Stem Cells: Medical Miracle Or Science Gone Too Far? (Medical Documentary) | Real Stories

they used the

stem

cells

of an unborn fetus that the mother is going to abort anyway as an abortion instead of discarding that fetus, they harvest the

stem

cell. We see one of the most divisive issues in America: abortion and the burning of the planet Sofia, the deadly shooting. at the Planned Parenthood clinics it bothers me because the anti-abortion people their child was safe the child had an illness if they were any type of parent maybe not everyone would be in line to be the first here and there is no doubt about it and I will I go head to head with anyone, but they choose to donate their organs to give life.

I think collecting stem

cells

is a great way to express how I feel about it as babies. Are you bored in any way? That's why I felt that it could also be that I God has made something available if you are going to have an abortion, don't waste what can save someone's life. I don't want you to abort, but if you're going to abort, don't waste anything. people must

real

ize that availability wherever they come is God's will, another laboratory has reduced its effort in studies requiring fetal tissues despite the importance of this research due to concerns about personal safety the importance of fetal tissue research by other leading research institutions, including Harvard, Yale School of Medicine and the University of Minnesota, if fetal stem cells are ever widely used, it will change the entire profit landscape of the pharmaceutical industry .

They don't make money with good people. They invest their money in sick people and continually inject medications of all kinds. This is how the

medical

profession survives on drugs. I haven't had a single episode of pain for the first time in 18 years. I'm totally pain free and drug free for people who have a disease that we're going to be dead in 12 to 15 years we should have an alternative to sitting on the sidelines and waiting for a triple blind placebo to fail in garbage suits you know , experiment, there should be something else that is thick, that we know how to help people and cure diseases and we can't do it, so we

real

ized that there was nothing like conventional medicine if we had visited absolutely all possible doctors.

It's so exciting that for the first time I see the light at the end of the tunnel. I see a light that Can I make a diet easier with medication? That's not something I want to hear, so going to another country for treatment sounds a lot better than that. I was very skeptical, very skeptical. It helped me tremendously with just one treatment. I attended since high school like Well, I almost failed staying up until 2:00 in the morning with my parents just so they could help me because I couldn't even do it myself, so now I'm getting A's and B's, which is phenomenal, as you say in the team way, yes, really beneficial, yes, absolutely, on medication, now alive, Ann's ADHD, Adderall, she was diagnosed with a rare form of muscular dystrophy after the first treatment over the next week, she went from falling fifteen and twenty-five days at no time.

She no longer falls, her gait was very wobbly everywhere and now she has walked super straight so she can walk in a straight line. Something is working right for you. Something is working well for me and I'm not going to do anything else. So what is important? It's chronic lymphocytic leukemia and it hasn't progressed and you're not sick, so once a year, as an insurance policy, I go back and get the stem cells. I've never seen anything like it. I have to be Honestly, I had the bat. I never thought something like this would work. I haven't seen anyone do it so well.

What can I tell you except that I look at this, a 20th century America and you would let him walk without help, so look where we are? today I say you could film keep going filming I'm still an associate professor emeritus in chemical engineering and an adjunct professor of mechanical engineering at Georgia Tech College. I have Parkinson's, the town's doll coming out to this day. I can tell the difference from the moment it first starts to do the trick, how do you feel the fact that you have to do it, but this is not available, like ritalin mistakes, I like the opinion, in my opinion, based What do I know about it now?

I think it's criminal, much better, you really are your bitch. I will prepare the layoffs, yes, how do you get out? It's not perfect, but it's much better. It's amazing. I'm not shaking so much in terms of the evolution of medicine if you think about the 20th century, we turned chemistry into service. In medicine, I mean, we learned how to deliver small molecules as drugs, but if we can learn how to deliver cells as drugs and actually repair and regenerate these degenerated tissues, it will have a huge impact on medicine. I think it's inevitable. There are many different types of stems.

The stem cells we hear about most are embryonic stem cells, umbilical cord stem cells, and adult stem cells. These different types of stem cells should not be confused with each other, as they are not all created equal nor are they the focus of this stem cell story. On this journey we focus on fetal stem cells, possibly the most controversial and controversial form of stem cell therapy to date. I just think I don't know how to start talking too much to tell you all at once, you know, it's hard. I see kids in wheelchairs and my doctor appointments and I think wow, I'm lucky and then I see kids in high school and I think wow, I got the worst of it.

I don't do the things I used to do anymore. I really don't do it anymore. leaving the house because it's hard, I mean, they live on my couch, in my kitchen, and in my room, and I don't choose to do that. I don't want to ignore my friends because I don't want to hang out. I hang out with them because it's difficult. I don't go to music shows like I used to because that's something I'm really passionate about, it's the only thing that matters to me and I can't even walk up the stairs without having to sit down. and I hold myself back because my heart is beating so fast and I feel like I'm about to faint, now that's what they're offering us and as for their cystic fibrosis team it's a double lung transplant, you know the horrors of that.

I can only imagine that I know my son doesn't want that and there's no guarantee of that either, no, they even said you know there are some people that go through that and wish they hadn't had a lung transplant, that's where you should go if you want. Think about it, we can ease his death if medicine isn't something he wanted here, so going to a different country for treatment sounds a lot better than that. I began to visualize crossing the border into Mexico and began to fantasize about the results. He's 21 and he should be living his life and going out or having a job and going to school or whatever he wants to do, he just doesn't exist in this house, it's very hard for me and then when we found out. there is another option, once it fully dawned on me, I remember getting angry, yeah man, that this is not available to us, you don't talk about people living with cystic fibrosis, the majority always experienced a constant worsening of their disease over time, but Brandon just gained seven pounds and at the time he received his first round of fetal stem cells in December 2014, his lung capacity was only 16 percent and now his lung capacity is 24 percent, while fetal stem cells cannot repair the genetic mutation that causes the cyst. fibrosis, Brandon is hopeful that fetal stem cells will prolong his need for a double lung transplant or perhaps prevent the transplant altogether.

Now imagine that it is a stem cell. Stem cells are unique because they have the ability to generate new cells of almost any type. They start out as unspecialized cells, but given the right chemical and genetic signals, stem cells can divide to form slightly more specialized cells of different size, shape and function and, after a few more cycles of division, can give rise to highly specialized cells. , such as heart muscle cells. For example, they help the heart pump blood throughout the body. By receiving a different set of signals, this same unspecialized stem cell can follow an alternative pathway and give rise to a different type of specialized cell, such as a neuron. which transmits electrical signals in the brain more frequently.

Most of the public does not understand what stem cells are, much less understand the differences between their types, so here is a brief overview. Umbilical cord stem cells are blood cells from the court or placenta that are preserved at birth; However, umbilical cord blood transplantation has limitations as a treatment. So far, adults with umbilical cord blood have proven to be very challenging, until recently only known to treat blood diseases, while a handful of clinical trials have recently opened for non-blood related diseases and Children who use umbilical cord blood require a genetic match and there is no guarantee that your umbilical cord blood will spontaneously transform into the specialized cells needed to help with your condition and be warned if you are currently expecting a child and plan to store the your child's umbilical cord blood, it is important to realize that obtaining access to your own child's umbilical cord blood cells is not an easy task, we spent approximately $4,000 before his cells and, when the time came, my illness in yes it turned out to be autism.

