Stem Cell Therapy for Multiple Sclerosis – Jennifer’s Story on Treatment in Panama

Hi. My name is Jennifer and I’ve been diagnosed with multiple sclerosis (MS) since 2003. I started coming to the Stem Cell Institute last year, 2017, in January. My second treatment was in August of last year and now I am here for my third treatment [May 2018].

“I feel strongly that I wouldn’t be where I am here today. I would have been in a wheelchair.”

From my first treatment, I saw major improvements as far as being able to stand without wobbling or bouncing back and forth. I also can feel my toes. I also have more bladder control. The second treatment, I didn’t really see much improvement like I did the first. The first was major. But now I am here for my third and I’m trying to go within six to seven, eight months the most in between my treatments until I see, let’s say 70% improvement.

So, thank you and I support the Stem Cell Institute, and I feel strongly that I wouldn’t be where I am here today. I would have been in a wheelchair.

Video: Stem Cell Therapy in Panama with Dr. Riordan and Mel Gibson

Host Michael Beattie discusses stem cell therapy using *human umbilical cord tissue-derived mesenchymal stem cells (hUCT-MSCs)  at the Stem Cell Institute in Panama with renowned applied stem cell scientist and founder, Neil Riordan, Pa, PhD and acclaimed actor, director and producer Mel Gibson.

Dr. Riordan discusses the miraculous progress of a spinal cord injury patient and pilot whose doctors said that he would never walk again.  He talks about where the stem cells come from, how they work and why they can treat so many seemingly different conditions.  Dr. Riordan explains how umbilical cords, and subsequently, hUCT-MSCs used at the Stem Cell Institute are carefully selected using molecular screening.  He also discusses why mesenchymal stem cells from umbilical cords function better than MSCs from adults, especially as they age or if they are suffering from a disease like multiple sclerosis.  For example. MSCs from a newborn multiply exponentially compared to MSCs from an older adult.

Mel Gibson discusses his father’s miraculous recovery, literally from his deathbed after receiving hUCT-MSCs at the age of 92.  He’s currently 99 and still going strong having been treated in Panama several times since then.  Mel also discusses his personal experiences in Panama.

Watch all this and more.

*umbilical cord tissue harvested after normal, healthy births

Stem Cell Therapy for Multiple Sclerosis – Joyce Adair

Joyce discusses her progress after mesenchymal stem cell therapy at the Stem Cell Institute in Panama.

Interviewer: Today is July 28th, 2017. Can you give me your full name and diagnosis?

Joyce: Yes. My name is Joyce Adair and I was diagnosed with multiple sclerosis.

Interviewer: So, this is your second treatment?

Joyce: Yes.

Interviewer: Could you tell me your experience after the first treatment?

Joyce: Well, after the first treatment last year in April of 2016, I noticed a big change in my energy. I was able to finally go out and do things with my family and friends that I had been unable to do for years. I noticed a change with my pain level. It didn’t go completely away but it did get better and I was able to cut back on some of my medications at that time.

Interviewer: And you also mentioned that you stopped using a wheelchair?

Joyce: Oh, yes. I wasn’t using the wheelchair. I was able to walk on my own – not using a cane or anything at that time. I could put full weight on my legs.

Interviewer: We just finished your second treatment. Can you mention if you have had any improvements this week?

Joyce: I’ve had a lot of improvement this week. When I came on Sunday, I was in terrible pain. I was even unsure if I should come or not because I was afraid to travel on the plane with the amount of pain that I was having in my right leg. But once I had my first treatment this week, I noticed a big change in my pain and I also have noticed a big change in my energy. I have a lot more energy and I can tell that it’s definitely getting better.

Interviewer: Thank you very much.

Sam Harrell at Texas State House Public Hearing on Stem Cell Therapy HB810

Multiple Sclerosis patient and stem cell therapy recipient, Sam Harrell, speaks before the Texas State House Public Health Committee about how stem cell therapy at the Stem Cell Institute in Panama improved his life.

