“I had my treatment done 8 weeks ago and I am getting my body back. I can’t believe it. Please see the attached videos. My feet were so screwed up when I came to Panama that I wasn’t sure how much longer I would be able to walk. Unbelievable is the only word I can think to describe this.” – John K.
Our patient stories.
From life-changing breakthroughs to everyday victories, hear how stem cell therapy has given our patients more than just recovery; it has given them their lives back.
Hear how our cellular therapies have changed patients’ lives.
Results: 244
I was gaining 7-12 lbs. of fluid around my heart every night from the congestive heart failure and legs were swollen, difficulty breathing. I was treated, went home, within a couple of weeks, I was only gaining about 3 lbs. around my heart every night, which was a vast improvement. I have weaned down since then to 20 mg of Lasix a day.
I walked… I was trying to walk prior to the treatment and wasn’t making it very far. Now I walk 3 miles a day. I work out at a gym with a trainer twice a week.
I’m back for a second treatment because I had a failure of my pacemaker and it had to be removed – pacemaker and defibrillator was removed and a new defibrillator put in, which indicated that the dead right atrium has regenerated enough. I no longer need a pacemaker. I just need a defibrillator for safety reasons.
For more information about stem cell therapy for heart failure at Stem Cell Institute, please visit: https://www.cellmedicine.com/stem-cell-therapy-for-heart-failure/
The Twins, Meadow and Summer were born in May 2014 and are Now five years old. They were both diagnosed non-verbal Autistic, Meadow having more issues than that of her older Twin Sister Summer.
Pre Stem Cell Treatment
Meadow had severe learning difficulties in addition to her non-verbal Autistic diagnosis. She suffered severe melt downs two to three times daily triggered off by the slightest thing, simply being tired, taking her shoes off and nappy changing are but a few. Meadow would often become aggressive during these meltdowns and would self-harm, pulling at her face and torso, slamming her heels into the ground or slapping her feet together, we have previously taken Meadow to ER following injuries she had inflicted to her feet. Meadows aggressive behaviour left us parents bruised and bitten on occasions, it was especially hard for my wife to cope with on her own, Meadow was very strong and hard to control even at 4 years old.
In addition to meltdowns, Meadow is very hyperactive, runs around on her toes and had virtually no attention span at all. Meadow would pull off her nappy and play with the contents, she would also make herself sick throughout the day and night, this was all part of her sensory issues and need for attention. Meadow could not understand our moods whether we were happy or angry, she never noticed her sister and rarely had anything to do with her. At her new school she was introduced to sign language, sign-along. She could not form any of the signs physically at all let alone understand them.
Life at home was incredibly hard for my wife and I with Meadow, we had very little sleep and no family support or friends to help us, our friends became distant and our family had either passed on or lived too far away.
“The most wonderful thing for us parents is watching Meadow and Summer playing with each other as sisters for the first time. They wait for each other in the mornings at the bottom of our stairs and scream and shout running around the house for the best part of the day laughing, they even argue with each other, it’s all quite amazing to watch.”
Summer is the younger Twin, she has her own issues, however in comparison to her sister Meadow, Summer was easier to manage. Summer stimmed a great deal and could only manage one word, NO!.
Summer found it hard to go outside when the weather was bad, she was uncomfortable with walking on soft ground like shingle or woodland areas. Summer would simply refuse to walk if these situations were presented.
Summer had better attention span but found it hard to share anything with anyone. Summer would melt-down when told No, or if you were to refuse her something of interest, she would also lose control if you were to take something away from her.
Summer did not play with Meadow at all, or show any sisterly or Twin bond, she did not have much of an imagination and played with toys inappropriately.
Both Twins were very happy despite all their issues, they had just started ABA at the local Special needs School Treetops, two – three weeks prior to Stem Cells. Treetops is an amazing school, we are very lucky to have found them both a place, we fought very hard to achieve this, which is another story…. .
Following Panama Stem Cell Treatment
In the first week of October 2018 just a year to date both Meadow and Summer are different Children.
