohen in 1986, they figured out swallowing snake venom

will cause rapid forming tumors in any part of the body that they call cancer.

So, how many people do you know? We're put on an ACE inhibitor for chronic kidney disease or

high blood pressure and later we're diagnosed with cancer. And then we're told we don't know what

caused your cancer. It's probably genetic. Swallowing snake venom or anything it looks like it

causes cancer. They give the Nobel Prize in medicine for proving that in 1986. You're welcome.

All right, let's keep going. This is chronic kidney disease. I don't want to digress too much.

Medications for kidney disease. ARBs are another class of drug that include low

sartin. You see that highlighted? But omel sartin, vowel sartin, eprosartin, azale sartin,

herbosartin are all chronic kidney disease drugs. What do these medications actually do?

Well, here's the published side effects of vasotech known as anala pril.

See the generic name of their anala pril? This is capped a pril, listen to pril.

vasotech belongs to a class of medications called angiotensin, converting enzyme inhibitors,

ACE inhibitors, snake venom, viper from a Brazil. Anala pril works by decreasing certain chemicals

that lighten or sorry tighten the blood vessels. So blood flows more smoothly and the heart can

pump blood more efficiently. That's what it looks like. Snake venom in a pool. Black box warning for

FDA for the FDA for anala pril made from snake venom. Discontinue anala pril as soon as possible

when pregnancy is detected because it will kill the baby. Including injury and death to the

developing fetus can be caused by drugs that act directly on the renen angiotensin system.

Well, if it does it to a baby, what's it doing to you? Now, when we read the side effects from

drugs.com, a package insert for the drug, the FDA has a list of side effects that are called

titled frequency not reported. This is after the FDA approved the drug and now medical doctors

are prescribing the drug and the medical doctors are giving the drug to patients and then watching and

reporting back to the FDA what happens only after the drug was given. And these are side effects not

included in the presents noted in the trials on humans of the drug that the FDA reviewed and then

approved the drug. So when you see the words frequency not reported, just remember these are

medical doctors prescribing the drug after the FDA approved it. They don't have the statistical

numbers of how many people this happens to. They just know this only happened after prescribing

this drug. So here we go, vasotech side effects, an allopryl made from snake venom, viper venom.

The most frequently reported side effects include congestive heart failure. Wait, wait, wait, wait,

what an allopryl, the most frequently reported side effects include congestive heart failure.

I thought they were given to you this for high blood pressure to prevent congestive heart failure.

Did you know this is the most frequently reported side effect of snake venom in a pill form

and coronary artery disease? Come on, man. They'll blame that on high blood pressure.

All right, so let's dive into the actual heart side effects. Up to 10% of all people in the

clinical trials had a heart attack. It's called myocardial infarction. Look at it. I highly,

one in 10 will have a heart attack from an allopryl, from the viper's venom. You also see adema,

hypotension, chest pain, tachycardia, rhythm disturbances, hypotension, cardiac arrest after

the FDA approved it. Oh, sorry, man. I gave my patient an allopryl snake venom in a pill form.

You didn't tell me to snake venom, but as soon as I gave it to him, they had a heart attack

and the heart died. Stopped. What about the skin swallowing snake venom? One percent of you will

lose your hair called alopecia. One percent of you will develop angioidema. Now, you might not

think this is a big deal, but an allopryl in the centipril, 22 million Americans woke up this

morning and took it. What is 1% of 22 million? How many of them? It's a lot of people, 200,000 people.

I think that's the math. I did it right. All right. What about your stomach swallowing this snake

venom in a pill called an allopryl? You get very common 10% of moral developed nausea. One in 10

will develop abdominal pain. You will develop 1% of you peptic ulcers and stomatitis. You'll develop

anemia. One percent of all of you hemolytic anemia. You will develop the liver hepatic failure.

One percent of all of you just from the drug. Liver failure. Liver transplant, anybody? Is that

right for you? Hyper sensitivity. One in 10 will develop angio neurotic edema. Meaning your face

is going to swell. Your extremities are going to swell. Your lips are going to swell. Your tongue

is going to swell. Your larynx glottis is tongue. Look at the bottom here. Angioidema associated with

laryngeal edema may be fatal. Okay. One in 10 had this experience on an allopryl for high blood

pressure or chronic kidney disease. Snake venom in a pill causes parts of your body to swell and it

can be fatal per drugs.com. Hyperclemia, high, high dangerous levels of potassium. One in 10,

dizziness and one in 10% or more of all of you. Vertigo, anybody? Is vertigo better?

Taste, alteration, vertigo, cerebral vascular accident. Oh my god, you had a stroke because of

the drug. One percent of all peripheral neuropathy. Okay. Anybody want leg and arm pain?

All right. Let's keep going. Very common. 10% or more will develop asthenia. Well,

y'all should go look what that is. Chronic fatigue, can't move low energy. All right. After the FDA

approved it, we highlighted a big red box. We gave our patient with chronic kidney disease

anallopryl. That the MD did not know came from snake venom, mirror snake venom from a

viper in Brazil. We gave it to him and oh my god, they died after we gave him this drug. Anallopryl

after the FDA approved it. Well, if death isn't big enough, look far to the right. Herpes

oster. What is that? Anybody signed up for shingles with anallopryl? Did you know snake venom causes

blistering reactions called shingles? Did you know that snake venom when ingested can actually

cause person's penis skin to just fall off? That's an actual real thing, by the way.

