“Latest Stem Cells News”

A clampdown on unproven and potentially unsafe stem cell research is being called for by an expert group.
Bionet, a group of expert Chinese and European doctors, lawyers and bioethicists, says countries throughout the world must develop more effective regulation for this emerging science (…)

They had provided a wealth of anecdotal evidence about their concerns that stem cell research was being moved too rapidly into clinical practice without proper study.
He said: “The key is informed consent. Doctors should be able to tell the patient about the short-term and long-term prognosis and the things we don’t know about the risks.”

Bionet is recommending that the safety and efficiency of stem cell treatments is investigated through state-of-the-art clinical trials before they are offered to patients (…)

And there should be quality standards for stem cells used in clinical practice.
These should include the bacterial and viral contamination applied during the production of the stem cells.

China introduced new regulations in May calling for clinical trials before stem cell treatments were offered to patients.
Professor Qui Renzong, vice-president of the ethics committee at the Chinese Ministry of Health, said: “In China there are about 150 institutions now providing stem cell therapy for diabetes through to spinal injuries.” (…)

“When stem cell ‘treatments’ are based overseas, regulatory oversight and jurisdiction is particularly problematic.
We take this very seriously and strongly encourage anyone considering participating in overseas stem cell ‘research trials’ or buying internet treatments to talk to their doctor and follow health guidelines.”

from http://news.bbc.co.uk/2/hi/health/8234206.stm

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Sierra Fedelem may look like any other 20-month-old, but her parents are doing everything they can to make sure her life is just like that of any other healthy human being.
Stem cell research has stirred quite the controversy in the United States, and though the current administration’s recent policy reversal on the issue could open the markets to treatments and commercialization, it’s still an option unavailable for American patients, like Sierra, unless they’re willing to travel across the world.

“The first time the neurologist said, ‘No, you don’t realize it, she’s never going to be able to walk, talk and see, and she’s always going to be at the mental level of a 4-month-old’,” Rosetta Fedelem said. “We were just shocked.”
The Fedelems hadn’t realized the extent of the brain damage Sierra suffered during birth.

“We said ‘We’re not going to stop, we’re going to start doing as much as you can for her’,” Rosetta said. “So we started praying and researching.”
Their research landed them in China, where Sierra received several treatments of adult stem cells extracted from somebody else’s umbilical cord. Adult stem cells differ from embryonic stem cells, in that they can be retrieved from adult organs or tissue.

While leading U.S. experts say the possibilities are far-reaching, the quality of overseas studies remains uncertain.
“It’s very hard to tell which is a good place, and which is not,” Texas A&M Health Science Center College of Medicine Institute for Regenerative Medicine Director Dr. Darwin Prockup said. “But of course, patients get to be desperate, and you can’t blame them for trying.”

Dr. Prockup said better adult stem cell treatments in the United States are coming. In March, President Barack Obama signed an executive order, reversing Bush administration policy, to allow scientists to continue stem cell research on ongoing projects. The results of the research will determine when the United States will open its doors to treatment.
“Of course there’s always danger with any therapy, so you have to be very careful, there’s always a risk-benefit you have to weigh carefully,” Prockup said. “That’s done in good medical centers. That’s why we’re a little slower.”

The Fedelems said they did weigh the pros and cons.
“I don’t accept new things easily, but when there’s enough evidence of results, I’m willing to try them,” Jason said. “And that’s exactly what happened here.”

In the three weeks they’ve been back from China, Sierra can sit up on her own for a few seconds, do an army crawl, and stand up for more than twice the amount of time she could before. Plus, her parents say she’s more alert and vocal.
Rosetta and Jason say they want Sierra to be able to walk, talk and see.

“Now we don’t know exactly which of those goals she’ll reach,” Rosetta said. “Our goal is, as parents, to push her to achieve her greatest potential, whatever that is. We’ll love her no matter what.”
The Fedelems said they spent more than$23,000 on treatments in China, but they raised $45,000. The rest of the funds went to a hyperbaric chamber, and other treatments Sierra will receive in Florida in two weeks.

To learn more about Sierra and how you can donate to help the family with medical expenses visit SightForSierra.com.
Dr. Prockup said the institute will be working on four clinical trials. By the end of the year he expects they’ll begin one with adult stem cell research for treatment on knee cartilage repair. The institute also plans to conduct stem cell research on diabetes, heart disease and strokes.

from News 8 Austin

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A blood sample databank under the China Marrow Donor Program (CMDP), was officially established Monday at Zhongguancun of Beijing.
The new databank is now the largest for Chinese people in the world, according to Hong Junling, deputy head of CMDP management center.

The databank includes information such as the names and gender of nearly one million donors and information about to which ethnic groups the donors come from, Hong said.
It also covers such medical information as blood types, gene types and health status of the donors.

The CMDP, launched in 2001 by the Red Cross Society of China, aims to help millions of Chinese with blood diseases.
But Hong said the blood sample databank could help genetic analysis for major diseases other than blood diseases.

The blood sample databank has collected 970,000 samples and provided more than 1,200 patients with haematogenous stem cells, including 50-odd cases from abroad, according to Hong.
The number of samples is expected to reach one million by 2010.

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Alex Normandin, 26, of Montreal, Canada has been cured of his Multiple Sclerosis following the implantation of his own Adult Stem Cells. The stem cell therapy was done in conjunction with a research program in Ottawa with Dr. Mark Freedman.