I couldn't get them, they didn't release them to me, although I want to say that I went to the end. At the top they announce that they will be able to do this, this and this, which did not happen. I couldn't get them when I finally got to the Vai Accord boss when I finally asked how many they had posted. The response I received from the clinical director was one of the ones I bought, paid for them and couldn't get them. Adult stem cells are the most popular and least controversial. Now researchers have found adult stem cells in more tissues than previously thought.

Bone marrow Skin Brain Liver Eyes and this has led to research into the use of the patient's own adult stem cells to repair damaged organs; However, there are currently several limitations to the use of adult stem cells. Adult stem cells are often present in trace amounts and can therefore be difficult to isolate and purify. Adult stem cells may also contain more DNA abnormalities caused by toxins and sunlight errors and make more copies of DNA over the course of life. There has recently been talk about how scientists can now reprogram adult stem cells to behave like embryonic stem cells, but they are still adulterated cells and can also suffer from DNA abnormalities.

The use of embryonic stem cells has been a hot topic of public debate. So much so that President George W. Bush banned all federal funding for embryonic stem cell research in 2007, only to be rescinded by President Barack Obama two years later. They are unadulterated stem cells that can be easily grown in a Petri dish and harvested within the first five days of development, but they also have limitations: the ability of embryonic stem cells to form non-cancerous tumors called teratomas is one of their defining traits. , it is a scary one particularly for those hoping to develop therapies from these cells, what makes fetal stem cells uniquely different is that the fetus provides stem cells taken from almost all relevant organs, the fetus contains pure stem cells and unadulterated from the beginning, after all these stem cells have been only nine months to create a complete human being and collecting them is quite easy a woman decides she wants to have an abortion and is then given the option to discard her fetus or donate it to the Science When fetal stem cells are injected, the idea is that they penetrate the nervous and immune system of our body and concentrate in areas that need repair.

This basic biological phenomenon is also observed between a mother and her child during pregnancy. Fetal cells migrate to the mother during pregnancy and can persist for decades. Fetal cells also appear to target sites of injury that cross the placental and blood-brain barriers x' fetal cells appear to change into whatever specific type of cell is necessary so that fetal cells and a mother with liver damage can transform into liver cells to To summarize in order, embryonic or adult stem cells from the umbilical cord to be effective, they must spontaneously transform into the different types of cells in our body, while fetal stem cells also function in the same way, they already contain the unadulterated basic components. of our nervous and immune systems, while the logical superiority of fetal stem cells makes sense when observed objectively. its research and use have caused a political storm.

Iran and Planned Parenthood kill babies in America, but 32 $100 prices per specimen are what we're talking about, yes, this makesthat deciphering fact from fiction in the media is almost impossible, as only special interest groups will do it. defend the types of stem cells that fit your agenda look every time there is a news story about a big success with stem cells, it is always stem cells and leave current fetal stem cell researchers working in the shadows for fear of their lives, what the doctors said. us in the United States is that Joey's life expectancy might not be beyond adolescence due to his heart and lungs and you know he would be in a wheelchair before he turned ten.

This is my son Joey, he has limb girdle muscular dystrophy. that's wasting of muscles throughout the body eventually it starts mainly in the shoulders and hips the disease was being quite aggressive oh so I pranked him to get him here quick enough once I did my research since then you know it stays Your heart Your lungs are full How do the doctors feel about your improvement? I told them what we were doing and you know at first they told me not to do it, you know if there's not enough research on it, there's not enough documentation on it, but after coming back from the first or even the second time, basically this is to keep doing what you're doing because they don't see it in any way, they see thousands of their patients a month a year, you know, I'm not sure the exact number and they never, ever get better.

Yes, it always gets worse and aggressive, most children his age with the same disease are not mobile at the moment and as you can see he stands upright so this is something that should be, should be available to everyone, there should be scientists. working around the clock on this instead of trying to make pills, you know, I have to tell people I have Parkinson's, no one would believe it, so it's big since the treatment. I have always been active and play golf. My golf score is the lowest. It was a 77 and I have shot par ever since.

I don't have tremors or tremors, so that makes a big difference in being able to walk 18 holes. The physical responsibilities that corner almost people with Parkinson's just can't do that. always noticeable before he had trouble walking since he came back last time he's like before. I've known Steve for about ten years, but I've been playing golf with him for a while. several years too and that is where I have noticed most of his distress. You know, you could see the similarities to who the actor would have had Parkinson's, Michael Fox, I think, and then he had a lot of those same things, tremors and all that, and then.

I guess it was probably two or three weeks ago when I saw Steve play and he wasn't playing with our group, but I saw him. I saw someone who I thought might be Steve. Everyone in the group commented that he now looks like Steve because he Don't you know he had trouble starting to walk and I thought no, that's not Steve because he walked normally and of course he was human the talk and It was obvious that something had happened and now he's actually walking? Like the rest of us, I really find the exhaustion miraculous, he's shooting now, he's playing better than the rest of us, so it's a dramatic improvement.

I have a wonderful physical therapist, most of the patients have progressive Parkinson's, but I think their spirits are high. and being very encouraged, I think because of the treatment, so he is working hard to continue with the translator. In fact, I built last week, I went to 278, which is the highest game I've ever thrown and Lola, you know, you would ask me if my doctor knew and I. I told you guys that I had never told him because he had mentioned that if he could take me to a convention he would win doctor of the year because he was doing so well.

Steve's story is somewhat unique. During this research I discovered that it is not. all people with Parkinson's improved. Fetal stem cells only seemed to help those with Parkinson's who were diagnosed recently, usually within a year or two, like Steve and Carolyn Porter, so my husband and I sat at the table and I remember that night I took my fork and started to take a bite in my hand I started to cut shaking so much I couldn't stop I took my left hand and finally I was able to take a bite well for a year and a half I carried My computer every night and wrote Parkinson's disease and stem cells came up on my computer and I thought I didn't type stem cells, why stem cells?

It had gotten to the point where I couldn't walk and I certainly couldn't talk I went in May 2013 when I went through the airport everything was in a wheelchair they told me there were no guarantees so we were very open we knew there were no guarantees and they said it would be up to six months probably if the stem cells helped me well we finished the treatment on a Saturday and returned to the hotel and left on a Sunday going home I told my husband I think I can walk he said oh no no you can't walk She informed me on the way home that he could get up and walk badly and he did, which was very surprising.

We got to the plane and I noticed I was getting better three days after having the stem. cellular treatment I started talking properly all of a sudden it was like everything had stopped it was like there were no more shaking there was no more head shaking it was maybe ten days after she came back she got out of her car and literally I mean it's just that I had chills because she could walk, we sat down, her hands didn't move, she didn't shake, she could carry on a conversation without stuttering and we both just did that and we cried and I promise you everything stopped.

