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Archive for the ‘Stem Cell Tourism’ Category

Stem Cell Treatment in India | Stem Cell Therapy in Uttar …

Thursday, May 2nd, 2019

We have expanded an expertise & capacities in accumulating and separating stem cells from the available organic material Adipose Tissue, Umbilical Cord Blood & Tissue, Amniotic Fluid, Amniotic Sac, Dental Pulp, Bone Marrow and Menstrual Blood.

We truly believe that stem cells is the perfect future to prevent age related degeneration. A period will come when the bodys own particular cells will assist in restoring youth and staying healthy without any drugs.

As the main health care consultant, stem cell center takes care of all section of the medical Tourism to New Delhi. We guarantee our patients get the best health care services by bringing in place, the famous multi-specialty hospitals, recent stem cell treatments, economical accommodations and travel alternatives for the patients.

We are passionate about the recent developments in stem cell therapies in India and endeavor to deliver safe and viable treatment alternate to patients all over the world at the highest medical standards.

At stem cell center, we have a vigorous team of researchers and clinicians at the helm of fundamental research in stem cells. We trust in creating a network of researchers and experts who are bound by a common interest and add to each others comprehension of the subject.

Our Stem cell Treatment services for Degenerative diseases

Spinal Cord Injury

Non-union Fracture

Peripheral Arterial Disease

Optic Nerve Damage

Diabetes

Brain Stroke/Injury/Coma

Avascular Necrosis

Coronary Arterial Disease

Retinitis Pigmentosa

Acute/Chronic Kidney Disease

Cerebral Palsy/Atrophy

Rheumatoid Arthritis

Macular Degeneration

Myocardial Infarction (MI)

Autism

Knee Cartilage Damage

Muscular Dystrophy as DMD, LGMD & BMD

Parkinsons Disease

Lung Fibrosis or COPD

Alzheimer Disease

Diabetic Foot Ulcer & Gangrene

Motor Neuron Disease

Sports Injury Treatment

Multiple Sclerosis

Liver Cirrhosis

Our Vision

The vision of stem cell center is to be a pioneer in the zone of stem cell research, stem cell banking and development of numerous stem cell based procedures and products that will address the neglected medical requirement.

Our Mission

In accordance with the activities of the group in the area of hematology, pathology and transfusion drug, stem cell based medicine will be the following in the pipeline .The group has the mission to think with cell based procedures and results of highest quality for clinical utilize. The mission is to have an authorize facility that meets the directions of both Indian and global standards.

If you have any queries related to stem cell therapy then contact us without any hesitation on our contact numbers:-

Md. No:- +91-9650988899, 91-9891404143

To get quick response, fill our quick contact form

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Adult Stem Cell Therapy Is A Resounding Healing Success …

Thursday, May 2nd, 2019

Adult stem cell therapy is enjoying widespread success around the world, but if the FDA gets its way, it may soon be banned here in the U.S....

There have been nearly 12,000 adult stem cell therapies performed in the United States with an over 90 percent success healing rate for mostly joint and spinal conditions. It involves using the patients own stem cells, so no patent-able drugs are involved.

They are targeting the most influential stem cell scientist in the U.S., Dr. Kristin Comella in Florida.

Differentiating the Types of Stem Cell Therapy

They could be considered seeds for growing body tissues. They are mostly able to function for cellular repair and growth no matter what organ is in need of repair or healing from chronic inflammation.

There is a considerable controversy surrounding stem cell therapy research, a branch of regenerative medicine. Much of the controversy has to do with not differentiating between adult stem cell therapy and embryonic stem cell therapy.

Read: Scientists Discover That Fasting Triggers Stem Cell Regeneration & Fights Cancer

Embryonic stem cell therapy is the controversial one. It cultures or creates stem cells from terminated or aborted fetuses.

Currently, the FDA is harassing stem cell clinics that do not derive their stem cell solutions from aborted fetus tissue. They extract the stem cells from the patients own adipose tissue and inject them into areas where that same patient needs repair. Its an autologous process called adult stem cell therapy.

U.S. Stem Cell based out of South Florida is one of the clinics being targeted by the FDA, and the clinics Chief Scientist is Dr. Kristin Comella, PhD.

Many other nations have been using adult stem cell therapy successfully over the past 15 years, leaving the USA dead last in this field. The FDA is trying to make sure it stays that way and allows costly pharmaceutical versions to prevail.

Dr. Kristin Comella and her clinic have been under attack from the FDA.

This short 3-minute video was produced interviewing Dr. Comella and some of her patients.

Examining and Comparing the Different Types of Stem Cell Therapy

Human embryonic stem cell (hESC) therapy has received most of the medias attention and government support. But it is the most controversial because it involves extracting tissues from terminated human embryos, aka aborted fetuses.

In addition to moral and ethical issues, human embryonic stem cell (hESC) solutions create cells so rapidly where theyre injected they lead to cancerous tumors. To avoid that, researchers have to use immuno-suppressant drugs to curb the embryonic stem cells tendency toward cancer.

Using pharmaceutical drugs to curb hESC cancer side effect issues leads to other unexplored and unexpected side effects from those patented stem cell solutions.

But the profit motive for embryonic stem cell therapies was strong and a lot of government funds had been put into its research. Pharmaceutical companies were motivated because they could patent stem cells created from embryonic tissues.

Bone marrow stem cell therapy was among the first to depart from flawed hESC (human embryonic stem cell) therapies developed over the past two decades. Bone marrow stem cell therapy was the segue into the adult stem cell therapy movement.

Bone marrow extractions are painful, requiring general anesthesia. Its relatively difficult and expensive compared to adipose (fat) tissue stem cell harvesting.

Bone marrows high white blood cell count also encourages inflammation, making it counter-productive for patients already suffering from chronic inflammation or autoimmune disorders.

Most importantly, adipose (fat) tissue yields up to 500 times more mesenchymal stem cells than bone marrow sources, according to Dr. Comella. These are potent stem cells that can differentiate into a wide variety of other cell types. Furthermore, the adipose white blood cell count is lower than bone marrow matter.

Overactive, confused immune responses attack organs continually and create chronic inflammation and autoimmune diseases. The lower white blood cell count automatically lowers the risk of further inflammation among patients already suffering from chronic inflammation and autoimmune diseases.

The outpatient treatment involves creating a very small and shallow incision that wont require stitches on an area of skin covering adipose tissue (fat). From there, liposuction can withdraw a portion of the fat. This part of the procedure requires only a local anesthetic.

Then what is extracted is spun at high speed in a special centrifuge to isolate the stem cells which are then purified for IV drip delivery or injection into the same patient from whom it was extracted. Total costs range from five to ten thousand dollars or more in some cases.

Dr. Comella and her colleagues mission is to get adult stem cell therapy available for everyone. Private and government health insurance providers cover medical treatments that are much more expensive.

Why not cover one that would save money with its lower expense and fewer side effects?

Over the years, there have been nearly 12,000 adult stem cell therapies performed in the United States with an over 90 percent success healing rate for mostly joint and spinal conditions as well as heart and lung issues.

But the three known adverse side effect cases continually get all the media attention.

The Panama College of Cell Science, which helped launch Kristin Comellas research and development, had this to say about her:

"Perhaps the most influential clinician on the subject of adult stem cell therapy, Dr. Comella has been able to quietly develop patient treatment protocols and treat patients via collaborating physicians and health care providers using legal patient-specific FDA guidelines, including studies permitted by Institutional Review Boards, patient-specific stem cell clinical trials, and direct treatments using the patients own stem cells that are harvested and re-injected for therapeutic purposes.

"Through Dr. Comellas leadership, she and her team have trained and certified more than 700 physicians worldwide in adult stem cell therapy." (Source)

The interview below allows the energetic Dr. Kristin Comella to give a thorough and upbeat description of adult stem cell therapy.

Big Pharma Is Using the FDA to Eliminate Unregulated Adult Stem Cell Competition

Since the late 1990s, adult stem cells used therapeutically were not under the control of the FDA and the adult stem cell movement took off.

There were complaints from some MDs that the adult stem cell practice should be regulated by the FDA. The Panama College of Cell Science responded to those outcries with this statement:

"The motive in opposing adult stem cell therapy is money. The big institutions want to keep federal funding of embryonic stem cell research at a high level with the promise that cures are just around the corner despite the fact that embryonic stem cells will never be useful in any way for patient treatment because they immediately cause tumors when transplanted." (Source)

Adult stem cell therapy is an autologous treatment method. The stem cells are not lab-created. They are only isolated and purified after extracting them from the patient being treated. Injecting them back into that patient powers up the bodys own healing mechanism to overcome chronic ailments.

The FDA didnt and shouldnt have anything to do with regulating stem cells from ones own body. That situation has recently been arbitrarily and suddenly changed.

Around 2014, the FDA started tweaking their guidance rules for stem cell therapy with the purpose of getting new rules made into laws through Congress that could be interpreted according to FDA whims and enforced arbitrarily. Their agenda is to consider adult stem cells as FDA-regulated drugs.

During our phone conversation, Dr. Comella explained how the FDA ignored testimonies from adult stem cell practitioners during their 2015 public hearings regarding new guideline proposals. Then they arranged to create new rules behind closed door meetings that included pharmaceutical industry allies and insiders.

The result was that by 2017, the FDAs hands-off policy with adult stem cell therapy came to a sudden halt after years of highly successful stem cell practice.

By 2018, the FDA got nastier with the the most influential clinician on the subject of adult stem cell therapy as its target. The FDA started doing inspections of Dr. Comellas South Florida clinic that are designed for labs that manufacture drugs.

The standards for hospitals and clinics are not as strict as drug manufacturers. Those inspections were inappropriate for a clinic. But those inspections made it easier to create damaging reports.

When the inspectors came by, they demanded to go into rooms while treatments were taking place with semi-nude or nude patients, which Dr. Comella prohibited. The inspectors also demanded to view patient medical records. She allowed that after redacting their names on the copies she gave them.

For her actions to protect patients privacy, inspectors allegedly cited Dr. Comella for resisting and obstructing FDA inspections.

Soon after the inspections, the FDA served Dr. Comella with a lawsuit for practicing medicine with unapproved drugs. The drugs were only those stem cell solutions drawn from patients to be used on them.

The FDA has allegedly offered to drop the lawsuit if Dr. Comella signed an agreement to stop doing adult stem cell therapy and no longer promote it.

She refused. She said she has witnessed people leave their wheelchairs for good from this therapy. The trial is set for a Federal Court hearing beginning June 2019, in Miami, Florida.

If Dr. Comella loses this court case, adult stem cell therapy in the USA may be forced out of the country and only be available to those who can afford medical tourism.

Reference: HealthImpactNews.com

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Top 10 Destinations for Stem Cell Therapy – PlacidWay

Monday, April 29th, 2019

Top 10 Destinations for Stem Cell Therapy

Stem Cell Therapy has made tremendous progress over the past decade. The years of approved clinical trials have shown that stem cell therapy works for certain conditions. Patients should understand that although stem cell therapy can do wonders for some diseases and illnesses, it is not for everything and everyone.