Sam’s testimony:

Chairman my name is Sam Harrell. I’m from Ennis Texas. I represent myself and I’m here in favor of House Bill 810. I’m just a football coach. That’s all I’ve ever been. There’s nothing easy about that but it’s all I’ve ever wanted to do, and I love what I do, and I’m doing what I love. I feel like the luckiest guy in the world. But I’d done that all my life and I was head coach in Ennis Texas, and everything was going great, and I had all these big plans and dreams, and in 2005 I was diagnosed with MS. At first it didn’t show up much so my wife and I didn’t tell a lot of people, but from 2005 to 2009 I’d gone where you couldn’t even notice anything to coaching out of a golf cart. Couldn’t stand up, couldn’t walk on my own, so in 2009 I had to retire from coaching, and in 2010 I had to retire completely from education, not because I wanted to, but because of MS.

During that time I was going to see the best guys, and they’re great guys in Dallas, and their heart’s in the right place, and they had me on MS meds and obviously not much was helping. That’s what they tell you about the meds. They won’t get you better. They just hope to slow it down.

Well, from 2005 to 2009, I went from coaching and walking and working out in the sun to not being able to walk and sit at home using a walker every day, so that slow down process wasn’t very slow in my mind. A friend of mine told me about Preston Walker, who went down to Central America for stem cells. Fortunately, in 2010, I found myself in Panama getting stem cells, and I fast-forwarded to 2014. I was doing so well again that I said, “I think I could coach again.” And I started again at Fort Worth Christian high school, and I’ve being doing that for the last three years. I get up every day, throw on my shorts and my tennis shoes and move again, and I never dreamed I’d do that. And it’s all because of adult stem cells in Panama. And that’s why I’m for this bill, house bill 810. I appreciate your time so much.

Stem Cell Treatments for Multiple Sclerosis – Jason Upshaw with Neil Riordan, PhD

MS Patient, Jason Upshaw and his wife, Michelle discuss his stem cell treatments at the Stem Cell Institute in Panama with founder and chief scientist, Neil Riordan, PhD. Jason was diagnosed with MS 21 years ago.

Transcript:

Jason: The very first time I came it was relapsing/remitting, and it progressed to secondary progressive, and that was the second trip that we came. I haven’t actually felt this good in years. I have no MS symptoms whatsoever, other than a bit of heat fatigue, still, but other than that, no numbness; no tingling; and I haven’t felt this good in years.

Jason: When I went the first time, it was to Costa Rica at y’all’s clinic and they had to put me on the plane in a wheelchair, and they had to transfer me between flights in a wheel chair. I couldn’t walk from here to the door without being exhausted and I still had a lot of numbness and tingling. When I got home from that trip I walked off the plane, got my own luggage, and walked out to the parking lot to the car that was waiting for us. It improved my life in one treatment.

Jason: Um, of course the numbness and tingling gradually went away, I haven’t had any numbness or tingling in years. The fatigue has gotten a lot better. A lot of it, if I’m smart, I don’t have any symptoms. I know my limits and if I push them too far… but I don’t think it’s just the MS. When you get tired, your body shuts down. I don’t blame a lot of it on MS. It’s just that when I get started, I just like to go, go, go, go. If I push it too far, I pay for it, but if I’m smart, I don’t go too far.

Dr. Riordan: You first came in August of 2008. When did you come a second time, in 2010? So, you felt the need to come back in 2010, so what were the symptoms like then?

Jason: The numbness and tingling wasn’t an issue. I could tell that I was dealing with more fatigue than I had been, so before I got down to where I was [before], I wanted to get a head start on it, so I came back. The heat was really bothering me then. My gait when I was walking… people could tell I wasn’t doing as well anymore. So before I got to rock bottom, to where I was before, I went to Costa Rica, I thought I’d get back down here and try to get ahead of the curve, and I’ve been going back ever since.

Jason: Yeah. I live in Texas so it’s going to be hot, but I think because of my medical history I have to pay closer attention than most, but for anyone if you stay out in the heat too long, you’re going to get drained. You’re going to get tired. It affects me more so than somebody without MS, but like I said, if I’m smart now and listen to my body, I really don’t have any problems.

Michelle: I’ve been with Jason through every step in this and with all his physicians in the states, and I would send anybody here. It’s extremely loving first of all, extremely hands-on in trying to help you.