Look at the next thing. So if death isn't bad enough, shingles isn't bad enough. You will develop

a positive A and A anti-nucleic antibody. Do y'all know what that is? Every autoimmune disease,

the medical doctors are looking in your blood for a positive A and A result.

Did you know snake venom in a pill called anallopryl is known to cause elevated A and A to show up

and now you're going to be diagnosed with an autoimmune disease of lupus, fibromyalgia,

showgrens, rheumatoid arthritis because you have positive A and A. And did you know that an

allopryl by itself when you swallow it has been reported by MDs prescribing it to their patients

never had a positive A and A before. Now have a positive A and A because of the snake venom

they're swallowing. Ask your doctor if lupus, fibromyalgia, or shingles, or death are right for you.

How about your eyes? Blurry of vision anybody and 10% or more of all of you? How about pink eye?

That's also a common side effect. Did you know one in 10 people on anallopryl will be diagnosed

depressed? Did you know one in 10 will develop bronchitis, dyspnea, pneumonia,

from the snake venom-laced anallopryl? Upper respiratory infections, anybody? Anybody want one

of those? Anallopryl has been published and reported to the FDA by medical doctors prescribing it

to be caused by anallopryl for chronic kidney disease and heart disease.

Urinary tract infections are common in one in 10 people. Now remember this is for chronic kidney

disease, anallopryl. ACE inhibitors are prescribed for chronic kidney disease. One of those is

polyneofritus, which is urinary tract infections. Did you know one in 10 people in the clinical trials

before the FDA approved this drug anallopryl for chronic kidney disease causes one in 10 people

confirmed in clinical trials to develop urinary tract infections from the drug?

Now let's look at Lysinopryl. Brand name, Prynnaville. Let's look at Lysinopryl. It's also a class

of ACE inhibitors. It works by decreasing certain chemicals that tighten the blood vessels,

just like anallopryl. Remember the same drug? And here we go. We're going to highlight those again.

I did not delete it. Sorry, you can read it again about ACE inhibitors.

Now let's look at the side effects of Prynnaville. What is Prynnaville?

Discontinue FDA black box warning for the Center for Lysinopryl everybody.

Discontinue as soon as possible when pregnancy is detected as drugs that act directly on the

reenin angiotensin system can cause injury and death to the developing fetus.

Well, if it kills the baby inside of you, what is it doing to you? I would like to ask.

Now let's look at cardiovascular side effects and human trials with Lysinopryl.

10% or more of all people, 11% of them developed hypotension. Let lethal low blood pressure.

10% 1 in 10 develop orthostatic hypotension, standing and getting dizzy and wanting to fall

in palpitations, which are typically arrhythmias of the heart. Did you know 1% of all people

on Lysinopryl in the trials had a heart attack or a stroke? Remember, I told you 22 million people

swallled at this morning. What's 1% that 10% would be 2 million? 2.2 million. So 1% should be

220,000 people will have heart attacks and strokes from Lysinopryl. That should keep funding for

the American Heart Association going. Just the side effect of the drugs they're telling you to take.

All right, 10% of you will develop headaches and syncopate. Change in your breathing.

Shallow breathing. Cratinine increased. That is a sign of chronic and acute kidney disease,

by the way. 10% of you will develop that just from Lysinopryl. So when your doctor say,

we're giving you Lysinopryl for chronic kidney disease, but we're taking your blood work every

three months and we're seeing your creatinine level go up. We don't know why you're continuing to

have worse than chronic kidney disease. Can you please tell your damn nephrologist or your cardiologist?

Did you know it's a side effect of Lysinopryl? 1 in 10 people develop increased creatinine levels.

Might be important for them to know. You don't want to get off that damn drug. Metabolic 10%

of you will develop deadly high levels of potassium after the FDA approved Lysinopryl. Medical

doctors reported our patients never had gout before we gave them Lysinopryl. Now they have gout.

Hypoglycemia in our diabetic patients receiving ACE inhibitors.

10% of you will develop diarrhea, nausea, and vomiting from Lysinopryl. This medicine everybody

read along from Drugs.com. This medicine, Lysinopryl, can cause serious types of allergic reactions,

including anaphylaxis. Anaphylaxis can be life threatening and requires immediate medical

tiction. Just no severe allergies from Lysinopryl. I guess the body wasn't designed to like

or benefit from snake venom. Very good. All right generic name, Low Sarton. A lot of you know

what Low Sarton is. His brand name is Kosar. What is Kosar? That's what it looks like.

Same warning. When pregnancy is detected, discontinue Low Sarton as soon as possible. Drugs that

act directly on the ACE inhibitor system can cause injury or death to developing fetus.

Remember these are chronic kidney disease drugs. The most common adverse reactions were upper

respiratory infections and dizziness. For the respiratory tract, one in 10 on Low Sarton will

develop upper respiratory infections from Low Sarton. Did you know that? Did you know after the

FDA approved it, bronchitis, pharyngeal discomfort, throat discomfort and pain have been reported

by your medical doctors prescribing it. In clinical trials, one in 10 develop abdominal pain.

