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Stem Cell Transplant Program – Cleveland, Ohio

Posted: October 17, 2016 at 7:46 am

UH Cleveland Medical Centers Stem Cell Transplant Program has received international recognition by the Foundation for the Accreditation of Cellular Therapy (FACT). Learn more.

University Hospitals Stem Cell Transplant Program offers excellence in cancer treatment for pediatric and adult patients. Located at UH Seidman Cancer Center in Cleveland, Ohio, the Stem Cell Transplant Program provides the latest innovations with superior outcomes for patients with leukemia, lymphoma and other hematologic (blood) types of cancer.

Experts in the Stem Cell Transplant Program provide specialized treatments, aiming to find the best therapy for each patient.

Our comprehensive program offers cord blood, blood, and marrow transplants for a range of hematologic cancers and other disorders using either the patients own stem cells or those donated by a family member or unrelated volunteer.

At UH Seidman Cancer Center, we take pride in offering a comprehensive approach to cancer treatment. Patients who seek care have access to a multidisciplinary team that includes:

After meeting with the patient, our experts develop a highly unique treatment plan based on each individuals specific needs and preferences. Transplant patients are evaluated and cared for by a team whose objective is to increase coordination of care and improve outcomes. Our team also works closely with the Blood and Bone Marrow Transplant Centerat University Hospitals Rainbow Babies & Childrens Hospital to treat children with hematologic cancers and other blood disorders.

As an affiliate of the National Marrow Donor Program, our bone marrow transplant program is among the most accomplished and respected nationwide. Some of the UH Stem Cell Transplant Programs accomplishments include the following:

Other accomplishments in the field of stem cell therapy include:

In addition, we are aggressively pursuing innovative treatment developments through stem cell therapy clinical trials combining chemotherapy, radiation therapy, biological therapy and stem cell transplantation.

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Stem Cell Therapy – North Kansas City Hospital, Kansas …

Posted: October 14, 2016 at 3:50 pm

Patients with severe critical limb ischemia (CLI) have an exciting new treatment option autologous stem cell therapy. Karl Stark, MD, FACS, with Kansas City Vascular, PC, is currently running two clinical trials with "incredible results," he says.

"This new stem cell therapy is a game changer for patients at high risk for losing a limb and for whom nothing else works," says Dr. Stark. "We have been looking for a viable treatment for a long time, and these new trials show the greatest promise." He has been involved in four clinical trials. The first two involved IV infusion of prostaglandins and the second was hyperbaric oxygen therapy but the results were not as profound as what his patients are experiencing with the two current stem cell trials.

CLI is the most severe form of peripheral artery disease. Its differentiated from acute limb ischemia in the duration of the process and the underlying etiology. Acute limb ischemia is usually embolic or thrombotic occlusion of the arteries of the leg.

Of patients with CLI, 25% will die within one year; 40% within 5 years. The one-year amputation rate is 25%, with the mortality risk 5-10% for BKA and 10-15% for AKA. In addition, quality of life and the ability to live independently decrease with an amputation.

Surgical revascularization involves using bovine carotid artery conduit when autologous vein is not available for bypass. It restores blood flow to the affected limb, and gives patients a better chance of survival than amputation. The same holds true for CLI patients, Dr. Stark reports.

Nondirect revascularization treatment options for patients with no reconstructable arteries include hyperbaric oxygen therapy. Clinical trial results included higher limb salvage rates and lower mortality rates. Patients were also twice as likely to heal their ischemic wounds.

Survival of patient with CLI and non-reconstructable arterial disease

For a specific group of patients, cell therapy appeared to be an option when other modalities proved inadequate or not possible:

The goal of cell therapy is angiogenesis. In Dr. Starks clinical trials, adult or autologous stem cells are used, which are harvested from bone marrow. Differentiated centrifugation separates cells into subgroups and then further separates them into tissue specific-types . An intra-arterial and/or intramuscular injection protocol then deposits cells in the neurovascular bundle.

Lifecells has developed the protocol Dr. Stark is using for harvesting and selecting the most effective stem cells. And because the work is with autologous stem cells, the process is safer, avoids moral issues and has fewer complications.

It takes 4 to 6 weeks to see results. Since limbs must be healthy enough to withstand this time period, seeing patients early in their disease is important. Early results show improved limb salvage rates at 60%. There is also improved limb perfusion as measured by ankle brachial index and TC02. Interim data also show improvement in ischemic rest pain and ulcer healing.

"We are seeing a lot of interest from around the country in our stem cell clinical trials," Dr. Stark noted. "North Kansas City Hospital is at the forefront of this research, and its an honor to work with referrals from some of the leading vascular surgery centers."

Dr. Starks presentation

Dr. Stark earned his medical degree from the University of Missouri-Kansas City. He completed his residency in general surgery at Truman Medical Center and a fellowship in vascular surgery at Middlesex General University Hospital, New Jersey. Dr. Stark is the Midwest medical director for Healogics and director of the Wound Healing Center at North Kansas City Hospital.

To learn more call, 816.872.1598.

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Stem Cell Therapy Tulsa OK | Cushing OK | Sapulpa OK

Posted: October 9, 2016 at 9:46 pm

Stem Cell Therapy in Tulsa, Oklahoma Stem Cell Injections for Arthritis, Tendonitis, Knee Pain & More

As an alternative to surgery, our patients can now benefit from injections of platelet - rich plasma, amniotic, bone marrow or adipose stem cells to treat chronic orthopaedic conditions. These treatments can reduce pain and provide long lasting relief from chronic tendinitis, early arthritis and cartilage damage in the joint.

Our surgeons offer these fairly new treatment options; PRP, amniotic membrane stem cell, bone marrow stem cell as well as adipose stem cell injections to successfully treat patients with knee, hip or shoulder osteoarthritis, rotator cuff tendonitis, Achilles tendonitis, chronic bursitis, meniscal tears and degenerative arthritis. (For clarification, amniotic stem cells comes from the amniotic sac not an embryo. While some people may have ethical issues with embryonic stem cell therapy, most people agree the use of amniotic stem cell therapy raises no ethical or moral questions.)

As we age, our bodies undergo wear and tear from previous injuries, exercising, playing sports or arthritis. We do not repair these injures as well as we did when we were young. We produce less of our repair cells (mesenchymal stem cells) as we get older so it takes longer to recover.

