As human beings, we have 100-140 trillion cells and each day our bodies produce 100 billion cells or more. This means that each day we potentially face 10,000 or more malformed or pre-cancerous cells. In a properly functioning body these cells are dealt with by our immune system or the cell itself senses problems and causes apoptosis. It is when these cells are ignored by our immune system, perhaps due to nutrient deficiencies or environmental influences, that a cancerous cell can take hold.
The Hino Foundation along with The Hino Medical Center has obtained and improved a ground breaking cancer protocol encompassing technology known as PNC. This technology has proven effective against many known cancer cell lines and has been used in humans with no known toxicity. We have taken this foundational technology and blended in additional specific elements to render a product we have named HICAN-7. HICAN-7 provides cancer patients with an alternative to Chemotherapy that is non-toxic and at the same time known to be effective.
HICAN-7 is a tiny molecule that attaches to a surface protein only found in malformed or transformed cells causing them to die quickly from violent cell necrosis while leaving normal cells unaffected. In the example below the foundational elements are used to attack human melanoma:
As you can see here, we penetrate the cancer cell and cause our product which makes the cell glow to enter the cell within 10 minutes of introduction. Interestingly this shows the subject cells disintegrating into the surrounding fluids at the 15 minute mark. This safe alternative to chemotherapy is available at the Hino Medical Center and we will continue to invest in disruptive technology that impacts our world.
There are many forms of cancer and everyone reacts differently which is why we have developed our Molecular Oncology Protocol consisting of several different treatments which we use to create a specialized treatment regimen for your particular case. Below you will find a brief overview of the steps.
We first gather all available medical records and blood tests for a proper evaluation. From this evaluation we determine what additional tests are needed along with what group of treatments will be recommended.
The body is detoxified with various forms of teas, herbs and enemas (coffee, wheatgrass and shark cartilage). Detoxification can also be done with chelation through IV drips.
The Auto Immune system is strengthened. Depending on what treatments have been done in the past, various forms of Immunotherapy, Vaccines and Stem/Live Cell therapies may be administered to build up the Auto Immune system before attacking the Cancer. This can also be done with vitamins, minerals and immune strengthening injections.
Enzyme therapy is added through supplementation of digestive and pancreatic enzymes.
Molecular Oncology treatment. The current medical reports and blood test results will determine which formulation of treatment will be used to attack the patient's cancer. Here is a list of treatments that are used:
Diet Therapy with High Alkaline foods. This can be incorporated with the Gerson diet, the Wigmore Diet, The Budwig diet, and the Hoxsey therapy.
Mental and Emotional Therapy by exercising and controlling symptoms with faith.
Biochemist Otto Heinrich Warburg, one of the twentieth century’s leading cell biologists, discovered that the root cause of cancer is too much acidity in the body, meaning that the pH, potential hydrogen, in the body is below the normal level of 7.365, which constitutes an “acidic” state. Warburg investigated the metabolism of tumors and the respiration of cells and discovered that cancer cells maintain and thrive in a lower pH, as low as 6.0, due to lactic acid production and elevated CO2. He firmly believed that there was a direct relationship between pH and oxygen. Higher pH, which is Alkaline, means higher concentration of oxygen molecules, while lower pH, which is acidic, means lower concentrations of oxygen…the same oxygen that is needed to maintain healthy cells.
In 1931 he was awarded the Nobel Prize in Medicine for this important discovery. Dr. Warburg was director of the Kaiser Wilhelm Institute (now Max Planck Institute) for cell physiology at Berlin. He investigated the metabolism of tumors and the respiration of cells, particularly cancer cells. Below are some direct quotes by Dr. Warburg during medical lectures where he was the keynote speaker:
“Cancerous tissues are acidic, whereas healthy tissues are alkaline. Water splits into H+ and OH- ions, if there is an excess of H+, it is acidic; if there is an excess of OH- ions, then it is alkaline.”
In his work The Metabolism of Tumors Warburg demonstrated that all forms of cancer are characterized by two basic conditions: acidosis and hypoxia (lack of oxygen). “Lack of oxygen and acidosis are two sides of the same coin: where you have one, you have the other.”
“All normal cells have an absolute requirement for oxygen, but cancer cells can live without oxygen - a rule without exception.”
“Deprive a cell 35% of its oxygen for 48 hours and it may become cancerous.”
