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Scientists have found that aerobic exercise triggers adult stem cells to become bone more often than fat. What they are suggesting is that exercise is a potent stimulus — enough of a stimulus to actually trigger a switch in these [adult] stem cells.
Exercise Helps Adult Stem Cells Build Bone, Not Fat
BIOETHICS DAVID PRENTICE, PH.D. SEP 1, 2011 | 6:06PM WASHINGTON, DC
Canadian scientists have published data that indicate exercise stimulates adult stem cells to form bone instead of fat.
The scientists used a mouse model to study exercise effects on adult bone marrow stem cell and blood production. Using treadmill-conditioned mice, they found that aerobic exercise triggers adult stem cells to become bone more often than fat. The bone environment provides better conditions, called a “niche”, for adult blood stem cell development. When the mice were sedentary, the stem cells tended to form fat, which impairs blood production in bone marrow cavities.
Dr. Gianni Parise, senior author on the study, said:
“The interesting thing was that a modest exercise program was able to significantly increase blood cells in the marrow and in circulation. What we’re suggesting is that exercise is a potent stimulus — enough of a stimulus to actually trigger a switch in these [adult] stem cells. Exercise has the ability to impact stem cell biology. It has the ability to influence how they differentiate.”via
Am I a Candidate for Stem Cell Treatment?
Posted:
9/3/2011 12:00:00 AM by
CJ Simpson | with
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Former Springbok rugby player Joost van der Westhuizen has undergone Repair Stem Cell treatment for a fatal motor neuron disease (MND).
Van der Westhuizen's neurologist Dr Jody Pearl says that the treatment was safe, but there was no guarantee it would have any real benefit.
"We don't know if we'll be able to help with the MND...(the) therapy is the most promising treatment we have to date in any kind of degenerative condition," she said.
"But I think we need to be cautiously optimistic."
Van der Westhuizen, 40, said he would continue to fight the disease, for which there is no known cure.
"I've been a fighter all my life," Van der Westhuizen told The Times daily.
"I'm going to fight this thing mentally and to the best of my ability.
"Don't worry, I'm not going to die on you too soon. I'm going to fight it."
Van der Westhuizen reportedly became the first South African to undergo the treatment, developed by United Kingdom neuroscientist Dr Steve Ray, two weeks ago.
Doctors injected some of his stem cells back into his body, with the hope that the cells would repair damaged muscle tissue.
Van der Westhuizen, who first realised there was something wrong with his right arm late last year, was diagnosed in July.
He played in South Africa's victorious 1995 Rugby World Cup team and at one stage held the record as the most capped Springbok player.
Posted:
8/25/2011 2:38:42 PM by
Don Margolis | with
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By: Priyanka Vora
Date: 2011-08-16
Place: Mumbai
Muscular dystrophy-afflicted child is responding to stem cell therapy, which is emerging as the most popular treatment for rare and fatal genetic disorders.
Meet Harshu Singh. This wheelchair-bound, frail eight-year-old cannot play or enjoy classes at school. Denying him these small childhood pleasures is Duchenne Muscular Dystrophy, a genetic disorder that weakens muscles of children, ultimately making them wheelchair dependent even before they cross the age of 10. But shining a faint ray of hope into his bleak condition is stem cell therapy, which is fast becoming the most popular treatment for diseases involving muscular dystrophy.
New lease of life: Harshu Singh
Harshu was diagnosed with DMD at the tender age of three, when he started finding it difficult to walk, or even change sides in bed. "Harshu's mother Sujata said, "It is a genetic disorder, and even my brother's kids have been diagnosed with it. Everywhere we went, the doctors insisted there is no cure for this fatal disorder. One day, I read about a miraculous recovery of a boy the same age as Harshu, who was suffering from DMD. I discovered that stem cell therapy was the only cure, and decided to opt for it."
