Interventional and Diagnostic Radiology
Medical Imaging & Therapeutics, Lady Lake, FL
Dr. Mark D. Jacobson serves as the CEO, Medical Director, and founder of Medical Imaging and Therapeutics, located in Lady Lake, Florida. With decades of expertise in joint, vascular, and spine interventions, he holds Board Certifications in both Diagnostic Radiology and Interventional Radiology. Specializing in minimally invasive, image-guided therapies, Dr. Jacobson is an expert in his field.
Dr. Jacobson earned his medical degree from Wake Forest University’s Bowman Gray School of Medicine in Winston-Salem, NC. Following this, he completed a General Surgery internship at NC Baptist Hospital, also affiliated with Wake Forest University. His Diagnostic Radiology residency took place at St. Francis Medical Center in Pittsburgh, PA, and he later pursued a fellowship in Interventional Radiology at the Pittsburgh Vascular Institute.
Dr. Jacobson is a board-certified radiologist with a Certificate of Added Qualification in Vascular and Interventional Radiology. He holds memberships in several prominent organizations, including the Florida Medical Society, Radiology Business Management Association, Society of Interventional Radiology, and the American College of Radiology. Additionally, he is a charter member of the Outpatient Endovascular and Interventional Society.
Since 2016, the University of Florida’s Division of Interventional Radiology has selected Dr. Jacobson and his center as a model independent residency training program for Interventional Radiology Fellows. His dedication to education has earned him multiple “Outstanding Teacher of the Year” awards.
Genesis® Regenerative Protein Arrays
Genesis® Regenerative Protein Array RPA represents a groundbreaking therapy in regenerative science and medicine due to its sophisticated array of proteins, growth factors, and cytokines derived from placental tissue. This innovative approach to healing and anti-aging is based on the understanding that the therapeutic power of regenerative medicine lies not in the direct transformation of injected cells into target tissues, but rather in their ability to modify the surrounding cellular environment through key biologic messages.
Genesis® RPA is created in a proprietary process of placing placental tissue in a specialized bioreactor, encouraging the emission of a rich array of healing components from all three layers of the placenta (endo/ecto/mesoderm) that are responsible for brain/nerve, soft tissue/organ, and musculoskeletal development in humans. The resulting product is an acellular, non-biologic, concentrated source of the broadest spectrum of bioactive components found in any regenerative product on the market, and these proteins have been proven in clinical studies to be pivotal in tissue regeneration and healing.
Genesis® RPA is in a category of products that the FDA refers to as cell factors. The FDA’s position on cell factors is similar to sterile nutraceuticals or drug ecacy study implementation programs for unapproved drugs. The FDA regulates the manufacturing, processing, and distribution, but allows licensed clinicians to make use and care decisions in collaboration with their patients. PDPA is produced in an FDA-registered facility following Human Cellular Therapy Tissue Product standards.
In summary, Genesis® RPA is a transformative development in regenerative medicine, offering potent, safe, and versatile treatment options for a range of medical conditions. By harnessing the power of placental derived growth factors and cytokines, Genesis® RPA opens new avenues in the pursuit of healing and tissue regeneration, making a significant stride forward in medical science.”