Dr. Warburg has made it clear that the root cause of cancer is oxygen deficiency, which creates an acidic state in the human body. Dr. Warburg also discovered that cancer cells are anaerobic (do not breathe oxygen) and cannot survive in the presence of high levels of oxygen, as found in an alkaline state.
My wife Stacey noticed a bump on our 5 year old daughter Mary one evening as she was preparing her for a bath before bedtime. It was a Thursday night in October of 2013. She asked me to take a look at it, which I did, and I quickly googled the symptoms and chalked it up to a possible hernia. The next day Stacey took Mary to the pediatrician mainly for a sore throat and a planters wart on her foot ,but also had them look at the bump in her groin area while they were there. The female pediatrician had Mary lay down and examined the bump. She then immediately called our local childrens hospital, which is a large institution, and told them that she had a 5 year old female that she is going to be sending down to them for some further testing of this bump. The doctor did not want to alarm Stacey so she didn’t show her true concern for Mary. Stacey agreed to make the trip to the hospital. The testing began late that afternoon on Friday Oct 4th 2013. One test lead to another as Stacey and Mary held onto their last couple of hours of normalcy unbeknownst to them and me. It wasn’t until a doctor entered the emergency room after all of the regular er doctors checked her out and introduced herself as doctor so and so from oncology. The doctor didn’t realize that Stacey had no clue of Mary’s diagnosis. The doctor also didn’t realize that “fear” was dragged into the room with her.
“Excuse me”, Stacey exclaimed. “Could you tell me why you are here in our room”. The two of them stepped out of the emergency room for privacy as the oncology doctor went on to tell Stacey that Mary had a very large tumor in her abdomen and they were going to need to do more testing. Our 5 year old Mary had a tumor in her belly and now someone from oncology is testing her......OH my God! How could this happen to us?
Conventional wisdom tells you that these doctors are the best and they are going to give you the best that the world has to offer in regards to treating this. I mean this was the #1 or #2 childrens hospital in the United States. And the US is the best in the world right. So who are we to question the best. We did get a second opinion from the leading oncology specialist in the Wilms tumor arena and his advice was very much the same as the first opinion. The protocol was a couple months of chemo to try and shrink this bilateral Wilms tumor that was attached to Mary’s kidneys. One side of the kidney was worse than the other and Mary was a rare condition. Before any of this though there would be a minor operation to install a port in the chest for the chemo meds and they would remove a small piece of the tumor. Once they did the biopsy of this tumor they would send it off to a lab and put it under a microscope to get more results. This was all standard procedure and I have come to find that, yes, it really is standard procedure in this country and probably other countries as well?
The port was installed a couple of days after the diagnosis and the chemo came immediately after that. Mary was given dose after dose of multiple chemo concoctions. The chemo meds all had lots of letters and lots of side effects. From October until late December Mary was in and out of the hospital fighting off all kinds of illnesses as they tried to shrink the tumors with the big name meds. The plan was once the tumors were reduced in size they would then go in and operate. The operation was to remove any tumors and most likely perform a nephrectomy of the diseased kidney. This is exactly what happened, so on Dec 23rd 2013 Mary had a 3 hour operation.. The surgeon removed 3/4 of her right kidney, part of the left kidney and any tumors as well. The operation was a success and Mary spent several days in PICU until she was stable and able to be moved to a regular oncology hospital bed. Now that they had the larger tumor out and in the lab the pathology team could perform a more in depth examination. What they found was not good news for Mary. The tumor was more aggressive than what they first thought and Mary’s odds went from 75% survival to 35%. Also they were going to have to go in and remove the rest of the right kidney because they feared it was likely to grow more tumors in the future. This operation would be a much simpler one and the recovery would be much quicker. So on Dec 26th 2013 the surgeon and Mary went back to the operating room and did exactly what they told us they would. Mary was now down to a little more than 3/4 of a kidney. The fun was not over just yet. Once she was fully recovered from the surgeries we would go back to our home hospital and start the radiation along with a more aggressive chemo. Mary had 18 rounds in total of both radiation and photon radiation during the early months of the new year of 2014. Mary was completely bald with a feeding tube down her nose because she couldn’t eat from the chemo and radiation. We thought this was our lowest point when a tumor developed in her chest somewhere along the way and Mary was now going to be heading into surgery once again. The pea sized tumor in her chest would be removed during this last relatively quick surgery. All went well, but the oncology team still didn’t have any answers on how to stop the tumors other than more chemo and possibly stem cell. It was now April and more chemo, then May and more chemo, then