Stem cell treatment takes advantage of the bodys ability to repair itself. With amniotic stem cell therapy, Dr. Mittal injects stem cells from amniotic tissues into your body. These stem cells have anti-inflammatory properties, similar to steroid and cortisone shots. Whats great is stem cell therapy can go beyond the benefits of standard injection therapy. Stem cells can actually restore degenerated tissue while providing pain relief. The growth factors in amniotic stem cells may replace damaged cells in your body. Stem cell injections also contain hyaluronic acid which lubricates tendons and joints which eases pain and helps to restore mobility.

One of the richest sources of stem cells is bone marrow, and the hip (pelvis) is one of the best and most convenient locations for obtaining bone marrow. During the harvesting procedure, the doctor removes (or aspirates) your cells from the pelvis. A trained nurse or technician then uses specifically designed equipment to concentrate the stem cells in the bone marrow and provides the cells back to the surgeon for implantation at the site of injury. This technique can be performed in one of our procedure rooms at the clinic.

A small sample of Adipose tissue (fat) is removed from above the Superior Iliac spine (love handles) or abdomen under a local anesthetic. Then a trained nurse or technician uses specifically designed equipment to concentrate the adipose stem cells and provides the cells back to the surgeon for implantation at the site of injury. This technique can be performed in one of our procedure rooms at the clinic.

Amniotic Stem Cell injections provide patients with a non-surgical treatment option to reduce various types of musculoskeletal pain. The injections are performed under Ultrasound guidance to ensure proper placement of the stem cells. With amniotic stem cells, there is no threat of patient rejection and amniotic fluid is highly concentrated source of stem cells, which makes this type of stem cell injection preferable.

Yes, more than 10,000 injections have been performed without a single reported adverse side effect. The use of amniotic stem cells is well researched, safe and effective, plus they have been used by ophthalmologists and plastic surgeons for around 20 years.

No, PRP is the injection or addition of blood platelets to enhance or jump-start the healing of soft tissue. Stem cell therapy is the process of using stem cells to create new cells to promote damaged or lost cells. They are different treatments but fall in the category of regenerative medicine.

To develop a PRP preparation, blood must first be drawn from a patient. The platelets are separated from other blood cells and their concentration is increased during a process called centrifugation. The increased concentration of platelets is then injected back into the region of the body being treated. This technique can also be performed in one of our clinic procedure rooms.

While PRP and stem cell therapy has been used for years to treat a multitude of injuries, their application is fairly new to orthopaedics. Due to this, some insurance companies may deny coverage making these procedures self-pay. In most cases its close to the amount of your deductible if you did in fact have a surgery. Our business office will be happy to work with you to obtain alternative payment arrangements prior to scheduling any procedure.

If you are suffering from any kind of joint, tendon or ligament pain and most other conservative treatments arent alleviating it then you may be a candidate for amniotic stem cell therapy. However if you have severe degenerative osteoarthritis you may not be eligible. If you believe you are a candidate then please fill out the form to the right to schedule a consultation appointment with one of our surgeons. They will look at your X-rays and examine you to determine if you are a candidate for one of these regenerative treatments.

Post-Procedure Instructions for Joints

Immediately After Your Cell Transplant Procedure: The stem cell injection includes producing a micro injury in the joint. As a result, expect the joint to be sore. This can be everything from minimally sore to very sore. Activity: The goal is to allow the stem cells to attach and then to protect them while they differentiate into cartilage. For this reason, youll be asked to keep the joint as still as possible for 30-60 minutes after the procedure. Do not take a bath for three days, but a shower 12 hours after the procedure is fine. 1st 3rd Day: For the first day, you should limit activity on the joint. If you have post-op soreness this may be easy to do, as you may have a natural limp or antalgic gait (your body does this to reduce pressure on the area to allow healing). If you dont have this, then simply, naturally taking a bit of weight off this area as you walk is a good idea this first day. Avoid all contact sports as well as jogging, running, or sports that involve impact on that joint. 4th Day 2nd Week: You can start to walk normally, no more than 30-60 minutes a day. Avoid all contact sports as well as jogging, running, or sports that involve impact on that joint. Bike riding is fine as are stationary bikes (no up/downs), elliptical machines, and swimming (no breast stroke). 3rd 6th Week: Avoid all contact sports as well as jogging, running, or sports that involve impact on that joint. You can walk as much as you like. Bike riding is fine, as are stationary bikes, elliptical machine, and swimming. Stem Cell Therapy Testimonials

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Regenerative Medicine | Nevada Pain – Las Vegas, Henderson

Posted: October 9, 2016 at 9:45 pm

What is Regenerative Medicine? Regenerative Medicine Explained by Las Vegas, Summerlin, and Henderson Nevadas Top Pain Doctors

Regenerative medicine is a rapidly evolving, advanced technology in the management of many acute and chronic pain conditions. Chronic pain is a common condition that can cause numerous detrimental impacts on an individuals ability to function on a day-to-day basis. Musculoskeletal pain, specifically, has historically been regarded as the number one cause of chronic disability in the United States. Further, chronic musculoskeletal pain has also been found to be the leading contributing factor to higher rates of physician appointments. Across both acute and chronic conditions, prevalence rates have estimated that approximately 100 million adults experience difficulties with regard to back pain every year. Regenerative medicine has not been approved to treat all cases of pain; however, depending on the individuals specific pain condition, regenerative medicine may be considered as an appropriate and effective treatment.

Drawing from research in the areas of biology, chemistry, computer science, engineering, genetics, medicine, and robotics, regenerative medicine involves the construction of biological substitutes for many of the tissues found in the body. The general idea behind regenerative medicine, or tissue engineering, is drawing from the work of science and technology so that researchers are able develop biological substitutes, which will act to restore, maintain, and improve the functioning of damaged or lost tissue.

Regenerative medicine is a relatively new procedure, though its origins date back as early as 1962, when the first synthetic skin substitute was used. While there are many misconceptions maintained regarding regenerative medicine, advances in technology have allowed for the development of new procedures for treating many common orthopedic conditions, which do not require an operation. In fact, many of the regenerative medicine interventions are minimally invasive. The common orthopedic conditions that have been successfully treated through the use of regenerative medicine procedures include arthritis, as well as injuries to the bodys cartilage, spinal discs, bone, tendons, ligaments, muscle, or other bodily tissue.

Regenerative medicine is believed to have originally emerged from a number of scientific and technological advances that span a diverse spectrum of fields. Also known as tissue engineering, regenerative medicine utilizes existing living tissue cells and biocompatible materials, along with both biochemical (such as growth factors found in the body) and physical factors to generate tissue-like constructs that may be used to repair tissue that has been damaged as the result of an injury or to replace an organ failing as the result of normal aging.

