Stem cell therapy for multiple sclerosis: Sam Harrell

After his multiple sclerosis diagnosis, renowned Texas high school football coach Sam Harrell had to stop coaching. Sam discusses how, with the aid of stem cell therapy, he’s fought back. Recently, he was able to travel to Super Bowl XLV where his son Graham suited up with the Green Bay Packers as backup quarterback.

“…after my third trip to Panama in September, my walking, my balance, and my stamina all improved dramatically”

Visit Sam’s Blog: Sam In Panama

TUESDAY, APRIL 1, 2012
Great Day in Fort Worth for Stem Cell Team

Sam Harrell at MS Walk

Stem Cell Institute MS walking team with Sam Harrell

Saturday, March 31 was the annual MS Walk in Ft Worth. This year, thanks to the Stem Cell Institute and some of the area stem cell patients, several of us MS sufferers and stem cell patients met for the Walk. Here’s a picture of several of us who have been to Panama, or Costa Rica, for treatments – (from L – R) Richard, Carolyn, Shelley, Carla, Judi, Holly, and me.

We wanted to give the Stem Cell Institute a presence in that sea of MS victims and caregivers. I wish all of them knew that many of us in those blue t-shirts were there walking, actually completing the whole mile, even though we were once unable to do such. I wanted to grab that microphone that the organizers were using and tell all of them “There is HOPE – it doesn’t have to be what you hear from your doctors so often. It can be more than ‘Let’s keep taking this medication so you might get worse at a slower rate’ ”

I personally never heard about the possibility of actually improving when I went to good doctors here in the US – but I chose to try the Stem Cell treatment in Panama, and I walked that mile on Saturday! A year ago, six months ago, I couldn’t have done that – but after my third trip to Panama in September, my walking, my balance, and my stamina all improved dramatically. And many of those in our group on Saturday have a similar story; some results more dramatic than others, but most all of us have seen and felt the changes that give us that Hope that all of those sufferers at the Walk are looking for.

THANKS STEM CELL INSTITUTE!

TUESDAY, JANUARY 17, 2012
2012 Update

Sam-Harrell-Award Well, I realize there may not be many readers of my Panama blog any longer, but just in case someone does return, I wanted to post an important update.

In March 2011 when I returned from my second trip to Panama (my last blog), I soon had a MS relapse. It was the biggest setback I had experienced since my diagnosis. I spent a week in the hospital in Dallas and had numbness from my toes to my chest. When I got home, I was better – the steroids had made the numbness go down to just my lower legs, but I was practically home bound – used a walker or cane most of the time and spent most hours sitting in a chair at home – feeling like this was going to be my lifestyle for the rest of my days!

Even after going to physical therapy and doing everything I was supposed to be doing, my progress was minimal. I was fitted with a brace for my left leg to help the foot drop that was causing me to stumble. My mobility was very limited and I needed help getting most anywhere. I could not hold my new grandson unless I was sitting down, and I couldn’t walk across the room without thinking about each move.

In September of 2011 I went back to Panama for a short visit to get what Dr. Paz called a “little booster.” My mom went with me for this third trip – we stayed in the hotel by the MultiPlaza mall and had a good time since it was mom’s first trip to Panama. But the best news was what happened once we returned.

I had begun a daily log of my condition weeks before I went to Panama – mainly measuring and logging my walking and mobility – here are the exact numbers leading up to my trip and once I got back – these numbers are coming straight from my calendar log – (on a scale of 1 – 10 – how well am I’m getting around):
5,4,5,4,5,5,5,5,5+,5,(panama), 5,5+,5+,6,6,6,
7,8,6,7,7,8,7,8,8,6,6,6,7,8,7,7,8,8,8,8,8,8,7,7,7,7,8,8,8,7(end of Oct)
8,8,8,8,8,8,8+,8,9,9,8,8,7,8,7+,8,8+,8+,8+,8,7,7,8+,8,8,7+,7,7,7,7+(Nov)
7+,8+8,7+,7+,7,7+,7+,8,8,7+,8,8,7+,7,7+,7,7,7+8,8+,7+,7+,8,7+,7+,7+,7,7+,7 (Dec)
7,8,8,7,7,7,7,8,8,8,7,8,8

I know these numbers don’t mean a great deal to you, but they are huge to me – the difference in getting around at about a 5 compared to 7 & 8 is really big – numbers don’t do it justice. My mobility is MUCH improved – I don’t need the brace any longer, I walk like a normal person until I get tired, I can stay on my feet longer, I can jump rope again, I can stand and walk with my grandson in my arms, I don’t have to think to walk from one place to another, and even Kathy sees a huge difference (she has been a little hesitant about the good of stem cells).