came June and the oncology doctors were pushing stem cell treatment. All the while Mary was in and out of the hospital trying to hang onto her childhood. The stem cell is where they crush her body with the heaviest chemo regime and then when her body is depleted of just about all its resources they put the stem cells that they extracted from her a few months prior and hope these stem cells can replenish any bad cells with good ones. The odds were not very good and Stace and I were unsure of what to do for our little girl. We were now at 15% survival. We started to look outside the box and I did some of my own research. One way or another we were lead to 2 guys that offered chance. Guy #1 Pat was the PNC 27 guy and guy #2 Fred was the vitamin guy. As these 2 guys and chance were being laid out to us, the sky started to clear up just a little for me anyway. What these guys offered just made too much sense to me, but I had to convince Stacey that maybe this was the way to go. It took a few favorable signs and lots of convincing from Pat and Fred, but God in my testimony put all the right people in place at the right time and there were less clouds than the day before. A conference call to the guys, then another conference call and before we knew it we were done with the chemo and doing what I call regime “hell ya”. Hell ya came to us in the mail after some exchanging of funds with Pat and Fred. Again, Stacey was very reluctant but somewhat patiently optimistic. I was all in and never looked back. Stacey wanted to continue with the chemo while doing the hell ya, but God had different plans as he changed Stacey’s outlook on what to do. We received many signs along the way as we started to take Mary’s destiny by the horns and push Mary’s oncology team out the door. We still kept them in place for monitoring and testing, but the madness of chemo and radiation was over once and for all. I can’t tell you how freeing that made me feel personally. To know that I was not poisoning my daughter anymore was more than I can put into words. We were finally, with the help of 2 strangers, (now allies, friends and heroes), attacking the cancer with PNC-27 and the vitamins, rebuilding the body with the vitamins and not crushing the whole body with chemo and radiation. I say Hell Ya!
The first couple of weeks in late June when we first started “hell ya” it took some getting use to for Mary. She was taking PNC by nebulizer 3 times a day and downing around 20 pills daily as well. It was a lot for Mary, but this kid did it and fought her way through something bigger than maybe she realizes or I realize for that matter. We continued on this path every day as we waited for her next scans to see if this was for real? Mary had CT scans, blood work, and an MRI on Aug 11th 2014, so we had been doing “hell ya” for just about 5 weeks. Mary’s scans were all clear and her blood work was improving tenfold to all the normal levels. The doctors didn’t know how to respond, because this was not suppose to be happening. All I can say is that it was a good day for our family that day.
Mary has been doing the “hell ya” regime since June of 2014 and we haven’t missed one day of hell ya since we started. We have cut back to a maintenance kinda version of hell ya that I call heck ya, but it is still the same stuff just less of it. We believe in it and the proof is in the pudding. Most people don’t believe my story when I tell them, but I don’t care. When truth slaps you in the face and you choose not to feel it, well then shame on you.
My daughter Mary was a real hero during this whole trial. She took everything they gave her and hung onto her childhood while doing it. I am happy to report that Mary is now in 1st grade and the memory of this whole ordeal is fading into the horizon like a forgotten sunset. She plays soccer, basketball and is as much of a 6 year old as any other child. Yes she only has 3/4 of one kidney, but that appears to be all she needs.
Mary has been scanned 3 times since hell ya and each time they can find no signs of any cancer in her body. She is scheduled for another MRI this coming August 2015 and I suspect they will find nothing again and again and again.
We thank God every night for what we call Mary’s Miracle as I kneel down before him and give thanks for everything.
We use a unique delivery system which moves minerals, such as Zinc and Copper, through the epidermal layers across semipermeable membranes very quickly to immediately be absorbed by diseased or healthy tissues at very low concentrations.
The Krebs cycle is a charting of the metabolic pathways that healthy plant or animals cells must follow to perform all functions supporting life. There are approximately thirty-two (32) steps in the process. The steps allow healthy cells to expel excessive amounts of toxic materials continuously, including minerals and other nutrients unless totally over-whelmed.
Diseased and/or mutated cells (such as cancer cells) do not follow the Krebs cycle. Rather they follow an alternative metabolic cycle with only about eighteen (18) steps and absorb all foods (particularly sugars). The diseased cells will also take up excessive amounts of minerals such as Zinc and Copper (in our formulation) in amounts that are toxic to them, causing the diseased cell to die. The surrounding healthy tissues (following the Krebs cycle's 32 steps) take up only the amounts of Zinc and Copper needed to function and excrete the excess minerals. Following the Krebs 32 steps versus the 18 steps that cancer and other diseases follow saves normal healthy tissues while killing the diseased cells.