Before choosing to undergo stem cell therapy patients should undergo a thorough research about the viability of the treatment in a certain country. Unfortunately, there are many clinics which state that they are accredited and that their treatment is approved, only to attract patients and money. Stem cell therapy can be categorized into:

1. Clinically-proven stem cell therapy

Such a clinical trial program costs millions of dollars, therefore only a few accredited institutions and centers had the possibility to undergo such programs.

2. Non-approved stem cell therapy in accredited centers

Competent physicians working in accredited centers can offer non-approved stem cell therapies, as long as the patient is informed about the risks and the lack of scientific support.

3. Fraudulent stem cell therapy

Stem cell therapy can be offered by clinics with no accreditation and by physicians with questionable competency. They are the ones who do exaggerated promotional claims about the efficacy and safety of the stem cell therapy, which has no scientific backing.

Studies made so far suggest that stem cells have the potential of developing into different types of cells and so repair the tissue and organs affected by various medical conditions. There are hundreds of different stem cells in our bodies, which are formed at different times in our lives and with different purposes. The embryonic stem cells are found only in the early stages of development, while adult stem cells develop and remain in our bodies the entire life.

Stem cell therapy gives hope where mainstream medical science fails to offer results. So far, the most common stem cell therapy is blood stem cell transplantation for conditions and diseases of the blood, the immune system or to restore the blood after treatments for certain cancer types. Some injuries or diseases of the bone, cornea or skin can be treated using grafted tissue which depends on stem cells from these parts of the body. But people should understand that like any other type of treatment, stem cell therapy can have side effects, and these can vary from individual to individual.

As people will try anything to see at least a slight improvement in their health or their dear ones, more and more are flocking to other countries and to clinics which promote safe and successful stem cell therapy for a multitude of serious conditions. Stem Cell Tourism, as it is called, is in a continuous expansion as patients want to try the promising therapy. But which are the best destinations for stem cell therapy?

South Korea has made tremendous progress in stem cell research, thanks to the country's flexible policies in this matter. Scientists have been able to develop stem cells which genetically match patients of all genders, ages, and races, which means that they can produce stem cells that fit each individual's needs and with a lower risk of rejection. South Korea might soon get to the forefront of stem cell research.

Singapore, also considered Asia's stem cell center, has more than 40 stem cell research centers. Over the years the country has attracted top scientists from all over the world, offering them a host of incentives and the authorization to use embryos for research. This has helped the country to become one of the top stem cell destinations.

China, world famous for its acupuncture and traditional Chinese medicine, plans to become a leader in stem cell research and development. In 2012, the Ministry of Health and the Ministry of Science started to evaluate all stem cell centers that were functioning illegally. This is of utmost importance for future medical tourists who will seek approved and safe stem cell therapy in China.

Stem Cell clinics: Beike Biotech, ReLife International Medical Center

It has been years since patients from the US and Canada have started choosing this destination to get stem cell therapy for serious medical conditions such as paralysis, autism or cerebral palsy. Mexico continues to make tremendous progress in this area and provide safe stem cell therapy.

Stem Cell clinics: Progencell-Stem Cell Therapies

Germany continues to attract patients coming from all over the world for stem cell therapy. The country is known as Europe's Stem Cell hub, thanks to the tremendous progress made in the Adult Stem Cell research and development.

Stem Cell clinics: Anova IRM Medical Center

Stem Cell therapy in Ukraine has helped hundreds of patients suffering from cirrhosis, pancreatic necrosis, burn disease, hepatitis, diabetes, critical lower limb ischemia and multiple sclerosis. The positive results of the therapy, continue to attract international patients.

Stem cell clinics: EmCell Clinic, Unique Cell Treatment Clinic

Austria is another destination preferred by medical tourists for stem cell therapy. Stem cell therapy in Austria has offered a chance to a normal life to patients suffering from Diabetes, Eye Diseases, Neurological Diseases, Gonarthritis or Peripheral vascular disease.

Stem Cell clinics: Stem Cell Therapy Center Vienna

After the US, Turkey has the highest number of JCI accredited healthcare institutions in the world. Turkey is fast-tracking stem cell research and development with new approaches being tested by renowned scientists and physicians. Patientsfrom Europe, Asia, and the Middle East come here to take advantage of the benefits offered by stem cell therapy.

Stem Cell clinics: Leading International Vision LIV Hospitals

Another stem cell therapy leader in Asia is Thailand, a country which, for the past few years has taken stem cell research to the next level by producing cardiac muscle from human embryonic stem cells, successfully using adult stem cells to treat arthritis and discovering a method to extract stem cells from a human amniotic fluid.

Although stem cell therapy might seem for many the last hope, we advise those who begin this journey to look for and seek help from specialists in this type of medical procedure. Experts will help you choose a safe medical destination and a high-quality hospital. Most of all you must understand that stem cell therapy can help some patients, but never cures them.

Being informed and doing a thorough research about what destination, clinic, and doctor to choose is a must when taking such a decision. Get as much information as you can about the center where you plan to undergo the treatment, try to get real patients testimonials, clinical data evaluation, find out about the centers' and doctors' credentials, detailed evaluation of the procedure they use, what methods and types of stem cells they provide, the real cost of the treatment with all expenditures included (airplane, accommodation, meals, hospital and other fees, etc).

By getting informed you will feel more secure, andtraveling abroad for medical carewill be a positive life-changing experience.

PlacidWay can offer you all the information you need for a successful medical experience overseas. Contact us and get more information about any Stem Cell Therapy on our website.Do not hesitate to contact us!

Disclaimer

Stem Cell Therapy is still an experimental treatment. Any information related to Stem Cell Therapy provided on this website is for educational purposes only. It is not intended to either replace a consultation with a licensed physician or be construed as medical advice or any emergency health need you may be experiencing.

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#ACTRIMS2019 Stem Cell Tourism Poses Threat of …

Sunday, April 7th, 2019

Academic neurologists are seeing many patients with neurological diseases interested in or receiving unapproved stem cell-based treatments, sometimes with negative health and/or financial consequences, according to a U.S. survey of neurologists.

The data were reported byWijdan Rai, MD, from Ohio State University in aposter titled Complications of Stem Cell Tourism in Multiple Sclerosis & Other Neurological Diseases: Results from First Nationwide Survey of Academic Neurologists on March 1 atthe 4thAnnual Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) Forumin Dallas, Texas.

Stem cell tourism is a blanket term used to describe clinics (in the U.S. or abroad) that offer unproven cell-based interventions to patients with debilitating diseases, such as Parkinsons disease and amyotrophic lateral sclerosis. The phenomenon of stem cell tourism is rising among patients with neurological diseases, including multiple sclerosis (MS).

According to Rai, an alarming number of stem cell clinics have been accessible to patients, and the need for education has been identified.

Academic neurologists often see patients withcomplications due to stem cell tourism. But, the experiences and challenges that neurologists face in the outpatient practices is unknown, Rai said.

Understanding the experiences of neurologists with patients of stem cell tourism is critical to develop a strategy to educatepatients about it. In fact, a fair amount of neurologists had said that they would find really helpful to have some sort of educational tool, because they were not prepared to answer certain questions about stem cell tourism and its complications, said Rai.

To fill this knowledge gap, researchers fromThe Ohio State Universitydeveloped a 25-question survey focused on academic neurologists in the U.S. and their experiences with and attitudes about stem cell tourism, and associated patient-reported complications. The survey wasdistributed using a web toolcalled Synapse to members of the American Academy of Neurology.

Academic neurologists were targeted because they have specialized and informed knowledge about experimental cell-based therapies. In total, 204 across the U.S. completed the survey, andwere specialized in a range of neurological fields, with about one-third of them specializing in MS.

The survey results showed that nine out of 10 neurologists (91%) had been asked about stem cell treatments by patients or family members/caregivers 37% of these patients had an MS diagnosis.

About two out of three respondents (65%) had a patient who had received stem cell therapies.

Patients most often wanted general information about stem cell therapies from their neurologists. Half of the patients requested permission to undergo a stem cell procedure, and 31% approached their neurologist after the procedure.

Among patients undergoing stem cell treatment,33% reported the treatment was performed in the U.S., 22% reported going abroad, and37% reported procedures both in the U.S. and abroad. The procedures abroad were performed inChina, Germany, the Bahamas, Mexico, Russia, and Costa Rica.

Rai said 75% of the physicians indicated that no patient experienced complications from these unapproved stem-cell-based treatments.

However, one in four (25%) reported seeing patients who experienced complications, such as infections, MS deterioration and relapse, stroke, meningoencephalitis, sepsis, tumors, hepatitis C, seizures, or spinal cord injury.

At least three neurologists had patients who died from unapproved stem cell procedures.

These results are sad, Rai toldMS News Today, because there is actually legit, approved research happening on stem cell therapy, and their complication rate is very low. So its tough to see that it can be done really well, but when its done in a sort of unregulated or unapproved sort of fashion, you can not only have a lot of these kind of complications, but also have a huge financial burden.

According to the researcher,patients reported significant financial burden with no benefit, with treatments costing $20,000 to $25,000, up to $80,000 per procedure.

Stem cell tourism is an emerging public health threat, and the resultsdemonstrate an alarming number of unreported complications and negative impact to MS patients, Rai said.

Therefore, the team believes in a multipronged approach to improve the education of MS patients to prevent exploitation and engaging multiple stakeholders in the field, including MS academic societies, licensing boards,and legislative bodies.

Specifically, the researchers suggested the creation of evidence-based education for neurologists and patients, including resources that neurologists can use when discussing stem cell interventions with patients, and videos on proper counseling during these visits, Rai noted.

The team also advocated for the creation of a publicly available national registry where stem cell tourism complications must be reported, and the development of guidelines on how to care for patients who have undergone experimental stem cell procedures with tumor formation, Rai said.

The researcher said that as a physician, you have to respect patients autonomy, and at the end of the day it is their decision, but we also have to keep in mind that we (physicians) have to do what is best for them and communicate that to (our) patients.

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Four Challenges to Making the Best Stem Cell Models for …

Thursday, March 28th, 2019

Neurological diseases are complicated. A single genetic mutation causes some, while multiple genetic and environmental factors cause others. Also, within a single neurological disease, patients can experience varying symptoms and degrees of disease severity.

And you cant just open up the brain and poke around to see whats causing the problem in living patients. Its also hard to predict when someone is going to get sick until its already too late.

To combat these obstacles, scientists are creating clinically relevant human stem cells in the lab to capture the development of brain diseases and the differences in their severity. However, how to generate the best and most useful stem cell models of disease is a pressing question facing the field.