Meadow and Summer came back from Panama. The first week home they were so hyper active we were worried and contacted the Clinic concerned for advice, the centre explained it was quite normal and after a couple more days the Twins settled.
The results were amazing following.
Meadow had no more meltdowns and stopped all self-harming to this day, she has had a tantrum but nothing more than expected from a 4 year old. She slept through the night for the first time and hardly ever wakes during the night today. Meadow wore Glasses which had been prescribed at Moorfields in London, a renowned eye hospital in the Capital London, her eyes unexplainably improved, she needed a new prescription, Moorefield’s were confused as she had undergone three examinations prior. Meadow won an award at her Special needs school for the most improved student, mastering all her signs, understanding a few and most importantly she managed to focus and increase her attention span. Meadow could walk to assembly, sit patiently and take instruction, all within two months to three months. Meadow was reported to be for the first time at her Sunshine day centre, aware of her surroundings and other children around her.
Meadow has improved throughout the year and smashed her school targets, we couldn’t be happier as parents we are so proud of her and so thankful to the stem cell institute in Panama for making this possible and our school for pushing Meadow to achieve what we thought was impossible in just a year.
Summer has developed further on her one vocal word ’NO ’, she can count to twenty, she sings nursery rhymes, she speaks in sentences, she uses phrases in context, i.e. when Summer tripped she said ‘oh that was close mummy’. Summer won the award at Treetops Special needs school for the best improved pupil in the whole school 2018. Summer was nappy trained in just Two weeks and has made a friend at School called Jackson. Summer likes to dress up and now plays with Toys appropriately. Summer loves being outside and loves the woods especially.
Summer has done so well, the school is transitioning her from ABA 1-1 tutoring, to moderate learning in a group which is amazing progress. Summer is quite amazing and the school has mentioned that she is quite special and has come so far in just a year.
For Us
The most wonderful thing for us parents is watching Meadow and Summer playing with each other as sisters for the first time. They wait for each other in the mornings at the bottom of our stairs and scream and shout running around the house for the best part of the day laughing, they even argue with each other, it’s all quite amazing to watch.
-Jade and John Lockey
Find out more about Stem Cell Therapy for Autism at Stem Cell Institute in Panama
We found this video on YouTube today. It’s great to see Kyle doing so well after his stem cell treatments for multiple sclerosis in Panama recently. Kyle has become a real advocate for stem cell therapy in Panama!
I have a diagnosis of arthritis and also other symptoms consistent with fibromyalgia – were like fibro fog and pressure point pains. I also had a lot of stomach problems like Crohn’s chronic constipation and other things that just seemed very autoimmune.
So, I came a year and a half ago my first time and it was amazing. So, my work involves my hands and my back and I felt like I could literally do cartwheels for months and months after I had the treatment, and even after that, I noticed that even my joints in my hands remained really happy.
So, my stem… I even had started eating, you know, gluten free for years and with no result, any good results from that. My stomach feels amazing and overall, I think that allows all my nutrients to absorb better and my joints for really good. And so I’m very, very happy that I came here and thank you so much.
Hi. My name is Leo Beus. I’m 76 this December. Three years ago, I had a second heart attack while I was sitting in church. I was taken to the hospital. Really capable doctors put in three stents. What they discovered was a prior heart attack and I had damage to my left ventricle. My ejection fraction was in the low 20s.
I then went to my cardiologist, who I have a great deal of confidence in, and we did drug optimization for a very long period of time with just a little bit of success. I was then sent to the Mayo Clinic, where we did more drug optimization – again with some success but not much. So, I was faced with the option of a heart transplant, which I didn’t qualify for [or] a pump from the left ventricle to the aorta, which I didn’t like the statistics on that procedure.
And then I went to scientists that I knew and I ran into the information about stem cells, umbilical cord stem cells at the Stem Cell Institute in Panama. I was encouraged by some very high-level scientists and doctors to go to Panama. I did.