After the FDA approved it, dental pain, mouth pain, dry mouth, flatulence, gastritis,

constipation, all side effects of Low Sarton. One in 10 develop muscle cramps, back pain, leg pain

and myalgia. How many of you senior citizens have been diagnosed with heart disease, chronic

kidney disease, put on Low Sarton and now you have relentless restless leg syndrome,

involuntary muscle cramping. You're now in re-quip and other drugs for that and those are side

effects of Low Sarton you were never told about. Myalgia is all over body pain. Fibromyalgia,

myalgia is short for fibromyalgia. If you want all over body pain, one in 10 of you will have that

from Low Sarton and you see it highlighted down there. FDA, after the FDA approved it,

medical doctors prescribing Low Sarton are like, oh my god, my patients now have arthritis. They

didn't have that before. Some of them are now diagnosed with fibromyalgia because of Low Sarton

and muscle weakness. One in 10 of you on Low Sarton will develop kidney impairment or renal failure.

Do you guys remember what the title of this presentation was? This is chronic kidney disease drugs.

The number one drugs prescribed to all of you with chronic kidney disease. Did you know one in 10

before the FDA approved this drug? They were told one in 10 in the clinical trials developed

kidney failure from our drug or kidney impairment.

Can you imagine any other industry in the world selling any food product to Americans could get

away with telling the FDA that our candy bar, our coffee drink, our energy drink causes one in

10 to have kidney failure. Will you still let us put it on the shelf and sell it? Only big pharma

runs America. Never a system. One in 10 will develop dizziness. Headache and vertigo. So let's go

back to the renal one. Everybody listening to the sound of my voice. If you've been diagnosed with

chronic kidney disease, acute kidney disease, and you've been prescribed Low Sarton, please for the

love of God, ask your medical doctor if they believe worsening kidney disease is right for them

or right for you. Sorry. It is if you want to sell more drugs to you.

All right, one in 10 will develop dizziness. Headache and vertigo. One percent of you will develop

a cerebral vascular events and act she is 0.1%. That's a percentage of you will develop strokes

from Low Sarton. And then after it was prescribed ataxia, that is a symptom of Parkinson's,

memory impairment. That's Alzheimer's, migraines, peripheral neuropathy. All of these are known

side effects caused by Low Sarton. Also tinnitus, which is ear ringing, tremors, taste perversion,

sounds like COVID. Maybe everybody got Low Sarton poisoning, develop COVID symptoms.

One in 10 with Low Sarton will develop edema swelling, chest pain and fatigue, and facial edema

and fever. This so you know, in case you're wondering, 10% of you will develop high lethal levels

of potassium and low levels of blood sugar. This is a chronic kidney disease drug Low Sarton

to lower blood pressure. One in 10 of you will develop orthostatic hypotension. You'll stand up,

roll over, get real dizzy and feel like you're going to pass out. Heart palpitations are caused

by Low Sarton and 1% of everybody. Second degree atrial ventricular block. You want cardiovascular

failure, myocardial infarction, heart attacks, caused by Low Sarton, reported by MDs after the FDA

approved the drug. Did you know that it was reported after FDA approved Low Sarton,

anxiety disorders, confusion, depression, dream abnormality, and panic disorders are caused by

Low Sarton, reported by your MDs to the FDA after prescribing it. One in 10 will develop edema.

One in, sorry, after the FDA approved it, urinary tract infections are reported by MDs when they

prescribe Low Sarton. That is a chronic kidney problem. Conjectivitis, blurred vision, burning

stinging in the eyes. Who doesn't want that? Who don't want their eyes burning and stinging?

That is a published side effect reported to the FDA after MDs prescribed Low Sarton.

After FDA approved it, flu-like symptoms have also been reported by MDs. Now let's dive into

the most, this is from frontiers and pharmacology. Those are the most common ACE inhibitor drugs

for chronic kidney disease that are actually prescribed to millions of Americans. Now we're going

to dive into this study here, which highlights the 30, this is from 2024, the 30 most commonly

reported drugs in the United States, that the FDA has approved that cause kidney stones,

which is just one kidney disease issue. These are 30 most commonly reported drugs. You are

prescribed at home that are known to cause kidney stones to form in the kidneys.

So look at the screen. Notice the first one is Humera. Wait, the drug for autoimmune diseases

of psoriasis and joint pain. Humera causes kidney stones. Did you know that? Ask your doctor if

kidney stones are right for you when you hate the plaque psoriasis on your skin. Embrale,

rheumacade. I don't know all of these and I'm not going to read them all. Let's see,

Xyram. Don't know that one. Avinex. Wait about. What about prevesid? Did you know prevesid

for gourd acid reflux? You know, prevesid is the ninth ranked drug. They know that causes kidney

stones to be formed in your kidneys. Stilera. See it at the bottom. Monoclonal antibody,

Vidal azumab. We're going to keep going. This is just the first 15. Sorry, let's go back to the

next 15 of the 30. Let's skip right over it. Next, see them. Oh my god. Causes kidney stones. Did

you all know that? Renvoque causes kidney stones. Ellaquist for atrial fibrillation causes kidney

stones. That will worsen a fib and high blood pressure. By the way, Ellaquist was the third

revenue and drug in the whole world last year. It causes kidney stones, worsening heart disease.

How about that? Cipro, the very common antibiotic, causes kidney stones. Truvada, a GOP-1 drug.