Current state of stem cell models for brain diseases

Cold Spring Harbor Lab, Hillside Campus, Location: Cold Spring Harbor, New York, Architect: Centerbrook Architects

A group of expert stem cell scientists met earlier this year at Cold Spring Harbor in New York to discuss the current state and challenges facing the development of stem cell-based models for neurological diseases. The meeting highlighted case studies of recent advances in using patient-specific human induced pluripotent stem cells (iPS cells) to model a breadth of neurological and psychiatric diseases causes and patient symptoms arent fully represented in existing human cell models and mouse models.

The point of the meeting was to identify what stem cell models have been developed thus far, how successful or lacking they are, and what needs to be improved to generate models that truly mimic human brain diseases. For a full summary of what was discussed, you can read a Meeting Report about the conference in Stem Cell Reports.

What needs to be done

After reading the report, it was clear that scientists need to address four major issues before the field of patient-specific stem cell modeling for brain disorders can advance to therapeutic and clinical applications.

1. Define the different states of brain cells: The authors of the report emphasized that there needs to be a consensus on defining different cell states in the brain. For instance, in this blog we frequently refer to pluripotent stem cells and neural (brain) stem cells as a single type of cell. But in reality, both pluripotent and brain stem cells have different states, which are reflected by their ability to turn into different types of cells and activate a different set of genes. The question the authors raised was what starting cell types should be used to model specific brain disorders and how do we make them from iPS cells in a reproducible and efficient fashion?

2. Make stem cell models more complex: The second point was that iPS cell-based models need to get with the times. Just like how most action-packed or animated movies come in 3D IMAX, stem cell models also need to go 3D. The brain is comprised of an integrated network of neurons and glial support cells, and this complex environment cant be replicated on the flat surface of a petri dish.

Advances in generating organoids (which are mini organs made from iPS cells that develop similar structures and cell types to the actual organ) look promising for modeling brain disease, but the authors admit that its far from a perfect science. Currently, organoids are most useful for modeling brain development and diseases like microencephaly, which occurs in infants and is caused by abnormal brain development before or after birth. For more complex neurological diseases, organoid technology hasnt progressed to the point of providing consistent or accurate modeling.

The authors concluded:

A next step for human iPS cell-based models of brain disorders will be building neural complexity invitro, incorporating cell types and 3D organization to achieve network- and circuit-level structures. As the level of cellular complexity increases, new dimensions of modeling will emerge, and modeling neurological diseases that have a more complex etiology will be accessible.

3. Address current issues in stem cell modeling: The third issue mentioned was that of human mosaicism. If you think that all the cells in your body have the same genetic blue print, then youre wrong. The authors pointed out that as many as 30% of your skin cells have differences in their DNA structure or DNA sequences. Remember that iPS cell lines are derived from a single patient skin or other cell, so the problem is that studies might need to develop multiple iPS cell lines to truly model the disease.

Additionally, some brain diseases are caused by epigenetic factors, which modify the structure of your DNA rather than the genetic sequence itself. These changes can turn genes on and off, and they are unfortunately hard to reproduce accurately when reprogramming iPS cells from patient adult cells.

4. Improve stem cell models for drug discovery: Lastly, the authors addressed the use of iPS cell-based modeling for drug discovery. Currently, different strategies are being employed by academia and industry, both with their pros and cons.

Industry is pursuing high throughput screening of large drug libraries against known disease targets using industry standard stem cell lines. In contrast, academics are pursuing candidate drug screening on a much smaller scale but using more relevant, patient specific stem cell models.

The authors point out that, a major goal in the still nascent human stem cell field is to utilize improved cell-based assays in the service of small-molecule therapeutics discovery and virtual early-phase clinical trials.

While in the past, the paths that academia and industry have taken to reach this goal were different, the authors predict a convergence between the paths:

Now, research strategies are converging, and both types of researchers are moving toward human iPS cell-based screening platforms, drifting toward a hybrid model New collaborations between academic and pharma researchers promise a future of parallel screening for both targets and phenotypes.

Conclusions and Looking to the Future

This meeting successfully described the current landscape of iPS cell-based disease modeling for brain disorders and laid out a roadmap for advancing these stem cell models to a stage where they are more effective for understanding the mechanisms behind disease and for therapeutic screening.

I agree with the authors conclusion that:

Moving forward, a critical application of human iPS cell-based studies will be in providing a platform for defining the cellular, molecular, and genetic mechanisms of disease risk, which will be an essential first step toward target discovery.

My favorite points in the report were about the need for more collaboration between academia and industry and also the push for reproducibility of these iPS cell models. Ultimately, the goal is to understand what causes neurological disease, and what drugs or stem cell therapies can be used to cure them. While iPS cell models for brain diseases still have a way to go before being more clinically relevant, they will surely play a prominent role in attaining this goal.

Meeting Attendees

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The Stem Cell Treatment Process – regenocyte.com

Thursday, March 14th, 2019

Once you have decided this is the best option for you, we will determine if any other testing is needed which can be done at our facilities in Florida or wherever you live. We will then plan a date for your stem cell procedure in the Dominican Republic. The process begins with the extraction of bone marrow from the top of you pelvis and also from adipose tissue (fat) at the hospital. In our lab, the stem cells will be activated and multiplied by using naturally occurring growth factors. In this process of activation, the stem cells are customized for the purpose for which they will be used in treatment. For example, they can be activated to build muscle tissue for the heart, to rebuild blood vessels in the extremities or lungs or into neural cells for the central nervous system. This process is done overnight.

The following day the activated cells are returned to the patients body by a process which delivers the stem cells to the part of the body that is being treated. You will be informed of your actual reinsertion method as part of the course of treatment developed specifically for you and your injury or disease.

Once your procedure is completed you will spend anywhere from a few hours, to two days in the hospital depending on your specific treatment and your baseline condition. A full report regarding your procedure will be prepared by the treating physicians and will be sent home with you. You will be given follow up instructions and a schedule of follow-up tests to evaluate your progress. Periodically, you will be contacted by our patient care team with interpretation of your test results and to answer any questions you may have.

Our stem cell clinic will help coordinate all of your travel and transportation arrangements. You arrive at the Santo Domingo International Airport in the Dominican Republic and your transportation coordinator will be waiting for you just outside of the airport. They will have a placard with your name on it. Our team will coordinate with you while you are in the Dominican Republic, including transportation to and from the airport, the hotel, and the hospital.

Be advised that a valid passport is required for entry into the Dominican Republic. Information regarding obtaining a United States passport can be found at: The United States Department of State

We have successfully treated patients from all over the world. We pride ourselves in providing the best, most advanced treatment worldwide and look forward to talking with you, your family or friends regarding the possibility of having Regenocyte Stem Cell Therapy change your life.

To get started with evaluation or more information. Contact our stem cell clinic here or call us at (866) 216-5710

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The Stem Cell Treatment Process - regenocyte.com

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Stem Cell Therapy for Autism in Turkey – health-tourism.com

Wednesday, February 27th, 2019

This information is intended for general information only and should not be considered as medical advice on the part of Health-Tourism.com. Any decision on medical treatments, after-care or recovery should be done solely upon proper consultation and advice of a qualified physician.

What is autism?

Autism is an array of disorders which are characterized by visible abnormalities in social interactions and communication. The common medical findings associated in children with the disorder are a chronic immunologically mediated inflammatory condition in the gut and reduced oxygenation in specific areas of the brain.

Current research aims at attempting to reverse the abnormalities through administration of anti-inflammatory agents, antibiotic and hyperbaric oxygen. However, none of these approaches address the underlying causes of the intestinal inflammation or oxygen deprivation.

It is thought that mesenchymal stem cells may help reverse inflammatory conditions and regulate the immune system. The umbilical cord-derived mesenchymal stem cells are administered intravenously by a licensed doctor.

Adult stem cells used to treat autism are harvested from human umbilical cord tissue also called allogenic mesenchymal. The human umbilical cords are donated by mothers after healthy and normal births. They are thoroughly screened and tested for bacteria and viruses.

They are idea for the treatment of autism because they allow for the administering of uniform doses and do not necessitate any stem cell harvesting from the patient, which can be quite concerning for the parents and terrifying for the autistic child. Because the stem cells are collected immediately after birth the umbilical cord-derived cells are much more effective than their counterparts such as bone marrow derived cells.

In addition the umbilical cord derived mesenchymal cells are not rejected by the patient because they do not recognize them as foreign. This is due to the fact that the HUCT stem cells are less mature than other cells. HUCT stem cells also differentiate/proliferate better that older cells and are therefore considered to be more potent.

A typical autism treatment protocol takes about 5 days and involves blood tests and physical examination. Intravenous infusions of the mesenchymal cells are then administered.

The cells are not rejected because the HUCT mesenchymal stem cells are immune system privileged and Human Leukocyte (HLA) matching is not required.

Screening and testing of the best stem cells can be conducted to ensure that the best immune modulating capacity, anti-inflammatory and regeneration stimulation cells are selected.

Administering of uniform dosages with high cell counts can be done with the allogenic stem cells.

The umbilical cord tissue provides a supply of mesenchymal stem cells in abundance.

There is no need to harvest stem cells from the patient under anesthesia which can be very unpleasant t the child.

Umbilical cord-derived mesenchymal stem cells are thought by researchers to be more robust than mesenchymal stem cells harvested from other sources.

Proper follow up after the procedure is necessary to ensure that the patient is progressing well.

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Stem Cell Science | Advanced Regenerative Orthopedics

Friday, February 1st, 2019

Stem cell science is an innovative treatment approach that involves utilizing stem cells to stimulate the bodys natural repair response.

Our doctors gladly educate patients on how stem cell therapy can become an alternative to invasive surgeries. You will learn what stem cell therapy actually is, and how can it alleviate knee, hip, shoulder, or neck/back pain.

Dr. Nick Willett is our chief science officer who specializes on Stem Cell Science and Regenerative Medicine. The overall goal of Advanced Regenerative Orthopedics is providing people who suffer from musculoskeletal diseases and injuries with an alternative to major surgeries. Our main concern is that too many people turn to surgery while it can be avoided, and too many people live with severe pain while it can be alleviated.

Contrary to popular belief, stem cell science does not involve the use of fetal or embryonic stem cells, but rather the use of stem cells derived from fat, bone marrow, cord blood and other sources. While there are many stem cell sources, not all stem cells are equal. In fact, stem cells derived from umbilical cord blood have the greatest ability to regenerate new tissue with little to no risk of rejection. These younger cells are far more powerful than the stem cells derived from fat and bone marrow, and they dont require a donor match as is the case with many other types of stem cells.

In many instances, stem cell science is used to promote tissue healing and recovery for orthopedic patients, and for these patients in particular, the use of high quality, cord blood stem cells is vital to their speedy recovery.

It is important to consider all options before committing to any medical procedure. Do not operate, first consult with a Medical Doctor to determine if Stem Cell Treatment is right for you. Too many people jump to surgery too quickly, dont operate, take your time and consider all options.

Make a call and schedule the NO-COST consultation or attend our FREE seminar to learn how science becomes medicine. Advanced Regenerative Orthopedics wants every patient to be fully aware of impending treatment.