A year ago I had four days of treatment. My ejection fraction is now 44. Everybody that sees me says I’m a walking miracle. That’s true I feel like I’m 25. I’ve been married 53 years. My wife is not sure she can stand what the stem cells have done for me. They’re fantastic.
The experience in Panama was one of the greatest experiences I’ve ever had. The facility was absolutely spotless professional. The doctors and staff that I dealt with were off the charts. I cannot do anything other than say it is probably the single best medical experience I’ve ever had. Good luck and that I may go back just for fun.
About Leo Beus
Leo Beus is the co-founder of Beus Gilbert PLLC, a premier boutique law firm concentrating on high stakes litigation, real estate and zoning law. Mr. Beus leads the Firm’s litigation department, with emphasis on representing plaintiffs in complex litigation involving securities, real estate, investment fraud, lender liability, professional malpractice, antitrust, trademark, intellectual property, and directorship liability. Mr. Beus has been the lead litigator in plaintiffs’ cases resulting in verdicts and settlements totaling in excess of $4 Billion for his clients. In addition, Mr. Beus has successfully represented defendants against antitrust and shareholder derivative claims where the stakes have been up to $1 Billion.
Mr. Beus has received numerous awards and recognitions in his profession and his community. Mr. Beus and his wife, Annette, serve as co-chairs of the President’s Club of Arizona State University. He is recognized by his peers as an AV® Preeminent Lawyer with the highest rating in Martindale-Hubbell and is ranked among the highest rated lawyers in America in Best Lawyers in America, Chambers & Partners USA Guide and Southwest Super Lawyers. Mr. Beus was named Litigator of the Week by Litigation Daily and named as a Benchmark Litigation Star in the upcoming 2016 edition. He has been recognized in national business and industry media, including the Wall Street Journal, New York Post, Crain’s New York Business, Litigation Daily, Benchmark and Law360, as well as the Arizona Republic, Arizona Attorney, Phoenix Business Journal, Tucson Citizen and Deseret News.
A 1970 cum laude graduate of the University of Michigan School of Law, Mr. Beus served as Managing Editor of the University of Michigan Journal of Law Reform. He received his B.A., magna cum laude, in 1967 from Brigham Young University where he was a member of Phi Kappa Phi Honorary Fraternity. Mr. Beus is admitted to practice before the United States Supreme Court, United States Court of Appeals for the Second and Ninth Circuits, United States Court of Federal Claims, United States District Courts for Arizona and Colorado, United States Tax Court and the Supreme Court of the State of Arizona. He was, at one time, fluent in Dutch and Flemish (alas, a bit rusty today).
It’s August 29 2019. My name is Dan Isbell. I’m a retired colonel from United States Air Force and a disabled veteran. Today, I’d like to share briefly the history of my career, how my injuries came about, and why I chose to seek help at the Stem Cell Institute, Panama City, Panama and it’s not all just about me. I want to help others because videos that I watched in preparation for my decision helped me make that decision. And I know there’s a lot of other especially military perhaps active duty and even disabled veterans that hopefully could have hope from learning with my experience and this might offer something for them.
So first let me briefly describe my career. I started out as a combat fighter pilot – Top Gun pilot. Then I was selected go to Test Pilot School. I became an experimental test pilot in the United States Air Force. Got to do a flight test a number of locations. Later, unfortunately, some flight tests are dangerous business. Lost 35 friends in my career. I’m lucky to still be alive but I had some incidents in the F-16 and in particular one where my aircraft exploded during a flight test mission. I was on the ground at the time so it didn’t crash but it disabled most the systems. I was trapped in the F-16 and canopy wouldn’t open. I was breathing in a lot of hot toxic gases as the airplane was on fire. The ground crew got me out and unfortunately, the damage to my lungs started to take a toll later in my career and really forced my retirement ultimately in 2004. So I’ve been retired about 15 years now.