Even if you need a glass of water, it’s not a bother, just little things like that. Extremely professional, wanting to make sure you go that extra step and know what you’re dealing with, that you’re not afraid of what you’re fixing to do. Being on the opposite end of this and not being the one who’s being treated you feel helpless, but here I haven’t felt helpless with anything Jason’s needed to go through. Everybody’s been so reassuring and reaffirming, and there’s been no questions. And if there are questions, they get answered. It’s a night and day difference. We’re not just a number, or a name, or the money being paid to make this happen. It’s truly being done because y’all care and it works! It just truly works, and I’d send anyone here in a heartbeat. The therapy of it, the physical therapy, it’s not you just go and exercise. You’re taught life skill exercise you can use until you’re 100 years old if you live that long, and continue to be stronger and better.

Jason: I’d like to qualify this: in the US I’ve had some of the best MS specialists that there are, who are still good friends of mine, but… it’s… my experience with MS in the United States is that they treat the symptoms and don’t look for a cure. I’ve been on every MS medication that there is, the last time I checked, and honestly the side effects were worse than what they were trying to fix, a lot of it. They weren’t doing anything. They said that the goal of each one of those was to lengthen the amount of time between relapses, which means you’re still going to have a relapse.

When we came here, I want to fix the problem. That’s what we found here. I speak to people with MS on a daily basis. I could make a full time job out of answering emails and phone calls about what stem cells have done for me, and I spend a great deal of time doing that. I don’t endorse the clinic, I don’t get paid a penny for doing it, but to me that would be the most selfish thing in the world to know it works if I didn’t take the time to share my story with other MS patients.

Y’all have changed my life. I’m back. I’m still in law enforcement. I work a 40 hour week that seems like a vacation. I’m not a proud man. The day my boss gave me my badge and gun back I cried like a baby because that was really the only thing that I’d ever given up on. I don’t give up. I never thought, ‘I won’t walk again,’ even when specialists told me, ‘Jason you might not walk again,’ because all that would do is make me more mad and more determined. The only thing that I nearly gave up on was never being able to wear a badge and gun again, and you guys gave me that back.

Every day when I take that first step it actually means something. It’s not I have to go to work tomorrow. I get to go to work tomorrow. It changes your whole thinking. She was talking about the staff. I get to tell people every time I talk to them that this is the finest group of doctors I ever dealt with. I’ve had some outstanding doctors in the US, but as far as… I’ll put the doctors here up against anyone in the world. The caring, the professionalism, if you have a question, they have an answer, and it’s… speaking from experience when I went to Costa Rica I was scared to death. I tried everything for my MS and nothing was working. I decide one day I’ve tried it all. I’d read about the clinic from another law enforcement officer who’d kept a blog about every day he spent in Costa Rica, which I followed religiously. I sent my application before he even got back and was approved. I met Preston Walker, the day after he got back was the day before I was supposed to leave. It was wonderful meeting him; if someone told you he had MS you wouldn’t know it to look at him, and he had the same results I did, and he’s still working today. But it was scary. I’m a country boy, I was raised on a farm, and for me to get on a plane to another country to get medical care down there… we all hear the horror stories. But after my first visit with the doctors I was at ease and it’s the finest group of doctors I’ve ever been associated with.

Michelle: And we’ve heard that from everybody. We have a group of people from every time we were here. I keep a group of people and stay in contact, and everybody is happy. Everybody who is dealing with children who have patients here to adults… we tell everyone when we were coming here that we were going on a family reunion because that’s just how we feel. This is like a family for us. Y’all have loved us and stood there with us through the hardest times and helped us have our life back and to us, that’s family.

Jason: We sat in our driveway and cried the day I sold my electric scooter because that was the only way I could get around. We sold it and when the gentleman come picked it up, we sat in our driveway and cried. It was so good to see that go, it was a godsend when I needed it, but it was so good seeing that go.

I’ll stand on top of the highest mountain and sing your praises to anyone that will listen, because like I said, it would be the most selfish thing in the world if I didn’t. I don’t just think it works, I’m walking proof that it works. I’ve talked to hundreds of people who have ended up coming down here, and I won’t say that everyone’s had the same results that I’ve had, but I can only think of two out of hundreds who just flat-out said it didn’t work.

That was my whole philosophy when I came down, I was so scared of getting my hopes up. I saw it worked for Preston Walker, but I’d been giving every witch potion you can think of saying this is going to make it all better. Medicine or herbal it didn’t matter. All I could see it was draining my checking account and not helping me at all. Of the hundreds I’ve talked to, with all but two, have said they were much better when they got back. I told myself if I had a better quality of life when I got home, then it worked. I don’t care how big or how small, if I had a better quality of life then it worked, and boy did it.