Tissue-based procedures related to regenerative medicine originated from early techniques in skin grafting. Originally developed in 1962, the first successful tissue-engineered procedures were performed in the 1970s. Beginning by harvesting a skin biopsy, Howard Green and his colleagues at Harvard Medical School perfected techniques in growing skin epidermis. This technology has also historically been applied clinically to help individuals with other conditions. Since the 1960s, regenerative therapy has drawn from stem cell technology to provide bone marrow transplants to help individuals suffering from leukemia.

For a number of years, scientists have been interested in stem cells because of their regenerative properties, as well as their ability to develop into any type of tissue that is found within the body. It is for these reasons that stem cells contain the potential for what is believed to be limitless clinical applications in the health care field. In fact, stem cell research is advancing the treatment options available as well as improving treatment outcome rates for diseases, such as Parkinsons disease, Type I diabetes, heart disease, Duchenes muscular dystrophy, Alzheimers disease, stroke, osteoarthritis, rheumatoid arthritis, and vision and hearing loss. This technology has also been utilized in the treatment of injuries, such as spinal cord injuries and severe burns. There are many scientists and researchers who firmly maintain the hope that in the future stem cell technology will lead to the possibility of repairing and replacing damaged or diseased tissue.

Indeed, the first tissue to be bioengineered was the skin. Following this, scientists were also able to successfully bioengineer cartilage. Both of these products, which were produced through tissue engineering, are available commercially to health care providers today. While these products arose on the market quickly and inspired enthusiasm for the possibility of generating all of the types of tissue that make up the human body through the use of tissue engineering, there are a number of problems that have prevented this progress. For example, both skin tissue and cartilage tissue do not require extensive vascularization, as other types of tissue do. This means that the generating process to engineer the tissue of both skin and cartilage can be completed using more simplified techniques, such as merely combining cells together.

Driven particularly by the discoveries of the bodys own ability to organize itself and regenerate tissue following cell death or loss, the primary goal of regenerative medicine, or tissue engineering, for pain, is to generate new tissue to replace tissue that has been injured, diseased, or is degenerating owing to advancing age.

Given that regenerative medicine involves the use of living cells, however, there are a number of ethical and legal issues surrounding the use of platelet-rich plasma and particularly that of embryonic stem cells. Of utmost importance in regenerative medicine is mimicking the environment from which the stem cells were drawn. While the FDA does not currently maintain any approval requirements with regard to adult stem cells, stem cell therapy does not currently have FDA approval. Moreover, physicians frequently go off label, when prescribing patients a form of treatment. This essentially means that the physician believes another type of drug, which has not undergone any clinical trials for that specific diagnosis, would greatly benefit the patient.

Of utmost importance in regenerative medicine is mimicking the environment from which the stem cells were drawn. This will allow the engineered cells to function as if they are still in their native tissue. In terms of musculoskeletal chronic pain, there are generally three types of regenerative medicine. These include the following.

One type of regenerative medicine is stem cell therapy. This procedure is believed to be ideal for patients experiencing low back or neck pain owing to a degeneration of the vertebral discs or joint pain owing to osteoarthritis, such as that in the knees, hips, or shoulders. Through cell division, stem cells are naturally able to renew themselves and to differentiate, or specialize, into a wide range of different types of tissue found within the body. As such, stem cells can also be found at many sites within the body, including human embryos, skin cells, bone marrow, peripheral blood, placental blood, placental tissue, and adipose tissue. There are two general types of stem cells found within the body, which include embryonic stem cells and adult stem cells.

Beginning in the 1960s, stem cell technology was used to effectively treat individuals needing bone marrow transplants, such as individuals suffering from leukemia. Currently, stem cell technology is regarded as an interventional procedure for the treatment of a number of chronic pain conditions. Generally, this procedure involves extracting the patients own stem cells and other supporting cells from one of the known sites for stem cells. This material is then purified, concentrated, and injected into the damaged tissue. It is important that this concentration is not altered in any way.

The procedure for stem cell therapy is generally non-surgical and there is very little recovery time. Thus, stem cell therapy can potentially help patients avoid surgery and the potential side effects that are associated with it. Most patients report some soreness at the site of the stem cell injection, which may or may not be accompanied by bruising. There have been no reports of serious side effects following stem cell therapy.

Another type of regenerative medicine for the treatment of chronic pain is amniotic membrane therapy. The human amniotic membrane is comprised of several unique properties that make it ideal for use in regenerative medicine. The amniotic membrane is composed of two types of cells: epithelial cells and stromal cells. Both the epithelial cells and the stromal cells exhibit characteristics that are similar to stem cells in that they are able to differentiate in vivo. Previous literature examining animal models on the use of amniotic membrane following a minimally invasive surgical procedure called a laminectomy has shown the amniotic membranes effectiveness in reducing epidural fibrosis and scar adhesion. Studies examining the use of the amniotic membrane in human models provide some evidence for its effectiveness. In particular, amniotic membrane use has been supported as an efficacious treatment for general tissue damage, such as tendonitis.

Similar to that of stem cells, the procedure for using amniotic membrane as an interventional therapy for the treatment of chronic pain conditions is generally non-surgical and there is very little recovery time. Thus, amniotic membrane procedures can provide the benefit of not undergoing surgery. This allows many patients to avoid going on disability or be subjected to the other side effects that can often occur following major surgery. Amniotic membrane therapy involves injecting a concentrated compound of the patients own amniotic membrane to the site of the injury. Most patients report some soreness at the site of the injection, which may or may not be accompanied by bruising.

The concentrated compound used in the platelet-rich plasma technique is created from a sample of blood from the patient. This blood is centrifuged to separate the almost-clear fluid called the serum (which is found as the top layer), the platelets and white blood cells (found in the middle), and the red blood cells (found at the bottom). Estimates have suggested that the middle layer is comprised of a platelet concentration of around one million platelets/uL. A typical platelet concentration would fall somewhere between 150,000-350,000 platelets/uL. Further, this fluid also contains highly concentrated (up to three to five times greater) growth factor. This concentrated compound is then injected into the site of the injury, where the platelets synthesize and release other active proteins. These actions are believed to account for the regenerative effect that platelet-rich plasma therapy has on damaged tissue. More specifically, the synthesizing of platelets and the release of proteins enhances the recruitment, proliferation, and differentiation of cells, which are the underlying processes in generating new tissue at the cellular level. Most patients report only some soreness at the site of the injection following the procedure, which may or may not be accompanied by bruising.