Harshu has already undergone five sessions of stem cell therapy, wherein doctors have injected stem cells of heterologous origin into his blood stream. "We first obtain stem cells from the umbilical cord of a new born infant in the lab, after which they are injected intravenously. In Harshu's case, the muscle degeneration appears to have stopped, and he has regained some movement in his hand and leg. These are clear signs of improvement," said Dr B S Rajput, consultant stem cell transplant surgeon, Criti Care hospital.
Adding that he has used stem cell therapy for over 100 patients suffering from various forms of muscular dystrophy, Rajput said, "This disorder has no documented treatment, but stem cell therapy has shown a ray of hope. We have noticed substantial improvement in a large majority of cases. The administration of mesenchymal stem cells has helped in the short term. Doctors are trying to gauge its efficacy in long-term treatment as well."
Did you know?
Duchenne Muscular Dystrophy is a congenital neuromuscular disorder that occurs in approximately 1 out of every 3,600 male infants, who are more prone to it than female infants. Patients usually live till the age of 25.
Posted:
8/16/2011 2:52:33 PM by
Don Margolis | with
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One of the Toughest:
Ava starts her journey towards a more normal life.
Two-year-old Ava McCulloch has a reason to smile - she's starting to feel better.
Ava was born with Spina Bifida, a neurological disorder that makes it difficult for her to walk.
"It affects nerves in the body below that point where her spinal cord was sticking out at birth, so there's some nerve damage that was done," said Ava's mother Jessica.
After doing some online research, Jessica discovered a procedure that could change her daughter's life - stem cell treatment. The procedure isn't available in the United States, so the McCulloch family took a trip around the world to China.
"They use these stem cells, which came from healthy Chinese babies, and they put them in by IV into her feet," said Jessica.
The doctors use stem cells from umbilical cords instead of embryos. Jessica said she was told not to expect any results right away - but that's exactly what happened.
"We started the treatment and the therapy, and after about the third stem cell treatment and the seventh day of acupuncture, she started crying," said Jessica.
Those tears meant that Ava was able to sense the pain for the first time. Jessica said her daughter is one step closer to walking without ankle braces.
"Now that we have seen things happen, which this isn't the end of it, more progress is suppose to come months down the road, and it's very exciting," said Jessica.
Jessica said that Ava will need to continue her therapy, and the family is trying to return to China within the next year for another procedure. Until then, Ava's smile is all the encouragement they need.
Posted:
8/13/2011 7:05:49 AM by
Don Margolis | with
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ST. THOMAS - Jackson Vandermark is like a lot of kids his age. He loves trucks, eating and being outdoors. The young St. Thomas resident, however, is unique in that he's now one year removed from a brain operation his family had to travel thousands of kilometres to see done.
Almost a year to the day since St. Thomas and Elgin community members sponsored the Vandermark family's trip to Dusseldorf, Germany for a complex, stem cell procedure for their son to help treat his cerebral palsy, the seven-year-old's mother reports he is more articulate and active than ever.
"His speech has definitely improved, adding from just a one-word sentence to two or three sentences put together .... We never used to have to watch what we said around Jackson, we could say whatever we wanted with no fears of him repeating it but he repeats everything now," Jackson's mother, Carrie Pasch, told the Times-Journal in an interview in their St. Thomas home.
"His core strength has definitely strengthened as well... (and), oh God, does he have a memory. Let's say his grandpa was going to pick him up tomorrow and take him to a boat show. Well, we wouldn't tell him right now becuase he would be up at three in the morning getting ready to go."
Last August, Jackson, diagnosed with the brain affliction when he was an infant, travelled with Pasch, his father, Greg Vandermark, and brother, Cooper, 3, overseas for an operation neither offered in Canada nor covered by OHIP.
The process involved two separate surgeries. The first pulled bone marrow from his hip and the resulting stem cells were then implanted near his brain stem with hopes that they would attach, replace and repair damaged cells.
The family raised about $40,000 with about $35,000 going towards paying for the procedure and the rest used for travel expenses.
