Stem cell therapy for multiple sclerosis: Preston Walker

MS Stem Cell Patient Preston Walker

Preston Walker

A Different Approach

Sergeant Preston Walker
Courtesy Sergeant Preston Walker

After undergoing conventional therapy for MS for several years, Fort Worth police sergeant Preston Walker learned about a new therapy for autoimmune disorders. Researchers were utilizing adult stem cells derived from cord blood at The Institute of Cellular Medicine in Costa Rica. Walker inquired about the potential of using stem cells for multiple sclerosis.

“We knew that if the treatment worked, the potential benefits for multiple sclerosis patients could be limitless,” says Walker.

Dr. Neil Riordan, CEO of the Institute, suggested a therapy under consideration – using stem cells derived from a patient’s fat tissue. In May 2008, Walker flew to the clinic where doctors removed samples of his abdominal fat through a mini-liposuction, drawing out stem cells, which were later re-injected. According to Dr. Riordan, Walker and a colleague were the first to undergo this treatment protocol. “My quality of life has improved significantly,” Walker told the Post. “The problems with depression, fatigue, and balance have been corrected. I feel really good.”

In June 2009, Walker, who continues to take Avonex as a maintenance drug, plans a return trip to Costa Rica for a “tune-up,” as he puts it. “I’m curious to see if they can further improve my cognitive abilities.”

Fox 4 News: A Fort Worth police officer has returned from Central America after having a cutting edge medical procedure to help cure his multiple sclerosis. Last year we told you about Sergeant Preston Walker tonight Larry Barriger updates us on how he is feeling following his stem cell transplant.

Sergeant Preston Walker has always been active. With a demanding job at the Fort Worth Police Department, a wife, and young children, he doesn’t have time to slow down. But about 8 years ago he didn’t have a choice. MS started taking a toll making him limp when he walked, fatigue easily, even everyday conversation was a chore.

“I can sit here and talk but trying to come up with actual words to say and really construct a sentence that people would understand was sometimes very difficult.”

Medicine helped keep the disease in remission but Preston wanted more. A chance for a cure.

“I wasn’t prepared to just let it stay in remission without me trying to do something, especially if there is an option out there to address it.”

Sergeant Walker was initially planning to have his treatment done in China but he says the political situation seemed unstable, so he started looking online. He found another center that was doing adult stem cell treatment in Central America.

The procedure, a stem cell transplant was expensive but last October police officers from Fort Worth and Dallas teamed up to help raise money for the trip and the treatment. Last March Preston and fellow MS patient Richard Humphries flew to the Institute for Cellular Medicine, both underwent a stem cell transplant, a cutting edge medical procedure not approved in the US. Both took a risk on such a new treatment, both said they have seen marked improvement.

“I haven’t felt this good in 10 years. I don’t have any of the fatigue issues, all of the cognitive lack of clarity, that cloud has been lifted.”

Walker says doctors at the Institute will be keeping up with him and Richard over the coming months and years to determine how successful the treatment was. He is hoping his improvements last and that the research leads to a cure for his and other’s multiple sclerosis.

It seems like a pretty simple task for a police officer just sitting and working on a computer. Just a couple of years ago, multiple sclerosis made that almost impossible for Fortworth Police Officer Preston Walker. New at 6 CBS 11’s Joe Thomas says Walker credits friends for recovery some feel is a miracle.

A year ago Preston Walker did not think he’d still be in uniform. Walker found out he has multiple sclerosis. He suffered chronic fatigue and began losing use of his legs.

I felt like my cognition was really declining at a rapid pace. I really felt if I made it through the end of the year, last year, I probably wouldn’t be employed any longer because the cognition just wasn’t there.

His fellow police officers held a hockey-game fundraiser to help him afford a revolutionary treatment. Walker and another MS patient, Richard Humphreys, went to Costa Rica. For the first time ever, doctors took samples of their fat, drew stem cells from it, and reinjected it. Their symptoms nearly vanished.

I’ll suffer from any of those symptoms that we talked about, the depression, the fatigue, the little cognitive cloud. I mean it’ll still hit occasionally, but its no where near every day or every moment of every day like it was.

If we or somebody doesn’t become a guinea pig, then how can that benefit others?

They led the way to a treatment that is now helped ease the suffering of dozens of others. Joel Thomas, CBS 11 News.