Platelet-rich plasma therapy has received an extensive amount of attention within the literature. In fact, platelet-rich plasma therapy has been shown to have beneficial effects on the expression of genes and matrix synthesis within tendons. Furthermore, platelet-rich plasma therapy is linked with the proliferation of cells and increases in total collagen production. Results from studies examining the effectiveness of platelet-rich plasma treatment have provided support for its benefits in treating lateral epicondylitis, patellar tendinopathy, Achilles tendinopathy, rotator cuff tendinopathy, rotator cuff tears, medial collateral ligament and anterior cruciate ligament tears, and osteoarthritis. Platelet-rich plasma therapy is also used to treat other acute and chronic pain conditions including tendonosis, muscle strain, muscle fibrosis, arthritis, arthrofibrosis, articular cartilage defects, meniscal injury, and chronic synovitis or joint inflammation. Given that platelet-rich plasma therapy for chronic pain is non-surgical, there is very little recovery time and very few risks.

Patients who are interested in whether or not regenerative medicine is an appropriate treatment option for providing relief for their pain condition are encouraged to seek out a consultation with a physician that is an expert in the area of regenerative medicine. This consultation will likely include an in-depth medical evaluation regarding the individuals underlying condition, and the potential for using regenerative medicine to treat the condition. This consultation will also include guidance from the expert physician regarding the procedures involved in regenerative medicine and what to expect. Indeed, many individuals hold misconceptions regarding the use and application of regenerative stem cell therapy; therefore, the consultation appointment serves to provide the patient with education regarding the process and to address any of the patients questions or concerns.

There are a number of pain conditions, including musculoskeletal conditions that are expected to benefit from regenerative medicine. During the initial consult with an expert physician in the area of regenerative medicine, your doctor will give you a medical evaluation consisting of a brief yet detailed personal history. The goal of this is to ensure an accurate diagnosis of the source of the pain, in order to determine the most appropriate regenerative medicine procedure. Indeed, in some cases of chronic pain, the precise cause is not identified. In these instances, the physician will want to ensure that certain diagnoses are ruled out. Your physician will also generally assess for your degree of risk for persistent difficulties.

Chronic pain can arise from a number of sources and many cases of chronic pain can originate because of a degenerative process or pathology. Damage to muscles, joints, or ligaments that comprise the spinal region can also be the main source of both acute and chronic pain. In general, back and neck pain is characterized by sensations of pain and discomfort that arises in the back and may radiate out toward the limbs. The specific symptoms or sensations of pain are widely varied. Some patients will experience the pain as a highly specific sharp stab, while others will describe the pain as more generalized and widespread. Further, the symptoms of chronic pain are expected to fluctuate over time. For instance, often dependent on environmental circumstances, a patient may fluctuate in and out of recurring symptoms and exacerbations of pain.

While the specific symptom clusters generally depend on the underlying cause, some common complaints include:

Pain experienced within the body is thought to provide a strong indication that there is likely tissue damage or an underlying injury. In general, a number of treatments available for these common conditions merely help the patient cope with the debilitating pain, rather than addressing the underlying injury. New technology in the field of regenerative medicine has provided advancements in the types of treatments available for chronic pain. Indeed, these forms of treatment target the underlying problem, by promoting the body to heal itself through the use of stem cells.

Patients who suffer from the following list of conditions are potential candidates for regenerative medicine procedures.

Spondylolisthesis refers to the degenerative process of the individual bones of the spine, called the vertebrae. Most commonly caused by degenerative disc disease, spondylolisthesis is a condition that occurs when the vertebra becomes dislocated and slips over another. It is often referred to under nonspecific low back pain, because a large portion of patients with this anatomical deformity do not present with any related symptoms, including pain. During spondylolysis, the nerves around the weakened and slipped vertebrae can become compressed. Annual prevalence rates of within the general population estimate that approximately 12% of the population have had difficulties with regard to this condition.

Spinal stenosis is a common condition characterized by a restriction of the spinal canal, which is caused by a narrowing of the spinal column. The characteristic feature of spinal stenosis is neurogenic claudication, which is an inflammation of the nerves fanning out from the spinal cord. People with spinal stenosis often experience pain while walking. It is generally recommended that patients attempt more conservative forms of treatment prior to beginning regenerative medicine intervention.

These are genetically linked problems that relate to the curvature of the spine (e.g., scoliosis or kyphosis), and generally involve the entire spine. These difficulties are relatively uncommon. Recent prevalence rates are not available; however, early estimates suggest that spinal deformities occur in about 0.8% to 1.9% of the general population.

Degenerative disc disease is a condition related to the changes that occur within the intervertebral discs as people age. This aging of the intervertebral disc can cause tears, which is believed to be the source of the pain associated with degenerative disc disease. The pain associated with this particular disease can occur throughout the spine, however in some instances, the pain was reported to be localized to the affected intervertebral disc. Previous treatments for degenerative disc disease have generally been limited to physical therapy, over-the-counter or prescription pain medications, steroid injections, and spinal fusion surgery. New advances in technology have lead to the use of stem cell therapy for the treatment of degenerative disc disease. This involves extracting the patients own stem cells. This is typically done from the patients hip, as it is the ideal location for obtaining bone marrow. This marrow is then concentrated and injected into the site of the injury.

Herniated disc is a condition characterized by damaged intervertebral discs, causing them to bulge or break. The intervertebral discs within the spine column undergo a significant amount of daily stress. Over time, this stress is believed to cause the disc to rupture, bulge, or herniate. In other words, the material comprising the intervertebral disc expands, putting pressure on the spinal column as well as the surrounding nerves. This pressure from the bulging disc is believed to be the source of significant pain. Further, this condition is more commonly found among aging individuals. While physical therapy has shown some promise in terms of improving the condition of the herniated disc, it requires a significant portion of time. Other treatments include surgical procedures, which cut out and remove bulging or herniated disc material. This type of procedure involves a number of risks as the disc is significantly weaker following the surgery and removal of tissue, which is believed to place the individual at an increased risk for future difficulties. New techniques within the field of regenerative medicine include utilizing the patients stem cells and support cells (which includes platelets) to regenerate and rebuild the network of cells comprising the injured disc.