Or actually, Truvada, I think, is a diabetes drug. Abageo. Trulicity is a GOP-1 drug. There you go.

He's the monster venom anybody. Look at the list. See if any of you like those.

Glivek, atripla, atripla, nipara, nipara, ziwav. I don't even know those drugs.

Anyway, there's your list. If you want to know if you're on any of those causing kidney stones.

Oh, but I want to do want to go to the very top. You will see sando-statin drugs are cholesterol

drugs. Well, there's one that causes kidney stones. All right. Now from medindia.net, medications

and their potential to cause increased urinary tract, fungal infections. So look at this

list. If you suffer with chronic UTIs, which are kidney disease supposedly, let's look and see if

you know any of these drugs. Now, arrows are pointing to the generic name. To the right is the drug

name that is really the brand name. So I do not know all these drugs, but some of you are on these

drugs and complaint of urinary tract infections. So I want to make sure you see the list.

Because if I am unfamiliar with them, it doesn't mean you're not familiar with them. So here we go.

All right. So I do not know how to pronounce all these.

Aburatorone acetate, drug names, Zatiga, and Yanza, causes UTIs.

Assemble prosat, which is Aotol and Camprol, causes UTIs.

Adolomumab, which is a monoclonal antibody called Humera, causes both kidney stones you've learned,

and urinary tract infections.

A fattenab, which I can't even read it on any there. You'll see the brain names there.

Albuterol. Albuterol inhalers for asthma cause urinary tract infections. Yeah. Look at some of

the drug names, pro-air atrovant. These are albuterol inhalers for asthma, children and adults.

Did you know it causes urinary tract infections, which is a chronic kidney disease?

There's Humera again. Nessina is the brand name of Metformin, which is a very common prescribed drug

for diabetes. Did you know Metformin causes urinary tract infections? Man, how many people are on that

one? Alpelacib, I can't read the drug name there, but you can. And Lodapine, drug name Tribenzor,

causes urinary tract infections, and Akinra, Kinaret, causes urinary tract infections. Anastrasol,

Arrimidex, is its actual brand name and millions of you are on this. Anastrasol.

Ask your doctor if urinary tract infections are right for you. A tour of a statin,

drug name, Lipitor. What? Clestrol drugs cause urinary tract infections and are known carcinogens.

Yeah. And cause kidney stones. Yep. Ask your doctor when they prescribe cholesterol drugs if

kidney disease is right for you. Illuminate, alumiant. This is all over the mainstream media right now

and social media. Bericitinib is its generic name, causes urinary tract infections,

invocana, causes urinary tract infections. This generic name is Senagle-Foxin. Looks like

Candestorod, Selexatil, Hydrochlorothyazide. Oh, my God. How many of you are on this

diuretic drug to lower your blood pressure? Did you know it causes urinary tract infections?

Now you do. Hydrochlorothyazide. Look at your drugs. If it says HCTZ, that's hydrochlorothyazide.

If you have high blood pressure and you're put on a diuretic, look to see if you have HCTZ,

which is actually patented salt, by the way, when they tell you salt is bad for you, you're buying

salt. Anyway, that drug causes urinary tract infections. Cablivi, generic name,

capital to Zumaab, causes urinary tract infections. Carbidopa and Levidopa, Parkinson's,

anybody. These are the number one drugs for Parkinson's. How many people do you know have Parkinson's?

Are on these two drugs, Levidopa, Carbidopa, and actually complain of urinary tract infections.

Oh, no, no, no, no, no, no. It's the drug. Everybody, they know it.

So last is all, Cezasse-Sapride, pro-pule side is the name of the drug. Anybody on that?

It causes urinary tract infections. Clomepermine, known as anaphyronyl, causes urinary tract infections.

Clopidogrel, known as pleavix. Pleavix, anybody? Do I know what pleavix is for?

Millions of people are taking pleavix every day. Do you know what causes urinary tract

infections? And it's known to do that. So, Novapitan, I'm really sorry, I can't read the very top

one's brand name because of the software I'm using. Okay, we'll keep going. Deslore Totten,

which is Clarenix. Did you know Clarenix for allergies, causes urinary tract infections?

Now, you do austeto, causes urinary tract infections.

Eltro-mopag, promacta, rovalonade, and alveyes, alveyes, causes urinary tract infections.

Both set tech and epinid, known as analapril. Now, you know, not only is from snake venom,

but it also causes urinary tract infections. Analapril. Analapril and hydrochlorothyside,

drug name is Vassaratech. Millions of you are on this one for high blood pressure and chronic

kidney disease, causes urinary tract infections. And then, epoetin metamethoxy polyethylene

glycol, known as mercara, causes urinary tract infections. Mirabogran, known as Mirabatric,

causes urinary tract infections. Rimoronavanzas, the brand name of Merchrezep,

Merchazepine, causes urinary tract infections. Mytoxentrone, causes urinary tract infections,

brand name, novant, novantrone. And then, natal tools of my ab, causes urinary tract infections.

Lowestran and aerovella, causes urinary tract infections,

pays, patinol, patide, which is the brand names of Ola patideen, causes urinary tract infections.

Omeprosol, known as Prylasek and Prylasek OTC for heartburn, causes urinary tract infection.