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Is Stem Cell Therapy Safe and Effective? | Berkeley Wellness

Friday, February 1st, 2019

Paul Knoepfler, PhD, is an associate professor at UC Davis School of Medicine with a special research interest in stem cells and cancer. In addition to his research, Dr. Knoepfler is the creator of the Knoepfler Lab Stem Cell Blog, through which he tries to inform people about legitimate stem cell research, and warn them about the rise of stem cell clinics offering unproven and sometimes risky stem cell treatments. Knoepfler is also the author of the book Stem Cells: An Insider's Guide, that examines the ethical issues and regulations surrounding stem cell transplants.

Frankly, there's a lot of stem cell snake oil out there. Weve seen a rise in stem cell tourismclinics worldwide selling treatments that are not proven safe and effective. I don't think the average patient can easily navigate the wild universe of stem cells and be confident they know whether a particular treatment would be safe and effective. Many clinics forgo the usual, accepted path of FDA pre-approval of an experimental therapy such as stem cells.

Not many. Bone marrow transplantation and hematopoietic stem cell transplants are the most established. Otherwise things are experimental and risky.

Many predatory stem cell clinics offer a whole menu of dozens of conditions for which they sell "treatments." For example, a single clinic may sell an adipose (fat) stem cell therapy for 15 conditions, none of which have anything to do with fat. The conditions may range from musculoskeletal disorders to neurological diseases to pulmonary conditionsand the doctor providing the stem cell treatment may have no expertise in those conditions.

There are many issues of concern. Some I mentioned earlier, including the lack of FDA approval, the lack of physician expertise in the area of the patient's disease, the lack of logical reason why a fat stem cell therapy would help a given condition, the lack of proper informed consent, and the lack of compelling data backing up the treatment.

Stem cells are also often administered in ways that don't make a whole lot of sense, such as intravenously (IV) for a brain condition. Stem cells can cause abnormal tissue growth thateven if benigncan be destructive to surrounding tissues. Stem cells can also cause cancer, pulmonary emboli, and immune reactions.

The FDA regulates biological drugs and products, including stem cell therapies. But the FDA does not regulate the doctors directly, as that is the responsibility of state medical boards. And the doctors at stem cell clinics are using the drugs and devices "off label" in ways that were not FDA approved. Is this illegal? We don't have a clear answer, particularly because the FDA has not taken any clear action in the last couple of years on this. (Previously the FDA had issued warnings to stem cell clinics.) The lack of FDA action has created a gray zone in which hundreds of clinics are now operating. That gray zone could suddenly collapse or instead things could stay murky for quite some time. Stuck in the middle are patients.

I recommend that patients talk to their primary care doctor about whether a stem cell therapy might be advisable or not. Patients should weigh the potential risks versus possible benefits, ideally using actual data. They should consider other options, and do as much homework as they can. Unfortunately many patients are understandably desperate for hope; predatory clinics take advantage of such patients. For many patients, cost is also an issue. A single stem cell treatment can cost $10,000, and many patients get more than one transplant. I strongly recommend against letting celebrity patients such as sports stars be the inspiration for stem cell therapy.

I noticed in late 2009 that there was a gap in the stem cell world. Social media and the Internet were dominated by the stem-cell clinic industry promoting this therapy, and by activists opposed to using stems cells from embryos for any medical reason at all. There was a need for a rational voice advocating for the stem cell field and evidenced-based medicine. I would also emphasize that there is much to be excited about with regard to stem cells and hundreds of legitimate clinical trials out there. I am hugely optimistic that stem cells will become a major part of mainstream medicine. But it is important not to jump the gun and do more harm than good by going too fast.

This opinion does not necessarily reflect the views of the UC Berkeley School of Public Health or of the Editorial Board at BerkeleyWellness.com.

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Stem Cell Treatment for Dementia | Stem Cell Doctors …

Monday, January 28th, 2019

Mary Holler, age 82, of Marco Island Florida is smiling again. Mary was suffering from dementia.

She and her husband sought Stem Cell Dementia Treatment.

She felt uneasy with her ability to function on a daily basis. Now, after undergoing a successful stem cell dementia treatment earlier this month, Mary is her old self again. She doesnt ask her husband, Peter, the same question 3-4 times in an hour anymore. Peter Holler, age 83, had become very concerned that his wife of 60 years was slowly losing her memory. She had been on medications for memory loss for several years but the deterioration in her recall accelerated in the last six months.It was starting to wear on him. He was losing his wife right in front of his eyes. Marys poor performance on an in-depth memory test revealed that that she was so advanced that should be in an assisted living facility. This frightened both the Hollers and their children.

Peter Holler sought out stem cell dementia treatment. He felt it was his wifes only option. Peter, no stranger to stem cells, had undergone a stem cell treatment by Dr. Zannos Grekos for his failing heart in 2008. He had experienced great success. Even my lung function improved dramatically, he recalls. Going back to the same group that he had trusted, he made arrangements to get the love of his life treated.

A track record of several successfully treated patients with dementia already existed. So the doctors knew exactly what to do. Heading the team is Dr. Hector Rosario, an interventional cardiologist and head of the stem cell program in the Dominican Republic. Dr Roberto Fernandez DeCastro head of the catheterization lab assisted in the procedure. Dr Grekos, Chief Scientific Officer for the company was present as well. Its very exciting to be able to have such a positive impact on a disease process that otherwise has such a grim prognosis, Grekos explained. The Dementia Treatmentprotocol used to treat Mrs. Holler had been developed specifically for patients with dementia by Dr Zannos Grekos.

Below arebefore(top) and after (bottom) angiogramsof Mrs. Hollers left internal carotid injections:

Stem cells collected from Marys bone marrow are subjected to an activation and concentration process. The stem cells were then injected into her cerebral circulation. Look at the difference, Dr Rosario exclaimed while pointing to the before and after pictures of the brain circulation. The increase in blood vessel flow was astonishing.Since only adult stem cells from the patient are used, the political, ethical, and medical issues are avoided and there is no risk of rejection.

Were able to normalize a patients neuro-cognitive (brain function) testing in 6 months after the stem cell dementia treatment said Zannos Grekos MD, commenting on the success of patients having received adult stem cell dementia treatment to reverse the effects of dementia. Peter Holler agrees, Not only does she not repeat questions any more, but she is also remembering things that she had forgotten. Its a godsend.

Dementia is a loss of brain function that occurs with age and certain diseases. Most types of dementia are nonreversible (degenerative).It affects memory, thinking, language, judgment, and behavior. Alzheimers disease is a common type of dementia.Dementia also can be due to many small strokes or poor circulation. This is called vascular dementia. Many dementias have a vascular component; these are referred to as mixed dementias. Stem cells are especially effective in treating these types of dementias.

Dr. Zannos Grekos colleagues in the world medical field are currently employing adult stem cell therapy and coordinating its application for patients who have exhausted all other traditional therapy options. His presentation at the 16th Annual World Congress on Anti-Aging Medicine & Regenerative Biomedical Technologies conference supports efforts by a global community of doctors that are striving to incorporate adult stem cell therapy into mainstream medicine.

Regenocyteis an international corporation located in Bonita Springs, Florida. Dedicated to leading the world in providing Adult Stem Cell therapies, Regenocyteutilizes the most effective and safest technologies and medical procedures in order to improve the lives of its patients. A video of Dr. Zannos Grekos presentation at the 16th Annual World Congress on Anti-Aging Medicine & Regenerative Biomedical Technologies is available for viewing on the companys website. Additional information on adult stem cell therapy as well as patient video experiences can be found at http://www.regenocyte.comor call (866) 216-5710.

To learn more about dementia please click here

For more information on Doctor Grekos, MD please click here

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Stem Cell Tourism: Caveat Emptor – Neurologist in Orange …

Friday, November 16th, 2018

Posted December 15, 2015 by Jack Florin

Stem cell pseudomedicine is on the rise, becoming highly profitable as patients and families are desperate for a cure for devastating and incurable neurological diseases, such as amyotrophic lateral sclerosis and multiple sclerosis. Treatment with cellular therapy usually costs between $15,000 and $20,000, is not covered by insurance, and is more widely available overseas than in the US, explaining the concept of stem cell tourism. Desperate patients will overlook the lack of rigorously tested scientific evidence and cling to anything, especially patient testimonials found on stem cell tourism web sites. One clinic does biobanking of placental cells in pregnant women with MS. The costs are very high to maintain cell viability with the hope of using them in the future for MS therapy. Other companies tout the concept that patients with MS or ALS can biobank their own skin or placental cells to generate off-the-shelf stem cells to be injected back into the patients in the distant future when the procedures are proven beneficial in clinical trials.

Many clinics advertise with state-of-the-art web sites, on which celebrities and even physicians give flowery testimonials. Often, they state they are conducting an observational cohort study, making the procedures sound official and allowing them to register their study with the government so that it can be found at the generally trusted web site ClinicalTrials.gov.

Physicians, in counseling their patients, must balance patient autonomy with physician beneficence. A hurdle in counseling patients is that the public has a lack of trust in the FDA and a perception that the FDA does not have the best interests of the patient in mind and stalls the development or approval of new therapies. Conspiratorial views are difficult to overcome.

There are real dangers. A child with a rare disease termed ataxia telangiectasia traveled to Russia and received injections into the spinal fluid of neural stem cells and later developed a brain tumor originating from those cells. Two pediatric patients in Germany died because of intracranial bleeding related to injections in a stem cell clinic. A patient in Thailand received stem cell injections directly into her kidney for lupus nephritis. This resulted in a kidney tumor. A clinic in China injected stem cells directly into the spinal cords of hundreds of patients with spinal cord injuries and ALS. There was no benefit, and there were alarming safety issues.

All stem cell therapies are not bogus. There are now several types of stem cells being studied for MS and ALS in reputable medical centers. Stem cell therapies for MS have been done for many years. They can help patients with fulminant MS but do not result in a cure.

Buyer beware.

See JAMA Neurology, November 2015, page 1342.

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Supraspinatus Tendon Tear: Shoulder Pain PRP and Stem Cell …

Sunday, October 14th, 2018

Supraspinatus Tendon Tear: Shoulder Pain Treated with PRP and Stem Cell Therapy

Tampa, Saint Petersburg and Clearwater, Fl

Platelet Rich Plasma (PRP) and Stem Cell Therapy are being used for a variety of shoulder problems. The rotator cuff is one of these shoulder problems that these regenerative therapies is used to treat by Dr. Dennis Lox. The rotator cuff is actually the tendinous insertion of 4 muscles muscles forming a cuff to protect the shoulder joint.