Plantar fasciitis is a common form of chronic pain within the heel and foot. The flat, thick connective tissue found on the bottom of the foot, which connects the ball of the foot to the heel is known at the plantar fascia. The plantar fascia creates support for the arch of the foot. When this connective tissue becomes strained, there is a risk for damage to occur in the form of tiny tears on the ligament itself. In general, treatments available for providing relief for the pain associated with plantar fascia only target the symptoms of pain. Thus, regenerative procedures are believed to be the ideal choice to treat the pain of plantar fascia, as they promote the bodys own process of healing damaged tissue. Indeed, several research studies have provided empirical support for the use of platelet rich plasma therapy as an effective therapy for plantar fascia.

The sacroiliac joint is large and located at the base of the spine, connecting the spine with the hip. In many instances of sacroiliac joint pain, the individual is able to identify the injury that occurred prior to the onset of pain. However, acute events do not account for all cases of sacroiliac joint pain. Presently, there are limited treatment options available for sacroiliac joint pain. Indeed, evidence in terms of the effectiveness of steroid injections, radiofrequency neurotomy, and pulsed radiofrequency for the treatment of pain related to this joint is generally poor. However, there is some evidence, albeit limited, that regenerative procedures are effective in providing the patient relief from pain. Further, some evidence exists that suggests that the benefits of prolotherapy last much longer than that of steroid injections.

Lumbar radiculopathy, which can also be known as sciatica, is believed to occur when a herniated disc (typically between the fifth lumbar (L5) and the first sacral spinal nerve (S1)) pushes against a nerve. This pain travels down the leg. The primary goal of therapy is to reduce the size of the bulging disc, thereby reducing the compressive effect the bulging disc had on the nerve root. While there are a number of treatments available for treating lumbar radiculopathy pain, should these treatments be ineffective in relieving patients from their pain, they may be an appropriate candidate for stem cell repair.

Cervical radioculopathy is a chronic pain condition that occurs when a disc in the neck is pushing against the cervical nerve causing pain to travel down the arms. This condition is commonly found among young adults either through a herniated disc or an injury. Older adults, however, struggling with these symptoms of neck pain, are expected to have osteophyte formation causing foraminal narrowing, decreased disc height, and degenerative changes in the intervertebral joints.

A small number of patients have back pain so severe and unremitting that they must have surgery in order to try and gain some relief. As a result of this surgery, some patients continue to suffer from ongoing symptoms of back pain. These cases are recognized as failed back surgery, as the goal of the original surgery was to provide the patient with relief from pain. In these cases, pain in the lower back is caused by scar tissue that develops around the spinal nerves of the epidural space following surgery. Other factors that likely explain pain that persists following back surgery include disc herniation, post-operative pressure that is persistently placed on the spinal nerve, and altered joint mobility. Individuals with a history of anxiety, depression, or difficulty falling asleep or staying asleep are considered to be at an increased risk for developing a chronic pain condition following back surgery. Symptoms of chronic pain that occurred as a result of failed back surgery primarily include diffuse, dull, and aching pain across the back and lower limbs. Additionally, some patients may experience sharp, pricking, or stabbing pain in the limbs. Provided that other treatments have failed at providing the individual with relief from pain, failed back surgery patients may be considered for treatment using regenerative medicine.

In general, the procedure takes approximately 30 minutes. The expert physician generally sees patients at a clinic and is able to complete the procedure without the use of general aesthesia. Further, by completing this procedure on an outpatient basis, there is no recovery period. In fact, individuals are able to return directly to work and their usual activities following the procedure.

Generally, regenerative medicine involves extracting the patients own stem cells and other supporting cells from one of the known sites for stem cells. This material is then purified, concentrated, and injected into the damaged tissue. It is important that this concentration is not altered in any way. Most individuals report very little discomfort from this procedure. Some minor soreness at the site of the injection may be reported. Further, patients may experience mild bruising.

Patients are expected to achieve a number of benefits through regenerative medicine, such as:

There are a number of treatments available to provide patients with relief from chronic pain. Following an accurate diagnosis by a physician specializing in pain conditions, it is generally recommended that patients who were referred for regenerative medicine first undergo an initial consultation with an expert pain specialist. While there is evidence that these treatments are beneficial to a wide variety of pain conditions, there are a number of individuals whose pain does not respond to treatment. For these individuals with intractable pain, more aggressive and long-term forms of treatment are available to combat their debilitating symptoms. Further, regenerative medicine is not approved for all pain conditions. Your doctor will help determine which treatment is right for you.

In terms of the procedure, regenerative medicine involves an extraction of the patients own stem cells and other supporting cells from one of the known sites for stem cells. This material is then purified, concentrated, and injected into the damaged tissue. It is important that this concentration is not altered in any way. Most individuals report very little discomfort from this procedure. Some minor soreness at the site of the injection may be reported. Further, patients may experience mild bruising, again, at the site of the injection. This procedure is generally regarded as safe and can be done on an outpatient basis.

Historically, very few studies exist regarding the effectiveness of regenerative medicine on many different pain conditions. However, evidence is mounting regarding its effectiveness for a range of pain conditions that failed to respond to first-line interventions. Improvements to the system and its procedure are impending, given the significant advances in technology. Thus, regenerative medicine may emerge in future studies as an ideal method of treating chronic pain.

NOTE: Adult stem cells are autologous, meaning that they are drawn from an adult patient and then returned to that same patient in the form of treatment. Presently, the FDA does not have any approval requirements in terms of the collection of adult stem cells. The FDA has not approved the use of stem cells to combat aging or to prevent, treat, or cure any disease or medical condition mentioned.

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Regenerative Medicine | Nevada Pain - Las Vegas, Henderson

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Stem Cell FAQs – Minnesota Regenerative Medicine

Posted: October 7, 2016 at 3:44 am

What is the benefit of stem cell treatment?

Stem cell injections provide a non-surgical treatment option to reduce pain and promote natural healing and regeneration, while still providing long-lasting relief from arthritic joint pain, chronic tendinitis, or damaged musculoskeletal tissue.

Who is a suitable candidate for stem cell treatment?

In general, stem cell injections are most appropriate for patients suffering from mild to moderate osteoarthritis affecting the knee, shoulder, hip, ankle, foot, hand, or digits. Stem cell injects are also appropriate for patients with chronic tendinitis, partially torn tendons, and damaged musculoskeletal tissues such as a rotator cuff, labrum, meniscus, ligament, and skeletal muscle.

Who is not a suitable candidate for stem cell treatment?

