Neil Riordan, PA, PhD Presents at the 5th Annual Perinatal Stem Cell Society Congress in Salt Lake City, UT on Thursday, February 28th

Neil Riordan, PA, PhD presented “Results From Panama Clinical Trials Using Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells (HUCT-MSCs) for Multiple Sclerosis and Autism” at the 5th Annual Perinatal Stem Cell Society Congress in Salt Lake City, UT on Thursday, February 28th.

Image of Neil Riordan, PA, PhD

Neil Riordan, PA, PhD

SALT LAKE CITY (PRWEB) MARCH 01, 2019

Neil Riordan, PA, PhD presented “Results From Panama Clinical Trials Using Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells (HUCT-MSCs) for Multiple Sclerosis and Autism” at the 5th Annual Perinatal Stem Cell Society Congress in Salt Lake City, UT on Thursday, February 28t.

During his talk, Dr. Riordan discussed his recently published phase I/II clinical trial entitled, “Clinical feasibility of umbilical cord tissue-derived mesenchymal stem cells in the treatment of multiple sclerosis”.

“It was an honor to speak with my distinguished peers on the advances of stem cell therapy in perinatal medicine today,” Neil H. Riordan, PA, PhD

https://www.ncbi.nlm.nih.gov/pubmed/29523171

He also touched on his recently completed and soon-to-be-published phase 1/II clinical trial on autism, “Allogeneic Umbilical Cord Mesenchymal Stem Cell Therapy for Autism” (NCT02192749).

About Perinatal Stem Cell Society

In 2013, the International Perinatal Stem Cell Society, Inc. a non-profit (501(c)(3) organization was founded on the basic principle that stem cells from perinatal tissues contain enormous, untapped life potential to treat many diseases and disorders. Perinatal stem cell sources include: amnion, amniotic fluid, cord blood, cord tissue/wharton’s jelly, as well as placental blood and placental tissue. Perinatal stem cells are formed around the time of birth and are classified as adult stem cells but they really are more primitive then stem cells found in bone marrow or adipose tissue or other traditional sources of adult stem cells and as such, have greater therapeutic potential.

Learn more at http://www.perinatalstemcells.com

About Riordan Technologies

Riordan Technologies strives to improve the human condition through innovation in scientific research, regenerative medicine, and stem cell therapy. Riordan Technologies comprises companies founded by Neil Riordan, PA, PhD: Dallas-based Aidan Products, Signature Biologics, and Riordan Medical Institute, and Panama-based Stem Cell Institute and Medistem Panama.

Read Dr. Riordan’s Amazon #1 Best Seller: Stem Cell Therapy: A Rising Tide – How Stem Cells Are Disrupting Medicine and Transforming Lives

Learn more at at http://www.neilriordan.com

Stem Cell Therapy in Panama Featured on Fox 4 Sports in Dallas-Fort Worth

On Sunday, February 24th, Fox 4 Sports in Dallas-Fort Worth aired a feature story about one of our patients, Sam Harrell.  Sam is head football coach at Ennis High School in Texas.  Sam was forced to retired from coaching several years ago due to multiple sclerosis but is now back on the field after receiving stem cell therapy in Panama.

For information about stem cell therapy for MS in Panama, please visit: Stem Cell Therapy for Multiple Sclerosis

Multiple Sclerosis News Today: Stem Cell Institute MS Trial is #4 in Top 10 MS Stories of 2018

Image of Top 10 Banner

Congratulations to Dr. Riordan and everyone at Stem Cell Institute and Medistem Labs in Panama!

Multiple Sclerosis News Today published its Top 10 Multiple Sclerosis Stories of 2018 and named Stem Cell Institute’s MS clinical trial its #4 top MS story of 2018.

The name of the article that reached #4 is “Treatment with Umbilical Cord Stem Cells Safe with Sustained Benefits for MS, Trial Shows”

The original peer-reviewed article, entitled “Clinical feasibility of umbilical cord tissue-derived mesenchymal stem cells in the treatment of multiple sclerosis” is published in the Journal of Translational Medicine and can be viewed here:  https://translational-medicine.biomedcentral.com/articles/10.1186/s12967-018-1433-7

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.

Multiple Sclerosis News Today Covers Stem Cell Institute Clinical Trial for MS

Image of GMP syringe prep lab at Stem Cell Institute clinic in Panama.

Stem cells being prepared for treatment.

Multiple Sclerosis News Today has published an article entitled “Treatment with Umbilical Cord Stem Cells Safe with Sustained Benefits for MS, Trial Shows“. This article can be read in its entirely at MultipleSclerosisNewsToday.com.