Pasch recalls the hardest part for Jackson was dealing with the needle doctors used to inject anesthetic.
"I went in (the operating room) while they put him to sleep and the prick scared him, hurt him. So he started to cry and he looked right at me he goes, 'mom, home.' It broke my heart...but he instantly fell asleep so he wasn't laying there for a long time crying and stuff. He said that and his eyes fluttered and he was right out."
But that was far from the only time Pasch says the whole ordeal affected her heart.
After the second procedure, Pasch became alarmed when Jackson was nauseous and constipated for two days following the brain operation.
"When he was sick and vomitting those two days after the procedure, to be honest, I was doubting myself. Like, what have we done...what if this isn't what we were supposed to do? It was one of the scariest times of my life," she said.
"You know Jackson's sick when he doesn't want to eat. So that's how we know when he's really not feeling well."
However, Jackson began improving after those two days and Pasch says his recovery was an immense weight off the entire family's shoulders.
"We had faith that he was going to be fine. So, I mean, you're scared but you can't think the worst is going to happen .... (After those two days,) then we could enjoy our time, as soon as he felt better," she adds.
The trip was extremely exciting for Jackson in more ways than one.
Aside from the major surgery, it was his first time on an airplane.
Pasch says that his affinity for loud motors made the booming plane engine something he thoroughly enjoyed and that he and Cooper were less nervous about the long flight than she was.
The trip also gave the family a chance to reconnect with Jackson's great aunt and uncle and grandparents on his father's side who live in Holland.
Come September, Jackson is going into Grade 2 at John Wise P.S. The young man has a smile that's as wide as it is bright and he doesn't hesitate to show it off. Ask him what his favourite part about school is -- which he refers to as work -- and he'll flash the grin and tell you it's eating.
A year after the fact, Pasch says Jackson is doing great. She says she wants to thank all the people who made the trip possible and let them know that she appreciates the time, effort and money they put in.
She also credits hospital staff at Dusseldorf's XCell-Center for being so adept and the friends she met during her time in Germany for helping make things go as smoothly as they could. One family in particular, she adds, made the second procedure go by much quicker.
"When Jackson was in the (second) procedure, this one family from the states there talked with us about Jackson. It probably would have been one of the longest half an hours of our lives (otherwise)," she said.
A full list of people and groups Pasch wants to thank can be found at www.stthomastimesjournal.com in the online edition of the article.
One year after the family travelled over 6,000 kilometres for the major surgery, Pasch adds it was all worthwhile.
"It definitely was worth it because I have no idea, if we hadn't taken him, if he would have been adding those words together or if his balance would have been better, or his core strength would have been better....We'll knever know but it definitely was worth it because, I mean, we'll try anything for him," she said.
"Words can not explain how thankful we are to everyone."
Posted:
8/12/2011 8:46:13 AM by
Don Margolis | with
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A survey of recent headlines about medical treatment received by Governor and potential presidential-hopeful Rick Perry of Texas could easily lead one to believe that he is a Texas-sized hypocrite when it comes to his opposition to human embryonic stem cell research. Once again, the mainstream media has things seriously wrong.
A Google search turns up articles with misleading titles, such as: “Stem Cell Critic Receives Stem Cell Therapy,” “Rick Perry has Stem Cell Procedure, Then Works to Bring it to Texas,” “Gov. Rick Perry Underwent Stem Cell therapy,” and “Report: Rick Perry Had Experimental Stem Cell Therapy.”
While there are a few exceptions, most of articles that address Gov. Perry’s treatment include titles that could easily lead one to believe that he accepted a treatment for his own medical condition that he has historically opposed for the treatment of others.
Of course, if you have the patience to read most of the articles carefully, you will see that the authors are forced to acknowledge that Gov. Perry’s treatment did not use stem cells taken from destroyed human embryos, and thus, he is not a “hypocrite” for opposing treatments that are based upon the use of such stem cells. In fact, it is the right position to take: opposing unethical research, while supporting ethical alternatives. Human embryonic stem cell research is morally wrong because it is rooted in the destruction of a human being; but other kinds of stem cell research, not involving the taking of a human being’s life, are not immoral.
