Millie Jimenez gives an update on her twin boys’ (Angelo and Anthony) improvements since their first umbilical cord stem cell treatments at the Stem Cell Institute in Panama almost 3 years ago. “Now, it’s just been amazing. I’ve been able to get a job again and get my life back. They are easier to take care of. Their cognitive skills have improved as well as their speech, their gross motor and fine motor skill have also improved. And I’m just happy. I’m a happy camper.”
VIDEO – The Science of Mesenchymal Stem Cells and Regenerative Medicine – Arnold Caplan PhD (Part 6)
In part 6, Prof. Caplan discusses Trophic properties of mesenchymal stem cells; MSCs for heart disease; MSCs homing to heart injury site and also to skin incision site; MSCs limit left ventricular thinning following infarction; Trophic properties of MSCs: anti-apoptotic, anti-fibrotic, anti-scarring, angiogenic, mitotic; phase 1 data for allogeneic MSCs show fewer arrhythmias, prompt heart rate recovery, and improved lung function; autologous adipose tissue-derived stromal vascular fraction for treatment of chronic heart disease; Active mesenchymal stem cell clinical trials around the world; Induction therapy with autologous MSCs in kidney transplants; MSCs can coax neural stem cells to become oligodendrocytes, curing mice with MS using allogeneic human MSCs.
King Goff received three applications of his own adipose tissue-derived stem cells over the course of 3 days for a knee injury and autoimmune issues at the Stem Cell Institute in Panama. In this video, Mr. Goff discusses conventional treatments he received before stem cells, pre-treatment symptoms, post-treatment improvements, the doctors and staff, and the clinic.
“My immune system is the thing that is noticeably better. My allergies have corrected. The sinusitis circumstances that I was having problems with have corrected, in part but not completely. My knees, I’m up to being able to be on fairly distant walks of one and a half to two miles as part of my exercise program without the pain that I experienced prior to the [stem cell] treatment. Those are the most significant gains that I can say; just a lack of pain and increased mobility.” – King Goff
A short film about three spinal cord injury patients who share their stories of tragedy, hope and recovery following stem cell treatments for spinal cord injury at the Stem Cell Institute in Panama City, Panama. See them demonstrate their improvements by lifting themselves up, standing and even walking after stem cell therapy.
Spinal cord injury patient, Chris Niles, discusses his improvements after undergoing stem cell therapy at the the Stem Cell Institute in Panama City, Panama. Chris now has sensation down to about a T10 level and has regained movement in his feet.
Theo Kostoulas is a T-6 complete spinal cord injury patient. He received a course of 16 stem cell therapy injections using umbilical cord-derived stem cells and his own bone marrow-derived stem cells. The cells were injected both intravenously and intrathecally (into the spinal fluid). During his stay in Panama and as part of his treatment protocol, Theo went to 19 physical therapy sessions over the course of month.
“I can definitely say that after the second injection, I immediately actually started getting some leg sensation and touch back from below my injury level. It was me lying in bed while my mother was putting my sock on my feet. I was actually able to feel that and it was pretty amazing because I haven’t had and feeling or sensation at all from my injury level of T-6. Now, more towards the end here, I have actually been able to have bladder sensation. I am a person that usually cath’ed myself every four hours but now because I do have this sensation coming back, I tend to wait until I have the need to have to go. So it can be anywhere from six to seven hours. If I need to drink a lot of water before coming to treatment, I know ahead of time whether I need to cath myself sooner or not.”
Arminda Bourin has suffered from rheumatoid arthritis since 2003. She underwent adult stem cell therapy at the Stem Cell Institute in February 2012 because her swollen, painful ankles made it very difficult for her to walk. This interview takes place approximately one year after treatment.
Before coming to Panama, Ms. Bourin tried everything from anti-inflammatory and auto-immune medication to homeopathy and finally surgery on her left ankle, “Which I regret because if I had waited [until after the stem cell therapy], it would not have been necessary. The other foot with the same symptoms is now better without any surgery. I think it was the stem cells.”
Ms. Bourin learned about the Stem Cell Institute from her husband’s cousin, Judi Lecoq. Judy received treatment for multiple sclerosis and, “…told us how wonderful the treatment was and that she was so much better.”
Regarding the doctors, staff and clinic, “They are wonderful. Everybody has been so kind.”
Upon being asked, “Has this treatment changed your life?” Ms. Bourin responded, “Well, yes. I was not walking too much. I needed a wheelchair. It was painful anyway. So to be able to go shopping, that’s a miracle!”