I was fine and I was the happiest person in the world I played the piano well all the time for two years I couldn't play the piano I'm just not a very good pimp my thing when I get home from work the first thing I do is I turn on the news and look at them and well, I'm sitting in my chair, but I'm always interrupted by Carolyn playing the piano, which in the future in question hid the effect that the empowered lady has a good reason, I better not have to look. the news every night my doctor was he just couldn't believe it he calls me his

miracle

patient I don't need any medication anymore right now the largest stem cell research agency in the world is SERM or the California Institute for Regenerative Medicine a multi-billion dollar agency which was created in 2004 by the citizens of California we are an agency that was created to help patients and our mission is to accelerate stem cell treatments for those patients with unmet

medical

needs since its inception more than a decade ago, faced some criticism from the media for what they perceive as a lack of progress; the LA Times called them a six-billion-dollar public investment born high, but it appears the mainstream media hasn't really investigated why the efforts are useful. they are moving so slow welcome to the SERM board meeting in December.

This observation was further confirmed when we discovered that we were essentially one of the only members of the media attending the 2015

science

subcommittee board meeting in Los Angeles. Mr. Morgue consists of a colorful array of members from doctors and scientists, retired Senator Art Torres, former CEO of Paramount Pictures, Sherry Lansing, to actress, writer, director, Lauren Miller, wife of Seth Rogen at the time of this meeting . SERM announced the start of 15 clinical trials, three of which involve fetal stem cells, while SERM has many with money and influential people at the helm, repeatedly expressed that their biggest impediment is not

science

or money, but the FDA, a regulatory agency that continues to insist on applying the drugged element model for a conventional drug to stem cell treatments, which is like forcing a round peg into a square hole 70% of respondents cited the FDA as the biggest impediment to developing stem cell therapies from the moment we discover a stem cell product that looks promising to the moment we can actually get an IND approved by the FDA to where we can start we can start doing clinical trials which at this point to stem cell therapies is too long, it's between 6 and 8 years, the industry average for anything other than a stem cell is 3.2 years, so we look at that and say okay, that's a Problem: Cellular therapies are either essentially unregulated by the FDA and very inconsistent, costing less than a hundred thousand dollars to complete in less than three months, or they are overly regulated by the FDA, where it costs more than a billion. dollars entered and captured, it takes more than twelve years and there is nothing in between and all the other disciplines of medicine have something in between;

In other words, to address this growing field in 2001, the FDA created a new paradigm of a tiered approach to addressing approval. of stem cell therapies by allowing certain stem cell therapies they considered safe, such as adult stem cells, to simply exist unregulated, while most other stem cell technologies, including fetal stem cells, are forced to go through a regulatory process of at least 12 years of $1,000,000,000 just to reach the market, we also know that stem cell therapies, from a commercial point of view, clearly clarify our disadvantage, so the big pharmaceutical companies will use disproportionately licensed non-cellular technologies at a much higher rate than cellular technologies.

Only 8% of serum programs actually have partners, the reason why it doesn't exist. The commercial interest is because stem cells are just biology that anyone with the right resources can harness, they simply cannot be patented or placed in the current pharmaceutical paradigm driven by Polly, the very idea that an increasing number of people are discovering this technology, many of whom no longer need the pharmaceutical medications they were expected to be prescribed for the rest of their lives is an extremely frightening reality for the current business paradigm that the pharmaceutical industry has relied on for decades and ever since.

The FDA's Department of Drug Evaluation has literally been bought by the pharmaceutical industry. medical industry because Congress passed the Drug User Fee Act with nearly a billion dollars of the FDA's $1.3 billion annual Drug Evaluation budget coming directly from the pharmaceutical industry it is supposed to regulate, There is no logical reason why the medical industry will relax its grip. In fact, the FDA recently began providing members of the US Congress with unilateral information that tells only about the dangers of stem cell treatments, much of which was outdated and does not reflect what has been documented in the clinical literature about these treatments.

These actions cast the FDA in a very unfavorable light and appear to give the impression that they are actively lobbying against a therapeutic modality that they are responsible for promoting. We are not against regulation. We're not against the FDA, but we won't ignore it either. There is a problem that we reject outright the notion that a regulatory path that takes more than 15 years and costs more than 2 billion dollars is the only way forward that is not an acceptable approach the demand the need is very real the patients really They are suffering, they are really suffering desperately, they really need help;

The entities, researchers and companies that have the solutions see in some aspects the barriers between their current therapies and those patients as insurmountable and, finally, with respect to centers that operate abroad or if the jurisdiction of the FDA, that It is a symptom of the problem: they take their products and technologies abroad, where they are not subject to the same regulatory restrictions. The common denominator is that we are not doing anything that significantly advances the field to help patients. Because of this reality, people like Lawrence Simon, who was diagnosed with multiple sclerosis a few years ago, are not going to sit back and wait for some well-intentioned agency to step up and alter a regulatory system they don't want to change.

There's no shaking that there was initially, how about you press really well right there really well normally in your experience if you don't mind me asking? I'm considering how many years ago you were diagnosed in 2011, what do you usually see? people will just continue down the path and get worse and worse and worse, which I've seen, then fail all the therapies that it basically reached. I would say it will plateau and stabilize where it is no longer in decline. I'm very impressed. With what I'm seeing I have a tape and they have added those 50 years almost to that autism and he has been my patient for about 30 so what do we say about all of us?

I don't know except to saythat. There's something working here, I don't think we're giving it anything, I really don't know, from what I've seen in the failures I've seen, I'm happy, but I can almost tell you, yeah, that's all I wanted. To hear this, even to be honest, I tell you the truth. I thought it was bullshit. She would break it. I'm the first to ask you. I see a lot of false things. At first he wasn't excited about all this. I said well, if you have money to spend, go ahead, but you're talking about a disease you can't cure, so with what we have, why not?

And you know, taste of the pudding. I have not seen anybody. Understand well, now you think I was a salesman for that thing, but you know what sales have been like. There is no seller. I'm glad to see him better, whatever it takes and he would let him talk about attendance, so he looks at where we are today. The MRI was very agnostic, he had injuries in January 2011 after experiencing weakness and vertigo. Lawrence's neurologist ordered an MRI that would find many areas of abnormality favoring active disease. Numerous lesions and plaques representing active multiple sclerosis were found a few weeks after this appointment, on March 25, Lawrence had another MRI. which found no new areas of abnormality or abnormal lesions Susie became a patient 31 years ago suffered from recurrent respiratory illnesses intermittent swelling of the lymph nodes frequently treated with antibiotics in 2004 became more severely ill and presented more persistently with lymph nodes that were swollen in his entire body considering the fact that he has a family history of malignant lymphocytic disease, it was appropriate to further investigate why his lymph nodes remained swollen and did not improve after treatment for infectious causes.