Still, suspicious and judgmental reporting regarding
Gov. Perry’s treatment—and adult stem cell treatments in general—is typical of the mainstream media, seemingly bent upon advancing embryo-destructive stem cell research while downplaying the dramatic successes achieved through adult stem cell research. The media often seem blind to the simple (but clear) ethical differences.
Perhaps the most baffling and disingenuous aspect of the articles, however, is their (mis)characterization of adult stem cell research. For example, one article states that “the use of adult stem cells has not been proven to be effective.” Another quotes unnamed “researchers” who say that “they’ve seen nothing more definitive than the so-called ‘placebo effect’” from adult stem cell research.
In reality, treatments developed from adult stem cells are being used every day to treat once incurable diseases and serious injuries. Scientists have been able to help patients suffering from over 70 different diseases and injuries—including brain cancer, leukemia, lymphoma, Crohn’s disease, lupus, heart damage, Parkinson’s disease, Sickle cell anemia, and end-stage bladder disease—using adult stem cells. It is deeply disappointing that the media continues to treat these life-affirming advances as insignificant, while chasing what may well be a pipe dream that life-destroying embryonic stem cell research will one day yield dramatic results.
Posted:
8/12/2011 8:19:31 AM by
Don Margolis | with
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By PAT BRENNAN / ORANGE COUNTY REGISTER
Survival for brain-cancer patients treated with chemotherapy comes with a dark side: "chemobrain," the debilitating loss of memory and mental function that often follows.
Now scientists at the UCI Medical Center are preparing a new weapon that could one day clear the cognitive fog.By manipulating stem cells, researchers Daniela Bota and Mark Linskey, both doctors who also treat cancer patients, say they may be able to place a bull's eye over tumor cells and wipe them out, while leaving the brain intact.
Their successes so far have all taken place in a petri dish, and it will likely be years before they can try their method on human patients.
But already, one expert is calling their discovery "the first truly novel approach to brain tumor therapy in more than four decades."
"Our cause and our passion is to take care of patients," Bota told a recent visitor to her lab on the hospital's campus in Orange. "That always comes first."
The first step would be to modify chemotherapy drugs so they can kill cancer without killing the brain cells around it.
But the two scientists, who are part of the hospital's Comprehensive Brain and Spinal Cord Tumor Program, have far bigger ideas.
"We hope to be able to do transplantation with human neural stem cells, and try to re-create memory and cognition," Linskey said. "That is sort of our big dream."
Their potential treatment hinges on the bizarre similarities between tumors and healthy tissues in the human body.
Both, for example, have their own versions of stem cells, the precursors that give rise to a variety of organs and other structures.
In normal tissues, these cells receive chemical signals that prompt them to become one thing or another.
The vast potential of stem cells, in fact, is driving an explosion of discoveries, Bota's and Linskey's among them.
The world's first trial of a treatment for acute spinal cord injuries using human embryonic stem cells, developed by UC Irvine stem-cell researchers Hans Keirstead and Gabriel Nistor, is now underway.
Many other conditions, from Alzheimer's to fatal childhood diseases, could one day be treated using stem cells.
But the "stem cells" in tumors are of a decidedly destructive variety.
Instead of differentiating into brains or bones or kidneys, they proliferate wildly, their chaotic growth becoming the tumors that disrupt the body and brain, and eventually kill.
Stem cells are also the tumor's greatest weakness.
By aiming chemical weapons at features found only on the tumor stem cells – a protein, for example, on the surface of the cell – Bota and Linskey hope to turn the tables on tumors, disrupting their mad growth while having little or no effect on normal cells.
Their early work on the problem is already making waves in the scientific community, with other researchers seeking out the two scientists and their co-authors by phone or email, and comments and references showing up in scientific journals.