Stem cell therapy for multiple sclerosis: Mary Posta

“It was a great experience with a fantastic pay off. I highly recommend this program to anyone in need.”

Hi, my name is Mary and I am an adult stem cell recipient. I can honestly say, now, after the procedure, the program was well worth every penny, and more. The four week stay was well organized, structured, and preformed in a timely manor. It was a very intense program of stem cell therapy and physical therapy. But, I feel every minute of every intense workout was desperately needed if there was to be any improvement. The medical staff was very knowledgeable and professional. The hospital, equipment, and procedure were all very state of the art technology. Almost everyone spoke English, so there was never a communication problem. I felt very safe in the country and in the whole program. In my case, I can walk, talk, sleep without pills, and many more improvements. I definitely received for more than the 5% improvements I was expecting. I still have some problems but the improvements by far out weigh the problems. This was the greatest decision I have ever made. I have no regrets. No one ever told me stem cells were a “cure” and in some cases there has been very little to no improvement. But if I had not of taken the chance of maybe getting 5% improvement, I would not be experiencing all the blessings I have now. It was a great experience with a fantastic pay off. I highly recommend this program to anyone in need.

Stem cell therapy for multiple sclerosis: Dana Bramlett

“I would recommend this treatment to anyone who has been diagnosed with Multiple Sclerosis.”

“I was diagnosed with Multiple Sclerosis in 2006. I was very scared when I found this out. My walking gradually became more impaired. I was dragging my left leg, and my balance was very bad. Some days I would be in a wheelchair. I have tried all the therapies including: Rebif, Tysabri and Avonex. Tysabri worked the best, but I was afraid of adverse side effects. I’ve heard many successful stories about stem cell treatment. I was recommended by the Physician I work for to contact the Stem Cell Institute. At first, I was leery about doing the treatment, but without many other options, I didn’t have a choice. I visited the Stem Cell Institute on May 31,2010. I was very impressed by the staffs’ caring attitude. Everybody was phenomenal. I completed the two week treatment including spinal injections and physical therapy. Although I first thought the treatment wasn’t effective, I am doing much better now. My balance is a lot better, and I am no longer dragging my leg. I have more energy and I am less fatigued at the end of the day. I am continuing to get better each day. Ultimately, I feel the treatment was a success, and I am very appreciative of the medical professionals who were involved in my treatment. I would recommend this treatment to anyone who has been diagnosed with Multiple Sclerosis.”

Stem cell therapy for multiple sclerosis: Tosin Ajayi

“He is able to take a few steps unassisted. Walker and wheelchair are now reserved for outings.”

“This is to let you know that Tosin Ajayi is doing much better. The second treatment received in January was very productive. It seems to be more effective than the first one. The quantity of cells received could (be) a factor. I started to observe changes within a week and the improvements have continued. Plus there were no side effects. His energy level is up and he is better able to care for himself. There is improvement in his speech, coordination and walking. He no longer uses walking aids in the house. He is able to take a few steps unassisted. Walker and wheelchair are now reserved for outings. I pray for continued progress and improvement in other symptoms that are yet to change.

We thank you very much. Please extend our gratitude and appreciation to Drs. Lara and Tomas.”

Stem cell treatments for MS: Lou Ann Giunta

“I am less spastic, have slightly better balance and more
stamina when exercising and moving about. I still have some incontinence 
issues, but it’s less severe.
”

“I hope you and all the Panama medical people are well.
 I am emailing to report an improvement from the Stem Cell treatments. This 
improvement is not just occasional but has been steady for 2-1/2 weeks or 
more. As of today, I have been home from stem cell treatment 5 months and 3 
days. 

Specifically, I am less spastic, have slightly better balance and more
stamina when exercising and moving about. I still have some incontinence 
issues, but it’s less severe.
 These improvements although subtle I feel are very real improvements and I
 hope they continue.”

Stem cell treatments for mutiple sclerosis: Janice Gonzales

“I am able to write legibly and have more energy than I have had in years. I exercise everyday and use a walker for short distances. I still use my scooter if I have to go far.”