Sarah Washington and her daughter Mary. Mary is 2 years old and was diagnosed with cerebral palsy when she was 4 months old. She was first treated at the Stem Cell Institute in Panama using human umbilical cord-derived stem cells. Mary received these stem cells intravenously over the course of 4 days. Her first treatment was in September of 2012. This interview was recorded in March 2013 at the clinic while she was there for a second round of treatments.
What kind of improvements have you noticed?
Overall, in general, what we noticed was, her upper body, she’s very stiff. She’s spastic in her legs and her arms and she has low tone in her trunk. In her upper body, we noticed a pretty significant improvement. Her range of motion, she couldn’t lift her arms over her before and now she can do that on both sides easily. And her hands, she was in tight little fists most of the time, whereas now if she is in a fist it’s very loose. But most of the time she kind of has her hands relaxed. That was a big improvement for us; small but significant for our family.
Her vision has improved, not necessarily distance but as far as like what I think as seeing details. So she would be able to tell the difference between you and me if we didn’t say anything. Whereas before, I don’t think she could do that. She would rely on smell and hearing more than her vision. Now she uses her vision a lot more. So that’s been an improvement that we’ve seen.
She is more involved in the world around her. [She] wants to be more involved in the world around her so that’s good. She has definitely, she doesn’t say, “mama, dada, ba, ba” yet but she definitely is making more vocalizations, making more sounds and trying to experiment with her voice, which is a positive thing.
She is trying different ways of communicating versus just screaming which is what she did before because that is all she knew how to do. And now, she is kind of fussing or sometimes she’ll just kind of like, yell and stop and wait for me to answer her instead of just going from “zero” to “scream”. So her communication has improved as well.
One thing that we were not expecting that we were pleased about is an improvement in her seizures. That wasn’t even something that we had even, I don’t know. I guess it just didn’t occur to us that maybe this would be helpful with that but before we came the first time in September she had been sick and we actually had to delay our trip twice because she had bronchialitis. She was just having a really hard time. And she was having a lot of seizures. We had to add a new seizure medicine to try to get them under control and she was having 6 or 7 short myotonic jerks every day. The first time we were here, by about Thursday, which was like day three of treatment, of stem cells we noticed that she hadn’t had a seizure that day. Whereas before, she was having 6 or 7 a day. And so, that was one thing. It was surprising but it was a nice surprise that those have improved since we’ve been here. She will still have breakthrough seizures every now and then when she’s sick, teething but she, we haven’t gone back to that, where she was having them on a regular basis. So that’s good. That’s been a good improvement.
Since we’ve been here this time, I haven’t really seen anything where I could say, “Oh, I think that’s the stem cells.” yet but I do know that last time it did take a couple of weeks for us to notice, you know, or to really pinpoint and say, “Yes, we think that is the stem cells. There’s no way she could have done that before.” So, and all of our therapists agree that her range of motion and her upper body for sure, and her vision would not have been the way they were without coming here.
In 2005, I was diagnosed with rheumatoid arthritis and started treatment right away. The traditional treatments did not seem to work. I changed from several treatments and the one that did was an experimental drug. It worked pretty good for about 4 or 5 months and then I fell back. That was about 2 years ago. Then we discontinued it. It really didn’t work. Then I started on Humira and it really didn’t seem to do much of anything. At that time, I could barely walk across street. I was in constant pain.
A year ago in August, I did the stem cells. After about 3 or 4 months, I started to notice a difference. I can’t say I am 100% but from what I was to what I am, I got my life back. I am basically pain free. I still have a little bit of, not necessarily pain but, discomfort in my toes occasionally and sometimes in various joints. It bounces around a little bit. But it’s nothing, nothing like it was before.
In the beginning, I couldn’t sleep for more than 10 minutes at a time and I had to sit in a chair to be able to sleep for those 10 or 15 minutes. It was very discouraging. In fact, I wanted to die. It was so intense that I didn’t want to go on that way. It was not life. And even with the traditional treatments that seemed to help somewhat but it was no relief.
And now with this – like I said – I have my life back. And I am not taking any poisons. I function, basically, normally. I am basically pain free compared to what it was.
They did a mini-liposuction, processed it and gave it to me intravenously. We extended the treatment over 3 or 4 weeks. Since I live here (Panama) it was a lot easier to do that instead of doing it continually which I believe is what they do for most people who live outside Panama. People who had not seen me in a while said that my face has changed and my look. I feel different. Of course, when you are living with pain, you’re awful tight and that’s changed. I just saw some people who I have not seen in a while last week. They remembered when they saw me last, I couldn’t walk. They said, “Wow! You are a new person now.” And I am.
Michael Foster – Rheumatoid Arthritis Patient