So I am very excited and encouraged about my improvements. I can live a fairly normal life right now. And I don’t know if it’s the stem cells that made the difference or simply God’s grace and favor, but I do know it all happened right around the 3rd trip to Panama, so the stem cells had something to do with it. As I have said numerous times before, maybe God is using the stem cells to help me just as He used the Jordan River to heal Naaman’s leprosy after he dipped in it seven times.

But I do want to say this – all of these news shows (60 Minutes, 20/20, etc) coming from the US, that keep saying there are no benefits to stem cell treatments, are only showing you what the FDA and US drug companies want them to say. They have not talked to me, or Richard Humphries, or Preston Walker or many others who have seen dramatic results – we are not healed, but our quality of life is greatly improved and many people are witnessing it. (Now that I am better and getting out, people in town constantly say, “I can’t believe how well you look and how good you are doing.”)

Don’t listen to those media shows and don’t just listen to me – come see the difference!

Thanks again to all who have helped and have been encouraging in my quest to overcome this disabling disease. I encourage all of you to take your health issues into your own hands – be pro-active. What do you have to lose? Many of you may be thinking just like I was – if I do nothing, I know where I will be in 3 years.

One last bit of information – the clinic in Panama is having good but maybe mixed results with MS treatments, but they are whipping, yes whipping, arthritis! If you have a friend or loved one who is dealing with arthritis and the doctors here have said, “your only hope of being mobile again is knee replacements and/or hip replacements”, then you owe it to your friend or yourself to call me or get in touch with the stem cell clinic. What do yo have to lose? There are no side effects or dangers to stem cell treatments. Do it today!

Stay Strong!
Sam Harrell

972 268-(edited for privacy)

*Please contact us if you would like to speak with Sam.

Sam Harrell shares son’s Super Bowl XLV moment

VYPE MAGAZINE – Dallas

By Bill Jones
CBS 11/TXA 21
Sports Anchor

A little more than two years after throwing one of the most dramatic game-winning touchdown passes in college football history in Texas Tech’s last second win over Texas in 2008, Graham Harrell was on football’s biggest stage during Super Bowl week in Arlington.

As the third string quarterback for the Green Bay Packers, he was just 40 miles away from his hometown of Ennis. And his father, former Ennis Lions head coach Sam Harrell, couldn’t contain his excitement, exclaiming, “All of a sudden, they win the NFC championship, and they’re coming all the way back to Dallas!”

“After all those times I experienced with Dad through high school,” recalled Graham, “then you get to come home and be in a Super Bowl. It’s special because there’s no telling how much longer he’s going to be able to come to football games.”

That’s because 54-year old Sam Harrell has multiple sclerosis, an autoimmune disease that affects the central nervous system. Diagnosed with the disease five years ago, Harrell was forced to retire from coaching last year after 16 years and three state championship seasons at Ennis High School.

“All of a sudden, you get stuck with a disease that changed your whole life really,” Sam Harrell said, “and then I started wondering, golly, what kind of dad am I going to be? What kind of granddad am I going to be? Can I even get up and play ball with them?”

Graham said the only thing tougher for his father than telling his family he had the disease was when he informed them last year that he was going to have to give up coaching.

“He loves high school football,” Graham said. “He loves football in general but high school, he feels like he can really touch and influence kids. He just has a passion for coaching high school football.”

The Harrell family is deeply rooted in the very heart of Texas high football. Sam’s father was an assistant on the legendary Gordon Wood’s coaching staff at Brownwood. Sam played quarterback at Brownwood High School in the 1970s and also became one of Wood’s assistant coaches.

After a head coaching stint at Reagan County, Harrell took over at Ennis in 1994. All three of Harrell’s sons played roles in the Lions’ three state championship seasons. The mastermind of one of the most prolific offensive attacks in Texas high school history, Sam Harrell was one of the first coaches to employ a no-huddle spread offense.

Playing for his father, Graham broke virtually every Texas high school passing record, but it’s his dad’s positive attitude while dealing with this debilitating disease that impresses him most. “He’s unbelievable,” Graham said. “A lot of times I wonder how he’s doing. I’m so far away from him. And then you talk to him, and you’d think he’s just fine.”