“It will be my pleasure to write about my experience. I have MS and went to Panama for 2 weeks of Stem Cell Treatments. All of the procedures were painless. The Dr’s and staff genuinely cared about the patients. The daily physical therapy combined with the treatments have already improved my fine motor skills. Before I left Panama, I was able to hold a glass of ice water without shaking or spilling. Since I have returned, I am able to write legibly and have more energy than I have had in years. I exercise everyday and use a walker for short distances. I still use my scooter if I have to go far. My dream is to walk unassisted in the near future.”

Stem cell therapy for multiple sclerosis: Richard Humphries

Stem Cell Institute Community Outreach (February 26, 2011 – Dallas, Tx) – Richard describes his miraculous recovery from secondary progressive multiple sclerosis and how stem cell therapy at the Stem Cell Institute took him from crawling to the bathroom and being effectively bedridden to playing and teaching golf once again.

Stem cell treatments for multiple sclerosis: Dennis Trammell

Biomedical Ethics in a Brave, New World

By Ken Camp, Managing Editor
Published: May 07, 2010

POSSUM KINGDOM — When Dennis Trammell exhausted treatments available in the United States for his multiple sclerosis and began looking at other options, he excluded from consideration any possible regimens involving embryonic stem cells.

“I didn’t even explore that,” said Trammell, pastor of First Baptist Church at Possum Kingdom Lake, near Graford.

The list of ‘can-do’ options in health care get longer each day; hence, also the ‘ought’ questions and the complexities.

His health problems started in 1999 with decreased vision in one eye, diagnosed as a case of optic neuritis. When similar symptoms occurred in his other eye two years later, he was diagnosed with relapsing-remitting MS. He began a series of conventional treatments, including once-daily injections that helped manage the illness temporarily.

But in July 2008, his illness advanced to secondary progressive MS. Two months later, he went to Costa Rica for stem-cell treatments not available in the United States—but not before he checked on the source of the stem cells.

Dennis Trammell – “Results have been mixed. …But since the treatment, a daily nap is no longer needed”

“I really questioned before agreeing to take part in the treatments what type of stem cells were used,” said Trammell, who serves on the Baptist General Convention of Texas Executive Board. While some countries allow experimental treatments using embryonic stem cells harvested from abortions, Costa Rica did not, he learned.

His treatment involved stem cells harvested from the umbilical cords of full-term births, administered by injection into his spinal cord to repair damage to the brain caused by MS. That was coupled with an intravenous infusion of his own stem cells, harvested through liposuction. The goal, he explained, was to “reset” his immune system.

Dennis Trammell

Results have been mixed, he reported. Initially, he experienced improvement in balance, but it proved short-lived. Use of his left arm has diminished in the last year, he noted. But a lasting benefit of the treatments has been a marked improvement in his energy level.

“I had gotten to the point where a nap was needed on a regular basis. But since the treatment, a daily nap is no longer needed,” he said.

Before he was diagnosed, Trammell already had determined certain boundaries existed in terms of medical treatment that he could not cross in good conscience. Other Christians sometimes fail to consider these kinds of issues until confronted with them in a doctor’s office or hospital waiting room.

“We’re still dealing with the age-old question: ‘Given what can be done, ought we?’ But the list of ‘can-do’ options in health care get longer each day; hence, also the ‘ought’ questions and the complexities of knowing right from wrong, good from bad,” said Tarris Rosell, professor at Central Baptist Theological Seminary, and the Rosemary Flanigan Chair in the Center for Practical Bioethics in Kansas City, Mo.

While subjects like nanotechnology, reproductive cloning, genetic engineering and artificial intelligence capture the imagination of some bioethicists, those are not the issues most people face, said ethicist David Gushee.

“I sometimes wonder whether there isn’t a bit of a science fiction fetish here, in which for some it is just fun and interesting to ponder ethical issues from a future that hasn’t reached us yet. I would prefer to deal with the ethical issues that face us right now,” said Gushee, professor of Christian ethics at Mercer University.

“Very difficult health care decision-making remains a reality that everyone faces at one time or another, and not just at the end of life. My own family’s recent experiences in the health care system remind me that it has its own momentum and practices that are simply taken for granted from within the system,” he said. “As Christians, we do need to have a broader vision that asks questions rather than simply taking for granted the way things are.”
In recent weeks, Gushee’s wife, Jeanie, had an appendectomy, and his sister, Janette, had surgery to remove a brain tumor.