And there's another one. Omeprosol, another one. Those of butinine hydrochloride, known as

Dytropan, causes urinary tract infections. Panto-Pryzol, known as Protonix,

your gird, anybody asked to reflux anybody. Protonix causes urinary tract infections.

Zimplar, which is the brand name of Pera-Cousatol, causes urinary tract infections.

The generic drug pegactinab causes urinary tract infections.

Co-Migolas XR is the brand name of Saxa, Galiptin, and Metformin together,

causes urinary tract infections. And then Sedgesterro and Acetate, known as Anovera,

causes urinary tract infections. Subutramine. Those are brand names there. They cause urinary tract infections.

Sedinaphyl. Oh my god, Viagra. That's the brand name. Viagra for the generic name Sedinaphyl.

Causes urinary tract infections. Well, your penis might get hard, but it's going to burn when

you pee. Ask your doctor if burning penises are right for you. Sympastatin. Zocore.

Flow-lippid and Symbador. Oh my god, these are cholesterol drugs. Cause urinary tract infections.

Citralamus, brand name HIFTOR, causes urinary tract infections. Tasmar. Tocapone is the generic name.

Causes urinary tract infections. Tolectin. Causes urinary tract infections.

This is Topiramate. Causes urinary tract infections. Trastuzemab, a monoclonal antibody,

known as Herceptin. Causes urinary tract infections. Taxoprost. Causes urinary tract infections.

Triptylaryllin, known as Trelstar and Triptador. Causes urinary tract infections.

If anybody you know is on any of those drugs and they're complaining of urinary tract infections,

which is a chronic kidney disease, tell your doctor to get off the damn drug.

Now let's dive into our natural solutions. This is very exciting for me. Cannot wait to dive

through this. All right. With all of you, there's not very many. There's only four recommendations here.

It's amazing. We're going to talk about vitamin D. We're going to talk about black cumin seed oil.

We're going to talk about selenium. Just watch. It's amazing. For all of you out there going,

how do I clear up stones? How do I dissolve stones naturally without drugs? How do I improve blood

pressure without these drugs? How do I improve my kidney function without these drugs?

Prevent urinary tract infections. I'm going to show you. This is sort of 2023 in vitro anti-bacterial

activities of selected medicinal plants, not drugs, used by traditional healers for treating

urinary tract infection in Ethiopia. Based on the findings on the current study, the second most

active plant extract in blocking the growth of tested bacteria were the extracts of Nagellicitiva.

Which is known as black cumin seed oil, which is the second ingredient in our bio-defense product.

The result of the present investigation revealed the strong anti-bacterial activity of Nagellicitiva

seeds, ethanol extracts against all studied bacteria at all concentrations. Do you remember I

showed you that CIPRO, a very common antibiotic, causes kidney stones? Nagellicitiva does it. In fact,

I'm going to show you it also does the opposite with stones. It's amazing. Ethanol extract of Nagellicitiva,

which is inside our bio-defense. It's effectiveness against staff-orius,

E. coli bacteria, and canymonia, with 18 millimeter of inhibition zone. That's what they found in the lab.

The ethanol extract of Nagellicitiva oil against staff-orius and E. coli concentrations of 25,

50, and 100 milligrams per millimeter, and against pneumonia, and ergonica was pseudomonas ergonica,

was 14 millimeters and 11 millimeters respectively at concentrations of 50 milligrams per millimeter.

These different concentrations of Nagellicitiva were effective,

no matter what the dose, clearing these bacteria. It was also observed that the extract of Nagellicitiva,

black cumin seed oil, exhibited higher anti-bacterial activity towards all strains of study

bacteria than the ethanol extract combined. So the methanol version was even better than the ethanol

version. The anti-bacterial activity of the methanol extract of this plant was most effective against

tested bacteria. This study demonstrated the anti-bacterial activity of both the methanol and

ethanol extract of Punica Grenadium, which is a different plant. Nagellicitiva, which is in our

bio-defense, black cumin seed oil, and ethanopskeboracol against E. coli, P. aruginosa,

aruginosa, staff-orius, Klebsialinomonia, and P. merabilis bacteria of Euro, Euro-meaning kidney,

kidney pathogenic bacteria. The results showed that all three tested plant extracts

inhibited the in vitro in the lab growth of at least one or more of these tested organisms.

These tested traditional plants can be the best candidate for further studies in the development

of a new anti-microbial agent against Euro, Euro-genitor, kidney bladder, urinary stress,

pathogenic bacteria that cause urinary tract infection. That's black cumin seed oil in our

bio-defense. Now, watch what black cumin seed oil does to kidney stones. This is from GSC

Biological and Pharmaceutical Sciences. You're not going to get this anywhere else. Only the doctor

already showed is going to show you this. Kidney stone risk reduction and size reduction

utilizing medical plants. Section 2.1, Nagellicitiva, known as black cumin seed oil, the second

ingredient in our bio-defense product. Watch this. This is infricken credible. Nagellicitiva was

tested on 80 people with four to 10 millimeter kidney stones. Four perspective. I had a

son named Bryce who had a nine millimeter stone. The medical doctors told me,

Dr. Artist, 99% chance that stone will not clear on its own. And I said, oh, I'll take that one

percent all day long. So we brought him home. We didn't do the surgery or the drugs they recommended.