Michelle: If it didn’t work we wouldn’t be coming back for maintenance. If I can advise a spouse that is wanting to help in any way, this is not a miracle cure. This is something like with anything you do to change your life and make that commitment. This is going to give you the tools and everything you need and it’s going to jumpstart you to such a level – that you have that will and desire to go again that it’s given him. It’s your responsibility when you’re given that gift, You have to take care of it. You have to maintain it and nurture it. I think that’s why Jason’s been so successful; coming in with his mind-frame, when he got that gift with the stem cells. He’s taken it and he’s taking care of that gift and has nurtured it and that’s why we keep coming back; to boost it and keep it going.

Jason: When I was coming back I told my Sheriff, my boss, that I was coming back, and he’s seen me at my worst and my best because I’ve been working for the same place for seventeen years. When I told him I was coming back down, he got a very concerned look at first like, ‘are you not doing okay?’ and I laughed. It’s the joke around the office that I haven’t felt this good in years. I’m going down for a tune-up, and they all got a good laugh out of that. That’s how I see it. I’m getting a tune-up and I’ll keep coming down for it as long as you’ll have me.

Michelle: When I say I love you guys, and I haven’t met y’all, it’s because you’ve meant so much to me. I married this man not-healthy, walking with the assistance of a cane or a walker. I was the one who got to pick him up at the airport that day, and watch him walk upright like the strong man that he is for the very first time and it was wonderful. So that was the most wonderful thing anybody can have. So I’ve loved y’all since that moment.

Multiple Sclerosis patient, Sam Harrell has no more use for his walker after stem cell therapy!

Here is an update from Sam Harrell who was speaking at our public seminar in Southlake, Texas in October, 2015. Sam has been to the Stem Cell Institute in Panama several times for umbilical cord mesenchymal stem cell therapy.

The beginning is about as inspirational at it gets! Go Sam!

“I used to need this [walker] get out of the house. Now, it needs me!” – Sam Harrell

Inside High School Football Report on Hall of Fame Coach and Stem Cell Recipient, Sam Harrell

Sam, who suffers from multiple sclerosis, was forced to retire as Ennis (Texas) High School’s head football coach due to his debilitating symptoms. Sam’s first two treatments using stem cells harvested from his own fat did not yield long lasting, positive results. However, after his third and fourth trips to the Stem Cell Institute in Panama for umbilical cord tissue-derived mesenchymal stem cells, Sam’s life turned around. Now, Sam is back in the game again!

Stem Cell Therapy for Multiple Sclerosis: Ron McGill

Ron McGill suffers from relapsing-remitting multiple sclerosis. He was started experiencing symptoms in 2009 but was not diagnosed with MS until January of 2013. He received several infusion and injections of human umbilical cord-tissue derived stem cells at the Stem Cell Institute in late October and Early November 2013.

In this video, Ron shares his story of discovery and recovery at a Stem Cell Institute seminar in San Antonio in October 2014.

For more information on MS therapy at the Stem Cell Institute in Panama, please visit: https://www.cellmedicine.com/stem-cell-therapy-for-multiple-sclerosis-3/

Good afternoon.

I was diagnosed with relapsing-remitting MS in January of 2013. My symptoms started with tingling and numbness in my hands and feet migraine headaches in April, 2009. Visits to the doctors concluded that job stress-related migraines were all it was.

My high tolerance for pain accepted the results and I went on with life. This was an extremely poor decision on my part. My symptoms remained constant but non-progressing until November of 2011. In attempting to kick a soccer ball, I lost my balance and I fell. I wrote it off as being out of shape and clumsy. A fall on a treadmill and down a stairwell in early 2012 was my final wakeup call. It solidified that there was more wrong with me than normal.

My quest to find out what was causing my issues and how to resolve them was started.

Starting from behind and (inaudible) to catch up, I did several things. I made immediate dietary changes. Sodas, fast food, canned food, alcohol – eliminated. Red meat, dairy, bread, pasta – reduced drastically. Chicken, fish, fresh fruits, vegetables – doubled. I went on a weight loss and body detox regimen. I replaced impact aerobic exercises I could no longer do with swimming.