This was the bone marrow. The biopsy confirmed that she had a condition called chronic lymphocytic leukemia. Most people with this condition have a progressive disease that can develop into a serious, life-threatening malignancy. It was interesting, as we have followed her for the last ten years, that there has not been any progression of her lymphocytic leukemia and, in fact, there has been an improvement in the number of abnormal cells relative to the normal cells in her blood, her lymph nodes have remained normal.he responded very quickly to the treatments he received in the body he probably has the most carefully documented body in my practice in terms of six to eight inch paper charts before the new computerized records began in 2006 , which if we printed them As Liana PI, we carry several boxes of computer paper and have been analyzing your labs frequently and I must admit that we found nothing wrong with you and no evidence of side effects from the treatments you received.

The important thing is that it is chronic lymphocytic leukemia and that it has not progressed and that you are not sick; most people don't have that experience, so the doctor who cares for someone with CL initially estimates that we'll be fine for a few years and then we're going to have problems, you're talking about 2004, so you're talking about eleven years ago when I had this diagnosis, yes, and based on the fifth, my father started off well with the chronic illness and ended up with a nice self. I'm not going to do that, understandably, Susie's doctor was quite nervous about speaking to us on camera, hence his modesty, not only did Suzie's chronic lymphocytic leukemia not progress to acute, the pathologists were baffled by the unusual finding that his cells normalized, meaning his diagnosis was reversed or cured.

A diagnosis of chronic lymphocytic leukemia requires an absolute B cell count of more than 5,000. Suzie's absolute B cell count dropped to 304. Suzie did not undergo any other medical intervention for her diagnosis other than receiving a series of fetal stem cell injections as part of my I feel uncomfortable being part of this project. I'm becoming the target, but stem cell therapy is actually becoming more common. It is important that people know about it and that we learn more about it. I would prefer it to be done in a scientific way. We can all learn from our experiences and if we don't have explorers we never learn anything it's an opportunity right, I mean, it's working well, something is working well for you, something is working well for me and I'm not doing anything else. so we're okay, yes we are, we're welcome when she decided to receive the stem cells initially as a doctor, somewhat skeptical.

I became more and more convinced of her benefit as the years went by, that she was getting better and better, and quite honestly. When you go to medical school I think they put a pair of blinders on you and that, unless it's taught in medical school or you read about it in medical literature, it can't be valid, it can't happen. Susie is living proof. She is healthier than me, considering I have some conditions of my own that I think could be beneficial. In fact, I am considering having these stem cells. I have visited about 14 doctors. I mean, she was going to go to extremes to try to get the paint off. just a little bit she even cut her hair short because she thought it would help her neck when I look back and think about all the doctor visits.

I remember being in the office with Danny and whatever doctor we were with and then saying well, it's in her head or something. I could see her eyes fill with tears and she would just put my hands on her face and tell her I'm NOT going to stop, you won't suffer another day if I have There's nothing to do about it. I had my wisdom teeth removed and was prescribed the medication they prescribed for her only if she had a really bad day. You know, she takes some narcotics. You know, in late 2013, a genetic test finally helped doctors diagnose Danny. with ankylosing spondylitis, this is a type of inflammatory arthritis that primarily affects the spine, causing the ligaments to become inflamed, the cartilage then fuses with the vertebrae, causing the spine to fuse and causing immobility after all medical treatments failed to help Danny with a lot of anti-inflammatories. to methotrexate, which is a chemotherapy drug typically given to cancer patients, as well as tumor necrosis factor inhibitors and some of the most potent narcotics available, then underwent fetal stem cell therapy in Mexico on the 25th.

July 2014. He had this smile from ear to ear. I had not seen that smile and for so long they brought her the menu back to our hotel, she says mom, let's go for a walk, let's go shopping and go out to eat and I said: who are you in a week after receiving the mother cells? I stopped taking all my medications, they didn't allow me to be me, they changed my personality a lot and that is something that the stem cells have given me, they have given me the ability to be me because I don't have to poison my body with everything.

The other medicines change who I am, Danny is now a Division One athlete whose rowing team reached the NCAA championships. Rowing is probably one of the most physically demanding sports you can practice, it works every muscle in your body. I had no idea even about all of them. My hours of research indicated that this type of therapy was that most people found out about fetal stem cell therapy by word of mouth. Danny's mother discovered her looking for a used truck for her son. If it weren't for me, which means Jan is good for finding that perfect option. truck for my son Wow, I can't believe you're here.

I can't believe God sent you here. He didn't send you here for this truck. He hit you here. He meets Jan Good and her adopted 16-year-old son. daughter Mariah two years ago, when Mariah was 14, she was diagnosed with fibromyalgia, as well as juvenile rheumatoid arthritis and systemic lupus erythematosus. I first met Mariah about three years ago, in April 2012, she and her mother had just moved from Tennessee and Ella came for an office visit. She had been diagnosed with lupus in Tennessee; However, shortly after moving to Florida she began having problems with joint pain, knee pain, back pain and her ability to do the things she liked to do, like play basketball, is very limited. .

So at that time we considered having her see a rheumatologist and the rheumatologist's concern was again lupus and she knew juvenile arthritis, so as part of the treatment regimen, at that time they prescribed a couple of chemotherapy agents, for what the rheumatologist gave Mariah. methotrexate, which is a chemotherapy drug, and prednisone, and he kept increasing the dose. She couldn't get out of bed, she could barely go to the bathroom, she could barely eat in April 2013. Lab reports found blood in Mariah's urine, indicating the beginning of her kidney failure. failure, that's when I said no more, no more, no more steroids.

I was desperate. I took a white sheet of paper and wrote on it. I was hoping that she would give my life something about stem cell treatment and I really hung up, got to her and the people's front yard. We started donating furniture and different things and we had cells in the garage and people would knock on a random door and give us twenty or a hundred dollars for their stem cell treatment and then I had to put this sheet on the back of the fence. The city had an attack, they made me take them both down, but yeah, it was a little bit and I guess it was because it was a more traditional, traditional way of dealing with the problem, but it worked, you know, we probably need to do it.

If we put her in a wheelchair and put her on the plane and we were all nervous because we had never been to Mexico, this will be like in your minds if this is really real and it's just going to work and you all emotional and you gave me my baby during the trip back to San Diego. I remember she said, so we went back to the motel we were staying at and she ate and I went to do the laundry, in addition to a laundry room there was an exercise room and she said mom can I go ahead with this and see what's happening?

I have to yeah, take it very, very slowly because your muscles, you know, I haven't been working out in a year and I've done it and the chicken lady she goes, come here. I want to show you something and I mean I'm going to sit there and look at the plane. Three hours after the stem cell treatment, she doesn't ride to Mars on the elliptical machine and then jump on the treadmill and then two more miles she seems to be clocking. pretty good, do you have any comments, didn't you try it? I don't have much experience in terms of the uses of therapy, however, if it seems that way, it seems to have made a difference in her life.

I guess it's something you can name something that was a benefit to her just when we thought this story couldn't get any more interesting Janet--good had also been incredibly dealing with her own health issues a year after Mariah's recovery, her adoptive mother Janet was I was diagnosed with systemic lupus erythematosus and dermatomyositis. I never dreamed that a year later I would be sentenced to death in three months or two years and would need stem cells, so I found Riya's stem cells and in turn saved her life. She needed them and she saved my life. You have to pass it on.