One of these muscles the Supraspinatus, is often injured and may develop tendonosis, partial tears, or unfortunately sometimes a complete tear. The Supraspinatus muscle may be treated with Platelet Rich Plasma (PRP) or Stem Cell Therapy. These regenerative therapies heal and repair by harnessing the bodies own natural healing properties and allowing them to repair in areas that cannot achieve this affect do to injury or poor blood supply. Blood supply is vital providing repair cells to regenerate and heal damaged tissue. Dr. Lox has great experience in treating these problems non-surgically. Improperly healing rotator cuff problems may lead to shoulder joint arthritis. Successful treatment and healing can help prevent degenerative arthritis of the shoulder. Surgery can lead to more shoulder joint trauma. Trauma has been shown to accelerate arthritis. Platelet Rich Plasma (PRP) and Stem Cell Therapy may be effective techniques to treat shoulder pain that wont go away.

Click Here for more ways (PRP) and Stemcells can help

Dr. Dennis Loxserves patients in the greater Tampa Bay area, including, Clearwater, St. Petersburg, Tampa, New Port Richey, Sarasota, and Spring Hill. He has been pleased to accommodate the needs of patients throughout Florida, the United States, the Western Hemisphere, and Europe, as well. Located in the 33765 and 33765 areas, our offices can be reached at (727) 462-5582 (Clearwater) and (727) 817-1909 (New Port Richey). Call to schedule your visit today.

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Canadian clinics begin offering stem-cell treatments …

Sunday, September 30th, 2018

The arthritis in Maureen Munsies ankles was so intense until barely a year ago, she literally had to crawl on hands and knees to get upstairs.

The pain, she recalls now, took my breath away, and played havoc with the avid hikers favourite pastime.

In desperation, Munsie turned to a Toronto-area clinic that provides a treatment many experts consider still experimental, unproven and of questionable safety.

The 63-year-old says the stem cells she received at Regenervate Medical Injection Therapy 18 months ago were transformational, all but eliminating the debilitating soreness and even allowing her to hike Argentinas Patagonia mountains two months ago.

For me its been a life saver, Munsie says. Ive been able to do it all again I dont have any of that pain, at all.

Canadians drawn to the healing promise of stem cells have for years travelled outside the country to such places as Mexico, China or Arizona, taking part in a dubious form of medical tourism.

But Regenervate is one of a handful of clinics in Canada that have begun offering injections of stem cells, satisfying growing demand but raising questions about whether a medical idea with huge potential is ready for routine patient care.

Especially when those patients can pay thousands of dollars for the service.

Clinics in Ontario and Alberta are treating arthritis, joint injuries, disc problems and even skin conditions with stem cells typically taken from patients fat tissue or bone marrow.

The underlying idea is compelling: stem cells can differentiate or transform into many other types of cell, a unique quality that evidence suggests allows them to grow or regenerate tissue damaged by disease or injury.

Researchers including hundreds in Canada alone are examining stem-cell treatments for everything from ailing hearts to severed spinal cords.

With few exceptions, however, the concept is still being studied in the lab or in human trials; virtually none of the treatments have been definitively proven effective by science or approved by regulators like Health Canada.

The fact that Canadian clinics are now offering stem-cell treatments commercially is concerning on a number of levels, not least because of safety issues, says Ubaka Ogbogu, a health law professor at the University of Alberta.

Three U.S. women were blinded after receiving stem-cell injections in their eyes, while other American patients have developed bony masses or tumours at injection sites, Ogbogu said.

Stem cells have to be controlled to act exactly the way you want them to act, and thats why the research takes time, he said. It is simply wrong for these clinics to take a proof of concept and run with it.

Ogbogu says Health Canada must crack down on the burgeoning industry but says the regulator has so far been conspicuous by its inaction.

Other experts say the procedures provided here typically for joint pain are likely relatively safe, but still warn that care must be taken that the stem cells do not develop into the wrong type of tissue, or at the wrong place.

Alberta Health Services convened a workshop on the issue late last year, concluding there is an urgent need to develop a certification system for cell preparation and delivery to avoid spontaneous transformation of (stem cells) into unwanted tissue.

But one of the pioneers of the service in Canada says theres no empirical evidence that such growths can develop, and suggests the treatments only real risk as with any invasive procedure is infection.

Meanwhile, patients at Regenervate have enjoyed impressive outcomes after paying fees from $750 to $3,900, says Dr. Douglas Stoddard, the clinics medical director.

About 80 per cent report less pain, stiffness and weakness within a few months of getting their stem-cell injection, he said. His treatments efficacy, though, has not been tested in a randomized controlled trial, the gold-standard scientific study which would compare the injections to a sham or other treatment and identify any placebo effect.

I believe medical progress is not just limited to the laboratory and randomized double-blind trials, Stoddard said. A lot of progress starts in the clinic, dealing with patients You see something works, you see something has merit, and then its usually the scientists that seem to catch up later.

The Orthopedic Sport Institute in Collingwood, Ont., the Central Alberta Pain and Rehabilitation Institute and Cleveland Clinic in Toronto all advertise similar stem-cell treatments for orthopedic problems.

Edmontons Regen Clinic says it plans to start doing so this fall.

Ottawas Innovo says it also treats a range of back conditions with injections between the vertebrae, and uses stem cells to alleviate nerve damage.

Orthopedic Sport says its doctor focuses on FDA and Health Canada approved stem-cell injection therapy for patient care.

In fact, no treatment of the sort the clinics here provide has ever been authorized.

Health Canada says the vast majority of stem-cell therapies would constitute a drug and therefore need to be authorized after a clinical trial or new drug submission.

A number of stem-cell trials are underway, but only one treatment Prochymal has been approved, said department spokesman Eric Morrissette. Designed to combat graft-versus-host disease where bone marrow transplants for treating cancer essentially attack the patients body its unlike any of the services the stem-cell providers here offer.

But as the U.S. Food and Drug Administration aggressively pursues the hundreds of clinics in America, Health Canada says only that its committed to addressing complaints it receives.

It will take action based on the risk posed to the general public, said Morrissette, who encouraged people to pass on to the department information about possible non-compliant products.

Stoddard said the injections his clinics provide are made up of minimally manipulated tissue from patients own bodies and any attempt to crack down would be regulation for the sake of regulation.

But academic experts remain skeptical about the effectiveness of the treatments.

Scientific evidence suggests the injections may help alleviate joint pain temporarily, but probably just because of anti-inflammatory secretions from the cells not regeneration, said Dr. David Hart, an orthopedic surgery professor at the University of Calgary who headed the Alberta workshop.

Theres a need for understanding whats going on here and theres a need for regulation, he said.

Most of the clinics say they use a centrifuge to concentrate the stem cells after removing them from patients fat tissue or bone marrow. But its unclear if the clinics even know how many cells they are eventually injecting into patients, says Jeff Biernaskie, a stem-cell scientist at the University of Calgary.

Munsie, on the other hand, has no doubts about the value of her own treatment, even with a $3,000 price tag.

The procedure from extraction of fat tissue in her behind to the injection of cells into her ankles took barely over an hour.

Within three months, the retired massage therapist from north of Toronto says she could walk her dogs again. Last week, she was hiking near Banff.

Im a real believer in it, and the possibility of stem cells, says Munsie. I just think Wow, if we can heal with our own body, its pretty amazing.

(The story was modified July 6 to clarify lack of clinical-trial evidence for Regenervate procedures.)

tblackwell@nationalpost.com

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Hospitals in Guatemala | Medical Tourism Guatemala

Sunday, September 30th, 2018

Guatemala City has the largest Medical District of all of Central America, a city within the city, dedicated almost exclusely to private medical providers. Besides the many private clinics and laboratories, the medical district consists of 5 large private hospitals and a top notch radiotherapy center, equipped with the most up to date technology.

Those private hospitals cater to the Guatemalan middle class, as well to the Americans and Europeans residing in Guatemala. The following medical specialties are taken care of in Guatemala-Citys medical district: cardiology, orthopedics, gynecology, obstetrics, bariatric and gastric surgery, organ transplant, pediatry, oncology. The choice of your hospital depends in large extent of which hospital your Specialist MD is affiliated with.

Specialist Doctors are often affiliated with more than one hospital within the medical district. A remarkable unknown fact is that the percentage of nocosomial infection rate in Guatemala Citys private hospitals is lower than the infection rate in most American hospitals. The ratio of nurse/patient is 1 to 3. Anyone who has been a patient in one of Guatemala Citys hospitals can testify about the quality of care and the warm attention given by Doctors and medical staff.

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Myths and Misconceptions About Stem Cell Research …

Wednesday, August 22nd, 2018

En Espaol

There is no shortage of myths and misconceptions when it comes to stem cell research and regenerative medicine. Here we address the most common concerns.

If you have more questions that aren't addressed here, please visit our other Stem Cell FAQ pages.

Is CIRM-funded stem cell research carried out ethically?Where do the embryos come from to create stem cell lines?I'm opposed to abortion. Can embryonic stem cell lines come from aborted fetuses?Does creating stem cell lines destroy the embryo?Are adult stem cells as goodor betterthan embryonic stem cells?Don't iPS cells eliminate the need to use embryos in stem cell research?Can't stem cell research lead to human cloning?

Stem cell research, like any fieldwithin biomedicine, poses social and ethical concerns. CIRM, as well as the broader research community, takes these seriously.

As a state funding body, CIRM has comprehensive policies to govern research, similar to our national counterpart, the National Institutes of Health. CIRM-funded researchers must comply with a comprehensive set of regulations that have been carefully developed and are in accordance with national and international standards.

These regulations were among the first formal policies governing the conduct of stem cell research and are in accordance with recommendations from the National Academies and from the International Society for Stem Cell Research. CIRMs Standards Working Group meets regularly to consider new ethical challenges as the science progresses and to revise standards to reflect the current state of the research.

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CIRM regulationsNational Academies of Science guidelinesInternational Society for Stem Cell Research guidelinesNational Academies of Science podcast about guidelines for embryonic stem cell research More about CIRM-grantee ethics training (4:03)

All the human embryonic stem cell lines currently in use come from four to five day-old embryos left over from in vitro fertilization (IVF) procedures. In IVF, researchers mix a man's sperm and a woman's eggs together in a lab dish. Some of those eggs will become fertilized. At about five days the egg has divided to become a hollow ball of roughly 100 cells called a blastocyst which is smaller than the size of the dot over an i. It is these very early embryos that are implanted into the woman in the hopes that she becomes pregnant.

Each cycle of IVF can produce many blastocysts, some of which are implanted into the woman. The rest are stored in the IVF clinic freezer. After a successful implantation, they must decide what to do with any remaining embryos. There are a few options:

Some embryonic stem cell lines also come from embryos that a couple has chosen not to implant because they carry harmful genetic mutations like the ones that cause cystic fibrosis or Tay Sachs disease. These are discovered through routine genetic testing prior to implantation. Still other embryos might be malformed in some way that causes them to be rejected for implantation into the mother. Embryos with genetic defects of malformations would have been discarded if the couple had not chosen to donate them to stem cell research.

People who donate leftover embryos for research go through an extensive consent process to ensure that they understand embryonic stem cell research. Under state, national and international regulations, no human embryonic stem cell lines can be created without explicit consent from the donor.