A medical student, Alex was diagnosed with multiple sclerosis more than 2 years ago and was distressed to learn that he had the aggressive form of MS and was on track to be in a wheelchair in a matter of months.

Process of Stem Cells for Multiple Sclerosis in Canada

Luckily, he was accepted into Dr. Freedman’s stem cell research program at Ottawa General Hospital. In this stem cell program, the patient is first given chemotherapy to kill off the immune system. Then, the stem cell transplant takes place to “reboot” the immune system.

From the stem cell article:

Normandin became patient 19. His transplant took place in December 2008. It worked.

Not only does the disease appear to have stopped its progression, but Normandin says he feels his co-ordination and strength improving.

Normandin is buoyed by the treatment’s eight-year track record — none of the 24 patients have suffered a relapse or a brain lesion. (The article fails to mention the one patient who died from the chemo)

Stem Cell Therapy in China Quote Remembered

Readers of this blog may remember Dr. Freedman from this Multiple Sclerosis Stem Cell post in which he commented on stem cell therapy in China:

Dr. Freedman is concerned that patients are forking over large amounts of money for unproven treatments like this, especially when there is no follow-up care or monitoring when they get home.

“It’s dangerous in the wrong hands,” he said. “The only reason these places could be in existence is to take people’s money and offer them something that’s unproven.”

I called that the “Most Hypocritical Statement So Far in 2009″ then, and I will stick to that for the following reasons:

1. Chemotherapy is dangerous.  1 of Dr. Freedman’s patients died while receiving it before the stem cell transplant- to call another treatment dangerous (which doesn’t use chemo, by the way) is hypocritical.
2. He says the therapies are unproven and only in existence to take people’s money-  however, in this article- it is revealed not only is his own treatment unproven, but it also is not free, in fact, far from free- “The trial procedure costs would be about $50,000 to $60,000 per patient.”  (A reader has since wrote in and says the Canadian Government pays for this treatment)
   

Actually that cost is more than other stem cell therapies in Costa Rica and China that we have covered in here (both are around $25-30,000) and do NOT use chemo.

So for those people who say that stem cell therapy overseas is very expensive– just look at Canada, or for that matter, look at Dr. Richard Burt’s multiple sclerosis study at Northwestern University in Chicago.  The cost for one multiple sclerosis patient is $90,000

I’m directing  this at critics who always point out that overseas stem cell therapies are expensive and dangerous rather than pointing out the “arrogance” of Dr. Freedman, who as far as I can tell is truly helping Multiple Sclerosis patients although he probably shouldn’t be opening his mouth about other stem cell treatments.

Stem Cell Treatment By The People, For The People

And yes, all of  these stem cell treatments in Canada, USA, Costa Rica, and China are “unproven” in the eyes of the medical world and the New England Journal of Medicine, although they all are proven in the eyes of the patients who receive the Adult Stem Cells whether they are in the form of umbilical cord stem cells (China), mixture of stem cells from the patient’s fat and cord blood stem cells(Costa Rica) and/or Adult Stem Cells given in the form of a stem cell transplant after chemotherapy (Canada, USA).   They all seem to work most of the time FOR THE PATIENTS NOW and that is what is important. Making Multiple Sclerosis patients wait for 10 years or so for the endless cycle of clinical trials in the US and Canada to end just so their doctors can see the words “proven” in a study is a travesty.

The Emergence of the Internet and Self Directed Healthcare

We can ask Jason Upshaw and friends about stem cell therapy in Costa Rica. Or, we can ask Betty Helm about how stem cell therapy in China worked for her MS. Thanks to the wonders of the internet, patients now have a bigger say and more access to information than ever before.

Dr. William Davis at the Heart Scan Blog has a great post on how health care is changing. Much like stockbrokers have disappeared due to online companies like E-trade and Ameritrade, patients can now take a more self directed approach to their health thanks to the internet.

original post by Don Margolis

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Adult Stem Cells Improve Young Boy with Cerebral Palsy

Corey de Gregorio, a 3 year old boy from Gordonvale, Australia has improved tremendously after going to a Stem Cell research company which implanted Adult Stem Cells from cord blood into him.

Corey’s parents, Mark and Roseanne had doubts before going to China for the stem cell treatment, but they  wanted Corey to have every chance to live a better life and therefore, they made the journey to China for the stem cell therapy which used only Adult Stem Cells.

The miracle treatment consisted of six “therapies” of cord blood stem cells.

Before the Adult Stem Cells for Cerebral Palsy

• Had very little use of his left arm/hand
• Little movement in his torso

After the Stem Cell Treatment

• Can now use his left hand, can use it to drink a cup by himself
• Increased flexibility in torso

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BEIJING – China is tightening regulations on the clinical use of high-risk or ethically controversial diagnostic and therapeutic technologies.
The Ministry of Health (MOH) issued a government order on Monday requiring hospitals to get approval before doing things such as artificial heart implants and homogeneous organ transplants.

The regulation goes in to effect May 1. Hospitals already using the technologies are required to report to the Ministry for verification of qualifications within six months after that date.
The MOH said its aim is to prevent abuses of those medical technologies. Previously, only some needed government approval, it said, without giving further details.

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