You have to tell everyone what you've been through and how she's helped you because she can save their life, or maybe that of a member of her family in a tragic turn. events of November 6, 2016 Mariah was shot to death, no, now, the batch that would keep these stem cells now that last time, someone with anger issues snuffed them out and took them, not only are people looking Fetal Stem Cells For various immunological and neurological ailments, some of the world's busiest professionals are seeking fetal stem cells to improve anti-aging performance and overall longevity. This is George Killer, an icon of American television comedy, winner of several Emmy Awards.

He is best known for his work as founding producer and writer of the groundbreaking television comedy classic. Rowan and Martin laugh. I gave the injections myself and when I got home, my wife looked at me and said, What happened to you? Ben Wright wasn't a euphoria, it wasn't any kind of drug or anything, it was just a feel good feeling it wasn't even euphoria, it was just a feeling of being in a relationship, so I took the shot and then I took some people here including my wife and my daughter, and I can understand the resistance to it, except for the fact that If fetal stem cells are ever widely used, they will change the entire profit landscape of the pharmaceutical industry: they don't make money on healthy people, they make money with sick people and continually pumping them with medications of all kinds. how the medical profession survives on drugs the medical professions are great, they do great things.

I wouldn't want a plumber to give birth to a baby, but they resist this because they believe it will change the entire profit structure of the medical profession and it will. it's just a matter of when they resisted Jonah's salt and having polio. I wish they would stop resisting soonerthat I contracted it. My favorite is that they said there hasn't been a double-blind study. There have been double-blind studies on a lot of drugs that killed people, there have been double-blind studies on chemotherapy that we know a lot of people haven't survived, it just makes me feel very, very uncomfortable to think that expecting some kind of double blind study that results in the death of one child and the cure of another, my question always is how do you select which child to treat with a placebo or which child to treat with these stem cells?

The use of fetal stem cells is as dangerous as cough medicine. it can kill you, this is William Raydor, the scientific director of stem cells of the United States, a company that operates in southern California, most of the patients you have seen so far were treated by the Raiders company; However, due to strict US federal regulations, these patients had to travel. to Tijuana Mexico to receive the injections at the beginning of my career. I was one of the first medical experts on television, starting first in radio and eventually appearing several times on the Merv Griffin Show dr.

William Raydor's successful television career continued well into the 1990s. I got a phone call from Eastern Europe and they called me and told me about fetal stem cells, so I said, I'll tell you what I want to see. This is what I want to interview. you I want to interview patients I just want to do whatever I want to do when I'm there would you agree that they said yes ten days later? I am an Air Ukraine plane. I was totally amazed when I saw William in 1995. Raydor traveled to kyiv, Ukraine and spent some time with the founders of a medical university clinic called M cell.

This is the late Professor Alexander Smita, who in 1991 is the man responsible for originally inventing and developing the technological innovation of fetal stem cell therapy along with M Cells Co-Founder and Partner, dr. Alexey karpenko, who you will meet later, professor smig a doob and professor karpenko taught william raydor the basic techniques of fetal stem cell transplantation according to professor alexei karpenko. Emcell was also looking to partner with William Raydor on a new clinic, but Rader decided to take the information. He learned and opened his own fetal stem cell company. I left everything else and dedicated myself to fetal stem cell research.

During the production of this

documentary

, the Medical Board of California revoked William Rader's medical license in their failed attempt to stop his surgery, but it was my choice. I got the cells in March 2015 and was treated the same as any of the other patients. Stem Cells USA does not perform any preliminary medical testing and this entire injection process takes approximately 30 minutes, as does anything done around federal laws. Regulations to gain full transparency as a journalist telling this part of the story was difficult as I was not allowed access to any of Raider's research labs where Rader claims to replicate his fetal stem cells rather than using fresh new beings. on board to really get to the bottom of this complicated story, I traveled to M Cell in kyiv, Ukraine, where this technology was started over 20 years ago and what better way to fully understand fetal stem cell therapy than to experience it? by the world's original pioneers while undergoing a three-day longevity anti-aging program with M cells.

M cells allowed me to document my entire treatment program and film their laboratories and facilities, unlike most clinics doctors in the United States. my blood and urine at their on-site lab it is from these lab results, plus a full ultrasound and electrocardiogram, that the M cell doctors designed a special protocol just for me that consisted of a variety of cell types fetal mother and a 3-day facial treatment. hyperbaric oxygen sessions with fetal stem cells and even massages to help keep my circulatory system flowing well and allow the stem cell transplants to take place properly, so on the first day, after completing all my preliminary tests, I was moved to a private room where I enjoyed some coffee. and a totally organic breakfast that I ordered off the menu while I waited for my GP to arrive.

This is Dr. Irena, who is a physician and doctor and regularly works behind the scenes on the expansion of M cell research and the development of fetal stem cell technology. It's Lena, one of M's sales managers and the translator assigned to me at the beginning of each day. Dr. Irena checked all of my vital signs and asked me several questions related to my general health after my physical exam. Dr. Irena carefully explained my entire treatment with fetal stem cells to me. program that was an incredibly complex array of a variety of types of fetal stem cells that were collected between seven and twelve weeks of gestation and programmed over a three-day period.

They pursue a variety of goals to improve my overall health. The combination of fetal stem cells that they administered to me. The first day helps me create new capillaries and other small vessels in all my organs, which helps supply more oxygen and nutrition to my entire body, thus improving overall functions in my organ tissues. These cells also have very positive effects on the inner wall of the large intestine. blood vessels serve to protect my vessels from atherosclerosis and if there is any current in the pink chlorosis, it prevents it from progressing, they have a very positive effect on the blood formation of the liver, bone marrow, immune and hormonal systems, essentially giving my entire immune system a complete reset, they started first with a standard sodium chloride saline drip to open up my veins, followed by some allergy meds just to be safe and after this all calmed down they brought in my first round of fetal stem cells and then it was I went to see their masseuse Yuri the massage was about an hour back to my room for a little lunch and relaxation followed by hyperbaric oxygen.

I had never been in a hyperbaric oxygen chamber before it felt like flying in an airplane only with perfect high density. quality of oxygenated air. I'm fantastic, thank you. Hyperbaric oxygen sessions are healthy anyway, but in this case it serves as additional nutrition for the fetal stem cells and then I went to the cosmetologist for the first day of my facial. My cosmetologist was Halina, who first gave my face a deep cleanse before applying the key ingredient of this cosmetic therapy. The chorion cells that Halina had already prepared shortly before my facial treatment began. Chorion cells are early fetal membrane cells that are rich in high-density nutritional vitamins and minerals.