In summary, we are able to transport our highly available Zinc and Copper to our target diseased cells (including cancer cells) and kill only the diseased cells, leaving the healthy normal cells surrounding them functioning without disruption.
Further, a sheath of bacterial cells (also non-Krebs cycle) often surrounds a mass of mutated cells in this shield. The mass of mutated cells are then exposed to the immune system and are destroyed.
This is an uncomplicated explanation of a highly complex system that was very difficult to develop. It took many years of study to devise a strategy that is effective against several terrible diseases.
Origin of the Disease
The treatment involves topical administration to targeted areas, starting with the skin areas surrounding the known origin of the disease. Additional applications are applied to the regional lymph nodes serving the area.
Prevention and Detection
Treating the sentinel lymph nodes and organs (collecting ducts) of the lymphatic system such as the thymus and spleen may reduce the potential of current or future metastasis of non-normal cells.
The manufacturer does not believe nor does it claim that this product is a permanent cure to any medical condition or disease. The treatment is not considered a permanent “cure” for any disease as it is possible that the removal of existing cellular tumors or other non-productive cells does not preclude the possibility of a future return of new mutated cells or tumors. Therefore, it is possible and even probable that re-treatments may be indicated.
Non-clinical trials have indicated that the product impacts several types of viral, bacterial and/or non-typical cell related conditions. However, these diseases may return and the manufacturer recommends a continuing “maintenance program” of treatment by applying the formula twice per week to various parts of the body.
The length of treatment depends widely on the location and severity of the condition and the strength of the immune system. Phases of the treatment can be considered as follows:
Some skin conditions can be successfully treated in days. Some subjects with internal conditions have treated for as long as four weeks before the development of a noticeable reaction indicating the treatment is working. Some subjects with advanced diseases have used the CC Treatment three times per day until reactions subside. Thereafter use twice each week may help to discover and/or prevent a reoccurrence of the condition.
For early stage disease, detection and maintenance of non-normal cells, a recommended dose of 10% of the Active Ingredient is suggested. For late stage disease and severe cases a stronger dose is initially suggested, containing 17% of the Active Ingredient. This can be reduced to the lower dose 10% after reactions decrease or subside.
Low dose periodic maintenance is recommended in the area of disease origin and surrounding lymph nodes. This will prevent a buildup of non-normal cells. Monthly, once per day applications for 5 to 7 day periods, if reaction occurs continue use till it subsides.
The use of this formula may produce one or more of the following expected reactions, which confirm that the treatment is working correctly:
All of these conditions should resolve themselves with no residual effect or scarring.
These effects indicate that the treatment is working and that the body is expelling the dead disease cells. Users should not stop treatment because of the effects listed above.
Treatment should not be stopped until after these effects stop.
As clinical trials are still ongoing it is too early to identify side effects which could be attributed solely to the formula, with the exception of the, expected reactions described above. The manufacturer received a few reports of stiffness of the joints and/or muscle soreness.
While many users experience no discomfort, the risk of discomfort or moderate pain due to the use of the formula is possible, depending on the severity of the affliction of mutated cells present in the skin or body. A few subjects have experienced extreme pain, however there is limited experience with all types of diseases and severe pain may only be typical with certain diseases.
Users have observed that the disease cells are typically killed and expelled by the body, either via the skin, urine, or feces. Subjects have experienced ulcerations and moderate to severe pain where tumors have come through the skin to be expelled after tumor cells were killed by the treatment. In most cases, this left no noticeable scars.
Yes, you should discuss this with your doctor before beginning the CC Treatment and throughout the treatment period. If you have a reaction which is not on the list above of expected reactions, talk to your doctor. If you experience pain during treatment, your doctor may be able to help you manage the pain.
This information is not intended to replace a one-on-one relationship with a qualified healthcare professional and is not intended as medical advice. In case of questions, contact your physician or get in touch with us here. If any instructions which you receive from this paper or web site conflict with those from your physician, your physician’s instructions should always be followed.
All ingredients are Generally Regarded as Safe (“GRAS”).
