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 therapy for multiple sclerosis: Richard Humphries
Stem Cell Therapy for Heart Disease: John Coleman
John “Skeeter” Coleman, III received stem cells for heart failure in Costa Rica in 2008″
“… Blood samples were taken to find donor placentas with tissue types compatible to mine. Three weeks later I received two IV injections per day for seven days. It was done on an outpatient basis in CIMA hospital. Simple, painless and I could drive myself to and from the hospital for the injections. Four months after the stem cell therapy my cardiologist asked me to return for tests to see if we had made any progress. Blood studies revealed BNP 620 (down from 3,875); Hemoglobin A1c 6.0; all other tests were normal. Ejection fraction had increased to 51 (up from 26 two months after ICD implant and up from 12 on original admission) and there were no further problems with dyspnea. She was ecstatic. I was elated. We hugged and both of us shed tears of joy before she emailed that same phalanx of physicians who kept me alive previously with my spectacular results.
“The quality of my life has been enhanced immeasurably. I definitely breathe easier and I’m climbing up and down the mountain daily with no problems and no stopping every 15 meters (48’) to catch my breath.”
Prior to stem cell therapy my ICD defibrillated five times preventing sudden cardiac death. A change in one medication followed by the stem cell therapy and I am “defib free” for 14 months. The quality of my life has been enhanced immeasurably. I definitely breathe easier and I’m climbing up and down the mountain daily with no problems and no stopping every 15 meters (48’) to catch my breath. How long I will live is not in my hands but I appreciate the fact I am no longer burdened by a powerful pharmaceutical lobby that maintains a stranglehold on the US Congress. One doctor explained it in simple terms. “Pharmaceutical firms make money selling drugs. Stem cell therapy has the capability of curing possibly eliminating all drug therapy. There are many things the United States has to be proud of. This isn’t one of them.Think about it.!”
Stem cell Therapy for cerebral palsy: Dylan Hancock (Mansfield News Journal)
Mansfield News Journal
ASHLAND — Three-year-old twins with cerebral palsy are making life adventurous, challenging and bittersweet for the Hancock family.
“They’re happy kids but it definitely makes it more difficult because as a parent you want them to have every opportunity that every other child has,” said mother Carrie Hancock. “It’s hard, but we’re handling it the best we can.”
Because they were born 10 weeks premature, both children suffered developmental delays.
By the time Tessa and Dylan were 20 months old, Tessa had been diagnosed with cerebral palsy, a permanent disorder that affects movement and posture. At that time, parents Carrie and Jeremy were getting ready to take their daughter overseas for a stem cell transplant, a procedure that would allow Tessa to live a better, less physically restricted life.
The results were remarkable…
In the midst of their planning, the family was soon faced with another obstacle. That January, Dylan also was diagnosed with cerebral palsy.
“What do you do? They’re your babies. You just go with it and do what you think is best,” Carrie said. “Before, we were always told that he just had developmental delays, but as much as you hated to hear it, it was almost a blessing because we were paying out of pocket for him because he hadn’t been officially diagnosed.
“That’s the silver lining I guess and now we’re able to get him the help he needs.”
The Ashland family ended up taking Tessa to Panama City, Panama, where she had her first round of stem cell treatments in 2009.
“She did really well and had a lot of improvement with her vision,” Carrie said. “Her tone in her hand had decreased and she wasn’t fisting all the time. When we went back in July, we took both the kids.”
The results were remarkable.
“As soon as we took him, he was like a whole other kid,” Carrie said of Dylan. “He was babbling and it helped him in so many different ways. He also just walked independently a couple months ago. For Tessa, it made her stronger. She was already smart and attentive.”
Today the twins attend therapy sessions at MedCentral Pediatric Therapy one day a week and preschool at Tri-County Preschool four days a week. They receive occupational, speech and physical therapy.
“A typical day for us includes them going to school a little after 8 and they’re picked up a little after 11,” Carrie said. “After we get them home and fed, Tessa goes down for a nap and then Dylan stays awake and I get alone time with him, which is nice. We work on walking and sitting up with them, but try to incorporate it into their play. We try to make it a fun time.”
The family takes the twins on outings by stroller and enjoy their play time together, but each day can be daunting.