In March, they published their highly suggestive findings. They found that two commonly used chemotherapy drugs did profound damage to neural stem cells, provided by Dr. Philip Schwartz at the Children's Hospital of Orange County and grown in their laboratory.
But the drugs had little effect on the tumor stem cells, or "glioma stem-like cells."
Meanwhile, two newer chemotherapy drugs had the opposite effect, causing little damage to the neural cells but knocking down tumor stem cells.
It's a long way from the petri dish to trials in human patients; tests on laboratory rats will come first.
And the findings by themselves also don't prove the connection between the resistance of tumors to some forms of chemotherapy and the "chemobrain" that later plagues patients.
But if the theory stands up to scientific scrutiny, it could make a huge difference in the lives of cancer survivors -- not only brain-cancer patients, but those who beat other forms of cancer and also suffer chemobrain.
Among them are breast-cancer patients, who show a 70 percent rate of memory loss after chemotherapy.
Children could be among the biggest beneficiaries of a chemobrain treatment, Bota said. They can have as high as an 80 percent survival rate after chemotherapy for brain cancer.
But the cognitive deficits that result can lower their quality of life and make it difficult, and perhaps impossible, to get on with their young lives: go to school, get a job.
"What you see at the end is the tumor in remission, the patient in dementia," Bota said.
For adults, such effects might explain why divorce rates among brain cancer patients are high.
"What we hear over and over again is, 'This is not the person that they used to be,'" she said.
It gets down to what Linskey believes could become a fundamental shift in the standards doctors use to decide whether or not a treatment is successful.
"The brain defines who we are as a person," he said. "The goal is to have the same person at the end of the treatment as you had when you started."
Cancer doctors Mark Linskey and Daniela Bota look over plans for experiments at the UC Irvine Medical Center. They hope to do battle with "chemobrain," a loss of memory and mental function that can follow chemotherapy treatment.
Posted:
8/4/2011 3:25:15 PM by
Don Margolis | with
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Danny Cox and his younger brother, Charlie McGowan, play a game on Danny's phone outside his granny unit, which has been adapted to meet his needs.
Terry Hankins/Argus-Courier file photo, February
By
Dan Johnson
ARGUS-COURIER STAFF
Published: Monday, August 1, 2011 at 11:59 a.m.
Last Modified: Monday, August 1, 2011 at 11:59 a.m.
A benefit golf tournament is planned for Sept. 9 to help a Petaluma teenager paralyzed in a diving accident last year receive additional stem cell treatments in Panama City.
The Second Annual Danny Cox Benefit Golf Tournament will be held at Rooster Run Golf Course, at 2301 E. Washington St., to raise funds for the Petaluma High School graduate who suffered a broken neck and was paralyzed from the chest down after doing a flat dive into shallow water at Lake Tahoe on Aug. 10.
The golf tournament is one of several local fund-raising events that have been organized to help Cox's family pay medical expenses as he tries to regain some of his physical functions. He has traveled to Panama City twice for stem-cell treatments, and after the second treatment he regained motor functions in a pinkie finger and his right tricep.
“Now, a year later, Danny has not plateaued in terms of physical and nerve progress,” said Maureen McGowan, his mother. “All in all, Danny has literally broken through the prognosis given by the docs treating him, and continues to push past his limitations.
“If he can regain control of his bladder, bowels and other fingers, he will be able to live independently.”
A $150 entry fee that includes green fees and carts will be charged for the golf tournament, which will begin at 1 p.m. Autoworld Dodge Chrysler Jeep in Petaluma is offering a 2011 Dodge Durango for anyone who shoots a hole in one.
Complimentary food will be offered and beverages will be available for purchase.
Immediately following the tournament, an awards reception and prize raffle will take place at Graffiti restaurant, at 101 Second St.
Anyone wishing to sign up for the tournament can do so at www.Dannycox707.com. More information can be obtained by calling Kelli Maciel at 280-4376.