The manufacturer has conducted several years of non-clinical trials with the formula. No patients reported any adverse effects from liberal and/or long-term use of the formula. This does not preclude the possibility of side effects from the prolonged use of extraordinary amounts of the formula and more research is required to make a final determination. Blood tests on one patient who used large doses of the treatment did not show elevated mineral levels. As with any experimental treatment, dosing levels are uncertain and risk of overdosing cannot be eliminated. Formal dosage studies have not yet taken place.
Do not use this formula if you are allergic to copper, zinc, or any of the ingredients. Do not use this formula if you are pregnant or on children under 12 years of age. This treatment or procedure may involve unknown risks to the subject (or to the embryo or fetus if the subject is or may become pregnant) which are currently unforeseeable.
The ionic minerals are highly Bioavailable and can penetrate the skin. Users have reported that the formula is systemic (affecting the region where applied and potentially the entire body). Systemic therapies employ carrier agents which travel through the body’s fluids and can affect cells throughout the body.
The CC Formula is still in the experimental stage. Thus the manufacturer has not applied for approval as a drug in any country. As a result, those distributing the product are prohibited from claiming that it treats or cures any disease and no such claims may be made on the label.
The risk of sickness or serious illness due to the use of this formula is considered minimal by the manufacturer, because all ingredients are considered Generally Regarded as Safe (“GRAS”) under United States 40 CFR 180.1001 entitled the “Exemption from the Requirements of a Tolerance.” The key mineral components in the formulation are considered nutritional elements for plants and animals. There have been no adverse effects reported by any of the over 100 users during over eight years of non-clinical trials.
The concentrations of each ingredient in the skin cream are below the maximum permissible levels established by the European Union for cosmetics. Thus is it considered safe for application to the skin. The product has successfully passed formal skin irritation and microbial testing.
Some of the ingredients are concentrated minerals that are readily expelled from the body when assimilated in excess of the normal daily nutritional requirements. More research is required to develop a complete understanding of all of the possible benefits and consequences of the use of this formula.
This formula contains a patent-pending technology which makes its key ingredients much more bioavailable than others. The manufacturer believes that this will deliver minerals directly into non-typical cells which adversely impact the health of humans, other animals, and plants. These minerals are pharmaceutical-grade, balanced, ionic minerals which have been combined with a unique delivery technology “Mineral Complex System”.
Store this product out of direct sunlight between 60 - 80 degrees fahrenheit (15.5 - 26.7 degrees celsius). Do not refrigerate or freeze.
Possibly. There have been instances where users reported discolored clothing and/or cloth.
The content below is provided for informational purposes only.
Stem cells have the remarkable potential to develop into many different cell types in the body. Serving as a sort of repair system for the body, they can theoretically divide without limit to replenish other cells as long as the person is still alive. When a stem cell divides, each new cell has the potential to either remain a stem cell or become another type of cell with a more specialized function, such as a muscle cell, a red blood cell, or a brain cell.
There are 4 main sources of stem cells:
How is quality control in umbilical cord blood stem cell programs?
Umbilical cord blood is donated from healthy mothers who give birth to full term, normal, healthy babies, it is then screened for major communicable diseases according to the American Association of Blood Banks standards. Only Type O, Universal Donor type is accepted. Blood that passes the test at this level is then sent to a laboratory where skilled technicians use special technology to separate CD34+/CD133+ cells, CD44- cells, and other subtypes. These progenitor cells are then expanded in a medium that is free from any animal products. After peak expansion is reached, the stem cells are frozen in liquid nitrogen and stored.
As for safety concerns, Umbilical cord stem cells have been used for over 18 years in both adults and children in the treatment of cancer and blood disorders, with no reports of secondary diseases or cancers from the use of the cord blood.
How many stem cells are contained in each vial?
Most commonly vials containing 5 million hUCSCs are utilized.
Is there a best time to go for treatment?
The decision to have or not to have stem cell therapies is difficult for all involved. The decision as to what type of cells to use, how to give the cells, what tests need to be done before hand and what treatments need to be done before and after the treatment all vary from case to case. Such questions are best answered by doctors after copies of the patient’s medical records and enrollment forms have been received and reviewed.
What is the general sequence for enrolling in the stem cell program?
How are the stem cells given?
Most infants and small children are given the stem cells via a subcutaneous injection into the tissues adjacent to the umbilicus. Older children and adults are typically given stem cells by IV drip. Blood may be drawn and reinjected to increase the number of growth factors given with the stem cells. Some neurological patients receive hUCSCs by direct catheter implant into the damaged areas of the brain, a procedure performed by an interventional radiologist and operating room team.