The name of the study, which is published in the Journal of Translational Medicine, is “Clinical feasibility of umbilical cord tissue-derived mesenchymal stem cells in the treatment of multiple sclerosis”.

The study concluded that “…intravenous infusion of UCMSC over several days is safe in subjects with MS. Additionally, UCMSC infusions may hold benefits, since this small study group saw improvement in bladder, bowel, and sexual dysfunction, walking, upper extremity physical function, energy and fatigue, general perspective of a positive health change and improved quality of life, and MRI lesions. More clinical studies, particularly with a larger cohort, are needed to substantiate the specific benefits of UCMSC infusion as a potential MS therapy.”

Joe Rogan Interview with Mel Gibson and Dr. Riordan

Joe Rogan interviews Stem Cell Institute founder Neil Riordan, PA, PhD and award-winning actor, director and producer Mel Gibson, who first brought his father to Panama at the age of 92.  Mel discusses his father’s miraculous recovery.  He is now 99.  Dr. Riordan discusses stem cell therapy using human *umbilical cord-derived mesenchymal stem cells including their application in conditions like multiple sclerosis and autism.

*umbilical cords are donated following normal, healthy births

Stem Cell Treatments for Multiple Sclerosis

Image of Stem Cell Therapy Patient Marth Phillips

A Miracle for Martha
A woman’s journey of deliverance from pain

By Deanna Kirk Daily Sun Nov 26, 2017 (Link to original story)

The last 12 months have been a giant series of ups and downs, an extreme roller coaster for Martha Phillips.

Last December, her father-in-law battled brain cancer, which affected the lives of all of her close family; and her only brother died very suddenly from a pulmonary embolism. They were buried a week apart.

The battle with Multiple Sclerosis

Martha had been fighting her own battle against Multiple Sclerosis since a diagnosis in 2010. This disease causes the body’s immune system to attack its own tissues, and the malfunction destroys myelin, the fatty substance that coats and protects nerve fibers in the brain and spinal cord, according to the Mayo Clinic.

Phillips’ had seen her own ups and downs in that battle as well, with medications that caused huge weight gain, severe intolerance to heat, and intense bouts with pain. She tried many different protocols and medications, but what seemed to make the most difference was an extreme dietary change, which led to a loss of 72 pounds, acupuncture, adjustments, and regular massage therapy. Under the care of Dr. William “Doc” Davis in Ennis, she went from 10 prescriptions down to two, and did quite well for nearly six years.

But after the bout with all the stress during December 2016, Phillips discovered her body just could not cope with all the continuous stress demands placed upon it, and she suffered a pretty severe setback. She was forced to go on disability from her job.

“The Tysybri I was having infused regularly has a black box warning,” Phillips said. “I had to sign paperwork when I started taking it, that I knew it could kill me.”

The neurologist offered several other choices of medications, but all were either equally as risky with not as many good results, or more risky with even worse results.

“To me, it felt like my only choice was going backwards, and to me that was unacceptable,” she said.

Phillips learned about a somewhat-new innovative treatment for people with Multiple Sclerosis, and it was not being done in the United States yet, but for $25,000 one could fly to Panama City, Panama and have the complete treatment done and stay right in the same hotel where the treatments are done.

The blessings of how all her funding came together to have the treatment were chronicled in a story that ran in the July 8, 2017 edition of the Daily Sun.

But this story is about the trip itself, the treatment, and how her life has been since the trip to Panama.

Life since Panama, and new stem cells

It’s been roughly three months since Phillips returned from Panama. She took her little sister Robine Reeves with her, and the things she noticed right off were 1) the Atlanta airport is awful, and 2) Panama is a lot like Texas with regard to the weather.

“It’s very Americanized — they take American dollars, Spanish is their primary language but it’s OK if you don’t speak it,” Phillips said. “The people in Panama are so super friendly, even the kids. A group of junior high kids got on the bus with us and many of them spoke to us. That was the day Vice President Pence was there, and we, stupid Americans, didn’t know he was there, but his motorcade was very impressive.”

Phillips notice that the Panamanian president’s motorcade also came through that morning, and they watched it all from the rooftop of their hotel where the pool was. And some guy from London had to tell them their own Vice President was there.

“The clinic has a very impressive concierge,” she said. “Someone was there holding a sign with my name on it at the airport. She took us to the VIP lounge and whisked us through customs and the fingerprint deal very quickly and painlessly, and called our driver who works for the clinic. He took us to the hotel, and showed us shopping and restaurants along the way.

“They don’t have really good restaurants, they just look for consistency,” she said.