(Contact Dan Johnson at dan.johnson@arguscourier.com)
Posted:
8/1/2011 4:36:04 PM by
Don Margolis | with
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Diagnosed with an extremely rare form of bone cancer, a Claresholm man is undergoing a unique treatment regime in Calgary, vowing to beat the disease.
Suffering from metastatic small blue cell cancer, Devin McCutcheon, 29, underwent the first of two stem cell transplants Thursday at the Tom Baker Cancer Centre, part of a rigorous treatment campaign created by doctors here in conjunction with Dr. Jonathan Finlay, a Los Angeles-based oncologist who has successfully treated this type of cancer in the past.
What makes McCutcheon’s case rare is the fact Finlay had only seen metastatic small blue cell cancer in children under five, meaning there was no treatment protocol for adults.
“It’s totally different (chemotherapy) recipes than what they’ve seen here before,” said McCutcheon.
“In one way it’s good because now they know a lot from what I’ve had and what they’ve had to do.”
The second transplant is scheduled for two months from now.
This is actually McCutcheon’s second battle against the disease, his first diagnosis coming two years ago while he was working in the northern Alberta oilsands.
Suffering from chronic headaches he thought was the result of an abscessed tooth, McCutcheon went for further tests after removing the tooth didn’t stop the pain.
It was then doctors discovered he had an aggressive brain tumour — called a medulloblastoma — which was removed in December 2009, followed by nearly six weeks of intense radiation therapy.
One year later, McCutcheon was given a clean bill of health on what he calls “the best day of my life.”
Cleared to return to work, McCutcheon was back in the oilsands for just a few weeks when he developed intense pain in his hip.
Further tests revealed the worst — bone cancer in both hips, his pelvis, spine, left shoulder blade and collar bone.
At first doctors told McCutcheon he would likely die from the disease, but that “just wasn’t an option” for him.
“I’m just doing what I gotta do to get through it,” he said.
“You can’t just lay down or you won’t win and I’m winning.
Along with beating the disease, McCutcheon said his goal is to one day meet Finlay.
“I would love to shake that man’s hand and say ‘thank you very much,’ because I was told by two specialists here I wouldn’t make it.”
dave.dormer@sunmedia.ca
Twitter: @SunDaveDormer
Posted:
7/31/2011 3:31:38 PM by
Don Margolis | with
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New push in Austin for adult stem cell therapy
Updated: Wednesday, 27 Jul 2011, 7:03 PM CDT
Published : Wednesday, 27 Jul 2011, 5:04 PM CDT
AUSTIN (KXAN) - After kicking and punching his way through 15 years of Krav Maga self-defense classes, Pete Hardy's knees were shot.
"Pretty much every morning I would have to get up and I would stay on eight to 10 Motrin a day to be able to function," said Hardy, a 59-year-old self-defense instructor Pete Hardy whose knee cartilage was paper thin.
Doctors told Hard that surgery to replace his aching joints would likely be his only option. But he chose a more unlikely route -- adult stem cell therapy.
Dr. Robert Johnson, an orthopedic surgeon, took Hardy's own stem cells from bone marrow in his hip and put them back into his knee joints. Johnson said the stem cells first reduced inflammation and pain and then became the cartilage Hardy is missing.
"What we're doing is going to where they are stored, harvesting them and transferring them to where we think they're needed," said Johnson.
"Within three days, I was pain free and taught class the very next day," said Hardy. "I taught four classes the next day, so there was no down time whatsoever.
"I can jump the way I used to jump. I can kick the way I used to kick. I can move. I can spin. I can turn. I can do anything that 20 and 30 year old guys that I train can do. It's remarkable."
A new movement advocating adult stem cell research and therapies
Hardy and Dr. Johnson are part of a new nonprofit in Austin called MedRebels . The group is funded primarily by two local medical product and research companies. They say more people could stay active and possibly disease free in the future if the medical community would give regenerative medicine and adult stem cells a chance.