Why is a subcutaneous injection used on most children while an IV approach on most adults?
Research has shown that injecting cells subcutaneously near the umbilicus produces notable results. It appears the cells migrate from the injection site and enter the circulation over a period of hours and perhaps days. Since an IV approach is not always easily done on some patients, especially infants and small children, the “subQ” approach is routinely employed on these patients.
In older patients, direct introduction of the cells into the circulation via IV is used. There are some neurological conditions for which a direct infusion of cells into the circulatory system is deemed the best approach to treating the patient.
The use of a subcutaneous IV or combination route is decided based on clinical study and past stem cell patient responses.
How long does it usually take before some change is seen?
It is reported that the first changes appear by the 3rd to 4th week after treatment and major changes are seen during the first 180 days following treatment. They may then plateau and diminish over time, although some patients report seeing new improvements more than one year following a single treatment.
Some patients have seen results almost from the moment the cells entered their bodies, how can the stem cells work that fast?
There is no way the cells could engraft, differentiate and begin “doing their thing” in a matter of minutes or hours. It is felt that the initial results are attributable to growth factors present in the stem cell medium. Also, the cells themselves may stimulate the body to create growth factors and other compounds that foster cell repair and replacement.
Is the reported healing and recovery due to the stem cells or to something else?
First, the umbilical cord stem cells begin to produce a specific growth factor almost immediately after injection which has the power to rescue neurons from a lack of oxygen, associated with conditions that include a stroke or traumatic brain injury. This glial derived growth factor activity can rescue up to 60-70% of dying neurons if administered soon after the injury.
In later stages and in younger patients such as those suffering from cerebral palsy, one type of stem cell (CD34+) has a tendency to produce “white matter cells”. These cells make up the “wiring” that connects one neuron to the next and to the muscles of the body. When you look at a cross section of the brain, the white matter makes up about 60% of the brain’s inner volume. The gray matter is the neurons which are spread over the surface of the brain. While the CD34+ stem cells have been reported to promote some neurons in addition to the glial white matter, the primitive progenitor cells (AC133+) more readily assist with neuronal growth.
Besides rescuing dying tissues by the action of glial derived neuron factors, the stem cells may also save cells by a process called “ cell fusion”. In this method, the stem cells seek out sick and dying cells and melt their body into the dying cell body. This combination cell then has the vitality of the stem cell and its cell nucleus. Such fusion is more often in brain cells that have hundreds of connections with other cells.
How do the stem cells know where to go in the body?
Many studies have shown that stem cells “home” in on specific chemical signals given off by injured, damaged or diseased tissues or organs.
Can stem cell treatment work if the injury or condition is old?
When these signals are weak they require intervention to increase their numbers. There are several ways to amplify these chemical signals. Pre-stem cell treatment programs, comprehensive 5 to 35 day outpatient programs, are recommended in such cases.
Is there anything done at the time of treatment to enhance the likelihood of stem cells entering the brain?
One of the difficulties in getting hUCSCs into the brain lies in the blood brain barrier which slows or blocks entry of many things into the central nervous system including stem cells. Children and adult patients with Multiple Sclerosis and many other neurological diseases have “leaky” blood brain barriers due to the inflammation. Fortunately, a formula has been developed which temporarily opens up the blood brain barrier long enough for a great many stem cells to get into the brain.
What dietary or lifestyle restrictions should be observed prior to and following stem cell treatment?
In general, think in terms of what you should eat if you were a young woman who has just become pregnant.
Recommendations for children being treated:
Recommendations for adults being treated:
What are some factors that can increase stem cell growth?
Serotonin generating foods: Squash, pumpkin, turnips, and celery.
Calcium rich foods: Salmon, sardines, green leafy vegetables, collards, filberts, kale, kelp, mustard greens, prunes, turnip greens, and watercress.
Magnesium rich foods: Avocados, brewer’s yeast, dulse, green leafy vegetables, salmon, and watercress.
Potassium rich foods: Avocados, brewer’s yeast, dulse, raisins, and winter squash.
B complex rich foods: Folic acid is in green leafy vegetables, asparagus, and spinach. Vitamin B6 is in poultry, fish oil, vegetables, sunflower seeds. Vitamin B12 is in poultry, fish and fish oil.
Seaweeds such as wakame and kombu contain sulfated fucoidans which support bone marrow stem cells production.
