For more than 40 years, Lesley Kelly of Glasgow, Scotland, lived with third-degree burns that stretched over 60 percent of her body.

Kelly was 2 years old when she fell into a bathtub filled with hot water that scorched most of the right side of her body. She lost full range of motion around many of her joints.

"When you have bad scarring, the buildup is very thick and has no elasticity," said Kelly, 45, whose right elbow was most affected by the buildup of scar tissue. "The problem with thermal burn scarring [is that] it's hard to get the range of motion."

Kelly underwent numerous reparative surgeries through the years, but the scar tissue continued to grow back. The procedures did not lessen the look of her scars.

In 2011, Kelly underwent a new, experimental procedure that used stem cells from her own fat tissue to repair the buildup around her right elbow.

Surgeons cleaned the scar buildup around the elbow and used liposuction to pull fat from off Kelly's waist. They separated the fat cells from the stem and regenerative cells, which were then injected into the wound on Kelly's arm. The procedure took less than two hours.

Within months, Kelly was able to regain 40 degrees of motion that she had lost more than 40 years ago.

Cytori Therapeutics, Inc.

"If this technology was available earlier in my life, my scars would not have been as bad," said Kelly.

There are an estimated 50,000 to 70,000 burn cases each year in the U.S., according to the American Burn Association.

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New Therapy May Help Burn Victims

Miami, FL (PRWEB) October 01, 2012

The Conference was geared to offer attendees the opportunity to attain updated information regarding current and future applications in cord blood stem cells as well as the ongoing research in regenerative medicine. It took place at the Charles Hotel in Cambridge Massachusetts, in the vicinity of Harvard University, minutes from the heart of Boston.

The event was attended by 300+ notable and prominent doctors, scientists and regulators in the field of stem and featured numerous keynote speakers. The program kicked-off with the chairmans opening remarks on the perspective on the cord blood market. Entities involved in the collection, processing, cryopreservation, transplantation and research shared their and experiences with the rapidly evolving future of cord blood stem cells and related tissues. Some presentation topics included were:

Umbilical cord blood preservation is a process by which blood is collected from the umbilical cord of a newborn baby and is stored cryogenically in a specially-designated bank. According to the National Marrow Donor Program, cord blood contains cells that can be transfused to a patient to treat various diseases, including lymphoma and leukemia. Currently, there are approximately 80 treatable diseases and the list of illnesses continue to grow. Cord blood is rich in stem cells and there is less risk for the recipients immune system to reject the cells, because certain immune cells found in the cord blood are not mature. Cord blood can be used to treat the child from whom the blood was collected as well as some first-degree relatives who are a close genetic match, such as family members. Additionally, patients can get the treatment in about three weeks - as opposed to six to eight for bone marrow from an adult donor.

A persons blood stem cell type is inherited, which means a patient is more likely to find a matched donor from within their own ethnic group, said GeneCells Director of Operations, Jose Cirino. More than half of cord blood donations and privately banked cord blood in the United States are from Caucasians while minorities remain underrepresented. By increasing the awareness of cord blood advantages among minorities, there is a potential for increased access to therapies for more people.

The shortage, or lack of availability, affects patients of African, Asian, Hispanic and Native American Indian descent. Since patients who need a transplant are more likely to find a match within their own race, Cirino adds it is important that the pool of donors reflects the overall community.

Why isn't everyone banking these cells? What transpires is that people are not informed about stem cell banking and some have never even heard of it. Most people are not aware they have stem cells in their body, they believe that stem cells only come from human embryos since that is what is mainly discussed in politics and the news. However, this is not the case. These cells are found in adults and there are no moral, ethical or political issues surrounding these cells.

The amazing thing about these cells, aside from their potential to treat a variety of different diseases, is that for the most part they can be harvested from the individual through relatively minimally invasive procedures and can be cryogenically frozen (at a temperature of -321 F) and stored for decades until a disease manifests or they are needed for cell-based therapies added GeneCells Director of Research & Laboratory Operations, Dr. Todd R. Flower.

