Our Story

JT

In 2020, I was a fairly hyper-healthy person who trained every year to ride competitively in long distance amateur bicycle races. I often drove and sometimes flew with my bike to events all over the country. I’d even had fellow cyclists blow smoke at me about maybe thinking about tuning up to compete in cycling in the Senior Olympics. In one
particular year, I’d ended third overall in my age group in the state of Missouri. Let’s give me the benefit of the doubt that I’d been racing more than two other guys…

Point being though, that I was way above average in fitness, suffered from no long term illnesses, and rarely even from minor day-to-day ones.

In January, 2021 , my wife Lyn and I came back to the US from a trip to Mexico and we both soon came down with the original Covid. It’d proved a relatively easy, modest and brief illness, though as I recovered she seemed to head straight into what would later
become known as “Long Haul” symptoms. We barely knew what that term was, and certainly, nor did doctors. Nobody knew at that time that the symptoms of Long Haul Covid would prove to be in most cases worse than the disease itself.

Dial forward a couple months and we were quickly approaching a planned return back to Mexico. However, with Lyn seemingly losing more ground everyday, and having very little of it left, we decided to go forward with the trip just to live our lives as comfortably
as possible. We fully recognized the great likelihood of her imminent passing. But then God or the universe or blind luck, whichever one cares to believe, intervened in a spectacular set of coincidences that are described in Lyn’s story. So while she began to undergo stem cell treatment and get back on her feet, I returned to the US in a few weeks. Warning, there will be a pattern arising here.

Before returning to the US, I was feeling fine and looked healthy and normal. There were no reasons to anticipate that my physical and mental health would soon decline precipitously.

Long Covid hit me in the same manner Hemingway described how he’d become bankrupt… “Gradually, then suddenly.”

While in the US, I began to not be as well as I had been. One day I was out and active and living a full and enjoyable life, and then next I could only gingerly walk downstairs in the morning to sit in a chair, and find myself drained by that tiny effort. So I’d fester all day staring at a TV screen and entirely oblivious and uncaring as to whether it was even
turned on.


My vital signs became erratic and quite worrisome. From the time I planted myself in a seat downstairs, my blood pressure would rise about 10 points every fifteen minutes or so. In short order it’d be climbing through 170/120 with the sky seemingly being the limit. I’d never had blood pressure problems before. So there I sat with a blood pressure cuff and a bottle of Lisinopril and a bottle of Clonodine, chasing the digits with the meds until my body finally succumbed to the chemicals. Then my BP would drop like a stone down to dangerous levels around 80/50’s, and I’d wonder how I was ever going to make my way back to bed.

During that time, unbeknownst to me, Covid was silently and quickly damaging my lungs. Before I knew it, and timeframe wise I mean within days of the proverbial Long
Covid greyhound bus hitting me, I could no longer walk twenty yards without succumbing to oxygen exhaustion. I’d done many ‘century rides’ at full gas in the heat of Texas summers and not gotten so blown-up physically as merely walking up and down our short driveway in my Covid body.

I hadn’t had the slightest idea of the extensive micro-clotting occurring throughout my body, and how my lungs were being permanently savaged. My brain became foggy. Depression set in, and at times my thoughts and words became aggressive, as if I were bipolar. I began to experience suicidal ideation. Fortunately for me, but in no way enjoyable to them, were family members who picked up that Dr. Jeff was descending
into a very dark Mr. Hyde.

How the tables had turned!

As my family helped me struggle through daily activities such as cleaning up and cooking and bringing me food, we quickly figured out that Lyn and I were in different emergencies.  
 
​Lyn, just a few short weeks earlier unable to walk or travel by herself, now knew she’d need to, and was actually once again able to, return unaided to the US.  Stem cells had done her a life-save, and now I needed salvation from whatever was hollowing me out. 
 
​Instead of me needing to help Lyn through the airport and carrying our bags, now she was helping me through DFW as I struggled with each st 

When we arrived back at the same Airbnb in Ajijic, our host Tony commented, “Well, this is quite a change in events,” pointing at Lyn, “You look healthy and he looks like he’s dying.”  I didn’t even have the breath to reply.​ 

Preparing for my first stem cell treatment, we had blood labs drawn.   The results gave my physician immediate concerned about a possible pulmonary embolism, and sent me for a chest X-ray.  
 
The X-ray found that I had pulmonary fibrosis. with Covid this is known as “glass lung” and considered incurable.  
 
The doctor demanded to see me right away, as my d-dimerwas hovering at emergency levels.  I was treated immediately with Aspirin and a blood thinner and told I’d likely be on them for a year.  During that time we’d do regular testing to ensure my blood thinned, or else I might suffer a stroke at any time.  Of course, flying on airplanes with thick blood was out of the question, so traveling anywhere except by car was out also of the question. 