And within two weeks, the stone passed. I'm going to show you one of the things we used to do

them. So these participants, 80 of them, had kidney stones of varying sizes. Four to 10 millimeters

in a randomized clinical trial. One gram every 12 hours for two weeks of Nagellicitiva was a

compared to the prescription drug called flowmax for kidney stones. Stone size decreased from 10

millimeters to five millimeters with either Nagellicitiva oil or the drug called flowmax.

Well, wait. Well, why do we even recommend flowmax if you can get the same thing done with Nagellicitiva oil?

Well, watch this. Look at the next statement. I'm showing you the flowmax label above.

Nagellicitiva oil reduced pain and increased kidney stone passage more than flowmax did.

Oh, what? What? Nagellicitiva oil called black cumin seed oil inside of our bio defense.

The second ingredient in there was more effective at reducing kidney stone pain and increasing

the ability of the person to pass the stone than flowmax, which makes billions of dollars and

is FDA approved. Imagine that Nagellicitiva oil a plant is not FDA approved. Aren't you glad you

watched the doctor or show clinical studies have shown beneficial effects of Nagellicitiva in the

prevention and treatment of kidney stones 60 patients with kidney stones were randomly enrolled in

two arms of a randomized triple-blind placebo controlled trial. The patients were treated with

Nagellicitiva oil capsules 500 milligrams or a placebo for two times a day for 10 weeks. Nagellicitiva

seed group watch these numbers 44% of all the patients peed out their kidney stones completely.

That's 45% and the size of the stones remained unchanged only in 3% of the people and decreased in

size and 51.8% of all the patients in contrast to the placebo group who did not get Nagellicitiva

only 15% of those patients peed out their stones compared to 45% when Nagellicitiva oil only 15%

peed out their stones in 10 weeks 11% had a reduction in their stone size. Nagellicitiva had 51%

of them decreased their kidney size and 15 sorry 15% had increased in their stone size in the

group that didn't get Nagellicitiva and 57% had no change in their stone size compared to only

3% in the Nagellicitiva group. So nephrologist kidney doctors those with kidney stones

ask your doctor of black cumin seed oil is right for you called Nagellicitiva. Ask him if bio-defense

is right for you because it is the difference in the average size of kidney stones after the study

was significant between the two groups. Nagellicitiva oil as compared to the placebo had demonstrated

to have significant positive effects on the disappearance or the reduction of the size of kidney

stones compared to the placebo. Less formation of calcium stones was found with the use of Nagellicitiva oil

and two animal models. In animal studies the use of Nagellicitiva seeds significantly protected

test animals against experimentally induced kidney stones. They have drugs that can

inject into animals and cause them to form kidney stones. Nagellicitiva significantly decreased

the number of kidney stones accumulating and calcium deposit in the rats.

So even when they had drugs that could cause an animal to create kidney stones and Nagellicitiva

prevented it. Nagellicitiva shows antioxidant anti-inflammatory, anti-apoptobic and apoptotic

and immune regulating properties. Nagellicitiva oil showed limited or no toxicity, meaning no

side effects. In conclusion, the plants with the best clinical trials and supporting pre-clinical

data showing effectiveness in reducing kidney stone size and reoccurrence are Nagellicitiva oil

number one black cumin seed oil. The second is horse gram, the third is veruna bark and then

tribulus is the fourth. Well, why would you go to second, third and fourth? Why don't you just go

to number one black cumin seed oil. Now vitamin D deficiency as a risk factor for urinary tract

infections in women at reproductive ages urinary tract infection is a severe health disease with

high complication because it is related to antibiotic resistance and it's threatening to the health

throughout your lifetime. According to the World Health Organization, urinary diseases caused death

of almost 85,000 people in the world every year. In this infection, urinary tract infection,

most parts of the urinary system including the urethra that you pee from, kidneys bladder and

ureters which the ureters are the little tubes that connect your kidneys to your bladder are affected

the urethra you pee from and bladder parts of the lower part of the urinary tract are the

evolved the most in these infections. Bladder lining cells secrete and express a human

antimicrobial peptide called cathol seedin which protects the lower urinary tract your urethra

and bladder. Your cells make it in the bladder. Vitamin D induces cathol seedin to be secreted by

the urinary bladder skin cells as it provides protection against both gram negative and positive

bacteria. This study's main purpose was to determine the relationship between blood levels of

vitamin D and UTIs and women of reproductive age. Out of 75 urine specimens collected from

patients complaining of signs and symptoms of UTIs, 52 samples, 69% were positive for bacterial

infections. That's 70%. From positive cultures, different bacterial types were isolated and most

of them were E. coli. You all remember why I made biodefense? It was to specifically clear E. coli

from your body. Out of the research study, you see these are the microorganisms and their percentage.

The blue is E. coli. It's the largest amounts from all the samples of urinary tract infection,

your analysis. But then you'll see the other ones. The orange one is staphylococcus,

staph. That's the second highest. Just for an example. In section 3.3 of this study, we tried

to examine if there was any correlation between the deficiency of vitamin D and the severity of

the urinary tract infection in the patient group. What they found, there were significantly higher

number of bacteria present in the patient's urine who had low vitamin D levels. The highest number

of bacteria that was found is in the urine sample of the vitamin D deficient patients. The ones with

the most bacteria creating UTI symptoms was in those with the lowest amount of vitamin D.