Conditions excluding a patient from being a suitable candidate for a stem cell treatment include: (1) a patient with lymphoma, leukemia, or active cancer not in remission for at least five years; (2) a patient with any current or active infection; (3) a patient needing to take blood thinners such as Coumadin; (4) a patient with a contraindication to having liposuction or autologous stem cell treatment or PRP therapy; (5) a patient with multiple or complex medical issues.

Which joints, tendons and musculoskeletal tissues can be treated with stem cells?

The most common joints treated with stem cells include the knee, shoulder, hip, ankle, hand, finger and toe. The most common tendons treated with stem cells involve those with chronic tendinitis or partial tears such as the shoulder rotator cuff, distal biceps tendon, medial or lateral elbow tendons, and Achilles tendon.

What are the risks of a stem cell treatment?

An orthopedic stem cell treatment to treat painful osteoarthritis or chronic tendinitis or degenerative musculoskeletal tissue uses your own stem cells. Since the cells come from your own fat, there is no chance of your body rejecting them as these cells promote or regenerate your bodys natural ability to heal. There is a small risk of infection during a stem cell treatment. You can expect some soreness at both the liposuction site and the stem cell injection site for a few days following the procedure.

What is the price of a stem cell treatment?

The final price of a stem cell treatment is determined by what type of stem cell injection is being done, the number of injections, and whether or not platelet-rich plasma (PRP) is used along with the stem cells.While the price can vary, the price for a stem cell injection with PRP into a single joint or tendonis $5900.The price for a stem cell injection with PRP into two or more areas may be more.

Orthopedic stem cell treatments with PRP using fluoroscopic or ultrasound guidance during injection are typically not a covered benefit of Medicare or private insurance.

Where is the stem cell therapy offered?

Our regenerative medicine specialists at Minnesota Regenerative Medicine provide stem cell treatments at our Hogue Clinics corporate headquarters only in Maple Grove, Minnesota. The entire stem cell treatment process takes five hours or less to perform.

What should I do if I think Im a suitable candidate?

If you live in the Minneapolis/St. Paul (Twin Cities) or surrounding areas, we recommend that you schedule an appointment for a consultation to determine if you are a suitable candidate for a stem cell with PRP treatment. To expedite this process, we recommend that you bring in your most recentradiology reportsfor any imaging studies performed, as well as any other pertinent medical records.

Where do the stem cells come from?

The stem cells used for a patients stem cell injection come from the patients own adipose tissue (fat).

What is the success rate of a stem cell treatment?

Since we began performing stem cell treatments in 2011, our experience is that most patients will experience some degree of pain relief and improvement starting within a few weeks to months following a stem cell with PRP treatment.

Sometimes, we recommend platelet-rich plasma (PRP) injections be performed monthly following the initial stem cell treatment to continue to nourish and stimulate the injected stem cells. Additional PRP treatments will incur a separate charge with each PRP treatment. Clinical improvement and pain relief continues for six months or longer, often up to a year or more, following a stem cell treatment. Of the dozens of patients we have treated so far with stem cell treatments, the majority of patients have self reported some degree of pain relief and improvement in musculoskeletal function. Very few patients have reported little to no improvement.

Does a stem cell treatment consist of one or multiple injections?

Typically we do from one to several stem cell injections per joint or tendon or targeted area. This may vary depending on the severity and complexity of the osteoarthritis or chronic tendinitis or degenerative musculoskeletal condition being treated.

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Minnesota invests in regenerative medicine – Health Talk

Posted: October 7, 2016 at 3:44 am

Last year, the 2014 Minnesota legislative session brought a big win for regenerative medicine, as legislators passed a bill allotting nearly $50 million over 10 years for regenerative medicine research, clinical translation and commercialization efforts.

Some of that research funding has now been awarded to Bruce Walcheck, Ph.D., professor in the University of Minnesota Department of Veterinary and Biomedical Sciences, whose proposal was one of six funded out of 90 applications. Bruce is the principal investigator on a new $500,000 grant for research on engineering human pluripotent stem cells to generate enhanced natural killer cells for cancer therapy. The ultimate goal: treating cancer using the patients immune system.

A unique scientific and medical resource, pluripotent stem cells are self-replicating and have the potential to differentiate into almost any cell in the body. They are an important starting cell population for engineering enhanced immune cells for cell-based therapies that have the potential to cure various types of cancer. The investigative team will generate natural killer cells, which are part of the human bodys first line of defense against cancer cells and virus-infected cells.

Our long-term goal is to engineer human-induced pluripotent stem cells to generate a renewable source of super natural killer cells to enhance current therapies and the patients immune system in killing cancer cells, Walcheckexplained. Natural killer cells play a vital role in the fight against cancer. In contrast to other lymphocytes, natural killer cells kill malignant cells without being restricted to specific antigens or requiring considerable expansion. Standardized natural killer cell-based immunotherapies can therefore be more readily administered to patients.

However, during their expansion for transfer into patients and in the tumor environment, natural killer cells can down-regulate key receptors, resulting in their dysfunction. Our objective is to genetically modify human-induced pluripotent stem cells to derive natural killer cells that maintain their expression of key receptors for enhanced anticancer activity.

The other members of the multidisciplinary investigative team are Dan Kaufman, M.D., Ph.D., professor, Medical School (coinvestigator); Jianming Wu, D.V.M., Ph.D., associate professor, College of Veterinary Medicine (coinvestigator); Jeffrey Miller, M.D., Ph.D., professor, Medical School (collaborator); Melissa Geller, M.D., associate professor and gynecologic oncologist, Medical School (collaborator); and Paul Haluska, M.D., Ph.D., associate professor of oncology, Mayo Clinic (collaborator).

Members of the Masonic Cancer Center, University of Minnesota, are involved in this research.

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Atlanta Stem Cell Therapy | Georgia Stem Cell Treatments …

Posted: October 7, 2016 at 3:43 am

Ortho Sport & Spine Physicians is proud to be one of Atlantas leading providers of stem cell therapy to be used in the treatment of lumbar and cervical spine injuries and degenerative disorders. We are an interventional spine and sports medicine practice that specializes in finding solutions to acute and chronic pain conditions with interventional spine treatments. Our dedicated team of double board certified interventional spine physicians and orthopedic specialists are committed to using the most minimally invasive methods possible to help patients with acute and chronic pain find relief from their symptoms, improved function and a better overall quality of life.