“All the talk of autonomy and informed consent bumps up against the realities of how little laypeople understand what doctors are saying and doing. Time pressures in situations of crisis, situations which also tend to limit our rational capacity as we are overwhelmed by fear and confusion and pain, also make it very difficult to exercise judgment either for ourselves or for someone else,” he said.

“Recently, I faced a situation where the doctor called me in the waiting room from my wife’s surgical suite during her appendectomy to ask me whether she should also take out the gall bladder. I had moments to decide, on the basis of very limited information, whether to authorize this irreversible surgery. I said no. But it was a tough call, and I had very little information, and of course, I had only met that doctor about 48 hours before.

“We need ways to slow down the decision-making process whenever possible, to empower patients and families with better information and more choices, to point us to websites and other sources of broader information.”

Tensions between sanctity-of-life issues and quality-of-life issues move from the realm of academic discussion or public policy debates when they affect people whom an individual Christian knows and loves, said ethicist Bill Tillman.

“Perhaps it is only when we find ourselves, a family member or someone else close to us involved in the bioethical realm that we even realize these tensions or where we might be with them,” said Tillman, who holds the T.B. Maston Chair of Christian Ethics at Hardin-Simmons University’s Logsdon School of Theology.

Patients and family members today face tough questions their parents and grandparents never had to consider one or two generations ago, in part because of a greater emphasis on patient autonomy and patients’ rights, Rosell observed.

“Medical paternalism was the rule and practice for centuries or millennia, while the consensus now is against paternalism in favor of patient autonomy,” he said.
Perhaps “the pendulum may have swung too far” in the direction of patients being called upon to make some life-and-death decisions, Rosell suggested.

“It’s not necessarily a good thing when patients and/or their families demand specific medical interventions, especially when they are not medically indicated and won’t help but might harm,” he said, citing the example of cardio-pulmonary resuscitation being used on the frail elderly or people suffering from the failure of multiple organs. “So, just because I want it does not mean it would be good for me to get it.”

Ministers often find themselves in difficult situations when seeking to provide comfort and spiritual counsel to families or individuals facing difficult medical decisions.

“Likely, conversation about suffering, pain and ‘Where is God in all this?’ will arise,” Tillman observed. “Isn’t it interesting that it takes something we would call an intellectual, theological or physical crisis before we are willing to talk about these things?

“But these are matters to which a minister can be sensitive and perhaps build a relationship which had not been possible before.”

Tillman advises seminary students to set the proper example by considering end-of-life issues personally long before a crisis occurs.

“My advice to the students I have in classes at Logsdon is that they are never too young to put a will together, to have a statement of advanced directives prepared and to be advising their friends, family members and congregants to be doing the same thing,” he said.

“One benefit is they have to think through the matters surrounding their own mortality—all of us will die. Will we leave our life circumstances in such order that someone can pick up where we leave off? Can someone speak on our behalf if we arrive in a context where we cannot? As we recognize we will not be in this life forever—and frankly do not know the circumstances or the when of our death—quite probably those considerations will cause us to think more clearly and deliberately about how we live the moments we have.”

Beginning-of-life issues raise as many questions for some Christians as end-of-life dilemmas, Gushee added.

“Reproductive technologies also have brought us a host of unanticipated consequences, such as genetic screening to sift through extra embryos, ‘octomoms’ for those who feel compelled to implant all the conceived embryos, half a million frozen embryos and the ethical issues these raise, including a steady call for their exploitation in research, custody disputes over frozen embryos, and on it goes,” he said.

While the Religious Right has been most vocal about some of these issues, concern transcends political agendas, he added.

“I hear among my students at McAfee, who are not driven by a conservative political ideology, a kind of healthy sense of caution and sobriety about this endless fiddling with the procreative process,” Gushee said. “One may say it may be that the scientific and technological pride of the 1960s and 1970s is giving way to a more cautious appreciation of the dangers and limits of our interventions in nature.”

Caution and humility likewise should characterize the counsel Christians offer to families who are coping with end-of-life, quality-of-life and beginning-of-life issues, Tillman noted.

“Presence—caring presence—can be priceless,” he said. “I’d say stay away from interpretive generalities. Praying that God’s will be done—and not outlining to the patient and to God what that will is—is always appropriate.”

Stem cell treatments for MS: KDFX News 3 Report on Rick Hardcastle

Stem cell treatments for MS: Bill Klapholz

It’s just amazing!