GeneCell International specializes in the collection, transport, processing and cryogenic storage of adult stem cells from various sources including; umbilical cord blood, cord tissue, dental pulp and adipose tissue (fat) that can later be used to treat a variety of diseases. The laboratory is also involved in scientific research and development with a range of stem cells from various adult tissues. The facility is governed and inspected by the FDA as well several other regulating bodies to ensure the safety of these cellular therapies.

Alongside its commitment to educating the public on the benefits of cord blood preservation, GeneCell is committed to being on the forefront of stem cell research. GeneCell International is the only Cord Blood, Cord Tissue and Dental Pulp Processing and Cryogenic Storage Laboratory to offer this cutting-edge, regenerative medicine technology in Miami, Florida.

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GeneCell International, Miami’s Only and Preferred Cord Blood Laboratory, Participates in The Stem Cells USA & World ...

HOUSTON, Oct. 1, 2012 /PRNewswire/ --Celltex Therapeutics Corp. announced today that it has received a letter, dated Sept. 24, 2012, from the U.S. Food and Drug Administration. The letter stated the agency's opinion that the process Celltex uses to multiply adult stem cells is subject to FDA regulation as biological drug manufacturing. The issue is a key one as stem cell therapy for patient care outside of an academic institution is a new frontier, yet there are a variety of technologies being used throughout the United States, often creating complex legal and regulatory questions.

David Eller, CEO and President of Celltex, stated:

Celltex makes identical copies of an individual's own stem cells and therefore should not be subject to FDA regulation as drugs. However, the FDA said our process causes the cells to be considered biological drugs and thus is subject to those regulations. We respectfully but firmly disagree with the FDA and intend to contest the agency's opinion within its administrative procedures. We are considering all options as we work with the agency toward a resolution.

FDA's letter also repeats its earlier observations from an April inspection of Celltex's laboratory. While Celltex provided detailed responses in April, May, June, July and August, now FDA tells us it needs more information. We will answer FDA's questions in whatever detail the agency requests."

We will meet FDA's requirements, no matter how high the hurdles may be, to ensure access to this technology. Celltex remains fully committed to advance the most promising new field in human health in decades regenerative medicine. We also remain committed to doing so safely, and we will continue to comply with federal and state agency requirements.

As we work with the FDA, Celltex will continue to make advances on the frontier of regenerative medicine, and we expect to have several significant announcements in the coming weeks on these matters:

"Celltex is committed to developing the promise of regenerative medicine into a reality for doctors and their patients," Mr. Eller said. "We sponsor clinical trials to better understand the therapeutic impact and monitor the safety of adult stem cell therapy, and we are confident that our research will help implement effective treatments for patients suffering from a variety of medical conditions."

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Celltex To Initiate New Clinical Program As It Responds To FDA Letter

(Part III)

Primum Non NocerePrimarily, do no harm. This is the principal dictum of Dr. Samuel D. Bernal, MD, PHP, JD, MBA.

Board-certified and diplomate of the American Board of International Medicine and a fellow of Harvard Medical School, this doctor of chemistry, oncology and human biochemistry, health and regulatory law (specifically medical malpractice) holds offices in Los Angeles, Prague and Manila.

His name is synonymous with personalized molecular medicine, the heart of which evolves around stem cells.

Dr. Bernal pioneered in the analysis of the electrical energy of the cell in the living state. And thus, in his regimen, which includes 300 mixes of vitamins, minerals, proteins and essential fats, the electrical production of the mitochondria is ensured.

Here is the result of our two-hour candid discussion about rejuvenation, health and beauty. While the 120-minute immersion cant give a complete understanding of the vast and complex world of the human body, it was nevertheless enough time to begin to grasp the basic truththat all the power of life rests within us all.

Q: What exactly are stem cells?

Stem cells (SC) are merely a small component of what we call regenerative medicine. And they have the ability to heal and repair the body back to a good health.

Q: Isnt it as simple as injecting stem cells into the human body?

Definitely not. There is the matter of molecular biology. No two individuals are alike. And this makes the idea of injecting a commercially-prepared stem cell solution into your body questionable and even dangerous.

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An expert talks about stem cells