What are stem cells?
Stem cells are the basic building blocks of human tissue and have the ability to repair, rebuild, and rejuvenate tissues in the body. When a disease or injury strikes, stem cells respond to specific signals and set about to facilitate the healing process by stimulating your own body to repair itself.
Stem cells that come from perinatal tissue(healthy post-natal C-sections) have distinct functional properties including immunomodulation and anti-inflammation which support the repair and regeneration of damaged tissue associated with disease and injury.
There are four known types of stem cells which include:
We provide allogeneic regenerative cytokines and mesenchymal stem cells from health post-natal C-sections.
We tap into our bodys stem cell reserve daily to repair and replace damaged or diseased tissue. When the bodys reserve is limited and as it becomes depleted, the regenerative power of our body decreases and we succumb to disease and injury.
Three sources of stem cells from a patients body are used clinically which include adipose tissue (fat), bone marrow and umbilical cord matrix(Whartons Jelly).
We provide stem cell therapy for a wide variety of musculoskeletal conditions for which traditional treatment offers less than optimal options. Some conditions include Osteoarthritis, Bursitis, Plantar Fasciitis and Degenerative Disc Disease
Since each condition and patient are unique, there is no guarantee of what results will be achieved or how quickly they may be observed. According to patient feedback, many patients report results in one to three months, however, it may take as long as six to nine months. Individuals interested in stem cell therapy are urged to consult with their physician before choosing investigational allogeneic umbilical cord derived regenerative medicine allografts as a treatment option.
In order to determine if you are a good candidate for a regenerative medicine treatment, you will need to complete a medical history form which will be provided by our patient advocate team. Once you complete and submit your medical history form, our medical team will review your records and determine if you are a qualified candidate for a regenerative medicine therapy.
The side effects of intra-articular injection of a regenerative medicine allograft are minimal and may include but are not limited to: infection, minor bleeding at the treatment sites and localized pain. However, these side effects typically last no longer than 24 hours.
We provide regenerative medicine allografts from healthy post-natal C-section births that provide regenerative factors and mesenchymal stem cells. Embryonic stem cells are typically associated with ethical concerns. We do not offer embryonic stem cells.
Our regenerative medicine allografts are regulated as human cell and tissue transplants, similar to skin and bone. As structural human cell and tissue products regulated under FDA CFR 1271 Part 361, our allografts do not require FDA approval, rather we are strictly regulated to prevent the spread of communicable diseases and to maintain the structural integrity of the allografts as theyre harvested from umbilical cords and transferred for musculoskeletal cushioning, protection and supplementation. These regenerative allografts are FDA regulated rather than FDA approved. The FDA is a regulatory oversight body and doesnt exercise legal authority. If an FDA regulated tissue transplant or therapy is noted as non-compliant and not corrected according to FDA guidelines, the FDA may refer a significant public health risk to the Department of Justice or a state attorney general.
Stem cell treatment is not covered by health insurance at this time.
Although stem cells are found throughout our bodies, mesenchymal stem cells can only be harvested for native (non-cultured) use from adipose, bone marrow and umbilical cord matrix. The term amniotic stem cells is an oxymoron in that amniotic fluid and matrix products dont contain stem cells. They do however contain unique cytokines and other growth factors.
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