Was fast tracked into the V.A. as a disabled veteran for the service connected injuries that I had. So, I went from being very, very fit flying 9-G airplanes, have been to the edge of space in the U2 in a space suitt seeing the curvature of the earth. Flown in a lot of different types of aircraft and my flight test career. Went to the gym, usually three times a week for weight training, and also did aerobics every day of the week, climb mountains, did snow skiing and many, many things, run marathon. So, I went from a level of extreme fitness to suddenly, I couldn’t get across the parking lot without being out of breath before I got to the curb. So, the degradation was very severe.
It began in about the year 2000 and unfortunately, the only things my lungs were responding to were prednisone steroids – very high doses. This started in 2000 to 2001, sort of got things under control but after I retired my health continue to degrade, and by 2012, literally, the situation became cataclysmic. It was a number of things that started to just break down, and my body was very diffuse case of what was finally, definitively diagnosed in 2012. The injuries had resulted in our bronchiectasis, as well as pulmonary sarcoidosis, and in my case those was a very diffuse form. It was affecting all of my body. My calcium levels were going super high. My uric acid was going high so I ended up with all of my joints locking up and being stuck in a wheelchair and very, very severe pain for several months until we got some of that under control with medications
I had about 18 emergency room visits, an ambulance ride where they had to stop my heart because I wouldn’t survive the ride if they didn’t stop it with an I.V. injection and then restart it to hopefully get it beating more regularly. Had an ICU visit after I crashed. I was admitted as an inpatient over 10 times and found over seven surgeries to try to deal with all of the things that had gone wrong with me. But in this particular case I went into septic shock and was in the ICU and they didn’t know if I would survive the night. They told my wife that might not be able to make it through. So in spite of all that, I’m still here. I had episodes where I was coughing up blood from my lungs and I’m home oxygen for a while, and a high dose of steroids had pumped my weight up to about 283 lbs. at the peak. I’ve lost about 70 of that now.
So anyway, that background should help you understand that my quality of life is not good. Bag of medicine every day: Nebulizer, steroids, all of these things, and to be trapped on prednisone steroid for the rest of my life was really not a good situation. When a flight surgeon, when I was still active duty, first prescribed it he said, “I don’t know how I feel about nuclear weapons but I’m about to prescribe one for you.” That was a very apt description because it’s not a precision drug. It has a number of very negative side effects, and after years of high dose steroids, it had caused bone loss to the point that I was diagnosed osteopenia. So the other things were that it had made the tendons in my body lose their suppleness and then I started having all sorts of tendon related pain and injuries.
So, I made the decision since there was nothing else and conventional medicine to help that if I found something that had promise and gave me hope, I would do everything in my power to actually go get that kind of treatment. My stepson, fortunately, had a friend in Los Angeles who had recently informed him about going to the Stem Cell Institute in Panama and how his very severe shoulder injuries were miraculous the results, and the pain going away and getting his function back.
So, my stepson shared that with me and said, “Look, so something you might want to check out. So I did. And having a research scientist background, he also informed me about Joe Rogan podcast that was available on YouTube. And it involved having Dr. Riordan, the head of the Stem Cell Institute in Panama, along with Mel Gibson and the story of Mel Gibson’s dad and how he went in his 90s, they were able to bring him back from the brink hospice to full functionality with these treatments.
So, I bought Dr. Riordan’s book. I read it cover to cover. I continued to do research on the Internet. Look at the pros and cons, look at the history of this. Watched every video that was posted at the Stem Cell Institute, many other personal YouTube videos that I could find related to this and the Stem Cell Institute. And made a calculated decision that I need to do something and that I was willing to take a chance that this procedure, particularly since there had been no known negative side effects and all the thousands of cases, that it was a risk worth taking. I applied under the autoimmune disease because that’s what pulmonary sarcoidosis is actually categorized as. I was accepted under that protocol and I traveled to Panama City, Panama October 15th of 2018 and began my treatment that week.
The treatment involved… First, there were three separate days where I got injections into alternate IV’s and my arm – just a normal I.V. injection about 40 millions of the mesenchymal stem cells each time, and also on that third day, they added the injections into my right hip that I had requested to try to get functionality back there. I’d had a surgery on the hip already but it didn’t give me full relief and I was still locking up after less than a block of walking, had to sit down on rollator and literally, try to let it come out of spasms so I could walk some more – very, very, very difficult. And visiting the Pentagon and places as a consultant, it really limited my ability to travel comfortably and perform properly.