According to our culture results of the urine, there is a clear correlation between the severity

of the deficiency of vitamin D and a positive culture for bacteria and microbes.

The more deficient the patient is in vitamin D levels, the more currents of bacterial UTIs

and mixed bacterial and positive cultures indicating vitamin D as a risk factor for UTIs.

Well, how many nephrologists UTI specialists are talking about vitamin D with you?

And if they're not shame on them, they are an act in their jobs. They are not up to date on research.

They're definitely not watching the doctor show. In conclusion, our research on women of

reproductive age with low vitamin D levels reveals that they are more at risk of contracting UTIs

than the healthy ones. This is not just for those that are able to have birth. We're talking to

people postmanopausal, those who have had their uterus removed. It doesn't matter. If you have

UTIs, you typically have low vitamin D levels. This shows a significant association of vitamin D

deficiency in urinary tract infections, especially in moderate and severe infections, which is an

important aspect of infection control, concluding that to treat women of reproductive age with the

urinary tract infections, whether acute or reoccurring, it is better to search for vitamin D deficiency

and treat it simultaneously. That's medical research. That's medical science. And if you're

MDs, if you're urinary specialists, if you're nephrologists are not checking your vitamin D levels,

when they check through your analysis for bacterial infections leading to a UTI diagnosis, shame on them.

Per the International Journal of Nanomedicine in 2016,

and hit inhibition of E. coli and staph aureus with selenium nanoparticles,

synthesized by pulse laser emulation and deionized water. Well, let's read this. Remember,

E. coli is the number one bacteria causing UTIs, staph aureus, number two.

Various concentrations of selenium nanoparticles were subjected into E. coli and staph aureus bacteria,

the two most common UTI infecting blamed infections. And they were incubated for either four,

eight or 24 hours, these two bacteria. The most concentrated selenium sample, 50 parts per milliliter,

exhibited the highest blocking of growth rate with a 46% and 63% of E. coli and staph aureus,

respectively, within 24 hours. Selenium by itself reduced the growth rate of E. coli by 46%

and staph aureus by 63% in just 24 hours. Selenium by itself. A possible mechanism toward

inhibiting E. coli bacteria is that selenium nanoparticles attached by chemosorption and

penetrate the outer membrane that contains lipolysaccharides. They're explaining to you how this

most likely works with E. coli. If you want to know how it works for E. coli, continued the

scientific nerdy stuff, biosynthetic pathway of lipoproteins, fat proteins in the E. coli bacteria

involves three enzymes, including these three. Preprolyproprotein diacyl glyceryl transferase is one,

prolypoprotein signal peptidase and apololiproprotein in acetyl transferase, which have been shown to

play an essential role in the survival of E. coli. Therefore, selenium nanoparticles inhibit E. coli

by modifying the role of those three enzyme conveyors. In gram-positive bacteria, such as

staph aureus, the cell wall structure is different. It has a thicker peptidoglycan membrane, peptide,

sugar membrane, without any outer lipofat polysaccharide membrane. Consequently, selenium penetrates

much more easily into staph aureus bacteria by chemosorption. That's how it works. The total inhibition

of E. coli and staph aureus is expected to occur at 179 parts per milliliter respectively.

It's confirmed that selenium nanoparticles can inhibit both gram-negative and gram-positive

bacteria with a higher efficacy against gram-positive bacteria. The minimal concentration required

is about 50 percent bacterial inhibition after 24 hours with E. coli and staph aureus at a minimum

of 50 parts per milliliter. So now you've seen vitamin D, you've seen black cumin seed oil,

now you've seen selenium, now you're about to get in acetyl cysteine. There's a bladder condition

called cystitis. In acetyl cysteine prevents bladder tissue fibrosis, which is what they blame

cystitis on. In a lipopolysaccharide-induced cystitis rat model, in the present study we developed

a cystitis rat model with chronic inflammation and prominent fibrosis cystitis by increasing the

frequency of inter-investigial LPS installation. So they're injecting something that's causing it.

The LPS induced cystitis rat model exhibited urotheol denodation, mass cell infiltration,

and fibrosis histologically and bladder dysfunction, which were similar to interstitial cystitis,

a bladder condition. Injection of NAC, in acetyl cysteine-improved inflammation,

fibrosis, and voided parameters in the LPS induced cystitis rats. You're welcome. LPS injury

promoted the deposition of fiberotic, extracellular matrix proteins, a nuclear accumulation of

piece-mad 2 protein, indicating the activation of TGFB signaling. That's not really that important

for you to all understand. Importantly, these fibrootic responses in the bladders of LPS group rats

were significantly improved by enacetyl cysteine treatment. Anybody with cystitis out there?

Ask your doctor if enacetyl cysteine's right for you. Treatment modalities for bladder

fibrosis, regardless of severity, are limited. But NAC is proven to have therapeutic effects by

reducing inflammation and reversing fibrosis, could be a possible breakthrough.

The first statement is treatment modalities for bladder fibrosis, regardless of severity,

are limited. Let me just tell you what that really is saying. Current prescription drugs,

approved for cystitis and bladder problems in bladder fibrosis, have not provided benefit.

It's very limited. And NAC, though, is proven to have therapeutic value. Reversing fibrosis.