“The biggest difference is the physical challenge of dressing and feeding. Tessa is in the process of being potty trained, but Dylan doesn’t want to yet,” Carrie said. “She can’t feed herself and we’re still changing diapers at age 3.
“Dylan’s not walking. If you ask him to pick up something, he doesn’t understand. It’s challenging.”
Recently, Dan and Stephanie Kreisher, of Ontario, held their third fundraiser for the family. Jeremy was on Dan’s 1994 state championship baseball team at Ontario High School.
The Kreishers and friends raised $1,400 for the Hancocks, along with providing them two iPads for Tessa and Dylan after learning the electronics would help their communication skills. The iPads were sponsored by Elite Excavating and Zara Construction.
“We have so much and are so fortunate that we wanted to help others,” Dan said. “Jeremy and Carrie are such positive people. They’re the happiest parents, just very admirable people.”
The feeling was mutual.
“I can’t say enough about Dan and Stephanie. The iPads are huge for us. We’re in the process of getting different communication devices to help with fine motor skills,” Carrie said. “They use them in school and it’s nice to be able to incorporate what they’re learning at home. Life isn’t easy, but we are very blessed.
“The best way to describe our family is that we’re taking the scenic route. We’re taking the back roads. We’ll get them there, but it just might take a little longer.”
Stem cell therapy for autism: Emma
Visit Emmas blog at www.EmmasHopeBook.com
A year ago tomorrow, when I began this blog, we had just returned from Costa Rica where we took Emma for her first stem cell treatment. We were filled with anticipation, fear and excitement, alternating between fantasies of miraculous recovery and tremendous uncertainty and worry. Like most things in life, we could not predict what the future would hold. We could not know that a year later we would be where we are now, that Emma would be where she now is.So a quick review… Emma has hit so many milestones in the past year it is difficult to say one is more significant than another. My immediate thought was the most important thing in the past year has been that Emma is learning to read and write (more on that later) and while that is certainly an incredible achievement, when I consider that she is also completely toilet trained, even during the night, that too seems equally significant. I know of families with autistic children – now in their teens – who wear a diaper to bed, with no end in sight. The endless changing of sheets each morning is something I am grateful not to be confronted with. In addition, Emma use to wake up in the middle of the night, often more than once, leaving all of us exhausted to the point of hallucinating. Until we had Emma I had never known exhaustion such as that – to be woken and kept up for hours at a time, only to then face a full day of work where you must function, make decisions and not fall asleep during meetings, is nothing short of surreal. Emma rarely wakes us these days, though she did keep her brother up last night. Poor Nic was showing all the signs of exhaustion we have come to know so well. We will speak with Emma, (which is another milestone) and remind her that she cannot do this.
Emma is speaking in longer, more coherent and increasingly complex sentences. She is expressing herself in more sophisticated ways and is showing genuine empathy for others. She is also initiating more. She has formed friendships with specific children at her school, requests to see her cousins, is clearly upset when told they are not available to come over. Emma seeks out our company, often requesting that one of us join her in her room to watch a movie with her on her computer or play specific games with her. While staying in Aspen with my mother, Emma approached her Granma and said, “Granma can’t snap her fingers. Granma hurt.” She then gently patted my mother’s arthritic fingers.
“No my fingers can’t do that any more,” my mother said, showing Emma her arthritic fingers.
Emma stared at them for a moment and then reached over and tried to snap them. We heard my mother’s knuckles crack as Emma did her best to assist in helping my mother snap her fingers.
“Oh no!” I said, looking over at my mother with concern. ”Are you alright?”
My mother was laughing so hard she couldn’t speak and simply nodded her head. Emma looked on with a grin, trying over and over again to snap her Granma’s fingers. It was a wonderful moment between my mother, whose knuckles kept cracking, much to Emma’s delight and Emma.
The next morning my mother entered the kitchen and said, “Good morning Emmy!”
To which Emma responded, “Good morning Grammy!”
To date we have taken Emma to Central America for stem cell treatments three times now. We have not decided whether we will return for a fourth treatment in the next few months until we have some blood work done to measure her cytokines.
Yesterday as I worked with Emma on her literacy program I handed Emma an index card which said, “the man”. I had laid out a toy plane, a truck, a man and a kid on the table. I handed Emma the index card and said, “Give me this one.”
