Instead of just covering up joint pain with medicine, regenerative medicine uses biologics derived from human embryonic tissue that is rich is cytokines, growth factors and proteins to actually regenerate human tissue
Do you suffer from pain in your joints and tendons?
At Advanced Health NY, we are pleased to offer a modern, science based regenerative medicine program for treating pain and inflammation. Medical literature and studies show how effective these treatments are and they are approved by the FDA and covered by some insurances.
Treatment with regeneratives has been effective in alleviating painful symptoms of arthritis and other forms of pain. Patients generally feel relief throughout the treatment period, are able to function better and even feel better emotionally. Unlike steroids which only provide immediate relief of pain, regeneratives work by regenerating human tissue, providing repair and relief over time, that lasts many years.
HUMAN EMBRYONIC TISSUE
Regenerative medicine products are “game changers” with their healing capabilities. Now with injectable Human Embryonic Tissue products, you can harness the powerful properties of regeneration.
Human Embryonic Tissue has unique characteristics that enhance structural support in body areas such as ligaments and joints, as well as providing insulation and lubrication to these structures and surrounding areas.
Human Embryonic Tissue products contain mesenchymal stem cells, growth factors, and other essential molecules necessary
for regeneration. They consist of high levels of extracellular matrix components; mainly collagen, hyaluronic acid and proteoglycans. Additionally, their vast reservoir of many peptide growth factors are essential for healing and regrowth.
Our products derived from Human Embryonic Tissue present a viable and more effective alternative to NSAID and steroid injections in reducing or eliminating the often debilitating pain associated with musculoskeletal injuries.
How Does It Work?
The biological components of regeneratives contain the building blocks (proteins, growth factors, antibodies) for stem cell activation and dedifferentiation. These mesenchymal and stromal cells used by your body to build, repair and regenerate human tissue. See the chart to the left for a detailed list of components and their function.
Where do these regeneratives come from?
Human Embryonic Tissue is sterile, safe, and obtained from consenting mothers at scheduled c-sections and does not utilize any fetal tissue.
Is it safe?
Human Embryonic Tissue is obtained and processed using a carefully controlled and stringent process. There are no side effects associated with this type of treatment.
Is it comfortable?
Human Embryonic Tissue is designed to be comfortably injected into a joint or soft tissue with minimal discomfort.
Tylenol may be used for pain relief unless there are known allergies.
It is best to avoid aspirin, ibuprofen, Advil, Aleve, Naproxen and icing for eight weeks after the injection.
The benefits of regenerative medicine take time. You should expect improvement after three months. If there is only minimal improvement, the procedure can be repeated up to two more times at three month intervals.
What conditions can benefit from Human Amniotic Fluid?
Rotator Cuff Pain
Using Human Embryonic Tissue is less invasive compared to Platelet Rich Plasma (PRP), bone marrow aspiration or adipose tissue extraction. No harvesting of tissue is required.
Human Embryonic Tissue related products have higher concentrations of growth factors, peptides and hyaluronic acid compared to PRP.
Human Embryonic Tissue has a high anti-inflammatory property due to its large concentrations of growth factors and cytokines.
Human Embryonic Tissue contains high levels of hyaluronic acid which assists in lubricating, supporting and aiding mobility in joints and tendons.
Studies report that mesenchymal stem cell products isolated from Human Embryonic Tissue are more effective than those isolated from adults.
Human Embryonic Tissue treatment may be covered by Medicare, as well as other insurance plans. Generally six to eight weeks of physical therapy is required for medical necessity. Some insurances require a cortisone injection to be tried first. At this time Medicare is reviewing coverage of these product and will not reimburse for it, however, cash pricing is available.
Collagen and Glycosaminoglycans of Wharton’s Jelly
Whartons Jelly as a reservoir of peptide growth factors
Sonolewski K, Bankowski E, Chyczewski L, Jaworkski S
Adult MSC for Tissue Engineering vs Regenerative Medicine
Jnl of Cellular Physiology
Caplan, AI, 2007
Amniotic fluid and placental membranes: unexpected sources of highly multipotent cells
Gestational tissue such as the placenta, placental membranes, and amniotic fluid are usually discarded following birth. Recently, researchers have identified gestational tissue as an untapped source of stem cells that are highly multipotent and possess potent immunosuppressive properties. Placental mesenchymal stem cells (MSCs), human amnion epithelial cells (hAECs), and amniotic fluid-derived stem cells (AFSCs) have been shown to differentiate into various cell types including adipogenic, osteogenic, myogenic, endothelial, pulmonary, neurogenic, hepatogenic, cardiac, and pancreatic lineages. Their immunomodulatory properties suggest that gestational stem cells may have an important application in the treatment of various inflammatory diseases such as graft versus host and autoimmune diseases. In clinical and preclinical studies, gestational stem cells have shown efficacy in the treatment of Crohn disease, lung disease, diabetes, repair of bone defects, heart disease, kidney disease, neural degeneration, and blood disorders. Stem cells derived from the placenta, placental membranes, and amniotic fluid are a valuable resource for the field of regenerative medicine.
Stem cells from amniotic fluid--Potential for regenerative medicine
Regenerative medicine has recently been established as an emerging field focussing on repair, replacement or regeneration of cells, tissues and whole organs. The significant recent advances in the field have intensified the search for novel sources of stem cells with potential for therapy. Recently, researchers have identified the amniotic fluid as an untapped source of stem cells that are multipotent, possess immunomodulatory properties and do not have the ethical and legal limitations of embryonic stem cells. Stem cells from the amniotic fluid have been shown to differentiate into cell lineages representing all three embryonic germ layers without generating tumours, which make them an ideal candidate for tissue engineering applications. In addition, their ability to engraft in injured organs and modulate immune and repair responses of host tissues suggest that transplantation of such cells may be useful for the treatment of various degenerative and inflammatory diseases affecting major tissues/organs. This review summarises the evidence on amniotic fluid cells over the past 15 years and explores the potential therapeutic applications of amniotic fluid stem cells and amniotic fluid mesenchymal stem cells.
Mesenchymal Stem/Stromal Cells in Regenerative Medicine: Past, Present, and Future
The concept of Regenerative Medicine combined with Cell based Therapy and Tissue Engineering represents the fourth pillar of healthcare and provides a promising approach for the treatment of serious diseases. Recently, cell based therapies are focused on the use of mesenchymal stem/stromal cells (MSCs). Human MSCs, that represent a mesoderm derived population of progenitors, are easily expanded in culture. They are capable to differentiate into osteoblasts, chondrocytes, and adipocytes and exhibit the potential to repair or regenerate damaged tissues. The best characterized source of human MSCs to date is the bone marrow; recently, fetal sources, such as amniotic fluid, umbilical cord, amniotic membranes, or placenta, have also attracted increased attention. Thus, MSCs may represent a valuable tool for tissue repair and cell therapeutic applications. To this end, the main focus of this review is to summarize and evaluate the key characteristics, the sources, and the potential use of MSCs in therapeutic approaches and modalities.
These statements have not been evaluated by the FDA but these products have been approved by the FDA for use as Anti-inflammatories. These products are not intended to diagnose, treat, cure or prevent any disease. Consult your physician before beginning any program.