These cells are highly anti-inflammatory and regenerative when applied to the skin and M cells are the only place in the world that offers chorion cells as part of a cosmetic facial treatment. The chorion cells were then carefully applied to my face. Halina then applied a rejuvenating mask containing aloe vera and other ingredients to end the session and this was the end of my first day of treatment and I was also provided with transportation to and from the clinic each day. At the end of the first day I was really looking forward to sightseeing in the beautiful town of Keeve, but the doctors at mSL asked me to take it easy and not push myself too hard.

I stayed in the center, near the central square of keeve, which offered a large number of hotels that bought on the day of food for the dr. Irina checked my vitals and they gave me a second round of the same fetal stem cells I received on the first day off for massage and then a second round of hyperbaric oxygen. This is Dr. Maria, who was supervising my sessions, not just Dr. Maria, a medical doctor, received her doctorate in fetal stem cell therapy. I returned to my room where dr. Irina inspected my abdomen to prepare me for my first subcutaneous injections of cells that will improve my neuronal or nervous system.

These cells improve all the processes regulated by my nervous system. They improve all interneuronal connections. They improve motor skills and my autonomic nervous system, such as heart rate. digestion, respiratory rate, and pupillary response, while also improving memory, concentration, sleep, and overall cognition, essentially giving my entire nervous system a healthy reboot after a standard saline drip was completed, this combination of cells was injected subcutaneously into the fat in my abdomen, the reason for the location of these injections is because the fat in our bodies maintains a more stable temperature and allows for the overall protection of these cells as they adjust to my body and begin to slowly release into my nervous system and finally the second day of my facial Halina started first applying steam. my face to open the pores and then apply more chorion cells after allowing my skin to absorb the concentration of chorion.

Halina prepares an alginate mask at a very cold temperature and then closes my pores, sealing the chorion cells inside and further stimulating blood microcirculation. and that was it for the second day, well at least for now, when I decided it was time to do some sightseeing, the city of kyiv is beautiful and rich in history and culture. During my trip I met an American from Pennsylvania who is in love with keeve as much as I am mr. DeMarco is also an EM cell patient. 18 years ago I was in a very serious motorcycle accident and, along with many other injuries, I suffered a fractured vertebrae, spinal cord damage, and a torn brachial plexus nerve group on the right side.

Those nerves control my right lung my scapula a right arm after multiple reconstructive surgeries I was left with severe spinal cord nerve pain. I was prescribed morphine mexitini neurontin many different narcotics unfortunately none of them worked, they would relieve the pain a little for short periods of time but nothing would stop me. I became addicted to morphine after two years. He took more than 200 milligrams of morphine a day. Let me describe the pain. The pain. There were two types of pain. There was a 24/7 type of compression pain that was more bearable than the previous one. Stabbing pains that I experienced, the stabbing pains that I could compare to a knitting needle that was heated over a flame and plugged into a wall and then stuck in your curious back and stuck there for about 30 seconds and pulled out and then stuck in. there for 30 seconds and take it out.

Skip forward, a year and a half ago I was here in kyiv for a personal matter and I discovered the M stem cell clinic, so they didn't make any promises to me, just that in the past I had helped people in my situation. I was advised to wait two to three months before starting to gradually reduce the medication I was taking which was decreasing the frequency of the episodes and I have not had a single episode of pain since the end of December 1st. once in 18 years I am totally pain free and I have medication for it dr.

Irina checked my vital signs as usual and then it was time for my second round of subcutaneous injections, but this round of subcutaneous injections was a series of fetal stem cells to help me with my entire musculoskeletal system, which helps improve my bones, cartilage, tendons, ligaments and my joints. all its connective tissues improve general metabolic processes while increasing the trophic and elasticity of my skin and also increase energy levels, which triggers regeneration, rejuvenation and overall high efficiency, which also, by the way, It includes a huge improvement in sexual functions, essentially giving my entire metabolic system a good reboot.

The reasons for the placement of these injections are the same because the cells are received on day 2, my third massage and then back to my room where I was given an intravenous drip of amino acids to further improve my body's environment, giving it the better to fetal stem cells. chance to do his job and finally went back to my room where dr. Irina spends a great deal of time summarizing my entire treatment program, reviewing my blood, urine, and other tests that were performed on me, and explaining to me why they gave me the types of injections and therapy that they did.

Each patient who receives therapy at M cell has a completely different personalized therapy. schedule depending on their current health or any more serious ailments they may have, since I'm already quite healthy. I underwent the M Cell Longevity Anti-Aging Program, but others with specific ailments would receive a different protocol. I met the kalahari who had just arrived from Houston Texas, whose youngest son,Beckham underwent a personalized M cell treatment protocol for autism. This is Beckham's father, Matt, and his mother, Teri, while they were on day three. I had the privilege of meeting dr. Alexi Karpenko, the co-founder and original partner of M Cell, but the only thing that will probably not be complete will become a greater part of its function will benefit, but for recovery we have to understand that we understand that we were looking for an improvement in quality of life .

Thank you. I greatly appreciate it, considering that autism currently affects one in forty-five children in the United States, costing each family that supports a child with autism over the course of their life up to 2.4 million. dollars to attend to said diagnosis. I was very interested to see how Beckham was doing after the fetal stem cell treatment, so four months later I traveled to the Kalahari of Houston, Texas, to see if Beckham had made any progress. We had a lot of aggression. Beckham scratched me, he bit me, so he went to bed every night and I had bloody sheets.

He had scratch marks. He would have in my face. On my back, wherever I was talking. I was trying to confront Becca back then, going back to her world, just looking past me, looking past you, it was, it was, it was really, really, really hard, but the eye contact wasn't there at all, period, It was even more. That, when you looked into his eyes it was almost as if you were looking into his eyes and you didn't see anyone. There was nobody at home. She didn't respond to his name. He didn't respond to anything. And he was pretty.

Drastic when that happened almost immediately after his stem cell transplant, we saw changes. He had this terrible eczema all over his skin in three days, he disappeared. I've fought that eczema for years with prednisone, whatever. I tried diet changes. It was

gone

His skin was clear His eyes suddenly became bright These smiles I hadn't seen in years We started swimming He didn't know how to swim Before he put his head under the water He will sit down before his stem cell transplant He wouldn't do it he walks for me I always had to carry him he would just block my body and refuse to walk I couldn't walk with him around the block at 3 I had to have a stroller suddenly he's walking now he's walking he takes my hand like a neurotypical child and we walk we can walk in the park I can walk with him to the supermarket to the mall that may not seem like a big deal to parents who are used to it but for those who can't have a child walking is a big thing so the fact that I could do that It made my life so much easier so I'm not lugging a 45 pound kid around with 18 bags of groceries.

I mean, it's really miserable and difficult, so that was another big thing for him. He is simply much more receptive to a different idea, which was not the case before him. Now he can plan his motor if he has an idea that was not there before his cognitive levels increased significantly. I've definitely seen him become more flexible because he would want to do things just the way he wanted and we couldn't change all the ideas. Any idea has been a long time since then. He is giving me many more new ideas. He is doing much better with some language and he started planning things like that too.