Policies vary as to whether women may be paid or otherwise compensated to donate eggs. Most jurisdictions allow donors to be reimbursed for direct costs such as travel to the clinic or lodging. Some also allow payments or IVF services to be provided to egg donors.

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How do scientists create stem cell lines from left over IVF embryos? (4:11)

No. Emybronic stem cells only come from four to five day old blastocysts or younger embryos.

In most cases, yes. The hollow blastocystwhich is where embryonic stem cells come fromcontains a cluster of 20-30 cells called the inner cell mass. These are the cells that become embryonic stem cells in a lab dish. The process of extracting these cells destroys the embryo.

Dont forget that the embryos were donated from IVF clinics. They had either been rejected for implantation and were going to be destroyed, or the couple had decided to stop storing the embryos for future use. The embryos used to create embryonic stem cell lines were already destined to be destroyed.

There is, however, a second method that creates embryonic stem cell lines without destroying the embryo. Instead, scientists take a single cell from a very early stage IVF embryo and can use that one cell to develop a new line. The process of removing one cell from an early stage embryo has been done for many years as a way of testing the embryo for genetic predisposition to diseases such as Tay Sachs. This process is called preimplantation genetic testing.

Adult stem cells are extremely valuable and have great potential for future therapies. However, these cells are very restricted in what they can do. Unlike embryonic stem cells, which can grow into virtually any cell type in the body, adult stem cells can only follow certain paths.

For example, Blood-forming stem cells can grow into mature blood cells, and brain stem cells may be able to grow into mature neurons, but a blood-forming stem cell cant grow into a neuron, and vice versa. Whats more, adult stem cells dont grow indefinitely in the lab, unlike embryonic stem cells, and they arent as flexible in the types of diseases they can treat.

And, while the news is full of stories about people who had great results from adult stem cell therapies, few of these therapies are part of big trials that can test whether a potential therapy is safe and effective. Until some of these large trials take place with both adult and embryonic stem cells we won't know which type of stem cell is superior. Even researchers who study adult stem cells advocate working with embryonic cells as well.

CIRM is excited about their potential for treating some diseases. However, our goal is to accelerate new treatments for diseases in need. At this time the most effective way of doing that is by exploring all types of stem cells. That's why CIRM has funded researchers pursuing a wide range of approaches to finding cures for diseases.

See how much of CIRM's funding has gone to different types of stem cells here: Overview of CIRM Stem Cell Research Funding.

Filter our list of all funded CIRM grants to see awards using different cell types.

How are adult stem cell different from embryonic stem cells? (3:29)

Induced pluripotent stem cells, or iPS cells, represent another type of cell that could be used for stem cell research. . iPS cells are adult cellsusually skin cellsthat scientists genetically reprogram to appear like embryonic stem cells. The technology used to generate human iPS cells, pioneered by Shinya Yamanaka in 2007, is very promising, which is why CIRM has funded many grants that create and use these cells to study or treat disease. However, iPS cell technology is very new and scientists are looking into whether those cells have the same potential as human embryonic stem cells and whether the cells are safe for transplantation.Many CIRM-funded researchers are working to find better ways of creating iPS cells that are both safe and effective.

Experts agree that research on all types of stem cells is critical. In September 2008, a panel of experts convened by the U.S. National Academy of Sciences stated that the use of human embryonic stem cells is still necessary. As panel chair Richard Hynes of the Massachusetts Institute of Technology stated:

It is far from clear at this point which types of cell types will prove to be the most useful for regenerative medicine, and it is likely that each will have some utility.

See a video about creating iPS cells (3:40)

No. Every significant regulatory and advisory body has restrictions on reproductive cloning. The National Academy of Sciences has issued guidelines banning the technique as has the International Society for Stem Cell Research. The California constitution and CIRM regulations specifically prohibit reproductive cloning with its funding.

Updated 2/16

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FAQs – Ocean Springs, MS – Gulf Coast Stem Cell …

Wednesday, July 25th, 2018

Our Technology

Gulf Coast Stem Cell & Regenerative Medicine Center (GCSC&RMC) uses adipose-derived stem cells for deployment & clinical research. Early stem cell research has traditionally been associated with the controversial use of embryonic stem cells. The new focus is on non-embryonic adult mesenchymal stem cells which are found in a persons own blood, bone marrow, and fat. Most stem cell therapy centers in the world are currently using stem cells derived from bone marrow.

A recent technological breakthrough enables us to now use adipose (fat) derived stem cells. Autologous stem cells from a persons own fat are easy to harvest safely under local anesthesia and are abundant in quantities up to 2500 times those seen in bone marrow.

Clinical success and favorable outcomes appear to be related directly to the quantity of stem cells deployed. Once these adipose-derived stem cells are administered back into the patient, they have the potential to repair human tissue by forming new cells of mesenchymal origin, such as cartilage, bone, ligaments, tendons, nerve, fat, muscle, blood vessels, and certain internal organs. Stem cells ability to form cartilage and bone makes them potentially highly effective therapy for degenerative orthopedic conditions. Their ability to form new blood vessels and smooth muscle makes them potentially very useful in treating Peyronies disease and impotence. Stem cells are used extensively in Europe and Asia to treat these conditions.

We have anecdotal and experimental evidence that stem cell therapy is effective in healing and regeneration. Stem cells seek out damaged tissues in order to repair the body naturally. The literature and internet are full of successful testimonials but we are still awaiting definitive studies demonstrating the efficacy of stem cell therapy. Such data may take five or ten years to accumulate. In an effort to provide relief for patients suffering from certain degenerative diseases that have been resistant to common modalities of medical care, we are initiating pilot studies as experimental tests of therapy effectiveness with very high numbers of adipose-derived stem cells obtained from fat. Adipose fat is an abundant and reliable source of stem cells.

GCSC&RMCs cell harvesting and isolation techniques are based on technology from Korea. This new technological breakthrough allows patients to safely receive their own autologous stem cells in extremely large quantities. Our therapy and research are patient funded and we have endeavored successfully to make it affordable. All of our sterile procedures are non-invasive and done under local anesthesia. Patients who are looking for non-surgical alternatives to their degenerative disorders can participate in our trials by filling out our application to determine if they are candidates.GCSC&RMC is proud to be state of the art in the new field of Regenerative Medicine. RETURN TO TOP

We are currently in the process of setting up FDA approved protocols for stem cell banking in collaboration with a reputable cryo-technology company. This enables a person to receive autologous stem cells at any time in the future without having to undergo liposuction which may be inconvenient or contraindicated. Having your own stem cells available for medical immediate use is a valuable medical asset.

Provisions are nearly in place for this option and storage of your own stem cells obtained by liposuction at GCSC&RMC or from fat obtained from cosmetic procedures performed elsewhere should be possible in the near future. RETURN TO TOP

Adult (NonEmbryonic) Mesenchymal Stem Cells are undifferentiated cells that have the ability to replace dying cells and regenerate damaged tissue. These special cells seek out areas of injury, disease, and destruction where they are capable of regenerating healthy cells and enabling a persons natural healing processes to be accelerated. As we gain a deeper understanding of their medical function and apply this knowledge, we are realizing their enormous therapeutic potential to help the body heal itself. Adult stem cells have been used for a variety of medicaltherapies to repair and regenerate acute and chronically damaged tissues in humans and animals. The use of stem cells is not FDA approved for treating any specific disease in the United States at this time and their use is therefore investigational. Many reputable international centers have been using stem cell therapy to treat various chronic degenerative conditions as diverse as severe neurologic diseases, renal failure, erectile dysfunction, degenerative orthopedic problems, and even cardiac and pulmonary diseases to name a few. Adult stem cells appear to be particularly effective at repairing cartilage in degenerated joints. RETURN TO TOP

Regenerative Medicine is the process of creating living, functional tissues to repair or replace tissue or organ function lost due to damage, or congenital defects. This field holds the promise of regenerating damaged tissues and organs in the body by stimulating previously irreparable organs to heal themselves. (Wikipedia) RETURN TO TOP

Traditionally, we have used various medications and hormones to limit disease and help the body repair itself. For example, hormone replacement therapy has, in many cases, shown the ability to more optimally help the immune system and thus help us repair diseased or injured tissues. Genetic research is an evolving area where we will eventually learn and utilize more ways of specifically dealing with gene defects causing degenerative disease. Stem cell therapy is another rapidly evolving and exciting area that has already shown considerable promise in treating many degenerative conditions. RETURN TO TOP

A stem cell is basically any cell that can replicate and differentiate. This means the cell can not only multiply, it can turn into different types of tissues. There are different kinds of stem cells. Most people are familiar with or have heard the term embryonic stem cell. These are cells from the embryonic stage that have yet to differentiate as such, they can change into any body part at all. These are then called pluripotential cells. Because they are taken from unborn or unwanted embryos, there has been considerable controversy surrounding their use. Also, while they have been used in some areas of medicine particularly, outside the United States they have also been associated with occasional tumor (teratoma) formations. There is work being conducted by several companies to isolate particular lines of embryonic stem cells for future use.

Another kind of stem cell is the adult stem cell. This is a stem cell that already resides in ones body within different tissues. In recent times, much work has been done isolating bone-marrow derived stem cells. These are also known as mesenchymal stem cells because they come from the mesodermal section of your body. They can differentiate into bone and cartilage, and probably all other mesodermal elements, such as fat, connective tissue, blood vessels, muscle and nerve tissue. Bone marrow stem cells can be extracted and because they are low in numbers, they are usually cultured in order to multiply their numbers for future use. As it turns out, fat is also loaded with mesenchymal stem cells. In fact, it has hundreds if not thousands of times more stem cells compared to bone marrow. Today, we actually have tools that allow us to separate the stem cells from fat. Because most people have adequate fat supplies and the numbers of stem cells are so great, there is no need to culture the cells over a period of days and they can be used right away. RETURN TO TOP

These adult stem cells are known as progenitor cells. This means they remain dormant (do nothing) unless they witness some level of tissue injury. Its the tissue injury that turns them on. So, when a person has a degenerative type problem, the stem cells tend to go to that area of need and stimulate the healing process. Were still not sure if they simply change into the type of injured tissue needed for repair or if they send out signals that induce the repair by some other mechanism. Suffice it to say that there are multiple animal models and a plethora of human evidence that indicates these are significant reparative cells. RETURN TO TOP

This will depend on the type of degenerative condition you have. A specialist will evaluate you and discuss whether youre a potential candidate for stem cell therapy. If after youve been recommended for therapy, had an opportunity to understand the potential risks and benefits, and decided on your own that you would like to explore this avenue, then you can be considered for stem cell therapy. Of course, even though its a minimally invasive procedure, you will still need to be medically cleared for the procedure. RETURN TO TOP

NO. However, GCSC&RMCs procedures fall under the category of physicians practice of medicine, wherein the physician and patient are free to consider their chosen course for medical care. The FDA does have guidelines about therapy and manipulation of a patients own tissues. At GCSC&RMC we meet these guidelines by providing same day deployment with the patients own cells that undergo very minimal manipulation and are inserted during the same procedure. RETURN TO TOP

No. Only adult mesenchymal stem cells are used. These cells are capable of forming bone, cartilage, fat, muscle, ligaments, blood vessels, and certain organs. Embryonic stem cells are associated with ethical considerations and limitations. RETURN TO TOP

Patients suffer from many varieties of degenerative illnesses. There may be conditions associated with nearly all aspects of the body. Board-certified specialists are ideal to evaluate, recommend and/or treat, and subsequently, follow your progress. Together, through the GCSC&RMC, we work to coordinate and provide therapy mainly with your own stem cells, but also through other avenues of regenerative medicine. This could include hormone replacement therapy or other appropriate recommendations.