The name MedRebels implies physicians should step up and rebel against the conventional treatments even though the stem cell therapies are not approved by the Food and Drug Administration . MedRebels are pushing adult stem cell therapies and research and not those utilizing embryonic stem cells.
The group hopes by focusing only on adult stem cells, they can avoid the ethical and political controversy that often surrounds embryonic stem cell research.
"We're considered to be a very conservative state, and Austin is considered to be a very liberal town," said MedRebels board member and Celling Technologies founder Kevin Dunworth. "That type of political environment wouldn't lend itself to something that doesn't sit right in the middle. Both sides of the aisle can agree that adults stem cells are a great way to positively affect Texas not 20 years from now, but now." "I think Texas is really in the forefront of adult stem cell research," Johnson said.
Johnson has been using adult stem cell therapies in his patients with spine fusions and in patients with other joint problems. The risks, he said, are minimal including the risk of infection at the injection points in the bone and any risk that comes along with sedation.
The therapy is done on an out-patient basis. Johnson has had to do a second procedure on a few patients when the pain came back after a year or so. The long-term effects are still unknown.
"This is a biologic step," said Johnson. "This gets away from metal and plastic. This is recruiting the body to heal itself, and I think it's a quantum leap ahead of everything else."
Other doctors and researchers are skeptical of MedRebels' motivation. They are also worried that MedRebels is pushing treatment that has not been approved by the Food and Drug Administration.
Another adult stem cell success story
Austin hair stylist Lizzie Horn stood on her feet through months of extreme hip pain trying to keep her career going. She also suffered through daily runs the active athlete had enjoyed for years.
"For about a year I just had a lot of hip pain," Horn said. "I do a lot of running, and full time I stand on my feet all day. With the running and standing on my feet, the pain pretty much got unbearable."
Horn also opted for adult stem cell therapy after encouraging her physician to try the procedure. The doctor took her own stem cells from bone marrow in her hip and after treating it placed it back in to her hip joint. Horn is back on her feet and running.
"Now I'm up to 40, 50 miles a week with no pain," Horn said. "It's been great. It's been over a year, and I've had no issues."
Stem cell research in Austin
Researchers at the University of Texas in Austin are studying both adult and embryonic stem cells. The National Institutes of Health runs an online data base compiling government and privately funded trials going on across the country.
One of MedRebels' biggest backers, Celling Technologies based in Austin, is working on more than 30 adult stem cell research projects.
The future of stem cell research
Researchers are not just looking at adult stem cells found in bone marrow but in
body fat. Plastic surgeons in Austin are using cells from body fat in reconstructive procedures.
Researchers discovered the capabilities of adult stem cells in body fat about the year 2000. Veterinarians shortly thereafter began using body fat stem cells from horses to repair the animals' own tendon and ligament tears and joint problems.
"Using fat derived stem cells or fat derived regenerative cells has been commercialized in the vet world for going on eight years," said MedRebels Scientist Dr. Ted Sand.
Researchers in Austin hope to duplicate the success vets have had with animals in humans. Sand said bone marrow stem cells can degenerate with age, but research suggests the fat derived stem cells do not. The chances for complications in therapy are lower in the stem cell collection from fat than from bone marrow. There are also more adult stem cells per volume in body fat.
"There is a lot more regenerative cells in fat on a per volume basis than there is in bone marrow," said Sand. "We can get fewer cells or we can get more cells at one collection and that again pushes the therapeutic benefit."
Dr. Johnson and other MedRebels look for a day when adult stem cells from bone marrow and body fat could be used to not just repair bones and tissue but life threatening diseases.
"I sort of feel like a little kid who wants to rush into the birthday party but is kind of holding back for the right moment," said Dr. Johnson. "I feel this is a dam that's going to burst. I don't know when. I think it's sort of starting to trickle, but I think eventually this will be the standard of care. I think most people around the country will be doing it."
Other links:
Another Austin nonprofit advocating stem cell research -
Posted:
7/28/2011 4:14:44 PM by
Don Margolis | with
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