Avocados also contain tyrosine, a mood elevator. The processing of tyrosine in nervous tissue is associated with the growth and guidance of nerve pathways.
Ginseng for two months can assist with both stem cell growth and stem cell differentiation into specialized cells.
Ginkgo Biloba also assists with stem cell growth and differentiation. However do not take this if you are taking other medications.
DHA (docosahexaenoic acid) rich fish and seafood. This omega 3 fatty acid plays a role in nerve cell growth, cognition and also modulates inflammatory responses.
After the stem cells have been given time to migrate to where they are needed and proliferate they will then differentiate into various cells such as new neurons, red blood cells, immune cells, etc. The following are prudent measures to implement about four weeks after a stem cell injection.
Bone Marrow treatments use a patient’s own cells, which removes concerns about grafts versus host complications. Bone Marrow procedures have been used with irradiation, chemotherapy and chronic immune suppression. Bone marrow procedures are potentially much safer and more effective for regeneration and anti-aging in cases where irradiation, chemotherapy and immune suppression are not required.
The bone marrow contains mononuclear cells, hematopoietic stem cells, endothelial and precursor progenitor cells and mesenchymal stem cells, all of which, in healthy patients, assist in cell repair.
Bone marrow blood is extracted, which is rich in hematopoietic and mesenchymal stem cells, from various locations in the body and then transfused back into the patient. A standard bone marrow transfusion filter is used to prevent bone marrow debris from entering the patient. It is generally considered pain free with a quick recovery.
Anywhere from 100 - 300 cc of bone marrow blood is extracted. This includes about 2 - 5 million CD34+ stem cells and about 100,000 to 500,000 mesenchymal stem cells. The blood also includes growth factors and multipotent progenitor cells.
CD34+ stem cells are capable of self-renewal and differentiation into various cell lineages, including immune and haematopoietic progenitors.
Mesenchymal stem cells are also multipotent. They are able to differentiate into adipocytes, condrocytes, osteocytes and neuronal/glial cells when specific growth factors are used. Mesenchymal stem cells can contribute to neurological repair by migrating to an injury, replacing degenerated neural cells, integrating into the neural network and leading to functional improvement. These same stem cells deliver tropical factors that support neuronal cell survival and induce endogenous cell growth and proliferation and inhibiting neuroinflammation. Mesenchymal stromal/stem cells show great promise for autoimmune as well as heart and neurological disorders.
Bone Marrow Stem Cell have been shown to help:
Many companies throughout the world offer Adult Stem Cells or Umbilical Cord Stem Cells however it is globally known that Embryonic Stem Cells (known as ESCs) are the most powerful cells and provide the best results. Stem cells are controversial due to some being derived from a blastocyst, which is a five day old embryo, however stem cells can also be obtained through In Vitro Fertilization (IVF).
What are Embryonic Stem Cells?
Within 24 hours of a sperm fertilizing an egg, the egg begins dividing into two cells, then four, and so on, until it becomes a hollow ball of cells called a blastocyst. This process is then interrupted for the harvest of ESCs.
If it is not interrupted within three weeks, blastocyst cells begin to differentiate, starting with nerve cells.
The cells from the moment of conception to the eighth week of pregnancy are called embryos. After the eighth week and until the moment of birth, they are called fetuses.
Depending on where or when they are harvested, the rejuvenation potential of Stem Cells will differ.
Optimally Embryonic Stem Cells are harvested after the 4 to 5 days of divisions from the blastocyst left over from in vitro fertilization. The blastocyst of 150 or so cells is then extracted and cultured in petri dishes. The 150 cells will divide into millions of ESCs which have the capability of becoming any type of cell, these are known as pluripotent. The cultured ESCs are then mixed with plasma as the final step before infusion.
What are the differences between ESCs, Adult and Umbilical Cord Stem Cells?
Adult Stem Cells are harvested from grown organs such as bone marrow, blood or fat tissue of the patient, and re-injected. Studies have concluded that adult stem cells are only able to develop into a limited number of cell types related to the tissue that the stem cells originally came from, in other words, they are multi-potent.
Umbilical Stem Cells are adult stem cells taken from a baby’s Umbilical Cord. Risk of rejection is usually greater when using Umbilical cord stem cells. ESCs are the only pluripotent Stem Cells. They are also the only stem cells to produce anti-cancer proteins.
Autologous cells have proven to be the best Stem Cells available, the ultimate healing and rejuvenating option, however the technology to produce them is time and labor extensive and requires highly skilled techniques.