Without hesitation Emma picked up the toy man and handed him to me. These are the moments, moments I could not allow myself to wish for a year ago, that take my breath away.
Emma is progressing beyond my wildest dreams.
Stem cell therapy for autism: Joseph Lowenstein
From Joseph’s mother:
I just want to share why Joey is an important part of our Jewish Community. Joey was our 10th man today and he allowed us to read from the torah. Joey sat nicely in the last row [there are only 4 rows] through out the service. We called Yosef up for the 7th aliya. he walked up to the torah and with a one word prompt said the set of first prayers. He stood at the torah with me , the reader and 2 other men, enjoying and watching. half way through, he put his hand on the wooden roller. after the reading he said the 2nd prayer and ended it loud and with joy. All the men on the Bimah shook his hand and when he sat down , some of the other men came over to Joey. Bertie, he makes you and me proud. Joey is truly a Jewish soul.
When I observed Joey, I observed the following: Joey for the most part was in a very pleasant and cooperative mood. He verbalized louder and his speech seemed clearer than in the past. He made better eye contact with me. When he needed to use the restroom, he verbalized this clearly to me. Socially, he enjoyed playing ball and reading with his classmates. Academically, he seemed interested in doing his math, and was less enthusiastic about his reading. I assume that different times and days he probably also enjoys doing the reading program. He is very comfortable around his teacher Michelle and seems to be adjusting to Caroline his new aide. I am extremely impressed with Joey’s resiliency in terms of his ability to adapt back to the Aspen school and he seems quite relaxed and comfortable at school. In addition, I was impressed with Joey’s ability to participate in his “base group,” he stayed focused and seemed interested in the content.
Hope this is helpful, let me know if I can be of anymore help.
Stem cell therapy for autism: James Wagner
My son James developed severe autistic symptomatology one month prior to his sixth birthday. The anguish and pain we felt as our family watched him disappear into the abyss of thoughtlessness is indescribable. All of the Physicians agreed that his regression was an autoimmune phenomenon. They counseled us on accepting James’ circumstance. We accepted what had happened however we never lost hope.
One evening we received a call from Dr. Lowe a physician that treated James. He said that “James needs to go to Panama and have adult stem cell therapy from the Stem Cell Institute.” We were extremely nervous going to a non US medical facility. We mustered up all of the courage we had and took James to Panama.
The initial round of stem cells significantly improved my son’s cognitive skills.
Once in Panama we were put at ease as the facilities were no different than those found in the finest United States hospitals. The initial round of stem cells significantly improved my son’s cognitive skills. Globally, his engagement and language production show marked improvement. Each day we see many subtle improvements like consistently smiling for pictures, allowing his sibling to blow out her birthday candles or understanding that Sunday comes before Monday.
We are going to bring James back to Panama and are extremely optimistic that he will continue on his current trajectory. It is truly remarkable that such a promising therapeutic intervention is not more widely available. We are extremely grateful to the Stem Cell Institute for transforming our hope into reality.
– Richard Wagner
Stem cell therapy for autism: Luke Fields
We are doing fine I hope you are as well. We enjoyed getting to know you this summer. Luke is about the same. I have noticed some small changes however. He seems to have a better grasp on the concept of time; as in how longer before Thanksgiving break or when a school function is going to occur.
…his teachers have reported his behavior at school is very good and he is taking less medicine than he ever has.
He is also taking more interest in what he is wearing and how it looks. Academically no difference except his teachers have reported his behavior at school is very good and he is taking less medicine than he ever has. Behavior with family is generally a little better like when eating out a little calmer sometimes.
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 therapy for cerebral palsy: Sarai Nathan
“Sarai walking with assistance after stem cell therapy in panama. She could not even stand before.” – Elizabeth, Sarai’s mother
Sarai Nathan suffers from mild spastic quadriplegic cerebral palsy. She came to the Stem Cell Institute at the beginning of August 2011 when she was about 16 months old. The following is a transcription of a phone call interview with Sarai’s mother, Elisabeth. It took place on January 18, 2012 about 5 1/2 months after her stem cell procedures.
How is Sarai doing since receiving stem cell therapy five months ago?