The other day I was here he saw this and the ramp was on the other side of the room and he went to try to get the ramp. He never had a plan for how he was going to ask, so that was very novel and very new. for him, so we've definitely seen progress in a lot of different areas. I've been working with him since he was 18 months old, so it's almost 3 years and at the same time it's also giving him a sense of where his body is in space. what I learned to plan and figure out how to do things by having a very good internal awareness of the body, yes, every day is something new.

We are both surprised because the Kalahari was making the trip to overcome 4 Beckham's autism. decided to see if fetal stem cells would also benefit his oldest son, Matt's Jr. My oldest son has convergence insufficiency and ADHD. I never thought he would make it to college. He was very skeptical, very skeptical. He helped me tremendously with just one treatment in terms of school. I got out of high school and then I also failed high school and stayed up until 2:00 in the morning with my parents just so they could help me because I couldn't even do it myself, so now I'm getting A's and B's, which which is phenomenal, and then...

I'm looking toward future semesters to take on a larger workload because it seems more feasible and possible, so you're saying on the four-month team yes. In fact, I've officially been off medication, now at least I'm stopping the dosage I would take. Going from pills like Ivan's previous Adderall for ADHD in these last four months has been tremendous until one of the most important things he said to me was mom, thank you very much, thank God, I no longer feel stupid while Matt Jr. received fetal stem cells in hopes of finding relief for his ADHD. He also suffered from overactive bladder and chronic skin conditions.

He was always urged to urinate every 15 to 20 minutes throughout the day, about two months after not having the urge between my skin I have had acne you have had uncontrollable it was bacterial acne I have tried the strongest it is accutane as high as you can go like the dose would ruin my liver makes me feel terrible but honestly in the last two months I have had skin, the skin has cleared up on my shoulders, my back, mainly around my entire face, it is a tremendous difference as well as all the eczema around my eyes mainly and on my arms that I have had. spots around the arms where they are now completely

gone

and it's just phenomenal, it's crazy and it's only been one treatment so we realized there was nothing like conventional medicine.

If we had visited absolutely every doctor possible, I feel like we made the right decision. We did it, I have no doubt that we had a lot of information to analyze and like everyone else, searching for information and trying to be well informed, it took us literally eight months just to analyze what we thought would be the best option for I can't Say how excited I am with the results. It's one thing for everyone around Beckham to notice such huge improvements after receiving fetal stem cell therapy just four months earlier, but another to review the results of his autism spectrum test or a dose two.

I got these results from Beckham's neurologist's tests. Beckham's last test with a dose two was in December 2013, where he scored a 22 and fell in the moderate to severe range on the autism spectrum; however, while he was visiting Kelleher in November 2016, another dose. The test was performed which revealed a score of 15, a seven point reduction showing that Beckham is now on the moderate autism spectrum. These results occurred after just one round of fetal stem cell therapy. Beckham has not been taking any medication during this time. I am very excited. It's so exciting for the first time I see the light at the end of the tunnel I see a light I haven't seen a light in a long time and after completing my three day treatment I spent a couple of days with dr. .

Karpenko while telling me the whole story of how emcell came about while showing me a key doctor. Karpenko had worked directly in cooperation with the Ukrainian Ministry of Health, allowing emcell to emerge freely and legally. It was since 1991 that this technology for clinical use. It was made and we used it for about 25 years this year, it's now 25 years and it's stable. We can predict what will happen with the expected time of results. Understand how it will behave. Our treatment will behave in different types of diseases at different ages. different patient conditions, so this was the beginning of the clinic, the use of fetal stem cell transplantation, not just a discovery of fetal stem cells for the first pioneer.

I took a tour of the M cell research facility and quality control labs. I wanted to gain a full understanding of how these cells are collected and tested before being administered to patients. The process specifically begins between seven and twelve weeks of gestation, where the fetal material from a legal voluntary abortion with the consent of the donor reaches the M cell within two hours after the abortion. procedure, this fetal material then enters the M cell biotechnology laboratory. This is Cristina, CEO of M cells and general supervisor of the entire M cell collection and quality control laboratory.

I would love for you to see the process of extraction of fetal stem cells, but I'm very Sorry, but we can't film it, okay, okay, thank you, yes, after M cell scientists extract more than a dozen different relevant categories of fetal material in their biotechnology laboratory, the fetal stem cells are immediately sent to the cryopreservation department where they are then suspended using a special patented method, once the cells are successfully suspended, they are simultaneously sent to three different departments during the research phase. Cells are tested for viability and consistency of functional activity. They need to ensure that they are using healthy, thriving cells capable of expanding and replicating once injected into the body.

This viability testing process also involves a state-of-the-art laser-based flow cytometer that is capable of analyzing cows and sorting stem cells. fetuses in real time up to a thousand particles per second While that is happening, this exact same batch of fetal stem cells is also being tested in the M cell microbiology laboratory, where each batch of fetal stem cells is tested to make sure it does not contain harmful bacteria or contamination. This same batch of fetal stem cells is also sent to the polymerase chain reaction laboratory where M cell scientists carefully test each batch of fetal stem cells for harmful viruses.

Polymerase chain reaction is the molecular diagnostic method that allows M cell scientists to identify a single copy of the DNA and RNA of harmful pathogens and the cells testing process is repeated three times to make absolutely sure. that their fetal stem cells meet the highest standards of viability and safety before being administered to patients. MSL has the largest fetal stem cell bank in the world. Very often people confuse fetal stem cells with embryonic stem cells when they are not even remotely the same. An embryonic stem cell is collected within the first five days of development in a Petri dish after artificial fertilization, unlike Fetal stem cells, embryonic stem cells have not formed any valuable organs or tissues to take advantage of regardless of the misleading advertising in the media, not to mention that embryonic stem cells can be quite dangerous, the ability of embryonic stem cells to form non-cancerous tumors called teratomas is one of their defining traits, it is frightening, especially for those hoping to develop therapies from these cells.

In many cultures, including the Ukrainian culture, the vocabulary word for fetal simply does not exist, so which only adds to the confusion since in some cultures the terms fetal and Briona are used interchangeably, hence the name emcell. I had the opportunity to read a handwritten draft of dr. Karpenko, who will soon publish an article summarizing the last 25 years of fetal stem cell transplantation, mentions the first patient they treated: a 14-year-old boy with severe aplastic anemia. A plastic anemia occurs when the body's immune system turns on itself and attacks. Blood platelets and red and white blood cells, also known as bone marrow failure, the only potential cure that conventional medicine offers for this disease is a life-threatening bone marrow transplant and the only way to To stay alive waiting for a bone marrow transplant is to undergo constant blood transfusions, this disease affects up to 900 people per year in the United States, so we decided to track this patient 25 years later, who is now a thriving husband and father who lives in Switzerland.

We had a lovely Skype call with Demetriou from her home in Switzerland and his parents, who still live in Ukraine. Demetriou was cured of plastic anemia 25 years ago after just two fetal stem cell transplants. Demetriou did not undergo any other therapies apart from fetal stem cell transplants, completely restoring his bone marrow since then. The fact that fetal stem cells take only nine months to create a complete human being should help illustrate the power of these cells compared to any other type of stem cell. When they enter the body, they are programmed to look for anything thatneeds repair, redefining the meaning of the word.