“The next day, I had a medical checkup and blood work. The second day, they gave me stem cells through an IV. I also had two subcutaneous injections in the groin/lymph region, which were more painful than the IV.”

Phillips also had physical therapy that day which consisted of evaluation, stretching exercises, balance and strength.

“The stems cells they use are umbilical cord stem cells, which women donate when they give birth,” she said. “Since they are brand new, they double every 24 hours. They’re a perfect source because they multiply so fast. I got 1.33 million stem cells.”

The way the stem cells work for MS and some other autoimmune diseases they’re using them for is that they reset the immune system, she said. They do not go in and repair the damage the MS has already done to her brain, but there is scientific evidence that shows if MS stops attacking the body, the body can heal the brain and spinal lesions.

“They believe that because there’s another virus that does the same kind of damage to your brain, but because it does not continue to attack the brain, people recover from it,” Phillips said.

There was another day of treatment just like the previous day, then the following day the sisters flew home. On the day of the blood work and checkup, the doctor discussed diet and supplements with Martha.

“He started describing a high fat, low carb diet, and I said, ‘Do you mean a keto diet?’ and he said ‘Yes,’” she said. “He said I would be throwing my $25,000 down the drain if I did NOT follow this diet and take supplements.”

Phillips had already followed this diet in the past, but wasn’t following it very strictly at the time.

Her supplement list looked something like this: 2000 mg per day of Magnesium; B vitamins; CoQ10; Stemkline; Probiotics; and a lot of it is supposed to be for energy as well as for brain health.

“When I went to Panama, I was taking 10 prescriptions,” she said. “I am taking one now, 90 days later.

“That all actually happened within the first two weeks.

“I feel amazing. I feel like I can conquer the world. I’ve had more energy than I’ve had the entire time I’ve had MS.”

Philips said when she made her trip to Panama, her thought was if she could get rid of enough of the pain and fatigue in order to return to work, she would be happy.

“But I got SO much more — I actually have no symptoms right now.”

She’s also no longer a slave to heat intolerance. Before, when she went to CrossFit, she had to wear a cooling vest full of ice packs and stand in front of a giant fan or A/C unit in order to work out. The least little bit of heat would cause her to become very, very sick.

“The first time I worked out after my transplant, Nick (Biles) came over to check on me, and I cried and said ‘I can’t remember the last time I worked out without heat intolerance,’” she said.

The heat intolerance makes the MS Symptoms you have temporarily worse until your body cools down. That can happen with one degree of change in body temperature, she said.

“It’s really weird to me now, to learn how to live without thinking about all those things,” Phillips said. “For so long, I’ve had to consider all sorts of eventualities in every scenario I find myself in.”

Dallas Morning News Features Stem Cell Institute Multiple Sclerosis Patient Judy Lecoq

Image of Stem Cell Therapy MS Patient Judy Lecoq

Judi Lecoq, 57, of Arlington, has been traveling to Panama once a year since 2010 for umbilical cord stem cell treatments to treat her multiple sclerosis — an option that’s not available in the U.S. Because the treatment is controversial and not FDA-approved, she must pay for the medical costs as well as travel. But Lecoq sees improvement with each treatment and says she’s doing much better than doctors originally predicted when she was diagnosed 20 years ago.

“When I come back, I feel a complete change in my energy level,” she says. “Before my last trip, it was hard to get anything done or to concentrate. My feet were numb; they’re not numb anymore.”

From – Ticket to Health: Do your homework before traveling for medical procedures

Read/download the entire chapter on stem cell therapy for multiple sclerosis from Dr. Riordan’s book

Image of Book Cover for Stem Cell Thearpy - Rising Tide

For more detailed information about our MS treatments, we welcome you to read/download the entire chapter on stem cell therapy for MS from Dr. Riordan’s new book, Stem Cell Therapy: A Rising Tide – How Stem Cells are Disrupting Medicine and Transforming Lives.  CLICK HERE (FREE PDF)

“Neil takes readers on a riveting journey through the past, present and future of stem cell therapy. His well-researched, educational and entertaining book could change your life. I highly recommend it.”Tony Robbins, NY Times #1 Bestselling Author

“100 years old will soon become the new 60. Stem cells are a key therapeutic to enable this future. Dr. Riordan’s book is your guide to why this is true and how you will benefit. A must read for anyone who cares about extending their healthy lifespan.”Peter H. Diamandis, MD; Founder, XPRIZE & Singularity University; Co-Founder, Human Longevity, Inc.; Author of NY Times Best Sellers Abundance and Bold

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.