Ortho Sport & Spine Physicians offers a variety of stem cell treatments that can be used to treat chronic back pain that is caused by injury or aging. Our stem cell therapy treatments involve removing stem cells from an adult patient and returning them to that same patient in a concentrated form to the damaged area in the spine. In some cases, stem cell therapy is used in conjunction with endoscopic spine surgery. The goal of stem cell therapy in the treatment of chronic back pain is to enable the parts of the spine (vertebra, discs, etc.) that have been damaged or degenerated due to injury or age to repair themselves. There are minimal complications associated with this type of stem cell therapy that has shown great promise and effectiveness in the treatment of chronic back pain.

Our Interventional Spine Physician, Dr. Armin V. Oskouei, is a nationally recognized leader in the field of regenerative medicine and travels widely to deliver lectures on the use of stem cell therapy in combination with endoscopic spine surgery. Dr. Oskouei has participated in many clinical trials evaluating the safety and effectiveness of stem cell therapy in the use of treating injuries and degenerative disorders of the spine. He has been actively using stem cell therapy in clinical practice for many years.

If you would like to find out if you are a candidate for stem cell therapy, please contact our Atlanta Stem Cell Therapy Specialists at Ortho Sport & Spine Physicians today and schedule a consultation with one of our Interventional Spine doctors. We look forward to helping you stay active and live your best life.

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California Proposition 71 (2004) – Wikipedia, the free …

Posted: October 7, 2016 at 3:42 am

Proposition 71 of 2004 (or the California Stem Cell Research and Cures Act) is a law enacted by California voters to support stem cell research in the state. It was proposed by means of the initiative process and approved in the 2004 state elections on November 2. The Act amended both the Constitution of California and the Health and Safety Code.

The Act makes conducting stem cell research a state constitutional right. It authorizes the sale of general obligation bonds to allocate three billion dollars over a period of ten years to stem cell research and research facilities. Although the funds could be used to finance all kinds of stem cell research, it gives priority to human embryonic stem cell research.

Proposition 71 created the California Institute for Regenerative Medicine (CIRM), which is in charge of making "grants and loans for stem cell research, for research facilities, and for other vital research opportunities to realize therapies" as well as establishing "the appropriate regulatory standards of oversight bodies for research and facilities development".[1] The Act also establishes a governing body called the Independent Citizens Oversight Committee (ICOC) to oversee CIRM.

Proposition 71 is unique in at least three ways. Firstly, it uses general obligation bonds, which are usually used to finance brick-and-mortar projects such as bridges or hospitals, to fund scientific research. Secondly, by funding scientific research on such a large scale, California is taking on a role that is typically fulfilled by the U.S. federal government. Thirdly, Proposition 71 establishes the state constitutional right to conduct stem cell research. The initiative also represents a unique instance where the public directly decided to fund scientific research.

Proposition 71 states that "This measure shall be known as the California Stem Cell Research and Cures Act. That is therefore the official citation. However the measure is also headed as the California Stem Cell Research and Cures Initiative.[2] The Act is long and complex. It amends the state constitution by adding "Article 35 Medical Research". This article establishes the CIRM and guarantees a right to conduct stem cell research. Proposition 71 also amends the Health and Safety Code, by introducing a provision in Part 5 of Division 106 called "Chapter 3 California Stem Cell Research and Cures Bond Act". This chapter, among other provisions, establishes the ICOC.

CIRM may have up to 50 employees, who are exempt from civil service. CIRM is divided in three working groups.

Human embryonic stem cell research became a public issue in 1998 when two teams of scientists developed "methods for culturing cell lines derived, respectively, from: (1) cells taken from the inner cell mass of early embryos, and (2) the gonadal ridges of aborted fetuses".[3] Since then, this type of research has sparked intense controversy in the United States.

Ever since 1996, Congress has attached to the Health and Human Services appropriations bill (which regulates the funding for the National Institutes of Health) a provision known as the "Dickey Amendment". This amendment, named after the former representative Jay Dickey, Republican from Arkansas, prohibits the use of federal monies to fund "research that destroys or seriously endangers human embryos, or creates them for research purposes".[4]

In 1999, however, the General Counsel of the Department of Health and Human Services issued a legal opinion arguing, "that the wording of the law might permit an interpretation under which human embryonic stem cell research could be funded".[5] This interpretation stipulated that the government could fund this research so long as the embryos used had been destroyed by researchers privately paid. Although the Clinton administration adopted this interpretation and wrote the corresponding guidelines, it did not have the time to enforce them. The issue would pass on to the next administration.

On August 9, 2001, President George W. Bush announced his administration's policy regarding human embryonic stem cell research. The President opted to fund only research on the existing 60 cell lines. The large number of cell lines quoted by the President surprised many scientists. Furthermore, they were concerned about the availability and quality of these lines. Scientists also worried about the impact the presidents policy could have on the American research community. The United States, they argued, lags behind other countries where governments support stem cell research. This, in turn, could cause American scientists to move to these countries.

Proposition 71 represents a response to the federal policy. The idea for this proposition came about after the California legislature blocked a billion-dollar measure to fund stem cell research. Robert N. Klein II, a real-estate developer from Palo Alto, whose son suffers from diabetes and whose mother has Alzheimer's, became the leader of the campaign effort to pass Proposition 71, and spent three million dollars of his own money in the campaign.

The Coalition for Stem Cell Research and Cures comprised a broad group of people and organizations that included: 22 Nobel laureates; celebrities such as Christopher Reeve, Sharyn Rossi, Monica Siegenthaler, Brad Pitt, Saba Motakef, and Michael J. Fox; a number of elected officials such as State Treasurer Phil Angelides, and State Controller Steve Westly, and State Senator Deborah Ortiz; more than fifty patient and disease advocacy groups (e.g., Juvenile Diabetes Research Foundation, Alzheimer's Association California Council, Sickle Cell Disease Foundation of California), medical groups and hospitals (e.g., California Medical Association, Children's Hospital-Los Angeles), groups representing Latinos and African Americans (e.g. National Coalition of Hispanic Organization, California NAACP), women's advocacy groups (e.g., Planned Parenthood, California NOW) and religious organizations (e.g. Catholics for a Free Choice).

The Republican Party opposed this initiative, but two key Republican figures endorsed it. They were George P. Shultz, the U.S. Secretary of State in the Reagan Administration and California Governor Arnold Schwarzenegger. Although Schwarzenegger did not endorse it until October 18, 2004, his support may have helped to solidify the proposition's lead in the polls.