The power of mother nature for the record. I couldn't find anyone who agreed to appear on camera and oppose fetal stem cell therapy. I have contacted countless anti-abortion politicians, including Ms. Blackburn of Tennessee, who chaired a congressional hearing on fetal stem cells in 2016. Cellular human fetal tissue for profit, breaks the law, donates fetuses for no profit, is within the law. I also contacted anti-abortion activists and Christian evangelists Franklin Graham Billy. Graham's son, who also declined to participate in my contact with several stem cell experts, had similar responses when I contacted the man from James Thompson's Time magazine who brought in used stem cells for his participation in this

documentary

as an expert. in stem cells.

His response was simply: "I'm sorry, but it is outside my area of ​​expertise to obtain legal access to fetal stem cell therapy in the United States is currently nearly impossible, Mr. MS, you are conducting several clinical trials, but these trials are currently 12 years and at least a billion dollars away, meeting FDA requirements for market approval and that's just for one ailment, it could theoretically take hundreds of years and billions of dollars to obtain. approval for all relevant ailments, the problem we have is that we don't have after 15 years of this regulatory paradigm in place I don't have anything close to being reviewed by the FDA for approval, but I think that when Sirum takes a step back and.

As you look at that regulatory framework, we thought if there was something in between that wasn't as daunting as the current regulatory approach rather than taking these innovative cell therapies overseas or having them under the FDA's watch, would they just not come into the fold. and they would do the work necessary to prove that they are safe and effective in a timely manner and in a way that cost-wise allowed them to be successful, there are only a handful of places in the world where stem cells can be obtained fetal Another company is San Diego-based Stem Medica, which first made headlines in 2015 after treating hockey legend Gordie Howe in Tijuana, Mexico.

Gordie Howe, one of the greatest hockey players of all time, was on his deathbed last year after suffering a stroke that his son, Dr. In fact, Marie Howe had begun writing his eulogy. father when he received a phone call from Diego Bay's stem cell company Gordie Howe. The stroke left him unable to walk, but eight hours after his first stem cell treatment he sat on his bed in the clinic, but he said, well, I'll walk to the bathroom, well, you can't walk, he said, well , hell, I can't, and he sits up and puts his feet up on the edge of the bed, and I was absolutely amazed. could do that When the Gordie Howe story first broke in 2015, we contacted CTV, the Canadian news organization that first covered the story, they told us Gordy received neural stem cells from a tissue sample fetal from a 12-week fetus and bone marrow. immune cells from a healthy 21-year-old donor from a US tissue bank, once the US media caught wind of this story, Stem Medica began receiving negative publicity for its use of fetal stem cells.

Stem Medica suddenly started claiming that the fetal brain tissue they were using was not from a 12 week fetus, but from a 14 to 16 week fetus, instead claiming that they are actually considered legally adult stem cells, even if your fetus is derived to make things more confusing if the bone marrow immune cells that the stem drug uses are from a 21 year old donor and it is being injected into patients like Gordie Howe without being a genetic match to these patients? why do we have so many bone marrow registries around the world if they are successfully giving mature 21 year old bone marrow cells to patients without genetic matching?

Stem Edeka did not respond to any of our questions or requests to participate in this documentary Gordie Howe passed away at the age of 88 so her family says she was simply old age. It is important to realize that not all types of stem cells are created equal. This is true for the various fetal stem cell companies, in the case of Stem Cell of America and Stem Medica both claim to use replicated cells rather than using fresh aborted cells, most likely due to the increasing difficulty in obtaining fresh fetal cells in The United States of America. A handful of American fetal stem cell experts who agreed to speak with me privately and not on camera, most said that replicating the cells was not a good idea since the cells could not only lose effectiveness but also risked mature beyond their productive capacity.

The paper also in Stem Medica only uses neuronal cells from a single fetal brain and bone marrow cells from a single adult donor. US Stem Cell claims to use only neuronal cells from the fetal brain and cells from the fetal liver. Liver cells that will eventually become the body's bone marrow. It is not to say that this method has not made many patients happy, but when we look at EM cells, the global pioneers of this innovation due to the ability of M cells to operate openly and legally in full cooperation with the Ministry Health Center of Ukraine harvests M cells and injects each patient with more than a dozen types of fetal stem cells, expanding the cells' ability to help the patient beyond just brain, liver or blood tissue. bone marrow can offer and M cells do not believe that replicating their cells is a good idea, while the United States has begun to publish some of its data on stem cells.

The United States has not yet authored any of its own peer-reviewed publications. peers, while M cell has been continuously publishing its peer-reviewed data for more than 25 years in cases of diabetes, for example, the child who has the initial phase. of diabetes one is condemned to a very low quality of life - or to debilitating complications, in many cases this will end with a kidney transplant with blindness with food duration exchange amputations, etc., but in case we intervene , that in the same starting with this disease we will change the fate of the child she will continue to be diabetic a diabetic patient but the course of diabetes will be very mild without any complications the results are not effective in five people they are effective in 30% but in cases of incurable diseases is something that concludes my three-year journey researching this story.

I tend to pay more attention to the millions of people around me. We certainly don't lack human beings, especially when I see homeless people sharing the same space as millionaires. It is clear that we are still struggling to care for the people who are already among us. The human race collectively aborts up to 50 million fetuses each year, whether we agree with abortion or not, no matter if we are pro-life or pro-choice, we are not going to do anything to change the harsh reality that People will continue to seek abortions, especially when 22 percent of all pregnancies in the United States end with abortion.

The argument that women will start getting pregnant on purpose just to abort and provide more fetal stem cells is absurd. No woman wants an abortion unless it is absolutely necessary. And if she chooses that path, what is that decision like? It's our business, so what do we have to say about all of this except that the only thing I can say is that we won't see this technology available to Americans anytime soon between the anti-abortionists who don't want this to happen and the pharmacists. industry that will take full advantage of this and not allow this to happen, this is probably the biggest threat to anything the industry has ever seen.

A lot of people asked me how I'm doing with the pair and, frankly, I feel amazing. I really can't talk. for a stem cell from the United States as much as for Edison, since I rushed in and out for 30 minutes without medical tests. I had blood tests before and after no significant change in my health, but with the M cell I had a full ultrasound that should show a little bit and enlarged angry and that was normalized in just four months completely normal my cholesterol was very very high according to my blood test, but no more months later my cholesterol normalized, you can't do that without pharmaceutical drugs, so it's quite remarkable, it's my hope that everyone I know, including my loved ones, gets a therapy of opportunity, but perhaps the most notable thing that happened to me that I experienced shortly after was that the cells, aside from things like the skin, became clearer.

I slept better. Energy increased dramatically, but my libido completely exploded. I exploded like an 18 year old again and that's no reason to know so I feel quite privileged as I'm only one in 15,000 people on the entire planet who have had fetal stem cells and built them well, thank you, no problem, no. you