She’s walking with very, very little support. Ever since we got the stem cell transplant, there’s been tons of progress. The major thing that I relay to people is that the stem cell treatment kind of put the cells in place to rebuild everything.
We flew right from the stem cell treatment to a place called the Napa Center and did a three-week intensive [physical therapy] program four hours per day and she was a completely different person four weeks later.
This is the most amazing, miraculous thing I have ever seen. She’s a completely different kid. Where did you go? – pediatrician
Once the stem cells migrated and rebuilt, all-of-the-sudden she was able to able to do all these things crazy quickly. It was unbelievable. She went from not being able to sit to sitting, standing cruising furniture by herself; without any assistance at all and she couldn’t even lift up her trunk prior to coming to Panama. Out of 100% being fully recovered, I would say she has had an 85% recovery since before the stem cells.
I know that the stem cells kind of laid the groundwork for that progress to be made but I definitely believe that doing the intensive right after the stem cells sealed the deal. I don’t think it was just the stem cells. I think that doing one right after the other made the progress amazing.
Did you try any other kinds of treatments before stem cells?
We tried hyperbaric [oxygen treatments] which worked but I noticed that the results regressed a little bit after a few months. It would make her spasticity better and then little by little I’d notice it start to come back 3 -5 months later. The whole thing was very expensive and time consuming though.
How did you find out about the Stem Cell Institute?
I am really active on a lot of Yahoo groups and I read about the parents who had positive results with stem cells and many had good experiences with the Stem Cell Institute. So I called them and they were really on top of getting back to me and answering all of my questions.
And my dad, who has a background in law enforcement, had it checked out as well because he said that he wouldn’t pay some crooks to inject my kid at some random place in Panama. After everything checked out, he helped me pay for it. And I am so glad that we got to do it.
What is your opinion of the doctors and medical staff at the clinic?
We tell people all the time that it was the best medical care we’ve ever received since our daughter was born. The hospitals, doctors, they were all far superior in patient care. They were prompt, professional, loving and they still check in with us all the time.
And the IV, I’ve never seen someone nail an IV that quickly. Randy Bowen [MD], who did all of her IV injections was just so good. My daughter had a huge crush on him and on the second day, actually started handing him her arm. Instead of crying when she was about to get an injection, she would look a little scared and just hand him her arm like, “Alright, just get it over with.” She was only 16 months old so it wasn’t like she could talk or anything.
What do her doctors and therapists at home think?
Well, I didn’t tell her pediatrician that we were going because I knew that he would try to talk me out of it. So I made an appointment right when we got back from the stem cells and the intensive. [at the appointment] I had her sitting on the table by herself and he walked in and said, “Oh, my God! What did you do?” I told him that we actually took her to get a stem cell transplant and he said, “This is the most amazing, miraculous thing I have ever seen. She’s a completely different kid. Where did you go?”
He was asking me about all the information for the clinic; everyone’s name and number. He also said, “I would have tried to talk you out of it so I am so glad you didn’t tell me. What happened to your child is unbelievable and it makes me want to fight and advocate for stem cells.” He’s been specializing in neuro-developmental delays for a long time and said that he would everything he could for the rest of his life to advocate for this therapy.
Now the center that did her intensive [physical therapy]…the things they said were, “I’ve never seen a child progress so quickly.” They watched her spasticity go away and they also watched her strength increase and all her therapists just kept saying, “It’s not usual for a kid to progress this quickly. She is doing exceptionally well.” All of our therapists – when we got home to Hawaii – they said the same things, “This is like a completely different child. This is unbelievable.”
And they asked me, of course, where we went.
Stem cell therapy for cerebral palsy: Tessa Hancock
The biggest thing we’ve noticed is her ability to track people and her vision. Her cognitive skills have improved. Before her stem cell treatment 7 months ago, she was like a 50 watt light bulb and she is like a 200 watts in comparison. She reacts more, holds her head up more and her hands are nice and open now, not fisted like before. Hand to mouth motion is much easier for her to do. Her range of motion, in general, is much better. She can now raise her hands over her head and she was never able to do that before.
Her therapists have seen dramatic changes. Our family has noticed changes. The neurologist has noticed changes. We are very thankful that we were able to get this treatment for her in Panama. We couldn’t imagine her not being who she is now. She is 200 times better than what she was.