For example, if you have a knee problem, you would see GCSC&RMCs Board Certified orthopedic surgeon rather than a generic clinic director. Also, you might be recommended for evaluation for hormone replacement therapy or an exercise program should such be considered optimal. Nonetheless, we believe stem cell therapy to be the likely foundation for regenerative medicine.It should also be noted, that all therapies are currently in the investigational stage. While we recognize our patients are seeking improvement in their condition through stem cell therapy, each deployment is part of an ongoing investigation to establish optimal parameters for future therapies, to evaluate for effectiveness and for any adverse effects. It is essential that patients understand they are participating in these investigational (research) analyses. Once sufficient information is appropriately documented and statistically significant, then data (validated by an Institutional Review Board) may be presented to the FDA for consideration of making an actual claim. RETURN TO TOP

Urology, cosmetic surgery, ear, nose, & throat, orthopedics, internal medicine, and cardiology are represented. Plans are currently being made for a number of other specialties. GCSC&RMC is the first multi-specialty stem cell center in the United States. RETURN TO TOP

Many have been told that they require surgery or other risky procedures for their ailments and are looking for non-invasive options. Some have heard about the compelling testimonials about stem cells in the literature and on various websites. Many have read about the results of stem cell therapy in animal models and in humans. GCSC&RMC gives a choice to those informed patients who seek modern regenerative therapy but desire convenience, quality, and affordability. GCSC&RMC fills a need for those patients who have been told that they have to travel to different countries and pay as much as twenty to one hundred thousand dollars for stem cell therapy offshore. (See stem cell tourism). RETURN TO TOP

Stem cells are harvested and deployed during the same procedure. Our patients undergo a minimally-invasive liposuction type of harvesting procedure by a qualified surgeon in our facility in Ocean Springs, Mississippi. The harvesting procedure generally lasts a few minutes and can be done under local anesthesia. Cells are then processed and are ready for deployment within 90 minutes or less. RETURN TO TOP

Bone marrow sampling (a somewhat uncomfortable procedure) yields approximately 5,000 60,000 cells that are then cultured over several days to perhaps a few million cells prior to deployment (injection into the patient). Recent advances in stem cell science have made it possible to obtain high numbers of very excellent quality multi-potent (able to form numerous other tissues) cells from a persons own liposuction fat. GCSC&RMC uses technology acquired from Asia to process this fat to yield approximately five hundred thousand to one million stem cells per cc of fat, and therefore, it is possible to obtain as many as 10 to 40 million cells from a single procedure. These adipose-derived stem cells can form many different types of cells when deployed properly including bone, cartilage, tendon (connective tissue), muscle, blood vessels, nerve tissue and others. RETURN TO TOP

GCSC&RMC patients have their fat (usually abdominal) harvested in our special sterile facility under a local anesthetic. The fat removal procedure lasts approximately twenty minutes. Specially designed equipment is used to harvest the fat cells and less than 100cc of fat is required. Postoperative discomfort is minimal and there is minimal restriction on activity. RETURN TO TOP

Stem cells are harvested under sterile conditions using a special closed system technology so that the cells never come into contact with the environment throughout the entire process from removal to deployment. Sterile technique and antibiotics are also used to prevent infection. RETURN TO TOP

No. Only a persons own adult autologous cells are used. These are harvested from each individual and deployed back into their own body. There is no risk of contamination or risk of introduction of mammalian DNA. RETURN TO TOP

These facilities are obtaining stem cells from bone marrow or blood in relatively small quantities and they are then culturing (growing) the cells to create adequate quantities. Research seems to indicate that success of stem cell therapy is directly related to the quantity of cells injected. GCSC&RMC uses adipose derived stem cells that are abundant naturally at approximately 2,500 times levels found in bone marrow (the most common source of mesenchymal stem cells). GCSC&RMC uses technology that isolates adipose stem cells in vast numbers in a short time span so that prolonged culturing is unnecessary and cells can be deployed into a patient within 90 minutes of harvesting. RETURN TO TOP

GCSC&RMC is doing pioneer research for treating many diseases. All investigational data is being collected so that results will be published in peer review literature and ultimately used to promote the advancement of cellular based regenerative medicine. FDA regulations mandate that no advertising medical claims be made and that even website testimonials are prohibited. RETURN TO TOP

No. Many are confused by this because they have heard of cancer patients receiving stem cell transplants. These patients had ablative bone marrow therapy and need stem cells to re-populate their blood and marrow. This is different from the stem cells we deploy to treat noncancerous human diseases at GCSC&RMC. RETURN TO TOP

Adult mesenchymal stem cells are not known to cause cancer. Some patients have heard of stories of cancer caused by stem cells, but these are probably related to the use of embryonic cells (Not Adult Mesenchymal Cells). These embryonic tumors known as teratomas are rare but possible occurrences when embryonic cells are used. RETURN TO TOP

Stem cell therapy is thought to be safe and not affect dormant cancers. If someone has had cancer that was treated and responded sucessfully, there is know reason to withhold stem cell deployment. In most cases, stem cells should not be used in patients with known active cancer. RETURN TO TOP

We know of no documented cases personally or in the literature where serious harm has resulted. All of our patients will be entered into a database to follow and report any adverse reactions. This information is vital to the development of stem cell science. There have been a few reports of serious complications from overseas and these are being thoroughly evaluated by epidemiologists to ascertain the facts. The International Stem Cell Society registry has over 1,000 cases currently registered and only 2% were associated with any complications, none of which were considered serious adverse events. RETURN TO TOP

None. Our aim is to make cell based medicine available to patients who are interested and to provide ongoing research data under approved Institutional Review Board (IRB) validated studies. We will follow our stem cell therapy patients over their lifetimes. This will enable us to accumulate significant data about the various degenerative diseases we treat. Instead of providing simply anecdotal or testimonial information, our goal is to categorize the various conditions and follow the patients progress through various objective (e.g. x-ray evidence or video displays) and subjective (e.g. patient and/or doctor surveys) criteria. We are aware of a lot of stories about marked improvement of a variety of conditions, but we make no claims about the intended therapy. At some point, once adequate amounts of data are accumulated, it might be appropriate to submit the information to the FDA at which point an actual claim may be substantiated and recognized by the Agency. Still, these are your own cells and not medicines for sale. They are only being used in your own body. Most likely, no claim needs to be made; rather a statistical analysis of our findings would suffice to suggest whether therapy is truly and significantly effective. We also hope to submit our patients data to an approved International Registry (See ICMS Stem Cell Registry) further fostering large collections of data to help identify both positive and negative trends. RETURN TO TOP

Our adipose derived stem cell harvesting and isolation technique yields extremely high numbers of stem cells. In reviewing outcomes data, therapy cell numbers appear to correlate with therapy success. Our cells are actually in a type of soup called Stromal Vascular Fraction SVF which is stem cells bathed in a rich mixture of natural growth factors (Not the same as human growth factor hormone which is only one type of growth factor). Some types of orthopedic and urologic diseases appear to respond better to stem cells that are super enriched with growth factors created by administering Platelet Rich Plasma to the patient. Autologous Platelet Rich Plasma is derived from a patients own blood drawn at the time of deployment. At GCSC&RMC we do not add any foreign substances or medications to the stem cells. RETURN TO TOP

Depending on the type of therapy required, stem cells can be injected through veins, arteries, into spinal fluid, subcutaneously, or directly into joints or organs. All of these are considered minimally invasive methods of introducing the stem cells. Stem cells injected intravenously are known to seek out and find (see photo) areas of tissue damage and migrate to that location thus potentially providing regenerative healing. Intravenously injected stem cells have been shown to have the capability of crossing the blood-brain barrier to enter the central nervous system and they can be identified in the patients body many months after deployment. Note yellow arrow showing the stem cells concentrated in the patients hand where he had a Dupytrens contracture (Dupuytrens contracture is a hand deformity that causes the tissue beneath the surface of the hand to thicken and contract). RETURN TO TOP

Different conditions are treated in different ways and there are different degrees of success. If the goal is regeneration of joint cartilage, one may not see expected results until several months. Some patients may not experience significant improvement and others may see dramatic regeneration of damaged tissue or resolution of disease. Many of the disorders and problems that the physicians at GCSC&RMC are treating represent pioneering work and there is a lack of data. FDA regulations prevent GCSC&RMC from making any claims about expectations for success, however, if you are chosen for therapy, it will be explained that we believe stem cell therapy may be beneficial or in some cases that we are unsure and therapy would be considered investigational. RETURN TO TOP

Stem cell therapy relies on the bodys own regenerative healing to occur. The regenerative process may take time, particularly with orthopedic patients, who may not see results for several months. In some diseases, more immediate responses are possible. RETURN TO TOP

No. Only certain medical problems are currently being treated at GCSC&RMC. Check our list or fill out a candidate application form on the website. All patients need to be medically stable enough to have the stem cell deployment in our facility. There may be some exceptional conditions that may eventually be treated in hospitalized patients, but that remains for the future. Some patients may be declined due to the severity of their problem. Other patients may not have conditions appropriate to treat or may not be covered by our specialists or our protocols. A waiting list or outside referral (if we know of someone else treating such a problem) might be applicable in such cases. RETURN TO TOP

Yes. Patients with uncontrolled cancer are excluded. If you have an active infection anywhere in your body you must be treated first. Severely ill patients may require special consideration. Also, anyone with a bleeding disorder or who takes blood thinning medications requires special evaluation before consideration for stem cells. RETURN TO TOP

The specialist seeing you at GCSC&RMC will make a determination based on your history and exam, studies, and current research findings. Any complex cases may be reviewed by our ethics advisory committee. Occasionally, we may seek opinions from thought leaders around the world. RETURN TO TOP

No. Participation in any of our protocols is not mandatory and there are no incentives, financial or otherwise, to induce patients to enroll in our studies. However, GCSC&RMC is dedicated to clinical research for the development of stem cell science. GCSC&RMC is taking an active role in cutting edge clinical research in the new field of regenerative medicine. Research studies will be explained and privacy will be maintained. Formal future research studies will be regulated by an Institutional Review Board which is an authorized agency that promotes validity, transparency and protection of human study enrollees. RETURN TO TOP