This campaign raised approximately $25 million. The contributors included such prominent figures as Bill Gates, who donated $400,000; Pierre M. and Pamela Omidyar, the founders of eBay who together gave $1 million; Gordon Gund, the owner of the Cleveland Cavaliers basketball team, who contributed $1 million; Herbert M. Sandler, chairman of the board of World Savings Bank, who gave $500,000; John Doerr, a Silicon Valley venture capitalist, who donated $2 million; and William Bowes Jr., a founder of Amgen (a biotech company), who gave $600,000.

Those who opposed Proposition 71 included the Roman Catholic Church, Orange County Republicans, and the California Pro-Life Council, an affiliate of the National Right to Life Committee. Among the politicians in this group were State Senator Tom McClintock (R-Thousand Oaks) and Orange County Treasurer-Tax Collector John Moorlach. The Hollywood actor Mel Gibson also joined the efforts to defeat this initiative. Conservative groups, however, were not the only ones opposing Prop. 71; organizations such as the California Nurses Association (CNA), the Green Party, the Center for Genetics and Society, Our Bodies Ourselves, among others, were also against the initiative.

Two prominent groups campaigning to defeat the initiative were the Pro-Choice Alliance Against Proposition 71 and Doctors, Patients, and Taxpayers for Fiscal Responsibility. These two groups lacked the wide range of endorsements that the proponents had (however, the Pro-Choice Alliance Against Proposition 71 was endorsed by seven organizations and a number of university professors). On the Doctors, Patients, and Taxpayers for Fiscal Responsibility website (which no longer exists) there were only fourteen members listed. Among these members were Dr. Vincent Fortanasce, a physician; Diane Beeson, a medical sociologists; Carol Hogan, a spokesperson for the California Catholic Bishops; and Dr. H Rex Greene, an oncologist and hospital administrator.

The four organizations campaigning against the initiative raised almost $400,000. The main contributors were the United States Conference of Catholic Bishops, which donated $50,000 and Howard Ahmanson Jr., founder and president of Fieldstead & Company, who gave $95,000.

Sociologist Ruha Benjamin offers the first in-depth analysis of Proposition 71 in People's Science: Bodies and Rights on the Stem Cell Frontier (Stanford University Press 2013). Too frequently the debate over stem cell research devolves in to simple judgmentsgood or bad, life-saving medicine or bioethical nightmare, symbol of human ingenuity or our fall from graceignoring the people affected. Benjamin moves the terms of debate to focus on the shifting relationship between science and society, on the people who benefitor don'tfrom Proposition 71 and what this says about democratic commitments to an equitable society. Benjamin discusses issues of race, disability, gender, and socio-economic class that serve to define certain groups as more or less deserving in their political aims and biomedical hopes.

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Stem cells can repair torn tendons or ligaments …

Posted: October 6, 2016 at 7:46 am

Weekend athletes who overexert themselves running or playing basketball may one day reap the benefits of research at the Hebrew University of Jerusalem that shows that adult stem cells can be used to make new tendon or ligament tissue.

Tendon and ligament injuries present a major clinical challenge to orthopedic medicine. In the United States, at least 200,000 patients undergo tendon or ligament repair each year. Moreover, the intervertebral disc, which is composed in part of tendon-like tissue, tends to degenerate with age, leading to the very common phenomenon of low-back pain affecting a major part of the population.

Until the present time, therapeutic options used to repair torn ligaments and tendons have consisted of tissue grafting and synthetic prostheses, but as yet, none of these alternatives has provided a successful long-term solution.

A novel approach for tendon regeneration is reported in the April issue of the Journal of Clinical Investigation. Researchers Prof. Dan Gazit and colleagues at the Skeletal Biotechnology Laboratory at the Hebrew University Faculty of Dental Medicine engineered mesenchymal stem cells (MSCs), which reside in the bone marrow and fat tissues, to express a protein called Smad8 and another called BMP2.

When the researchers implanted these cells into torn Achilles tendons of rats they found that the cells not only survived the implantation process, but also were recruited to the site of the injury and were able to repair the tendon. The cells changed their appearance to look more like tendon cells (tenocytes), and significantly increased production of collagen, a protein critical for creating strong yet flexible tendons and ligaments.

Tendon tissue repair was detected using a special type of imaging known as proton DQF MRI, developed by Prof. Gil Navon at Tel Aviv University, which recognizes differences among collagen-containing tissue such as tendon, bone, skin, and muscle. The authors note that BMP and Smad proteins are involved in other tissues such as nerve and liver, suggesting that this type of delivery technology may be helpful for other degenerative diseases.

In an accompanying commentary in the Journal of Clinical Investigation, Dwight A. Towler and Richard Gelberman from the Washington University School of Medicine in St. Louis, Missouri, state, "Given our limited understanding of how MSCs become tenocytes, the recent progress demonstrated in these studies is quite remarkable and may be potentially useful in cell-based therapeutic approaches to musculoskeletal injuries."

###

The study was supported by GENOSTEM, an integrated project of the European Union for the engineering of mesenchymal stem cells in connective tissue disorders.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.

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Stem Cell Therapy Treatment at Allure Medical Spa in Michigan

Posted: October 6, 2016 at 7:46 am

Stem Cell Therapy in Michigan

Thank you for visiting. Many people have been awaiting a practical way to get stem cells for various conditions. This site is intended to offer information so you can learn about current options, understand what stem cells are, and to allow you to determine if this stem cell therapy be for you.

The term Stem Cells refers to cells in your body that are lying dormant, and designed to regenerate or repair diseased tissues. Stem Cell Therapy refers to isolating and deploying stem cells into your body with the intention of regenerating the tissues they are designed to repair.

Your stem cells are your bodys natural healing cells. They are recruited by chemical signals emitted by damaged tissues to repair and regenerate your damaged cells. Stem cells derived from your own tissues may well be the next major advance in medicine. Allure Medical Spa has the technology to produce a solution rich with your own stem cells. Under investigational protocols these can be deployed to treat a number of degenerative conditions and diseases.

At this time, the cost of experimental stem cell treatments is not covered by insurance companies. We believe that our research is university quality. We are patient funded and we have no source of grants or pharmaceutical company funding. Although we are a for-profit organization, our goal is not to patent stem cell technology for corporate profit but rather to learn the medical potential of these cells and contribute to the science of regenerative medicine. We have set our fees very reasonably to lower the threshold of access to stem cell medicine. Our fee includes harvesting, isolating cells and deployment of your own cells. Also, under special conditions, your stem cells may be cryogenically stored for future treatments.

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