“You can’t imagine someone having that positive attitude having that disease,” said Highland Park football coach Randy Allen, who coached with Harrell in Brownwood. “He’s very optimistic, and he’s doing better.”

Harrell’s doing better because of stem cell transplants he underwent last summer in Panama. He’s heading back there for another round of treatments in March. Still employed as Ennis ISD’s Career and Technology Education Director, Sam says his health is much improved compared to a year ago.

“That stem cell treatment stuff is expensive, and we couldn’t afford it,” Harrell said as he walked with a slight limp on the Ennis campus last month. “The coaches across the whole state of Texas were just unbelievably kind and generous.”

“Hopefully, the stem cells will continue to help him, and he’ll be able to come as long as I play,” Graham said during Super Bowl Media Day at Cowboys Stadium. “MS can attack you in a hurry. In a couple of years, he may never be able to come to a game again, but my first year I land in a Super Bowl, and he’s able to come because it’s right here in Dallas. It’s going to be such an awesome experience.”

Not only Sam Harrell, but also Graham’s mother Kathy, and his two brothers, Zac and Clark, were at Cowboys Stadium as the Packers won Super Bowl XLV. But none in the crowd of 103,000 spectators was as happy to be there as Sam.

“It brings back memories of him playing so many games at Texas Stadium and being part of the Ennis Lions there,” Sam reflected, “and then how many great places he got play at while he was at Texas Tech and now getting to do it at the biggest stage there is. It reminds us we’re awfully blessed.”

It’s a family blessed with a faithful, positive spirit equipped to take on life’s toughest challenges, and now proud possessors of a Super Bowl ring to go alongside all that high school championship hardware.

Stem cell therapy for multiple sclerosis: Shirley Wigfall

Shirley Wigfall shares her success story. Shirley was diagnosed relapsing remitting multiple sclerosis in 2003 after having trouble walking. After MS drugs were unsuccessful and she was rejected for clinical trials, Shirley found the Stem Cell Institute. Shirley no longer needs a cane to walk and credits stem cells for “truly changing her life”.

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 autism: Millie Jimenez

Millie Jimenez discusses her twin boys’ improvements after they both underwent stem cell therapy for autism at the Stem Cell Institute in Panama City, Panama. One of the boys, who was non-verbal prior to treatment is now speaking in English and Spanish. The other has stopped stimming and both are now making a “more affectionate” connection with their mother.

Stem cell therapy for autism: Juliana Ubinas

Juliana discussed the improvements her daughter has made over the past year and a half after undergoing 2 stem cell clinical protocols at the Stem Cell Institute in Panama City, Panama.

“The changes have been extremely positive and obvious. After my daughter’s first treatment in January 2010, her tantrums diminished. She could transition from one activity to another without throwing a tantrum. She had more self-control. After the second treatment in June 2010, she was in contact more with her surroundings; as if a veil had been lifted. She was surprised, happy and wanting to be with her friends. Her social interaction improved. Before, she was very isolated. After she returned to school following her second treatment, she was able to do “show and tell” for the first time ever. Now she welcomes other children and wants to be part of the group. Her speech is improving. Now she can express to others what she wants.”

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 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.

Stem cell therapy for autism: Victoria

Victoria explains the remarkable progress her son has made since undergoing stem cell therapy for autism in Panama at the Stem Cell Institute. He no longer needs to be placed into outside care. All of the professionals who care for him agree that “it must be the stem cells”. He has experienced a “rocketing of understanding”. He is now peaceful, calm and does not attack anyone. He can now be safely around his infant sister.

Stem cell therapy for autism: Kenneth Kelley TV News Story

July 2012 — Update from Marty Kelley on her son Ken’s progress following stem cell therapy for autism at the Stem Cell Institute in Panama.

“Ken has gone to summer camp (overnight) for the week! He was so excited to go! Ken claims that he is no longer scared of the dark and can handle summer camp…It feels very strange to not have him home this week. He is having such a good time.

This is a major event in our lives. If you understand the type of autism Ken had, you would know what a miracle this is. To clarify, Ken is at camp on his own without any support or an aide–he is just like all the other campers. Pray for the families that are still struggling and cannot do this with their children. Stem cells have changed our lives.” — Marty Kelley (Ken’s mother)