At this time, we are not treating autism, spinal cord injuries, and some advanced diseases. See list of problems currently being studied at GCSC&RMC. RETURN TO TOP

Patients who are considered to be candidates based on information provided in the candidate application form will be invited for a consultation with one of our panel physicians. $250 is charged for this consultation which includes office evaluation (but may also include physicians evaluation of X-Rays, records, or telephonic consultations). Unfortunately, insurance generally will not cover the actual cost of stem cell therapy in most cases since stem cell therapy is still considered experimental. The cost varies depending on the disease state being treated and which type of stem cell deployment is required. RETURN TO TOP

Because of recent innovations in technology, GCSC&RMC is able to provide outpatient stem cell therapy at a fraction of the cost of that seen in many overseas clinics. The fee covers fat cell harvesting, cell preparation, and stem cell deployment which may include the use of advanced interventional radiology and fluoroscopy techniques. Financing is available through a credit vendor. RETURN TO TOP

Stem cells can be cryopreserved in the form of liposuction fat for prolonged periods of time. Currently, this service is outsourced to an outside provider known to have excellent quality control. Many patients have been inquiring about banking cells while they are still young since stem cell numbers drop naturally with each decade of life and some advocate obtaining and saving cells to be used later in life as needed. (see chart). RETURN TO TOP

Most patients, especially those with orthopedic conditions, require only one deployment. Certain types of degenerative conditions, particularly auto-immune disease, may respond best to a series of stem cell deployments. The number and necessity of any additional procedures would be decided on a case by case basis. Financial consideration is given in these instances. RETURN TO TOP

A good resource is the International Cellular Medicine Society (ICMS). Stem Cells 101

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Human stem cells restore mobility in Parkinson’s monkeys: study – Times LIVE

Tuesday, September 5th, 2017

Dopamine is a naturally occurring chemical that plays several key roles in the brain and body.

But the use of foetal tissue is fraught with practical and ethical problems.

So Takahashi and his colleagues, in a medical first, substituted so-called induced pluripotent stem cells (iPSCs), which can be easily made from human skin or blood.

Within a year, some monkey's who had could barely stand up gradually recovered mobility.

"They became more active, moving more rapidly and more smoothly," Takahashi said by email. Animals that had taken to just sitting "start walking around in the cage."

"These findings are strong evidence that human iPSC-derived dopaminergic neurons can be clinically applicable to treat Parkinson's patients," he said.

Experts not involved in the research described the results as encouraging.

The treatment, if proven viable, "has the potential to reverse Parkinson's by replacing the dopamine cells that have been lost -- a groundbreaking feat," said David Dexter, deputy research director at Parkinson's UK.

"Not only did the new cells survive... but they also integrated with the existing neuronal network," he said.

Neurons made from foetal tissue grafted into brains have been known to survive for more than a decade, and the researchers said they expected those derived from iPSCs to last just as long.

Tilo Kunath, Parkinson's Senior Research Fellow at the University of Edinburgh, said the outcome was "extremely promising," and highlighted the advantage of avoiding stem cells extracted from human foetal tissue.

"It means that this therapy can be used in any country worldwide," including Ireland and most of South America, where medical use of human embryonic stem cells is banned.

The results, reported in the journal Nature, were not the same for the dozen monkeys in the experiment, each of which received donor neurons from a different person.

"Some were made with cells from healthy donors, while others were made from Parkinson's disease patients," said lead author Tetsuhiro Kikuchi, also from Kyoto University.

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Human stem cells restore mobility in Parkinson's monkeys: study - Times LIVE

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Adult Stem Cell Therapy Abroad

Saturday, September 2nd, 2017

Stem Cells Pool Re-population

In order to self-repair, living organisms have stem cells in central and peripheral locations which can be attracted to sites of injured tissues by alarm signals. In this way, these cells proliferate, migrate, and accumulate in those damaged sites. If this situation of alarm perpetuates, stem cells could be permanently exhausted from their original locations leading to irreversible disease.

Basically, it could be a matter of stem cell quantity and effective availability at a certain time point when active regeneration is needed. adult stem cell therapy abroad The expected consequences of this situation could be the lack of an appropriate number of stem cells for further tissue replacement and regeneration and eventually the development of disease and ageing.

For example, we could think that any alteration of this stem cell homoeostasis by constant and repetitive trauma, physical hyperactivity, chronic inflammation and chronic disease could provoke a persistent disequilibrium inside all these reserve locations. This could promote an irreversible and premature stem cell exhaustion, being impossible then for the organism to self-repair and survive.

As we age we have less circulating stem cells. Introduction of new stem cells to our bodies circulation can improve health and repopulate our stem cell pool.

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Adult Stem Cell Therapy Abroad

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Human Stem Cells Fight Parkinson’s Disease in Monkeys – Scientific American

Saturday, September 2nd, 2017

LONDON (Reuters)Scientists have successfully used reprogrammed stem cells to restore functioning brain cells in monkeys, raising hopes the technique could be used in future to help patients with Parkinsons disease.

Since Parkinsons is caused by a lack of dopamine made by brain cells, researchers have long hoped to use stem cells to restore normal production of the neurotransmitter chemical.

Now, for the first time, Japanese researchers have shown that human induced pluripotent stem cells (iPS) can be administered safely and effectively to treat primates with symptoms of the debilitating disease.

So-called iPS cells are made by removing mature cells from an individualoften from the skinand reprogramming them to behave like embryonic stem cells. They can then be coaxed into dopamine-producing brain cells.

The scientists from Kyoto University, a world-leader in iPS technology, said their experiment indicated that this approach could potentially be used for the clinical treatment of human patients with Parkinsons.

In addition to boosting dopamine production, the tests showed improved movement in affected monkeys and no tumors in their brains for at least two years.

The human iPS cells used in the experiment worked whether they came from healthy individuals or Parkinsons disease patients, the Japanese team reported in the journal Nature on Wednesday.

This is extremely promising research demonstrating that a safe and highly effective cell therapy for Parkinsons can be produced in the lab, said Tilo Kunath of the MRC Centre for Regenerative Medicine, University of Edinburgh, who was not involved in the research.

The next step will be to test the treatment in a first-in-human clinical trial, which Jun Takahashi of Kyoto University told Reuters he hoped to start by the end of 2018.

Any widespread use of the new therapy is still many years away, but the research has significantly reduced previous uncertainties about iPS-derived cell grafts.

The fact that this research uses iPS cells rather human embryonic stem cells means the treatment would be acceptable in countries such as Ireland and much of Latin America, where embryonic cells are banned.

Excitement about the promise of stem cells has led to hundreds of medical centers springing up around the world claiming to be able to repair damaged tissue in conditions such as multiple sclerosis and Parkinsons.

While some treatments for cancer and skin grafts have been approved by regulators, many other potential therapies are only in early-stage development, prompting a warning last month by health experts about the dangers of stem-cell tourism.

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Human Stem Cells Fight Parkinson's Disease in Monkeys - Scientific American

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FDA cracks down on shady stem cell treatment clinics sweeping the US – New Atlas

Saturday, September 2nd, 2017

On Friday August 25th, US Marshals seized five vials of a smallpox vaccine from a stem cell treatment center in California. The action was undertaken on behalf of the FDA, which followed up the seizure with a larger announcement targeting the "unscrupulous clinics" selling unproven stem cell treatments that have rapidly arisen across the United States in recent years.

The unconventional smallpox "treatment" was being delivered by a company called StemImmune. The FDA alleges that the smallpox vaccine treatment was discovered after inspecting two California Stem Cell Treatment Centers in Rancho Mirage and Beverly Hills, California. The vaccine was apparently being combined with adult stem cells derived from a patient's body fat and this combined product was then administered to a patient either intravenously or injected directly into the tumors.

Not only does this strange treatment have no clinical backing, but the FDA noted "serious concerns" as to how the company obtained this vaccine in the first place.

"The FDA will not allow deceitful actors to take advantage of vulnerable patients by purporting to have treatments or cures for serious diseases without any proof that they actually work," says Scott Gottlieb, FDA Commissioner. "I especially won't allow cases such as this one to go unchallenged, where we have good medical reasons to believe these purported treatments can actually harm patients and make their conditions worse."

Dr. Mark Berman of the Cell Surgical Network, who works with the California Stem Cell Treatment Centers, fired back angrily at the FDA claiming Gottlieb's comments were "disparaging and misrepresentative."

The statement went on to claim that StemImmune's work involved, saying "many top national andinternational doctors and scientists are participating in this study, including our nation's ownDepartment of Defense."

A study was published in 2016 documenting the rapid rise of commercial stem cell treatment centers in the US. Paul Knoepfler and Leigh Turner's research paper was published in the journal, Cell Stem Cell, and it chronicled a startling 351 businesses marketing unapproved stem cell interventions across 570 clinics.

This frightening study revealed a burgeoning marketplace in the US, replacing the traditional trend of "medical tourism." Exploiting potential loopholes in the regulatory system, these clinics were offering unproven stem cell treatments for just about every disease you can think of.

"Brakes ought to exist in a marketplace like this, but where are the brakes? Where are the regulatory bodies?" says Leigh Turner, co-author of the study. "And how did this entire industry come into being in a country where stem cell-based interventions and the medical devices that produce them are supposed to be regulated by the FDA?"

These stem cell clinics seem to be operating inside a grey area whereby their treatments are not exactly classifiable under general FDA regulations. Many of these clinics simply extract stem cells from a patient's adipose tissue, subject those cells to minimal manipulation, and then implant them back into the same patient. This allows the procedure to be classified under a surgical procedure exemption meaning it doesn't need regulatory approval. Essentially it is not a "drug" or "medical" procedure, but instead just a straightforward "surgical" procedure.

The FDA has recently looked to address this loophole. Since 2015 the regulatory body has been working on reclassifying the way it views the repurposing of a patient's own tissue. Draft guidelines, not yet passed into law, are designed to classify these stem cell treatments as "drugs," meaning any treatment will need to undergo a stringent approval process.

Alongside the more dramatic smallpox incident, the FDA recently reset the battle lines with stem cell clinics. One company, called US Stem Cell Clinic (USSC), was delivered an expansive warning letter from the FDA arguing that the repurposing of adipose tissue in this context must be considered a drug.

The company responded by claiming the procedure is exempt from regulation, "because the procedures practiced at USSC do not involve more than 'minimal manipulation'." It seems the fundamental questions being argued here are how much manipulation of the tissue is actually taking place and for what is the claimed function of the resulting implantation?

The latest FDA announcement is drawing a line in the sand. Stem cell clinics delivering unproven treatments are on notice. It's yet to be seen actually how far the FDA will be able to go in legally moving on some of these clinics, but a new framework, set to clarify the regulatory processes surrounding these new treatments, will be delivered soon.

Source: FDA

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FDA cracks down on shady stem cell treatment clinics sweeping the US - New Atlas

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