So, I was looking for some help, not only with my lungs but also for that right hip that was an issue. So let me tell you what then next happened. That first injection, which took about 18 minutes and it seemed like the Star Trek Enterprise. You’re in a floor-to-ceiling glass room with… It’s not surgery. You’re in a nice comfy chair. You can see out on the Atlantic Ocean the entrance to the Panama Canal, all the ships out there and all the skyscrapers everywhere. In Panama is not like the Panama that I remember from 20 years earlier when I’d been there just before we turned over Howard Air Force Base to the Panamanians to actually run the Panama Canal and maintain it. Now, it’s like a little Dubai. There are skyscrapers everywhere. It’s very modern. There is every kind of restaurant, hotel. In fact, the hotel in the building that we stayed in is a 5-star Hilton but beautiful, beautiful with lots of restaurants and swimming pools and hot tubs. This is a very nice experience. It’s like a vacation if you want to think of it that way.
So, they met us at the airport, helped us with, right through customs very quickly. Nice ride already ready to go to the facility. Got there and checked in. Went to the hotel room and then the next day, began the process. So, after that first injection, I felt a little bit of malaise maybe a half hour later, like a generalized like you’re getting sick with something but it’s very mild and it’s subsided after about 45 minutes. And the instructions were just go back to your hotel room, which was filmed at 27th floor. The clinic’s on the 63rd floor of the same skyscraper.
So I did, and about five hours later I was lying in my bed. My wife, of course, accompanied me. And I set up in the middle of bed and I said, “Sweetie.” And she goes, “What?” She thought something bad it happened. I said, “I can breathe and it doesn’t gurgle, and I, it does, it’s not painful.” This is literally five hours after the first injection. So, I think most of those cells, you know, went directly there right away and started working on calming down my lungs and getting rid of the inflammation.
So, over the next course of days and after the injection my hip, I traveled back and I had not told my doctor, my pulmonologist, that I was going in advance of my trip. So, I had scheduled an appointment with her. She was pretty upset because she didn’t believe in this and thought there was maybe a lot of “witch doctory” out there about it and she was worried about my health. She was the only doctor I’ve ever had that gave me her personal cell phone number and said, “You text or call me anytime 24 hours a day or night when you run into crisis and I’ll be there for you.” And she has been for all these years since roughly 2012.
So, I really was not wanting to do this in the dark. Being, having a research scientist background, I wanted data so I told her, “Well, you know look, this is why I scheduled the appointment with you, because I want you to schedule labs for me, regular labs, so we can check on my progress, see how I’m doing. And then in the course of that, we’ll have some data to go along with my subjective feel about it.
She thought it’s just a placebo effect and one of her other elderly patients had blown his life savings at some place here in the United States that probably wasn’t at all the same kind of well-researched procedure. And it hadn’t done him any good. So, she just had negative background information and really didn’t understand it well. But she was willing to support me through the process.
So, the labs have all shown them my body pretty much has return to homeostasis. One of the things that I learned to keep track of was my oxygen saturation. So, before this procedure, I could be in the low 80s, especially at times when I had to go on home oxygen and literally carry an oxygen bottle around when me everywhere I went. And the best I could do on a good day was about 94 percent, which is not bad. I could survive on that, little hypoxic. The Sporiva helped and the nebulizer. And of course, the emergency inhaler that I carried everywhere I went because I was very sensitive to second-hand cigarette smoke after my lungs were damaged. Never been a smoker but I would have a bad reaction to it.
So the labs were showing good. My calcium, everything was back normal and by the way, I had chosen so that I didn’t interfere with the effects of the medicine, the stem cells in this case, not medicine. I had chose to stop all my pharmaceuticals before the procedure. And then I took them with me. You know, if there was an emergency I had them available but I didn’t take them because I wanted to see what the actual effect of the stem cells would be and not have a conflict between, “Is this the medicine that I’ve been taking or is this the stem cells that are doing this. So, having done that, I never needed to take the pharmaceuticals and still haven’t to this day needed to take all those medicines that I was on daily before.