I made the most of my insurance. I literally became a human pin cushion. Everybody was sticking me. I looked outside traditional medicine: acupuncturist, building my immune system and pure vitamin regimens. While I made great strides in changing my life, I was testing healthier, a progression of worse symptoms continued to happen. Severe leg and back aches, leg stingers, twitching, lost grip and more loss of balance.

It was determined that MS was my cause. My instability had me falling one to two times a month. I reached my lowest point waking up immobile from the waist down on a Wednesday morning in February of 2013.

With my motor skills seemingly erased from my memory, a deep cloud of panic overtook me. My confidence went out the window. I had to dig down extremely deep. I was able to regain mobility later that evening. I progressed to a penguin walk and very limited speed and distance over the next 6 months with the help of a walking stick and physical therapy.
Hours of online research for possible relief led to stem cell therapy.

After many months of research, doctor consultations, numerous conversations with people who had had stem cell therapy, heard about it, had relatives who had experienced it, I sent the email to the Stem Cell Institute.

After being accepted, I still had more conversations with Dr. Barnett and Cindy, asking more and more questions. They were extremely patient to everything I had.

The care provided for me upon my arrival and during my stay and departure in Panama was extremely good. The facility was simple, clean, efficient with a very helpful and friendly staff. The procedure was well-explained to me and carefully administered.

I was able to see results on my way back (on) November 3rd. I was able to walk farther and feel better. I was able to my walking stick in the back of my car for good two weeks later. Knock on wood, I haven’t fallen since October 23rd of 2013. My stamina, walking speed and stability have continued to increase. I do have momentary balance loss and heat can still wipe me out. My MS is still with me.

Do I feel (that) Panama was the right choice? For me, absolutely. I feel the infusion of healthy cells gave my body a huge boost to recover the majority of lost motor skills I had experienced. It also helped amplify the lifestyle changes I was already making to give me a faster and more positive result.

These successes have given me a more positive mental state that have allowed me to heal more and more.

What advice could I give you about stem cells? Research, research, research. There isn’t a price you can put on due diligence when it comes to your health. Make lifestyle changes at the cellular level in your body and amplify it with stem cell therapy.

In closing, I’d like to thank my wife for undying support and hours of research. I’d like to thank Dr. Riordan, (and) Stem Cell Institute for being at the cutting edge of healing diseases and I’d like to thank you all for allowing me to share with you today.

Colorado MS patient returning to Panama for more stem cell therapy

By Travis Khachatoorian
Created: Mon, 05 May 2014 10:21:00 MST
Updated: Mon, 05 May 2014 11:27:10 MST

CLIFTON, Colo. – Even with all the advances in medical sciences over the years, multiple sclerosis remains mysterious in both causes and symptoms. There is no known cure for the disease, but one Clifton resident isn’t waiting on the US government anymore and is planning to fly to Panama for a stem cell therapy.

Pam Claypoole was diagnosed with MS almost a decade ago and has slowly lost the feeling in her legs and right arm. She said since the FDA currently doesn’t approve any stem cell therapies for her disease, she’s planning a second trip to Panama in hopes to improve her condition.

Claypoole said she’s made one trip to the Stem Cell Institute in Panama more than a year ago and was amazed by the effects.

“I felt it made a big difference for me right away,” said Claypoole. “My walking was better, the feeling in my feet was better, I had more energy.”

She emphasized her treatment doesn’t involve unborn fetus stem cells but rather the stem cells taken from healthy birthed babies umbilical cords.

Her family is currently planning a live auction on May 14th at the Western Slope Cattleman’s Livestock Auction in Loma. The event starts at 6 pm, and they’re hoping to collect $20,000 dollars to fund Pam’s therapy in Central America.

more…

Sam Harrell’s Stem Cell Journey: Stem Cell Therapy for Multiple Sclerosis

Sam Harrell sent us this homemade video documenting his progress from 2010 until now (2014). Sam was coaching football at Ennis high school in Texas when MS struck him hard, forcing him to retire. Since then, after several rounds of stem cell therapy at the Stem Cell Institute in Panama, Sam has returned to coaching football, something he though that he would never be able to do again.

For more information about umbilical cord tissue-derived mesenchymal stem cell therapy for MS, please visit: http://www.cellmedicine.com/stem-cell-therapy-for-multiple-sclerosis-3/