Within days of my first treatment, brain fog began to lift, as well as the depression.   I was taken off the blood thinners, as my d-dimer numbers had returned to within normal range.  Pulmonary fibrosis would of course be permanent, and we could at least consider ourselves lucky that it hadn’t gotten so bad as to bring lung transplants into conversation.  Ah, silver linings. 

Recovery

After several weeks, I went back and had some new films shot, starring my right and leftlungs.Those x-rays, by the way, cost US$20 each, no insurance or appointmentneeded.You get the films handed to you within 20 minutes.And what do you know, they were clear as a bell and you-know-who no longer hadfreezer burn lungs!All the sudden I could get out again for long hikes and my onlyphysical barrier was being out of shape (…that part hasn’t improved so much; somedayI’ll get on that, I keep saying).

My stem cell journey, Part II

In December, 2021, I was in a motorcycle accident while on a business trip in the US, leaving me with head trauma and multiple fractures in both my left tibia/fibula and arm/wrist, with only soft tissues holding the bones together. I was taken to a large, prestigious hospital (that will not be shamed here, because I’m above that) in Dallas, only to be told I would be seen in the parking lot!  It was a serious enough situation that over the coming days I tiptoed quite close to the line of becoming a motorcycle fatality statistic.   Weeks later Baylor Scott & White emailed me to ask if I wanted to schedule to come in for followup treatment.  Bless their hearts because for all they should have known, they’d be emailing a dead man.  But let’s not dwell on the US healthcare systems and prestigious hospital systems, shall we? 
 
Once again, my wife was called to urgently rescue my sorry self!  As the ER grudgingly sloppily wrapped up some of my broken bones and left me to deal with other the unattended ones and dispatched me home — Lyn got her ‘go bag’ and headed to the airport for an overnight flight back to the US. 

I was dispatched from the hospital with much haste on their behalf with a pair of crutches.  Nevermind a broken left leg in barely an ace bandage.  Or a broken left arm entirely unsplinted.  Or the TBI which had knocked me out cold for minutes, or the injection of Morphine the hospital had given me without even asking if I was in pain or had allergies.   
 
​Two fraught steps later came the inevitable full-frontal faceplant getting in the house.  Which of course re-separated various broken bones in my leg, beat up all my soft tissues once again, and since this time I WASN’T wearing a helmet, produced a second TBI in about as many hours.  

As a long time wound care nurse, Lyn didn’t like the look of the tissue which was losing circulation and immediately called our physicians in Mexico to consult and an emergency plan was made to return for surgery and stem cells. She expected me to lose parts of my leg with an amputation if gangrene set in. She set about gathering appropriate necessary equipment for the trip including a wheelchair.  
 
My wife wheeled me in a wheelchair with leg elevated, semi-splinted fractured arm, crutches and other medical equipment through the airport without any physical issues after having recovered from Long Haul also. During the trip, I also went into shock on the airplane and a kind stewardess helped my wife stabilize me. 

We landed in Guadalajara after midnight, and were met and taken to a fantastic hospital, where I had surgery that evening. 
 
​We were told without that immediate intervention, I would have lost the leg as it had been improperly set by the harried doctor at Baylor.  

The surgery involved 13 people in total with three different surgeons working on different parts of me at the same time.  As I was being rolled into the ‘theatre’ I was asked if I wanted pictures of the procedure.  Well, HECK YES I did!  
 
After I’d been stitched up and rolled back to my room, ​I received a dose of 200 million stem cells.   
 
​I now have multiple screws and plates holding things in place, recovered without any further problems, and was able to quickly resume walking and never required physical therapy. ​​ 

Stem cells have saved us both in many ways.

First, they saved my wife’s life and saved me from having to let her go. They fully restored my brain and body from Long Covid.  And they allowed my body to heal after a devastating accident where in all likelihood, I would have lost a significant portion of my body, which would have changed my life drastically.  I no longer even think about a good or bad arm or leg, as there is no deficit in either. 

We made it our mission to help others. 

When stem cells saved my wife and she began to get better, she told me that we needed to help others, allowing them to find this same hope for recovery. 
 
​We decided to help as many people as possible and we put off our retirement to do just that. We have even invested our retirement into helping others.  

After recovering, we have still experience health incidents that one does in life.  Most frequently, additional bouts Covid that have arisen as we’ve both traveled and hosted people to help them through their illnesses.  What we know, is that we’ve got access to a powerful life substance that is not medicine but works better than any medicine.  So we can go forward doing what we do, without fear and without holding ourselves back.

Our clients become family.

Our stem cell journey doesn’t end here. Over the past few years, we have not only helped hundreds of clients but also provided education for others to find their own journey. We have helped locals who cannot afford this treatment to receive it at cost or even for free. We have also helped many members of our own families recover from Covid, Long Haul and other medical problems.  We continue to support the community we built with weekly calls and post-treatment support months after clients have returned home.