My oxygen saturation is, within a month or two, it improved to, where they measure usually 99 to 100 percent, which is really miraculous and been pain-free breathing, having the ability to start exercising again. The steroids had brought my weight up to 283 lbs. at its peak. I’ve lost 70 of that already. Still got a few to go to get back to where I used to be and want to be. But I did a couple of other experiments. A month after I got back from Panama, I took a trip out to Utah where I’d been squadron commander before. I love the mountains out there and decided I wanted to test myself up to 11000 feet elevation, and look at the oxygen saturation and see how I’m doing because I couldn’t tolerate that kind of altitude exposure before. So i went out, did that, took the gondola up to the peak of the mountain for a ski resort. It was actually snowing, so it was really beautiful and, And so I measured my wife’s who’s not gotten wind damage as kind of a baseline. She’s slightly younger than me. And then looked at my oxygen saturation and I was doing right on exactly either the same as her or maybe a percent better than her. We went down to 8000 feet, had lunch at a beautiful cafe in the snow and and again, took samples there. And I was actually better than her at 8,000 feet so the subjective and the objective data were convincing me along the way that, yeah this is working.
By May of this year, I had made another trip out to Utah and actually went Zion National Park to do some hiking because my hip and recovered so that I no longer needed the rollater, no walker assistance, could not need the cane anymore, and literally chose a moderate intensity hike that was up a mountain to about 8000 feet elevation just to see how my lungs responded and how well my body responded. And I was able to climb that. Now granted, I’m not in full shape like I used to be. So I did stop occasionally and just rest and stretch some. But I made it all the way up without any assistance and no problems and felt great at the top and then all the way down.
So, that really gave me a lot of a lot of confirmation that I’d made the right choice. Anyway, I’m concerned that there’s a lot of veterans like me who, you know, have had injuries either active duty or, you know, they’re suffering now as disabled veterans from combat-related injuries. And I would like to make sure that this word gets out and they can have some hope like I’ve had. For me, it’s been miraculous and I really appreciate Dr. Riordan and the Stem Cell Institute. That he came up with this and then it’s made all the difference for me.
Thank you for listening. Have a great day.
The other day after the second stem cells treatment, half way through the second stem cells treatment, in the morning, he woke up and told me, “It’s sunny.” He never said that before like that, only when he would be asked what the weather was like. So Alex has a very big vocabulary but only if he’s asked to name things. And since the first stem cell treatment, he’s made quite a few spontaneous comments. This is one of the things I notice. I’ve really seen a difference. Not everybody does but I’ve learned that for many years now, I’m very confident that a mother is the best judge and I’ve definitely seen lots of differences.
So, we’ll be back. We’ll be back soon.
Hi my name is Layla I am Valentino Roshi’s mom. He is 4 and a half years old and we have been to the Stem Cell Institute three times.
The first time we came over in November 2017 and at that point, he was diagnosed with the highest level of autism. He was nonverbal. He didn’t have eye contact. After the first treatment, we had a lot of eye contact, a lot of attention span, [and] his attention span increased. He would sit down through the whole classroom for 4 hours, and, you know, sit down still and pay attention
The second treatment we saw a lot of gains on the speech. So, like right now he’s saying “mama,” he’s saying “sister,” like he’s repeating words. When he goes to the bathroom he says, “water and soap.” So like a lot of those things like, you know I guess, we never thought we would hear. He says, “I love you,” and he kisses us. You know the gains are there.
I guess the third time we are expecting more fluid speech, but as of right now we are very happy with the improvements, and you know, it’s just giving us a lot of hope, hope that was lost at some point. You Know, that’s really it.
For more information about stem cell therapy for autism at the Stem Cell Institute in Panama, please visit: https://www.cellmedicine.com/stem-cell-therapy-for-autism/