Could be a possible breakthrough. How about that? Investigating the effects of enacetyl cysteine

and selenium on reflux nephropathy. Now, some of you are blamed on your UTIs. Your chronic kidney

problem is the bladder infection is moving up, back up into the kidneys. They call that reflux.

Vesicchio red-roll reflux. They're investigating enacetyl cysteine and selenium

on this condition called reflux. Vesicchio uratorol reflux is defined as reflux of urine from the

bladder back up into the upper urinary tract, which is your kidneys and urators. VUR alone does

not cause urinary tract infection. However, it does lead to the development of infections in the

case of bacteria. If there's bacteria, they're E. coli in the urine. It will do it, which we just

told you was the number one cause of all UTIs. VUR is observed in approximately 40 to 50%

of cultures proven to have a UTI. What? 50% of all UTIs have this VUR or bacteria re-infection.

All right, everybody listen. Enacetyl cysteine is a synthetic derivative of the endogenous

amino acid L cysteine and a precursor of sulfhydrol containing tripeptide glutathione, GSH,

which serves as one of the self-defense mechanisms of cells against oxidative stress.

Enac has been used for the treatment of numerous diseases characterized by oxidative stress.

Selenium is a trace element, which is a component of the glutathione peroxidase system. Selenium is

also an antioxidant and plays an essential role in the activity of several enzymes and proteins

involved in regulating the immune response and cell antioxidant defense. Well, if you want to

reduce inflammation from VUR, reflux, UTIs, Nynacetyl cysteine and Selenium is proven to reduce

the inflammation from both of those. Now, let's look solely at Selenium. For those of you with

kidney transplants, did you know that Selenium has been proven to prevent the damage to the

transplanted kidney caused by your own immune system? Dietary Selenium increases cellular

glutathione peroxidase activity and reduces the enhanced susceptibility to lipid peroxidation

of plasma and low-density lipoprotein and kidney transplant recipients. When you supplement Selenium,

your liver produces more glutathione, which is the most powerful antioxidant to reduce stress on

the body any cause of inflammation for any reason ever. The glutathione system plays a major role

in the protection of cells against oxidative stress in humans. The aim of the present study was

to find out the relationship between glutathione system and plasma lipid peroxidation in six

kidney transplant recipients. By using dietary Selenium to activate the glutathione system,

we thus analyze the effect of the Selenium 0.2 milligrams per day, which is exactly what is

inside of our individual capsules for Selenium for a period of three months. So one capsule of

our Selenium for three months, followed by an additional three months on a placebo. On plasma

and on LDL, bad cholesterol lipid peroxidation. Selenium treatment resulted in a 50% reduction

in AAPH-induced plasma lipid peroxidation in the kidney transplant recipients.

Analysis of the patient's red blood cell count, glutathione system revealed low levels of

reduced glutathione and decreased activities of red blood cell glutathione peroxidase and glutathione

reductase by 23%, 18% and 20% respectively in comparison to normal red blood cells. Selenium

treatment resulted in significant elevation of red blood cell glutathione peroxidase and glutathione

reductase activities and in reduced glutathione content by 64, 57 and 11% respectively.

This effect was also paralleled by a 39% reduction in the red blood cell oxidized,

the damaged glutathione content. We thus conclude these medical researchers say that dietary

Selenium, which activates the glutathione system, is a potent antioxidant against plasma and LDL

bad cholesterol lipid peroxidation in kidney transplant recipients. If you know anybody on dialysis,

know anybody with a kidney transplant, ask your doctor Selenium and acetylcystine vitamin D

and black cumin seed oil will write for you. Here's our bio-defense with our Nagellosativa oil

highlighted, black cumin seed oil. It is the primary ingredient there and that's why it's in there.

Defense against E. coli, staff-orias. It also helps dissolve kidney stones, you just learned.

Here's our vitamin D3 supplement. Suspended in organic MCT oil. Here's our enacetylcystine

at 750 milligrams a dose. Here's our Selenium at 200 micrograms, which is that 0.2 milligrams you

just saw in the research study. And here is our hydrate complete. Every one of the 40 essential

nutrients are crucial for adequate kidney health. I drink two of these every day. I'm

drinking one right now while I'm recording this show and every day I believe all of you.

Anybody dealing with chronic kidney disease, cardiovascular disease, I don't care what it is.

If you go to the hospital, they're going to inject you with salt and chloride, which are just two

of the 11 minerals required for adequate hydration. Here's all of our ingredients, all the 40 of them.

No other product comes close. Scan our QR code. If you like this presentation,

want to learn more or stay up to date on what we're doing. And this is our new book. Moving beyond

the COVID-19 lies. It is now printable in Spanish, audible in Spanish, published in French,

an audible French version is coming. There's an audible English version by me. There's a digital

format where you can hyperlink live all the links, images inside the book from research studies.

That is now, by the way, if you look at Amazon right now, our book is now number one in the

pulmonary medicine section category of Amazon. It's been pretty humbling to watch that our book,

Moving Beyond COVID-19 lies has been an Amazon bestseller for the last year and a half,

since it was released in August of 2024. If you haven't got the book, you need the book.

And buy a separate copy and give it to your favorite doctor on earth. I'm Dr. Artis. God bless you.

We'll see you next time. This is How to Protect and Prevent Kidney Diseases. May this bless your

life as I expect it will. God bless you. We'll see you next time on the Dr. Artis Show.

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